Sapra S - Search Results

1

The spectrum of neurological manifestations and genotype-phenotype correlation in Indian children with Gaucher disease.

Venkatachari M, Chakraborty S, Correa ARE, Mishra P, Kocchar KP, Kabra M, Chakrabarty B, Kalaivani M, Sapra S, Mishra P, Gulati S, Gupta N. Venkatachari M, et al. Among authors: sapra s. Am J Med Genet A. 2023 Apr;191(4):1038-1043. doi: 10.1002/ajmg.a.63115. Epub 2023 Jan 13. Am J Med Genet A. 2023. PMID: 36637080

2

Behavioral problems in children with Down syndrome.

Bhatia MS, Kabra M, Sapra S. Bhatia MS, et al. Among authors: sapra s. Indian Pediatr. 2005 Jul;42(7):675-80. Indian Pediatr. 2005. PMID: 16085968 Free article.

3

Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: report of two classical Rett syndrome patients of Indian origin.

Khajuria R, Sapra S, Ghosh M, Gupta N, Gulati S, Kalra V, Kabra M. Khajuria R, et al. Among authors: sapra s. Genet Test Mol Biomarkers. 2009 Apr;13(2):277-80. doi: 10.1089/gtmb.2008.0142. Genet Test Mol Biomarkers. 2009. PMID: 19371229

4

Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome.

Khajuria R, Sapra S, Ghosh M, Gupta N, Ghulati S, Kalra V, Kabra M. Khajuria R, et al. Among authors: sapra s. Hum Genet. 2010 Jan;127(1):117-8. Hum Genet. 2010. PMID: 20108394 No abstract available.

5

Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome.

Khajuria R, Sapra S, Ghosh M, Gupta N, Gulati S, Kalra V, Kabra M. Khajuria R, et al. Among authors: sapra s. Hum Genet. 2010 Jan;127(1):117. Hum Genet. 2010. PMID: 20108429 No abstract available.

6

Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome.

Khajuria R, Sapra S, Ghosh M, Gupta N, Gulati S, Kalra V, Kabra M. Khajuria R, et al. Among authors: sapra s. Hum Genet. 2010 Jan;127(1):118. Hum Genet. 2010. PMID: 20108430 No abstract available.

7

A novel MECP2 change in an indian boy with variant rett phenotype and congenital blindness: implications for genetic counseling and prenatal diagnosis.

Khajuria R, Gupta N, Sapra S, Gulati S, Ghosh M, Kalra V, Kabra M. Khajuria R, et al. Among authors: sapra s. J Child Neurol. 2011 Feb;26(2):209-13. doi: 10.1177/0883073810378535. J Child Neurol. 2011. PMID: 21285040

8

Novel non-identical MECP2 mutations in Rett syndrome family: a rare presentation.

Khajuria R, Gupta N, Sapra S, Gulati S, Ghosh M, Kalra V, Kabra M. Khajuria R, et al. Among authors: sapra s. Brain Dev. 2012 Jan;34(1):28-31. doi: 10.1016/j.braindev.2011.01.006. Epub 2011 Feb 5. Brain Dev. 2012. PMID: 21300488

9

Aetiology of global developmental delay in young children: experience from a tertiary care centre in India.

Tikaria A, Kabra M, Gupta N, Sapra S, Balakrishnan P, Gulati S, Pandey RM, Gupta AK. Tikaria A, et al. Among authors: sapra s. Natl Med J India. 2010 Nov-Dec;23(6):324-9. Natl Med J India. 2010. PMID: 21561041

10

Effectiveness and safety of donepezil in boys with fragile x syndrome: a double-blind, randomized, controlled pilot study.

Sahu JK, Gulati S, Sapra S, Arya R, Chauhan S, Chowdhury MR, Gupta N, Kabra M, Gupta YK, Dwivedi SN, Kalra V. Sahu JK, et al. Among authors: sapra s. J Child Neurol. 2013 May;28(5):570-5. doi: 10.1177/0883073812449381. Epub 2012 Jun 29. J Child Neurol. 2013. PMID: 22752489 Clinical Trial.

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