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H Pihko

Showing results (61-70 of 98) with videos related to

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Neurology|January 6, 2011
Dominant encephalopathy mimicking mitochondrial diseaseT Lönnqvist, P Isohanni, L Valanne, et al.
Journal of the Neurological Sciences|January 1, 1994
Infantile onset spinocerebellar ataxia with sensory neuropathy: a new inherited diseaseT Koskinen, P Santavuori, K Sainio, et al.
Pediatric Research|October 1, 1991
Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletionA Majander, A Suomalainen, K Vettenranta, et al.
The British Journal of Radiology|August 1, 1990
Magnetic resonance of diseased skeletal muscle: combined T1 measurement and chemical shift imagingA E Lamminen, J I Tanttu, R E Sepponen, et al.
Muscle & Nerve|May 1, 1991
Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophyP T Nokelainen, L Alanen-Kurki, H V Somer, et al.
Brain & Development|January 1, 1995
Ocular findings in muscle-eye-brain (MEB) disease: a follow-up studyH Pihko, M Lappi, C Raitta, et al.
The British Journal of Radiology|September 1, 1993
T1 rho dispersion imaging of diseased muscle tissueA E Lamminen, J I Tanttu, R E Sepponen, et al.
Pediatric Research|May 1, 1995
Correlation between the clinical symptoms and the proportion of mitochondrial DNA carrying the 8993 point mutation in the NARP syndromeP Mäkelä-Bengs, A Suomalainen, A Majander, et al.
The Journal of Pediatrics|November 1, 1993
Transient ischemic cerebral lesions during induction chemotherapy for acute lymphoblastic leukemiaH Pihko, T Tyni, K Virkola, et al.
Human Genetics|September 1, 1997
Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritanceK Silander, P Meretoja, H Pihko, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
Neurology|January 6, 2011
Dominant encephalopathy mimicking mitochondrial diseaseT Lönnqvist, P Isohanni, L Valanne, et al.
Journal of the Neurological Sciences|January 1, 1994
Infantile onset spinocerebellar ataxia with sensory neuropathy: a new inherited diseaseT Koskinen, P Santavuori, K Sainio, et al.
Pediatric Research|October 1, 1991
Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletionA Majander, A Suomalainen, K Vettenranta, et al.
The British Journal of Radiology|August 1, 1990
Magnetic resonance of diseased skeletal muscle: combined T1 measurement and chemical shift imagingA E Lamminen, J I Tanttu, R E Sepponen, et al.
Muscle & Nerve|May 1, 1991
Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophyP T Nokelainen, L Alanen-Kurki, H V Somer, et al.
Brain & Development|January 1, 1995
Ocular findings in muscle-eye-brain (MEB) disease: a follow-up studyH Pihko, M Lappi, C Raitta, et al.
The British Journal of Radiology|September 1, 1993
T1 rho dispersion imaging of diseased muscle tissueA E Lamminen, J I Tanttu, R E Sepponen, et al.
Pediatric Research|May 1, 1995
Correlation between the clinical symptoms and the proportion of mitochondrial DNA carrying the 8993 point mutation in the NARP syndromeP Mäkelä-Bengs, A Suomalainen, A Majander, et al.
The Journal of Pediatrics|November 1, 1993
Transient ischemic cerebral lesions during induction chemotherapy for acute lymphoblastic leukemiaH Pihko, T Tyni, K Virkola, et al.
Human Genetics|September 1, 1997
Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritanceK Silander, P Meretoja, H Pihko, et al.
Pageof 10