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Andrea Zatkova

Showing results (1-10 of 32) with videos related to

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Journal of Inherited Metabolic Disease|July 2, 2011
An update on molecular genetics of Alkaptonuria (AKU)Andrea Zatkova
The Application of Clinical Genetics|March 12, 2020
Alkaptonuria: Current PerspectivesAndrea Zatkova, Lakshminarayan Ranganath, Ludevit Kadasi
European Journal of Human Genetics : EJHG|February 3, 2022
Breakpoints characterisation of the genomic deletions identified by MLPA in alkaptonuria patientsAndrea Soltysova, Martina Sekelska, Andrea Zatkova
European Journal of Human Genetics : EJHG|September 10, 2021
Alkaptonuria in RussiaAndrea Soltysova, Alexandr Kuzin, Elena Samarkina, et al.
Metabolites|October 27, 2022
Analysis of the Phenotype Differences in Siblings with AlkaptonuriaAndrea Zatkova, Birgitta Olsson, Lakshminarayan R Ranganath, et al.
Metabolites|June 26, 2024
Correction: Zatkova et al. Analysis of the Phenotype Differences in Siblings with Alkaptonuria. <i>Metabolites</i> 2022, <i>12</i>, 990Andrea Zatkova, Birgitta Olsson, Lakshminarayan R Ranganath, et al.
Leukemia Research|November 28, 2006
A patient with de novo AML M1 and t(16;21) with karyotype evolutionAndrea Zatkova, Christa Fonatsch, Wolfgang R Sperr, et al.
General Physiology and Biophysics|March 28, 2013
Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patientsCsaba Bognar, Marian Baldovic, Jan Benetin, et al.
BMC Medical Informatics and Decision Making|April 16, 2017
ApreciseKUre: an approach of Precision Medicine in a Rare DiseaseOttavia Spiga, Vittoria Cicaloni, Andrea Bernini, et al.
The Israel Medical Association Journal : IMAJ|April 10, 2018
Degenerative Osteoarthritis with Multiple Joint Arthroplasties Due to Alkaptonuria, a Rare Inborn Error of Tyrosine MetabolismRaja Hakim, Nimrod Rozen, Andrea Zatkova, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Journal of Inherited Metabolic Disease|July 2, 2011
An update on molecular genetics of Alkaptonuria (AKU)Andrea Zatkova
The Application of Clinical Genetics|March 12, 2020
Alkaptonuria: Current PerspectivesAndrea Zatkova, Lakshminarayan Ranganath, Ludevit Kadasi
European Journal of Human Genetics : EJHG|February 3, 2022
Breakpoints characterisation of the genomic deletions identified by MLPA in alkaptonuria patientsAndrea Soltysova, Martina Sekelska, Andrea Zatkova
European Journal of Human Genetics : EJHG|September 10, 2021
Alkaptonuria in RussiaAndrea Soltysova, Alexandr Kuzin, Elena Samarkina, et al.
Metabolites|October 27, 2022
Analysis of the Phenotype Differences in Siblings with AlkaptonuriaAndrea Zatkova, Birgitta Olsson, Lakshminarayan R Ranganath, et al.
Metabolites|June 26, 2024
Correction: Zatkova et al. Analysis of the Phenotype Differences in Siblings with Alkaptonuria. <i>Metabolites</i> 2022, <i>12</i>, 990Andrea Zatkova, Birgitta Olsson, Lakshminarayan R Ranganath, et al.
Leukemia Research|November 28, 2006
A patient with de novo AML M1 and t(16;21) with karyotype evolutionAndrea Zatkova, Christa Fonatsch, Wolfgang R Sperr, et al.
General Physiology and Biophysics|March 28, 2013
Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patientsCsaba Bognar, Marian Baldovic, Jan Benetin, et al.
BMC Medical Informatics and Decision Making|April 16, 2017
ApreciseKUre: an approach of Precision Medicine in a Rare DiseaseOttavia Spiga, Vittoria Cicaloni, Andrea Bernini, et al.
The Israel Medical Association Journal : IMAJ|April 10, 2018
Degenerative Osteoarthritis with Multiple Joint Arthroplasties Due to Alkaptonuria, a Rare Inborn Error of Tyrosine MetabolismRaja Hakim, Nimrod Rozen, Andrea Zatkova, et al.
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