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Smail Hadj-Rabia

Showing results (91-100 of 125) with videos related to

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The British Journal of Dermatology|July 15, 2025
Prevalence of Kidney Complications in a Large Cohort of Patients with Recessive Dystrophic Epidermolysis BullosaIdris Boudhabhay, Nathalia Bellon, Marina Avramescu, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 6, 2025
Expanding PIGM-related disorders to coding mutationsRomain Nicolle, Laura Russell, Véronique Abadie, et al.
Orphanet Journal of Rare Diseases|February 28, 2013
Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneitySmail Hadj-Rabia, Bert L Callewaert, Emmanuelle Bourrat, et al.
Genes|December 23, 2022
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly UpdateNicolai Peschel, John T Wright, Maranke I Koster, et al.
The Journal of Investigative Dermatology|January 8, 2010
A prevalent mutation with founder effect in xeroderma pigmentosum group C from north AfricaNadem Soufir, Cecile Ged, Agnes Bourillon, et al.
Pediatric Dermatology|July 13, 2023
Effectiveness of biologic therapies in children with palmoplantar plaque psoriasis: An analysis of real-life data from the BiPe cohortsBochra Hanafi, Alain Beauchet, Vito Di Lernia, et al.
European Journal of Human Genetics : EJHG|August 24, 2018
New splicing pathogenic variant in EBP causing extreme familial variability of Conradi-Hünermann-Happle SyndromeMathilde Pacault, Marie Vincent, Thomas Besnard, et al.
Pediatrics|June 4, 2002
Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his motherSophie Dupuis-Girod, Nadège Corradini, Smail Hadj-Rabia, et al.
Annals of the New York Academy of Sciences|July 29, 2022
Impact of claudin-10 deficiency on amelogenesis: Lesson from a HELIX toothNicolas Obtel, Adeline Le Cabec, Thè Nghia Nguyen, et al.
Journal of the American Academy of Dermatology|August 16, 2011
Folliculocystic and collagen hamartoma of tuberous sclerosis complexAntonio Torrelo, Smail Hadj-Rabia, Isabel Colmenero, et al.
Pageof 13

Showing results (91-100 of 125) with videos related to

Sort By:
Pageof 13
The British Journal of Dermatology|July 15, 2025
Prevalence of Kidney Complications in a Large Cohort of Patients with Recessive Dystrophic Epidermolysis BullosaIdris Boudhabhay, Nathalia Bellon, Marina Avramescu, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 6, 2025
Expanding PIGM-related disorders to coding mutationsRomain Nicolle, Laura Russell, Véronique Abadie, et al.
Orphanet Journal of Rare Diseases|February 28, 2013
Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneitySmail Hadj-Rabia, Bert L Callewaert, Emmanuelle Bourrat, et al.
Genes|December 23, 2022
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly UpdateNicolai Peschel, John T Wright, Maranke I Koster, et al.
The Journal of Investigative Dermatology|January 8, 2010
A prevalent mutation with founder effect in xeroderma pigmentosum group C from north AfricaNadem Soufir, Cecile Ged, Agnes Bourillon, et al.
Pediatric Dermatology|July 13, 2023
Effectiveness of biologic therapies in children with palmoplantar plaque psoriasis: An analysis of real-life data from the BiPe cohortsBochra Hanafi, Alain Beauchet, Vito Di Lernia, et al.
European Journal of Human Genetics : EJHG|August 24, 2018
New splicing pathogenic variant in EBP causing extreme familial variability of Conradi-Hünermann-Happle SyndromeMathilde Pacault, Marie Vincent, Thomas Besnard, et al.
Pediatrics|June 4, 2002
Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his motherSophie Dupuis-Girod, Nadège Corradini, Smail Hadj-Rabia, et al.
Annals of the New York Academy of Sciences|July 29, 2022
Impact of claudin-10 deficiency on amelogenesis: Lesson from a HELIX toothNicolas Obtel, Adeline Le Cabec, Thè Nghia Nguyen, et al.
Journal of the American Academy of Dermatology|August 16, 2011
Folliculocystic and collagen hamartoma of tuberous sclerosis complexAntonio Torrelo, Smail Hadj-Rabia, Isabel Colmenero, et al.
Pageof 13