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Journal of Pediatric Orthopedics. Part B
|
January 27, 2000
Absence of congenital prethrombotic disorders in children with Legg-Perthes disease
N Sirvent, F Fisher, T el Hayek, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 26, 2009
[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder]
S Pierron, H Giudicelli, M Moreigne, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Homocysteine response to methionine challenge in four obligate heterozygotes for homocystinuria and relationship with cystathionine beta-synthase mutations
M P Sperandeo, M Candito, G Sebastio, et al.
European Journal of Pediatrics
|
July 1, 1995
Early-onset fatal encephalomyopathy associated with severe mtDNA depletion
V Paquis-Flucklinger, J F Pellissier, J Camboulives, et al.
Chirurgie; Memoires De L'Academie De Chirurgie
|
January 1, 1993
[Salmonella aortitis complicated by rupture. Diagnostic and therapeutic problems]
I Farah, H Giudicelli, L Voirin, et al.
American Journal of Medical Genetics
|
October 23, 1997
Stüve-Wiedemann syndrome and defects of the mitochondrial respiratory chain
B Chabrol, S Sigaudy, V Paquis, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 5, 2008
[A cause of intracerebral calcifications that should be known: pseudohypoparathyroidism Ib]
P Faissolle, K Wagner-Mahler, J-C Mas, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
Journal of Pediatric Orthopedics. Part B
|
January 27, 2000
Absence of congenital prethrombotic disorders in children with Legg-Perthes disease
N Sirvent, F Fisher, T el Hayek, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 26, 2009
[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder]
S Pierron, H Giudicelli, M Moreigne, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Homocysteine response to methionine challenge in four obligate heterozygotes for homocystinuria and relationship with cystathionine beta-synthase mutations
M P Sperandeo, M Candito, G Sebastio, et al.
European Journal of Pediatrics
|
July 1, 1995
Early-onset fatal encephalomyopathy associated with severe mtDNA depletion
V Paquis-Flucklinger, J F Pellissier, J Camboulives, et al.
Chirurgie; Memoires De L'Academie De Chirurgie
|
January 1, 1993
[Salmonella aortitis complicated by rupture. Diagnostic and therapeutic problems]
I Farah, H Giudicelli, L Voirin, et al.
American Journal of Medical Genetics
|
October 23, 1997
Stüve-Wiedemann syndrome and defects of the mitochondrial respiratory chain
B Chabrol, S Sigaudy, V Paquis, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 5, 2008
[A cause of intracerebral calcifications that should be known: pseudohypoparathyroidism Ib]
P Faissolle, K Wagner-Mahler, J-C Mas, et al.
Page
of 2