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

S Verbeek

Showing results (51-60 of 122) with videos related to

Pageof 13
Sort By:
Human Genetics|October 18, 2002
Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21Dineke S Verbeek, Jurgen H Schelhaas, Elly F Ippel, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 7, 2000
A codominant role of Fc gamma RI/III and C5aR in the reverse Arthus reactionU Baumann, J Köhl, T Tschernig, et al.
Brain : a Journal of Neurology|August 13, 2004
Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3D S Verbeek, B P van de Warrenburg, P Wesseling, et al.
Journal of Neurology|April 1, 2015
Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystoniaEsther Nibbeling, Susen Schaake, Marina A Tijssen, et al.
Molecular and Cellular Biology|February 1, 1985
Human c-fms proto-oncogene: comparative analysis with an abnormal alleleJ S Verbeek, A J Roebroek, A M van den Ouweland, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 26, 2021
Developmental neurobiology of cerebellar and Basal Ganglia connectionsDeborah A Sival, Suus A M van Noort, Marina A J Tijssen, et al.
British Journal of Haematology|September 1, 1985
A hereditary abnormal c-fms proto-oncogene in a patient with acute lymphocytic leukaemia and congenital hypothyroidismJ S Verbeek, H van Heerikhuizen, B E de Pauw, et al.
BMC Neurology|October 15, 2019
Cortical pencil lining on SWI MRI in NBIA and healthy agingMarlous C M van der Weijden, Peter Jan van Laar, Roald A Lambrechts, et al.
Blood|December 3, 1998
FcgammaRIII (CD16)-deficient mice show IgG isotype-dependent protection to experimental autoimmune hemolytic anemiaD Meyer, C Schiller, J Westermann, et al.
European Journal of Human Genetics : EJHG|March 18, 2004
Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutationsDineke S Verbeek, Sytse J Piersma, Eric F A M Hennekam, et al.
Pageof 13

Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
Human Genetics|October 18, 2002
Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21Dineke S Verbeek, Jurgen H Schelhaas, Elly F Ippel, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 7, 2000
A codominant role of Fc gamma RI/III and C5aR in the reverse Arthus reactionU Baumann, J Köhl, T Tschernig, et al.
Brain : a Journal of Neurology|August 13, 2004
Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3D S Verbeek, B P van de Warrenburg, P Wesseling, et al.
Journal of Neurology|April 1, 2015
Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystoniaEsther Nibbeling, Susen Schaake, Marina A Tijssen, et al.
Molecular and Cellular Biology|February 1, 1985
Human c-fms proto-oncogene: comparative analysis with an abnormal alleleJ S Verbeek, A J Roebroek, A M van den Ouweland, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 26, 2021
Developmental neurobiology of cerebellar and Basal Ganglia connectionsDeborah A Sival, Suus A M van Noort, Marina A J Tijssen, et al.
British Journal of Haematology|September 1, 1985
A hereditary abnormal c-fms proto-oncogene in a patient with acute lymphocytic leukaemia and congenital hypothyroidismJ S Verbeek, H van Heerikhuizen, B E de Pauw, et al.
BMC Neurology|October 15, 2019
Cortical pencil lining on SWI MRI in NBIA and healthy agingMarlous C M van der Weijden, Peter Jan van Laar, Roald A Lambrechts, et al.
Blood|December 3, 1998
FcgammaRIII (CD16)-deficient mice show IgG isotype-dependent protection to experimental autoimmune hemolytic anemiaD Meyer, C Schiller, J Westermann, et al.
European Journal of Human Genetics : EJHG|March 18, 2004
Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutationsDineke S Verbeek, Sytse J Piersma, Eric F A M Hennekam, et al.
Pageof 13