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P Guibaud

Showing results (91-100 of 147) with videos related to

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Journal Francais D'Ophtalmologie|September 19, 2000
[Persistent hyperplastic primary vitreous syndrome in a girl with Aicardi syndrome]F Beby, C Zech, R Touraine, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
A new neonatal case of N-acetylglutamate synthase deficiency treated by carbamylglutamateN Guffon, C Vianey-Saban, J Bourgeois, et al.
Annales De Pediatrie|February 2, 1970
[Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy]M Jeune, C Collombel, M Michel, et al.
Human Mutation|January 1, 1995
A 13-bp deletion (1952 del 13) in the methylmalonyl CoA mutase gene of an affected patientR L Touraine, M O Rolland, P Divry, et al.
Archives Francaises De Pediatrie|December 1, 1978
[Familial congenital muscular dystrophy caused by phosphofructokinase deficiency]P Guibaud, H Carrier, M Mathieu, et al.
Transplantation|May 1, 1992
Orthotopic liver transplantation for type 1 Gaucher's diseaseC DuCerf, B Bancel, P Caillon, et al.
Pediatrie|January 1, 1988
[Hypertrophic kidneys in utero and neonatal renal failure caused by diffuse mesangial sclerosis]B Parchoux, J Bourgeois, J Gilly, et al.
Journal De Genetique Humaine|March 1, 1982
[Acetylcholinesterase of amniotic fluid: application to prenatal diagnosis of neural tube closing defects. I. Quantitative tests]S Guibaud, A Simplot, M Bonnet, et al.
Journal De Genetique Humaine|January 1, 1989
[Results of pregnancies characterized by a decrease in the level of alpha-fetoprotein in the maternal blood]S Guibaud, C Boisson, A Simplot, et al.
Journal De Genetique Humaine|June 1, 1982
[Amniotic fluid acetylcholinesterase and prenatal diagnosis of neural tube defects. II. Qualitative test]S Guibaud, A Simplot, M Bonnet, et al.
Pageof 15

Showing results (91-100 of 147) with videos related to

Sort By:
Pageof 15
Journal Francais D'Ophtalmologie|September 19, 2000
[Persistent hyperplastic primary vitreous syndrome in a girl with Aicardi syndrome]F Beby, C Zech, R Touraine, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
A new neonatal case of N-acetylglutamate synthase deficiency treated by carbamylglutamateN Guffon, C Vianey-Saban, J Bourgeois, et al.
Annales De Pediatrie|February 2, 1970
[Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy]M Jeune, C Collombel, M Michel, et al.
Human Mutation|January 1, 1995
A 13-bp deletion (1952 del 13) in the methylmalonyl CoA mutase gene of an affected patientR L Touraine, M O Rolland, P Divry, et al.
Archives Francaises De Pediatrie|December 1, 1978
[Familial congenital muscular dystrophy caused by phosphofructokinase deficiency]P Guibaud, H Carrier, M Mathieu, et al.
Transplantation|May 1, 1992
Orthotopic liver transplantation for type 1 Gaucher's diseaseC DuCerf, B Bancel, P Caillon, et al.
Pediatrie|January 1, 1988
[Hypertrophic kidneys in utero and neonatal renal failure caused by diffuse mesangial sclerosis]B Parchoux, J Bourgeois, J Gilly, et al.
Journal De Genetique Humaine|March 1, 1982
[Acetylcholinesterase of amniotic fluid: application to prenatal diagnosis of neural tube closing defects. I. Quantitative tests]S Guibaud, A Simplot, M Bonnet, et al.
Journal De Genetique Humaine|January 1, 1989
[Results of pregnancies characterized by a decrease in the level of alpha-fetoprotein in the maternal blood]S Guibaud, C Boisson, A Simplot, et al.
Journal De Genetique Humaine|June 1, 1982
[Amniotic fluid acetylcholinesterase and prenatal diagnosis of neural tube defects. II. Qualitative test]S Guibaud, A Simplot, M Bonnet, et al.
Pageof 15