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Ceskoslovenska Patologie
|
April 6, 2002
Mitochondrial cardiomyopathy--case report
I Steiner, J Zeman, J Spacek, et al.
Journal of Endocrinological Investigation
|
January 25, 2021
Decrease in serum calcitriol (but not free 25-hydroxyvitamin D) concentration in hip fracture healing
J Vaculik, L Wenchich, M Bobelyak, et al.
Journal of Endocrinological Investigation
|
January 26, 2022
A decrease in serum 1,25(OH)<sub>2</sub>D after elective hip replacement and during bone healing is associated with changes in serum iron and plasma FGF23
J Vaculik, L Wenchich, M Bobelyak, et al.
Physiological Research
|
December 4, 2003
Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects
L Wenchich, Z Drahota, T Honzík, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti
|
February 4, 2012
[Corneal ulceration complicating surgical correction of ptosis in patient with Kearns-Sayre syndrome--a case report]
T Cesneková, T Jurecka, K Skorkovská, et al.
Journal of Inherited Metabolic Disease
|
July 15, 2000
Abnormalities in succinylpurines in fumarase deficiency: possible role in pathogenesis of CNS impairment
J Zeman, J Krijt, L Stratilová, et al.
Casopis Lekaru Ceskych
|
September 26, 2006
[Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)]
T Honzík, M Tesarová, H Hansíková, et al.
Early Human Development
|
August 19, 2007
Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates
T Honzik, L Wenchich, M Böhm, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
November 1, 2001
Novel mutations in a boy with dihydrolipoamide dehydrogenase deficiency
L Cerna, L Wenchich, H Hansiková, et al.
Neuropediatrics
|
August 26, 2004
Mitochondrial DNA depletion in Alpers syndrome
M Tesarova, J A Mayr, L Wenchich, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Ceskoslovenska Patologie
|
April 6, 2002
Mitochondrial cardiomyopathy--case report
I Steiner, J Zeman, J Spacek, et al.
Journal of Endocrinological Investigation
|
January 25, 2021
Decrease in serum calcitriol (but not free 25-hydroxyvitamin D) concentration in hip fracture healing
J Vaculik, L Wenchich, M Bobelyak, et al.
Journal of Endocrinological Investigation
|
January 26, 2022
A decrease in serum 1,25(OH)<sub>2</sub>D after elective hip replacement and during bone healing is associated with changes in serum iron and plasma FGF23
J Vaculik, L Wenchich, M Bobelyak, et al.
Physiological Research
|
December 4, 2003
Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects
L Wenchich, Z Drahota, T Honzík, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti
|
February 4, 2012
[Corneal ulceration complicating surgical correction of ptosis in patient with Kearns-Sayre syndrome--a case report]
T Cesneková, T Jurecka, K Skorkovská, et al.
Journal of Inherited Metabolic Disease
|
July 15, 2000
Abnormalities in succinylpurines in fumarase deficiency: possible role in pathogenesis of CNS impairment
J Zeman, J Krijt, L Stratilová, et al.
Casopis Lekaru Ceskych
|
September 26, 2006
[Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)]
T Honzík, M Tesarová, H Hansíková, et al.
Early Human Development
|
August 19, 2007
Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates
T Honzik, L Wenchich, M Böhm, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
November 1, 2001
Novel mutations in a boy with dihydrolipoamide dehydrogenase deficiency
L Cerna, L Wenchich, H Hansiková, et al.
Neuropediatrics
|
August 26, 2004
Mitochondrial DNA depletion in Alpers syndrome
M Tesarova, J A Mayr, L Wenchich, et al.
Page
of 2