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Daniela Zahorakova

Showing results (1-10 of 7) with videos related to

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Bratislavske Lekarske Listy|September 30, 2024
Porphyria cutanea tarda triggered by hepatitis-E virusPavel Hrabak, Katerina Benesova, Daniela Zahorakova, et al.
Journal of Child Neurology|February 9, 2010
APOE epsilon4: a potential modulation factor in Rett syndromeDaniela Zahorakova, Marie Jachymova, David Kemlink, et al.
Journal of Human Genetics|March 18, 2016
MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanningDaniela Zahorakova, Petra Lelkova, Vladimir Gregor, et al.
Neuro Endocrinology Letters|August 31, 2010
No association with the ETM2 locus in Czech patients with familial essential tremorDaniela Zahorakova, Olga Ulmanova, David Kemlink, et al.
Plos One|September 20, 2014
Parkin (PARK 2) mutations are rare in Czech patients with early-onset Parkinson's diseaseOndrej Fiala, Daniela Zahorakova, Lenka Pospisilova, et al.
Journal of Human Genetics|March 28, 2007
Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphismsDaniela Zahorakova, Robert Rosipal, Jan Hadac, et al.
Journal of Magnetic Resonance Imaging : JMRI|April 5, 2017
Brain iron accumulation in Wilson's disease: A longitudinal imaging case study during anticopper treatment using 7.0T MRI and transcranial sonographyPetr Dusek, David Skoloudik, Jana Maskova, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Bratislavske Lekarske Listy|September 30, 2024
Porphyria cutanea tarda triggered by hepatitis-E virusPavel Hrabak, Katerina Benesova, Daniela Zahorakova, et al.
Journal of Child Neurology|February 9, 2010
APOE epsilon4: a potential modulation factor in Rett syndromeDaniela Zahorakova, Marie Jachymova, David Kemlink, et al.
Journal of Human Genetics|March 18, 2016
MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanningDaniela Zahorakova, Petra Lelkova, Vladimir Gregor, et al.
Neuro Endocrinology Letters|August 31, 2010
No association with the ETM2 locus in Czech patients with familial essential tremorDaniela Zahorakova, Olga Ulmanova, David Kemlink, et al.
Plos One|September 20, 2014
Parkin (PARK 2) mutations are rare in Czech patients with early-onset Parkinson's diseaseOndrej Fiala, Daniela Zahorakova, Lenka Pospisilova, et al.
Journal of Human Genetics|March 28, 2007
Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphismsDaniela Zahorakova, Robert Rosipal, Jan Hadac, et al.
Journal of Magnetic Resonance Imaging : JMRI|April 5, 2017
Brain iron accumulation in Wilson's disease: A longitudinal imaging case study during anticopper treatment using 7.0T MRI and transcranial sonographyPetr Dusek, David Skoloudik, Jana Maskova, et al.
Pageof 1