Results 21 to 30 of about 45,884 (249)

Inherited Metabolic Causes of Stroke in Children: Mechanisms, Types, and Management

open access: yesFrontiers in Neurology, 2021
A stroke should be considered in cases of neurologic decompensation associated with inherited metabolic disorders. A resultant stroke could be a classical ischemic stroke (vascular stroke) or more commonly a “metabolic stroke.” A metabolic stroke begins ...
Brahim Tabarki   +6 more
doaj   +1 more source

Atypical Strokes in a Young African American Male: A Case of Mitochondrial Encephalopathy Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome

open access: yesStroke Research and Treatment, 2011
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare but important cause of stroke-like symptoms which can often be missed Thambisetty and Newman 2004.
Jully M. Sanchez   +3 more
doaj   +1 more source

Mitochondrial Encephalopathy and Cytochrome C

open access: yesPediatric Neurology Briefs, 1997
Benefits from treatment of mitochondrial encephalomyopathy (MEM) with cytochrome C (6.25 mg) and vitamins Bl (25 mg) and B2 (12.5 mg), in daily injections, are reported from Osaka University Medical School and other centers in Japan.
J Gordon Millichap
doaj   +1 more source

Epilepsy Associated With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes

open access: yesFrontiers in Neurology, 2021
Objectives: The present study explored the clinical characteristics and prognostic factors of epilepsy in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS).Methods: Thirty-four MELAS patients were included ...
Jiaai Li   +5 more
doaj   +1 more source

Clinical Characteristics of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes

open access: yesLife, 2021
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome, a maternally inherited mitochondrial disorder, is characterized by its genetic, biochemical and clinical complexity.
Hueng-Chuen Fan   +3 more
doaj   +1 more source

Nitric Oxide Deficiency in Mitochondrial Disorders: The Utility of Arginine and Citrulline

open access: yesFrontiers in Molecular Neuroscience, 2021
Mitochondrial diseases represent a growing list of clinically heterogeneous disorders that are associated with dysfunctional mitochondria and multisystemic manifestations.
Mohammed Almannai   +3 more
doaj   +1 more source

Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report

open access: yesJournal of Medical Case Reports, 2019
Background Maternally inherited diabetes and deafness, and mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes are examples of mitochondrial diseases that are relatively common in the adult population. Mitochondrial myopathy,
Mai Fukuda, Yoshiro Nagao
doaj   +1 more source

Chorea-ballism as a dominant clinical manifestation in heteroplasmic mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome with A3251G mutation in mitochondrial genome: a case report

open access: yesJournal of Medical Case Reports, 2019
Background Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes, the most common maternally inherited mitochondrial disease, can present with a wide range of neurological manifestations including both central and peripheral nervous ...
Durjoy Lahiri   +5 more
doaj   +1 more source

Stroke and Stroke-like Episodes in Muscle Disease [PDF]

open access: yesThe Open Neurology Journal, 2012
Though not obvious at a first glance, myopathies may be associated with ischemic stroke. Stroke-like episodes resemble ischemic stroke only to some extent but are a unique feature of certain mitochondrial disorders with a pathogenesis at variance from that of ischemic stroke.
openaire   +2 more sources

Stroke-like episodes in mitochondrial encephalomyopathy with lactic acidosis

open access: yesАнналы клинической и экспериментальной неврологии, 2017
We described two patients (female, 47 years and male, 42 years)with mitochondrial encephalomyopathy, lactic acidosis andstroke-like episodes (MELAS). Diagnosis was confirmed bygenetic study (A3243G mitochondrial DNA mutation wasfound), muscle biopsy and ...
L. A. Kalashnikova   +9 more
doaj   +1 more source

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