Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Pazhayannur V, Swaminath"'
Publikováno v:
The Annals of The Royal College of Surgeons of England. 93:133-138
INTRODUCTION The results of a survey on evidence-based surgery (EBS) among members of the American Academy of Orthopedic Surgeons (AAOS) and the British Orthopaedic Association (BOA) are presented. The study also analyzes the citations earned by arti
Publikováno v:
Movement Disorders. 22:2133-2135
Autor:
Mona, Ragothaman, Pazhayannur V, Swaminath, Nagaraja, Sarangmath, Suma, Koshy, Mohan, Adhyam, Dodaballapur K, Subbakrishna, Christopher J, Mathias, Uday B, Muthane
Publikováno v:
The Journal of the Association of Physicians of India. 59
Can dysautonomic symptoms occurring within a year of developing motor symptoms distinguish Multiple system atrophy-Parkinsonian (MSA-P) from Parkinson's disease (PD)?Seventy-two Parkinsonian patients diagnosed as probable PD or MSA-P.PD (n = 58, 80.6
Autor:
Pazhayannur V, Swaminath, Mona, Ragothaman, Suma, Koshy, Nagaraja, Sarangmath, Mohan, Adhyam, D K, Subbakrishna, Christopher J, Mathias, Uday B, Muthane
Publikováno v:
The Journal of the Association of Physicians of India. 58
One hundred and eighty-one parkinsonian patients were evaluated to determine if urogenital symptoms at presentation to the Neurology clinic can differentiate them as PD or MSA-P. An autonomic questionnaire was used to document urinary and genital sym
Autor:
Sachi Jayaram, Geetika Nainwal, Uday B. Muthane, Madhuri Behari, B.K. Thelma, Pazhayannur V. Swaminath, Sumit Randhir Singh, Ramesh C. Juyal, Mitashree Das, Sohan Punia, Shyla T. Govindappa
Publikováno v:
Neurogenetics. 7(4)
The depletion of dopamine levels in the brain due to degeneration of dopaminergic neurons of substantia nigra pars compacta is a hallmark of Parkinson’s disease (PD). The cumulative contribution of genetic variations in genes from the dopaminergic
Autor:
Ramesh C. Juyal, Pazhayannur V. Swaminath, Sohan Punia, Sachi Jayaram, B.K. Thelma, Madhuri Behari, Vinay Goyal, Uday B. Muthane, Shyla T. Govindappa
Publikováno v:
Neuroscience letters. 409(2)
Recent discovery of pathogenic mutations in the leucine-rich repeat kinase 2 (LRRK2) gene in Parkinson's disease (PD) patients in different ethnic groups have raised a hope of diagnostic screening and genetic counseling. We investigated the six most
Autor:
Shashi Chaudhary, Madhuri Behari, Maninder Dihana, Pazhayannur V. Swaminath, Shyla T. Govindappa, Sachi Jayaram, Sumit Singh, Uday B. Muthane, Ramesh C. Juyal, Thelma B.K.
Publikováno v:
Pharmacogenetics and genomics. 15(10)
Objectives To investigate the association of (i) seven SNPs and SNP haplotypes in the phase II conjugating enzyme N-acetyl transferase 2 gene; and (ii) slow acetylator phenotype, with the development of young onset (YO) and late onset (LO) Parkinson'
Autor:
Nagaraja Sarangmath, Sachi Jayaram, Uday B. Muthane, Pazhayannur V. Swaminath, Mona Ragothaman
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 19(10)
Task-specific dystonia significantly impairs the performance of approximately 8% of musicians [Lederman RJ. Muscle Nerve 2003;27:549-561]. We describe hand dystonia in two professional musicians experienced while playing tabla, a percussion instrumen
Autor:
Saumya A. H. Udupa, Shobini L. Rao, Mona Ragothaman, Pazhayannur V. Swaminath, Srikanth Subbamma Govindappa, Uday B. Muthane
Publikováno v:
Movement Disorders. 21:1296-1297