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

Laura Gonzalez

Showing results (261-270 of 317) with videos related to

Pageof 32
Sort By:
Clinical and Experimental Medicine|March 1, 2017
Serum levels of P-glycoprotein and persistence of disease activity despite treatment in patients with systemic lupus erythematosusEdsaul Emilio Perez-Guerrero, Jorge Ivan Gamez-Nava, Jose Francisco Muñoz-Valle, et al.
Neuromuscular Disorders : NMD|June 17, 2011
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathyMontse Olivé, Zagaa Odgerel, Amaia Martínez, et al.
Journal of Human Immunity|May 22, 2026
Thymic output in human newborns is shaped by environmental exposures and a common TCRD genetic variantZiyang Tan, Camille Kergaravat, Laura Gonzalez, et al.
Scientific Reports|April 17, 2021
Functional disability is related to serum chemerin levels in rheumatoid arthritisMaria Luisa Vazquez-Villegas, Jorge I Gamez-Nava, A Miriam Saldaña-Cruz, et al.
Genes|May 15, 2020
Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in SpainLidia Gonzalez-Quereda, Maria Jose Rodriguez, Jordi Diaz-Manera, et al.
The Journal of International Medical Research|May 24, 2017
Association of adipokines, interleukin-6, and tumor necrosis factor-α concentrations with clinical characteristics and presence of spinal syndesmophytes in patients with ankylosing spondylitis: A cross-sectional studyLaura Gonzalez-Lopez, Nicte S Fajardo-Robledo, A Miriam Saldaña-Cruz, et al.
American Journal of Human Genetics|November 27, 2010
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with coresNyamkhishig Sambuughin, Kyle S Yau, Montse Olivé, et al.
Brain : a Journal of Neurology|September 28, 2014
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutationsJohann Böhm, Valérie Biancalana, Edoardo Malfatti, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|July 4, 2026
Early Metabolic Risk in Childhood Brain Cancer Survivors with Childhood-Onset Growth Hormone DeficiencyAlice Casiraghi, Olivier Pollé, Clément Bailly, et al.
Plos One|September 10, 2021
Serum chemerin levels: A potential biomarker of joint inflammation in women with rheumatoid arthritisFabiola Gonzalez-Ponce, Jorge I Gamez-Nava, Emilio E Perez-Guerrero, et al.
Pageof 32

Showing results (261-270 of 317) with videos related to

Sort By:
Pageof 32
Clinical and Experimental Medicine|March 1, 2017
Serum levels of P-glycoprotein and persistence of disease activity despite treatment in patients with systemic lupus erythematosusEdsaul Emilio Perez-Guerrero, Jorge Ivan Gamez-Nava, Jose Francisco Muñoz-Valle, et al.
Neuromuscular Disorders : NMD|June 17, 2011
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathyMontse Olivé, Zagaa Odgerel, Amaia Martínez, et al.
Journal of Human Immunity|May 22, 2026
Thymic output in human newborns is shaped by environmental exposures and a common TCRD genetic variantZiyang Tan, Camille Kergaravat, Laura Gonzalez, et al.
Scientific Reports|April 17, 2021
Functional disability is related to serum chemerin levels in rheumatoid arthritisMaria Luisa Vazquez-Villegas, Jorge I Gamez-Nava, A Miriam Saldaña-Cruz, et al.
Genes|May 15, 2020
Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in SpainLidia Gonzalez-Quereda, Maria Jose Rodriguez, Jordi Diaz-Manera, et al.
The Journal of International Medical Research|May 24, 2017
Association of adipokines, interleukin-6, and tumor necrosis factor-α concentrations with clinical characteristics and presence of spinal syndesmophytes in patients with ankylosing spondylitis: A cross-sectional studyLaura Gonzalez-Lopez, Nicte S Fajardo-Robledo, A Miriam Saldaña-Cruz, et al.
American Journal of Human Genetics|November 27, 2010
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with coresNyamkhishig Sambuughin, Kyle S Yau, Montse Olivé, et al.
Brain : a Journal of Neurology|September 28, 2014
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutationsJohann Böhm, Valérie Biancalana, Edoardo Malfatti, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|July 4, 2026
Early Metabolic Risk in Childhood Brain Cancer Survivors with Childhood-Onset Growth Hormone DeficiencyAlice Casiraghi, Olivier Pollé, Clément Bailly, et al.
Plos One|September 10, 2021
Serum chemerin levels: A potential biomarker of joint inflammation in women with rheumatoid arthritisFabiola Gonzalez-Ponce, Jorge I Gamez-Nava, Emilio E Perez-Guerrero, et al.
Pageof 32