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E Jaakkola

Showing results (1-10 of 8) with videos related to

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European Journal of Neurology|August 24, 2017
Ventral striatal dopaminergic defect is associated with hallucinations in Parkinson's diseaseE Jaakkola, J Joutsa, E Mäkinen, et al.
American Journal of Medical Genetics. Part A|October 20, 2009
Calvarial doughnut lesions and osteoporosis: a new three-generation family and reviewE Jaakkola, C M Laine, M K Mäyränpää, et al.
Clinical Genetics|May 12, 2010
ERCC6 founder mutation identified in Finnish patients with COFS syndromeE Jaakkola, A Mustonen, P Olsen, et al.
Tissue Antigens|June 12, 2004
A novel human leucocyte antigen-DRB1 genotyping method based on multiplex primer extension reactionsE Jaakkola, I Herzberg, A M Crane, et al.
Genes and Immunity|February 22, 2003
Interleukin 10 polymorphisms in ankylosing spondylitisV Goedecke, A M Crane, E Jaakkola, et al.
Annals of the Rheumatic Diseases|October 27, 2005
Finnish HLA studies confirm the increased risk conferred by HLA-B27 homozygosity in ankylosing spondylitisE Jaakkola, I Herzberg, K Laiho, et al.
Rheumatology (Oxford, England)|August 2, 2003
The effect of transforming growth factor beta1 gene polymorphisms in ankylosing spondylitisE Jaakkola, A M Crane, K Laiho, et al.
Neurology|July 15, 2011
Dominant GDAP1 mutations cause predominantly mild CMT phenotypesM Zimoń, J Baets, G M Fabrizi, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
European Journal of Neurology|August 24, 2017
Ventral striatal dopaminergic defect is associated with hallucinations in Parkinson's diseaseE Jaakkola, J Joutsa, E Mäkinen, et al.
American Journal of Medical Genetics. Part A|October 20, 2009
Calvarial doughnut lesions and osteoporosis: a new three-generation family and reviewE Jaakkola, C M Laine, M K Mäyränpää, et al.
Clinical Genetics|May 12, 2010
ERCC6 founder mutation identified in Finnish patients with COFS syndromeE Jaakkola, A Mustonen, P Olsen, et al.
Tissue Antigens|June 12, 2004
A novel human leucocyte antigen-DRB1 genotyping method based on multiplex primer extension reactionsE Jaakkola, I Herzberg, A M Crane, et al.
Genes and Immunity|February 22, 2003
Interleukin 10 polymorphisms in ankylosing spondylitisV Goedecke, A M Crane, E Jaakkola, et al.
Annals of the Rheumatic Diseases|October 27, 2005
Finnish HLA studies confirm the increased risk conferred by HLA-B27 homozygosity in ankylosing spondylitisE Jaakkola, I Herzberg, K Laiho, et al.
Rheumatology (Oxford, England)|August 2, 2003
The effect of transforming growth factor beta1 gene polymorphisms in ankylosing spondylitisE Jaakkola, A M Crane, K Laiho, et al.
Neurology|July 15, 2011
Dominant GDAP1 mutations cause predominantly mild CMT phenotypesM Zimoń, J Baets, G M Fabrizi, et al.
Pageof 1