(Q37211810)

English

Multiple neurologic, psychiatric, and endocrine complaints in a young woman: a case discussion and review of the clinical features and management of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke

scientific article published on January 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Multiple neurologic, psychiatric, and endocrine complaints in a young woman: a case discussion and review of the clinical features and management of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

lactic acidosis

1 reference

based on heuristic

inferred from title

mitochondrial myopathy

1 reference

based on heuristic

inferred from title

Theodore A Stern

3

object named as

Theodore A Stern

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Chaya G Bhuvaneswar

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Jared L Goetz

2

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

publication date

1 January 2008

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Primary Care Companion to the Journal of Clinical Psychiatry

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

3

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

237-244

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

MR imaging of temporal lobe epilepsy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Mitochondrial disease: a practical approach for primary care physicians.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Prevalence of mitochondrial DNA disease in adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Psychiatric comorbidity in 36 adults with mitochondrial cytopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

MELAS and L-arginine therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Beneficial effects of creatine, CoQ10, and lipoic acid in mitochondrial disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Factitious disorders: reformulating the DSM-IV criteria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Review of the literature on major mental disorders in adult patients with mitochondrial diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Heart transplantation for progressive cardiomyopathy as a manifestation of MELAS syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Reappraisal of Lhermitte's sign in multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Pathology of mitochondrial encephalomyopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Evaluation of the patient with muscle weakness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Mitochondrial DNA 3243A>G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Coenzyme Q 10 improves lactic acidosis, strokelike episodes, and epilepsy in a patient with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Abductor sign: a reliable new sign to detect unilateral non-organic paresis of the lower limb

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

A review of cochlear implantation in mitochondrial sensorineural hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Chronic fatigue syndrome: evaluation and treatment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Diagnosis of "non-organic" limb paresis by a novel objective motor assessment: the quantitative Hoover's test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

9 September 2017

Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

28 September 2017

Dystonia as a presenting feature of the 3243 mitochondrial DNA mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

26 June 2018

Cerebral blood flow and oxygen metabolism before and after a stroke-like episode in patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

26 June 2018

Psychiatric symptoms in a patient with diabetes mellitus associated with point mutation in mitochondrial DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

26 June 2018

Idebenone improves cerebral mitochondrial oxidative metabolism in a patient with MELAS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

26 June 2018

CPEO and carnitine deficiency overlapping in MELAS syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

26 June 2018

Mitochondrial myopathies with necrotizing encephalopathy of the Leigh type.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

26 June 2018

Therapeutic effect of sodium dichloroacetate on visual and auditory hallucinations in a patient with MELAS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

26 June 2018

Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Acute hearing loss in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Early cardiac involvement in children carrying the A3243G mtDNA mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Regional cerebral blood flow and cerebrovascular reactivity during chronic stage of stroke-like episodes in MELAS -- implication of neurovascular cellular mechanism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Population prevalence of the MELAS A3243G mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Mitochondrial DNA sequence analysis of patients with 'atypical psychosis'.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

A case of stroke-like episode of MELAS of which progressive spread would be prevented by edaravone

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

High prevalence of the COII/tRNA(Lys) intergenic 9-bp deletion in mitochondrial DNA of Taiwanese patients with MELAS or MERRF syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Persistent organic personality change as rare psychiatric manifestation of MELAS syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Slowly progressive spread of the stroke-like lesions in MELAS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Response to sumatriptan in headache of MELAS syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Effectiveness of creatine monohydrate in mitochondrial encephalomyopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Effects of midazolam on acute phase of stroke in two patients with mitochondrial encephalopathy, lactic acidosis and stroke-like episodes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

MELAS: a neuropsychological and radiological follow-up study. Mitochondrial encephalomyopathy, lactic acidosis and stroke

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Long-term treatment with idebenone and riboflavin in a patient with MELAS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Neurologic presentations of mitochondrial disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B1 and B2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2446487

3 September 2018

[Polymorphism of epilepsy associated with the A3243G mutation of mitochondrial DNA (MELAS): reasons for delayed diagnosis]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular motor disorders in mitochondrial encephalopathy with lactic acid and stroke-like episodes with the 3271 (T-C) point mutation in mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dichloroacetate causes toxic neuropathy in MELAS: a randomized, controlled clinical trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homoplasmy, heteroplasmy, and mitochondrial dystonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metabolic interventions against complex I deficiency in MELAS syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The course of vision disturbances in a patient with the MELAS syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased activities of antioxidant enzymes and decreased ATP concentration in cultured myoblasts with the 3243A-->G mutation in mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MELAS syndrome: imaging and proton MR spectroscopic findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebral blood flow and glucose metabolism in mitochondrial disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pregnancy with mitochondrial encephalopathy, lactic acidosis, and strokelike episodes syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Statins provoking MELAS syndrome. A case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lactate increase and oxygen desaturation in mitochondrial disorders--evaluation of two diagnostic screening protocols

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-isopropyl-p-[123I]iodoamphetamine SPECT in MELAS syndrome: comparison with CT and MR imaging

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial neurological diseases: a clinician's perspective

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Corticosteroid treatment of mitochondrial encephalomyopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic sequencing in the service of human rights

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adult-onset hypertrophic cardiomyopathy manifested as initial major presentation of mitochondrial disease with A-to-G 3243 tRNA (Leu(UUR)) point mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18615168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.4088/PCC.V10N0309

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

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