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Eulalie Lasseaux

Showing results (1-10 of 51) with videos related to

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The Journal of Investigative Dermatology|December 30, 2019
Albinism: An Underdiagnosed ConditionBenoit Arveiler, Vincent Michaud, Eulalie Lasseaux
Presse Medicale (Paris, France : 1983)|July 24, 2017
[Clinical and genetic aspects of albinism]Benoit Arveiler, Eulalie Lasseaux, Fanny Morice-Picard
HLA|August 22, 2023
Characterization of the novel HLA-DRB1*11:01:01:12N allele by sequencing-based typingMarine Cargou, Vincent Elsermans, Charlotte A Cambridge, et al.
Pigment Cell & Melanoma Research|January 11, 2026
First Report of Oculocutaneous Albinism Type I Among Baka Pygmies From CameroonAlain Froment, Paul Verdu, Claudio Plaisant, et al.
Clinical and Experimental Dermatology|August 7, 2024
Hypohidrotic ectodermal dysplasia in a family: expanding spectrum of LEF1-related disordersAli Hassan, Fanny Morice-Picard, Victor Marin, et al.
European Journal of Medical Genetics|August 14, 2022
Co-occurrence of oculocutaneous albinism type 2 and mild sickle cell disease explained by HbS/βthal genotype in an individual from the Democratic Republic of CongoRobert Aquaron, Eulalie Lasseaux, Joseph Kelekele, et al.
Clinical and Experimental Dermatology|May 4, 2023
A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosisFanny Morice-Picard, Pierre-Louis Lanvin, Eulalie Lasseaux, et al.
Ophthalmic Genetics|April 4, 2019
Clinical and molecular findings of FRMD7 related congenital nystagmus as adifferential diagnosis of ocular albinismVincent Michaud, Sabine Defoort-Dhellemmes, Isabelle Drumare, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 26, 2024
Crossed VEP asymmetry in a patient with AHR-linked infantile nystagmus and foveal hypoplasiaVasily M Smirnov, Eulalie Lasseaux, Vincent Michaud, et al.
European Journal of Medical Genetics|March 5, 2021
CHN1 and duane retraction syndrome: Expanding the phenotype to cranial nerves development diseaseChloé Angelini, Aurélien Trimouille, Benoit Arveiler, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
The Journal of Investigative Dermatology|December 30, 2019
Albinism: An Underdiagnosed ConditionBenoit Arveiler, Vincent Michaud, Eulalie Lasseaux
Presse Medicale (Paris, France : 1983)|July 24, 2017
[Clinical and genetic aspects of albinism]Benoit Arveiler, Eulalie Lasseaux, Fanny Morice-Picard
HLA|August 22, 2023
Characterization of the novel HLA-DRB1*11:01:01:12N allele by sequencing-based typingMarine Cargou, Vincent Elsermans, Charlotte A Cambridge, et al.
Pigment Cell & Melanoma Research|January 11, 2026
First Report of Oculocutaneous Albinism Type I Among Baka Pygmies From CameroonAlain Froment, Paul Verdu, Claudio Plaisant, et al.
Clinical and Experimental Dermatology|August 7, 2024
Hypohidrotic ectodermal dysplasia in a family: expanding spectrum of LEF1-related disordersAli Hassan, Fanny Morice-Picard, Victor Marin, et al.
European Journal of Medical Genetics|August 14, 2022
Co-occurrence of oculocutaneous albinism type 2 and mild sickle cell disease explained by HbS/βthal genotype in an individual from the Democratic Republic of CongoRobert Aquaron, Eulalie Lasseaux, Joseph Kelekele, et al.
Clinical and Experimental Dermatology|May 4, 2023
A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosisFanny Morice-Picard, Pierre-Louis Lanvin, Eulalie Lasseaux, et al.
Ophthalmic Genetics|April 4, 2019
Clinical and molecular findings of FRMD7 related congenital nystagmus as adifferential diagnosis of ocular albinismVincent Michaud, Sabine Defoort-Dhellemmes, Isabelle Drumare, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 26, 2024
Crossed VEP asymmetry in a patient with AHR-linked infantile nystagmus and foveal hypoplasiaVasily M Smirnov, Eulalie Lasseaux, Vincent Michaud, et al.
European Journal of Medical Genetics|March 5, 2021
CHN1 and duane retraction syndrome: Expanding the phenotype to cranial nerves development diseaseChloé Angelini, Aurélien Trimouille, Benoit Arveiler, et al.
Pageof 6