Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Ogier

Showing results (31-40 of 127) with videos related to

Pageof 13
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1994
Pre- and postnatal diagnosis of succinic semialdehyde dehydrogenase deficiency using enzyme and metabolite assaysK M Gibson, C Baumann, H Ogier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 7, 1999
[Severe lactic acidosis disease disclosing milk-protein intolerance to cows' milk]C Rizk, L Valdes, H Ogier de Baulny, et al.
Archives D'Anatomie Et De Cytologie Pathologiques|January 1, 1985
[Congenital anomaly of the metabolism of vitamin B 12. Histopathological study]E Sonsino, H Ogier, J C Mercier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Clinical synthesis and investigation protocol: "extrapyramidal" signs, clinical orientation]P Evrard, M C Nassogne, H Ogier de Baulny, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1986
[Type IV Ehlers-Danlos syndrome of acrogeria type]M C Boullie, P Y Venencie, E Thomine, et al.
Pediatrics|December 1, 1981
Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiencyF X Coude, H Ogier, C Marsac, et al.
Archives of Disease in Childhood|January 1, 1997
In vivo functional investigations of lactic acid in patients with respiratory chain disordersG Touati, O Rigal, A Lombès, et al.
Neuromuscular Disorders : NMD|January 1, 1993
Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiencyN B Romero, C Marsac, M Paturneau-Jouas, et al.
The Journal of Pediatrics|August 1, 1981
Occurrence of hyperammonemia in the course of 17 cases of methylmalonic acidemiaL Cathelineau, P Briand, H Ogier, et al.
Pediatric Neurology|September 12, 2001
Striatal and pontocerebellar hypoperfusion in Hallervorden-Spatz syndromeP Castelnau, M Zilbovicius, M J Ribeiro, et al.
Pageof 13

Showing results (31-40 of 127) with videos related to

Sort By:
Pageof 13
Journal of Inherited Metabolic Disease|January 1, 1994
Pre- and postnatal diagnosis of succinic semialdehyde dehydrogenase deficiency using enzyme and metabolite assaysK M Gibson, C Baumann, H Ogier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 7, 1999
[Severe lactic acidosis disease disclosing milk-protein intolerance to cows' milk]C Rizk, L Valdes, H Ogier de Baulny, et al.
Archives D'Anatomie Et De Cytologie Pathologiques|January 1, 1985
[Congenital anomaly of the metabolism of vitamin B 12. Histopathological study]E Sonsino, H Ogier, J C Mercier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Clinical synthesis and investigation protocol: "extrapyramidal" signs, clinical orientation]P Evrard, M C Nassogne, H Ogier de Baulny, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1986
[Type IV Ehlers-Danlos syndrome of acrogeria type]M C Boullie, P Y Venencie, E Thomine, et al.
Pediatrics|December 1, 1981
Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiencyF X Coude, H Ogier, C Marsac, et al.
Archives of Disease in Childhood|January 1, 1997
In vivo functional investigations of lactic acid in patients with respiratory chain disordersG Touati, O Rigal, A Lombès, et al.
Neuromuscular Disorders : NMD|January 1, 1993
Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiencyN B Romero, C Marsac, M Paturneau-Jouas, et al.
The Journal of Pediatrics|August 1, 1981
Occurrence of hyperammonemia in the course of 17 cases of methylmalonic acidemiaL Cathelineau, P Briand, H Ogier, et al.
Pediatric Neurology|September 12, 2001
Striatal and pontocerebellar hypoperfusion in Hallervorden-Spatz syndromeP Castelnau, M Zilbovicius, M J Ribeiro, et al.
Pageof 13