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[Hereditary disorders of mitochondrial ATP synthase].

• Authors : Houstĕk J; Fyziologický ústav AV CR, Praha. ; Zeman J

Subjects: Mutation*; Adenosine Triphosphatases/Adenosine Triphosphatases/Adenosine Triphosphatases/*genetics ; Mitochondrial Diseases/Mitochondrial Diseases/Mitochondrial Diseases/*genetics

• Source: Casopis lekaru ceskych [Cas Lek Cesk] 2004; Vol. 143 (8), pp. 517-20.Publisher: Ceskoslovenska Lekarska Spolecnost Country of Publication: Czech Republic NLM ID: 0004743 Publication Model: Print

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[Genetic background of mitochondrial diabetes].

• Authors : Vanková M; Endokrinologický ústav, Praha. ; Lukásová P

Subjects: DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/*genetics ; Mitochondrial Diseases/Mitochondrial Diseases/Mitochondrial Diseases/*genetics

• Source: Casopis lekaru ceskych [Cas Lek Cesk] 2007; Vol. 146 (3), pp. 235-9.Publisher: Ceskoslovenska Lekarska Spolecnost Country of Publication: Czech Republic NLM ID: 0004743 Publication Model: Print

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[Mitochondrial metabolism in mammalian spermatozoa--a minireview].

• Authors : Spácilová J; Sládková J; Macáková M

Subjects: Mitochondria/Mitochondria/Mitochondria/*metabolism ; Mitochondrial Diseases/Mitochondrial Diseases/Mitochondrial Diseases/*physiopathology ; Spermatozoa/Spermatozoa/Spermatozoa/*physiology

• Source: Ceskoslovenska fysiologie [Cesk Fysiol] 2015; Vol. 64 (2), pp. 84-9.Publisher: Ceska Lekarska Spolecnost J.E. Purkyne Country of Publication: Czech Republic NLM ID: 2984710R Publication Model:

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Metabolické myopatie.

• Authors : Kolářová, Hana; Ješina, Pavel

Subjects: INBORN errors of metabolism; GLYCOGEN storage disease; MUSCLE weakness

• Source: Neurologie Pro Praxi; Mar2022, Vol. 23 Issue 1, p24-32, 7p

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PSYCHIATRICKÁ MANIFESTACE DĚDIČNÝCH METABOLICKÝCH PORUCH.

• Authors : Kulhánek, Jan; Albrecht, Jakub; Honzík, Tomáš

• Source: Ceská a Slovenská Psychiatrie; 2015, Vol. 111 Issue 6, p295-304, 10p

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Mitochondrie - od vzniku po dnešní terapeutické možnosti.

• Authors : Smejkal, Vít; Hromadníková, Ilona; Palmová, Anežka

• Source: Journal of Czech Physicians / Časopis Lékařů Českých; 2021, Vol. 160 Issue 7/8, p332-339, 8p

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Realimentačni syndrom po paleodietě.

• Authors : Kalousová, M.; Macášek, J.; Zeman, M.

• Source: Klinická Biochemie a Metabolismus; 2018, Vol. 26 Issue 4, p185-188, 4p

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AUTOSOMÁLNĚ DOMINANTNÍ SPINOCEREBELÁRNÍ ATAXIE: REVIEW.

• Authors : Krakorová, K.; Čedíková, M.; Polívka, J.

• Source: Plzensky Lekarsky Sbornik; 2018, Issue 84, p55-62, 8p

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Vzácná příčina slepoty u pacienta s nosní polypózou Leberova hereditární neuropatie zrakového nervu.

• Authors : Bruthansová, P.; Vokurka, J.; Diblík, P.

• Source: Otorhinolaryngology & Phoniatrics / Otorinolaryngologie a Foniatrie; Nov2011, Vol. 60 Issue 3, p169-171, 3p

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[The mitochondrial genome and mitochondrial diseases].

• Authors : Jirásek JE; Ustav pro péci o matku a dítĕ, Praha-Podolí.

Subjects: DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics; Humans ; Muscular Diseases/Muscular Diseases/Muscular Diseases/genetics

• Source: Ceskoslovenska gynekologie [Cesk Gynekol] 1990 Dec; Vol. 55 (10), pp. 768-9.Publisher: Ceska Lekarska Spolecnost Jana Evangelisty Purkyne Country of Publication: Czech Republic NLM ID: 0042671 Publication

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