Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
4 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Publication Date timeline is not available.
Page 1
Spectrum of ARSA variations in Asian Indian patients with Arylsulfatase A deficient metachromatic leukodystrophy.
J Hum Genet. 2019 Apr;64(4):323-331. doi: 10.1038/s10038-019-0560-1. Epub 2019 Jan 23.
J Hum Genet. 2019.
PMID: 30674982
Spectrum of SMPD1 mutations in Asian-Indian patients with acid sphingomyelinase (ASM)-deficient Niemann-Pick disease.
Ranganath P, Matta D, Bhavani GS, Wangnekar S, Jain JM, Verma IC, Kabra M, Puri RD, Danda S, Gupta N, Girisha KM, Sankar VH, Patil SJ, Ramadevi AR, Bhat M, Gowrishankar K, Mandal K, Aggarwal S, Tamhankar PM, Tilak P, Phadke SR, Dalal A.
Ranganath P, et al.
Am J Med Genet A. 2016 Oct;170(10):2719-30. doi: 10.1002/ajmg.a.37817. Epub 2016 Jun 24.
Am J Med Genet A. 2016.
PMID: 27338287
Item in Clipboard
Autistic children exhibit distinct plasma amino acid profile.
Naushad SM, Jain JM, Prasad CK, Naik U, Akella RR.
Naushad SM, et al.
Indian J Biochem Biophys. 2013 Oct;50(5):474-8.
Indian J Biochem Biophys. 2013.
PMID: 24772971
Item in Clipboard
Aberrations in folate metabolic pathway and altered susceptibility to autism.
Mohammad NS, Jain JM, Chintakindi KP, Singh RP, Naik U, Akella RR.
Mohammad NS, et al.
Psychiatr Genet. 2009 Aug;19(4):171-6. doi: 10.1097/YPG.0b013e32832cebd2.
Psychiatr Genet. 2009.
PMID: 19440165
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.