Results 251 to 260 of about 161,523 (294)

An unusual presentation of pheochromocytoma accompanied by catecholamine‐induced cardiomyopathy

open access: yes
ESC Heart Failure, EarlyView.
Hugh O.J. Roberts   +2 more
wiley   +1 more source

Mitochondrial dysfunction: Related diseases, influencing factors, and detection

open access: yesInterdisciplinary Medicine, EarlyView.
Mitochondrial dysfunction is implicated in the pathogenesis of numerous diseases, including neurological disorders, cancers, and cardiovascular conditions, through mechanisms such as mitochondrial DNA mutations, dysregulation of mitochondrial network dynamics, and impaired mitophagy.
Zhaojin Li   +9 more
wiley   +1 more source

New insights into applications of base editor in hereditary disorders

open access: yesInterdisciplinary Medicine, EarlyView.
Abstract Hereditary disorders are a group of diseases caused by genetic mutations or chromosomal variations. Although the incidence of each genetic disorder is relatively low, patients affected by the disease generally experience a range of severe symptoms, including blindness, disability, and even premature death. In addition, the available treatments
Maoping Cai   +8 more
wiley   +1 more source

Update on left ventricular outflow tract obstruction. [PDF]

open access: yesJ Cardiovasc Imaging
Song JK, Sun BJ, Kim DH, Jung SH.
europepmc   +1 more source

Integrated single-cell functional-proteomic profiling reveals a shift in myofibre specificity in human nemaline myopathy: A proof-of-principle study. [PDF]

open access: yesJ Physiol
Seaborne RAE   +9 more
europepmc   +1 more source

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