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Identification of novel mutations in HEXA gene in children affected with Tay Sachs disease from India.
PLoS One. 2012;7(6):e39122. doi: 10.1371/journal.pone.0039122. Epub 2012 Jun 18.
PLoS One. 2012.
PMID: 22723944
Free PMC article.
Clinical, biochemical and mutation profile in Indian patients with Sandhoff disease.
Tamhankar PM, Mistri M, Kondurkar P, Sanghavi D, Sheth J.
Tamhankar PM, et al. Among authors: kondurkar p.
J Hum Genet. 2016 Feb;61(2):163-6. doi: 10.1038/jhg.2015.130. Epub 2015 Nov 19.
J Hum Genet. 2016.
PMID: 26582265
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Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1.
Tamhankar PM, Vasudevan L, Kondurkar P, Niazi S, Christopher R, Solanki D, Dholakia P, Muranjan M, Kamate M, Kalane U, Sheth J, Tamhankar V, Gulati R, Vasikarla M, Danda S, Naushad SM, Girisha KM, Patil S.
Tamhankar PM, et al. Among authors: kondurkar p.
J Pediatr Genet. 2021 Sep;10(3):213-221. doi: 10.1055/s-0040-1715528. Epub 2020 Sep 2.
J Pediatr Genet. 2021.
PMID: 34504725
Free PMC article.
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Krabbe disease--clinical profile.
Tullu MS, Muranjan MN, Kondurkar PP, Bharucha BA.
Tullu MS, et al. Among authors: kondurkar pp.
Indian Pediatr. 2000 Sep;37(9):939-46.
Indian Pediatr. 2000.
PMID: 10992329
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Clinical features of organic acidemias: experience at a tertiary care center in Mumbai.
Muranjan MN, Kondurkar P.
Muranjan MN, et al. Among authors: kondurkar p.
Indian Pediatr. 2001 May;38(5):518-24.
Indian Pediatr. 2001.
PMID: 11359979
No abstract available.
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Effect of deferiprone on urinary zinc excretion in multiply transfused children with thalassemia major.
Bartakke S, Bavdekar SB, Kondurkar P, Muranjan MN, Manglani MV, Sharma R.
Bartakke S, et al. Among authors: kondurkar p.
Indian Pediatr. 2005 Feb;42(2):150-4.
Indian Pediatr. 2005.
PMID: 15767711
Free article.
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