Results 111 to 120 of about 371,748 (188)

The Role of Autophagy in the Pathogenesis of Mitochondrial Diseases. [PDF]

Cells
Avdonina ED, Kutsev SI, Shestopalov AV.
europepmc   +1 more source

[Mitochondrial encephalomyopathies].

Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 1995
L K, Hansen, K, Wulff, H, Schrøder, K, Rasmussen   +3 more
openaire   +3 more sources

Mitochondrial Disorder in a Child With Brainstem Lesions Mimicking Thiamine Deficiency. [PDF]

Cureus
Asfour MA, Nedimyer Horner J, Gupta K, Silva G, Chandra T, Rossi G.   +5 more
europepmc   +1 more source

The Clinical Burden of Inherited Neurometabolic Disorders in Adults-A Territorial Care Approach. [PDF]

J Clin Med
Orsucci D, Caldarazzo Ienco E, Giuntini M, Vista M.   +3 more
europepmc   +1 more source

Identifying NDUFA12 mutation in a Saudi family: An unusual presentation of mitochondrial Complex I deficiency mimicking as idiopathic intracranial hypertension in a patient with papilledema and visual loss. [PDF]

J Family Community Med
Alshamrani FJ, Alajmi MS, Almuslim NI, Alsubaie MM, Fardan GM, Alabdali MM.   +5 more
europepmc   +1 more source

Irisin as a Regulator of Brain Energy Homeostasis: Implications for Age-Related Neurodegenerative Diseases. [PDF]

Cells
Osuch B, Młotkowska P, Marciniak E, Misztal T.   +3 more
europepmc   +1 more source

Non-Mammalian Models for Mitochondria Research in CNS Disorders. [PDF]

Biomolecules
Svob Strac D, Filic V, Filosevic Vujnovic A, Vrhovac Madunic I, Madunic J, Cipak Gasparovic A, Havelka Mestrovic A, Andretic Waldowski R.   +7 more
europepmc   +1 more source

Rare diseases in the Turkish-Cypriot community: a nationwide study. [PDF]

J Community Genet
Koyutourk B, Ergoren MC.
europepmc   +1 more source

Expanding the Phenotypic Spectrum of NDUFS6-Related Disease: From Neonatal Mitochondrial Encephalopathy to Childhood-Onset Axonal Neuropathy. [PDF]

Int J Mol Sci
Baris S, Ipek R, Baris ST, Baris I.
europepmc   +1 more source