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European Journal of Pediatrics|October 24, 2000
Nutrition, physical growth, and bone density in treated phenylketonuriaH Przyrembel, H J BremerClinica Chimica Acta; International Journal of Clinical Chemistry|February 8, 1975
Alpha-ketoadipic aciduria: degradation studies with fibroblasts,U Wendel, H W Rüdiger, H Przyrembel, et al.Monatsschrift Fur Kinderheilkunde|March 1, 1978
[Pyruvate-dehydrogenase deficiency. Lethal course of the disease during infancy (author's transl)]U Wendel, H Przyrembel, K Becker, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 16, 1976
Glutaric aciduria type II: report on a previously undescribed metabolic disorderH Przyrembel, U Wendel, K Becker, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1978
Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine diseaseU Langenbeck, U Wendel, A Mench-Hoinowski, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|February 8, 1975
Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studiesH Przyrembel, D Bachmann, I Lombeck, et al.European Journal of Pediatrics|February 9, 1999
Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997P Burgard, H J Bremer, P Bührdel, et al.Wiener Klinische Wochenschrift|January 6, 1989
[Diseases of the heart caused by metabolic defects]H PrzyrembelJournal of Inherited Metabolic Disease|January 1, 1987
Therapy of mitochondrial disordersH PrzyrembelThe American Journal of Clinical Nutrition|February 7, 2001
Consideration of possible legislation within existing regulatory frameworksH PrzyrembelPageof 13