Hana Stufkova

General University Hospital in Prague

Czech Republic

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Articles (9)

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Collaborators (6)

MARIE Vanišová

Všeobecná Fakultní Nemocnice v Praze

CZECH REPUBLIC

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Lenka Noskova

Charles University

CZECH REPUBLIC

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Jiri Zeman

prof. MD. PhD

General Faculty Hospital, 1st Medical Faculty of Charles University

CZECH REPUBLIC

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Marketa Tesarova

General University Hospital in Prague

CZECH REPUBLIC

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Hana Hansikova

CZECH REPUBLIC

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Nikol Volfová

University of Arkansas for Medical Sciences Department of Pediatrics

CZECH REPUBLIC

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Hana Stufkova

Research Interests

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Articles (9)

ATAD3A-related pontocerebellar hypoplasia: new patients and insights into phenotypic variability

Case report: A rare variant m.4135T>C in the <i>MT-ND1</i> gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes.

Case report: A rare variant m.4135T & gt;C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes

ATAD3A-related pontocerebellar hypoplasia: new patients and insights into phenotypic variability

A Novel MTTK Gene Variant m.8315A>C as a Cause of MERRF Syndrome

EARLY MITOCHONDRIAL DYSFUNCTION IN PERIPHERAL BLOOD MONONUCLEAR CELLS IN PROGRESSION OF HUNTINGTON'S DISEASE

Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington's disease

Knock-Out of ACBD3 Leads to Dispersed Golgi Structure, but Unaffected Mitochondrial Functions in HEK293 and HeLa Cells

CAN CUMULATION OF NEURODEGENERATIVE DISORDERS SIGNIFICANTLY PROMOTE MITOCHONDRIAL DYSFUNCTION IN CULTURED SKIN FIBROBLASTS?

Collaborators (6)

MARIE Vanišová

Lenka Noskova

Jiri Zeman

Marketa Tesarova

Hana Hansikova

Nikol Volfová

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