Bevinahalli Nandeesh
Overview
Explore the profile of Bevinahalli Nandeesh including associated specialties, affiliations and a list of published articles.
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8
Citations
23
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0
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Recent Articles
1.
Polavarapu K, ONeil D, Thompson R, Spendiff S, Nandeesh B, Vengalil S, et al.
Neuromuscul Disord
. 2024 Apr;
39:10-18.
PMID: 38669730
Recessive desminopathies are rare and often present as severe early-onset myopathy. Here we report a milder phenotype in three unrelated patients from southern India (2 M, 1F) aged 16, 21,...
2.
Van Haute L, OConnor E, Diaz-Maldonado H, Munro B, Polavarapu K, Hock D, et al.
Nat Commun
. 2023 Feb;
14(1):1009.
PMID: 36823193
Mutations in the mitochondrial or nuclear genomes are associated with a diverse group of human disorders characterized by impaired mitochondrial respiration. Within this group, an increasing number of mutations have...
3.
Santhappan Girija M, Tiwari R, Vengalil S, Nashi S, Preethish-Kumar V, Polavarapu K, et al.
Neurol Res Pract
. 2022 Oct;
4(1):49.
PMID: 36210472
Background: We sought to determine the utility of PET-MRI in diagnosing Idiopathic Inflammatory Myositis (IIM), and look for association between FDG uptake and clinical, pathological and laboratory parameters. Methods: A...
4.
Sriram N, Padmanabha H, Chandra S, Mahale R, Nandeesh B, Bhat M, et al.
Ann Indian Acad Neurol
. 2022 Jun;
25(2):311-314.
PMID: 35693676
No abstract available.
5.
Polavarapu K, Mathur A, Joshi A, Nashi S, Preethish-Kumar V, Bardhan M, et al.
Neurogenetics
. 2021 Aug;
22(4):271-285.
PMID: 34333724
Twelve patients from seven unrelated South Indian families with a limb-girdle muscular dystrophy-congenital myasthenic syndrome (LGMD/CMS) phenotype and recessive inheritance underwent deep clinical phenotyping, electrophysiological evaluation, muscle histopathology, and next-generation...
6.
Polavarapu K, Vengalil S, Preethish-Kumar V, Arunachal G, Nashi S, Mohan D, et al.
Eur J Paediatr Neurol
. 2021 Feb;
31:54-60.
PMID: 33631708
Three unrelated girls, all born to consanguineous parents had respiratory distress, severe hypotonia at birth along with prominent fatigable muscle weakness and characteristic myopathic facies. In addition, patient 1 had...
7.
Vengalil S, Lavania M, Singh I, Nashi S, Preethish-Kumar V, Polavarapu K, et al.
Am J Trop Med Hyg
. 2020 Apr;
103(1):209-213.
PMID: 32285768
Identification of DNA by polymerase chain reaction (PCR) is a reliable and an affordable method to confirm leprosy. DNA from 87 nerve samples (61 from paraffin blocks and 26 fresh...
8.
Anadure R, Narayanan C, Varadraj G, Nandeesh B
J Clin Diagn Res
. 2017 Mar;
11(1):OD01-OD03.
PMID: 28273992
Mononeuritis multiplex is a common manifestation of many illnesses which includes Hansen's disease and certain types of systemic vasculitis. The Antineutrophil Cytoplasmic Antibody (ANCA)-Associated Vasculitis (AAV) is a group of...