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G Sanner

Showing results (1-10 of 12) with videos related to

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Developmental Medicine and Child Neurology|October 1, 1979
Pathogenetic and preventive aspects of non-progressive ataxic syndromesG Sanner
Acta Paediatrica Scandinavica|March 1, 1979
Benign paroxysmal torticollis in infancyG 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 myoclonusK 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 dystoniaM 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 variationM Kyllerman, L Forsgren, G Sanner, et al.
Clinical Genetics|May 1, 1985
Effect of folic acid treatment in the fragile X syndromeK 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 childrenV 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 9qJ Wahlström, L Ozelius, P Kramer, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Developmental Medicine and Child Neurology|October 1, 1979
Pathogenetic and preventive aspects of non-progressive ataxic syndromesG Sanner
Acta Paediatrica Scandinavica|March 1, 1979
Benign paroxysmal torticollis in infancyG 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 myoclonusK 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 dystoniaM 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 variationM Kyllerman, L Forsgren, G Sanner, et al.
Clinical Genetics|May 1, 1985
Effect of folic acid treatment in the fragile X syndromeK 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 childrenV 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 9qJ Wahlström, L Ozelius, P Kramer, et al.
Pageof 2