Sara E Sabbagh
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Explore the profile of Sara E Sabbagh including associated specialties, affiliations and a list of published articles.
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9
Citations
23
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Recent Articles
1.
Chen K, Chiu Y, Vleugels R, Co D, Kim H, Sabbagh S, et al.
J Invest Dermatol
. 2024 Nov;
PMID: 39530954
Juvenile dermatomyositis (JDM), the most common pediatric inflammatory myopathy, is associated with significant morbidity despite therapeutic advances. Distinct clinical phenotypes have emerged, which can correlate with myositis-specific antibodies. Because translational...
2.
Sabbagh S, Haribhai D, Gershan J, Verbsky J, Nocton J, Yassai M, et al.
Front Immunol
. 2024 Jul;
15:1446946.
PMID: 38962010
[This corrects the article DOI: 10.3389/fimmu.2024.1306490.].
3.
Tarvin S, Sherman M, Kim H, Balmuri N, Brown A, Chow A, et al.
Arthritis Care Res (Hoboken)
. 2024 Jun;
76(11):1532-1539.
PMID: 38937134
Objective: The objective was to develop consensus treatment plans (CTPs) for patients with refractory moderately severe juvenile dermatomyositis (JDM) treated with biologic disease-modifying antirheumatic drugs (bDMARDs). Methods: The Biologics Workgroup...
4.
Sabbagh S, Haribhai D, Gershan J, Verbsky J, Nocton J, Yassai M, et al.
Front Immunol
. 2024 Jun;
15:1306490.
PMID: 38873594
Recurrent exposures to a pathogenic antigen remodel the CD8 T cell compartment and generate a functional memory repertoire that is polyclonal and complex. At the clonotype level, the response to...
5.
Karasawa R, Yudoh K, Sato T, Tanaka M, Sabbagh S, Flegel W, et al.
Rheumatology (Oxford)
. 2023 May;
62(11):3757-3762.
PMID: 37144941
Objectives: AECAs are detected in multiple forms of vasculitis or vasculopathy, including JDM. High levels of tropomyosin alpha-4 chain (TPM4) gene expression in cutaneous lesions and TPM4 protein expression in...
6.
Sherman M, Graf R, Sabbagh S, Galindo-Feria A, Pinal-Fernandez I, Pak K, et al.
Rheumatology (Oxford)
. 2022 Aug;
62(SI2):SI226-SI234.
PMID: 35961028
Objectives: Four-and-a-half LIM domains 1 (FHL1) is a muscle-specific protein. Autoantibodies against FHL1 were recently discovered in adults with idiopathic inflammatory myopathies (IIMs) and were found to be associated with...
7.
Karasawa R, Yudoh K, Sato T, Tanaka M, Tamaki M, Sabbagh S, et al.
Rheumatology (Oxford)
. 2021 Nov;
61(7):2969-2977.
PMID: 34791087
Objectives: JDM is an inflammatory myopathy characterized by prominent vasculopathy. AECAs are frequently detected in inflammatory and autoimmune diseases. We sought to determine whether AECAs correlate with clinical features of...
8.
Sabbagh S, Pinal-Fernandez I, Casal-Dominguez M, Albayda J, Paik J, Miller F, et al.
Clin Rheumatol
. 2021 Apr;
40(10):4095-4100.
PMID: 33851273
We analyzed the prevalence of anti-mitochondrial autoantibodies (AMA) in adult- and juvenile-onset myositis longitudinal cohorts and investigated phenotypic differences in myositis patients with AMA. We screened sera from myositis patients...
9.
Sabbagh S, Neely J, Chow A, DeGuzman M, Lai J, Lvovich S, et al.
Rheumatology (Oxford)
. 2020 Sep;
60(2):829-836.
PMID: 32889531
Objectives: Pneumocystis jirovecii pneumonia (PJP) is associated with significant morbidity and mortality in adult myositis patients; however, there are few studies examining PJP in juvenile myositis [juvenile idiopathic inflammatory myopathy...