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C Labrèze

Showing results (11-20 of 18) with videos related to

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American Journal of Medical Genetics. Part A|December 25, 2009
An unusual severe vascular case of pseudoxanthoma elasticum presenting as generalized arterial calcification of infancyG Le Boulanger, C Labrèze, A Croué, et al.
The Journal of Investigative Dermatology|July 17, 1998
A variable monilethrix phenotype associated with a novel mutation, Glu402Lys, in the helix termination motif of the type II hair keratin hHb1H Winter, C Labrèze, V Chapalain, et al.
Cardiovascular and Interventional Radiology|April 1, 2017
Percutaneous Image-Guided Cryoablation as Second-Line Therapy of Soft-Tissue Venous Vascular Malformations of Extremities: A Prospective Study of Safety and 6-Month EfficacyF H Cornelis, C Labrèze, V Pinsolle, et al.
Annales De Dermatologie Et De Venereologie|August 4, 2006
[Cutaneous leishmania in HIV patient in Ouagadougou: clinical and therapeutic aspects]P Niamba, A Traoré, O Goumbri-Lompo, et al.
Pediatric Dermatology|July 8, 2000
Asymmetric periflexural exanthem of childhood: microbiologic case-control studyD Coustou, B Masquelier, M E Lafon, et al.
Nature Genetics|August 1, 1997
Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrixH Winter, M A Rogers, L Langbein, et al.
The British Journal of Dermatology|November 21, 2013
Aplasia cutis congenita with dystrophic epidermolysis bullosa: clinical and mutational studyC Chiaverini, A Charlesworth, A Fernandez, et al.
Molecular Syndromology|June 27, 2013
Genotypes and phenotypes of 162 families with a glomulin mutationP Brouillard, L M Boon, N Revencu, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
American Journal of Medical Genetics. Part A|December 25, 2009
An unusual severe vascular case of pseudoxanthoma elasticum presenting as generalized arterial calcification of infancyG Le Boulanger, C Labrèze, A Croué, et al.
The Journal of Investigative Dermatology|July 17, 1998
A variable monilethrix phenotype associated with a novel mutation, Glu402Lys, in the helix termination motif of the type II hair keratin hHb1H Winter, C Labrèze, V Chapalain, et al.
Cardiovascular and Interventional Radiology|April 1, 2017
Percutaneous Image-Guided Cryoablation as Second-Line Therapy of Soft-Tissue Venous Vascular Malformations of Extremities: A Prospective Study of Safety and 6-Month EfficacyF H Cornelis, C Labrèze, V Pinsolle, et al.
Annales De Dermatologie Et De Venereologie|August 4, 2006
[Cutaneous leishmania in HIV patient in Ouagadougou: clinical and therapeutic aspects]P Niamba, A Traoré, O Goumbri-Lompo, et al.
Pediatric Dermatology|July 8, 2000
Asymmetric periflexural exanthem of childhood: microbiologic case-control studyD Coustou, B Masquelier, M E Lafon, et al.
Nature Genetics|August 1, 1997
Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrixH Winter, M A Rogers, L Langbein, et al.
The British Journal of Dermatology|November 21, 2013
Aplasia cutis congenita with dystrophic epidermolysis bullosa: clinical and mutational studyC Chiaverini, A Charlesworth, A Fernandez, et al.
Molecular Syndromology|June 27, 2013
Genotypes and phenotypes of 162 families with a glomulin mutationP Brouillard, L M Boon, N Revencu, et al.
Pageof 2