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Journal of the American Academy of Dermatology
|
August 21, 2013
Angiosarcoma in patients with xeroderma pigmentosum: less aggressive and not so rare?
Raymond Karkouche, Delphine Kerob, Maxime Battistella, et al.
American Journal of Medical Genetics. Part A
|
March 27, 2024
Familial recurrence of incontinentia pigmenti due to de novo pathogenic variants in the IKBKG gene
Julie Steffann, Judite De Oliveira Santos, Anne-Laure Zelbin, et al.
Orphanet Journal of Rare Diseases
|
August 29, 2020
Early management of sight threatening retinopathy in incontinentia pigmenti
Sarah Michel, Clothilde Reynaud, Alejandra Daruich, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 8, 2010
Crouzon syndrome with acanthosis nigricans: a case-based update
Federico Di Rocco, Corinne Collet, Laurence Legeai-Mallet, et al.
Presse Medicale (Paris, France : 1983)
|
June 6, 2026
Dyadic adjustment and quality of life in albinism:a pilot study on their shared lived experiences with their loved ones
Hugo Fournier, Nicolas Pillaud, Marie Hasdenteufel, et al.
JAMA Dermatology
|
February 25, 2026
Dupilumab Use in Severe Epidermolysis Bullosa Simplex
Orsola Crespi, Nathalia Bellon, Julie Bonigen, et al.
JAMA Dermatology
|
January 3, 2020
Use of Epidermal Growth Factor Receptor Inhibitor Erlotinib to Treat Palmoplantar Keratoderma in Patients With Olmsted Syndrome Caused by TRPV3 Mutations
Céline Greco, Stéphanie Leclerc-Mercier, Sarah Chaumon, et al.
The Journal of Investigative Dermatology
|
September 18, 2023
PRIMA-1<sup>MET</sup>/APR-246 Can Partially Rescue In Vitro Cell Adhesion of Patient-Derived Junctional Epidermolysis Bullosa Epidermal Cells
Clément Berthy, Laurent Gagnoux-Palacios, Marine Madrange, et al.
Human Molecular Genetics
|
September 28, 2002
The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes
Asma Smahi, Gilles Courtois, Smail Hadj Rabia, et al.
Acta Dermato-Venereologica
|
June 8, 2010
Phacomatosis pigmentokeratotica with nephroblastoma and juvenile hypertension
Simon Jacobelli, Stéphanie Leclerc-Mercier, Rémi Salomon, et al.
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of 13
Search research articles
Search
Showing results (31-40 of 125) with videos related to
Sort By:
Page
of 13
Journal of the American Academy of Dermatology
|
August 21, 2013
Angiosarcoma in patients with xeroderma pigmentosum: less aggressive and not so rare?
Raymond Karkouche, Delphine Kerob, Maxime Battistella, et al.
American Journal of Medical Genetics. Part A
|
March 27, 2024
Familial recurrence of incontinentia pigmenti due to de novo pathogenic variants in the IKBKG gene
Julie Steffann, Judite De Oliveira Santos, Anne-Laure Zelbin, et al.
Orphanet Journal of Rare Diseases
|
August 29, 2020
Early management of sight threatening retinopathy in incontinentia pigmenti
Sarah Michel, Clothilde Reynaud, Alejandra Daruich, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 8, 2010
Crouzon syndrome with acanthosis nigricans: a case-based update
Federico Di Rocco, Corinne Collet, Laurence Legeai-Mallet, et al.
Presse Medicale (Paris, France : 1983)
|
June 6, 2026
Dyadic adjustment and quality of life in albinism:a pilot study on their shared lived experiences with their loved ones
Hugo Fournier, Nicolas Pillaud, Marie Hasdenteufel, et al.
JAMA Dermatology
|
February 25, 2026
Dupilumab Use in Severe Epidermolysis Bullosa Simplex
Orsola Crespi, Nathalia Bellon, Julie Bonigen, et al.
JAMA Dermatology
|
January 3, 2020
Use of Epidermal Growth Factor Receptor Inhibitor Erlotinib to Treat Palmoplantar Keratoderma in Patients With Olmsted Syndrome Caused by TRPV3 Mutations
Céline Greco, Stéphanie Leclerc-Mercier, Sarah Chaumon, et al.
The Journal of Investigative Dermatology
|
September 18, 2023
PRIMA-1<sup>MET</sup>/APR-246 Can Partially Rescue In Vitro Cell Adhesion of Patient-Derived Junctional Epidermolysis Bullosa Epidermal Cells
Clément Berthy, Laurent Gagnoux-Palacios, Marine Madrange, et al.
Human Molecular Genetics
|
September 28, 2002
The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes
Asma Smahi, Gilles Courtois, Smail Hadj Rabia, et al.
Acta Dermato-Venereologica
|
June 8, 2010
Phacomatosis pigmentokeratotica with nephroblastoma and juvenile hypertension
Simon Jacobelli, Stéphanie Leclerc-Mercier, Rémi Salomon, et al.
Page
of 13