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European Journal of Human Genetics : EJHG
|
April 17, 2014
Clinical utility gene card for: Prader-Willi Syndrome
Karin Buiting, Suzanne B Cassidy, Daniel J Driscoll, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
September 1, 1995
Evidence against a role of nitric oxide in the indirect negative inotropic-effect of M-cholinoceptor stimulation in human ventricular myocardium
H Kilter, O Lenz, K La Rosée, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
April 1, 1993
Cardiac inotropic as well as coronary and pulmonary artery actions of epinine in human isolated tissues
R H Schwinger, M Böhm, C Schulz, et al.
American Journal of Medical Genetics
|
November 22, 1996
Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease
V Arolt, R Lencer, A Nolte, et al.
Human Genetics
|
September 1, 1997
CAG repeat analyses in frozen and formalin-fixed tissues following primer extension preamplification for evaluation of mitotic instability of expanded SCA1 alleles
C Zühlke, Y Hellenbroich, F Schaaff, et al.
European Journal of Human Genetics : EJHG
|
September 2, 2004
Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutations
C H Zühlke, A Dalski, M Habeck, et al.
Human Mutation
|
February 22, 2002
Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D
Benigna von Brederlow, Hanno Bolz, Andreas Janecke, et al.
Plos One
|
April 22, 2021
Impact of electric cardioversion on platelet activation
Harald Haidl, Johanna Gaugler, Gerhard Cvirn, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
April 26, 2005
Feasibility of high-dose interleukin-2 in heavily pretreated pediatric cancer patients
W Schwinger, V Klass, M Benesch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 7, 2006
Heterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?
Ana Djarmati, Katja Hedrich, Marina Svetel, et al.
Page
of 85
Search research articles
Search
Showing results (611-620 of 849) with videos related to
Sort By:
Page
of 85
European Journal of Human Genetics : EJHG
|
April 17, 2014
Clinical utility gene card for: Prader-Willi Syndrome
Karin Buiting, Suzanne B Cassidy, Daniel J Driscoll, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
September 1, 1995
Evidence against a role of nitric oxide in the indirect negative inotropic-effect of M-cholinoceptor stimulation in human ventricular myocardium
H Kilter, O Lenz, K La Rosée, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
April 1, 1993
Cardiac inotropic as well as coronary and pulmonary artery actions of epinine in human isolated tissues
R H Schwinger, M Böhm, C Schulz, et al.
American Journal of Medical Genetics
|
November 22, 1996
Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease
V Arolt, R Lencer, A Nolte, et al.
Human Genetics
|
September 1, 1997
CAG repeat analyses in frozen and formalin-fixed tissues following primer extension preamplification for evaluation of mitotic instability of expanded SCA1 alleles
C Zühlke, Y Hellenbroich, F Schaaff, et al.
European Journal of Human Genetics : EJHG
|
September 2, 2004
Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutations
C H Zühlke, A Dalski, M Habeck, et al.
Human Mutation
|
February 22, 2002
Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D
Benigna von Brederlow, Hanno Bolz, Andreas Janecke, et al.
Plos One
|
April 22, 2021
Impact of electric cardioversion on platelet activation
Harald Haidl, Johanna Gaugler, Gerhard Cvirn, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
April 26, 2005
Feasibility of high-dose interleukin-2 in heavily pretreated pediatric cancer patients
W Schwinger, V Klass, M Benesch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 7, 2006
Heterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?
Ana Djarmati, Katja Hedrich, Marina Svetel, et al.
Page
of 85