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Evening of the Slovak Society of Clinical Biochemistry SSKB on the topic: Inherited metabolic disorders

Date
Time
17:00
Venue
Malá poslucháreň (Small Lecture Hall), NTÚ LF UK
Sasinkova 4, Bratislava · map
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Programme

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

Chair doc. MUDr. V. Bzdúch, CSc.

  1. New approaches in the treatment of hyperammonaemia in childrenBrennerová K.
  2. Barth syndromeTárnoková S.
  3. Glutaric aciduria type I detected by newborn screeningUrbanová D.
  4. TMEM 70 deficiency – a mitochondrial disorder with a high incidence in the Roma populationBzdúch V.
Original programme in Slovak

Večer Slovenskej spoločnosti klinickej biochémie SSKB na tému: Dedičné metabolické poruchy

Predsedá doc. MUDr. V. Bzdúch, CSc.

  1. Nové prístupy v liečbe hyperamoniémie u detíBrennerová K.
  2. Barthov syndrómTárnoková S.
  3. Glutarová acidúria I. typu zachytená novorodeneckým skríningomUrbanová D.
  4. Deficit TMEM 70 – mitochondriová porucha s vysokým výskytom v rómskej populáciiBzdúch V.

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

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