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BMC Neurology|March 25, 2014
Observational Dutch Young Symptomatic StrokE studY (ODYSSEY): study rationale and protocol of a multicentre prospective cohort studyRenate M Arntz, Mayte E van Alebeek, Nathalie E Synhaeve, et al.
Clinical Genetics|August 29, 2024
Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variantsMiriam Bauwens, Vincent De Man, Isabelle Audo, et al.
American Journal of Human Genetics|May 14, 2013
Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophyKornelia Neveling, Lilian A Martinez-Carrera, Irmgard Hölker, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 6, 2023
Identifying unmet needs and challenges in the definition of a plaque in mycosis fungoides: An EORTC-CLTG/ISCL surveyPietro Quaglino, Julia Scarisbrick, Gabriele Roccuzzo, et al.
The Journal of Investigative Dermatology|September 18, 2009
Oligonucleotide array-CGH identifies genomic subgroups and prognostic markers for tumor stage mycosis fungoidesRocío Salgado, Octavio Servitje, Fernando Gallardo, et al.
Open Heart|June 28, 2019
Heritability in genetic heart disease: the role of genetic backgroundJoeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, et al.
JACC. Heart Failure|August 11, 2023
Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort StudyMark Jansen, Remco de Brouwer, Fahima Hassanzada, et al.
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