Peter Blumel
Overview
Explore the profile of Peter Blumel including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
218
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0
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Recent Articles
1.
Culen C, Herle M, Ertl D, Frohlich-Reiterer E, Blumel P, Wagner G, et al.
Clin Endocrinol (Oxf)
. 2021 Jan;
93(4):449-455.
PMID: 33464630
Objective: Young women with Turner syndrome (TS) are known to be at risk for loss to medical follow-up. Recent literature indicates that there are disparities regarding transition readiness between different...
2.
Mayer M, Gleiss A, Hausler G, Borkenstein M, Kapelari K, Kostl G, et al.
Ann Hum Biol
. 2014 Apr;
42(1):45-55.
PMID: 24761986
Background: BMI reference charts are widely used to diagnose overweight, obesity and underweight in children and adolescents. Aim: To provide up-to-date national reference values for Austria. Methods: A cross-sectional sample...
3.
Gleiss A, Lassi M, Blumel P, Borkenstein M, Kapelari K, Mayer M, et al.
Ann Hum Biol
. 2013 Apr;
40(4):324-32.
PMID: 23590681
Background: Previous studies have demonstrated differences between national and the WHO reference curves in children older than 5 years. Moreover, reference curves for body proportions (sitting height, subischial leg length...
4.
Spengler S, Begemann M, Bruchle N, Baudis M, Denecke B, Kroisel P, et al.
J Pediatr
. 2012 Jun;
161(5):933-42.
PMID: 22683032
Objective: To determine the contribution of submicroscopic chromosomal imbalances to the etiology of Silver-Russell syndrome (SRS) and SRS-like phenotypes. Study Design: We performed molecular karyotyping in 41 patients with SRS...
5.
Cantagrel V, Lefeber D, Ng B, Guan Z, Silhavy J, Bielas S, et al.
Cell
. 2010 Jul;
142(2):203-17.
PMID: 20637498
N-linked glycosylation is the most frequent modification of secreted and membrane-bound proteins in eukaryotic cells, disruption of which is the basis of the congenital disorders of glycosylation (CDGs). We describe...
6.
Riedl S, Vosahlo J, Battelino T, Stirn-Kranjc B, Brugger P, Prayer D, et al.
Eur J Pediatr
. 2008 Jan;
167(11):1269-76.
PMID: 18231810
Septo-optic dysplasia (SOD) is a heterogeneous brain midline anomaly associated with ophthalmological, endocrinological, and/or neurodevelopmental symptoms. The clinical phenotype correlates with abnormal brain magnetic resonance imaging (MRI) findings. However, variations...
7.
Riedl S, Blumel P, Zwiauer K, Frisch H
Acta Paediatr
. 2005 Sep;
94(7):974-7.
PMID: 16188826
Unlabelled: Reports on sudden death in Prader-Willi syndrome (PWS) patients after the start of growth hormone (GH) treatment have been published recently. We observed a 4.7-y-old girl who showed a...