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U Wendel

Showing results (151-160 of 186) with videos related to

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The Journal of Pediatrics|December 1, 1990
Prenatal treatment of a patient with vitamin B12-responsive methylmalonic acidemiaS B van der Meer, L J Spaapen, B Fowler, et al.
Neurology|July 1, 1996
Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscleH A Bentlage, U Wendel, H Schägger, et al.
Neuropediatrics|April 29, 1998
Systemic infantile complex I deficiency with fatal outcome in two brothersM E Rubio-Gozalbo, W Ruitenbeek, U Wendel, et al.
Journal of Inherited Metabolic Disease|April 14, 2007
Dietary long-chain polyunsaturated fatty acid supplementation in infants with phenylketonuria: a randomized controlled trialB Koletzko, T Sauerwald, H Demmelmair, et al.
European Journal of Pediatrics|April 1, 1992
Development of height and weight in children with diabetes mellitus: report on two prospective multicentre studies, one cross-sectional, one longitudinalA Thon, E Heinze, K D Feilen, et al.
Biochemical and Biophysical Research Communications|July 30, 1997
Autosomal recessive liver phosphorylase kinase deficiency caused by a novel splice-site mutation in the gene encoding the liver gamma subunit (PHKG2)E A van Beurden, M de Graaf, U Wendel, et al.
European Journal of Pediatrics|February 1, 1982
A familial progressive neurodegenerative disease with 2-oxoglutaric aciduriaA Kohlschütter, A Behbehani, U Langenbeck, et al.
Neuropediatrics|August 18, 2001
Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiencyM Baethmann, U Wendel, G F Hoffmann, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identification of four novel mutations in severe methylenetetrahydrofolate reductase deficiencyL A Kluijtmans, U Wendel, E M Stevens, et al.
European Journal of Pediatrics|December 1, 1993
White matter abnormalities in patients with treated hyperphenylalaninaemia: magnetic resonance relaxometry and proton spectroscopy findingsU Bick, K Ullrich, U Stöber, et al.
Pageof 19

Showing results (151-160 of 186) with videos related to

Sort By:
Pageof 19
The Journal of Pediatrics|December 1, 1990
Prenatal treatment of a patient with vitamin B12-responsive methylmalonic acidemiaS B van der Meer, L J Spaapen, B Fowler, et al.
Neurology|July 1, 1996
Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscleH A Bentlage, U Wendel, H Schägger, et al.
Neuropediatrics|April 29, 1998
Systemic infantile complex I deficiency with fatal outcome in two brothersM E Rubio-Gozalbo, W Ruitenbeek, U Wendel, et al.
Journal of Inherited Metabolic Disease|April 14, 2007
Dietary long-chain polyunsaturated fatty acid supplementation in infants with phenylketonuria: a randomized controlled trialB Koletzko, T Sauerwald, H Demmelmair, et al.
European Journal of Pediatrics|April 1, 1992
Development of height and weight in children with diabetes mellitus: report on two prospective multicentre studies, one cross-sectional, one longitudinalA Thon, E Heinze, K D Feilen, et al.
Biochemical and Biophysical Research Communications|July 30, 1997
Autosomal recessive liver phosphorylase kinase deficiency caused by a novel splice-site mutation in the gene encoding the liver gamma subunit (PHKG2)E A van Beurden, M de Graaf, U Wendel, et al.
European Journal of Pediatrics|February 1, 1982
A familial progressive neurodegenerative disease with 2-oxoglutaric aciduriaA Kohlschütter, A Behbehani, U Langenbeck, et al.
Neuropediatrics|August 18, 2001
Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiencyM Baethmann, U Wendel, G F Hoffmann, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identification of four novel mutations in severe methylenetetrahydrofolate reductase deficiencyL A Kluijtmans, U Wendel, E M Stevens, et al.
European Journal of Pediatrics|December 1, 1993
White matter abnormalities in patients with treated hyperphenylalaninaemia: magnetic resonance relaxometry and proton spectroscopy findingsU Bick, K Ullrich, U Stöber, et al.
Pageof 19