Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 25 (of 25 Records) |
Query Trace: Minimal Change Disease[original query] |
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Interleukin-13 genetic polymorphisms in Singapore Chinese children correlate with long-term outcome of minimal-change disease. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2005 Apr 20 (4): 728-34. Wei Chang-Li, Cheung Wai, Heng Chew-Kiat, Arty Novi, Chong Samuel S, Lee Bee-Wah, Puah Ken-Lee, Yap Hui-K |
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome. Pediatric nephrology (Berlin, Germany) 2008 Sep 23 (9): 1455-60. Chernin Gil, Heeringa Saskia F, Gbadegesin Rasheed, Liu Jinhong, Hinkes Bernward G, Vlangos Christopher N, Vega-Warner Virginia, Hildebrandt Friedhe |
Genetic effect of the NPHS2 gene variants on proteinuria in minimal change disease and immunoglobulin A nephropathy. Nephrology (Carlton, Vic.) 2009 Dec 14 (8): 728-34. Zhu Li, Yu Lei, Wang Chen-Dan, Lv Ji-Cheng, Li Gui-Sen, Zhang Hong, Wang Hai-Y |
The influence of vascular endothelial growth factor (VEGF) polymorphism on the progression of chronic glomerulonephritides. Folia biologica 2011 57 (4): 145-50. Safránková H, Merta M, Reiterová J, Stekrová J, Maixnerová D, Ryšavá R, Skibová J, Tesa? |
TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease. Folia biologica 2012 58 (4): 173-6. Obeidová L, Reiterová J, Ln?ni?ka P, Štekrová J, Šafránková H, Kohoutová M, Tesa? |
GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome. Pediatric nephrology (Berlin, Germany) 2012 Sep 27 (9): 1595-9. Cheong Hae Il, Kang Hee Gyung, Schlondorff Johann |
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome. Folia biologica 2012 58 (2): 64-8. Reiterová J, Safránková H, Obeidová L, St?krová J, Maixnerová D, Merta M, Tesa? |
[Correlation between Chinese medicine syndromes and the NPHS1 gene and NPHS2 gene polymorphism as well as corticosteroid sensitivity in patients with minimal change disease]. Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine / Zhongguo Zhong xi yi jie he xue hui, Zhongguo Zhong yi yan jiu yuan zhu ban 2012 Jul 32 (7): 914-7. Luo Yue-zhong, Wang Chao, Zeng |
The CTLA-4 +49GG genotype is associated with susceptibility for nephrotic kidney diseases. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2013 Nov 28 (11): 2800-5. Spink Clemens, Stege Gesa, Tenbrock Klaus, Harendza Sigr |
Mutational analysis of ACTN4, encoding a-actinin 4, in patients with focal segmental glomerulosclerosis using HRM method. Folia biologica 2013 59 (3): 110-5. Safa?íková M, Reiterová J, Safránková H, Stekrová J, Zidková A, Obeidová L, Kohoutová M, Tesa? |
Association of aldosterone synthase (CYP11B2) gene -344T/C polymorphism with the risk of primary chronic glomerulonephritis in the Polish population. Journal of the renin-angiotensin-aldosterone system : JRAAS 2014 Dec 15 (4): 553-8. Pawlik Magdalena, Mostowska Adrianna, Lianeri Margarita, Oko Andrzej, Jagodzi?ski Pawe? |
Impact of the 4G/5G polymorphism in the plasminogen activator inhibitor-1 gene on primary nephrotic syndrome. Molecular medicine reports 2014 Mar 9 (3): 894-8. Luo Yuezhong, Wang Chao, Tu Hait |
Steroid-resistant nephrotic syndrome: impact of genetic testing. Annals of Saudi medicine 0 33 (6): 533-8. Kari Jameela A, El-Desoky Sherif M, Gari Mamdooh, Malik Khalid, Vega-Warner Virginia, Lovric Svjetlana, Bockenhauer Detl |
Angiotensin-converting enzyme genotype is not a significant genetic risk factor for idiopathic nephrotic syndrome in Croatian children. Nephron 2015 130 (1): 29-34. Batini? Danko, Serti? Jadranka, ?ori? Marijana, Konjevoda Paško, Batini? Danica, Miloševi? Dan |
Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children. Clinical and experimental nephrology 2016 Jan . Dhandapani Mohanapriya Chinambedu, Venkatesan Vettriselvi, Rengaswamy Nammalwar Bollam, Gowrishankar Kalpana, Ekambaram Sudha, Sengutavan Prabha, Perumal Venkatachal |
Cytotoxic T- Lymphocyte Antigen-4 (CTLA4) Gene Expression and Urinary CTLA4 Levels in Idiopathic Nephrotic Syndrome. Indian journal of pediatrics 2018 Jul . Mishra Om P, Chhabra Prashant, Narayan Gopeshwar, Srivastava Pradeep, Prasad Rajniti, Singh Ankur, Abhinay Abhishek, Batra Vineeta |
Effect of angiotensin converting enzyme gene I/D polymorphism in South Indian children with nephrotic syndrome. Journal of biomedical research 2019 Jun 33 (3): 201-207. Kumar Ramanathan Aravind Selvin, Karuppiah Balakrishnan, Vijayan Murali, Raju Kamaraj, Mani Dhivakar, Chinniah Rathika, Thirunavukkarasu Manikandan, Malini Ravi Padma, Illiayaraja Krishnan Jeyaram, Senguttuvan Prab |
NPHS2 gene sequencing results in children of the Azerbaijani population with different types of nephrotic syndrome caused by chronic glomerulonephritis. Bratislavske lekarske listy 2019 2 120 (2): 102-105. Baylarov R, Baylarova R, Berdeli A, Bayramov R, Haziyev |
Minimal Change Disease With Nephrotic Syndrome Associated With Coronavirus Disease 2019 After Apolipoprotein L1 Risk Variant Kidney Transplant: A Case Report. Transplantation proceedings 2020 9 52 (9): 2693-2697. Yamada Masaaki, Rastogi Prerna, Ince Dilek, Thayyil Abdullah, Adela Mansilla M, Smith Richard J H, Kuppachi Sarat, Thomas Christie |
Homocysteine and IgA nephropathy: observational and Mendelian randomization analyses. Chinese medical journal 2020 1 133 (3): 277-284. Zhang Yue-Miao, Zhou Xu-Jie, Shi Su-Fang, Liu Li-Jun, Lyu Ji-Cheng, Zhang Ho |
APOL1 genotype-associated morphologic changes among patients with focal segmental glomerulosclerosis. Pediatric nephrology (Berlin, Germany) 2021 3 36 (9): 2747-2757. Zee Jarcy, McNulty Michelle T, Hodgin Jeffrey B, Zhdanova Olga, Hingorani Sangeeta, Jefferson Jonathan Ashley, Gibson Keisha L, Trachtman Howard, Fornoni Alessia, Dell Katherine M, Reich Heather N, Bagnasco Serena, Greenbaum Larry A, Lafayette Richard A, Gipson Debbie S, Brown Elizabeth, Kretzler Matthias, Appel Gerald, Sambandam Kamalanathan K, Tuttle Katherine R, Chen Dhruti, Atkinson Meredith A, Hogan Marie C, Kaskel Frederick J, Meyers Kevin E, O'Toole John, Srivastava Tarak, Sethna Christine B, Hladunewich Michelle A, Lin J J, Nast Cynthia C, Derebail Vimal K, Patel Jiten, Vento Suzanne, Holzman Lawrence B, Athavale Ambarish M, Adler Sharon G, Lemley Kevin V, Lieske John C, Hogan Jonathan J, Gadegbeku Crystal A, Fervenza Fernando C, Wang Chia-Shi, Matar Raed Bou, Singer Pamela, Kopp Jeffrey B, Barisoni Laura, Sampson Matthew |
Association Between NPHS2 p.R229Q and Focal Segmental Glomerular Sclerosis/Steroid-Resistant Nephrotic Syndrome. Frontiers in medicine 2022 8 9 937122. Zhou Qiongxiu, Weng Qinjie, Zhang Xiaoyan, Liu Yunzi, Tong Jun, Hao Xu, Shi Hao, Shen Pingyan, Ren Hong, Xie Jingyuan, Chen N |
Molecular Study of Childhood Steroid-Resistant Nephrotic Syndrome: A Hospital-Based Study. Journal of pediatric genetics 2022 8 11 (3): 185-191. Singh Akanksha, Singh Ankur, Mishra Om Prakash, Prasad Rajniti, Narayan Gopeshwar, Batra Vineeta V, Tabatabaeifar Mansoureh, Schaefer Fra |
Minimal Change Disease Is Associated with Mitochondrial Injury and STING Pathway Activation. Journal of clinical medicine 2022 2 11 (3): . Yu Byung Chul, Moon Ahrim, Lee Kyung Ho, Oh Young Seung, Park Moo Yong, Choi Soo Jeong, Kim Jin K |
Nephrotic syndrome with Minimal Change Disease and Atopy in NorthAfrican adults. La Tunisie medicale 2023 9 101 (2): 253-258. Asma Hadhri, Sanda Mrabet, Narjes Ben Aicha, Asma Fradi, Awatef Azzabi, Wissal Sahtout, Raja Boukadida, Yosra Guedri, Dorsaf Zellama, Nihed Abdessaied, Helmi Ben Saad, Abdellatif Acho |
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- Page last updated:Apr 29, 2024
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