Search

Your search keyword '"Strauss, John"' showing total 2 results
Start Over Author "Strauss, John" Region hungary
2 results on '"Strauss, John"'

1. Continuing the legacy of Franz Liszt.

Author

Strauss, John and Strauss, Virginia

Subjects
FRANZ Liszt Academy of Budapest (Hungary)
Abstract

Profiles the Franz Liszt Academy of Budapest. Important role played by Liszt in the musical life of the city; Other artists who performed in the city; Liszt's domination in Hungary during the 19th century; Famous Hungarians who attended the academy; Reputation of the academy in Hungary; Comments from academy professor Kalman Drafi regarding distinct national schools of piano playing.

Published
1994

2. Association study of serotonin system genes in childhood-onset mood disorder.

Author

Shaikh SA, Strauss J, King N, Bulgin NL, Vetró A, Kiss E, George CJ, Kovacs M, Barr CL, and Kennedy JL

Subjects
Adolescent, Adult, Age of Onset, Bipolar Disorder epidemiology, Bipolar Disorder genetics, Case-Control Studies, Child, Depressive Disorder epidemiology, Depressive Disorder genetics, Female, Gene Frequency, Genotype, Humans, Hungary epidemiology, Male, Mood Disorders epidemiology, Mood Disorders physiopathology, Parents, Pennsylvania epidemiology, Receptor, Serotonin, 5-HT1B physiology, Receptor, Serotonin, 5-HT2A physiology, Serotonin Plasma Membrane Transport Proteins physiology, Siblings, Mood Disorders genetics, Polymorphism, Single Nucleotide, Receptor, Serotonin, 5-HT1B genetics, Receptor, Serotonin, 5-HT2A genetics, Serotonin physiology, Serotonin Plasma Membrane Transport Proteins genetics
Abstract

Background: The serotonin system has been implicated in neuropsychiatric disorders, including mood disorders., Methods: We investigated polymorphisms in two serotonin-receptor genes, HTR1B and HTR2A, and the serotonin transporter (SLC6A4) in two independent samples of patients with childhood-onset mood disorders (COMD): 203 patients from Pittsburgh, USA with matched controls and 448 small families from Hungary., Results: Case-control and family-based analyses showed no association between COMD and any of the studied polymorphisms (all P values >0.05). Haplotype analysis of SLC6A4 was also negative in both samples., Conclusions: Overall, the examination of genetic variants at the HTR1B, HTR2A, and SLC6A4 loci indicated no association between the selected polymorphisms and COMD.

Published
2008
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results