Академический Документы
Профессиональный Документы
Культура Документы
Papers:
2. Miller-Fisher Syndrome. Swamy H.S., Nandi S.S., Arunodoya G.R., Acharya J.N.
4. Visual and auditory evoked potentials in Early Onset Parkinson's disease and their
Dec. 1993.
tetrahydropyridine in C57/bl and CD-1 mice. Muthane UB., Ramsay KA, Jiang H,
Jackson-Lewis V, Donaldson D, Fernando S, Ferreira M and Przedborski S.
10. Early Onset Parkinson's Disease: Are Juvenile- and Young-Onset Different? Muthane
UB, Swamy HS, Satishchandra P, Subhash MN, Rao S and Subbakrishna. Movement
cerebrospinal fluid. Dixit N.S., Muthane UB., Satishchandra P, Taly A.V., Gourie-
Devi M, Chandramukhi, A, and S.K. Shankar. Journal of Cytology. 12, 48-51, 1995.
13. Juvenile and Young Onset Parkinson's disease. Muthane UB. The Clinical
Proceedings of the Nizam's Institute of Medical Sciences, Vol. 10, (Suppl 1), 8-11,
1995.
17. Low numbers and No loss of melanized nigral neurons with increasing age in normal
human brains from India. Muthane UB, T.C. Yasha, S.K. Shankar. Annals of
18. Palatal tremor, Progressive mulitple cranial nerve palsies and cerebellar ataxia: A
19. Hallervordern Spatz disease and acanthocytes. Muthane UB, Shetty R, Panda K,
Yasha TC, Jayakumar PN, Taly AB. Neurology. 1999 Nov 10;53(8):32A.
20. Tardive Parkinsonism, orofacial dyskinesia and akathisia following brief exposure to
lithium carbonate. Muthane UB, Prasad BN, Vasanth A, Satishchandra P.J Neurol
21. Hunting genes in Parkinson's disease from the roots. Muthane UB, Jain S, Gururaj G.
22. A clinical study of patients with genetically confirmed Huntington's disease from
India. Murgod UA, Saleem Q, Anand A, Brahmachari SK, Jain S, Muthane UB. J
23. Nobel Men of Medicine-2000. Muthane UB. Annals of Indian Academy of Neurology,
25. Expanding colonies and expanding repeats. Saleem Q, Muthane UB, Verma IC,
28. The Burden of Movement Disorders in India. Muthane UB. Moving Along, 2002;4(2):8-
9.
29. Lower Risk of Parkinson ’s Disease in an Admixed Population of European and
30. Molecular analysis of Huntington’s disease and linked polymorphisms in the Indian
UB, Jain S, Brahmachari SK. Acta Neurol Scand. 2003 Oct; 108(4): 281-286.
31. Complex phenotypes in an Indian family with homozygous SCA2 mutations. Mona
Mitali Mukerji, Ramesh C. Juyal, Thelma BK, Muthane UB. Ann Neurol
2004;55:130–133.
32. Clinical features of Adult GM1 Gangliosidosis: Report of three Indian patients and
33. Botulinum Toxins: Pharmacology and its current therapeutic evidence for use. J.N.
34. Task Specific Dystonia in Tabla Players. Mona Ragothaman, Nagaraja Sarangmat,
Sachi Jayaram, PV Swaminath, Muthane UB. Mov Disord 2004; 19(10): 1254-1256.
phenotype with young onset and late onset Parkinson’s disease among Indians. Shashi
Govindappa, Sachi Jayaram, Sumit Singh, Muthane UB, Ramesh C Juyal and Thelma
37. Melanized Nigral neuronal numbers In Nigerian and British individuals. Muthane UB,
38. Parkinsonism and Personality changes following an Acute Hypoxic insult during
39. Parkin mutations in familial and sporadic Parkinson’s disease among Indians. Shashi
Govindappa, Sachi Jayaram, Vinay Goyal, Arindam Maitra, Muthane UB, R.C.
40. Direct costs of Managing Parkinson’s disease (PD) in India: Concerns in a developing
Muthane UB. Movement Disorder, 2006 Jul 27; Vol. 21, No. 10:1755-1758.
41. Studies on genomic DNA topology and stability in brain regions of Parkinson’s
Shankar, Muthane UB, K. Subba Rao and K.S. Jagannatha Rao. Archives of
Biochemistry and Biophysics. 15 May 2006, Volume 449, Issues 1-2, Pages 143-156.
42. Genetic susceptibility to Parkinson's disease among South and North Indians: I. Role
DRD4 120-bp duplication marker. Ramesh C. Juyal, Mitashree Das, Sohan Punia,
44. The “Indian Turban trick”: a novel sensory trick in blepharospasm. Mona
Ragothaman, Shyla TG, and Muthane UB. Mov Disord. 2007 Jul 30;22(10):1516.
Muthane UB, Juyal RC, B. K Thelma. Neurosci Lett. 2006 Dec 1;409(2):83-88.
Shankar, SG Srikanth, P. Satishchandra and Muthane UB. Mov Disord. 2007 Aug
20;22(13):1964-1968.
and Possibilities. Muthane UB, M. Ragothaman, and Gururaj, G. JAPI, 2007 Oct.
observations and mini review. Praveen K.S., Sinha, S., Yasha, T.C., Muthane UB,
Ravishankar, S., Sangeetha, S., Shetty, K.T and Taly, A.B. Ann Indian Acad Neurol,
2007; 10:259-262.
50. Primary cardiac cytotoxic T-cell lymphoma presenting with neurological deficits: a
case report. Deepti AN, Noone ML, Mahadevan A, Naresh KN, Yasha TC,
Satishchandra P, Muthane UB, Shankar SK.Cardiovasc Pathol. 2007 Oct 24; [Epub
ahead of print].
51. Homozygous SCA 2 mutations changes phenotype and hastens its progression.
771.
52. High occurrence and Low Recognition of Parkinsonism (and Possible PD) in Old Age
K Subbakrishna and Muthane UB. JAPI, Vol. 56, 233-236, April 2008.
Mahadevan, Yasha TC, Raju TR, Shankar SK and Muthane UB. Neuroscience,
Subbakrishna DK, Mathias CJ and Muthane UB. Mov Disord. 2009 Sep 15;24(12):1747-51.
disorder of childhood. Bindu PS, Noone ML, Nalini A, Muthane UB, Kovoor JM. J
57. Expression of GDBF receptors GFRα1 and RET is preserved in substantia nigra pars
compacta of aging Asian Indians. P.Anand Alladi, Anita Mahadevan, Shankar SK,
58. Role of polymorphisms in dopamine synthesis and metabolism genes and association
of DBH haplotypes with Parkinson’s disease among North Indians. Sohan Punia
Mohan Adhyam, Subbakrishna DK, Mathias CJ, Muthane UB. J Assoc Physicians
60. Leads from xenobiotic metabolism genes for Parkinson's disease among north
Indians. Punia S, Das M, Behari M, Dihana M, Govindappa ST, Muthane UB, Thelma
proliferation in the striatum and frontal cortex of Parkinson's disease brains. Mythri
Bharath MM, Shankar SK. Neurochem Res. 2011 Aug;36(8):1452-63. Epub 2011 Apr
12.
62. Secondary Parkinsonism with Mumps Infection. Masoom M. Abbas, Purba Basu,
66. Early Onset Parkinson's disease due to DJ1 mutations: An Indian study. Masoom M. Abbas,
Shyla T. Govindappa, Sumedha Sudhaman, B.K. Thelma, Ramesh C. Juyal, Madhuri Behari, Uday B.
Muthane. Parkinsonism & Related Disorders, November 2016, Vol 32, Page-20-24.
Book Chapters:
Parkinson’s Disease and Other Akinetic Disorders. 1st Edition. Editor Noshir H Wadia
Movement Disorders in India. Jaypee Brothers Medical Publishers (P) Ltd, New
Autonomic Nervous System. 5th Ed. Edited by Mathias CJ and Bannister R. Oxford
Kalyan B Bhattcharyya.
Medicine, 8th Ed, Ed. Shah SN and Anand MP, 1261-63, 2008.
and Arun B. Taly. Indian Academy of Neurology as part of CME Program of the
sixteenth Annual Conference of IAN, New Delhi, October 2008, ISSN: 0971-5924.