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Clinical Chemistry
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July 1, 1996
Cardiac troponins in severe rhabdomyolysis
M Löfberg, R Tähtelä, M Härkönen, et al.
Brain Pathology (Zurich, Switzerland)
|
April 1, 1992
Disorders associated with multiple deletions of mitochondrial DNA
M Haltia, A Suomalainen, A Majander, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
January 1, 1984
[Meningitis following myelography]
M Kallio, H Somer, V Valtonen, et al.
Thrombosis and Haemostasis
|
April 1, 2000
Altered platelet shape change in hereditary gelsolin Asp187Asn-related amyloidosis
S Kiuru, K Javela, H Somer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 16, 1975
Studies on N-aspartyl-beta-glucosaminidase in aspartylglycosaminuria
H Somer, J Palo, H Savolainen, et al.
Acta Medica Scandinavica
|
January 1, 1985
Morbid obesity, gastric plication and a severe neurological deficit
H Somer, L Bergström, P Mustajoki, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1975
Brain creatine kinase in blood after acute brain injury
H Somer, M Kaste, H Troupp, et al.
Archives of Neurology
|
December 1, 1995
Myosin heavy-chain fragments and cardiac troponins in the serum in rhabdomyolysis. Diagnostic specificity of new biochemical markers
M Löfberg, R Tähtelä, M Härkönen, et al.
European Journal of Neurology
|
June 26, 2003
Pure quadriceps myopathy in two sisters
I Mahjneh, H Somer, A Paetau, et al.
Archives of Neurology
|
November 1, 1973
A serum isozyme study in muscular dystrophy. Particular reference to creatine kinase, aspartate aminotransferase, and lactic acid dehydrogenase isozymes
H Somer, M Donner, J Murros, et al.
Page
of 13
Search research articles
Search
Showing results (41-50 of 123) with videos related to
Sort By:
Page
of 13
Clinical Chemistry
|
July 1, 1996
Cardiac troponins in severe rhabdomyolysis
M Löfberg, R Tähtelä, M Härkönen, et al.
Brain Pathology (Zurich, Switzerland)
|
April 1, 1992
Disorders associated with multiple deletions of mitochondrial DNA
M Haltia, A Suomalainen, A Majander, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
January 1, 1984
[Meningitis following myelography]
M Kallio, H Somer, V Valtonen, et al.
Thrombosis and Haemostasis
|
April 1, 2000
Altered platelet shape change in hereditary gelsolin Asp187Asn-related amyloidosis
S Kiuru, K Javela, H Somer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 16, 1975
Studies on N-aspartyl-beta-glucosaminidase in aspartylglycosaminuria
H Somer, J Palo, H Savolainen, et al.
Acta Medica Scandinavica
|
January 1, 1985
Morbid obesity, gastric plication and a severe neurological deficit
H Somer, L Bergström, P Mustajoki, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1975
Brain creatine kinase in blood after acute brain injury
H Somer, M Kaste, H Troupp, et al.
Archives of Neurology
|
December 1, 1995
Myosin heavy-chain fragments and cardiac troponins in the serum in rhabdomyolysis. Diagnostic specificity of new biochemical markers
M Löfberg, R Tähtelä, M Härkönen, et al.
European Journal of Neurology
|
June 26, 2003
Pure quadriceps myopathy in two sisters
I Mahjneh, H Somer, A Paetau, et al.
Archives of Neurology
|
November 1, 1973
A serum isozyme study in muscular dystrophy. Particular reference to creatine kinase, aspartate aminotransferase, and lactic acid dehydrogenase isozymes
H Somer, M Donner, J Murros, et al.
Page
of 13