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Lídia Balogh

Showing results (1-10 of 9) with videos related to

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Orvosi Hetilap|November 21, 2017
[Diet treatment of classical galactosemia]Erika Kiss, Lídia Balogh, Péter Reismann
Orvosi Hetilap|November 28, 2017
[Diagnostics of inborn errors of metabolism: laboratory approaches]Eszter Szabó, Lídia Balogh, Attila Szabó, et al.
Orvosi Hetilap|October 20, 2007
[Neonatal lupus erythematosus: case report and review of the literature]Géza Vass, Zsuzsanna Antal, Mária Katona, et al.
Annals of Human Genetics|June 12, 2019
EPG5 c.1007A > G mutation in a sibling pair with rapidly progressing Vici syndromeEszter Vojcek, Tália Magdolna Keszthelyi, Eszter Jávorszky, et al.
Pediatrics|October 28, 2015
Severe Hyperinsulinemic Hypoglycemia in a Neonate: Response to Sirolimus TherapyÜnőke Méder, Géza Bokodi, Lídia Balogh, et al.
Orvosi Hetilap|November 26, 2023
[Focal congenital hyperinsulinism]Zsuzsa Tallós, Andrea Luczay, Lídia Balogh, et al.
European Journal of Pediatrics|January 16, 2013
Relation between biomarkers and clinical severity in patients with Smith-Lemli-Opitz syndromeAnna V Oláh, Gabriella P Szabó, József Varga, et al.
Orvosi Hetilap|November 21, 2017
[Rhabdomyolysis - may it be a metabolic myopathy? Case report and diagnostic algorithm]Ágnes Sebők, Endre Pál, Gergő Attila Molnár, et al.
Kidney International|August 5, 2020
An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypesMartina Živná, Kendrah Kidd, Mohamad Zaidan, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Orvosi Hetilap|November 21, 2017
[Diet treatment of classical galactosemia]Erika Kiss, Lídia Balogh, Péter Reismann
Orvosi Hetilap|November 28, 2017
[Diagnostics of inborn errors of metabolism: laboratory approaches]Eszter Szabó, Lídia Balogh, Attila Szabó, et al.
Orvosi Hetilap|October 20, 2007
[Neonatal lupus erythematosus: case report and review of the literature]Géza Vass, Zsuzsanna Antal, Mária Katona, et al.
Annals of Human Genetics|June 12, 2019
EPG5 c.1007A > G mutation in a sibling pair with rapidly progressing Vici syndromeEszter Vojcek, Tália Magdolna Keszthelyi, Eszter Jávorszky, et al.
Pediatrics|October 28, 2015
Severe Hyperinsulinemic Hypoglycemia in a Neonate: Response to Sirolimus TherapyÜnőke Méder, Géza Bokodi, Lídia Balogh, et al.
Orvosi Hetilap|November 26, 2023
[Focal congenital hyperinsulinism]Zsuzsa Tallós, Andrea Luczay, Lídia Balogh, et al.
European Journal of Pediatrics|January 16, 2013
Relation between biomarkers and clinical severity in patients with Smith-Lemli-Opitz syndromeAnna V Oláh, Gabriella P Szabó, József Varga, et al.
Orvosi Hetilap|November 21, 2017
[Rhabdomyolysis - may it be a metabolic myopathy? Case report and diagnostic algorithm]Ágnes Sebők, Endre Pál, Gergő Attila Molnár, et al.
Kidney International|August 5, 2020
An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypesMartina Živná, Kendrah Kidd, Mohamad Zaidan, et al.
Pageof 1