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Didier Bessis

Showing results (121-130 of 165) with videos related to

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Journal of the American Academy of Dermatology|April 14, 2020
Clinical and pathological dermatological features of deficiency of adenosine deaminase 2: A multicenter, retrospective, observational studyFrançois Chasset, Antoine Fayand, Philippe Moguelet, et al.
JAMA Dermatology|May 14, 2025
Clinical, Histopathologic, and Molecular Features and Treatment of Multiple Xanthogranuloma in AdultsElissa Annabi, Thibault Mahévas, François Chasset, et al.
Orphanet Journal of Rare Diseases|April 27, 2025
Neurofibromatosis-Noonan syndrome: a prospective monocentric study of 26 patients and literature reviewDidier Bessis, Dominique Vidaud, Pierre Meyer, et al.
European Journal of Medical Genetics|August 30, 2011
Systematic search for neutropenia should be part of the first screening in patients with poikilodermaJuliette Piard, Muriel Holder-Espinasse, Bernard Aral, et al.
European Journal of Pediatrics|July 11, 2023
Accurate diagnosis of acute hemorrhagic edema of infancy: a French multicenter observational studySophie Leducq, Annabel Maruani, Christine Bodemer, et al.
Seminars in Arthritis and Rheumatism|September 27, 2021
DADA2 diagnosed in adulthood versus childhood: A comparative study on 306 patients including a systematic literature review and 12 French casesAntoine Fayand, François Chasset, David Boutboul, et al.
Journal of the American Academy of Dermatology|April 6, 2018
Cutis laxa associated with monoclonal gammopathy: 14 new cases and review of the literatureMarie Jachiet, Stéphanie Harel, Anne Saussine, et al.
Familial Cancer|January 22, 2010
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndromePia Vahteristo, Taru A Koski, Laura Näätsaari, et al.
The British Journal of Dermatology|April 16, 2024
Clinical phenotype of the PIK3R1-related vascular overgrowth syndromePaul Kuentz, Camille Engel, Mathieu Laeng, et al.
Acta Dermato-Venereologica|November 8, 2017
Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results from the French National Paediatric Cohort CONAPEAnnabel Maruani, Marine Durieux-Verde, Juliette Mazereeuw-Hautier, et al.
Pageof 17

Showing results (121-130 of 165) with videos related to

Sort By:
Pageof 17
Journal of the American Academy of Dermatology|April 14, 2020
Clinical and pathological dermatological features of deficiency of adenosine deaminase 2: A multicenter, retrospective, observational studyFrançois Chasset, Antoine Fayand, Philippe Moguelet, et al.
JAMA Dermatology|May 14, 2025
Clinical, Histopathologic, and Molecular Features and Treatment of Multiple Xanthogranuloma in AdultsElissa Annabi, Thibault Mahévas, François Chasset, et al.
Orphanet Journal of Rare Diseases|April 27, 2025
Neurofibromatosis-Noonan syndrome: a prospective monocentric study of 26 patients and literature reviewDidier Bessis, Dominique Vidaud, Pierre Meyer, et al.
European Journal of Medical Genetics|August 30, 2011
Systematic search for neutropenia should be part of the first screening in patients with poikilodermaJuliette Piard, Muriel Holder-Espinasse, Bernard Aral, et al.
European Journal of Pediatrics|July 11, 2023
Accurate diagnosis of acute hemorrhagic edema of infancy: a French multicenter observational studySophie Leducq, Annabel Maruani, Christine Bodemer, et al.
Seminars in Arthritis and Rheumatism|September 27, 2021
DADA2 diagnosed in adulthood versus childhood: A comparative study on 306 patients including a systematic literature review and 12 French casesAntoine Fayand, François Chasset, David Boutboul, et al.
Journal of the American Academy of Dermatology|April 6, 2018
Cutis laxa associated with monoclonal gammopathy: 14 new cases and review of the literatureMarie Jachiet, Stéphanie Harel, Anne Saussine, et al.
Familial Cancer|January 22, 2010
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndromePia Vahteristo, Taru A Koski, Laura Näätsaari, et al.
The British Journal of Dermatology|April 16, 2024
Clinical phenotype of the PIK3R1-related vascular overgrowth syndromePaul Kuentz, Camille Engel, Mathieu Laeng, et al.
Acta Dermato-Venereologica|November 8, 2017
Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results from the French National Paediatric Cohort CONAPEAnnabel Maruani, Marine Durieux-Verde, Juliette Mazereeuw-Hautier, et al.
Pageof 17