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Items: 12

1.
Association of serum mannose-binding lectin, anti-phospholipase A2 receptor antibody and renal outcomes in idiopathic membranous nephropathy and atypical membranous nephropathy: a single center retrospective cohort study
Yuchao Zhao, Meishun Cai, Zhenbin Jiang, Bao Dong, Yu Yan, Yina Wang, Li Zuo
Ren Fail. 2022; 44(1): 428–433. Published online 2022 Mar 10. doi: 10.1080/0886022X.2022.2048016
PMCID:
PMC8920381
AbstractArticlePDF–604K
2.
A novel mutation of congenital nephrotic syndrome in a Slovenian child eventually receiving a renal transplant
Valentina Golob, Gregor Nosan, Sara Bertok, Maja Frelih, Emanuela Boštjančič, Rina Rus
Croat Med J. 2021 Apr; 62(2): 187–191. doi: 10.3325/cmj.2021.62.187
PMCID:
PMC8107997
AbstractArticlePDF–372K
3.
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome
Xiaoyuan Jia, Tomohiko Yamamura, Rasheed Gbadegesin, Michelle T. McNulty, Kyuyong Song, China Nagano, Yuki Hitomi, Dongwon Lee, Yoshihiro Aiba, Seik-Soon Khor, Kazuko Ueno, Yosuke Kawai, Masao Nagasaki, Eisei Noiri, Tomoko Horinouchi, Hiroshi Kaito, Riku Hamada, Takayuki Okamoto, Koichi Kamei, Yoshitsugu Kaku, Rika Fujimaru, Ryojiro Tanaka, Yuko Shima, The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan, Jiwon Baek, Hee Gyung Kang, Il-Soo Ha, Kyoung Hee Han, Eun Mi Yang, Korean Consortium of Hereditary Renal Diseases in Children, Asiri Abeyagunawardena, Brandon Lane, Megan Chryst-Stangl, Christopher Esezobor, Adaobi Solarin, Midwest Pediatric Nephrology Consortium (Genetics of nephrotic syndrome study group), Claire Dossier, Georges Deschénes, NEPHROVIR, Marina Vivarelli, Hanna Debiec, Kenji Ishikura, Masafumi Matsuo, Kandai Nozu, Pierre Ronco, Hae Il Cheong, Matthew G. Sampson, Katsushi Tokunaga, Kazumoto Iijima
Kidney Int. Author manuscript; available in PMC 2021 May 6.
Published in final edited form as: Kidney Int. 2020 Nov; 98(5): 1308–1322. Published online 2020 Jun 14. doi: 10.1016/j.kint.2020.05.029
PMCID:
PMC8101291
AbstractArticlePDF–1.2M
4.
GWAS-Based Discoveries in IgA Nephropathy, Membranous Nephropathy, and Steroid-Sensitive Nephrotic Syndrome
Elena Sanchez-Rodriguez, Christopher T. Southard, Krzysztof Kiryluk
Clin J Am Soc Nephrol. 2021 Mar 8; 16(3): 458–466. Published online 2020 Jul 17. doi: 10.2215/CJN.14031119
PMCID:
PMC8011010
AbstractArticle
5.
Severe hypertriglyceridaemia and pancreatitis in a patient with lipoprotein lipase deficiency based on mutations in lipoprotein lipase (LPL) and apolipoprotein A5 (APOA5) genes
Charlotte Koopal, Remy Bemelmans, A David Marais, Frank LJ Visseren
BMJ Case Rep. 2019; 12(4): e228199. Published online 2019 Apr 3. doi: 10.1136/bcr-2018-228199
PMCID:
PMC6453290
AbstractArticlePDF–279K
6.
A PRISMA-compliant meta-analysis of MDR1 polymorphisms and idiopathic nephrotic syndrome: Susceptibility and steroid responsiveness
Shi-Sheng Han, Yan-Qiu Xu, Yan Lu, Xiang-Chen Gu, Yi Wang
Medicine (Baltimore) 2017 Jun; 96(24): e7191. Published online 2017 Jun 16. doi: 10.1097/MD.0000000000007191
Correction in:
Medicine (Baltimore). 2017 Jun; 96(26): e7453.
PMCID:
PMC5478346
AbstractArticlePDF–334K
7.
Initial Steroid Sensitivity in Children with Steroid-Resistant Nephrotic Syndrome Predicts Post-Transplant Recurrence
Wen Y. Ding, Ania Koziell, Hugh J. McCarthy, Agnieszka Bierzynska, Murali K. Bhagavatula, Jan A. Dudley, Carol D. Inward, Richard J. Coward, Jane Tizard, Christopher Reid, Corinne Antignac, Olivia Boyer, Moin A. Saleem
J Am Soc Nephrol. 2014 Jun; 25(6): 1342–1348. Published online 2014 Feb 7. doi: 10.1681/ASN.2013080852
PMCID:
PMC4033379
AbstractArticle
8.
Urokinase Gene 3′-UTR T/C Polymorphism Is Associated with Malignancy and ESRD in Idiopathic Membranous Nephropathy
Cheng-Hsu Chen, Shih-Yin Chen, Kuo-Hsiung Shu, Mei-Chin Wen, Chi-Hung Cheng, Ming-Ju Wu, Tung-Min Yu, Ya-Wen Chuang, Fuu-Jen Tsai
Biomed Res Int. 2014; 2014: 425095. Published online 2014 Apr 14. doi: 10.1155/2014/425095
PMCID:
PMC4009112
AbstractArticlePDF–582K
9.
Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome
Fatih Ozaltin, Tulin Ibsirlioglu, Ekim Z. Taskiran, Dilek Ertoy Baydar, Figen Kaymaz, Mithat Buyukcelik, Beltinge Demircioglu Kilic, Ayse Balat, Paraskevas Iatropoulos, Esin Asan, Nurten A. Akarsu, Franz Schaefer, Engin Yilmaz, Ayşin Bakkaloglu, the PodoNet Consortium
Am J Hum Genet. 2011 Jul 15; 89(1): 139–147. doi: 10.1016/j.ajhg.2011.05.026
PMCID:
PMC3135805
AbstractArticlePDF–1.2M
10.
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome
Saskia F. Heeringa, Christopher N. Vlangos, Gil Chernin, Bernward Hinkes, Rasheed Gbadegesin, Jinhong Liu, Bethan E. Hoskins, Fatih Ozaltin, Friedhelm Hildebrandt, Members of the APN Study Group
Nephrol Dial Transplant. 2008 Nov; 23(11): 3527–3533. Published online 2008 May 23. doi: 10.1093/ndt/gfn271
PMCID:
PMC2720813
AbstractArticlePDF–183K
11.
Improved prognosis for congenital nephrotic syndrome of the Finnish type in Irish families
J Savage, J Jefferson, A Maxwell, A Hughes, J Shanks, D Gill
Arch Dis Child. 1999 May; 80(5): 466–469. doi: 10.1136/adc.80.5.466
PMCID:
PMC1717912
SummaryPDF–100K
12.
Hypertension induces glomerulosclerosis in phospholipase C-ε1 deficiency
Douglas K. Atchison, Christopher L. O’Connor, Rajasree Menon, Edgar A. Otto, Santhi K. Ganesh, Roger C. Wiggins, Alan V. Smrcka, Markus Bitzer
Am J Physiol Renal Physiol. 2020 May 1; 318(5): F1177–F1187. Published online 2020 Mar 30. doi: 10.1152/ajprenal.00541.2019
PMCID:
PMC7294338
AbstractArticle

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