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Medicine|March 1, 1992
Neonatal lupus erythematosus syndrome: analysis of C4 allotypes and C4 genes in 18 familiesR M Watson, J N Scheel, M Petri, et al.The Journal of Clinical Endocrinology and Metabolism|May 1, 1986
Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B proteinP A Donohoue, C van Dop, R H McLean, et al.Biochemical and Biophysical Research Communications|February 13, 1987
Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasiaN Jospe, P A Donohoue, C Van Dop, et al.Diabetes|October 1, 1981
Increased concentration of albumin in kidney basement membranes in diabetes mellitusA F Michael, D M BrownAmerican Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1993
Alport syndrome: from bedside to genome to bedsideC E Kashtan, A F MichaelThe American Journal of Anatomy|February 1, 1990
Expression of novel basement membrane components in the developing human kidney and eyeM M Kleppel, A F MichaelArchives of Pathology & Laboratory Medicine|November 1, 1978
Focal glomerular sclerosis and sarcoidosisS M Lee, A F MichaelThe Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 1, 1983
Retardation of fading and enhancement of intensity of immunofluorescence by p-phenylenediamineJ L Platt, A F MichaelUremia Investigation|January 1, 1984
Analysis of renal cell populations using monoclonal antibodiesJ L Platt, A F MichaelKidney International|January 1, 1988
Acute tubulointerstitial nephritis associated with aminonucleoside nephrosisA A Eddy, A F MichaelPageof 21