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P Guibaud

Showing results (121-130 of 147) with videos related to

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Electromyography and Clinical Neurophysiology|December 1, 1994
Carpal tunnel syndrome in Mucopolysaccharidoses. A report of four cases in childI 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 deficiencyJ 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 tracheaJ 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.
Pageof 15

Showing results (121-130 of 147) with videos related to

Sort By:
Pageof 15
Electromyography and Clinical Neurophysiology|December 1, 1994
Carpal tunnel syndrome in Mucopolysaccharidoses. A report of four cases in childI 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 deficiencyJ 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 tracheaJ 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.
Pageof 15