نتائج البحث

Multisystem clinicopathologic and genetic analysis of MELAS.

• Authors : Xu, Shuai¹ (AUTHOR) ; Jiang, Jialiu¹ (AUTHOR) ; Chang, Leilei¹ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 12/24/2024, Vol. 19 Issue 1, p1-15. 15p.

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Cardiac manifestations in adult MELAS syndrome (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome)– a cross-sectional study.

• Authors : Stoevesandt, Dietrich¹ (AUTHOR) ; Schlitt, Axel^2,3 (AUTHOR); Röntgen, Philipp¹ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 2/10/2025, Vol. 20 Issue 1, p1-7. 7p.

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Hearing impairment in MELAS: new prospective in clinical use of microRNA, a systematic review

• Authors : Arianna Di Stadio; Valentina Pegoraro; Laura Giaretta

Subjects: MELAS; Hearing loss; Hearing impairment

• Source: Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)

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Open-label pilot study using hydroxytyrosol as dietary supplements in patients with mitochondrial diseases.

• Authors : Wong, Tsz Sum¹ (AUTHOR); Man, Emily² (AUTHOR); Wong, Ian Chi Kei³ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 6/6/2025, Vol. 20 Issue 1, p1-11. 11p.

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Endocrine manifestations and long-term outcomes of patients with mitochondrial diseases

• Authors : Ja Hye Kim; Dohyung Kim; Soojin Hwang

Subjects: Adult; Male; Mitochondrial Diseases

• Source: Orphanet J Rare DisOrphanet Journal of Rare Diseases, Vol 20, Iss 1, Pp 1-9 (2025)

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The m.3290T > C variant might be a protective factor against the pathogenic m.3243 A > G variant: a case study

• Authors : Ning Zhang; Zhikang Zhang; Ying Zhang

Subjects: Mitochondrial DNA; Mitochondrial disease; m.3290T > C

• Source: Orphanet Journal of Rare Diseases, Vol 20, Iss 1, Pp 1-5 (2025)

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Impact of cardiovascular involvement on the clinical course of paediatric mitochondrial disorders.

• Authors : Brambilla A; Paediatric Cardiology Unit, Anna Meyer Children Hospital, Viale Pieraccini 24, 50139, Florence, Italy. .; Inborn Metabolic and Muscular Disorders Unit, Anna Meyer Children Hospital, Florence, Italy. .

Subjects: Cardiomyopathy, Hypertrophic* ; Heart Failure* ; MELAS Syndrome*

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2020 Jul 31; Vol. 15 (1), pp. 196. Date of Electronic Publication: 2020 Jul 31.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

تفاصيل العنوان

Hearing impairment in MELAS: new prospective in clinical use of microRNA, a systematic review.

• Authors : Di Stadio, Arianna; Pegoraro, Valentina; Giaretta, Laura

Subjects: HEARING disorder diagnosis; TREATMENT of hearing disorders; BIOMARKERS

• Source: Orphanet Journal of Rare Diseases; 2/21/2018, Vol. 13, p1-9, 9p

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The immune system as a driver of mitochondrial disease pathogenesis: a review of evidence

• Authors : Allison Hanaford; Simon C. Johnson

Subjects: Mitochondrial disease; Leigh syndrome; MELAS

• Source: Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)

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MicroRNAs are appropriate in mitochondrial related hearing loss? Answer to the skepticism.

• Authors : Di Stadio, Arianna¹ ; Angelini, Corrado¹

• Source: Orphanet Journal of Rare Diseases. 7/18/2018, Vol. 13 Issue 1, pN.PAG-N.PAG. 1p.

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