نتائج البحث

Psychiatric involvement in adult patients with mitochondrial disease.

• Authors : Mancuso M; Department of Neuroscience, Neurological Clinic, University of Pisa, Via Roma 67, 56126 Pisa, Italy. ; Orsucci D

Subjects: Mental Disorders/Mental Disorders/Mental Disorders/*etiology ; Mental Disorders/Mental Disorders/Mental Disorders/*psychology ; Mitochondrial Diseases/Mitochondrial Diseases/Mitochondrial Diseases/*complications

• Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2013 Jan; Vol. 34 (1), pp. 71-4. Date Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited

تفاصيل العنوان

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

• Authors : Ardissone, Anna¹ (AUTHOR) ; Bruno, Claudio² (AUTHOR); Diodato, Daria³ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 10/9/2021, Vol. 16 Issue 1, p1-12. 12p.

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Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: case report of an Italian patient.

• Authors : Piro E; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro'. University Hospital 'P.Giaccone', University of Palermo, Piazza delle Cliniche, 2, 90127, Palermo, Italy. .; Serra G

Subjects: Cytochrome-c Oxidase Deficiency/Cytochrome-c Oxidase Deficiency/Cytochrome-c Oxidase Deficiency/*genetics ; Leigh Disease/Leigh Disease/Leigh Disease/*genetics ; Neoplasm Proteins/Neoplasm Proteins/Neoplasm Proteins/*geneticsLeigh syndrome , French Canadian type

• Source: Italian journal of pediatrics [Ital J Pediatr] 2020 Sep 24; Vol. 46 (1), pp. 140. Date of Electronic Publication: 2020 Sep 24.Publisher: BioMed Central Country of Publication: England NLM ID: 101510759 Publication Model: Electronic Cited Medium: Internet ISSN: 1824-7288

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Role of adenine nucleotide translocator 1 in mtDNA maintenance.

• Authors : Kaukonen J; National Public Health Institute, Department of Human Molecular Genetics, Mannerheimintie 166, 00300 Helsinki, Finland.; Juselius JK

Subjects: DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*metabolism ; Mitochondrial ADP, ATP Translocases/Mitochondrial ADP, ATP Translocases/Mitochondrial ADP, ATP Translocases/*genetics

• Source: Science (New York, N.Y.) [Science] 2000 Aug 04; Vol. 289 (5480), pp. 782-5.Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 0404511 Publication Model: Print Cited Medium:

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