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Pediatrics
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August 1, 1993
Nasogastric drip feeding as the only treatment of neonatal maple syrup urine disease
R Parini, L P Sereni, D C Bagozzi, et al.
Journal of Inherited Metabolic Disease
|
February 22, 2000
Dietary therapy in two patients with a mild form of sulphite oxidase deficiency. Evidence for clinical and biological improvement
G Touati, E Rusthoven, E Depondt, et al.
Chirurgie; Memoires De L'Academie De Chirurgie
|
January 1, 1993
[Intrasplenic transplantation of hepatocytes in spf-ash mice with congenital ornithine transcarbamylase deficiency]
J L Michel, D Rabier, C Rambaud, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Therapeutic use of carbamylglutamate in the case of carbamoyl-phosphate synthetase deficiency
G Kuchler, D Rabier, F Poggi-Travert, et al.
Transplantation Proceedings
|
February 1, 1994
Definitive cure of hyperammonemia by liver transplantation in urea cycle defects: report of three cases
D Jan, F Poggi, P Jouvet, et al.
Annales De Genetique
|
January 1, 1990
[Cri-du-chat disease: plasma and urinary amino acids]
J Lejeune, M O Rethoré, M Peeters, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1997
Continuous venovenous haemodiafiltration in the acute phase of neonatal maple syrup urine disease
P Jouvet, F Poggi, D Rabier, et al.
Journal of Inherited Metabolic Disease
|
July 17, 1999
Defects in activation and transport of fatty acids
M Brivet, A Boutron, A Slama, et al.
Pediatrics
|
February 2, 1999
Hair and skin disorders as signs of mitochondrial disease
C Bodemer, A Rötig, P Rustin, et al.
Prenatal Diagnosis
|
December 2, 2009
Gestational age-related reference values for amniotic fluid organic acids
C Ottolenghi, N Abermil, A Lescoat, et al.
Page
of 16
Search research articles
Search
Showing results (91-100 of 157) with videos related to
Sort By:
Page
of 16
Pediatrics
|
August 1, 1993
Nasogastric drip feeding as the only treatment of neonatal maple syrup urine disease
R Parini, L P Sereni, D C Bagozzi, et al.
Journal of Inherited Metabolic Disease
|
February 22, 2000
Dietary therapy in two patients with a mild form of sulphite oxidase deficiency. Evidence for clinical and biological improvement
G Touati, E Rusthoven, E Depondt, et al.
Chirurgie; Memoires De L'Academie De Chirurgie
|
January 1, 1993
[Intrasplenic transplantation of hepatocytes in spf-ash mice with congenital ornithine transcarbamylase deficiency]
J L Michel, D Rabier, C Rambaud, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Therapeutic use of carbamylglutamate in the case of carbamoyl-phosphate synthetase deficiency
G Kuchler, D Rabier, F Poggi-Travert, et al.
Transplantation Proceedings
|
February 1, 1994
Definitive cure of hyperammonemia by liver transplantation in urea cycle defects: report of three cases
D Jan, F Poggi, P Jouvet, et al.
Annales De Genetique
|
January 1, 1990
[Cri-du-chat disease: plasma and urinary amino acids]
J Lejeune, M O Rethoré, M Peeters, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1997
Continuous venovenous haemodiafiltration in the acute phase of neonatal maple syrup urine disease
P Jouvet, F Poggi, D Rabier, et al.
Journal of Inherited Metabolic Disease
|
July 17, 1999
Defects in activation and transport of fatty acids
M Brivet, A Boutron, A Slama, et al.
Pediatrics
|
February 2, 1999
Hair and skin disorders as signs of mitochondrial disease
C Bodemer, A Rötig, P Rustin, et al.
Prenatal Diagnosis
|
December 2, 2009
Gestational age-related reference values for amniotic fluid organic acids
C Ottolenghi, N Abermil, A Lescoat, et al.
Page
of 16