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Acta Ophthalmologica
|
December 1, 1986
Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology
M 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 inheritance
H 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 results
H 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 myopathies
M Löfberg, K Liewendahl, A Lamminen, et al.
Journal of Neurosurgery
|
October 1, 1981
Creatine kinase isoenzymes in acute brain injury
M Kaste, J Hernesniemi, H Somer, et al.
Acta Neurologica Scandinavica
|
November 10, 1998
Metabolic causes of recurrent rhabdomyolysis
M 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 dystrophy
B Udd, J Rapola, P Nokelainen, et al.
Journal of Medical Genetics
|
August 1, 1988
Osteoporosis-pseudoglioma syndrome: clinical, morphological, and biochemical studies
H Somer, A Palotie, M Somer, et al.
Page
of 13
Search research articles
Search
Showing results (61-70 of 123) with videos related to
Sort By:
Page
of 13
Acta Ophthalmologica
|
December 1, 1986
Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology
M 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 inheritance
H 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 results
H 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 myopathies
M Löfberg, K Liewendahl, A Lamminen, et al.
Journal of Neurosurgery
|
October 1, 1981
Creatine kinase isoenzymes in acute brain injury
M Kaste, J Hernesniemi, H Somer, et al.
Acta Neurologica Scandinavica
|
November 10, 1998
Metabolic causes of recurrent rhabdomyolysis
M 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 dystrophy
B Udd, J Rapola, P Nokelainen, et al.
Journal of Medical Genetics
|
August 1, 1988
Osteoporosis-pseudoglioma syndrome: clinical, morphological, and biochemical studies
H Somer, A Palotie, M Somer, et al.
Page
of 13