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

Astrid Rasmussen

Showing results (21-30 of 125) with videos related to

Pageof 13
Sort By:
The Journal of Antimicrobial Chemotherapy|June 16, 2025
Carbapenem resistance in Escherichia marmotae: characterization of IncL plasmids carrying blaOXA-48Astrid Rasmussen, Anette M Hammerum, Frank Hansen, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
Elevated Levels of IL-9 Fail to Suppress Pathogenic T helper 17 cells in Sjögren's DiseaseAlexandria Voigt, Yiran Shen, Patricia Glenton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 13, 2009
Clinical and genetic characteristics of Mexican Huntington's disease patientsMaría Elisa Alonso, Adriana Ochoa, Marie-Catherine Boll, et al.
Lung|June 15, 2023
Multiple Correspondence Analysis and HLA-Associations of Organ Involvement in a Large Cohort of African-American and European-American Patients with SarcoidosisAstrid Rasmussen, Bryan A Dawkins, Chuang Li, et al.
Clinical Immunology (Orlando, Fla.)|January 26, 2023
Anti-vimentin antibodies are associated with higher severity of Sjögren's diseaseHarini Bagavant, Antonina M Araszkiewicz, Astrid Rasmussen, et al.
Neurogenetics|April 22, 2006
Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican familiesPetra Yescas, Adriana Huertas-Vazquez, María Teresa Villarreal-Molina, et al.
Journal of Neurosurgery|April 1, 2006
Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastomaAstrid Rasmussen, Sonia Nava-Salazar, Petra Yescas, et al.
Annals of Neurology|May 3, 2007
Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17Astrid Rasmussen, Irene De Biase, Marcela Fragoso-Benítez, et al.
American Journal of Medical Genetics. Part A|August 30, 2016
Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosisAriadna González-Del Angel, Bernardette Estandía-Ortega, Miguel Angel Alcántara-Ortigoza, et al.
Plos One|November 27, 2013
Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestryKhalaf Bushara, Matthew Bower, Jilin Liu, et al.
Pageof 13

Showing results (21-30 of 125) with videos related to

Sort By:
Pageof 13
The Journal of Antimicrobial Chemotherapy|June 16, 2025
Carbapenem resistance in Escherichia marmotae: characterization of IncL plasmids carrying blaOXA-48Astrid Rasmussen, Anette M Hammerum, Frank Hansen, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
Elevated Levels of IL-9 Fail to Suppress Pathogenic T helper 17 cells in Sjögren's DiseaseAlexandria Voigt, Yiran Shen, Patricia Glenton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 13, 2009
Clinical and genetic characteristics of Mexican Huntington's disease patientsMaría Elisa Alonso, Adriana Ochoa, Marie-Catherine Boll, et al.
Lung|June 15, 2023
Multiple Correspondence Analysis and HLA-Associations of Organ Involvement in a Large Cohort of African-American and European-American Patients with SarcoidosisAstrid Rasmussen, Bryan A Dawkins, Chuang Li, et al.
Clinical Immunology (Orlando, Fla.)|January 26, 2023
Anti-vimentin antibodies are associated with higher severity of Sjögren's diseaseHarini Bagavant, Antonina M Araszkiewicz, Astrid Rasmussen, et al.
Neurogenetics|April 22, 2006
Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican familiesPetra Yescas, Adriana Huertas-Vazquez, María Teresa Villarreal-Molina, et al.
Journal of Neurosurgery|April 1, 2006
Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastomaAstrid Rasmussen, Sonia Nava-Salazar, Petra Yescas, et al.
Annals of Neurology|May 3, 2007
Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17Astrid Rasmussen, Irene De Biase, Marcela Fragoso-Benítez, et al.
American Journal of Medical Genetics. Part A|August 30, 2016
Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosisAriadna González-Del Angel, Bernardette Estandía-Ortega, Miguel Angel Alcántara-Ortigoza, et al.
Plos One|November 27, 2013
Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestryKhalaf Bushara, Matthew Bower, Jilin Liu, et al.
Pageof 13