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Journal of Inherited Metabolic Disease
|
September 14, 2002
A novel Y243S mutation in the pyruvate dehydrogenase El alpha gene subunit: correlation with thiamine pyrophosphate interaction
C Benelli, F Fouque, I Redonnet-Vernhet, et al.
Archives Francaises De Pediatrie
|
November 1, 1989
[Evolutive atlanto-axial luxation revealing chronic inflammatory rheumatism in children]
J M Pedespan, J F Chateil, F Ceccato, et al.
Pediatrie
|
March 1, 1977
[Hypo-hyperparathyroidism in a boy with an 8-20 translocation in mosaicism]
D Fontan, A Brendel, F Serville, et al.
Archives of Dermatology
|
October 8, 1998
Congenital cutaneous defects as complications in surviving co-twins. Aplasia cutis congenita and neonatal volkmann ischemic contracture of the forearm
C Léauté-Labrèze, F Depaire-Duclos, J Sarlangue, et al.
Pediatrie
|
January 1, 1973
[Karyotype 49, XXXXY in an infant]
F Serville, J M Guillard, C de Joigny, et al.
Archives Francaises De Pediatrie
|
July 1, 1979
[Results of brain tomography in acute lymphoblastic leukemia in children]
J M Guillard, D Candito, P Constant, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur
|
May 31, 2002
[Botulinum toxin in the management of spastic hip adductors in non-ambulatory cerebral palsy children]
B Deleplanque, A Lagueny, V Flurin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 10, 2001
[Cerebellar vermis hypoplasia with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes]
D Graber, C Antignac, G Deschenes, et al.
Brain & Development
|
January 11, 2000
Schizencephaly: clinical and imaging features in 30 infantile cases
D Denis, J F Chateil, M Brun, et al.
Journal of the Peripheral Nervous System : JPNS
|
August 26, 2000
Congenital insensitivity to pain with anhydrosis. Report of two unrelated cases
A Vital, D Fontan, J Julien, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 82) with videos related to
Sort By:
Page
of 9
Journal of Inherited Metabolic Disease
|
September 14, 2002
A novel Y243S mutation in the pyruvate dehydrogenase El alpha gene subunit: correlation with thiamine pyrophosphate interaction
C Benelli, F Fouque, I Redonnet-Vernhet, et al.
Archives Francaises De Pediatrie
|
November 1, 1989
[Evolutive atlanto-axial luxation revealing chronic inflammatory rheumatism in children]
J M Pedespan, J F Chateil, F Ceccato, et al.
Pediatrie
|
March 1, 1977
[Hypo-hyperparathyroidism in a boy with an 8-20 translocation in mosaicism]
D Fontan, A Brendel, F Serville, et al.
Archives of Dermatology
|
October 8, 1998
Congenital cutaneous defects as complications in surviving co-twins. Aplasia cutis congenita and neonatal volkmann ischemic contracture of the forearm
C Léauté-Labrèze, F Depaire-Duclos, J Sarlangue, et al.
Pediatrie
|
January 1, 1973
[Karyotype 49, XXXXY in an infant]
F Serville, J M Guillard, C de Joigny, et al.
Archives Francaises De Pediatrie
|
July 1, 1979
[Results of brain tomography in acute lymphoblastic leukemia in children]
J M Guillard, D Candito, P Constant, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur
|
May 31, 2002
[Botulinum toxin in the management of spastic hip adductors in non-ambulatory cerebral palsy children]
B Deleplanque, A Lagueny, V Flurin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 10, 2001
[Cerebellar vermis hypoplasia with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes]
D Graber, C Antignac, G Deschenes, et al.
Brain & Development
|
January 11, 2000
Schizencephaly: clinical and imaging features in 30 infantile cases
D Denis, J F Chateil, M Brun, et al.
Journal of the Peripheral Nervous System : JPNS
|
August 26, 2000
Congenital insensitivity to pain with anhydrosis. Report of two unrelated cases
A Vital, D Fontan, J Julien, et al.
Page
of 9