(Q40807256)

23 September 2017

1 reference

title

Neuropathy associated with mitochondrial disorders (English)

1 reference

23 September 2017

Schröder JM

1

1 reference

23 September 2017

1 April 1993

1 reference

23 September 2017

1 reference

23 September 2017

3

1 reference

23 September 2017

2

1 reference

23 September 2017

177-190

1 reference

Mitochondrial DNA mutation and Leigh's syndrome

23 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Mitochondrial myopathies with necrotizing encephalopathy of the Leigh type.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

MELAS: clinical features, biochemistry, and molecular genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Melas: an original case and clinical criteria for diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Peripheral neuropathy in Leigh's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Mitochondrial abnormalities in human sural nerves: fine structural evaluation of cases with mitochondrial myopathy, hereditary and non-hereditary neuropathies, and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Lactic acidemia, mitochondrial myopathy, and basal ganglia calcification

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Sural nerve biopsy studies in Leigh's subacute necrotizing encephalomyelopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Peripheral neuropathy associated with mitochondrial myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Adult Onset Lipid Storage in Gastric Mucosa and Skeletal Muscle Fibers Associated with Gastric Pain, Progressive Muscle Weakness and Partial Deficiency of Cytochrome C Oxidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

MELAS of infantile onset: mitochondrial angiopathy or cytopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

MELAS: a family with paternal inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

New aspects of the genetic, etiologic, and clinical puzzle of Leber's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Mosaicism of mitochondria in mitochondrial myopathy: an electronmicroscopic analysis of cytochrome c oxidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Functional respiratory chain studies in mitochondrial cytopathies. Support for mitochondrial DNA heteroplasmy in myoclonus epilepsy and ragged red fibers (MERRF) syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Segmental cytochrome c‐oxidase deficiency in CPEO: Teased muscle fiber analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Intracristal rods. A new structure in beef heart mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Mitochondrial changes in ischemic skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Nuclear and mitochondrial changes of muscle fibers in AIDS after treatment with high doses of zidovudine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

Vascular involvement in mitochondrial myopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROME

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00742.X

10.1111/J.1750-3639.1993.TB00742.X

21 January 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference

PubMed ID

8293179