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Sumita Danda

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Movement Disorders Clinical Practice|October 17, 2022

Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian ChildrenDivyani Garg, Sangeetha Yoganathan, Uzma Shamim, et al.

American Journal of Medical Genetics. Part A|September 25, 2014

GALNS mutations in Indian patients with mucopolysaccharidosis IVAAbdul Mueed Bidchol, Ashwin Dalal, Hitesh Shah, et al.

Gene|May 5, 2015

Recurrent and novel GLB1 mutations in IndiaAbdul Mueed Bidchol, Ashwin Dalal, Rakesh Trivedi, et al.

Epilepsia|January 17, 2024

KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literatureSangeetha Yoganathan, Robyn Whitney, Maya Thomas, et al.

American Journal of Human Genetics|July 5, 2016

Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and CraniosynostosisAimee L Fenwick, Maciej Kliszczak, Fay Cooper, et al.

Nature Genetics|July 18, 2018

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migrationAshleigh E Schaffer, Martin W Breuss, Ahmet Okay Caglayan, et al.

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Search research articles

Showing results (111-120 of 116) with videos related to

Sort By:

Pageof 12

You have reached the last page of results.This site can display upto 116 results.

Movement Disorders Clinical Practice|October 17, 2022

Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian ChildrenDivyani Garg, Sangeetha Yoganathan, Uzma Shamim, et al.

American Journal of Medical Genetics. Part A|September 25, 2014

GALNS mutations in Indian patients with mucopolysaccharidosis IVAAbdul Mueed Bidchol, Ashwin Dalal, Hitesh Shah, et al.

Gene|May 5, 2015

Recurrent and novel GLB1 mutations in IndiaAbdul Mueed Bidchol, Ashwin Dalal, Rakesh Trivedi, et al.

Epilepsia|January 17, 2024

KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literatureSangeetha Yoganathan, Robyn Whitney, Maya Thomas, et al.

American Journal of Human Genetics|July 5, 2016

Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and CraniosynostosisAimee L Fenwick, Maciej Kliszczak, Fay Cooper, et al.

Nature Genetics|July 18, 2018

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migrationAshleigh E Schaffer, Martin W Breuss, Ahmet Okay Caglayan, et al.

Pageof 12