Suchergebnisse - "Liao, Nai-Yi"

PubPharm (5)

1

Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia

enthalten in: Journal of the Formosan Medical Association = Taiwan yi zhi | 2023

von Liao, N. | Lai, K. | Liao, Y. | +2

CommentIn: J Formos Med Assoc. 2023 Sep;122(9):965-966. - PMID 37400293

2

Reply to : Mitochondrial disorders are not spinocerebellar ataxias but may resemble them in some aspects

enthalten in: Journal of the Formosan Medical Association = Taiwan yi zhi | 2023

von Hsiao, C. | Liao, N. | Lee, Y.

CommentOn: J Formos Med Assoc. 2023 Sep;122(9):965-966. - PMID 37400293

3

Transient Postictal Hyperglycemia as a Diagnostic Clue of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes

enthalten in: Acta neurologica Taiwanica | 2022

von Liao, N. | Lin, L. | Chen, C. | +2

4

Reply : MELAS can be delineated from CADASIL by genotype and phenotype

enthalten in: Neurobiology of aging | 2021

von Liao, N. | Liao, K. | Liao, Y. | +1

CommentOn: Neurobiol Aging. 2021 Jan;97:145.e5-145.e6. - PMID 32950272

5

Mitochondrial DNA m.3243A>G mutation rarely causes CADASIL-like phenotype

enthalten in: Neurobiology of aging | 2021

von Liao, N. | Liao, K. | Liao, Y. | +1

CommentIn: Neurobiol Aging. 2021 Mar;99:104. - PMID 33288335

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