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A Munnich

Showing results (81-90 of 573) with videos related to

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Journal of Medical Genetics|October 1, 1991
An animal model for maternal phenylketonuriaC Roux, F Rey, S Lyonnet, et al.
Human Genetics|April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndromeB Parfait, D Chretien, A Rötig, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Expression of respiratory chain deficiencies in human cultured cellsT Bourgeron, D Chretien, P Amati, et al.
Annales De Medecine Interne|January 1, 1987
[Research methods in metabolic myopathies in children]A Lombes, H Ogier, J P Bonnefont, et al.
Pathologie-Biologie|January 14, 1999
[From monogenic to polygenic: model of Hirschsprung disease]R Salomon, J Amiel, T Attié, et al.
European Journal of Pediatrics|February 1, 1994
Valproate-induced hepatic failure in a case of cytochrome c oxidase deficiencyB Chabrol, J Mancini, D Chretien, et al.
European Journal of Biochemistry|July 15, 1987
Dietary and hormonal regulation of L-type pyruvate kinase gene expression in rat small intestineH Ogier, A Munnich, S Lyonnet, et al.
Human Genetics|December 1, 1991
Fatal hyperammonemia resulting from a C-to-T mutation at a MspI site of the ornithine transcarbamylase geneD Hentzen, A Pelet, D Feldman, et al.
Tijdschrift Voor Kindergeneeskunde|December 1, 1991
[Pearson's syndrome: a multi-system disorder based on a mt-DNA deletion]P W Danse, C Jakobs, A Rötig, et al.
Biochimica Et Biophysica Acta|August 22, 1997
Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in humanP Rustin, T Bourgeron, B Parfait, et al.
Pageof 58

Showing results (81-90 of 573) with videos related to

Sort By:
Pageof 58
Journal of Medical Genetics|October 1, 1991
An animal model for maternal phenylketonuriaC Roux, F Rey, S Lyonnet, et al.
Human Genetics|April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndromeB Parfait, D Chretien, A Rötig, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Expression of respiratory chain deficiencies in human cultured cellsT Bourgeron, D Chretien, P Amati, et al.
Annales De Medecine Interne|January 1, 1987
[Research methods in metabolic myopathies in children]A Lombes, H Ogier, J P Bonnefont, et al.
Pathologie-Biologie|January 14, 1999
[From monogenic to polygenic: model of Hirschsprung disease]R Salomon, J Amiel, T Attié, et al.
European Journal of Pediatrics|February 1, 1994
Valproate-induced hepatic failure in a case of cytochrome c oxidase deficiencyB Chabrol, J Mancini, D Chretien, et al.
European Journal of Biochemistry|July 15, 1987
Dietary and hormonal regulation of L-type pyruvate kinase gene expression in rat small intestineH Ogier, A Munnich, S Lyonnet, et al.
Human Genetics|December 1, 1991
Fatal hyperammonemia resulting from a C-to-T mutation at a MspI site of the ornithine transcarbamylase geneD Hentzen, A Pelet, D Feldman, et al.
Tijdschrift Voor Kindergeneeskunde|December 1, 1991
[Pearson's syndrome: a multi-system disorder based on a mt-DNA deletion]P W Danse, C Jakobs, A Rötig, et al.
Biochimica Et Biophysica Acta|August 22, 1997
Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in humanP Rustin, T Bourgeron, B Parfait, et al.
Pageof 58