A rare mitochondrial disorder: Leigh syndrome - a case report

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1824-7288

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: A rare mitochondrial disorder: Leigh syndrome - a case report ; volume:36 ; number:1 ; day:15 ; month:9 ; year:2010 ; pages:1-5 ; date:12.2010
The Italian journal of pediatrics ; 36, Heft 1 (15.9.2010), 1-5, 12.2010

Creator: Shrikhande, Dhananjay Y.

Contributor: Kalakoti, Piyush
Syed, MM Aarif
Ahya, Kunal
SINGH, GURMEET
SpringerLink (Online service)

DOI: 10.1186/1824-7288-36-62

URN: urn:nbn:de:1111-2016032339624

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 11:00 AM CEST

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Shrikhande, Dhananjay Y.
Kalakoti, Piyush
Syed, MM Aarif
Ahya, Kunal
SINGH, GURMEET
SpringerLink (Online service)

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A rare mitochondrial disorder: Leigh syndrome - a case report

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Other Objects (12)

Netherton Syndrome, a Rare Genetic Disorder—Case Report

Diagnosis of Brugada Syndrome, a Rare Inherited Arrhythmogenic Disorder

SLC 25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome

Modeling mitochondrial disorders of the Leigh syndrome spectrum using human patient-derived cells and iPSC technology

Mitochondrial disease in a heteroplasmic MT DNA mutation causing mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and leigh syndrome phenotypes

Clinical, imaging, biochemical and molecular features in Leigh syndrome: a study from the Italian network of mitochondrial diseases

Synthetic aporphine alkaloids are potential therapeutics for Leigh syndrome

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Aurora Leigh

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SLC 25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome

Modeling mitochondrial disorders of the Leigh syndrome spectrum using human patient-derived cells and iPSC technology

Mitochondrial disease in a heteroplasmic MT DNA mutation causing mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and leigh syndrome phenotypes

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[Eduard Leigh]

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Aurora Leigh

Leigh, Vivien

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