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Neurology
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January 6, 2011
Dominant encephalopathy mimicking mitochondrial disease
T 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 disease
T 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 deletion
A 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 imaging
A 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 dystrophy
P 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 study
H Pihko, M Lappi, C Raitta, et al.
The British Journal of Radiology
|
September 1, 1993
T1 rho dispersion imaging of diseased muscle tissue
A 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 syndrome
P 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 leukemia
H 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 inheritance
K Silander, P Meretoja, H Pihko, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 98) with videos related to
Sort By:
Page
of 10
Neurology
|
January 6, 2011
Dominant encephalopathy mimicking mitochondrial disease
T 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 disease
T 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 deletion
A 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 imaging
A 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 dystrophy
P 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 study
H Pihko, M Lappi, C Raitta, et al.
The British Journal of Radiology
|
September 1, 1993
T1 rho dispersion imaging of diseased muscle tissue
A 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 syndrome
P 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 leukemia
H 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 inheritance
K Silander, P Meretoja, H Pihko, et al.
Page
of 10