Results 181 to 190 of about 8,722 (247)

Alport’s Syndrome (Hereditary Nephritis)

core   +1 more source

Parvovirus B19 Infection Presenting as Acute Tubulointerstitial Nephritis in an Immunocompetent Patient: A Case Report. [PDF]

Cureus
Benhadda S, Tahri Y, Benamar L, Ouzeddoun N, Bouattar T.   +4 more
europepmc   +1 more source

[Hereditary nephritis (Alport)].

Srpski arhiv za celokupno lekarstvo, 1979
M, Popović-Rolović, S, Smiljanić
openaire   +1 more source

Approach to Renal Tubular Acidosis - A Review. [PDF]

Indian J Endocrinol Metab
Das S, Agarwal V, Paul TV, Cherian KE.
europepmc   +1 more source

TNFSF4/OX40L and IKZF1/IKAROS Genetic Variant Associations with Egyptian Juvenile Systemic Lupus Erythematosus (JSLE). [PDF]

Biology (Basel)
Attia ZR, Amshawee AM, Hasan AF, Hussein DT, Abd El Azeem RA, Zedan MM, Mutawi TM, El-Beltagy NS, El Basuni MA.   +8 more
europepmc   +1 more source

A beginner's guide to the clinical approach and key concepts of glomerular disease: a mini review. [PDF]

Asian Biomed (Res Rev News)
Udomkarnjananun S, Kanjanabuch T, Hesselink DA.   +2 more
europepmc   +1 more source

Importance of family history and health checkup for school-aged children for type IV collagen-associated nephropathy in hereditary kidney disease. [PDF]

J Nephrol
Kawamoto R, Mori T, Chiga M, Fujimaru T, Nanamatsu A, Fujiki T, Mori Y, Mandai S, Ando F, Susa K, Rai T, Sohara E, Uchida S.   +12 more
europepmc   +1 more source

Real-world immune response to SARS-CoV-2 vaccination in Thai patients with systemic lupus erythematosus: a cross-sectional observational study. [PDF]

Lupus Sci Med
Pongkulkiat P, Foocharoen C, Nanthapisal S, Phanthanawiboon S, Meesing A, Suwannaroj S, Mootsikapun P, Mahakkanukrauh A.   +7 more
europepmc   +1 more source

Urinary Exosomes in Nephrology: A New Frontier for Diagnosis and Prognosis of Kidney Diseases. [PDF]

Int J Mol Sci
Gaudio C, D'Arpino E, Stefani S, Fani FM, Rosso G, Di Marcantonio E, Becherelli P, Caselli G, Merciai C, Fortunato L, Scopetani N, Rosati A.   +11 more
europepmc   +1 more source

A Rare NPHS2 Mutation (E130K) in Hereditary Steroid-Resistant Nephrotic Syndrome: A Case Report. [PDF]

Case Rep Nephrol
Mujahed RH, Salloum OH, Ishreiteh NF, Hosheyh HM, Hashem ADA, Shamestti YF, Hroub MR.   +6 more
europepmc   +1 more source