Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Morice-Picard

Showing results (1-10 of 26) with videos related to

Pageof 3
Sort By:
Annales De Dermatologie Et De Venereologie|April 23, 2019
[Genetics and dermatology]F Morice-Picard
The British Journal of Dermatology|September 20, 2014
Rare genetic diseases, signalling pathways, and keloid scar formationD Lacombe, F Morice-Picard
Journal of the European Academy of Dermatology and Venereology : JEADV|July 6, 2019
Compound heterozygosity for novel KRT85 variants associated with pure hair and nail ectodermal dysplasiaS Amico, C Ged, A Taïeb, et al.
Clinical and Experimental Dermatology|November 13, 2010
A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalpS Nahum, F Morice-Picard, A Taieb, et al.
The British Journal of Dermatology|August 30, 2007
Severe linear form of granuloma annulare along Blaschko's lines preceding the onset of a classical form of granuloma annulare in a childF Morice-Picard, F Boralevi, S Lepreux, et al.
Annales De Dermatologie Et De Venereologie|June 2, 2026
Multiple cutaneous juvenile xanthogranuloma: a monocentric studyJ Le Bourdon, D Canu, O Letertre, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 24, 2017
ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patientJ Petre, E Lasseaux, C Ged, et al.
Clinical and Experimental Dermatology|February 23, 2020
Lentiginosis and café-au-lait macules as part of the phenotypic spectrum of PAX3-related disordersF Morice-Picard, O Letertre, E Lasseaux, et al.
The British Journal of Dermatology|August 18, 2018
Mosaic mutations in FGFR3 and FGFR2 are associated with naevoid acanthosis nigricans or RAVEN (round and velvety epidermal naevus)M Larsabal, O Cogrel, C Caumont, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 21, 2017
High-dose pulsed corticosteroid therapy combined with methotrexate for severe alopecia areata of childhoodJ H Chong, A Taïeb, F Morice-Picard, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Annales De Dermatologie Et De Venereologie|April 23, 2019
[Genetics and dermatology]F Morice-Picard
The British Journal of Dermatology|September 20, 2014
Rare genetic diseases, signalling pathways, and keloid scar formationD Lacombe, F Morice-Picard
Journal of the European Academy of Dermatology and Venereology : JEADV|July 6, 2019
Compound heterozygosity for novel KRT85 variants associated with pure hair and nail ectodermal dysplasiaS Amico, C Ged, A Taïeb, et al.
Clinical and Experimental Dermatology|November 13, 2010
A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalpS Nahum, F Morice-Picard, A Taieb, et al.
The British Journal of Dermatology|August 30, 2007
Severe linear form of granuloma annulare along Blaschko's lines preceding the onset of a classical form of granuloma annulare in a childF Morice-Picard, F Boralevi, S Lepreux, et al.
Annales De Dermatologie Et De Venereologie|June 2, 2026
Multiple cutaneous juvenile xanthogranuloma: a monocentric studyJ Le Bourdon, D Canu, O Letertre, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 24, 2017
ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patientJ Petre, E Lasseaux, C Ged, et al.
Clinical and Experimental Dermatology|February 23, 2020
Lentiginosis and café-au-lait macules as part of the phenotypic spectrum of PAX3-related disordersF Morice-Picard, O Letertre, E Lasseaux, et al.
The British Journal of Dermatology|August 18, 2018
Mosaic mutations in FGFR3 and FGFR2 are associated with naevoid acanthosis nigricans or RAVEN (round and velvety epidermal naevus)M Larsabal, O Cogrel, C Caumont, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 21, 2017
High-dose pulsed corticosteroid therapy combined with methotrexate for severe alopecia areata of childhoodJ H Chong, A Taïeb, F Morice-Picard, et al.
Pageof 3