Results 51 to 60 of about 317 (112)

An 8-month-old boy with infantile nephrotic syndrome caused by semaphorin 3B-associated membranous nephropathy. [PDF]

CEN Case Rep, 2023
Tanaka Y, Yamamoto M, Nozu K, Hara S.
europepmc   +1 more source

Causal effects of rheumatoid arthritis or ankylosing spondylitis on membranous nephropathy: a two-sample Mendelian randomization study. [PDF]

Clin Kidney J, 2023
Wang XF, Duan SB, He J, Wu X, Wu T.
europepmc   +1 more source

Management of Steroid-Resistant Nephrotic Syndrome in Children. [PDF]

Cureus, 2021
Sachdeva S, Khan S, Davalos C, Avanthika C, Jhaveri S, Babu A, Patterson D, Yamani AJ.   +7 more
europepmc   +1 more source

The Pitfall of White Blood Cell Cystine Measurement to Diagnose Juvenile Cystinosis. [PDF]

Int J Mol Sci, 2023
Bondue T, Kouraich A, Berlingerio SP, Veys K, Marie S, Alsaad KO, Al-Sabban E, Levtchenko E, van den Heuvel L.   +8 more
europepmc   +1 more source

Hereditary Gingival Fibromatosis: A Report of a Severe Case. [PDF]

Cureus, 2022
Aboujaoude S, Aoun G.
europepmc   +1 more source

Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis. [PDF]

Am J Hum Genet, 2003
Dowling O, Difeo A, Ramirez MC, Tukel T, Narla G, Bonafe L, Kayserili H, Yuksel-Apak M, Paller AS, Norton K, Teebi AS, Grum-Tokars V, Martin GS, Davis GE, Glucksman MJ, Martignetti JA.   +15 more
europepmc   +1 more source

Lipoid proteinosis in a 36-year-old woman: An index case from Qatar. [PDF]

Qatar Med J
Abdelhamed E, Veettil ST.
europepmc   +1 more source

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. [PDF]

Am J Hum Genet, 2003
Hanks S, Adams S, Douglas J, Arbour L, Atherton DJ, Balci S, Bode H, Campbell ME, Feingold M, Keser G, Kleijer W, Mancini G, McGrath JA, Muntoni F, Nanda A, Teare MD, Warman M, Pope FM, Superti-Furga A, Futreal PA, Rahman N.   +20 more
europepmc   +1 more source

A Rare Presentation of a 12-Year-Old With Systemic Infantile Hyalinosis: A Case Report and Review of the Literature. [PDF]

Cureus
Alfadhli F, Alrehaili L, Bindekhayel JN, Alzamil L, Alrehaili A, Hussain Z.   +5 more
europepmc   +1 more source

Zimmermann-Laband syndrome-associated hereditary gingival fibromatosis.

J Indian Soc Periodontol, 2023
Kshirsagar JT, Dharani K, Thangavel P.
europepmc   +1 more source