Rita Christopher
Overview
Explore the profile of Rita Christopher including associated specialties, affiliations and a list of published articles.
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Articles
135
Citations
1291
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0
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Recent Articles
11.
Natarajan A, Christopher R
Pract Lab Med
. 2023 Jan;
33:e00305.
PMID: 36618341
Background And Objectives: Very long-chain fatty acyl-lysophosphatidylcholines (VLCFA-LysoPCs) are measured in dried blood spots (DBS) for identifying X-linked adrenoleukodystrophy (X-ALD) and other inherited peroxisomal disorders. Our study aimed to establish...
12.
Aditi Devi N, Phillip M, Varambally S, Christopher R, Gangadhar B
Asian J Psychiatr
. 2023 Jan;
81:103429.
PMID: 36608612
No abstract available.
13.
Siroya H, Devi B, Aripirala P, Ramesh S, Bhat D, Shukla D, et al.
Asian J Neurosurg
. 2022 Sep;
17(2):199-208.
PMID: 36120623
Endothelial nitric oxide synthase ( gene polymorphisms are found to predict predisposition to aneurysmal rupture and development of vasospasm in a patient of subarachnoid hemorrhage (SAH). gene polymorphisms are also...
14.
Nattala P, Kishore M, Murthy P, Christopher R, Veerabathini J, Suresh S
J Neurosci Rural Pract
. 2022 Aug;
13(3):441-447.
PMID: 35946027
To compare the executive functions in adolescents of fathers with alcohol dependence (AOFADs) with a control group of adolescents without a paternal history of alcohol dependence and examine the association...
15.
Gowda V, Vignesh S, Nagarajan B, Srinivasan V, Battina M, Bhat M, et al.
J Pediatr Genet
. 2022 Jun;
11(2):87-90.
PMID: 35769961
Biotinidase deficiency is a treatable neurometabolic disorder. It usually presents during the first year of life with seizures, ataxia, hypotonia, vision and hearing disturbance, alopecia, and skin rashes. It can...
16.
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.
17.
Arora C, Padmanabha H, Christopher R, Mahale R, Bhat M, Arunachal G, et al.
Ann Indian Acad Neurol
. 2022 Jun;
25(2):275-278.
PMID: 35693670
No abstract available.
18.
Ramaswamy P, Christopher R, Pal P, Debnath M, Yadav R
Diagnostics (Basel)
. 2022 May;
12(5).
PMID: 35626359
Progressive supranuclear palsy (PSP) is the second most common Parkinsonian disorder with complex etiology. The underlying molecular mechanism of PSP pathogenesis remains unclear. The present study aims to find the...
19.
Narendiran S, Debnath M, Shivaram S, Kannan R, Sharma S, Christopher R, et al.
J Neurogenet
. 2022 May;
36(1):21-31.
PMID: 35499206
The Hereditary Spastic Paraplegias (HSPs) are a group of clinically and genetically heterogeneous disorders characterized by length dependent degeneration of the corticospinal tracts. Genetic data related to HSPs are limited...
20.
Padmanabha H, Mahale R, Christopher R, Arunachal G, Bhat M, Mondal M, et al.
Ann Indian Acad Neurol
. 2022 Apr;
24(6):908-916.
PMID: 35359558
Objectives: The objective of this study is to describe the clinical, biochemical, radiological, and genetic profile of patients presenting with progressive spastic paraparesis due to homocysteine remethylation pathway defect. Methods:...