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C Philippe

Showing results (151-160 of 188) with videos related to

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Nature Communications|February 20, 2026
Substorm expansion embedded in a global cycle of field-aligned currents and auroral electrojetsTonghui Wang, Lei Dai, C Philippe Escoubet, et al.
Revue Des Maladies Respiratoires|November 28, 2015
Adaptive servo-ventilation: How does it fit into the treatment of central sleep apnoea syndrome? Expert opinionsP Priou, M-P d'Ortho, T Damy, et al.
American Journal of Human Genetics|April 29, 1998
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterilityS Bione, C Sala, C Manzini, et al.
Human Molecular Genetics|July 1, 1996
Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1S M van der Maarel, I H Scholten, I Huber, et al.
Human Molecular Genetics|May 16, 1998
The UTX gene escapes X inactivation in mice and humansA Greenfield, L Carrel, D Pennisi, et al.
Translational Psychiatry|April 9, 2020
Machine learning classification of ADHD and HC by multimodal serotonergic dataA Kautzky, T Vanicek, C Philippe, et al.
European Journal of Medical Genetics|February 14, 2006
Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular updateC Philippe, L Villard, N De Roux, et al.
Clinical Genetics|March 28, 2012
MEF2C mutations are a rare cause of Rett or severe Rett-like encephalopathiesL Lambert, T Bienvenu, L Allou, et al.
Journal of Autism and Developmental Disorders|December 21, 2006
Development of a video-based evaluation tool in Rett syndromeS Fyfe, J Downs, O McIlroy, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 30, 2021
Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutationsM Theiler, L Weibel, S Christen-Zaech, et al.
Pageof 19

Showing results (151-160 of 188) with videos related to

Sort By:
Pageof 19
Nature Communications|February 20, 2026
Substorm expansion embedded in a global cycle of field-aligned currents and auroral electrojetsTonghui Wang, Lei Dai, C Philippe Escoubet, et al.
Revue Des Maladies Respiratoires|November 28, 2015
Adaptive servo-ventilation: How does it fit into the treatment of central sleep apnoea syndrome? Expert opinionsP Priou, M-P d'Ortho, T Damy, et al.
American Journal of Human Genetics|April 29, 1998
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterilityS Bione, C Sala, C Manzini, et al.
Human Molecular Genetics|July 1, 1996
Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1S M van der Maarel, I H Scholten, I Huber, et al.
Human Molecular Genetics|May 16, 1998
The UTX gene escapes X inactivation in mice and humansA Greenfield, L Carrel, D Pennisi, et al.
Translational Psychiatry|April 9, 2020
Machine learning classification of ADHD and HC by multimodal serotonergic dataA Kautzky, T Vanicek, C Philippe, et al.
European Journal of Medical Genetics|February 14, 2006
Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular updateC Philippe, L Villard, N De Roux, et al.
Clinical Genetics|March 28, 2012
MEF2C mutations are a rare cause of Rett or severe Rett-like encephalopathiesL Lambert, T Bienvenu, L Allou, et al.
Journal of Autism and Developmental Disorders|December 21, 2006
Development of a video-based evaluation tool in Rett syndromeS Fyfe, J Downs, O McIlroy, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 30, 2021
Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutationsM Theiler, L Weibel, S Christen-Zaech, et al.
Pageof 19