Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mona, Ragothaman"'
Are current recommendations to diagnose orthostatic hypotension in Parkinson's disease satisfactory?
Autor:
Jenny Jamnadas-Khoda, Subbakrishna K. Dodaballapur, Mona Ragothaman, Christopher J. Mathias, Suma Koshy, Uday B. Muthane
Publikováno v:
Movement Disorders. 24:1747-1751
We interviewed 50 Parkinson's disease (PD) patients using a questionnaire to verify the reliability of orthostatic symptoms in warning the presence of orthostatic hypotension (OH). OH is defined as 20 mm Hg systolic or 10 mm Hg diastolic BP fall with
Autor:
Uday B. Muthane, Subbakrishna K. Doddaballapur, Mona Ragothaman, Gururaj Gopalkrishna, Elan D. Louis, Nagaraja Sarangmath, Rohini Rattihalli
Publikováno v:
Movement Disorders. 20:1550-1556
The prevalence of Parkinson's disease (PD) is low among Indians, except in the Parsis. Data for Indians come from studies using different screening tools and criteria to detect PD. An epidemiological study in India, which has nearly a billion people,
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
Publikováno v:
The Journal of the Association of Physicians of India. 56
The elderly population in developing countries is likely to increase by 200-280%. Age related diseases like Parkinsonism are also likely to increase in ageing population. The prevalence and awareness of Parkinsonism (and possible PD) amongst them are
Publikováno v:
The Journal of the Association of Physicians of India. 55
Improving economy and health in developing countries like India, has increased the life span and changed the emphasis from communicable to noncommunicable diseases. This is likely to increase the prevalence of movement disorders and, age-related dise
Autor:
Dodaballapur K. Subbakrishna, Uday B. Muthane, Mona Ragothaman, Rohini Rattihalli, Shyla T. Govindappa
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 21(10)
Medicines and surgical interventions improve thequality of life of Parkinson’s disease (PD) patients. Theseare still expensive options and are unaffordable to thoseliving in developing countries. Managing PD in Indians whohave a low annual gross na
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:
Mitali Mukerji, Ramesh C. Juyal, Sangeeta Sharma, Sreelatha Komatireddy, Shashi Chaudhary, Subhabrata Chakrabarti, Vishwamohini Khare, B.K. Thelma, Uday B. Muthane, Uma Mittal, Nagaraja Sarangmath, Mona Ragothaman
Publikováno v:
Annals of neurology. 55(1)
We describe a consanguineous Indian family having spinocerebellar ataxia type 2 (SCA2) expansions with complex phenotypes (early-onset, dopa-responsive parkinsonism, ataxia and retinitis pigmentosa). The two probands having homozygous SCA2 mutations