Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Abdul Alrajab"'
Autor:
Jens-Peter Schenk, Tsvetomir Loukanov, Joachim Eichhorn, Astrid Helling-Bakki, Wolfgang Springer, Abdul Alrajab, Marcus A. Mall, Olaf Sommburg
Publikováno v:
Respiration. 97:108-118
Background: Congenital cardiovascular malformations (CCVM) may cause infrequently airway pathologies (AP) in children and are of prognostic and therapeutic relevance. While computed tomography (CT) is considered first-line imaging modality in many ce
Autor:
Abdul Alrajab, Janna Mittnacht, Daniela Klose, Ioana Inta, Egbert Schulze, Jürgen Grulich-Henn, Daniela Choukair, Vira Yakovenko, Thomas Breil, Markus Bettendorf
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 32(3)
Background 11β-hydroxylase deficiency (11βOHD) is a rare disease representing the second most common cause of congenital adrenal hyperplasia (CAH) (5–8%) with an incidence of about 1:100,000. In contrast to 21-hydroxylase deficiency (21OHD), 11β