Works matching DE "MITOCHONDRIAL encephalomyopathies"
Results: 106
Malignant stroke in a ticagrelor non-responder as a complication following aneurysm treatment with the Pipeline Embolization Device™.
- Published in:
- Interventional Neuroradiology, 2017, v. 23, n. 3, p. 297, doi. 10.1177/1591019917697473
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- Publication type:
- Article
Ressonância Magnética Convencional, Difusão e Espectroscopia Protónica na Síndrome de MELAS.
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- Acta Médica Portuguesa, 2012, v. 25, n. Supp 1, p. 59
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- Publication type:
- Article
Mutations in coenzyme Q10 biosynthetic genes.
- Published in:
- 2007
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- Publication type:
- journal article
Diagnosing Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes (MELAS) Requires Not Only Phenotypic But Also Genotypic Verification.
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- Ochsner Journal, 2018, v. 18, n. 1, p. 4
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- Publication type:
- Article
Mitochondrial ataxia - Unravelling the puzzle.
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- Annals of Movement Disorders, 2024, v. 7, n. 2, p. 78, doi. 10.4103/aomd.aomd_63_24
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- Article
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement.
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- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 5, p. 492, doi. 10.1002/acn3.189
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- Article
Diagnostic Criteria For Pediatric Mitochondrial Disorders.
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- Iranian Journal of Child Neurology, 2013, v. 7, n. 4, p. 8
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- Article
Anesthetic Management for Pediatric Mitochondrial Disease.
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- International Student Journal of Nurse Anesthesia, 2017, v. 16, n. 3, p. 18
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- Article
Hemodialysis in MNGIE transiently reduces serum and urine levels of thymidine and deoxyuridine, but not CSF levels and neurological function.
- Published in:
- 2017
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- Publication type:
- Case Study
Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model.
- Published in:
- 2017
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- Publication type:
- journal article
Localization and amount of myoglobin and myoglobin mRNA in ragged-red fiber of patients with mitochondrial encephalomyopathy.
- Published in:
- 1996
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- Publication type:
- journal article
Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
- Published in:
- 1996
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- Publication type:
- journal article
Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient population.
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- Journal of Neurology, 2016, v. 263, n. 2, p. 257, doi. 10.1007/s00415-015-7969-z
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- Article
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?
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- Journal of Neurology, 2014, v. 261, n. 3, p. 504, doi. 10.1007/s00415-013-7225-3
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- Publication type:
- Article
Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation.
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- Journal of Neurology, 2013, v. 260, n. 4, p. 1071, doi. 10.1007/s00415-012-6763-4
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- Publication type:
- Article
A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria.
- Published in:
- 2010
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- Publication type:
- journal article
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) triggered by valproate therapy.
- Published in:
- 1997
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- Publication type:
- journal article
MELAS syndrome diagnosed in ICU in a 56-year-old patient presenting with status epilepticus.
- Published in:
- 2013
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- Publication type:
- Letter
Growth differentiation factor 15 as a useful biomarker for mitochondrial disorders.
- Published in:
- 2015
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- Publication type:
- journal article
Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy.
- Published in:
- 2001
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- Publication type:
- journal article
The mitochondrial DNA A8344G mutation in Leigh syndrome revealed by analysis in paraffin-embedded sections: revisiting the past.
- Published in:
- 1998
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- Publication type:
- journal article
Mitochondrial Neurogastrointestinal Encephalomyopathy: A Nonrenal Indication for Peritoneal Dialysis.
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- Indian Journal of Nephrology, 2018, v. 28, n. 4, p. 310, doi. 10.4103/ijn.IJN_404_17
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- Publication type:
- Article
Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions.
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- BMC Neurology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2377-14-116
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- Publication type:
- Article
Young onset mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome: a case report.
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- Critical Care Innovations, 2024, v. 7, n. 4, p. 43, doi. 10.32114/CCI.2024.7.4.43.48
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- Publication type:
- Article
Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion.
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- European Journal of Human Genetics, 2015, v. 23, n. 3, p. 325, doi. 10.1038/ejhg.2014.128
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- Publication type:
- Article
A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathy.
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- European Journal of Human Genetics, 2013, v. 21, n. 5, p. 571, doi. 10.1038/ejhg.2012.153
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- Publication type:
- Article
Cerebral imaging in paediatric mitochondrial disorders.
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- Neuroradiology Journal, 2018, v. 31, n. 6, p. 596, doi. 10.1177/1971400918786054
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- Publication type:
- Article
The Role of Brain MRI in Mitochondrial Neurogastrointestinal Encephalomyopathy.
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- Neuroradiology Journal, 2013, v. 26, n. 5, p. 520, doi. 10.1177/197140091302600505
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- Publication type:
- Article
Influenza A H1N1 Related Acute Necrotizing Encephalopathy: Radiological Findings in Adulthood.
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- Neuroradiology Journal, 2012, v. 25, n. 4, p. 397, doi. 10.1177/197140091202500401
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- Publication type:
- Article
Homeostatic structural plasticity can account for topology changes following deafferentation and focal stroke.
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- Frontiers in Neuroanatomy, 2014, v. 8, p. 1, doi. 10.3389/fnana.2014.00115
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- Publication type:
- Article
Childhood mitochondrial encephalomyopathies: clinical course, diagnosis, neuroimaging findings, mtDNA mutations and outcome in six children.
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- Italian Journal of Pediatrics, 2013, v. 39, n. 1, p. 60, doi. 10.1186/1824-7288-39-60
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- Publication type:
- Article
Isolated and repeated stroke-like episodes in a middle-aged man with a mitochondrial ND3 T10158C mutation: a case report.
- Published in:
- 2017
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- Publication type:
- journal article
Management von Patienten mit MELAS-Syndrom : Ein Fallbericht und allgemeine Besonderheiten aus anästhesiologischer Sicht.
- Published in:
- 2020
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- Publication type:
- journal article
Advances in the Treatment of MELAS Syndrome: Could Cognitive Rehabilitation Have a Role?
- Published in:
- 2016
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- Publication type:
- journal article
GlyNAC (Glycine and N-Acetylcysteine) Supplementation in Mice Increases Length of Life by Correcting Glutathione Deficiency, Oxidative Stress, Mitochondrial Dysfunction, Abnormalities in Mitophagy and Nutrient Sensing, and Genomic Damage.
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- Nutrients, 2022, v. 14, n. 5, p. N.PAG, doi. 10.3390/nu14051114
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- Publication type:
- Article
L-Arginine Reduces Nitro-Oxidative Stress in Cultured Cells with Mitochondrial Deficiency.
- Published in:
- Nutrients, 2021, v. 13, n. 2, p. 534, doi. 10.3390/nu13020534
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- Publication type:
- Article
Bright and dark vessels on stroke imaging: different sides of the same coin?
- Published in:
- 2016
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- Publication type:
- journal article
Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity.
- Published in:
- 2021
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- Publication type:
- journal article
Tumors masquerading as neurological diseases: A caution for clinicians in planning diagnosis and treatment.
- Published in:
- 2020
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- Publication type:
- journal article
Pregnancy-precipitated status epilepticus: a rare presentation of MELAS syndrome.
- Published in:
- 2007
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- Publication type:
- Case Study
Precipitation of stroke-like event by chickenpox in a child with MELAS syndrome.
- Published in:
- 2005
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- Publication type:
- journal article
Renal cell carcinoma in a pediatric patient with an inherited mitochondrial mutation.
- Published in:
- 2005
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- Publication type:
- journal article
Mitochondriale Erkrankungen benötigen ein umfassendes perioperatives Management.
- Published in:
- 2016
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- Publication type:
- Case Study
NOTA CLÍNICA: Litio: Un tratamiento antiguo para una nueva indicación.
- Published in:
- Actas Espanolas de Psiquiatria, 2021, v. 49, n. 3, p. 125
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- Publication type:
- Article
Search for mitochondrial DNA mutations in migraine subgroups.
- Published in:
- 1999
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- Publication type:
- journal article
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature.
- Published in:
- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00038
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- Publication type:
- Article
Encefalopatía mitocondrial, acidosis láctica y episodios stroke like (MELAS).
- Published in:
- Archivos de Neurociencias, 2012, v. 17, n. 2, p. 138
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- Publication type:
- Article
Sonification as a possible stroke rehabilitation strategy.
- Published in:
- Frontiers in Neuroscience, 2014, v. 8, p. 1, doi. 10.3389/fnins.2014.00332
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- Publication type:
- Article
Forecasting stroke-like episodes and outcomes in mitochondrial disease.
- Published in:
- 2022
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- Publication type:
- journal article
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy.
- Published in:
- 2021
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- Publication type:
- journal article