Gopikrishnan Unnikrishnan
Overview
Explore the profile of Gopikrishnan Unnikrishnan including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
22
Citations
52
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Chawla T, Baskar D, Polavarapu K, Preethish-Kumar V, Nashi S, Vengalil S, et al.
Ann Indian Acad Neurol
. 2025 Mar;
PMID: 40079678
Background And Objectives: Magnetic resonance imaging (MRI) in dysferlinopathy has consistently demonstrated a particular pattern of affliction. We aimed to study muscle MRI characteristics of lower limbs in limb girdle...
2.
Baskar D, Vengalil S, Polavarapu K, Preethish-Kumar V, Nashi S, Arunachal G, et al.
J Neuromuscul Dis
. 2025 Mar;
:22143602241313119.
PMID: 40033712
Introduction: Titinopathies are heterogenous group of disorders affecting the skeletal and cardiac muscles variably and caused by Titin ( gene mutations located in Chromosome 2. The manifestations extend from congenital...
3.
Sriram M, Shivarthi T, Narayanan S, Rohan P, Nikhilesh M, Kannoth S, et al.
Epileptic Disord
. 2025 Feb;
PMID: 39932459
No abstract available.
4.
Kumar S, Kannoth S, Nambiar V, Gopinath S, Anandakuttan A, Umesh S, et al.
Neurol Sci
. 2025 Jan;
PMID: 39843650
Background: In this research, we extend our initial study in 2016 of a distinct cohort diagnosed with autoimmune atypical parkinsonism, assessing the long-term effects of immunotherapy over a decade. Objective:...
5.
Sridhar S, Nashi S, Kulanthaivelu K, Vengalil S, Baskar D, Polavarapu K, et al.
Neuromuscul Disord
. 2025 Jan;
47:105257.
PMID: 39756250
Idiopathic inflammatory myopathies (IIMs) constitute a group of immune-mediated disorders, affecting muscles. Our study aims to investigate the specific patterns of muscle involvement in subgroups of IIM. An ambispective and...
6.
Shivarthi T, Sriram M, Nikhilesh M, Rohan P, Jinna S, Kannoth S, et al.
Mult Scler Relat Disord
. 2024 Dec;
93:106249.
PMID: 39736174
Background And Objectives: Myelin oligodendrocyte glycoprotein (MOG) associated disease (MOGAD) is an antibody-mediated inflammatory demyelinating disorder of the CNS with varied presentations like optic neuritis (ON), transverse myelitis, and cortical...
7.
Jiju J, Santhosh S, Lalwani C, Thampi S, Kannoth S, Nambiar V, et al.
Neurol India
. 2024 Dec;
72(6):1259-1262.
PMID: 39691002
Anti γ aminobutyric acid B(GABA B) receptor encephalitis is a rare form of autoimmune encephalitis. Our aim is to study the clinical characteristics and treatment outcomes of anti GABA B...
8.
Baskar D, Vengalil S, Polavarapu K, Preethish-Kumar V, Arunachal G, Sukrutha R, et al.
Glob Med Genet
. 2024 Sep;
11(4):297-303.
PMID: 39238562
ORAI-1 is a plasma membrane calcium release-activated calcium channel that plays a crucial role in the excitation-contraction of skeletal muscles. Loss-of-function mutations of cause severe combined immunodeficiency, nonprogressive muscle hypotonia,...
9.
Baskar D, Reddy N, Preethish-Kumar V, Polavarapu K, Nishadham V, Vengalil S, et al.
J Neuromuscul Dis
. 2024 Aug;
11(5):959-968.
PMID: 39213088
Introduction: GNE myopathy is a rare slowly progressive adult-onset distal myopathy with autosomal recessive inheritance. It has distinctive features of quadriceps sparing with preferential anterior tibial involvement. Most patients eventually...
10.
Chawla T, Nashi S, Baskar D, Polavarapu K, Vengalil S, Bardhan M, et al.
Neurogenetics
. 2024 Aug;
25(4):435-469.
PMID: 39103709
Congenital Muscular Dystrophies (CMD) are phenotypically and genotypically heterogenous disorders with a prevalence of 0.68 to 2.5/100,000, contributing to significant morbidity and mortality. We aimed to study the phenotype-genotype spectrum...