Zobrazeno 1 - 10
of 486
pro vyhledávání: '"M. S. Keshavan"'
Autor:
Ayman H. Fanous
Publikováno v:
Psychological Medicine. 41:888-889
Autor:
S.J. Wilson, A.R. Lillywhite
Publikováno v:
Journal of Psychopharmacology. 7:302-302
Autor:
V. K. Yeragani, M. S. Keshavan
Publikováno v:
Biological Basis and Therapy of Neuroses ISBN: 9781351070249
Biological Basis and Therapy of Neuroses
Biological Basis and Therapy of Neuroses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdb6254cc36c67ead919859cef1707b5
https://doi.org/10.1201/9781351070249-1
https://doi.org/10.1201/9781351070249-1
Autor:
Lillywhite, A.R., Wilson, S.J.
Publikováno v:
Journal of Psychopharmacology; May 1993, Vol. 7 Issue: 3 p302-302, 1p
Autor:
John P. Hatch, David Axelson, Roberto B. Sassi, Pablo Najt, Jair C. Soares, Mark Nicoletti, Paolo Brambilla, M S Keshavan, Boris Birmaher, Hua Hsuan Chen, Sheila C. Caetano, Neal D. Ryan
Publikováno v:
Neuroscience Letters. 413:183-186
Imaging studies indicate smaller orbitofrontal cortex (OFC) volume in mood disorder patients compared with healthy subjects. We sought to determine whether child and adolescent patients with bipolar disorder have smaller OFC volumes than healthy cont
Publikováno v:
Biological Psychiatry. 48:369-380
Magnetic resonance spectroscopy allows investigation of in vivo neurochemical pathology of schizophrenia. "First generation" studies, focusing on phosphorus and proton magnetic resonance spectroscopy, have suggested alterations in membrane phospholip
Autor:
R, Das Chakraborty, D, Chakraborty, A J, Bernal, K, Schoch, T D, Howard, E H, Ip, S R, Hooper, M S, Keshavan, R L, Jirtle, V, Shashi
Publikováno v:
Translational Psychiatry
Chromosome 22q11.2 deletion syndrome (22q11DS) is the most common microdeletion syndrome in humans. It is typified by highly variable symptoms, which might be explained by epigenetic regulation of genes in the interval. Using computational algorithms
Publikováno v:
Acta psychiatrica Scandinavica. 114(5)
To examine the volumetric and metabolic correlates of caudate nucleus in antipsychotic-naïve schizophrenia patients in comparison with healthy controls.Twelve antipsychotic-naïve schizophrenia patients and 13 healthy controls underwent (31)P magnet
Autor:
V, Shashi, M S, Keshavan, T D, Howard, M N, Berry, M J, Basehore, E, Lewandowski, T R, Kwapil
Publikováno v:
Clinical genetics. 69(3)
Chromosome 22q11.2 deletion syndrome (22q11DS) is a common microdeletion syndrome associated with a markedly elevated risk of schizophrenia in adulthood. Cognitive impairments such as a low IQ and deficits in attention and executive function are comm
Publikováno v:
The American journal of psychiatry. 161(6)
The superior temporal gyrus, a heteromodal auditory and language association cortex, has been found to be smaller in patients with schizophrenia than in normal subjects. However, genetic and/or neurodevelopmental underpinnings of superior temporal gy