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Showing results (171-180 of 182) with videos related to

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Survey of Ophthalmology|April 21, 2015
The potential of 3T high-resolution magnetic resonance imaging for diagnosis, staging, and follow-up of retinoblastomaMarcus C de Jong, Pim de Graaf, Hervé J Brisse, et al.
Ophthalmic Plastic and Reconstructive Surgery|April 15, 2004
Cutaneous benign mixed tumor (chondroid syringoma) of the eyelid: clinical presentation and managementJohn T H Mandeville, Joo Heon Roh, John J Woog, et al.
Clinical Genetics|March 25, 2018
Single, short in-del, and copy number variations detection in monogenic dyslipidemia using a next-generation sequencing strategyO Marmontel, S Charrière, T Simonet, et al.
American Journal of Human Genetics|October 18, 2016
Comprehensive Genetic Landscape of Uveal Melanoma by Whole-Genome SequencingBeryl Royer-Bertrand, Matteo Torsello, Donata Rimoldi, et al.
Diabetes & Metabolism|January 3, 2012
Consensus statement on the care of the hyperglycaemic/diabetic patient during and in the immediate follow-up of acute coronary syndromeB Vergès, A Avignon, F Bonnet, et al.
Archives of Cardiovascular Diseases|July 19, 2012
Consensus statement on the care of the hyperglycaemic/diabetic patient during and in the immediate follow-up of acute coronary syndromeB Vergès, A Avignon, F Bonnet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 8, 2008
[Recommendations for the management of bone demineralization in cystic fibrosis]I Sermet-Gaudelus, R Nove-Josserand, G-A Loeille, et al.
American Journal of Human Genetics|January 25, 2024
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunctionMiriam Bauwens, Elifnaz Celik, Dinah Zur, et al.
American Journal of Human Genetics|February 26, 2026
Loss-of-function variants in SAXO6, encoding a microtubule inner protein of photoreceptor cilia, causes a late-onset retinal dystrophyAbigail R Moye, Caitlyn L McCafferty, Siying Lin, et al.
American Journal of Human Genetics|September 3, 2016
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia DefectsKonstantinos Nikopoulos, Pietro Farinelli, Basilio Giangreco, et al.
Pageof 19

Showing results (171-180 of 182) with videos related to

Sort By:
Pageof 19
Survey of Ophthalmology|April 21, 2015
The potential of 3T high-resolution magnetic resonance imaging for diagnosis, staging, and follow-up of retinoblastomaMarcus C de Jong, Pim de Graaf, Hervé J Brisse, et al.
Ophthalmic Plastic and Reconstructive Surgery|April 15, 2004
Cutaneous benign mixed tumor (chondroid syringoma) of the eyelid: clinical presentation and managementJohn T H Mandeville, Joo Heon Roh, John J Woog, et al.
Clinical Genetics|March 25, 2018
Single, short in-del, and copy number variations detection in monogenic dyslipidemia using a next-generation sequencing strategyO Marmontel, S Charrière, T Simonet, et al.
American Journal of Human Genetics|October 18, 2016
Comprehensive Genetic Landscape of Uveal Melanoma by Whole-Genome SequencingBeryl Royer-Bertrand, Matteo Torsello, Donata Rimoldi, et al.
Diabetes & Metabolism|January 3, 2012
Consensus statement on the care of the hyperglycaemic/diabetic patient during and in the immediate follow-up of acute coronary syndromeB Vergès, A Avignon, F Bonnet, et al.
Archives of Cardiovascular Diseases|July 19, 2012
Consensus statement on the care of the hyperglycaemic/diabetic patient during and in the immediate follow-up of acute coronary syndromeB Vergès, A Avignon, F Bonnet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 8, 2008
[Recommendations for the management of bone demineralization in cystic fibrosis]I Sermet-Gaudelus, R Nove-Josserand, G-A Loeille, et al.
American Journal of Human Genetics|January 25, 2024
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunctionMiriam Bauwens, Elifnaz Celik, Dinah Zur, et al.
American Journal of Human Genetics|February 26, 2026
Loss-of-function variants in SAXO6, encoding a microtubule inner protein of photoreceptor cilia, causes a late-onset retinal dystrophyAbigail R Moye, Caitlyn L McCafferty, Siying Lin, et al.
American Journal of Human Genetics|September 3, 2016
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia DefectsKonstantinos Nikopoulos, Pietro Farinelli, Basilio Giangreco, et al.
Pageof 19