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Literature DB >> 16283102

Fatal cerebral hemorrhage in mitochondrial encephalomyopathy. Clinical and pathological data of a case.

Haruhisa Kato, Masanobu Uchigata, Mutsumi Iijima, Seiichiro Shimizu, Ikuya Nonaka, Yuichi Goto.

Abstract

Entities: Disease

Mesh：

Year: 2005 PMID： 16283102 DOI： 10.1007/s00415-005-0010-1

Source DB: PubMed Journal: J Neurol ISSN： 0340-5354 Impact factor: 4.849

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6 in total

1. Recurrent brain hematomas in MELAS associated with an ND5 gene mitochondrial mutation.

Authors: I Pénisson-Besnier; P Reynier; P Asfar; O Douay; A Sortais; F Dubas; J Emile; Y Malthièry
Journal: Neurology Date: 2000-07-25 Impact factor: 9.910

2. The T-C(8356) mitochondrial DNA mutation in a Japanese family.

Authors: M Sano; M Ozawa; S Shiota; Y Momose; M Uchigata; Y Goto
Journal: J Neurol Date: 1996-06 Impact factor: 4.849

3. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.

Authors: M Zeviani; F Muntoni; N Savarese; G Serra; V Tiranti; F Carrara; C Mariotti; S DiDonato
Journal: Eur J Hum Genet Date: 1993 Impact factor: 4.246

4. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.

Authors: Mariarosa A B Melone; Alessandra Tessa; Stefania Petrini; Giacomo Lus; Simone Sampaolo; Giuseppe di Fede; Filippo M Santorelli; Roberto Cotrufo
Journal: Arch Neurol Date: 2004-02

5. Progression from MERRF to MELAS phenotype in a patient with combined respiratory complex I and IV deficiencies.

Authors: E Byrne; I Trounce; X Dennett; B Gilligan; J B Morley; S Marzuki
Journal: J Neurol Sci Date: 1988-12 Impact factor: 3.181

6. Mitochondrial encephalomyopathies: CT and MRI findings and correlations with clinical features.

Authors: C C Huang; Y Y Wai; N S Chu; C W Liou; C Y Pang; K D Shih; Y H Wei
Journal: Eur Neurol Date: 1995 Impact factor: 1.710

6 in total

4 in total

Fatal cerebral hemorrhage in mitochondrial encephalomyopathy. Clinical and pathological data of a case.

1. Recurrent brain hematomas in MELAS associated with an ND5 gene mitochondrial mutation.

2. The T-C(8356) mitochondrial DNA mutation in a Japanese family.

3. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.

4. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.

5. Progression from MERRF to MELAS phenotype in a patient with combined respiratory complex I and IV deficiencies.

6. Mitochondrial encephalomyopathies: CT and MRI findings and correlations with clinical features.

1. Cerebellar hematoma in a carrier of the A3243G MELAS mutation.

Review 2. Cerebral imaging in paediatric mitochondrial disorders.

3. Causes of Death in Adults with Mitochondrial Disease.

4. Spontaneous intracerebral hemorrhage in CADASIL.