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Bocquet

Showing results (831-840 of 844) with videos related to

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Physical Review Letters|September 28, 2010
Limits on light-speed anisotropies from Compton scattering of high-energy electronsJ-P Bocquet, D Moricciani, V Bellini, et al.
Scientific Reports|May 3, 2018
Dietary, environmental, and genetic risk factors of Extensive Macular Atrophy with Pseudodrusen, a severe bilateral macular atrophy of middle-aged patientsAymeric Douillard, Marie-Christine Picot, Cécile Delcourt, et al.
EMBO Molecular Medicine|June 17, 2026
Systems serology identifies FcR-related autoantibody signatures and functions for Sjögren's syndromeMartin Killian, Suzanne K Shoffner-Beck, Timon Damelang, et al.
The Journal of Allergy and Clinical Immunology. in Practice|May 30, 2025
Parameters Linked With Higher Itch Severity in Chronic Spontaneous Urticaria-Chronic Urticaria Registry ResultsJules Stolz, Pascale Salameh, Riccardo Asero, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 18, 2025
Sex matters in CSU: Women face greater burden and poorer urticaria control, especially in midlife-CURE insightsEmek Kocatürk, Pascale Salameh, Riccardo Asero, et al.
Investigative Ophthalmology & Visual Science|February 21, 2025
Elevated Plasma Complement Factors in CRB1-Associated Inherited Retinal DystrophiesLude Moekotte, Joke H de Boer, Sanne Hiddingh, et al.
Human Mutation|March 25, 2022
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsiaMaria Solaki, Britta Baumann, Peggy Reuter, et al.
Diagnostic and Interventional Imaging|March 20, 2019
Five simultaneous artificial intelligence data challenges on ultrasound, CT, and MRIN Lassau, T Estienne, P de Vomecourt, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Biallelic germline variants in the hematologic malignancy predisposition gene <i>DDX41</i> cause retinal dystrophy through dysregulation of retinal homeostasisZoéline Mars, Andrea Zanetti, Karolina Kaminska, et al.
Frontiers in Cell and Developmental Biology|February 23, 2023
Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosisDaan M Panneman, Rebekkah J Hitti-Malin, Lara K Holtes, et al.
Pageof 85

Showing results (831-840 of 844) with videos related to

Sort By:
Pageof 85
Physical Review Letters|September 28, 2010
Limits on light-speed anisotropies from Compton scattering of high-energy electronsJ-P Bocquet, D Moricciani, V Bellini, et al.
Scientific Reports|May 3, 2018
Dietary, environmental, and genetic risk factors of Extensive Macular Atrophy with Pseudodrusen, a severe bilateral macular atrophy of middle-aged patientsAymeric Douillard, Marie-Christine Picot, Cécile Delcourt, et al.
EMBO Molecular Medicine|June 17, 2026
Systems serology identifies FcR-related autoantibody signatures and functions for Sjögren's syndromeMartin Killian, Suzanne K Shoffner-Beck, Timon Damelang, et al.
The Journal of Allergy and Clinical Immunology. in Practice|May 30, 2025
Parameters Linked With Higher Itch Severity in Chronic Spontaneous Urticaria-Chronic Urticaria Registry ResultsJules Stolz, Pascale Salameh, Riccardo Asero, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 18, 2025
Sex matters in CSU: Women face greater burden and poorer urticaria control, especially in midlife-CURE insightsEmek Kocatürk, Pascale Salameh, Riccardo Asero, et al.
Investigative Ophthalmology & Visual Science|February 21, 2025
Elevated Plasma Complement Factors in CRB1-Associated Inherited Retinal DystrophiesLude Moekotte, Joke H de Boer, Sanne Hiddingh, et al.
Human Mutation|March 25, 2022
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsiaMaria Solaki, Britta Baumann, Peggy Reuter, et al.
Diagnostic and Interventional Imaging|March 20, 2019
Five simultaneous artificial intelligence data challenges on ultrasound, CT, and MRIN Lassau, T Estienne, P de Vomecourt, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Biallelic germline variants in the hematologic malignancy predisposition gene <i>DDX41</i> cause retinal dystrophy through dysregulation of retinal homeostasisZoéline Mars, Andrea Zanetti, Karolina Kaminska, et al.
Frontiers in Cell and Developmental Biology|February 23, 2023
Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosisDaan M Panneman, Rebekkah J Hitti-Malin, Lara K Holtes, et al.
Pageof 85