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D Ville

Showing results (41-50 of 46) with videos related to

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Journal Des Maladies Vasculaires|January 1, 1996
[Diagnosis of venous thrombosis and/or pulmonary embolism by determination of d-dimers using ELISA. Review based on a study of 80 consecutive patients hospitalized in an emergency unit]C Gavaud, J Ninet, D Ville, et al.
Epilepsy Research|July 21, 2001
Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JMET Moore, S Hecquet, A McLellann, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Diagnostic investigations for an unexplained developmental disability]A Verloes, D Héron, T Billette de Villemeur, et al.
Epilepsy Research|September 28, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizuresC Windemuth, H Schulz, K Saar, et al.
Clinical Genetics|July 4, 2015
Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndromeS Dimassi, A Labalme, D Ville, et al.
Human Molecular Genetics|July 11, 2000
Genome search for susceptibility loci of common idiopathic generalised epilepsiesT Sander, H Schulz, K Saar, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Journal Des Maladies Vasculaires|January 1, 1996
[Diagnosis of venous thrombosis and/or pulmonary embolism by determination of d-dimers using ELISA. Review based on a study of 80 consecutive patients hospitalized in an emergency unit]C Gavaud, J Ninet, D Ville, et al.
Epilepsy Research|July 21, 2001
Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JMET Moore, S Hecquet, A McLellann, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Diagnostic investigations for an unexplained developmental disability]A Verloes, D Héron, T Billette de Villemeur, et al.
Epilepsy Research|September 28, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizuresC Windemuth, H Schulz, K Saar, et al.
Clinical Genetics|July 4, 2015
Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndromeS Dimassi, A Labalme, D Ville, et al.
Human Molecular Genetics|July 11, 2000
Genome search for susceptibility loci of common idiopathic generalised epilepsiesT Sander, H Schulz, K Saar, et al.
Pageof 5