Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

L MICHAUD

Showing results (401-410 of 509) with videos related to

Pageof 51
Sort By:
Presse Medicale (Paris, France : 1983)|February 7, 1998
[Thymic and bronchial neuroendocrine tumors in multiple endocrine neoplasia type 1. GENEM1]A Murat, M F Heymann, S Bernat, et al.
The International Journal of Behavioral Nutrition and Physical Activity|May 6, 2025
Developing an implementation fidelity measure for a family healthy weight programCaitlin A Golden, Paul A Estabrooks, Kate A Heelan, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Identification of a novel in-frame de novo mutation in SPTAN1 in intellectual disability and pontocerebellar atrophyFadi F Hamdan, Hirotomo Saitsu, Kiyomi Nishiyama, et al.
American Journal of Medical Genetics. Part A|October 18, 2016
Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changesFarah R Zahir, Tracy Tucker, Sonia Mayo, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1996
[Heart-lung transplantation and cystic fibrosis. Indications and results]A Haloun, P Despins, D Horeau, et al.
American Journal of Human Genetics|April 25, 2017
Dysfunction of the Cerebral Glucose Transporter SLC45A1 in Individuals with Intellectual Disability and EpilepsyMyriam Srour, Noriaki Shimokawa, Fadi F Hamdan, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|January 18, 2015
[Imagery of treated prostate cancer]R Renard-Penna, L Michaud, L Cormier, et al.
European Journal of Neurology|November 8, 2018
MYOD1 involvement in myopathyF Lopes, M Miguet, B E Mucha, et al.
American Journal of Medical Genetics. Part A|January 21, 2016
A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature reviewNancy Merner, Baudouin Forgeot d'Arc, Scott C Bell, et al.
Clinical Genetics|March 19, 2013
Polymicrogyria with dysmorphic basal ganglia? Think tubulin!D Amrom, I Tanyalçin, H Verhelst, et al.
Pageof 51

Showing results (401-410 of 509) with videos related to

Sort By:
Pageof 51
Presse Medicale (Paris, France : 1983)|February 7, 1998
[Thymic and bronchial neuroendocrine tumors in multiple endocrine neoplasia type 1. GENEM1]A Murat, M F Heymann, S Bernat, et al.
The International Journal of Behavioral Nutrition and Physical Activity|May 6, 2025
Developing an implementation fidelity measure for a family healthy weight programCaitlin A Golden, Paul A Estabrooks, Kate A Heelan, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Identification of a novel in-frame de novo mutation in SPTAN1 in intellectual disability and pontocerebellar atrophyFadi F Hamdan, Hirotomo Saitsu, Kiyomi Nishiyama, et al.
American Journal of Medical Genetics. Part A|October 18, 2016
Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changesFarah R Zahir, Tracy Tucker, Sonia Mayo, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1996
[Heart-lung transplantation and cystic fibrosis. Indications and results]A Haloun, P Despins, D Horeau, et al.
American Journal of Human Genetics|April 25, 2017
Dysfunction of the Cerebral Glucose Transporter SLC45A1 in Individuals with Intellectual Disability and EpilepsyMyriam Srour, Noriaki Shimokawa, Fadi F Hamdan, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|January 18, 2015
[Imagery of treated prostate cancer]R Renard-Penna, L Michaud, L Cormier, et al.
European Journal of Neurology|November 8, 2018
MYOD1 involvement in myopathyF Lopes, M Miguet, B E Mucha, et al.
American Journal of Medical Genetics. Part A|January 21, 2016
A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature reviewNancy Merner, Baudouin Forgeot d'Arc, Scott C Bell, et al.
Clinical Genetics|March 19, 2013
Polymicrogyria with dysmorphic basal ganglia? Think tubulin!D Amrom, I Tanyalçin, H Verhelst, et al.
Pageof 51