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H Somer

Showing results (61-70 of 123) with videos related to

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Acta Ophthalmologica|December 1, 1986
Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathologyM Haltia, A Tarkkanen, H Somer, et al.
Progress in Clinical and Biological Research|January 1, 1989
Adult onset limb-girdle muscular dystrophy with autosomal dominant inheritanceH Somer, V Laulumaa, L Paljärvi, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1988
[Carnitine--an important carrier molecule for fatty acids]S Toiviainen, H Tikkanen, L Rovamo, et al.
Clinical Genetics|March 1, 1990
Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial resultsH Kääriäinen, M Lindlöf, H Somer, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1977
[Serum aspartate aminotransferase activity persistently increased in a healthy person]A Konttinen, J Murros, M Salaspuro, et al.
Archives of Neurology|July 25, 1998
Antimyosin scintigraphy compared with magnetic resonance imaging in inflammatory myopathiesM Löfberg, K Liewendahl, A Lamminen, et al.
Journal of Neurosurgery|October 1, 1981
Creatine kinase isoenzymes in acute brain injuryM Kaste, J Hernesniemi, H Somer, et al.
Acta Neurologica Scandinavica|November 10, 1998
Metabolic causes of recurrent rhabdomyolysisM Löfberg, H Jänkälä, A Paetau, et al.
Journal of the Neurological Sciences|December 1, 1992
Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophyB Udd, J Rapola, P Nokelainen, et al.
Journal of Medical Genetics|August 1, 1988
Osteoporosis-pseudoglioma syndrome: clinical, morphological, and biochemical studiesH Somer, A Palotie, M Somer, et al.
Pageof 13

Showing results (61-70 of 123) with videos related to

Sort By:
Pageof 13
Acta Ophthalmologica|December 1, 1986
Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathologyM Haltia, A Tarkkanen, H Somer, et al.
Progress in Clinical and Biological Research|January 1, 1989
Adult onset limb-girdle muscular dystrophy with autosomal dominant inheritanceH Somer, V Laulumaa, L Paljärvi, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1988
[Carnitine--an important carrier molecule for fatty acids]S Toiviainen, H Tikkanen, L Rovamo, et al.
Clinical Genetics|March 1, 1990
Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial resultsH Kääriäinen, M Lindlöf, H Somer, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1977
[Serum aspartate aminotransferase activity persistently increased in a healthy person]A Konttinen, J Murros, M Salaspuro, et al.
Archives of Neurology|July 25, 1998
Antimyosin scintigraphy compared with magnetic resonance imaging in inflammatory myopathiesM Löfberg, K Liewendahl, A Lamminen, et al.
Journal of Neurosurgery|October 1, 1981
Creatine kinase isoenzymes in acute brain injuryM Kaste, J Hernesniemi, H Somer, et al.
Acta Neurologica Scandinavica|November 10, 1998
Metabolic causes of recurrent rhabdomyolysisM Löfberg, H Jänkälä, A Paetau, et al.
Journal of the Neurological Sciences|December 1, 1992
Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophyB Udd, J Rapola, P Nokelainen, et al.
Journal of Medical Genetics|August 1, 1988
Osteoporosis-pseudoglioma syndrome: clinical, morphological, and biochemical studiesH Somer, A Palotie, M Somer, et al.
Pageof 13