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Developmental Medicine and Child Neurology
|
October 1, 1979
Pathogenetic and preventive aspects of non-progressive ataxic syndromes
G Sanner
Acta Paediatrica Scandinavica
|
March 1, 1979
Benign paroxysmal torticollis in infancy
G Sanner, B Bergström
Die Pharmazie
|
August 1, 1985
[Use of x-ray fluorescence analysis for determination of bromine in drug synthesis, with a look at chlorine (sulfur) and fluorine]
G Sanner, H Usbeck
Acta Neurologica Scandinavica
|
August 1, 1991
Hereditary spastic paraplegia with epileptic myoclonus
K Sommerfelt, M Kyllerman, G Sanner
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]
|
June 1, 1996
[The remineralization of the vertebral metastases of breast carcinoma after radiotherapy]
I Wachenfeld, G Sanner, H D Böttcher, et al.
Brain & Development
|
July 1, 1993
Early onset dystonia decreasing with development. Case report of two children with familial myoclonic dystonia
M Kyllerman, G Sanner, L Forsgren, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1990
Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation
M Kyllerman, L Forsgren, G Sanner, et al.
Clinical Genetics
|
May 1, 1985
Effect of folic acid treatment in the fragile X syndrome
K H Gustavson, K Dahlbom, A Flood, et al.
Neuropediatrics
|
February 1, 1986
Salla disease variants. Sialoylaciduric encephalopathy with increased sialidase activity in two non-Finnish children
V Ylitalo, B Hagberg, J Rapola, et al.
Clinical Genetics
|
February 1, 1994
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q
J Wahlström, L Ozelius, P Kramer, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Developmental Medicine and Child Neurology
|
October 1, 1979
Pathogenetic and preventive aspects of non-progressive ataxic syndromes
G Sanner
Acta Paediatrica Scandinavica
|
March 1, 1979
Benign paroxysmal torticollis in infancy
G Sanner, B Bergström
Die Pharmazie
|
August 1, 1985
[Use of x-ray fluorescence analysis for determination of bromine in drug synthesis, with a look at chlorine (sulfur) and fluorine]
G Sanner, H Usbeck
Acta Neurologica Scandinavica
|
August 1, 1991
Hereditary spastic paraplegia with epileptic myoclonus
K Sommerfelt, M Kyllerman, G Sanner
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]
|
June 1, 1996
[The remineralization of the vertebral metastases of breast carcinoma after radiotherapy]
I Wachenfeld, G Sanner, H D Böttcher, et al.
Brain & Development
|
July 1, 1993
Early onset dystonia decreasing with development. Case report of two children with familial myoclonic dystonia
M Kyllerman, G Sanner, L Forsgren, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1990
Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation
M Kyllerman, L Forsgren, G Sanner, et al.
Clinical Genetics
|
May 1, 1985
Effect of folic acid treatment in the fragile X syndrome
K H Gustavson, K Dahlbom, A Flood, et al.
Neuropediatrics
|
February 1, 1986
Salla disease variants. Sialoylaciduric encephalopathy with increased sialidase activity in two non-Finnish children
V Ylitalo, B Hagberg, J Rapola, et al.
Clinical Genetics
|
February 1, 1994
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q
J Wahlström, L Ozelius, P Kramer, et al.
Page
of 2