Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
Records 1 - 30 (of 138 Records) |
Query Trace: Hemolytic Anemia[original query] |
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Novel variant in glycophorin c gene protects against ribavirin-induced anemia during chronic hepatitis C treatment.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2021 Sep 143 112195. Lin Jennifer J, Loucks Catrina M, Trueman Jessica N, Drögemöller Britt I, Wright Galen E B, Yoshida Eric M, Ford Jo-Ann, Lee Samuel S, Kim Richard B, Al-Judaibi Bandar, Schwarz Ute I, Ramji Alnoor, Tam Edward, Ross Colin J, Carleton Bruce |
Putative pathogen-selected polymorphisms in the PKLR gene are associated with mycobacterial susceptibility in Brazilian and African populations. PLoS neglected tropical diseases 2021 8 15 (8): e0009434. Bezerra Ohanna Cavalcanti de Lima, Alvarado-Arnez Lucia Elena, Mabunda Nédio, Salomé Graça, de Sousa Amina, Kehdy Fernanda de Souza Gomes, Sales-Marques Carolinne, Manta Fernanda Saloum de Neves, Andrade Rafaela Mota, Ferreira Laís Pereira, Leal-Calvo Thyago, Cardoso Cynthia Chester, Nunes Kelly, Gouveia Mateus H, Mbulaiteve Sam M, Yeboah Edward D, Hsing Ann, Latini Ana Carla Pereira, Leturiondo André Luiz, Rodrigues Fabíola da Costa, Noronha Ariani Batista, Ferreira Cynthia de Oliveira, Talhari Carolina, Rêgo Jamile Leão, Castellucci Léa Cristina de Carvalho, Tarazona-Santos Eduardo, Carvalho Elizeu Fagundes de, Meyer Diogo, Pinheiro Roberta Olmo, Jani Ilesh V, Pacheco Antonio Guilherme, Moraes Milton Ozór |
Hyperhomocysteinemia-related lung disease and hemolytic anemia with bone marrow features masquerading as myelodysplasia. American journal of blood research 2021 7 11 (3): 266-270. Yamanishi Masayoshi, Tamura Atsushi, Miyoshi Takashi, Imashuku Shinsa |
Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report. World journal of clinical cases 2021 7 9 (19): 5245-5251. Wang Jun-Fang, Ma Li, Gong Xiao-Hui, Cai Cheng, Sun Jing-Ji |
Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X-linked Thrombocytopenia-A single center study. Immunological investigations 2021 6 51 (5): 1272-1283. Bildik Hacer Neslihan, Cagdas Deniz, Ozturk Kura Aysenur, Oskay Halacli Sevil, Sanal Ozden, Tezcan Ilh |
Multiple-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
The Journal of clinical investigation 2021 May . Page Grier P, Kanias Tamir, Guo Yuelong J, Lanteri Marion C, Zhang Xu, Mast Alan E, Cable Ritchard G, Spencer Bryan R, Kiss Joseph E, Fang Fang, Endres-Dighe Stacy M, Brambilla Donald, Nouraie Mehdi, Gordeuk Victor R, Kleinman Steve, Busch Michael P, Gladwin Mark T, |
The protective effect of the spleen in sickle cell patients. A comparative study between patients with asplenia/hyposplenism and hypersplenism. Frontiers in physiology 2022 9 13 796837. Peretz Sari, Livshits Leonid, Pretorius Etheresia, Makhro Asya, Bogdanova Anna, Gassmann Max, Koren Ariel, Levin Cari |
Genetic modulation of anemia severity, hemolysis level, and hospitalization rate in Angolan children with Sickle Cell Anemia. Molecular biology reports 2022 Sep . Germano Isabel, Santos Brígida, Delgadinho Mariana, Ginete Catarina, Lopes Pedro, Arez Ana Paula, Brito Miguel, Faustino Pau |
Functional characterization of the p.(Gln195His) or Tainan and novel p.(Ser184Cys) or Toluca glucose-6-phosphate dehydrogenase (G6PD) gene natural variants identified through Mexican newborn screening for glucose-6-phosphate dehydrogenase deficiency. Clinical biochemistry 2022 9 109-110 64-73. Alcántara-Ortigoza Miguel A, Hernández-Ochoa Beatriz, González-Del Angel Ariadna, Ibarra-González Isabel, Belmont-Martínez Leticia, Gómez-Manzo Saúl, Vela-Amieva Marce |
A case of G6PD Utrecht associated with ?-thalassemia responding to splenectomy. Pediatric blood & cancer 2022 6 69 (9): e29837. Yang Kun, Liu Xiaodong, Chen Kai, Luo Shan, Kong Wenqiang, Huang Wenying, Xiao Ji |
Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis. Genetic testing and molecular biomarkers 2022 5 26 (5): 270-276. Herrera-Tirado Isis Mariela, Espinoza-Mata Laura Lucia, Rizo-delaTorre Lourdes Del Carmen, Becerra-Solano Luis Eduardo, Ibarra-Cortés Bertha, Perea-Díaz Francisco Javi |
Diagnosis and Treatment of a Patient With Severe Combined Immunodeficiency Due to a Novel Homozygous Mutation in the IL-7R? Chain. Frontiers in immunology 2022 4 13 867837. Mansour Rana, Bsat Yasmin El, Fadel Anthony, El-Orfali Youmna, Noun Dolly, Tarek Nidale, Kabbara Nabil, Abboud Miguel, Massaad Michel |
STEREOTYPED CASES IN UKRAINIAN COHORT OF CHRONIC LYMPHOCYTIC LEUKEMIA PATIENTS DEPENDING ON THE IONIZING RADIATION EXPOSURE. Problemy radiatsiinoi medytsyny ta radiobiolohii 2022 12 27 307-323. Bilous N I, Abramenko I V, Chumak A A, Dyagil I S, Martina Z |
Glucose-6-phosphate Dehydrogenase (G6PD) A-Variant Frequency and Novel Polymorphism in Haiti. The American journal of tropical medicine and hygiene 2022 10 107 (5): 1142-1144. Vincent Jeanne P, Existe Alexandre V, Komaki-Yasuda Kanako, Boncy Jacques, Kano Shigeyu |
Molecular Detection of Hemoglobin O-Arab in the Sudanese Population. International journal of general medicine 2023 8 16 3323-3330. Izzeldin Elbashir, Tagwa Yousif Elsayed Yous |
Detection of Transversions and Transitions in HBG2 Cis-Elements Associated with Sickle Cell Allele in Ghanaians. Biochemical genetics 2023 7 . G K Ababio, I Ekem, J Acquaye, S Y Oppong, A G B Amoah, J Brandful, I K Qua |
Association of CYP2C19, CYP2D6 and CYP3A4 Genetic Variants on Primaquine Hemolysis in G6PD-Deficient Patients. Pathogens (Basel, Switzerland) 2023 7 12 (7): . Marielle M Macêdo, Anne C G Almeida, Gabrielly S Silva, Amanda C Oliveira, Victor I Mwangi, Ana C Shuan, Laila R A Barbosa, Fernanda Rodrigues-Soares, Gisely C Me |
A Rare Case of Abnormal Hemoglobin Variant Hb Mizuho: [HBB: c.206T?>?C ? 68(E12) Leu-Pro]: A First Report in the Chinese Population. Hemoglobin 2023 7 1-5. Ya-Ping Chen, Peng Wu, Heng Wang, Jiang-Fen Wu, Dan Xie, Lei Wang, Bangquan An, Shengwen Hua |
Rare Case of Hemolytic Anemia and Distal Renal Tubular Acidosis in an adult due to Homozygous SLC4A1 Mutation. Indian journal of nephrology 2023 7 33 (3): 209-212. Wasiyeeullah Shaikh, Lohitaksha Suratkal, Abhay Bha |
Assessment of interleukin-10 promoter variant (-1082A/G) and cytokine production in patients with hemolytic uremic syndrome. Frontiers in pediatrics 2023 7 11 1210158. Micaela Aldana Mongelos, Fernando Nicolás Sosa, Gonzalo Ezequiel Pineda, Gabriela Fiorentino, Adriana Santiago, Miguel Martín Abelleyro, Liliana Carmen Rossetti, Ramón Exeni, Carlos Daniel De Brasi, Marina Sandra Palermo, María Victoria Ram |
Genotype-degree of hemolysis correlation in hereditary spherocytosis. BMC genomics 2023 6 24 (1): 304. Yimeng Shi, Yuan Li, Xiawan Yang, Xiaoxia Li, Guangxin Peng, Xin Zhao, Xu Liu, Yufei Zhao, Jing Hu, Xiangrong Hu, Baohang Zhang, Kang Zhou, Yang Yang, Youzhen Xiong, Jianping Li, Huihui Fan, Wenrui Yang, Lei Ye, Liping Jing, Li Zhang, Fengkui Zha |
Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population. Annals of hematology 2023 3 . Dongerdiye Rashmi, Bokde Meghana, More Tejashree Anil, Saptarshi Arati, Devendra Rati, Chiddarwar Ashish, Warang Prashant, Kedar Prabhak |
In vivo evaluation of the effect of sickle cell hemoglobin S, C and therapeutic transfusion on erythrocyte metabolism and cardiorenal dysfunction. American journal of hematology 2023 3 . D'Alessandro Angelo, Nouraie S Mehdi, Zhang Yingze, Cendali Francesca, Gamboni Fabia, Reisz Julie A, Zhang Xu, Bartsch Kyle W, Galbraith Matthew D, Gordeuk Victor R, Gladwin Mark |
Mutations in the alternative complement pathway in multiple myeloma patients with carfilzomib-induced thrombotic microangiopathy. Blood cancer journal 2023 2 13 (1): 31. Moscvin Maria, Liacos Christine Ivy, Chen Tianzeng, Theodorakakou Foteini, Fotiou Despina, Hossain Shahrier, Rowell Sean, Leblebjian Houry, Regan Eileen, Czarnecki Peter, Bagnoli Filippo, Bolli Niccolo', Richardson Paul, Rennke Helmut G, Dimopoulos Meletios A, Kastritis Efstathios, Bianchi Gia |
In vivo evaluation of the effect of sickle cell hemoglobin S, C and therapeutic transfusion on erythrocyte metabolism and cardiorenal dysfunction. bioRxiv : the preprint server for biology 2023 2 . D'Alessandro Angelo, Nouraie S Mehdi, Zhang Yingze, Cendali Francesca, Gamboni Fabia, Reisz Julie A, Zhang Xu, Bartsch Kyle W, Galbraith Matthew D, Gordeuk Victor R, Gladwin Mark |
Cytokine polymorphisms in patients with autoimmune hemolytic anemia. Frontiers in immunology 2023 11 14 1221582. Anna Zaninoni, Bruno Fattizzo, Loredana Pettine, Cristina Vercellati, Anna P Marcello, Wilma Barcelli |
Molecular characteristics of hereditary red blood cell membrane disorders in Thailand: a multi-center registry. Annals of hematology 2023 11 . Duantida Songdej, Pacharapan Surapolchai, Patcharee Komwilaisak, Pornpun Sripornsawan, Supanun Lauhasurayotin, Nattiya Teawtrakul, Tarinee Rungjirajittranon, Adisak Tantiworawit, Phakatip Sinlapamongkolkul, Kitti Torcharus, Pranee Sutcharitchan, Bunchoo Pongtanakul, Nongnuch Sirachainan, Pimlak Charoenkw |
Evaluating the prevalence of inborn errors of immunity in adults with chronic immune thrombocytopenia or Evans syndrome. Blood advances 2023 10 . Debbie Jiang, Kira Maria Rosenlind, Sarah K Baxter, Terry Gernsheimer, Suleyman Gulsuner, Eric Allenspach, Sioban B Ke |
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- Page last updated:Apr 29, 2024
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