HuGE Literature Finder
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Records 1-100
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Role of Genetic Susceptibility in the Development of Bronchopulmonary Dysplasia.
The Journal of pediatrics 2018 Sep . Parad Richard B, Winston Abigail B, Kalish Leslie A, Gupta Munish, Thompson Ivana, Sheldon Yvonne, Morey Joann, Van Marter Linda |
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Gene variants of the phosphatidylcholine synthesis pathway do not contribute to RDS in the Chinese population.
World journal of pediatrics : WJP 2018 Feb . Chen Yu-Jun, Meyer Julia, Wambach Jennifer A, DePass Kelcey, Wegner Daniel J, Fan Xin, Zhang Qun-Yuan, Hillary Heins, Cole F Sessions, Hamvas Aar |
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Genetic association of single nucleotide polymorphisms of FZD4 and BDNF genes with retinopathy of prematurity.
Ophthalmic genetics 2018 Feb 1-6. Lasabova Zora, Stanclova Andrea, Grendar Marian, Mikolajcikova Silvia, Calkovska Andrea, Lenhartova Nina, Ziak Peter, Matasova Katarina, Caprnda Martin, Kruzliak Peter, Zibolen Mir |
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[The polymorphism of detoxification genes system genes in very preterm infants.]
Klinicheskaia laboratornaia diagnostika 2018 63 (10): 658-660. Mezhinskij S S, Shilova N A, Chasha T V, Fetisova I N, Kharlamova N V, Ratnikova S Yu, Fetisov N |
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Association of cytokine gene polymorphisms with bronchopulmonary dysplasia in Han Chinese newborns.
Pediatric pulmonology 2017 Nov . Chen Hui, Zheng W |
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Mutation spectrum of NDP, FZD4 and TSPAN12 genes in Indian patients with retinopathy of prematurity.
The British journal of ophthalmology 2017 Oct . Rathi Sonika, Jalali Subhadra, Musada Ganeswara Rao, Patnaik Satish, Balakrishnan Divya, Hussain Anjli, Kaur Inderje |
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Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene.
Scientific reports 2017 Aug 7 (1): 9271. Mahlman Mari, Karjalainen Minna K, Huusko Johanna M, Andersson Sture, Kari M Anneli, Tammela Outi K T, Sankilampi Ulla, Lehtonen Liisa, Marttila Riitta H, Bassler Dirk, Poets Christian F, Lacaze-Masmonteil Thierry, Danan Claude, Delacourt Christophe, Palotie Aarno, Muglia Louis J, Lavoie Pascal M, Hadchouel Alice, Rämet Mika, Hallman Mik |
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Association of SP-B gene 9306 A/G polymorphism (rs7316) and risk of RDS.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2017 Jul 1-13. Fatahi Neda, Niknafs Nikoo, Kalani Majid, Dalili Hosein, Shariat Mamak, Amini Elaheh, Esmaeilnia Shirvani Tahereh, Hardani Amir Kamal, Taheritafti Roya, Ghasemi-Fakhr Nasrin, Ghadami Mohsen, Tavakkoly-Bazzaz Javad, Rashidi-Nezhad Ramin, Nayeri Fatemeh, Rashidi-Nezhad A |
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Is the C242T polymorphism of the CYBA gene linked with oxidative stress-associated complications of prematurity?
Antioxidants & redox signaling 2017 Apr . Huizing Maurice J, Cavallaro Giacomo, Moonen Rob M, Gonzalez-Luis Gema E, Mosca Fabio, Vento Maximo, Villamor Eduar |
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GSTP1 and CYP2B6 Genetic Polymorphisms and the Risk of Bronchopulmonary Dysplasia in Preterm Neonates.
American journal of perinatology 2017 Jan . Zachaki Sophia, Daraki Aggeliki, Polycarpou Elena, Stavropoulou Chrysa, Manola Kalliopi N, Gavrili Stavrou |
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Association between Interleukin-10-1082 G/A and Tumor Necrosis Factor-? 308 G/A Gene Polymorphisms and Respiratory Distress Syndrome in Iranian Preterm Infants.
Mediators of inflammation 2017 2017 6386453. Khoshdel Abolfazl, Kheiri Soleiman, Omidvari Peyman, Moradi Fahimeh, Hamidi Majid, Teimori Hosse |
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Evaluation of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort.
Ophthalmic genetics 2016 Dec 37 (4): 415-418. Aydin Hatip, Gunay Murat, Celik Gokhan, Gunay Betul Onal, Aydin Umeyye Taka, Karaman A |
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Genetic Polymorphisms of SP-A, SP-B, and SP-D and Risk of Respiratory Distress Syndrome in Preterm Neonates.
Medical science monitor : international medical journal of experimental and clinical research 2016 Dec 22 5091-5100. Chang Hong-Yu, Li Fang, Li Feng-Sheng, Zheng Cheng-Zhong, Lei Yan-Zhe, Wang Ji |
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Association between the p.Thr1406Asn polymorphism of the carbamoyl-phosphate synthetase 1 gene and necrotizing enterocolitis: A prospective multicenter study.
Scientific reports 2016 Nov 6 36999. Moonen Rob M, Cavallaro Giacomo, Huizing Maurice J, González-Luis Gema E, Mosca Fabio, Villamor Eduar |
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Association of SP-C gene codon 186 polymorphism (rs1124) and risk of RDS.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2016 Nov 1-5. Fatahi Neda, Dalili Hosein, Kalani Majid, Niknafs Nikoo, Shariat Mamak, Tavakkoly-Bazzaz Javad, Amini Elaheh, Esmaeilnia Shirvani Tahereh, Hardani Amir Kamal, Taheritafti Roya, Ghasemi-Fakhr Nasrin, Ghadami Mohsen, Nayeri Fatemeh, Rashidi-Nezhad A |
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Evaluation of family history of permanent hearing loss in childhood as a risk indicator in universal screening.
Acta otorrinolaringologica espanola 2016 Oct . Valido Quintana Mercedes, Oviedo Santos Ángeles, Borkoski Barreiro Silvia, Santana Rodríguez Alfredo, Ramos Macías Áng |
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Functional and genetic predisposition to rhinovirus lower respiratory tract infections in prematurely born infants.
European journal of pediatrics 2016 Oct . Drysdale Simon B, Alcazar Mireia, Wilson Theresa, Smith Melvyn, Zuckerman Mark, Hodemaekers Hennie M, Janssen Riny, Bont Louis, Johnston Sebastian L, Greenough An |
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Early Erythropoietin Administration does not Increase the Risk of Retinopathy in Preterm Infants.
Pediatrics and neonatology 2016 Jun . Chou Hsin-Hsu, Chung Mei-Yung, Zhou Xiao-Guang, Lin Hung-Ch |
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Association of Rho-kinase Gene Polymorphisms with Respiratory Distress Syndrome in Preterm Neonates.
Pediatrics and neonatology 2016 May . Kaya Gül, Sivasli Ercan, Oztuzcu Serdar, Melekoglu Nuriye A, Ozkara Esma, Sarikabadayi Unal, Demiryürek Abdullah |
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Recurrent Copy Number Variants Associated with Bronchopulmonary Dysplasia.
Pediatric research 2016 Mar . Ahmad Ausaf, Bhattacharya Soumyaroop, Sridhar Arthi, Iqbal Anwar M, Mariani Thomas |
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COX-1 and COX-2 polymorphisms in susceptibility to cerebral palsy in very preterm infants.
Molecular neurobiology 2016 Jan . Kapitanovi? Vidak Helena, Catela Ivkovi? Tina, Vidak Zoran, Kapitanovi? San |
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Surfactant Protein A and B Gene Polymorphisms and Risk of Respiratory Distress Syndrome in Late-Preterm Neonates.
PloS one 2016 11 (11): e0166516. Tsitoura Maria-Eleni I, Stavrou Eleana F, Maraziotis Ioannis A, Sarafidis Kosmas, Athanassiadou Aglaia, Dimitriou Gabri |
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A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia.
Acta paediatrica (Oslo, Norway : 1992) 2015 Dec . Trittmann J K, Gastier-Foster J M, Zmuda E J, Frick J, Roger L K, Vieland V J, Chicoine L G, Nelin L |
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Association of C609T-Inborn Polymorphism of NAD(P)H: Quinone Oxidoreductase 1 with the Risk of Bronchopulmonary Dysplasia in Preterm Neonates.
American journal of perinatology 2015 Dec . Gavrili Stavroula, Zachaki Sophia, Daraki Aggeliki, Polycarpou Elena, Manola Kalliopi, Stavropoulou Chryssa, Sambani Constantina, Baroutis Geor |
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UGT1A1*28 Genotypes and Respiratory Disease in Very Preterm Infants: A Cohort Study.
Neonatology 2015 Dec 109 (2): 124-129. Petersen Jesper Padkær, Ebbesen Finn, Hollegaard Mads Vilhelm, Andersson Sofia, Hougaard David Michael, Thorlacius-Ussing Ole, Henriksen Tine Bri |
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Elucidating the role of genomics in neonatal sepsis.
Seminars in perinatology 2015 Oct . Srinivasan Lakshmi, Kirpalani Haresh, Cotten Charles Micha |
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Steroid Pathway Genes and Neonatal Respiratory Distress After Betamethasone Use in Anticipated Preterm Birth.
Reproductive sciences (Thousand Oaks, Calif.) 2015 Oct . Haas David M, Lai Dongbing, Sharma Sunita, Then Jenny, Kho Alvin, Flockhart David A, Tantisira Kelan, Foroud Tatia |
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The Haplotype TGGAG in the ABCA3 Gene Increases the Risk of Respiratory Distress Syndrome in Preterm Infants in Southern China.
Pediatrics and neonatology 2015 Oct . Tian Wenjun, Chen Xiuqi, Qin Huijuan, Wei Qiufen, Zhang Shuying, Tang Shangying, Liao Liangrong, Zhang Yanming, Chen Yuj |
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Association of vitamin D binding protein polymorphisms with bronchopulmonary dysplasia: a case-control study of gc globulin and bronchopulmonary dysplasia.
Journal of perinatology : official journal of the California Perinatal Association 2015 Sep 35 (9): 763-7. Serce Pehlevan O, Karatekin G, Koksal V, Benzer D, Gursoy T, Yavuz T, Ovali |
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Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia.
American journal of respiratory and critical care medicine 2015 Sep 192 (5): 589-96. Li Jingjing, Yu Kun-Hsing, Oehlert John, Jeliffe-Pawlowski Laura L, Gould Jeffrey B, Stevenson David K, Snyder Michael, Shaw Gary M, O'Brodovich Hugh |
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Polymorphisms of Vascular Endothelial Growth Factor and Retinopathy of Prematurity.
Journal of pediatric ophthalmology and strabismus 2015 Jul 52 (4): 245-53. Ali Aliaa A, Hussien Nouran F, Samy Rania M, Husseiny Khalid |
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Human Surfactant Proteins A2 (SP-A2) and B (SP-B) Genes as Determinants of Respiratory Distress Syndrome.
Indian pediatrics 2015 May 52 (5): 391-4. Abuelhamed Walaa A, Zeidan Nancy, Shahin Walaa A, Rizk Hoda I, Rabie Walaa |
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FUT 2 polymorphism and outcome in very-low-birth-weight infants.
Pediatric research 2015 Apr 77 (4): 586-90. Demmert Martin, Schaper Anne, Pagel Julia, Gebauer Corinna, Emeis Michael, Heitmann Friedhelm, Kribs Angela, Siegel Jens, Müller Dirk, Keller-Wackerbauer Annette, Gerleve Hubert, Wieg Christian, Herting Egbert, Göpel Wolfgang, Härtel Christo |
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Ophthalmic and molecular genetic findings in Kniest dysplasia.
Eye (London, England) 2015 Apr 29 (4): 475-82. Sergouniotis P I, Fincham G S, McNinch A M, Spickett C, Poulson A V, Richards A J, Snead M |
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Genetic Polymorphisms of Heme-oxygenase 1 (HO-1) may Impact on Acute Kidney Injury, Bronchopulmonary Dysplasia and Mortality in Premature Infants.
Pediatric research 2015 Mar . Askenazi David J, Halloran Brian, Patil Neha, Keeling Susan, Saeidi Behtash, Koralkar Rajesh, Ambalavanan Namasivay |
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Integrated genomic analyses in bronchopulmonary dysplasia.
The Journal of pediatrics 2015 Mar 166 (3): 531-7.e13. Ambalavanan Namasivayam, Cotten C Michael, Page Grier P, Carlo Waldemar A, Murray Jeffrey C, Bhattacharya Soumyaroop, Mariani Thomas J, Cuna Alain C, Faye-Petersen Ona M, Kelly David, Higgins Rosemary D, |
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Very low birthweight bronchopulmonary dysplasia survivors show no substantial association between lung function and current inflammatory markers.
Acta paediatrica (Oslo, Norway : 1992) 2015 Mar 104 (3): 264-8. Suursalmi Piia, Kopeli Tarja, Korhonen Päivi, Lehtimäki Lauri, Nieminen Riina, Luukkaala Tiina, Moilanen Eeva, Korppi Matti, Paassilta Marita, Tammela Ou |
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Correlation of ECR1 A3650G polymorphism with neonatal respiratory distress syndrome.
Genetic testing and molecular biomarkers 2015 Jan 19 (1): 18-23. Dai Ying, Wang Qi-Wei, He Shu, Zhang Zhao, Gao Ch |
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Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study.
Clinica chimica acta; international journal of clinical chemistry 2015 Jan . Carrera Paola, Di Resta Chiara, Volonteri Chiara, Castiglioni Emanuela, Bonfiglio Silvia, Lazarevic Dejan, Cittaro Davide, Stupka Elia, Ferrari Maurizio, Somaschini Marco, |
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Correlation of interactions between NOS3 polymorphisms and oxygen therapy with retinopathy of prematurity susceptibility.
International journal of clinical and experimental pathology 2015 8 (11): 15250-4. Yu Chunhong, Yi Jinglin, Yin Xiaolong, Deng Yan, Liao Yujun, Li Xiaobi |
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Investigation of TNF-alpha gene (G308A) and GSTP1 gene (Ilel05Val) polymorphisms in Turkish patients with retinopathy of prematurity.
Turkish journal of medical sciences 2015 45 (1): 164-9. Türe Mehmet, Yildiz Meral, Karkucak Mutlu, Gülten Emine Tuna, Si?irli Deniz, Özmen Ahmet Tuncer, Yakut Tahs |
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Surfactant protein B gene polymorphisms is associated with risk of bronchopulmonary dysplasia in Chinese Han population.
International journal of clinical and experimental pathology 2015 8 (3): 2971-8. Zhang Sheng, Zhang Xiaoying, Li Qiuping, Kong Xiangyong, Zhang Yupei, Wei Xiujuan, Song Jie, Feng Zhich |
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Arginase I gene single-nucleotide polymorphism is associated with decreased risk of pulmonary hypertension in bronchopulmonary dysplasia.
Acta paediatrica (Oslo, Norway : 1992) 2014 Oct 103 (10): e439-43. Trittmann J K, Nelin L D, Zmuda E J, Gastier-Foster J M, Chen B, Backes C H, Frick J, Vaynshtok P, Vieland V J, Klebanoff M |
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Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants.
Investigative ophthalmology & visual science 2014 Oct 55 (10): 6194-203. Hartnett M Elizabeth, Morrison Margaux A, Smith Silvia, Yanovitch Tammy L, Young Terri L, Colaizy Tarah, Momany Allison, Dagle John, Carlo Waldemar A, Clark Erin A S, Page Grier, Murray Jeff, DeAngelis Margaret M, Cotten C Michael, |
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Surfactant protein-D-encoding gene variant polymorphisms are linked to respiratory outcome in premature infants.
The Journal of pediatrics 2014 Oct 165 (4): 683-9. Sorensen Grith Lykke, Dahl Marianne, Tan Qihua, Bendixen Christian, Holmskov Uffe, Husby Steff |
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Association of vitamin D receptor gene polymorphisms and bronchopulmonary dysplasia.
Pediatric research 2014 Aug 76 (2): 171-6. Koroglu Ozge Altun, Onay Huseyin, Cakmak Bilin, Bilgin Betul, Yalaz Mehmet, Tunc Seckin, Ozkinay Ferda, Kultursay Nilg |
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Common genetic variants and risk of brain injury after preterm birth.
Pediatrics 2014 Jun 133 (6): e1655-63. Boardman James P, Walley Andrew, Ball Gareth, Takousis Petros, Krishnan Michelle L, Hughes-Carre Laurelle, Aljabar Paul, Serag Ahmed, King Caroline, Merchant Nazakat, Srinivasan Latha, Froguel Philippe, Hajnal Jo, Rueckert Daniel, Counsell Serena, Edwards A Dav |
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Genotype-phenotype correlations for infants and children with ABCA3 deficiency.
American journal of respiratory and critical care medicine 2014 Jun 189 (12): 1538-43. Wambach Jennifer A, Casey Alicia M, Fishman Martha P, Wegner Daniel J, Wert Susan E, Cole F Sessions, Hamvas Aaron, Nogee Lawrence |
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Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.
The Journal of pediatrics 2014 Jun 164 (6): 1316-21.e3. Wambach Jennifer A, Wegner Daniel J, Heins Hillary B, Druley Todd E, Mitra Robi D, Hamvas Aaron, Cole F Sessio |
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Relationship between angiotensin-converting enzyme gene polymorphism and respiratory distress syndrome in premature neonates.
The clinical respiratory journal 2014 May . Hussein Nouran Fahmy, Abdel Ghany Eman Abdel Ghany, Abu Elhamed Walaa Alsharany, Samy Rania Moham |
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[Clinical analysis of heterozygous ABCA3 mutations in children].
Zhonghua er ke za zhi. Chinese journal of pediatrics 2014 Apr 52 (4): 244-7. Xu Xiujuan, Liu Enmei, Luo Zhengxiu, Luo Jian, Fu Zh |
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GSTM1 and GSTT1 gene polymorphisms as major risk factors for bronchopulmonary dysplasia in a Chinese Han population.
Gene 2014 Jan 533 (1): 48-51. Wang Xijuan, Li Wenbin, Liu Wei, Cai Baohuan, Cheng Tingting, Gao Chunfang, Mo Luxia, Yang Hui, Chang Liw |
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A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia.
BMC medical genetics 2014 15 120. Huusko Johanna M, Karjalainen Minna K, Mahlman Mari, Haataja Ritva, Kari M Anneli, Andersson Sture, Toldi Gergely, Tammela Outi, Rämet Mika, Lavoie Pascal M, Hallman Mikko, |
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Analysis of nitric oxide synthase gene polymorphisms in neonatal respiratory distress syndrome among the Chinese Han population.
Italian journal of pediatrics 2014 40 (1): 27. Shen Wei, Du Jiang, Wang Bin, Zeng Qi |
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Association of a vascular endothelial growth factor polymorphism with the development of bronchopulmonary dysplasia in Japanese premature newborns.
Scientific reports 2014 4 4459. Fujioka Kazumichi, Shibata Akio, Yokota Tomoyuki, Koda Tsubasa, Nagasaka Miwako, Yagi Mariko, Takeshima Yasuhiro, Yamada Hideto, Iijima Kazumoto, Morioka Ichi |
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Gentamicin, genetic variation and deafness in preterm children.
BMC pediatrics 2014 14 (1): 66. Bitner-Glindzicz Maria, Rahman Shamima, Chant Kathy, Marlow Ne |
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Toll-like receptor genetic variants are associated with Gram-negative infections in VLBW infants.
Journal of perinatology : official journal of the California Perinatal Association 2013 Oct 33 (10): 772-7. Sampath V, Mulrooney N P, Garland J S, He J, Patel A L, Cohen J D, Simpson P M, Hines R |
A genome-wide association study (GWAS) for bronchopulmonary dysplasia.
Pediatrics 2013 Aug 132 (2): 290-7. Wang Hui, St Julien Krystal R, Stevenson David K, Hoffmann Thomas J, Witte John S, Lazzeroni Laura C, Krasnow Mark A, Quaintance Cecele C, Oehlert John W, Jelliffe-Pawlowski Laura L, Gould Jeffrey B, Shaw Gary M, O'Brodovich Hugh |
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Single nucleotide polymorphism in toll-like receptor 6 is associated with a decreased risk for ureaplasma respiratory tract colonization and bronchopulmonary dysplasia in preterm infants.
The Pediatric infectious disease journal 2013 Aug 32 (8): 898-904. Winters Alexandra H, Levan Tricia D, Vogel Stefanie N, Chesko Kirsty L, Pollin Toni I, Viscardi Rose |
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Genetic polymorphisms of vascular endothelial growth factor and risk for retinopathy of prematurity in South of Iran.
Molecular biology reports 2013 Jul 40 (7): 4613-8. Kalmeh Zahra Asadi, Azarpira Negar, Mosallaei Mahnaz, Hosseini Hamid, Malekpour Zah |
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The macrophage migration inhibitory factor -173G/C polymorphism is not significantly associated with necrotizing enterocolitis in preterm infants.
Journal of pediatric surgery 2013 Jul 48 (7): 1499-502. Prencipe Giusi, Auriti Cinzia, Inglese Rita, Gallusi Giulia, Dotta Andrea, De Benedetti Fabriz |
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Association of surfactant protein B gene polymorphisms (C/A-18, C/T1580, intron 4 and A/G9306) and haplotypes with bronchopulmonary dysplasia in chinese han population.
Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban 2013 Jun 33 (3): 323-8. Cai Bao-huan, Chang Li-wen, Li Wen-bin, Liu Wei, Wang Xi-juan, Mo Lu-xia, Zhao Ling-xia, Xu Hong-tao, Yang H |
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Functional Genetic Variation in NFKBIA and Susceptibility to Childhood Asthma, Bronchiolitis, and Bronchopulmonary Dysplasia.
Journal of immunology (Baltimore, Md. : 1950) 2013 Apr 190 (8): 8. Ali S, Hirschfeld AF, Mayer ML, Fortuno ES, Corbett N, Kaplan M, Wang S, Schneiderman J, Fjell CD, Yan J, Akhabir L, Aminuddin F, Marr N, Lacaze-Masmonteil T, Hegele RG, Becker A, Chan-Yeung M, Hancock RE, Kollmann TR, Daley D, Sandford AJ, Lavoie PM, Turvey SE |
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Associations of VEGF/VEGF-receptor and HGF/c-Met promoter polymorphisms with progression/regression of retinopathy of prematurity.
Current eye research 2013 Jan 38 (1): 137-42. Kaya Mahmut, Çokakli Murat, Berk Ayse Tulin, Yaman Aylin, Yesilirmak Didem, Kumral Abdullah, Atabey Ne |
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Endothelial NOS gene Glu298Asp polymorphism in preterm neonates with respiratory Distress syndrome.
Pediatric pulmonology 2013 Jan . Demirçubuk AG, Co?kun MY, Demiryürek S, Dokuyucu R, Oztuzcu S, Tavilo?lu ZS, Arslan A, Sivasl? E |
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The impact of glucocorticoid polymorphisms on markers of neonatal respiratory disease following antenatal betamethasone administration.
American journal of obstetrics and gynecology 2013 Jan . Haas DM, Dantzer J, Lehmann AS, Philips S, Skaar TC, McCormick CL, Hebbring SJ, Jung J, Li L |
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TNF-238 polymorphism may predict bronchopulmonary dysplasia among preterm infants in the Egyptian population.
Pediatric pulmonology 2013 Jan . Elhawary NA, Tayeb MT, Abdel-Ghafar S, Rashad M, Alkhotani AA |
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Association of a FGFR-4 gene polymorphism with bronchopulmonary dysplasia and neonatal respiratory distress.
Disease markers 2013 35 (6): 633-40. Rezvani Milad, Wilde Juliane, Vitt Patricia, Mailaparambil Beena, Grychtol Ruth, Krueger Marcus, Heinzmann Andr |
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Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity.
Molecular vision 2013 19 476-85. Kondo Hiroyuki, Kusaka Shunji, Yoshinaga Aki, Uchio Eiichi, Tawara Akihiko, Tahira Tomo |
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Surfactant protein B deficiency and gene mutations for neonatal respiratory distress syndrome in China Han ethnic population.
International journal of clinical and experimental pathology 2013 6 (2): 267-72. Yin Xiaojuan, Meng Fanping, Wang Yan, Xie Lu, Kong Xiangyong, Feng Zhich |
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Association between bronchopulmonary dysplasia and MBL2 and IL1-RN polymorphisms.
Pediatrics international : official journal of the Japan Pediatric Society 2012 Dec 54 (6): 863-8. Cakmak Bilin Cetinkaya, Calkavur Sebnem, Ozkinay Ferda, Koroglu Ozge Altun, Onay Huseyin, Itirli Gulcin, Karaca Emin, Yalaz Mehmet, Akisu Mete, Kultursay Nilg |
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[Pulmonary surfactant associated gene variants in mixed ethnic population of Han and Zhuang].
Zhonghua er ke za zhi. Chinese journal of pediatrics 2012 Nov 50 (11): 843-6. Chen Yu-jun, Chen Shao-ke, DePass Kelcey, Wegner Daniel J, Hamvas Aaron, Nong Guang-min, Wang Ya-zhou, Fan Xin, Luo Jing- |
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Association of VEGF gene polymorphisms with advanced retinopathy of prematurity: a meta-analysis.
Molecular biology reports 2012 Oct . Liu P, Wu D, Zhou W, Li Y, Lian C, Yang Y, Feng Z |
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Surfactant Protein A Associated with Respiratory Distress Syndrome in Korean Preterm Infants: Evidence of Ethnic Difference.
Neonatology 2012 Oct 103 (1): 1. Jo HS, Cho SI, Chang YH, Kim BI, Choi JH |
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Association of polymorphisms in neuroprotection and oxidative stress genes and neurodevelopmental outcomes after preterm birth.
Obstetrics and gynecology 2012 Sep 120 (3): 542-50. Costantine Maged M, Clark Erin A S, Lai Yinglei, Rouse Dwight J, Spong Catherine Y, Mercer Brian M, Sorokin Yoram, Thorp John M, Ramin Susan M, Malone Fergal D, Carpenter Marshall, Miodovnik Menachem, O'Sullivan Mary J, Peaceman Alan M, Caritis Steve |
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Polymorphism of the angiotensin-converting enzyme gene and angiotensin-converting enzyme activity in transient tachypnea of neonate and respiratory distress syndrome.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2012 Sep 25 (9): 1712-5. Satar Mehmet, Ta?k?n Erdal, Özlü Ferda, Tuli Abdullah, Özcan Kenan, Y?ld?zda? Hacer |
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Interleukin-6 polymorphism and bronchopulmonary dysplasia risk in very low-birthweight infants.
Pediatrics international : official journal of the Japan Pediatric Society 2012 Aug 54 (4): 471-5. Usuda Touhei, Kobayashi Takehiro, Sakakibara Seiichi, Kobayashi Akira, Kaneko Takayuki, Wada Masaki, Onozuka Junya, Numata Osamu, Torigoe Katsumi, Yamazaki Hajime, Sato Takashi, Nagayama Yoshihisa, Uchiyama Mako |
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Genetic basis of apnoea of prematurity and caffeine treatment response: role of adenosine receptor polymorphisms: genetic basis of apnoea of prematurity.
Acta paediatrica (Oslo, Norway : 1992) 2012 Jul 101 (7): e299-303. Kumral Abdullah, Tuzun Funda, Yesilirmak Didem Cemile, Duman Nuray, Ozkan Has |
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A TLR5 (g.1174C?>?T) variant that encodes a stop codon (R392X) is associated with bronchopulmonary dysplasia.
Pediatric pulmonology 2012 May 47 (5): 460-8. Sampath Venkatesh, Garland Jeffery S, Le Min, Patel Aloka L, Konduri Girija G, Cohen Jonathan D, Simpson Pippa M, Hines Ronald |
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Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates.
Journal of perinatology : official journal of the California Perinatal Association 2012 May 32 (5): 349-55. Ryckman K K, Dagle J M, Kelsey K, Momany A M, Murray J |
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Polymorphism analysis of the ABCA3 gene: association with neonatal respiratory distress syndrome in preterm infants.
Chinese medical journal 2012 May 125 (9): 1594-8. Jiang Lin, Wu Yi-Dong, Xu Xue-Feng, DU Li-Zho |
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The impact of drug metabolizing enzyme polymorphisms on outcomes after antenatal corticosteroid use.
American journal of obstetrics and gynecology 2012 May 206 (5): 447.e17-24. Haas David M, Lehmann Amalia S, Skaar Todd, Philips Santosh, McCormick Catherine L, Beagle Kyle, Hebbring Scott J, Dantzer Jessica, Li Lang, Jung Jees |
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ATP-binding cassette member A3 (E292V) gene mutation and pulmonary morbidity in very-low-birth-weight infants.
Acta paediatrica (Oslo, Norway : 1992) 2012 Apr 101 (4): 380-3. Härtel Christoph, Felderhoff-Müser Ursula, Gebauer Corinna, Hoehn Thomas, Kribs Angela, Laux Reinhard, Möller Jens, Segerer Hugo, Teig Norbert, von der Wense Axel, Wieg Christian, Stichtenoth Guido, Herting Egbert, Göpel Wolfgang, |
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Serum mannose-binding lectin (MBL) gene polymorphism and low MBL levels are associated with neonatal sepsis and pneumonia.
Journal of perinatology : official journal of the California Perinatal Association 2012 Mar 32 (3): 210-7. Özkan H, Köksal N, Çetinkaya M, Kiliç ?, Çelebi S, Oral B, Budak |
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[Relationship between pulmonary surfactant-associated protein B polymorphisms and the susceptibility to neonatal respiratory distress syndrome].
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2012 Jan 14 (1): 1. Lu WC, Xiang W, Wu M, Zheng X, Lin J, Chen XY, Wei HB, Zhan D, Li CL |
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A study of collectin genes in spontaneous preterm birth reveals an association with a common surfactant protein D gene polymorphism.
Pediatric research 2012 Jan 71 (1): 1. Karjalainen MK, Huusko JM, Tuohimaa A, Luukkonen A, Haataja R, Hallman M |
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Genetic variations in fetal and maternal tumor necrosis factor-? and interleukin 10: is there an association with preterm birth or periventricular leucomalacia?
Journal of perinatology : official journal of the California Perinatal Association 2012 Jan 32 (1): 27-32. Nuk M, Orendi K, Rosenberger S, Griesbacher A, Holzapfel-Bauer M, Resch B, Lang U, Pertl |
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IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants.
Pediatric research 2012 Jan 71 (1): 1. Floros J, Londono D, Gordon D, Silveyra P, Diangelo SL, Viscardi RM, Worthen GS, Shenberger J, Wang G, Lin Z, Thomas NJ |
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Influence of common non-synonymous Toll-like receptor 4 polymorphisms on bronchopulmonary dysplasia and prematurity in human infants.
PloS one 2012 7 (2): e31351. Lavoie Pascal M, Ladd Mihoko, Hirschfeld Aaron F, Huusko Johanna, Mahlman Mari, Speert David P, Hallman Mikko, Lacaze-Masmonteil Thierry, Turvey Stuart |
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ACE gene polymorphism in premature neonates with respiratory distress syndrome.
Genetic testing and molecular biomarkers 2011 Dec 15 (12): 867-70. Yimenicioglu Sevgi, Oztuzcu Serdar, Sivasli Ercan, Igci Mehri, Igci Yusuf Ziya, Demiryürek Seniz, Ozkara Esma, Gogebakan Bulent, Arslan Ahmet, Coskun Mehmet Yav |
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Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia.
American journal of respiratory and critical care medicine 2011 Nov 184 (10): 1164-70. Hadchouel Alice, Durrmeyer Xavier, Bouzigon Emmanuelle, Incitti Roberto, Huusko Johanna, Jarreau Pierre-Henri, Lenclen Richard, Demenais Florence, Franco-Montoya Marie-Laure, Layouni Inès, Patkai Juliana, Bourbon Jacques, Hallman Mikko, Danan Claude, Delacourt Christop |
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Mannose-binding lectin codon 54 gene polymorphism in relation to risk of nosocomial invasive fungal infection in preterm neonates in the neonatal intensive care unit.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2011 Sep 24 (9): 1124-7. Aydemir Cumhur, Onay Huseyin, Oguz Serife Suna, Ozdemir Taha Resid, Erdeve Omer, Ozkinay Ferda, Dilmen Ug |
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Plasminogen activator inhibitor I 4G/5G polymorphism in neonatal respiratory distress syndrome.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2011 Aug 17 (4): 352-7. Armangil Didem, Yurdakök Murat, Okur Hamza, Gürgey Aytem |
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Polymorphisms of interleukin 18 in the genetics of preterm birth and bronchopulmonary dysplasia.
Archives of disease in childhood. Fetal and neonatal edition 2011 Jul 96 (4): F299-300. Krueger M, Heinzmann A, Mailaparambil B, Härtel C, Göpel |
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Genetic variation of vascular endothelial growth factor pathway does not correlate with the severity of retinopathy of prematurity.
Journal of perinatology : official journal of the California Perinatal Association 2011 Apr 31 (4): 246-50. Kusuda T, Hikino S, Ohga S, Kinjo T, Ochiai M, Takahata Y, Tokunaga S, Ihara K, Hata Y, Hara |
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A polymorphism in the macrophage migration inhibitory factor promoter is associated with bronchopulmonary dysplasia.
Pediatric research 2011 Feb 69 (2): 142-7. Prencipe Giusi, Auriti Cinzia, Inglese Rita, Devito Rita, Ronchetti Maria Paola, Seganti Giulio, Ravà Lucilla, Orzalesi Marcello, De Benedetti Fabriz |
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Surfactant protein B gene polymorphism in preterm babies with respiratory distress syndrome.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2011 Jan 44 (1): 66-72. Lyra P P R, Diniz E M A, Abe-Sandes K, Angelo A L D, Machado T M B, Cardeal |
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HLA and bronchopulmonary dysplasia susceptibility: a pilot study.
Disease markers 2011 31 (4): 199-203. Rocha Gustavo, Proença Elisa, Areias Augusta, Freitas Fátima, Lima Bruno, Rodrigues Teresa, Alves Helena, Guimarães Hercíl |
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Endothelial nitric oxide synthase genotypes in the etiology of retinopathy of prematurity in premature infants.
Ophthalmic genetics 2010 Dec 31 (4): 173-7. Yanamandra Krishna, Napper Dawn, Pramanik Arun, Bocchini Joseph A, Dhanireddy Ramasubbared |
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Role of mannose-binding lectin in nosocomial sepsis in critically ill neonates.
Human immunology 2010 Nov 71 (11): 1084-8. Auriti Cinzia, Prencipe Giusi, Inglese Rita, Azzari Chiara, Ronchetti Maria Paola, Tozzi Alberto, Seganti Giulio, Orzalesi Marcello, De Benedetti Fabriz |
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- Page last updated:Jul 11, 2019
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