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A Suomalainen

Showing results (21-30 of 76) with videos related to

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Dento Maxillo Facial Radiology|January 16, 2008
Accuracy of linear measurements using dental cone beam and conventional multislice computed tomographyA Suomalainen, T Vehmas, M Kortesniemi, et al.
Pediatric Research|November 1, 1994
Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxiasK Nikali, T Koskinen, A Suomalainen, et al.
Genome Research|January 10, 1998
Steady-state transcript levels of the porphobilinogen deaminase gene in patients with acute intermittent porphyriaS Mustajoki, R Kauppinen, P Mustajoki, et al.
Genome Research|September 1, 1996
Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locusT Varilo, K Nikali, A Suomalainen, et al.
Neuropediatrics|June 1, 1996
Laminar cortical necrosis in MELAS syndrome: MR and neuropathological observationsL Valanne, A Paetau, A Suomalainen, et al.
AJNR. American Journal of Neuroradiology|March 21, 1998
Neuroradiologic findings in children with mitochondrial disordersL Valanne, L Ketonen, A Majander, et al.
Somatic Cell Genetics|November 1, 1983
Assignment of gene(s) coding for antigen defined by monoclonal antibody 2B2H A Suomalainen, C Lundqvist, C G Gahmberg, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Mitochondrial diseases]H Pihko, A Suomalainen, H Somer, et al.
Human Molecular Genetics|May 1, 1993
Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcriptionA Suomalainen, A Majander, H Pihko, et al.
Hereditas|January 1, 1983
Karyotype of a mouse/rabbit hybrid clone secreting rabbit immunoglobulin kappa light chainH A Suomalainen, L Brys, W van der Loo, et al.
Pageof 8

Showing results (21-30 of 76) with videos related to

Sort By:
Pageof 8
Dento Maxillo Facial Radiology|January 16, 2008
Accuracy of linear measurements using dental cone beam and conventional multislice computed tomographyA Suomalainen, T Vehmas, M Kortesniemi, et al.
Pediatric Research|November 1, 1994
Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxiasK Nikali, T Koskinen, A Suomalainen, et al.
Genome Research|January 10, 1998
Steady-state transcript levels of the porphobilinogen deaminase gene in patients with acute intermittent porphyriaS Mustajoki, R Kauppinen, P Mustajoki, et al.
Genome Research|September 1, 1996
Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locusT Varilo, K Nikali, A Suomalainen, et al.
Neuropediatrics|June 1, 1996
Laminar cortical necrosis in MELAS syndrome: MR and neuropathological observationsL Valanne, A Paetau, A Suomalainen, et al.
AJNR. American Journal of Neuroradiology|March 21, 1998
Neuroradiologic findings in children with mitochondrial disordersL Valanne, L Ketonen, A Majander, et al.
Somatic Cell Genetics|November 1, 1983
Assignment of gene(s) coding for antigen defined by monoclonal antibody 2B2H A Suomalainen, C Lundqvist, C G Gahmberg, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Mitochondrial diseases]H Pihko, A Suomalainen, H Somer, et al.
Human Molecular Genetics|May 1, 1993
Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcriptionA Suomalainen, A Majander, H Pihko, et al.
Hereditas|January 1, 1983
Karyotype of a mouse/rabbit hybrid clone secreting rabbit immunoglobulin kappa light chainH A Suomalainen, L Brys, W van der Loo, et al.
Pageof 8