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Electromyography and Clinical Neurophysiology
|
December 1, 1994
Carpal tunnel syndrome in Mucopolysaccharidoses. A report of four cases in child
I Bona, C Vial, P Brunet, et al.
Journal De Genetique Humaine
|
March 1, 1981
[Problems posed by prenatal diagnosis of abdominal wall malformations]
S Guibaud, M Bonnet, C Coicaud, et al.
Pediatrie
|
January 1, 1989
[Biotidinase deficiency: a disease with neurologic and cutaneous expression susceptible to biotin]
L de Parscau, B Beaufrère, C Vianey-Liaud, et al.
European Journal of Pediatrics
|
February 1, 1988
Neonatal hyperphenylalaninaemia presumably caused by a new variant of biopterin synthetase deficiency
J L Dhondt, P Guibaud, M O Rolland, et al.
Pediatrie
|
June 1, 1971
[Abdominal aorta aneurysm during Bourneville's tuberous sclerosis]
F Freycon, P Mollard, M Hermier, et al.
Journal De Genetique Humaine
|
August 1, 1988
[Alpha-fetoprotein and trisomy 21]
S Guibaud, C Boisson, A Simplot, et al.
Pediatrie
|
December 1, 1984
[Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency]
J P Collet, P Divry, J F Blanc, et al.
Annals of Vascular Surgery
|
June 21, 2001
Surgical repair of an aneurysm of the innominate artery with fistulization into the trachea
J P Guibaud, M N Laborde, J Dubrez, et al.
Pediatrie
|
January 1, 1988
[Neurologic manifestations of arterial hypertension in children]
P Cochat, M C Delmas, L de Parscau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 5, 1997
[Study of plasma acylcarnitines using tandem mass spectrometry. Application to the diagnosis of metabolism hereditary diseases]
F Delolme, C Vianey-Saban, N Guffon, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 147) with videos related to
Sort By:
Page
of 15
Electromyography and Clinical Neurophysiology
|
December 1, 1994
Carpal tunnel syndrome in Mucopolysaccharidoses. A report of four cases in child
I Bona, C Vial, P Brunet, et al.
Journal De Genetique Humaine
|
March 1, 1981
[Problems posed by prenatal diagnosis of abdominal wall malformations]
S Guibaud, M Bonnet, C Coicaud, et al.
Pediatrie
|
January 1, 1989
[Biotidinase deficiency: a disease with neurologic and cutaneous expression susceptible to biotin]
L de Parscau, B Beaufrère, C Vianey-Liaud, et al.
European Journal of Pediatrics
|
February 1, 1988
Neonatal hyperphenylalaninaemia presumably caused by a new variant of biopterin synthetase deficiency
J L Dhondt, P Guibaud, M O Rolland, et al.
Pediatrie
|
June 1, 1971
[Abdominal aorta aneurysm during Bourneville's tuberous sclerosis]
F Freycon, P Mollard, M Hermier, et al.
Journal De Genetique Humaine
|
August 1, 1988
[Alpha-fetoprotein and trisomy 21]
S Guibaud, C Boisson, A Simplot, et al.
Pediatrie
|
December 1, 1984
[Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency]
J P Collet, P Divry, J F Blanc, et al.
Annals of Vascular Surgery
|
June 21, 2001
Surgical repair of an aneurysm of the innominate artery with fistulization into the trachea
J P Guibaud, M N Laborde, J Dubrez, et al.
Pediatrie
|
January 1, 1988
[Neurologic manifestations of arterial hypertension in children]
P Cochat, M C Delmas, L de Parscau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 5, 1997
[Study of plasma acylcarnitines using tandem mass spectrometry. Application to the diagnosis of metabolism hereditary diseases]
F Delolme, C Vianey-Saban, N Guffon, et al.
Page
of 15