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B Puech

Showing results (31-40 of 40) with videos related to

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Acta Chirurgica Belgica|January 1, 1977
[Isotopic criteria for the assessment of the effects of lumbar sympathectomy (author's transl)]L Mamère, X Quancard, B Masson, et al.
Clinical Chemistry|July 1, 1992
Rapid diagnosis of mitochondrial mutation at position 11778-associated Leber hereditary optic neuropathyV Dumur, G Lalau, P Boone, et al.
American Journal of Medical Genetics|March 21, 1998
Blau syndrome of granulomatous arthritis, iritis, and skin rash: a new family and review of the literatureS Manouvrier-Hanu, B Puech, F Piette, et al.
Journal Francais D'Ophtalmologie|March 19, 2004
[Congenital achromatopsia: electroretinogram in early diagnosis]S Defoort-Dhellemmes, T Lebrun, C F Arndt, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 22, 2019
Thoracic ultrasound accuracy for the investigation of initial neonatal respiratory distressC Grimaldi, F Michel, V Brévaut-Malaty, et al.
Lancet (London, England)|August 8, 1992
Diagnosis of Leber's hereditary optic neuropathy without neurological abnormalitiesP Labalette, J C Hache, B Hemery, et al.
Bulletin De La Societe De Pathologie Exotique (1990)|February 27, 2014
Family tetrodotoxin poisoning in Reunion Island (Southwest Indian Ocean) following the consumption of Lagocephalus sceleratus (Pufferfish)B Puech, B Batsalle, P Roget, et al.
The Journal of Pediatrics|February 1, 1996
Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathyJ L Michaud, E Héon, F Guilbert, et al.
Molecular Vision|January 5, 2000
North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysisK W Small, N Udar, S Yelchits, et al.
Human Mutation|March 10, 2001
Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophyD Marchant, K Gogat, S Boutboul, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Acta Chirurgica Belgica|January 1, 1977
[Isotopic criteria for the assessment of the effects of lumbar sympathectomy (author's transl)]L Mamère, X Quancard, B Masson, et al.
Clinical Chemistry|July 1, 1992
Rapid diagnosis of mitochondrial mutation at position 11778-associated Leber hereditary optic neuropathyV Dumur, G Lalau, P Boone, et al.
American Journal of Medical Genetics|March 21, 1998
Blau syndrome of granulomatous arthritis, iritis, and skin rash: a new family and review of the literatureS Manouvrier-Hanu, B Puech, F Piette, et al.
Journal Francais D'Ophtalmologie|March 19, 2004
[Congenital achromatopsia: electroretinogram in early diagnosis]S Defoort-Dhellemmes, T Lebrun, C F Arndt, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 22, 2019
Thoracic ultrasound accuracy for the investigation of initial neonatal respiratory distressC Grimaldi, F Michel, V Brévaut-Malaty, et al.
Lancet (London, England)|August 8, 1992
Diagnosis of Leber's hereditary optic neuropathy without neurological abnormalitiesP Labalette, J C Hache, B Hemery, et al.
Bulletin De La Societe De Pathologie Exotique (1990)|February 27, 2014
Family tetrodotoxin poisoning in Reunion Island (Southwest Indian Ocean) following the consumption of Lagocephalus sceleratus (Pufferfish)B Puech, B Batsalle, P Roget, et al.
The Journal of Pediatrics|February 1, 1996
Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathyJ L Michaud, E Héon, F Guilbert, et al.
Molecular Vision|January 5, 2000
North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysisK W Small, N Udar, S Yelchits, et al.
Human Mutation|March 10, 2001
Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophyD Marchant, K Gogat, S Boutboul, et al.
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