Showing results (41-50 of 75) with videos related to
Sort By:
Pageof 8
Acta Paediatrica (Oslo, Norway : 1992)|May 13, 2009
Insufficient energy and nutrient intake in children with motor disabilityP Kilpinen-Loisa, H Pihko, U Vesander, 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.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.Archives of Disease in Childhood|August 1, 1992
Reversible mitochondrial myopathy with cytochrome c oxidase deficiencyM K Salo, J Rapola, H Somer, et al.Pageof 8