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M E Rubio-Gozalbo

Showing results (1-10 of 35) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1994
Dihydropyrimidine dehydrogenase deficiency presenting with psychomotor retardation and ocular abnormalitiesH D Bakker, M E Rubio Gozalbo, A H van Gennip
Journal of Inherited Metabolic Disease|September 13, 2007
Proposal for the prevention of osteoporosis in paediatric patients with classical galactosaemiaB Panis, M J P G van Kroonenburgh, M E Rubio-Gozalbo
Molecular Aspects of Medicine|September 15, 2004
Carnitine-acylcarnitine translocase deficiency, clinical, biochemical and genetic aspectsM E Rubio-Gozalbo, J A Bakker, H R Waterham, et al.
Journal of Inherited Metabolic Disease|November 13, 2016
The galactosemia network (GalNet)M E Rubio-Gozalbo, A M Bosch, A Burlina, 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|January 26, 2006
Body composition in children with galactosaemiaB Panis, P Ph Forget, F H Nieman, et al.
Magnetic Resonance Imaging|July 14, 1999
Proton MR spectroscopy in a child with pyruvate dehydrogenase complex deficiencyM E Rubio-Gozalbo, A Heerschap, J M Trijbels, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Neuroleptic malignant syndrome during zuclopenthixol therapy in X-linked cerebral adrenoleukodystrophyM E Rubio-Gozalbo, D A van Waardenburg, P P Forget, et al.
Archives of Disease in Childhood|June 29, 2002
Bone mineral density in patients with classic galactosaemiaM E Rubio-Gozalbo, S Hamming, M J P G van Kroonenburgh, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 7, 2002
N-acetyl-glutamate synthetase deficiency or porto-systemic shunt associated encephalopathy?R Dammers, M E Rubio-Gozalbo, S G F Robben, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Journal of Inherited Metabolic Disease|January 1, 1994
Dihydropyrimidine dehydrogenase deficiency presenting with psychomotor retardation and ocular abnormalitiesH D Bakker, M E Rubio Gozalbo, A H van Gennip
Journal of Inherited Metabolic Disease|September 13, 2007
Proposal for the prevention of osteoporosis in paediatric patients with classical galactosaemiaB Panis, M J P G van Kroonenburgh, M E Rubio-Gozalbo
Molecular Aspects of Medicine|September 15, 2004
Carnitine-acylcarnitine translocase deficiency, clinical, biochemical and genetic aspectsM E Rubio-Gozalbo, J A Bakker, H R Waterham, et al.
Journal of Inherited Metabolic Disease|November 13, 2016
The galactosemia network (GalNet)M E Rubio-Gozalbo, A M Bosch, A Burlina, 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|January 26, 2006
Body composition in children with galactosaemiaB Panis, P Ph Forget, F H Nieman, et al.
Magnetic Resonance Imaging|July 14, 1999
Proton MR spectroscopy in a child with pyruvate dehydrogenase complex deficiencyM E Rubio-Gozalbo, A Heerschap, J M Trijbels, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Neuroleptic malignant syndrome during zuclopenthixol therapy in X-linked cerebral adrenoleukodystrophyM E Rubio-Gozalbo, D A van Waardenburg, P P Forget, et al.
Archives of Disease in Childhood|June 29, 2002
Bone mineral density in patients with classic galactosaemiaM E Rubio-Gozalbo, S Hamming, M J P G van Kroonenburgh, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 7, 2002
N-acetyl-glutamate synthetase deficiency or porto-systemic shunt associated encephalopathy?R Dammers, M E Rubio-Gozalbo, S G F Robben, et al.
Pageof 4