Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Irena Vrečar"'
Publikováno v:
Zdravniški Vestnik, Vol 79, Iss 3 (2010)
Background: Diff erent reentry circuits within A-V node region are able to sustain A-V nodal reentrant tachycardia (AVNRT). On this basis, electrophysiological criteria for at least three AVNRT types – slow/fast, fast/slow, and slow/ slow–have be
Externí odkaz:
https://doaj.org/article/082a84d8a3664e338c5c022c8f0efb4a
Autor:
Irena Vrečar, William Reardon, Bronwyn Kerr, Elizabeth A. Jones, Sofia Douzgou, J A Innes, Helen Kingston, Jill Clayton-Smith
Publikováno v:
Journal of pediatric genetics. 6(3)
Mutations in the MEF2C (myocyte enhancer factor 2) gene have been established as a cause for an intellectual disability syndrome presenting with seizures, absence of speech, stereotypic movements, hypotonia, and limited ambulation. Phenotypic overlap
Publikováno v:
International Journal of Rehabilitation Research. 35:116-123
The Halliwick concept is widely used in different settings to promote joyful movement in water and swimming. To assess the swimming skills and progression of an individual swimmer, a valid and reliable measure should be used. The Halliwick-concept-ba
Publikováno v:
Medicina Fluminensis : Medicina Fluminensis
Volume 50
Issue 2
Volume 50
Issue 2
Metoda molekularne kariotipizacije omogućava analizu genomskih mutacija s visokom rezolucijom na razini cijelog humanog genoma. Manje genomske mutacije (mikrodelecije, mikroduplikacije) koje nije moguće otkriti klasičnom kariotipizacijom prisutne