Related references
Note: Only part of the references are listed.Pyruvate therapy for Leigh syndrome due to cytochrome c oxidase deficiency
Hirofumi Komaki et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (2010)
Coenzyme Q10 in Neuromuscular and Neurodegenerative Disorders
M. Mancuso et al.
CURRENT DRUG TARGETS (2010)
Drugs interfering with mitochondrial disorders
Josef Finsterer et al.
DRUG AND CHEMICAL TOXICOLOGY (2010)
Treatment of mitochondrial disorders
Josef Finsterer
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY (2010)
Mitochondrial DNA shifting in older adults following resistance exercise training
M. A. Tarnopolsky
APPLIED PHYSIOLOGY NUTRITION AND METABOLISM-PHYSIOLOGIE APPLIQUEE NUTRITION ET METABOLISME (2009)
Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI features
Nicole I. Wolf et al.
EPILEPSIA (2009)
Management of mitochondrial stroke-like-episodes
J. Finsterer
EUROPEAN JOURNAL OF NEUROLOGY (2009)
EFNS guidelines on the molecular diagnosis of mitochondrial disorders
J. Finsterer et al.
EUROPEAN JOURNAL OF NEUROLOGY (2009)
Evaluation of putative inhibitors of mitochondrial permeability transition for brain disorders - Specificity vs. toxicity
Saori Morota et al.
EXPERIMENTAL NEUROLOGY (2009)
Major depression in adolescent children consecutively diagnosed with mitochondrial disorder
S. Koene et al.
JOURNAL OF AFFECTIVE DISORDERS (2009)
Progressive carotid artery stenosis with a novel tRNA phenylalanine mitochondrial DNA mutation
Takahiro Iizuka et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2009)
EFFICACY OF LAMOTRIGINE IN DISABLING MYOCLONUS IN A PATIENT WITH AN mtDNA A3243G MUTATION
Daniel J. Costello et al.
NEUROLOGY (2009)
Ketogenic Diet in Alpers-Huttenlocher Syndrome
Charuta N. Joshi et al.
PEDIATRIC NEUROLOGY (2009)
Mitochondrial Energy Production Correlates With the Age-Related BMI
Saskia B. Wortmann et al.
PEDIATRIC RESEARCH (2009)
L-arginine efficiency in MELAS syndrome. A case report
F. Moutaouakil et al.
REVUE NEUROLOGIQUE (2009)
Mitochondrial disorders in the nervous system
Salvatore DiMauro et al.
ANNUAL REVIEW OF NEUROSCIENCE (2008)
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase γ (POLG1)
R. McFarland et al.
ARCHIVES OF DISEASE IN CHILDHOOD (2008)
Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene Is Associated With Autism
Joni A. Turunen et al.
AUTISM RESEARCH (2008)
Resistance training in patients with single, large-scale deletions of mitochondrial DNA
Julie L. Murphy et al.
BRAIN (2008)
Intestinal pseudo-obstruction in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with phenytoin therapy
Tomohiro Chiyonobu et al.
BRAIN & DEVELOPMENT (2008)
Mitochondrial respiratory chain defects: Underlying etiology in various epileptic conditions
Young Mock Lee et al.
EPILEPSIA (2008)
A surviving case of mitochondrial cardiomyopathy diagnosed from the symptoms of multiple organ dysfunction syndrome
Yasuyuki Tsujita et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2008)
Cognitive decline as a manifestation of mitochondrial disorders (mitochondrial dementia)
Josef Finsterer
JOURNAL OF THE NEUROLOGICAL SCIENCES (2008)
Variable outcome of growth hormone administration in respiratory chain deficiency
S. Romano et al.
MOLECULAR GENETICS AND METABOLISM (2008)
Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: Case study and effect of deep brain stimulation
Maria Stella Aniello et al.
MOVEMENT DISORDERS (2008)
How can we treat mitochondrial encephalomyopathies? Approaches to therapy
Rita Horvath et al.
NEUROTHERAPEUTICS (2008)
Primary myopathies and the heart
Josef Finsterer et al.
SCANDINAVIAN CARDIOVASCULAR JOURNAL (2008)
Aromatic antiepileptic drugs and mitochondrial toxicity: Effects on mitochondria isolated from rat liver
N. A. G. Santos et al.
TOXICOLOGY IN VITRO (2008)
Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia
Simon Edvardson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Mitochondrial complex I encephalomyopathy and cerebral 5-methyltetrahydrofolate deficiency
V. T. Ramaekers et al.
NEUROPEDIATRICS (2007)
Safety, tolerability, and pharmacokinetics of high-dose idebenone in patients with Friedreich ataxia
Nicholas A. Di Prospero et al.
ARCHIVES OF NEUROLOGY (2007)
Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA
Chih-Ming Lin et al.
METABOLIC BRAIN DISEASE (2007)
Beneficial effects of creatine, CoQ10, and lipoic acid in mitochondrial disorders
M. Christine Rodriguez et al.
MUSCLE & NERVE (2007)
Safe and effective use of the ketogenic diet in children with epilepsy and mitochondrial respiratory chain complex defects
Hoon-Chul Kang et al.
EPILEPSIA (2007)
Neurosurgical treatment of tremor in mitochondrial encephalopathy
Norbert Kovacs et al.
MOVEMENT DISORDERS (2006)
Infusion of platelets transiently reduces nucleoside overload in MNGIE
M. C. Lara et al.
NEUROLOGY (2006)
Central nervous system manifestations of mitochondrial disorders
J. Finsterer
ACTA NEUROLOGICA SCANDINAVICA (2006)
Effects of riboflavin in children with complex II deficiency
Marianna Bugiani et al.
BRAIN & DEVELOPMENT (2006)
Antimyoclonic effect of levetiracetam in MERRY syndrome
M Mancuso et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2006)
Levetiracetam: Antiepileptic properties and protective effects on mitochondrial dysfunction in experimental status epilepticus
JE Gibbs et al.
EPILEPSIA (2006)
Dichloroacetate causes toxic neuropathy in MELAS - A randomized, controlled clinical trial
P Kaufmann et al.
NEUROLOGY (2006)
Approaches to the treatment of Mitochondrial Diseases - Invited review
Salvatore DiMauro et al.
MUSCLE & NERVE (2006)
Exercise and training in mitochondrial myopathies
T Taivassalo et al.
MEDICINE AND SCIENCE IN SPORTS AND EXERCISE (2005)
Platelet mitochondrial evaluation during cytochrome c and dichloroacetate treatments of MELAS
K Nakano et al.
MITOCHONDRION (2005)
Creatine has no beneficial effect on skeletal muscle energy metabolism in patients with single mitochondrial DNA deletions:: a placebo-controlled, double-blind 31P-MRS crossover study
C Kornblum et al.
EUROPEAN JOURNAL OF NEUROLOGY (2005)
L-arginine improves the symptoms of stroke-like episodes in MELAS
Y Koga et al.
NEUROLOGY (2005)
Two full-term pregnancies in a patient with mitochondrial myopathy and chronic ventilatory insufficiency
S Diaz-Lobato et al.
RESPIRATION (2005)
Overview of Japanese experience-controlled and uncontrolled trials
K Yagi
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY (2004)
Coenzyme Q10 improves lactic acidosis, strokelike episodes, and epilepsy in a patient with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes)
A Berbel-Garcia et al.
CLINICAL NEUROPHARMACOLOGY (2004)
Dichloroacetate treatment for mitochondrial cytopathy: long-term effects in MELAS
M Mori et al.
BRAIN & DEVELOPMENT (2004)
Beneficial effect of L-arginine for stroke-like episode in MELAS
M Kubota et al.
BRAIN & DEVELOPMENT (2004)
Successful treatment with succinate in a patient with MELAS
H Oguro et al.
INTERNAL MEDICINE (2004)
Slowly progressive spread of the stroke-like lesions in MELAS
T Iizuka et al.
NEUROLOGY (2003)
A sporadic case of cystinuria, respiratory chain and growth hormone deficiencies
M Zaffanello et al.
PEDIATRIC NEPHROLOGY (2003)
A mutation in mitochondrial DNA-encoded cytochrome c oxidase II gene in a child with Alpers-Huttenlocher-like disease -: art. no. e262
J Uusimaa et al.
PEDIATRICS (2003)
The effect of short-term dimethylglycine treatment on oxygen consumption in cytochrome oxidase deficiency: A double-blind randomized crossover clinical trial
JM Liet et al.
JOURNAL OF PEDIATRICS (2003)
Hypothalamic growth hormone deficiency and supplementary GH therapy in two patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
M Matsuzaki et al.
NEUROPEDIATRICS (2002)
Corticosteroid treatment of mitochondrial encephalomyopathies
FH Rossi et al.
NEUROLOGIST (2002)
Effects of oral creatine supplementation in a patient with MELAS phenotype and associated nephropathy
N Barisic et al.
NEUROPEDIATRICS (2002)
Mitochondrial disorders: A potentially under-recognized etiology of infantile spasms
NS Shah et al.
JOURNAL OF CHILD NEUROLOGY (2002)
Phenotype variability in 130 adult patients with respiratory chain disorders
J Finsterer et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2001)
Carnitine-responsive carnitine insufficiency in a case of mtDNA 8993T > C mutation associated Leigh syndrome
G Toth et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2001)
A placebo-controlled crossover trial of creatine in mitochondrial diseases
T Klopstock et al.
NEUROLOGY (2000)
Endocrine disorders in two sisters affected by MELAS syndrome
P Balestri et al.
JOURNAL OF CHILD NEUROLOGY (2000)
A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I
C Scharfe et al.
JOURNAL OF MEDICAL GENETICS (2000)
Increased cerebral blood flow in MELAS shown by Tc-99m HMPAO brain SPECT
NJ Peng et al.
NEURORADIOLOGY (2000)
Long-term treatment with idebenone and riboflavin in a patient with MELAS
A Napolitano et al.
NEUROLOGICAL SCIENCES (2000)