Sinha KK - Search Results

1

Molecular anatomy of CTG expansion in myotonin protein kinase gene among myotonic dystrophy patients from eastern India.

Basu P, Gangopadhaya PK, Mukherjee SC, Das SK, Sinha KK, Bhattacharyya NP. Basu P, et al. Among authors: sinha kk. Hum Mutat. 2000 Oct;16(4):372. doi: 10.1002/1098-1004(200010)16:4<372::AID-HUMU13>3.0.CO;2-G. Hum Mutat. 2000. PMID: 11013451

2

Expansion of CTG repeat in myotonin protein kinase gene on Alu(ins)-HinfI-I background in a myotonic dystrophy patient from India. Mutations in brief no. 210. Online.

Basu P, Gangopadhaya PK, Murkherjee SC, Sinha KK, Bhattacharyya NP. Basu P, et al. Among authors: sinha kk. Hum Mutat. 1999;13(1):84. doi: 10.1002/(SICI)1098-1004(1999)13:1<84::AID-HUMU15>3.0.CO;2-U. Hum Mutat. 1999. PMID: 10189221

3

Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.

Basu P, Chattopadhyay B, Gangopadhaya PK, Mukherjee SC, Sinha KK, Das SK, Roychoudhury S, Majumder PP, Bhattacharyya NP. Basu P, et al. Among authors: sinha kk. Hum Genet. 2000 Jun;106(6):597-604. doi: 10.1007/s004390000320. Hum Genet. 2000. PMID: 10942107

4

Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India.

Pramanik S, Basu P, Gangopadhaya PK, Sinha KK, Jha DK, Sinha S, Das SK, Maity BK, Mukherjee SC, Roychoudhuri S, Majumder PP, Bhattacharyya NP. Pramanik S, et al. Among authors: sinha s, sinha kk. Eur J Hum Genet. 2000 Sep;8(9):678-82. doi: 10.1038/sj.ejhg.5200515. Eur J Hum Genet. 2000. PMID: 10980573

5

Molecular analysis of GAA repeats and four linked bi-allelic markers in and around the frataxin gene in patients and normal populations from India.

Chattopadhyay B, Gupta S, Gangopadhyay PK, Das SK, Roy T, Mukherjee SC, Sinha KK, Singhal BS, Bhattacharyya NP. Chattopadhyay B, et al. Among authors: sinha kk. Ann Hum Genet. 2004 May;68(Pt 3):189-95. doi: 10.1046/j.1529-8817.2003.00087.x. Ann Hum Genet. 2004. PMID: 15180699

6

Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India.

Chattopadhyay B, Ghosh S, Gangopadhyay PK, Das SK, Roy T, Sinha KK, Jha DK, Mukherjee SC, Chakraborty A, Singhal BS, Bhattacharya AK, Bhattacharyya NP. Chattopadhyay B, et al. Among authors: sinha kk. Neurosci Lett. 2003 Jul 17;345(2):93-6. doi: 10.1016/s0304-3940(03)00436-1. Neurosci Lett. 2003. PMID: 12821179

7

Variation of CAG repeats and two intragenic polymorphisms at SCA3 locus among Machado-Joseph disease/SCA3 patients and diverse normal populations from eastern India.

Chattopadhyay B, Basu P, Gangopadhyay PK, Mukherjee SC, Sinha KK, Chakraborty A, Roy T, Roychoudhury S, Majumder PP, Bhattacharyya NP. Chattopadhyay B, et al. Among authors: sinha kk. Acta Neurol Scand. 2003 Dec;108(6):407-14. doi: 10.1034/j.1600-0404.2003.00167.x. Acta Neurol Scand. 2003. PMID: 14616293

8

Wilson's disease in Eastern India.

Sinha S, Jha DK, Sinha KK. Sinha S, et al. Among authors: sinha kk. J Assoc Physicians India. 2001 Sep;49:881-4. J Assoc Physicians India. 2001. PMID: 11837754

9

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.

Sinha KK, Worth PF, Jha DK, Sinha S, Stinton VJ, Davis MB, Wood NW, Sweeney MG, Bhatia KP. Sinha KK, et al. Among authors: sinha s. J Neurol Neurosurg Psychiatry. 2004 Mar;75(3):448-52. doi: 10.1136/jnnp.2002.004895. J Neurol Neurosurg Psychiatry. 2004. PMID: 14966163 Free PMC article.

10

Mitral valve echocardiogram as a reflector of left ventricular function.

Sinha KK, Sinha S. Sinha KK, et al. Among authors: sinha s. J Indian Med Assoc. 1987 Apr;85(4):99-101. J Indian Med Assoc. 1987. PMID: 3585030 No abstract available.

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