Nina Ondrušková - Author - Inventaire

Nina Ondrušková

languages spoken, written or signed: Czech, English

occupation: researcher, biochemist

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Articles 6

Date

Title

Authors

2015-01-01

Isoelectric Focusing of Serum Apolipoprotein C-III as a Sensitive Screening Method for the Detection of O-glycosylation Disturbances

Nina Ondrušková, Tomáš Honzík, Jitka Kytnarová, Martin Matoulek, Jiri Zeman
2014-07-24

Mutation of Nogo-B receptor, a subunit of cis-prenyltransferase, causes a congenital disorder of glycosylation

Viktor Stránecký, Hana Hartmannová, Kateřina Hodaňová, Veronika Barešová, Nina Ondrušková, Tomáš Honzík, Jiri Zeman, Helena Hůlková, William C. Sessa, Jana Sovová
2014-02-24

Diagnostic serum glycosylation profile in patients with intellectual disability as a result of MAN1B1 deficiency.

Manfred Wuhrer, Ann Saada, Paul J Hensbergen, Agnes L Hipgrave Ederveen, Simon Edvardson, Dagmar Procházková, Nina Ondrušková, Gert Matthijs, Joris A Veltman
2012-10-13

RFT1-CDG in adult siblings with novel mutations.

Kateřina Veselá, Jiri Zeman, Tomáš Honzík, Nina Ondrušková, Martin Magner
2012-08-23

Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency

Tomáš Honzík, Jakub Krijt, Jitka Sokolová, Kateřina Veselá, Jiri Zeman, Viktor Kožich, Martin Magner, Lenka Bauerová, Nina Ondrušková, Pavel Ješina
2011-03-23

Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I.

Nina Ondrušková, Jiri Zeman

Human - wd:Q56943248

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