Results 171 to 180 of about 8,550 (230)

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

Severe clinical phenotype caused by the COL4A5 compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature review

Linchuang shenzangbing zazhi
Zhang Hong-wen
doaj  

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HYPERPROLINÆMIA AND HEREDITARY NEPHRITIS

Lancet, The, 1964
A M Asatoor, M D Milne
exaly   +6 more sources

Hereditary Nephritis

New England Journal of Medicine, 1959
Ralph Goldman, George C. Haberfelde
exaly   +2 more sources

HEREDITARY AND FAMILIAL NEPHRITIS.

Lancet, The, 1924
J Eason, G.L Malcolm Smith
exaly   +2 more sources

Hereditary nephritis and pregnancy

American Journal of Obstetrics and Gynecology, 1969
A 25-year-old woman is presented with congenital ocular defects, perceptive hearing loss since aged 8, and evidence of chronic renal disease since aged 19. During her second pregnancy she developed the nephrotic syndrome which spontaneously subsided post partum, despite persistent evidence of reduced renal function and proteinuria. A percutaneous renal
G N, Gill, J P, Hayslett
openaire   +2 more sources