Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 27, 2015
[Diagnosing an inborn metabolic error with consciousness disorders]
J-B Arnoux, A Brassier, A-S Guemann, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 30, 2011
[Enzyme replacement therapy for lysosomal storage disorders]
V Valayannopoulos, A Brassier, A Chabli, et al.
Revue Des Maladies Respiratoires
|
October 13, 2022
[Pulmonary phenotypes of inborn errors of metabolism]
W Mauhin, A Brassier, J London, et al.
JIMD Reports
|
November 27, 2015
Renal Involvement in a French Paediatric Cohort of Patients with Lysinuric Protein Intolerance
C Nicolas, N Bednarek, V Vuiblet, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 28, 2015
Two new cases of serine deficiency disorders treated with l-serine
A Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Journal of Child Neurology
|
December 17, 2013
Acute psychosis in propionic acidemia: 2 case reports
C Dejean de la Bâtie, V Barbier, V Valayannopoulos, et al.
Molecular Genetics and Metabolism Reports
|
June 27, 2017
Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosis
F Habarou, A Brassier, M Rio, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 19, 2020
Management of 35 critically ill hyperammonemic neonates: Role of early administration of metabolite scavengers and continuous hemodialysis
L Abily-Donval, L Dupic, C Joffre, et al.
JIMD Reports
|
May 17, 2017
Ketone Bodies as a Possible Adjuvant to Ketogenic Diet in PDHc Deficiency but Not in GLUT1 Deficiency
F Habarou, N Bahi-Buisson, E Lebigot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 14, 2012
[Prenatal symptoms and diagnosis of inherited metabolic diseases]
A Brassier, C Ottolenghi, N Boddaert, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 27, 2015
[Diagnosing an inborn metabolic error with consciousness disorders]
J-B Arnoux, A Brassier, A-S Guemann, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 30, 2011
[Enzyme replacement therapy for lysosomal storage disorders]
V Valayannopoulos, A Brassier, A Chabli, et al.
Revue Des Maladies Respiratoires
|
October 13, 2022
[Pulmonary phenotypes of inborn errors of metabolism]
W Mauhin, A Brassier, J London, et al.
JIMD Reports
|
November 27, 2015
Renal Involvement in a French Paediatric Cohort of Patients with Lysinuric Protein Intolerance
C Nicolas, N Bednarek, V Vuiblet, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 28, 2015
Two new cases of serine deficiency disorders treated with l-serine
A Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Journal of Child Neurology
|
December 17, 2013
Acute psychosis in propionic acidemia: 2 case reports
C Dejean de la Bâtie, V Barbier, V Valayannopoulos, et al.
Molecular Genetics and Metabolism Reports
|
June 27, 2017
Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosis
F Habarou, A Brassier, M Rio, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 19, 2020
Management of 35 critically ill hyperammonemic neonates: Role of early administration of metabolite scavengers and continuous hemodialysis
L Abily-Donval, L Dupic, C Joffre, et al.
JIMD Reports
|
May 17, 2017
Ketone Bodies as a Possible Adjuvant to Ketogenic Diet in PDHc Deficiency but Not in GLUT1 Deficiency
F Habarou, N Bahi-Buisson, E Lebigot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 14, 2012
[Prenatal symptoms and diagnosis of inherited metabolic diseases]
A Brassier, C Ottolenghi, N Boddaert, et al.
Page
of 2