Literature DB >> 14874135

Subacute necrotizing encephalomyelopathy in an infant.

D LEIGH.   

Abstract

Entities:  

Keywords:  CENTRAL NERVOUS SYSTEM/diseases

Mesh：

Year:  1951        PMID： 14874135      PMCID： PMC499520          DOI： 10.1136/jnnp.14.3.216

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  188 in total

Review 1.  Disorders related to mitochondrial membranes: pathology of the respiratory chain and neurodegeneration.

Authors:  S Di Donato
Journal:  J Inherit Metab Dis       Date:  2000-05       Impact factor: 4.982

2.  Antemortem diagnosis of Leigh's disease: role of magnetic resonance studies.

Authors:  D Ghosh; S Pradhan
Journal:  Indian J Pediatr       Date:  1996 Sep-Oct       Impact factor: 1.967

3.  Leigh syndrome in a 3-year-old boy with unusual brain MR imaging and pathologic findings.

Authors:  M Topçu; I Saatci; R A Apak; F Söylemezoglu; Z Akçören
Journal:  AJNR Am J Neuroradiol       Date:  2000-01       Impact factor: 3.825

Review 4.  Human mitochondrial complex I in health and disease.

Authors:  J Smeitink; L van den Heuvel
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

5.  Complex I deficiency due to loss of Ndufs4 in the brain results in progressive encephalopathy resembling Leigh syndrome.

Authors:  Albert Quintana; Shane E Kruse; Raj P Kapur; Elisenda Sanz; Richard D Palmiter
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-01       Impact factor: 11.205

6.  Leigh syndrome caused by mitochondrial DNA G13513A mutation: frequency and clinical features in Japan.

Authors:  Akira Sudo; Shiho Honzawa; Ikuya Nonaka; Yu-Ichi Goto
Journal:  J Hum Genet       Date:  2004-01-17       Impact factor: 3.172

Review 7.  Mitochondria, OxPhos, and neurodegeneration: cells are not just running out of gas.

Authors:  Estela Area-Gomez; Cristina Guardia-Laguarta; Eric A Schon; Serge Przedborski
Journal:  J Clin Invest       Date:  2019-01-02       Impact factor: 14.808

Review 8.  Long survival in patients with leigh syndrome and the m.10191T>C mutation in MT-ND3 : a case report and review of the literature.

Authors:  Rebecca J Levy; Purificación Gutierrez Ríos; Hasan O Akman; Monica Sciacco; Darryl C De Vivo; Salvatore DiMauro
Journal:  J Child Neurol       Date:  2013-11-27       Impact factor: 1.987

9.  MR findings in Leigh syndrome with COX deficiency and SURF-1 mutations.

Authors:  Laura Farina; Luisa Chiapparini; Graziella Uziel; Marianna Bugiani; Massimo Zeviani; Mario Savoiardo
Journal:  AJNR Am J Neuroradiol       Date:  2002-08       Impact factor: 3.825

10.  Medical treatment with thiamine, coenzyme Q, vitamins E and C, and carnitine improved obstructive sleep apnea in an adult case of Leigh disease.

Authors:  Charalampos Mermigkis; Izolde Bouloukaki; Vasileios Mastorodemos; Andreas Plaitakis; Vangelis Alogdianakis; Nikolaos Siafakas; Sophia Schiza
Journal:  Sleep Breath       Date:  2013-02-07       Impact factor: 2.816
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