Mathula Thangarajh
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Explore the profile of Mathula Thangarajh including associated specialties, affiliations and a list of published articles.
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31
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572
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Recent Articles
1.
Clemens P, Gordish-Dressman H, Niizawa G, Gorni K, Guglieri M, Connolly A, et al.
J Neuromuscul Dis
. 2023 Nov;
11(1):201-212.
PMID: 37980682
Background: Becker muscular dystrophy is an X-linked, genetic disorder causing progressive degeneration of skeletal and cardiac muscle, with a widely variable phenotype. Objective: A 3-year, longitudinal, prospective dataset contributed by...
2.
Association between neurodevelopmental impairments and motor function in Duchenne muscular dystrophy
Thangarajh M, McDermott M, Guglieri M, Griggs R
Ann Clin Transl Neurol
. 2023 Oct;
10(12):2285-2296.
PMID: 37804000
Objective: We explored various prognostic factors of motor outcomes in corticosteroid-naive boys with Duchenne Muscular Dystrophy (DMD). Methods: The associations between parent-reported neurodevelopmental concerns (speech delay, speech and language difficulties...
3.
Guglieri M, Bushby K, McDermott M, Hart K, Tawil R, Martens W, et al.
JAMA
. 2022 Apr;
327(15):1456-1468.
PMID: 35381069
Importance: Corticosteroids improve strength and function in boys with Duchenne muscular dystrophy. However, there is uncertainty regarding the optimum regimen and dosage. Objective: To compare efficacy and adverse effects of...
4.
Thangarajh M, Bello L, Gordish-Dressman H
Muscle Nerve
. 2021 Jul;
64(4):467-473.
PMID: 34255858
Introduction/aims: There is considerable heterogenicity in clinical outcomes in Duchenne muscular dystrophy (DMD). The aim of this study was to assess whether dystrophin gene (DMD) pathogenic variant location influences upper...
5.
Pilato C, Walker M, Nguyen A, Hanna M, Huang S, Lutins E, et al.
Autops Case Rep
. 2020 Dec;
10(4):e2020221.
PMID: 33344329
There is scant information about the comprehensive distribution of dystrophic muscles in muscular dystrophy. Despite different clinical presentations of muscular dystrophy, a recent multi-center study concluded that phenotypic distribution of...
6.
Heier C, Zhang A, Nguyen N, Tully C, Panigrahi A, Gordish-Dressman H, et al.
J Pers Med
. 2020 Nov;
10(4).
PMID: 33228131
The development of therapeutics for muscle diseases such as facioscapulohumeral dystrophy (FSHD) is impeded by a lack of objective, minimally invasive biomarkers. Here we identify circulating miRNAs and proteins that...
7.
Thangarajh M, Elfring G, Trifillis P
J Clin Med
. 2020 Sep;
9(9).
PMID: 32933029
The developmental maturation of forward and backward digit spans-indices of working memory-in boys with nonsense (nm) Duchenne muscular dystrophy (DMD) (nmDMD) was assessed using prospective, longitudinal data. Methods: Fifty-five boys...
8.
Hendriksen J, Thangarajh M, Kan H, Muntoni F
Neuromuscul Disord
. 2020 Sep;
30(9):782-794.
PMID: 32912717
No abstract available.
9.
Clemens P, Niizawa G, Feng J, Florence J, DAlessandro A, Morgenroth L, et al.
Muscle Nerve
. 2020 Jun;
62(3):369-376.
PMID: 32564389
We performed an observational, natural history study of males with in-frame dystrophin gene deletions causing Becker muscular dystrophy (BMD). A prospective natural history study collected longitudinal medical, strength, and timed...
10.
Thangarajh M
Continuum (Minneap Minn)
. 2019 Dec;
25(6):1619-1639.
PMID: 31794463
Purpose Of Review: The dystrophinopathies are among the most common neuromuscular conditions, and they include Duchenne and Becker muscular dystrophies. This article reviews the epidemiology, clinical manifestations, genetic cause, management,...