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H Houst'ková

Showing results (1-10 of 18) with videos related to

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Ceskoslovenska Pediatrie|March 1, 1983
[Experience with measuring the level of serum theophylline in infants and toddlers]H Houst'ková, J Zeman, E Márová, et al.
Ceskoslovenska Pediatrie|March 1, 1987
[Phenylketonuria undiagnosed, unrecognizable and neglected. Review of failures in diagnosis, therapy, and prevention of hereditary disorders of phenylalanine]J Hyánek, M Kubík, M Simková, et al.
Clinical Neuropathology|April 12, 2008
Early onset Alexander disease: a case report with evidence for manifestation of the disorder in neurohypophyseal pituicytesR Matej, L Dvoráková, L Mrázová, et al.
Casopis Lekaru Ceskych|January 8, 2003
[A new missense mutation of 574C>T in the SURF1 gene--biochemical and molecular genetic study in seven children with Leigh syndrome]M Capková, H Hansíková, C Godinot, et al.
Ceskoslovenska Pediatrie|July 1, 1985
[Homocystinuria]H Houst'ková, J Zeman, J Hyánek, et al.
Ceskoslovenska Pediatrie|April 1, 1982
[Pneumonia in children hospitalized at the 4th pediatric clinic in Prague during 1980]H Houst'ková, J Zeman, E Kamenická, et al.
Casopis Lekaru Ceskych|October 31, 2002
[Variation in manifestations of heteroplasmic mtDNA mutation 8993 T>G in two families]M Tesarová, H Hansíková, A Hlavatá, et al.
Ceskoslovenska Pediatrie|July 1, 1987
[Transitory hyperphenylalaninemia with a tetrahydrobiopterin synthesis deficiency]J Zeman, H Houst'ková, J Hyánek, et al.
Ceskoslovenska Pediatrie|July 1, 1985
[Cystathioninuria]H Houst'ková, J Zeman, J Hyánek, et al.
Molecular Genetics and Metabolism|August 18, 2001
A novel mutation in SURF1 causes skipping of exon 8 in a patient with cytochrome c oxidase-deficient leigh syndrome and hypertrichosisS L Williams, J W Taanman, H Hansíková, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Ceskoslovenska Pediatrie|March 1, 1983
[Experience with measuring the level of serum theophylline in infants and toddlers]H Houst'ková, J Zeman, E Márová, et al.
Ceskoslovenska Pediatrie|March 1, 1987
[Phenylketonuria undiagnosed, unrecognizable and neglected. Review of failures in diagnosis, therapy, and prevention of hereditary disorders of phenylalanine]J Hyánek, M Kubík, M Simková, et al.
Clinical Neuropathology|April 12, 2008
Early onset Alexander disease: a case report with evidence for manifestation of the disorder in neurohypophyseal pituicytesR Matej, L Dvoráková, L Mrázová, et al.
Casopis Lekaru Ceskych|January 8, 2003
[A new missense mutation of 574C>T in the SURF1 gene--biochemical and molecular genetic study in seven children with Leigh syndrome]M Capková, H Hansíková, C Godinot, et al.
Ceskoslovenska Pediatrie|July 1, 1985
[Homocystinuria]H Houst'ková, J Zeman, J Hyánek, et al.
Ceskoslovenska Pediatrie|April 1, 1982
[Pneumonia in children hospitalized at the 4th pediatric clinic in Prague during 1980]H Houst'ková, J Zeman, E Kamenická, et al.
Casopis Lekaru Ceskych|October 31, 2002
[Variation in manifestations of heteroplasmic mtDNA mutation 8993 T>G in two families]M Tesarová, H Hansíková, A Hlavatá, et al.
Ceskoslovenska Pediatrie|July 1, 1987
[Transitory hyperphenylalaninemia with a tetrahydrobiopterin synthesis deficiency]J Zeman, H Houst'ková, J Hyánek, et al.
Ceskoslovenska Pediatrie|July 1, 1985
[Cystathioninuria]H Houst'ková, J Zeman, J Hyánek, et al.
Molecular Genetics and Metabolism|August 18, 2001
A novel mutation in SURF1 causes skipping of exon 8 in a patient with cytochrome c oxidase-deficient leigh syndrome and hypertrichosisS L Williams, J W Taanman, H Hansíková, et al.
Pageof 2