Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 73 Records) |
Query Trace: Syndrome and EGFR[original query] |
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Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort. European journal of medical genetics 2020 9 63 (11): 104047. Sun Shuzhen, Xu Linan, Bi Yunli, Wang Jing, Zhang Zhiqing, Tang Xiaoshan, Cao Qi, Zhai Yihui, Chen Jing, Fang Xiaoyan, Liu Jialu, Fang Ye, Xiang Tianchao, Qian Yanyan, Wu Bingbing, Wang Huijun, Zhou Wenhao, Shen Jian, Dong Kuiran, Liu Xiaorong, Zheng Bixia, Zhang Aihua, Wang Xiaowen, Wu Yubing, Ma Duan, Shen Qian, Rao Jia, Xu Ho |
Exploring the real-world effect of the SARS-CoV-2 pandemic on the molecular diagnostics for cancer patients and high-risk individuals. Expert review of molecular diagnostics 2020 12 21 (1): 101-107. Cavic Milena, Krivokuca Ana, Boljevic Ivana, Spasic Jelena, Mihajlovic Milica, Pavlovic Marijana, Damjanovic Ana, Radosavljevic Davorin, Jankovic Radmi |
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases. Frontiers in medicine 2020 12 7 580376. Mastrangelo Antonio, Giani Marisa, Groppali Elena, Castorina Pierangela, Soldà Giulia, Robusto Michela, Fallerini Chiara, Bruttini Mirella, Renieri Alessandra, Montini Giovan |
Molecular diagnosis and clinical outcome of a lung cancer patient with TP53-E285K mutated Li-Fraumeni syndrome harboring a somatic EGFR-KDD mutation. American journal of translational research 2020 11 12 (10): 6689-6693. Yang Dafu, Han Xue, Li Dan, Cui Saiqiong, Liu Sisi, Wu Xue, Dai Zhaox |
The Relationship between Metabolic Syndrome and Plasma Metals Modified by EGFR and TNF-? Gene Polymorphisms. Toxics 2021 Sep 9 (9): . Chen Tzu-Hua, Kung Wei-Shyang, Sun Hung-Yu, Huang Joh-Jong, Lu Jia-Yi, Luo Kuei-Hau, Chuang Hung- |
A randomised controlled unblinded multicentre non-inferiority trial with activated vitamin D and prednisolone treatment in patients with minimal change nephropathy (ADAPTinMCN). Trials 2021 7 22 (1): 442. Kristensen Tilde, Birn Henrik, Ivarsen P |
Urine concentrating defect as presenting sign of progressive renal failure in Bardet-Biedl syndrome patients. Clinical kidney journal 2021 6 14 (6): 1545-1551. Zacchia Miriam, Blanco Francesca Del Vecchio, Torella Annalaura, Raucci Raffaele, Blasio Giancarlo, Onore Maria Elena, Marchese Emanuela, Trepiccione Francesco, Vitagliano Caterina, Iorio Valentina Di, Alessandra Perna, Simonelli Francesca, Nigro Vincenzo, Capasso Giovambattista, Viggiano Davi |
Association between polymorphism at IGF-1 rs35767 gene locus and long-term decline in renal function: a Japanese retrospective longitudinal cohort study. BMC nephrology 2021 Jun 22 (1): 207. Honda Kosuke, Kuriyama Satoru, Ichida Kimiyoshi, Nakano Tomoko, Sugano Naoki, Yokoo Takas |
Nephroplex: a kidney-focused NGS panel highlights the challenges of PKD1 sequencing and identifies a founder BBS4 mutation. Journal of nephrology 2021 5 34 (6): 1855-1874. Zacchia Miriam, Blanco Francesca Del Vecchio, Trepiccione Francesco, Blasio Giancarlo, Torella Annalaura, Melluso Andrea, Capolongo Giovanna, Pollastro Rosa Maria, Piluso Giulio, Di Iorio Valentina, Simonelli Francesca, Viggiano Davide, Perna Alessandra, Nigro Vincenzo, Capasso Giovambattis |
Genotype-phenotype correlations and nephroprotective effects of RAAS inhibition in patients with autosomal recessive Alport syndrome. Pediatric nephrology (Berlin, Germany) 2021 3 36 (9): 2719-2730. Zhang Yanqin, Böckhaus Jan, Wang Fang, Wang Suxia, Rubel Diana, Gross Oliver, Ding J |
APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses. Pediatric nephrology (Berlin, Germany) 2021 2 36 (8): 2327-2336. Watanabe Andreia, Guaragna Mara Sanches, Belangero Vera Maria Santoro, Casimiro Fernanda Maria Serafim, Pesquero João Bosco, de Santis Feltran Luciana, Palma Lilian Monteiro Pereira, Varela Patrícia, de Menezes Neves Precil Diego Miranda, Lerario Antonio Marcondes, de Souza Marcela Lopes, de Mello Maricilda Palandi, de Brito Lutaif Anna Cristina Gervásio, Ferrari Cassio Rodrigues, Sampson Matthew Gordon, Onuchic Luiz Fernando, Nogueira Paulo Cesar Ko |
Glioma Imaging by O-(2-18F-Fluoroethyl)-L-Tyrosine PET and Diffusion-Weighted MRI and Correlation With Molecular Phenotypes, Validated by PET/MR-Guided Biopsies. Frontiers in oncology 2021 12 11 743655. Cheng Ye, Song Shuangshuang, Wei Yukui, Xu Geng, An Yang, Ma Jie, Yang Hongwei, Qi Zhigang, Xiao Xinru, Bai Jie, Xu Lixin, Hu Zeliang, Sun Tingting, Wang Leiming, Lu Jie, Lin Qingta |
Mutation search within monogenic diabetes genes in Polish patients with long-term type 1 diabetes and preserved kidney function. Polish archives of internal medicine 2021 Nov . Hohendorff Jerzy, Kwiatkowska Magdalena, Pisarczyk-Wiza Dorota, Ludwig-S?omczy?ska Agnieszka, Milcarek Magdalena, Kapusta Przemys?aw, Zapa?a Barbara, Kie?-Wilk Beata, Trznadel-Morawska Iwona, Szopa Magdalena, Zozuli?ska-Zió?kiewicz Dorota, Ma?ecki Maciej |
Arterial stiffness in regards to kidney function in middle-aged subjects with metabolic syndrome: Lithuanian high-risk cohort. Blood pressure monitoring 2021 1 26 (3): 191-195. Laucyte-Cibulskiene Agne, Ryliskyte Ligita, Badaras Ignas, Navickas Petras, Badariene Jolita, Laucevicius Aleksandr |
Clinicopathological Impact of Gene Polymorphism of Nephrin and Glucocorticoid Receptor Genes in Egyptian Children with Nonfamilial Nephrotic Syndrome. Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 0 32 (6): 1615-1627. El-Refaey Ahmed M, Elsamanoudy Ayman Z, Elmorsy Zakarya, Gaber Eman, Sarhan Amr, Hammad Aymman, Zedan Mohamed M, Bakr Ashr |
Distinct NSCLC EGFR Variants in a Family With Li-Fraumeni Syndrome: Case Report. JTO clinical and research reports 2022 7 3 (8): 100368. Edmondson Shelby, von Itzstein Mitchell S, Reys Brian, Mayer Melissa, Gagan Jeffrey, Gerber David |
ACLY and CKD: A Mendelian Randomization Analysis. Kidney international reports 2022 7 7 (7): 1673-1681. Mohammadi-Shemirani Pedrum, Chong Michael, Perrot Nicolas, Pigeyre Marie, Steinberg Gregory R, Paré Guillaume, Krepinsky Joan C, Lanktree Matthew |
Normal fasting triglyceride levels and incident type 2 diabetes in the general population. Cardiovascular diabetology 2022 6 21 (1): 111. Szili-Torok Tamas, Bakker Stephan J L, Tietge Uwe J |
GWAS of Hematuria. Clinical journal of the American Society of Nephrology : CJASN 2022 4 17 (5): 672-683. Gagliano Taliun Sarah A, Sulem Patrick, Sveinbjornsson Gardar, Gudbjartsson Daniel F, Stefansson Kari, Paterson Andrew D, Barua Moumi |
Osimertinib-induced syndrome of inappropriate secretion of antidiuretic hormone in oncogene-addicted lung adenocarcinoma: A case report. Lung cancer (Amsterdam, Netherlands) 2022 3 166 132-134. Skribek Marcus, Bozoky Benedek, Tsakonas Georgi |
Effect of CYP2C19 status on platelet reactivity in Taiwanese acute coronary syndrome patients switching to prasugrel from clopidogrel: Switch Study. Journal of the Formosan Medical Association = Taiwan yi zhi 2022 2 121 (9): 1786-1797. Kuo Feng-Yu, Lee Cheng-Han, Lan Wei-Ren, Su Cheng-Huang, Lee Wen-Lieng, Wang Yi-Chih, Lin Wei-Shiang, Chu Pao-Hsien, Lu Tse-Min, Lo Ping-Han, Tsukiyama Shuji, Yang Wei-Chen, Cheng Li-Chung, Huang Chien-Lung, Yin Wei-Hsian, Liu Ping-Y |
Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age. Frontiers in medicine 2022 11 9 953643. Günthner Roman, Knipping Lea, Jeruschke Stefanie, Satanoskij Robin, Lorenz-Depiereux Bettina, Hemmer Clara, Braunisch Matthias C, Riedhammer Korbinian M, ?omi? Jasmina, Tönshoff Burkhard, Tasic Velibor, Abazi-Emini Nora, Nushi-Stavileci Valbona, Buiting Karin, Gjorgjievski Nikola, Momirovska Ana, Patzer Ludwig, Kirschstein Martin, Gross Oliver, Lungu Adrian, Weber Stefanie, Renders Lutz, Heemann Uwe, Meitinger Thomas, Büscher Anja K, Hoefele Jul |
LZTR1 mutation mediates oncogenesis through stabilization of EGFR and AXL. Cancer discovery 2022 11 . Ko Aram, Hasanain Mohammad, Oh Young Taek, D'Angelo Fulvio, Sommer Danika, Frangaj Brulinda, Tran Suzanne, Bielle Franck, Pollo Bianca, Paterra Rosina, Mokhtari Karima, Soni Rajesh Kumar, Peyre Matthieu, Eoli Marica, Papi Laura, Kalamarides Michel, Sanson Marc, Iavarone Antonio, Lasorella An |
Traditional Chinese Medicine Syndromes are Associated with Driver Gene Mutations and Clinical Characteristics in Patients with Lung Adenocarcinoma. Evidence-based complementary and alternative medicine : eCAM 2022 10 2022 9905868. Yang Jili, Lu Haiyan, Jing Niancai, Wang Bo, Guo Huanyu, Sun Shoukun, Zhang Y |
Investigation of the impact of AXL, TLR3, and STAT2 in congenital Zika syndrome through genetic polymorphisms and protein-protein interaction network analyses. Birth defects research 2023 8 . Julia A Gomes, Eduarda Sgarioni, Juliano A Boquett, Thayne W Kowalski, Lucas R Fraga, Ana Cláudia P Terças-Trettel, Juliana H da Silva, Bethânia F R Ribeiro, Marcial F Galera, Thalita M de Oliveira, Maria Denise F Carvalho de Andrade, Isabella F Carvalho, Lavínia Schüler-Faccini, Fernanda S L Vian |
Atypical haemolytic uraemic syndrome in the era of terminal complement inhibition- An observational cohort study. Blood 2023 6 . Vicky Brocklebank, Patrick R Walsh, Kate Smith-Jackson, Thomas M Hallam, Kevin J Marchbank, Valerie Wilson, Theophile Bigirumurame, Tina Dutt, Emma K Montgomery, Michal Malina, Edwin Ks Wong, Sally Johnson, Neil Sheerin, David Kavana |
Osimertinib combined with bevacizumab as the first-line treatment in non-small cell lung cancer patients with brain metastasis harboring epidermal growth factor receptor mutations. Thoracic cancer 2023 4 . Zhang Ling, You Yunhong, Liu Xueli, Liu Fengjuan, Nie Keke, Ji Youx |
USH2A mutation and specific driver mutation subtypes are associated with clinical efficacy of immune checkpoint inhibitors in lung cancer. Journal of Zhejiang University. Science. B 2023 2 24 (2): 143-156. Yang Dexin, Feng Yuqin, Lu Haohua, Chen Kelie, Xu Jinming, Li Peiwei, Wang Tianru, Xia Dajing, Wu Yih |
APOL1 Risk Variants and Acute Kidney Injury in Black Americans with COVID-19. Clinical journal of the American Society of Nephrology : CJASN 2023 1 16 (12): 1790-1796. Larsen Christopher P, Wickman Terrance J, Braga Juarez R, Matute-Trochez Luis A, Hasty Anna E, Buckner Lyndsey R, Arthur John M, Haun Randy S, Velez Juan Carlos |
Pediatric-type high-grade gliomas with PDGFRA amplification in adult patients with Li-Fraumeni syndrome: clinical and molecular characterization of three cases. Acta neuropathologica communications 2024 4 12 (1): 57. Yuji Kibe, Fumiharu Ohka, Kosuke Aoki, Junya Yamaguchi, Kazuya Motomura, Eiji Ito, Kazuhito Takeuchi, Yuichi Nagata, Satoshi Ito, Nobuhiko Mizutani, Yoshiki Shiba, Sachi Maeda, Tomohide Nishikawa, Hiroki Shimizu, Ryuta Sai |
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- Page last updated:Apr 16, 2024
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