Search research articles
Contact Us
Filters
Showing results (151-160 of 165) with videos related to
Page
of 17
Sort By:
Nature Genetics
|
October 16, 2019
Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome
Pierre Vabres, Arthur Sorlin, Stanislav S Kholmanskikh, et al.
Nature Genetics
|
October 2, 2019
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome
Pierre Vabres, Arthur Sorlin, Stanislav S Kholmanskikh, et al.
Rheumatology (Oxford, England)
|
April 3, 2023
Anti-SAE autoantibody in dermatomyositis: original comparative study and review of the literature
Juliette Demortier, Mathieu Vautier, Olivier Chosidow, et al.
Nature Genetics
|
February 9, 2020
Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome
Pierre Vabres, Arthur Sorlin, Stanislav S Kholmanskikh, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
November 12, 2014
The clinical spectrum and therapeutic management of hypocomplementemic urticarial vasculitis: data from a French nationwide study of fifty-seven patients
Marie Jachiet, Béatrice Flageul, Alban Deroux, et al.
RMD Open
|
January 5, 2025
Efficacy of valaciclovir in preventing herpes zoster in patients receiving anifrolumab
Ludovic Trefond, Francois Chasset, Marie Jachiet, et al.
Journal of the American Academy of Dermatology
|
November 14, 2020
Trunk involvement and peau d'orange aspect are poor prognostic factors in eosinophilic fasciitis (Shulman disease): A multicenter retrospective study of 119 patients
Elina Zuelgaray, Sylvie Chevret, Marie Jachiet, et al.
Journal of the American Academy of Dermatology
|
February 1, 2022
Dermatoscopic and clinical features of congenital or congenital-type nail matrix nevi: A multicenter prospective cohort study by the International Dermoscopy Society
Félix Pham, Amélie Boespflug, Gérard Duru, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 14, 2021
Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities
Virginie Carmignac, Cyril Mignot, Emmanuelle Blanchard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 9, 2021
Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities
Virginie Carmignac, Cyril Mignot, Emmanuelle Blanchard, et al.
Page
of 17
Search research articles
Search
Showing results (151-160 of 165) with videos related to
Sort By:
Page
of 17
Nature Genetics
|
October 16, 2019
Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome
Pierre Vabres, Arthur Sorlin, Stanislav S Kholmanskikh, et al.
Nature Genetics
|
October 2, 2019
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome
Pierre Vabres, Arthur Sorlin, Stanislav S Kholmanskikh, et al.
Rheumatology (Oxford, England)
|
April 3, 2023
Anti-SAE autoantibody in dermatomyositis: original comparative study and review of the literature
Juliette Demortier, Mathieu Vautier, Olivier Chosidow, et al.
Nature Genetics
|
February 9, 2020
Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome
Pierre Vabres, Arthur Sorlin, Stanislav S Kholmanskikh, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
November 12, 2014
The clinical spectrum and therapeutic management of hypocomplementemic urticarial vasculitis: data from a French nationwide study of fifty-seven patients
Marie Jachiet, Béatrice Flageul, Alban Deroux, et al.
RMD Open
|
January 5, 2025
Efficacy of valaciclovir in preventing herpes zoster in patients receiving anifrolumab
Ludovic Trefond, Francois Chasset, Marie Jachiet, et al.
Journal of the American Academy of Dermatology
|
November 14, 2020
Trunk involvement and peau d'orange aspect are poor prognostic factors in eosinophilic fasciitis (Shulman disease): A multicenter retrospective study of 119 patients
Elina Zuelgaray, Sylvie Chevret, Marie Jachiet, et al.
Journal of the American Academy of Dermatology
|
February 1, 2022
Dermatoscopic and clinical features of congenital or congenital-type nail matrix nevi: A multicenter prospective cohort study by the International Dermoscopy Society
Félix Pham, Amélie Boespflug, Gérard Duru, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 14, 2021
Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities
Virginie Carmignac, Cyril Mignot, Emmanuelle Blanchard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 9, 2021
Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities
Virginie Carmignac, Cyril Mignot, Emmanuelle Blanchard, et al.
Page
of 17