About: Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents     Goto   Sponge   NotDistinct   Permalink

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Description
  • This paper describes that 39 of 82 paediatric patients (48%) with randomly found fasting hyperglycaemia suffered from single gene defect conditions, MODY2 being the most prevalent. An additional 11 patients (13%) progressed to overt T1DM. The aetiological diagnosis in asymptomatic hyperglycaemia is a clue to introducing an early therapy
  • This paper describes that 39 of 82 paediatric patients (48%) with randomly found fasting hyperglycaemia suffered from single gene defect conditions, MODY2 being the most prevalent. An additional 11 patients (13%) progressed to overt T1DM. The aetiological diagnosis in asymptomatic hyperglycaemia is a clue to introducing an early therapy (en)
  • Tento článek popisuje, že 39 z 82 pediatrických pacientů (48%) s náhodně zjištěnou lačnou hyperglykémií mělo defekty jednoho genu, nejvíce často MODY2. Dalších 11 pacientů (13%) vyvinulo jasný T1DM. Etiologická diagnóza u asymptomatické hyperglykémie je klíčem k zahájení časné terapie (cs)
Title
  • Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents
  • Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents (en)
  • Etiologická heterogenita asymptomatické hyperglykémie u dětí a adolescentů (cs)
skos:prefLabel
  • Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents
  • Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents (en)
  • Etiologická heterogenita asymptomatické hyperglykémie u dětí a adolescentů (cs)
skos:notation
  • RIV/00216208:11120/06:00000168!RIV07-MSM-11120___
http://linked.open.../vavai/riv/strany
  • 446-452
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(NB7420), Z(MSM0021620814)
http://linked.open...iv/cisloPeriodika
  • 7
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 464277
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11120/06:00000168
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • hyperglycaemia; genetics; MODY; T1DM; permanent neonatal diabetes mellitus (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • DE - Spolková republika Německo
http://linked.open...ontrolniKodProRIV
  • [F3CF36549E16]
http://linked.open...i/riv/nazevZdroje
  • European Journal of Pediatrics
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 165
http://linked.open...iv/tvurceVysledku
  • Kološtová, Katarína
  • Lebl, Jan
  • Pintérová, Daniela
  • Černá, Marie
  • Hansen, T.
  • Pedersen, O.
  • Průhová, Štěpánka
  • Feigerlová, E.
  • Dittertová, Lucie
http://linked.open...n/vavai/riv/zamer
issn
  • 0340-6199
number of pages
http://localhost/t...ganizacniJednotka
  • 11120
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