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László Wenchich
Observed names:
L Wenchich,
L. WENCHICH,
L. Wenchich,
Laszlo Wenchich
Institution:
Institute of Rheumatology
Observed institutions:
Czech Academy of Sciences,
Charles University,
Institute of Rheumatology,
Pediatrics and Genetics,
General University Hospital in Prague,
Czech Academy of Sciences, Institute of Physiology
show all 6
ORCID:
0000-0002-8250-2981
Observed ORCID:
0000-0002-8250-2981
OpenAlex ID:
A5082025066
YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation
2012
·
Lukas Stiburek
, Jana Cesnekova
, et al.
·
Molecular Biology of the Cell
·
186
PDF
Novel insights into the assembly and function of human nuclear-encoded cytochrome c oxidase subunits 4, 5a, 6a, 7a and 7b
2010
·
Daniela Fornuskova
, Lukas Stiburek
, et al.
·
Biochemical Journal
·
104
PDF
Knockdown of Human Oxa1l Impairs the Biogenesis of F1Fo-ATP Synthase and NADH:Ubiquinone Oxidoreductase
2007
·
Lukas Stiburek
, Daniela Fornuskova
, et al.
·
Journal of Molecular Biology
·
93
Neonatal onset of mitochondrial disorders in 129 patients: clinical and laboratory characteristics and a new approach to diagnosis
2012
·
Tomas Honzik
, Marketa Tesarova
, et al.
·
Journal of Inherited Metabolic Disease
·
86
Mitochondrial Respiration in the Platelets of Patients with Alzheimer’s Disease
2016
·
Zden|k FiŠar
, Jana Hroudová
, et al.
·
Current Alzheimer Research
·
84
Activities of mitochondrial respiratory chain complexes in platelets of patients with Alzheimer's disease and depressive disorder
2019
·
Zdeněk Fišar
, Hana Hansíková
, et al.
·
Mitochondrion
·
64
The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues
2008
·
Daniela Fornuskova
, Olga Brantova
, et al.
·
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
·
40
PDF
Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates
2007
·
T. Honzik
, L. Wenchich
, et al.
·
Early Human Development
·
34
Mitochondrial DNA Depletion in Alpers Syndrome
2004
·
M. Tesarova
, J. A. Mayr
, et al.
·
Neuropediatrics
·
28
Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects.
2003
·
L Wenchich
, Z Drahota
, et al.
·
Physiological Research
·
28
PDF
Novel mutations in a boy with dihydrolipoamide dehydrogenase deficiency.
2001
·
L Cerna
, L Wenchich
, et al.
·
PubMed
·
27
Mitochondrial Energy Metabolism in Very Premature Neonates
2002
·
László Wenchich
, Jiří Zeman
, et al.
·
Neonatology
·
24
Fumaric aciduria: Mild phenotype in a 8‐year‐old girl with novel mutations
2006
·
M. Maradin
, K. Fumić
, et al.
·
Journal of Inherited Metabolic Disease
·
23
PDF
The Effect of Very-Low-Calorie Diet on Mitochondrial Dysfunction in Subcutaneous Adipose Tissue and Peripheral Monocytes of Obese Subjects with Type 2 Diabetes Mellitus
2017
·
M. URBANOVÁ
, M. MRÁZ
, et al.
·
Physiological Research
·
21
PDF
Abnormalities in succinylpurines in fumarase deficiency: Possible role in pathogenesis of CNS impairment
2000
·
J. Zeman
, J. Krijt
, et al.
·
Journal of Inherited Metabolic Disease
·
18
Activities of respiratory chain complexes in isolated platelets in females with anorexia nervosa
2007
·
Marek Böhm
, Hana Papezova
, et al.
·
International Journal of Eating Disorders
·
13
PDF
Menopausal Transition: Prospective Study of Estrogen Status, Circulating MicroRNAs, and Biomarkers of Bone Metabolism
2022
·
Jiri Baloun
, Aneta Pekacova
, et al.
·
Frontiers in Endocrinology
·
12
Interindividual differences contribute to variation in microbiota composition more than hormonal status: A prospective study
2023
·
Zuzana Jackova
, Jan J. Stepan
, et al.
·
Frontiers in Endocrinology
·
10
Inflammatory myopathy associated with statins: report of three cases
2014
·
Klara Kuncova
, Marie Sedlackova
, et al.
·
Modern Rheumatology
·
9
Vitamin D and its receptor in skeletal muscle are associated with muscle disease manifestation, lipid metabolism and physical fitness of patients with myositis
2025
·
Lucia Vernerová
, Martina Vokurková
, et al.
·
Arthritis Research & Therapy
·
8
[Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome].
2002
·
M Capková
, M Tesarová
, et al.
·
PubMed
·
6
The relationship of mitochondrial dysfunction and the development of insulin resistance in Cushing’s syndrome
2019
·
Jana Ježková
, Viktória Ďurovcová
, et al.
·
Diabetes Metabolic Syndrome and Obesity
·
5
PDF
Two patients with clinically distinct manifestation of pyruvate dehydrogenase deficiency due to mutations in PDHA1 gene.
2011
·
M Magner
, K Vinšová
, et al.
·
PubMed
·
5
Decrease in serum calcitriol (but not free 25-hydroxyvitamin D) concentration in hip fracture healing
2021
·
J. Vaculik
, L. Wenchich
, et al.
·
Journal of Endocrinological Investigation
·
3
[Corneal ulceration complicating surgical correction of ptosis in patient with Kearns-Sayre syndrome--a case report].
2011
·
T Cesneková
, T Jurecka
, et al.
·
PubMed
·
3
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Works count:
34
Citation count:
945
H-index:
15
I10-index:
18
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