Skip to content

This evening has taken place

Evening of the Section of Inherited Metabolic Disorders, SSKB

Date
Time
17:00
Venue
Malá poslucháreň (Small Lecture Hall), NTÚ LF UK
Sasinkova 4, Bratislava · map
Add all evenings to your calendar
Share

Programme

The lectures are held in Slovak. The titles are translated from the Slovak programme.

Chair doc.MUDr.V.Bzdúch,CSc.

  1. Cerebrotendinous xanthomatosis in childrenBrennerová K.
  2. Empagliflozin in the treatment of glycogenosis Ib.Bzdúch V.
  3. Glutaric aciduria type II detected by newborn screening 4.Bzdúch V.: The first patient with a new congenital disorder of glycosylation SLC37A4-CDG.Hlásna K.
Original programme in Slovak

Večer Sekcie dedičných metabolických porúch SSKB

Predsedá doc.MUDr.V.Bzdúch,CSc.

  1. Cerebrotendinózna xantomatóza u detíBrennerová K.
  2. Empagliflozín v liečbe glykogenózy Ib.Bzdúch V.
  3. Glutarová acidúria II.typu zachytená novorodeneckým skríningom 4.Bzdúch V.: Prvá pacientka s novou kongenitálnou poruchou glykozylácie SLC37A4-CDG.Hlásna K.

The Slovak Accreditation Council for Continuing Medical Education awards 2 credits for attending an evening lecture.

← All evening lectures