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M Rietschel

Showing results (21-30 of 207) with videos related to

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Biological Psychiatry|December 15, 1994
Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depressionS Cichon, M M Nöthen, M Rietschel, et al.
European Archives of Psychiatry and Clinical Neuroscience|February 3, 1999
Reliability and validity of the premorbid adjustment scale (PAS) in a German sample of schizophrenic and schizoaffective patientsH Krauss, K Marwinski, T Held, et al.
Lancet (London, England)|January 15, 1998
Apolipoprotein E epsilon 4 and clinical phenotype in schizophreniaM Rietschel, H Krauss, D J Müller, et al.
American Journal of Medical Genetics|October 1, 1991
MASA syndrome: clinical variability and linkage analysisM Rietschel, W Friedl, S Uhlhaas, et al.
FEBS Letters|December 21, 1992
No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHONK D Gerbitz, A Paprotta, B Obermaier-Kusser, et al.
Psychiatric Genetics|June 13, 1998
Familial occurrence of primary premature ejaculationM D Waldinger, M Rietschel, M M Nöthen, et al.
Psychiatric Genetics|November 5, 1997
Association study of schizophrenia and the histidase geneM Nobile, P Maffei, M M Nöthen, et al.
Lancet (London, England)|September 12, 2000
Pharmacogenetics of the clozapine responseJ Schumacher, T G Schulze, T F Wienker, et al.
Lancet (London, England)|May 27, 1995
Tyrosine hydroxylase gene and manic-depressive illnessM Rietschel, M M Nöthen, W Maier, et al.
Molecular Psychiatry|August 26, 2015
Rare SHANK2 variants in schizophreniaS Peykov, S Berkel, F Degenhardt, et al.
Pageof 21

Showing results (21-30 of 207) with videos related to

Sort By:
Pageof 21
Biological Psychiatry|December 15, 1994
Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depressionS Cichon, M M Nöthen, M Rietschel, et al.
European Archives of Psychiatry and Clinical Neuroscience|February 3, 1999
Reliability and validity of the premorbid adjustment scale (PAS) in a German sample of schizophrenic and schizoaffective patientsH Krauss, K Marwinski, T Held, et al.
Lancet (London, England)|January 15, 1998
Apolipoprotein E epsilon 4 and clinical phenotype in schizophreniaM Rietschel, H Krauss, D J Müller, et al.
American Journal of Medical Genetics|October 1, 1991
MASA syndrome: clinical variability and linkage analysisM Rietschel, W Friedl, S Uhlhaas, et al.
FEBS Letters|December 21, 1992
No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHONK D Gerbitz, A Paprotta, B Obermaier-Kusser, et al.
Psychiatric Genetics|June 13, 1998
Familial occurrence of primary premature ejaculationM D Waldinger, M Rietschel, M M Nöthen, et al.
Psychiatric Genetics|November 5, 1997
Association study of schizophrenia and the histidase geneM Nobile, P Maffei, M M Nöthen, et al.
Lancet (London, England)|September 12, 2000
Pharmacogenetics of the clozapine responseJ Schumacher, T G Schulze, T F Wienker, et al.
Lancet (London, England)|May 27, 1995
Tyrosine hydroxylase gene and manic-depressive illnessM Rietschel, M M Nöthen, W Maier, et al.
Molecular Psychiatry|August 26, 2015
Rare SHANK2 variants in schizophreniaS Peykov, S Berkel, F Degenhardt, et al.
Pageof 21