Anesthetic consideration for neuromuscular diseases

JA Katz, GS Murphy - Current Opinion in Anesthesiology, 2017 - journals.lww.com
Anesthetic consideration for neuromuscular diseases : Current Opinion in Anesthesiology
Anesthetic consideration for neuromuscular diseases : Current Opinion in Anesthesiology Log …

JCS/JHFS 2018 guideline on the diagnosis and treatment of cardiomyopathies

H Kitaoka, H Tsutsui, T Kubo, T Ide, T Chikamori… - Circulation …, 2021 - jstage.jst.go.jp
The classes of recommendations and levels of evidence in these guidelines were
determined and described according to the “Guidelines for the treatment of acute and …

[HTML][HTML] Essential roles of the dystrophin-glycoprotein complex in different cardiac pathologies

IC Valera, AL Wacker, HS Hwang, C Holmes… - Advances in medical …, 2021 - Elsevier
The dystrophin-glycoprotein complex (DGC), situated at the sarcolemma dynamically
remodels during cardiac disease. This review examines DGC remodeling as a common …

[HTML][HTML] Functional correction of dystrophin actin binding domain mutations by genome editing

V Kyrychenko, S Kyrychenko, M Tiburcy, JM Shelton… - JCI insight, 2017 - ncbi.nlm.nih.gov
Dystrophin maintains the integrity of striated muscles by linking the actin cytoskeleton with
the cell membrane. Duchenne muscular dystrophy (DMD) is caused by mutations in the …

[HTML][HTML] Atrioventricular block

AH Kashou, A Goyal, T Nguyen, I Ahmed, L Chhabra - 2017 - europepmc.org
Objectives: Recall the causes of AV block. Summarize the ECG features of atrioventricular
block. List the treatment and management options available for atrioventicular block. Explain …

Bioenergetic and metabolic impairments in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients

L Willi, I Abramovich, J Fernandez-Garcia… - International journal of …, 2022 - mdpi.com
Duchenne muscular dystrophy (DMD) is caused by mutations in the dystrophin gene and
dilated cardiomyopathy (DCM) is a major cause of morbidity and mortality in DMD patients …

Electrophysiological abnormalities in induced pluripotent stem cell‐derived cardiomyocytes generated from Duchenne muscular dystrophy patients

B Eisen, R Ben Jehuda, AJ Cuttitta… - Journal of Cellular …, 2019 - Wiley Online Library
Duchenne muscular dystrophy (DMD) is an X‐linked progressive muscle degenerative
disease, caused by mutations in the dystrophin gene and resulting in death because of …

Proteomic and morphological insights and clinical presentation of two young patients with novel mutations of BVES (POPDC1)

A Gangfuß, A Hentschel, L Heil, M Gonzalez… - Molecular Genetics and …, 2022 - Elsevier
Popeye domain containing protein 1 (POPDC1) is a highly conserved transmembrane
protein essential for striated muscle function and homeostasis. Pathogenic variants in the …

Dilated cardiomyopathy as the initial presentation of Becker muscular dystrophy: a systematic review of published cases

G Del Rio-Pertuz, C Morataya, K Parmar… - Orphanet Journal of …, 2022 - Springer
There are scarce publications regarding the presentation and outcome of Becker muscular
dystrophy in adulthood when idiopathic dilated cardiomyopathy is the initial disease …

Cardiac involvement in the muscular dystrophies

NJ Silvestri, H Ismail, P Zimetbaum… - Muscle & …, 2018 - Wiley Online Library
Cardiac disease is a common clinical manifestation present in a variety of neuromuscular
disorders, most notably the muscular dystrophies. Heart disease may produce the …