Danda S - Search Results

1

Recurrent and novel GLB1 mutations in India.

Bidchol AM, Dalal A, Trivedi R, Shukla A, Nampoothiri S, Sankar VH, Danda S, Gupta N, Kabra M, Hebbar SA, Bhat RY, Matta D, Ekbote AV, Puri RD, Phadke SR, Gowrishankar K, Aggarwal S, Ranganath P, Sharda S, Kamate M, Datar CA, Bhat K, Kamath N, Shah H, Krishna S, Gopinath PM, Verma IC, Nagarajaram HA, Satyamoorthy K, Girisha KM. Bidchol AM, et al. Among authors: danda s. Gene. 2015 Aug 10;567(2):173-81. doi: 10.1016/j.gene.2015.04.078. Epub 2015 Apr 30. Gene. 2015. PMID: 25936995

2

Acromesomelic dwarfism: report of a family with two affected siblings.

Danda S, Phadke SR, Agarwal SS. Danda S, et al. Indian Pediatr. 1997 Dec;34(12):1127-30. Indian Pediatr. 1997. PMID: 9715561 No abstract available.

3

A case report of fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome associated with Klinefelter syndrome and review of the literature.

Ekbote AV, Danda S. Ekbote AV, et al. Among authors: danda s. Foot Ankle Spec. 2012 Feb;5(1):37-40. doi: 10.1177/1938640011422594. Epub 2011 Sep 30. Foot Ankle Spec. 2012. PMID: 21965580 Review.

4

Fanconi- Bickel Syndrome: mutation in an Indian patient.

Ekbote AV, Mandal K, Agarwal I, Sinha R, Danda S. Ekbote AV, et al. Among authors: danda s. Indian J Pediatr. 2012 Jun;79(6):810-2. doi: 10.1007/s12098-011-0568-9. Epub 2011 Oct 5. Indian J Pediatr. 2012. PMID: 21972075

5

ATR-X syndrome in two siblings with a novel mutation (c.6718C>T mutation in exon 31).

Thakur S, Ishrie M, Saxena R, Danda S, Linda R, Viswabandya A, Verma IC. Thakur S, et al. Among authors: danda s. Indian J Med Res. 2011 Oct;134(4):483-6. Indian J Med Res. 2011. PMID: 22089611 Free PMC article.

6

Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.

Dalal A, Bhavani G SL, Togarrati PP, Bierhals T, Nandineni MR, Danda S, Danda D, Shah H, Vijayan S, Gowrishankar K, Phadke SR, Bidchol AM, Rao AP, Nampoothiri S, Kutsche K, Girisha KM. Dalal A, et al. Among authors: danda d, danda s. Am J Med Genet A. 2012 Nov;158A(11):2820-8. doi: 10.1002/ajmg.a.35620. Epub 2012 Sep 17. Am J Med Genet A. 2012. PMID: 22987568

7

A descriptive analysis of 14 cases of progressive-psuedorheumatoid-arthropathy of childhood from south India: review of literature in comparison with juvenile idiopathic arthritis.

Ekbote AV, Danda D, Kumar S, Danda S, Madhuri V, Gibikote S. Ekbote AV, et al. Among authors: danda d, danda s. Semin Arthritis Rheum. 2013 Jun;42(6):582-9. doi: 10.1016/j.semarthrit.2012.09.001. Epub 2012 Dec 25. Semin Arthritis Rheum. 2013. PMID: 23270760 Review.

8

Novel mutations in the neuraminidase-1 (NEU1) gene in two patients of sialidosis in India.

Ranganath P, Sharma V, Danda S, Nandineni MR, Dalal AB. Ranganath P, et al. Among authors: danda s. Indian J Med Res. 2012 Dec;136(6):1048-50. Indian J Med Res. 2012. PMID: 23391804 Free PMC article. No abstract available.

9

Molecular analyses of novel ASAH1 mutations causing Farber lipogranulomatosis: analyses of exonic splicing enhancer inactivating mutation.

Bashyam MD, Chaudhary AK, Kiran M, Reddy V, Nagarajaram HA, Dalal A, Bashyam L, Suri D, Gupta A, Gupta N, Kabra M, Puri RD, RamaDevi R, Kapoor S, Danda S. Bashyam MD, et al. Among authors: danda s. Clin Genet. 2014 Dec;86(6):530-8. doi: 10.1111/cge.12316. Epub 2013 Dec 20. Clin Genet. 2014. PMID: 24355074

10

Clinical utility of multiplex ligation-dependent probe amplification technique in identification of aetiology of unexplained mental retardation: a study in 203 Indian patients.

Boggula VR, Shukla A, Danda S, Hariharan SV, Nampoothiri S, Kumar R, Phadke SR. Boggula VR, et al. Among authors: danda s. Indian J Med Res. 2014 Jan;139(1):66-75. Indian J Med Res. 2014. PMID: 24604040 Free PMC article.

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