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Štufková, Hana
28
results:
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Format
Online (28)
Mediatypes
Articles (Online) (9)
OpenAccess-fulltext (19)
Sorted by: Relevance
Sorted by: Year
?
1
ATAD3A-related pontocerebellar hypoplasia: new patients and..:
Skopkova, Martina
;
Stufkova, Hana
;
Rambani, Vibhuti
...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
2
Case report: A rare variant m.4135T>C in the MT-ND1 gene le..:
Rákosníková, Tereza
;
Kelifová, Silvie
;
Štufková, Hana
...
Frontiers in Genetics. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
Mitochondrial organization and structure are compromised in..:
Vanisova, Marie
;
Stufkova, Hana
;
Kohoutova, Michaela
...
Ultrastructural Pathology. 46 (2022) 5 - p. 462-475 , 2022
Link:
https://doi.org/10.1080/..
?
4
A Novel MTTK Gene Variant m.8315A>C as a Cause of MERRF Syn..:
Štufková, Hana
;
Kolářová, Hana
;
Lokvencová, Kateřina
...
Genes. 13 (2022) 7 - p. 1245 , 2022
Link:
https://doi.org/10.3390/..
?
5
Knock-Out of ACBD3 Leads to Dispersed Golgi Structure, but ..:
Daňhelovská, Tereza
;
Zdražilová, Lucie
;
Štufková, Hana
...
International Journal of Molecular Sciences. 22 (2021) 14 - p. 7270 , 2021
Link:
https://doi.org/10.3390/..
?
6
Deterioration of mitochondrial bioenergetics and ultrastruc..:
Rodinova, Marie
;
Krizova, Jana
;
Stufkova, Hana
...
Disease Models & Mechanisms. 12 (2019) 7 - p. , 2019
Link:
https://doi.org/10.1242/..
?
7
A transgenic minipig model of Huntington's disease shows ea..:
Askeland, Georgina
;
Rodinova, Marie
;
Štufková, Hana
...
Disease Models & Mechanisms. 11 (2018) 10 - p. , 2018
Link:
https://doi.org/10.1242/..
?
8
Sideroblastic anemia associated with multisystem mitochondr..:
Tesarova, Marketa
;
Vondrackova, Alzbeta
;
Stufkova, Hana
...
Pediatric Blood & Cancer. 66 (2018) 4 - p. , 2018
Link:
https://doi.org/10.1002/..
?
9
Mitochondrial bioenergetics in skeletal muscle of premanife..:
Hansikova, Hana
;
Rodinova, Marie
;
Krizova, Jana
...
Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1859 (2018) - p. e88 , 2018
Link:
https://doi.org/10.1016/..
?
10
Molecular basis of deficit of F1Fo-ATP synthase and its imp..:
Štufková, Hana
http://hdl.handle.net/20.500.11956/178864. , 2023
Link:
https://hdl.handle.net/2..
?
11
Molecular basis of deficit of F1Fo-ATP synthase and its imp..:
Štufková, Hana
http://hdl.handle.net/20.500.11956/181801. , 2023
Link:
https://hdl.handle.net/2..
?
12
Case report: A rare variant m.4135T>C in the MT-ND1 gene le..:
Rákosníková, Tereza
;
Kelifová, Silvie
;
Štufková, Hana
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233053/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
13
ATAD3A-related pontocerebellar hypoplasia: new patients and..:
Skopkova, Martina
;
Stufkova, Hana
;
Rambani, Vibhuti
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127305/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
14
A Novel MTTK Gene Variant m.8315A>C as a Cause of MERRF Syn..:
Štufková, Hana
;
Kolářová, Hana
;
Lokvencová, Kateřina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319148/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
15
Knock-Out of ACBD3 Leads to Dispersed Golgi Structure, but ..:
Daňhelovská, Tereza
;
Zdražilová, Lucie
;
Štufková, Hana
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303370/. , 2021
Link:
http://www.ncbi.nlm.nih...
1-15
