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Showing results (121-130 of 157) with videos related to

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Neurology|November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann diseaseM R Baumgartner, N M Verhoeven, C Jakobs, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 7, 2002
Long-chain 3-hydroxyacylCoA dehydrogenase deficiency: a new case presenting with liver dysfunction, cholestasis and fibrosisM H Odievre, C Sevin, J Laurent, et al.
European Journal of Pediatrics|December 22, 1999
Liver transplantation in propionic acidaemiaJ M Saudubray, G Touati, P Delonlay, et al.
European Journal of Medical Genetics|January 18, 2015
Multiple congenital anomalies in two boys with mutation in HCFC1 and cobalamin disorderM Gérard, G Morin, A Bourillon, et al.
Anales Espanoles De Pediatria|November 1, 1989
[Respiratory chain diseases in infancy. Clinical presentation and diagnosis]M T García Silva, J P Bonnefont, A Rotig, et al.
Human Molecular Genetics|November 25, 2000
Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding delta(1)-pyrroline-5-carboxylate synthaseM R Baumgartner, C A Hu, S Almashanu, et al.
Annales De Genetique|January 1, 1992
[Amino acids and trisomy 21]J Lejeune, M O Rethoré, M C de Blois, et al.
The Journal of Pediatrics|December 1, 1994
Clinical outcome of long-term management of patients with vitamin B12-unresponsive methylmalonic acidemiaS B van der Meer, F Poggi, M Spada, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2002
[Hematologic manifestations of inborn errors of metabolism]P de Lonlay, O Fenneteau, G Touati, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Liver transplantation in two cases of propionic acidaemiaJ S Schlenzig, F Poggi-Travert, J Laurent, et al.
Pageof 16

Showing results (121-130 of 157) with videos related to

Sort By:
Pageof 16
Neurology|November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann diseaseM R Baumgartner, N M Verhoeven, C Jakobs, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 7, 2002
Long-chain 3-hydroxyacylCoA dehydrogenase deficiency: a new case presenting with liver dysfunction, cholestasis and fibrosisM H Odievre, C Sevin, J Laurent, et al.
European Journal of Pediatrics|December 22, 1999
Liver transplantation in propionic acidaemiaJ M Saudubray, G Touati, P Delonlay, et al.
European Journal of Medical Genetics|January 18, 2015
Multiple congenital anomalies in two boys with mutation in HCFC1 and cobalamin disorderM Gérard, G Morin, A Bourillon, et al.
Anales Espanoles De Pediatria|November 1, 1989
[Respiratory chain diseases in infancy. Clinical presentation and diagnosis]M T García Silva, J P Bonnefont, A Rotig, et al.
Human Molecular Genetics|November 25, 2000
Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding delta(1)-pyrroline-5-carboxylate synthaseM R Baumgartner, C A Hu, S Almashanu, et al.
Annales De Genetique|January 1, 1992
[Amino acids and trisomy 21]J Lejeune, M O Rethoré, M C de Blois, et al.
The Journal of Pediatrics|December 1, 1994
Clinical outcome of long-term management of patients with vitamin B12-unresponsive methylmalonic acidemiaS B van der Meer, F Poggi, M Spada, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2002
[Hematologic manifestations of inborn errors of metabolism]P de Lonlay, O Fenneteau, G Touati, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Liver transplantation in two cases of propionic acidaemiaJ S Schlenzig, F Poggi-Travert, J Laurent, et al.
Pageof 16