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Pediatric Nephrology (Berlin, Germany)|June 1, 1995
A case of craniomandibular dermatodysostosis associated with focal glomerulosclerosisE Pedagogos, G Flanagan, D M Francis, et al.Pediatrics|September 1, 1980
The Pediatric Examination of Educational Readiness: validation of an extended observation procedureM D Levine, F Oberklaid, T E Ferb, et al.Pediatric Research|October 1, 1979
Malignant hyperphenylalaninemia--clinical features, biochemical findings, and experience with administration of biopterinsD M Danks, P Schlesinger, F Firgaira, et al.Lancet (London, England)|April 2, 1994
Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1D Ravine, R N Gibson, R G Walker, et al.Pediatric Research|May 1, 1989
Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patientsS J Mihalik, H W Moser, P A Watkins, et al.Human Genetics|June 1, 1994
Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemiaK Nanao, K Okamura-Ikeda, Y Motokawa, et al.Lancet (London, England)|January 19, 1991
Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.Acta Neuropathologica|January 1, 1989
Striatal degeneration in glutaric acidaemia type IIC W Chow, F E Frerman, S I Goodman, et al.Journal of Inherited Metabolic Disease|January 1, 1992
X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutationH H Dahl, L L Hansen, R M Brown, et al.Biomedical Mass Spectrometry|October 1, 1979
Abnormal deoxyribose metabolites in the urine of a child with a possible new inborn error of metabolismR J Truscott, B Halpern, J Hammond, et al.Pageof 19