Michele L Yang
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Explore the profile of Michele L Yang including associated specialties, affiliations and a list of published articles.
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18
Citations
298
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Recent Articles
1.
Dang U, Damsker J, Guglieri M, Clemens P, Perlman S, Smith E, et al.
Neurology
. 2024 Feb;
102(5):e208112.
PMID: 38335499
Background And Objectives: Vamorolone is a dissociative agonist of the glucocorticoid receptor that has shown similar efficacy and reduced safety concerns in comparison with prednisone in Duchenne muscular dystrophy (DMD)....
2.
Gorokhova S, Schessl J, Zou Y, Yang M, Heydemann P, Sufit R, et al.
Med
. 2023 Mar;
4(4):245-251.e3.
PMID: 36905929
Background: Utrophin, a dystrophin homolog, is consistently upregulated in muscles of patients with Duchenne muscular dystrophy (DMD) and is believed to partially compensate for the lack of dystrophin in dystrophic...
3.
Joshi C, Yang M, Eschbach K, Tong S, Jacobson M, Stillman C, et al.
Neurol Clin Pract
. 2021 Apr;
11(2):e73-e82.
PMID: 33842074
Objective: To examine whether telemedicine remains safe and of high quality despite rapid expansion of services by comparing telemedicine encounters before and during the COVID-19 pandemic. Methods: Pre-post study investigating...
4.
James K, Gralla J, Ridall L, Do T, Czaja A, Mourani P, et al.
Cardiol Young
. 2020 Jan;
30(2):171-176.
PMID: 31964455
Background: Duchenne muscular dystrophy is associated with progressive cardiorespiratory failure, including left ventricular dysfunction. Methods And Results: Males with probable or definite diagnosis of Duchenne muscular dystrophy, diagnosed between 1...
5.
Mortality and respiratory support in X-linked myotubular myopathy: a RECENSUS retrospective analysis
Graham R, Muntoni F, Hughes I, Yum S, Kuntz N, Yang M, et al.
Arch Dis Child
. 2019 Sep;
105(4):332-338.
PMID: 31484632
Purpose: Individuals with X-linked myotubular myopathy (XLMTM) who survive infancy require extensive supportive care, including ventilator assistance, wheelchairs and feeding tubes. Half die before 18 months of age. We explored...
6.
Beck D, Subramanian T, Vijayalingam S, Ezekiel U, Donkervoort S, Yang M, et al.
Neurogenetics
. 2019 May;
20(3):129-143.
PMID: 31041561
We previously reported a pathogenic de novo p.R342W mutation in the transcriptional corepressor CTBP1 in four independent patients with neurodevelopmental disabilities [1]. Here, we report the clinical phenotypes of seven...
7.
Beggs A, Byrne B, de Chastonay S, Haselkorn T, Hughes I, James E, et al.
Muscle Nerve
. 2017 Nov;
57(4):550-560.
PMID: 29149770
Introduction: X-linked myotubular myopathy (XLMTM), characterized by severe hypotonia, weakness, respiratory distress, and early mortality, is rare and natural history studies are few. Methods: RECENSUS is a multicenter chart review...
8.
Martin J, Messacar K, Yang M, Maloney J, Lindwall J, Carry T, et al.
Neurology
. 2017 Jun;
89(2):129-137.
PMID: 28615421
Objective: We describe long-term functional, neurodiagnostic, and psychosocial outcomes of a cohort of 12 children from Colorado diagnosed with acute flaccid myelitis (AFM) in 2014. Methods: Children were assessed every...
9.
Watne L, Yang M
J Pediatr Rehabil Med
. 2016 Mar;
9(1):13-21.
PMID: 26966796
Objective: To assess the effect of nutritional interventions on growth and on respiratory status in patients with congenital myopathy (CM), congenital muscular dystrophy (CMD), and congenital myasthenic syndrome (CMS). Methods:...
10.
Zukosky K, Meilleur K, Traynor B, Dastgir J, Medne L, Devoto M, et al.
JAMA Neurol
. 2015 May;
72(6):689-98.
PMID: 25938801
Importance: New genomic strategies can now be applied to identify a diagnosis in patients and families with previously undiagnosed rare genetic conditions. The large family evaluated in the present study...