These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
172 related articles for article (PubMed ID: 33982833)
21. Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane. Funk SD; Lin MH; Miner JH Matrix Biol; 2018 Oct; 71-72():250-261. PubMed ID: 29673759 [TBL] [Abstract][Full Text] [Related]
22. Forced expression of laminin beta1 in podocytes prevents nephrotic syndrome in mice lacking laminin beta2, a model for Pierson syndrome. Suh JH; Jarad G; VanDeVoorde RG; Miner JH Proc Natl Acad Sci U S A; 2011 Sep; 108(37):15348-53. PubMed ID: 21876163 [TBL] [Abstract][Full Text] [Related]
23. Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. Hasselbacher K; Wiggins RC; Matejas V; Hinkes BG; Mucha B; Hoskins BE; Ozaltin F; Nürnberg G; Becker C; Hangan D; Pohl M; Kuwertz-Bröking E; Griebel M; Schumacher V; Royer-Pokora B; Bakkaloglu A; Nürnberg P; Zenker M; Hildebrandt F Kidney Int; 2006 Sep; 70(6):1008-12. PubMed ID: 16912710 [TBL] [Abstract][Full Text] [Related]
24. Laminin-521 Protein Therapy for Glomerular Basement Membrane and Podocyte Abnormalities in a Model of Pierson Syndrome. Lin MH; Miller JB; Kikkawa Y; Suleiman HY; Tryggvason K; Hodges BL; Miner JH J Am Soc Nephrol; 2018 May; 29(5):1426-1436. PubMed ID: 29472414 [No Abstract] [Full Text] [Related]
25. Skeletal impairment in Pierson syndrome: Is there a role for lamininβ2 in bone physiology? Beaufils C; Farlay D; Machuca-Gayet I; Fassier A; Zenker M; Freychet C; Bonnelye E; Bertholet-Thomas A; Ranchin B; Bacchetta J Bone; 2018 Jan; 106():187-193. PubMed ID: 29051055 [TBL] [Abstract][Full Text] [Related]
26. Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome. Rossanti R; Shono A; Miura K; Hattori M; Yamamura T; Nakanishi K; Minamikawa S; Fujimura J; Horinouchi T; Nagano C; Sakakibara N; Kaito H; Nagase H; Morisada N; Asanuma K; Matsuo M; Nozu K; Iijima K J Hum Genet; 2019 Jul; 64(7):673-679. PubMed ID: 31015583 [TBL] [Abstract][Full Text] [Related]
27. Nephron development and extrarenal features in a child with congenital nephrotic syndrome caused by null LAMB2 mutations. Kino J; Tsukaguchi H; Kimata T; Nguyen HT; Nakano Y; Miyake N; Matsumoto N; Kaneko K BMC Nephrol; 2017 Jul; 18(1):220. PubMed ID: 28683731 [TBL] [Abstract][Full Text] [Related]
28. Chimeric protein identification of dystrophic, Pierson and other laminin polymerization residues. McKee KK; Aleksandrova M; Yurchenco PD Matrix Biol; 2018 Apr; 67():32-46. PubMed ID: 29408412 [TBL] [Abstract][Full Text] [Related]
30. Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome. Maselli RA; Ng JJ; Anderson JA; Cagney O; Arredondo J; Williams C; Wessel HB; Abdel-Hamid H; Wollmann RL J Med Genet; 2009 Mar; 46(3):203-8. PubMed ID: 19251977 [TBL] [Abstract][Full Text] [Related]
31. Ocular findings in a case of Pierson syndrome with a novel mutation in laminin ß2 gene. Arima M; Tsukamoto S; Akiyama R; Nishiyama K; Kohno RI; Tachibana T; Hayashida A; Murayama M; Hisatomi T; Nozu K; Iijima K; Ohga S; Sonoda KH J AAPOS; 2018 Oct; 22(5):401-403.e1. PubMed ID: 30120985 [TBL] [Abstract][Full Text] [Related]
32. A milder variant of Pierson syndrome. Kagan M; Cohen AH; Matejas V; Vlangos C; Zenker M Pediatr Nephrol; 2008 Feb; 23(2):323-7. PubMed ID: 17943323 [TBL] [Abstract][Full Text] [Related]
34. Pierson syndrome in an adolescent girl with nephrotic range proteinuria but a normal GFR. Lehnhardt A; Lama A; Amann K; Matejas V; Zenker M; Kemper MJ Pediatr Nephrol; 2012 May; 27(5):865-8. PubMed ID: 22228401 [TBL] [Abstract][Full Text] [Related]
35. A comparison of splicing assays to detect an intronic variant of the OCRL gene in Lowe syndrome. Nakanishi K; Nozu K; Hiramoto R; Minamikawa S; Yamamura T; Fujimura J; Horinouchi T; Ninchoji T; Kaito H; Morisada N; Ishimori S; Nakanishi K; Morioka I; Awano H; Matsuo M; Iijima K Eur J Med Genet; 2017 Dec; 60(12):631-634. PubMed ID: 28803024 [TBL] [Abstract][Full Text] [Related]
36. An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis. Yamamura T; Nozu K; Miyoshi Y; Nakanishi K; Fujimura J; Horinouchi T; Minamikawa S; Mori N; Fujimaru R; Nakanishi K; Ninchoji T; Kaito H; Mariko TI; Morioka I; Matsuo M; Iijima K BMC Nephrol; 2017 Dec; 18(1):353. PubMed ID: 29202719 [TBL] [Abstract][Full Text] [Related]
37. [LAMB2 gene mutation as a cause of congenital nephrotic syndrome with distinct eye abnormalities and hypotonia]. Zurowska A; Załuska-Leśniewska I; Zenker M Przegl Lek; 2006; 63 Suppl 3():37-9. PubMed ID: 16898484 [TBL] [Abstract][Full Text] [Related]
38. Five-Year Follow-Up and Successful Kidney Transplantation in a Girl with a Severe Phenotype of Pierson Syndrome. Sobieszczańska-Droździel A; Grenda R; Lipska-Ziętkiewicz BS; Korolczuk A; Jarmużek W; Sikora P Nephron; 2021; 145(5):579-584. PubMed ID: 34058744 [TBL] [Abstract][Full Text] [Related]