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Katalin Komlósi

Showing results (1-10 of 33) with videos related to

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Current Molecular Medicine|November 16, 2019
Mass Spectrometric Analysis of L-carnitine and its Esters: Potential Biomarkers of Disturbances in Carnitine HomeostasisJudit Bene, Andras Szabo, Katalin Komlósi, et al.
Orvosi Hetilap|January 22, 2013
[Larsen-syndrome: final diagnosis following multiple surgical interventions]Péter Kisfali, Katalin Komlósi, Kinga Hadzsiev, et al.
Orvosi Hetilap|March 3, 2011
[Molecular genetic diagnosis of neurofibromatosis type I]Noémi Polgár, Katalin Komlósi, Kinga Hadzsiev, et al.
Pediatric Research|May 23, 2007
Determination of carnitine ester patterns during the second half of pregnancy, at delivery, and in neonatal cord blood by tandem mass spectrometry: complex and dynamic involvement of carnitine in the intermediary metabolismGábor C Talián, Katalin Komlósi, Tamás Decsi, et al.
World Journal of Gastroenterology|January 21, 2006
Plasma carnitine ester profile in adult celiac disease patients maintained on long-term gluten free dietJudit Bene, Katalin Komlósi, Beáta Gasztonyi, et al.
Orvosi Hetilap|January 26, 2012
[Significance of thiopurine s-methyltransferase gene test in a clinical case]Csilla Sipeky, Anita Maász, Gréta Tarlós, et al.
Orvosi Hetilap|June 4, 2013
[Novel TSC1 mutation associated with variable phenotypes in tuberous sclerosis]Erzsébet Kövesdi, Kinga Hadzsiev, Katalin Komlósi, et al.
Orvosi Hetilap|November 29, 2015
[De novo SCN1A gene deletion in therapy-resistant Dravet syndrome]Judit Bene, Kinga Hadzsiev, Katalin Komlósi, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 21, 2013
Differences in circulating carnitine status of preterm infants fed fortified human milk or preterm infant formulaJudit Bene, Katalin Komlósi, Bela I Melegh, et al.
BMC Medical Genetics|December 18, 2017
Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case reportZsolt Bánfai, Kinga Hadzsiev, Endre Pál, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Current Molecular Medicine|November 16, 2019
Mass Spectrometric Analysis of L-carnitine and its Esters: Potential Biomarkers of Disturbances in Carnitine HomeostasisJudit Bene, Andras Szabo, Katalin Komlósi, et al.
Orvosi Hetilap|January 22, 2013
[Larsen-syndrome: final diagnosis following multiple surgical interventions]Péter Kisfali, Katalin Komlósi, Kinga Hadzsiev, et al.
Orvosi Hetilap|March 3, 2011
[Molecular genetic diagnosis of neurofibromatosis type I]Noémi Polgár, Katalin Komlósi, Kinga Hadzsiev, et al.
Pediatric Research|May 23, 2007
Determination of carnitine ester patterns during the second half of pregnancy, at delivery, and in neonatal cord blood by tandem mass spectrometry: complex and dynamic involvement of carnitine in the intermediary metabolismGábor C Talián, Katalin Komlósi, Tamás Decsi, et al.
World Journal of Gastroenterology|January 21, 2006
Plasma carnitine ester profile in adult celiac disease patients maintained on long-term gluten free dietJudit Bene, Katalin Komlósi, Beáta Gasztonyi, et al.
Orvosi Hetilap|January 26, 2012
[Significance of thiopurine s-methyltransferase gene test in a clinical case]Csilla Sipeky, Anita Maász, Gréta Tarlós, et al.
Orvosi Hetilap|June 4, 2013
[Novel TSC1 mutation associated with variable phenotypes in tuberous sclerosis]Erzsébet Kövesdi, Kinga Hadzsiev, Katalin Komlósi, et al.
Orvosi Hetilap|November 29, 2015
[De novo SCN1A gene deletion in therapy-resistant Dravet syndrome]Judit Bene, Kinga Hadzsiev, Katalin Komlósi, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 21, 2013
Differences in circulating carnitine status of preterm infants fed fortified human milk or preterm infant formulaJudit Bene, Katalin Komlósi, Bela I Melegh, et al.
BMC Medical Genetics|December 18, 2017
Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case reportZsolt Bánfai, Kinga Hadzsiev, Endre Pál, et al.
Pageof 4