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List of works by Michio Hirano

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy

scientific article published in May 2003

ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiency

scientific article

Accelerated physiology and increased energy expenditure in animals and humans with mitochondrial defects: A meta-analysis

scientific article published on 10 September 2023

Acute quadriplegic myopathy: a complication of treatment with steroids, nondepolarizing blocking agents, or both

scientific article published on 01 November 1992

Apparent mtDNA heteroplasmy in Alzheimer’s disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes ⬇️

scientific article published on December 23, 1997

Association of myopathy with large‐scale mitochondrial dna duplications and deletions: Which is pathogenic? ⬇️

scientific article published on 01 August 1997

Biochemical studies of patients with Cuban epidemic neuropathy

scientific article published in November 2001

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy.

scientific article published on 18 January 2018

Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA ⬇️

scientific article published on December 1, 2001

Deoxynucleoside Therapy for Thymidine Kinase 2-Deficient Myopathy

scientific article published on 17 June 2019

Differential expression of genes specifying two isoforms of subunit VIa of human cytochrome c oxidase

scientific article (publication date: October 1992)

Differentiation of astrocytes and oligodendrocytes from germinal matrix cells in primary culture

scientific article published on January 1986

Editing the Mitochondrial Genome

scientific article published on 01 October 2020

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

scientific article

Human aging DNA methylation signatures are conserved but accelerated in cultured fibroblasts

scientific article published on 12 June 2019

Hypermetabolism and energetic constraints in mitochondrial disorders

scientific article published on 9 February 2024

Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome

scientific article published on 31 July 2002

Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6

scientific article published on 27 November 2019

Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.

scientific article published in January 1999

Leukocyte cytokine responses in adult patients with mitochondrial DNA defects

scientific article published in June 2022

Leukocyte cytokine responses in adult patients with mitochondrial DNA defects

scientific article published on 16 December 2021

MELAS: clinical features, biochemistry, and molecular genetics

scientific article published on April 1, 1992

MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria

scientific article published on 13 January 2016

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation

scientific article published in January 1999

Melas: an original case and clinical criteria for diagnosis

scientific article (publication date: 1992)

Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency

scientific article published on 31 October 2020

Mitochondria and the heart

scientific article

Mitochondria in neuromuscular disorders ⬇️

scientific article published on August 10, 1998

Mitochondrial diseases

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts

scientific article

Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter.

scientific article

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

scientific article published on 31 August 2009

Multifocal motor neuropathy with conduction block: is it a distinct clinical entity?

scientific article published on March 1, 1992

New treatments for mitochondrial disease-no time to drop our standards

scientific article published on 02 July 2013

Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegia ⬇️

scientific article published on October 1, 1997

Optic neuropathy in familial dysautonomia

scientific article published on 01 June 1997

Perceived association of mood and symptom severity in adults with mitochondrial diseases

scientific article published on 4 February 2024

Pituitary adenoma revealed by paracentral junctional scotoma of traquair

scientific article published on 01 January 1997

Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).

scientific article

Regulatory Environment for Novel Therapeutic Development in Mitochondrial Diseases

scientific article published on 24 December 2020

Retrospective natural history of thymidine kinase 2 deficiency.

scientific article

The treatment of periocular and facial pain with topical capsaicin

scientific article published on 01 March 1998

Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase

scientific article published on October 1, 1992

What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?

scientific article

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