Titlebook: Diagnosis and Management of Mitochondrial Disorders; Michelangelo Mancuso,Thomas Klopstock Book 2019 Springer Nature Switzerland AG 2019 M

面包屑

observatory

Mitochondrial Neurodegenerative Disorders I: Parkinsonism and Cognitive Deficits,sease progression and discuss the data from human post-mortem studies, which provide evidence of mitochondrial dysfunction and molecular changes in mtDNA quality and quantity in idiopathic Parkinson’s disease, primary mitochondrial and .-related disorders. We also discuss the mechanistic insights gained from transgenic animal models.

空氣傳播

Mitochondrial Heart Involvement,causal therapeutic strategies are still lacking for patients with MID and cardiac involvement. Nevertheless, e.g., device therapies can be particularly helpful (and prolong life) in MID patients with arrhythmias—in case of early and timely diagnosis of the underlying cardiac disease.

remission

neoplasm

FEIGN

Mitochondria: Muscle Morphology,hies to indicate that skeletal muscle and brain tissue, due to their high energy demand, are most often involved..Given this background, skeletal muscle tissue is the most useful and extensively used target for morphological investigations. Indeed, skeletal muscle is a post-mitotic terminally differ

groggy

Mitochondrial Disease Genetics,ity, progression, and genetic etiologies. Mitochondria are cellular organelles in which oxidative phosphorylation occurs to generate chemical energy in the form of adenosine triphosphate (ATP). Both nuclear and mitochondrial DNA genomes contribute to approximately 1500 proteins that comprise mitocho

laxative

NOCT

Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS),pical symptoms of short stature, failure to thrive, recurrent headaches and vomiting, stroke-like episodes causing hemiplegia or vision loss, epilepsy, hearing loss, and diabetes. Additional manifestations include other endocrinopathies and cardiac involvement. MELAS is typically caused by a mitocho

精致