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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 JME
T 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 seizures
C Windemuth, H Schulz, K Saar, et al.
Clinical Genetics
|
July 4, 2015
Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome
S Dimassi, A Labalme, D Ville, et al.
Human Molecular Genetics
|
July 11, 2000
Genome search for susceptibility loci of common idiopathic generalised epilepsies
T Sander, H Schulz, K Saar, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 46) with videos related to
Sort By:
Page
of 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 JME
T 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 seizures
C Windemuth, H Schulz, K Saar, et al.
Clinical Genetics
|
July 4, 2015
Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome
S Dimassi, A Labalme, D Ville, et al.
Human Molecular Genetics
|
July 11, 2000
Genome search for susceptibility loci of common idiopathic generalised epilepsies
T Sander, H Schulz, K Saar, et al.
Page
of 5