ESP
E 2
01
5
Poster
presented at:
747--P3Shahab Noorian DOI: 10.3252/pso.eu.54espe.2015
Diabetes 2
10.3252/pso.eu.54espe - abstracts.eurospe.orgabstracts.eurospe.org/hrp/0084/eposters/hrp0084p3-600_eposter.pdf · Achalasia cardia noticed incidentally Co-incidentally MRI brain showed
Documents
DIDMOAD syndrome with megacystisand megaureter · as a familial event by Wolfram (1938) and the syndrome has been reviewed by Rose et al. (1966), Page et al. (1976) and Cremers et
10.3252/pso.eu.54espeabstracts.eurospe.org/hrp/0084/eposters/hrp0084p3-1010_eposter.pdf · Disease-specific growth charts of Marfan syndrome in Korea su Jin Kiml, sung Won Park2,
10.3252/pso.eu.54espeabstracts.eurospe.org/hrp/0084/eposters/hrp0084p3-646_e...Gorham-Stout disease (GSD): a Diagnostic and Treatment Protocolt N. Di lorgil, Elisabetta Godanol , Alberto
Hasanbegovic Snijezanaabstracts.eurospe.org/hrp/0084/eposters/hrp0084p3-771_eposter.pdf · Hasanbegovic Snijezana T1DM patients from Pediatric Clinic in Sarajevo with insulin pump
Adipocyte fatty acid binding protein (aFABP) is related …abstracts.eurospe.org/hrp/0084/eposters/hrp0084p3-882_eposter.pdf · Jakob Käpplinger1, David Petroff1, 2, Sabine Herget1,
The Presence of Periodic Limb Movement Disorder in a ...Wolfram syndrome (WFS) is characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness (DIDMOAD), together
Cronicon OPEN ACCESS EC PAEDIATRICS Case Report Acute on … · Wolfram syndrome is a rare autosomal recessive known as DIDMOAD which stands for diabetes insipidus, Diabetes mellitus,
Wolfram (DIDMOAD) syndrome with ventral central pontine ...indoamericanhospital.in/uploads/publications/ni... · Wolfram syndrome 1 (WFS1) is a rare autosomal recessive genetic disorder,
10.3252/pso.eu.54espeabstracts.eurospe.org/hrp/0084/eposters/hrp0084p3-1021_e...Beatriz Villafuerte Q; Raquel Barrio C; María Martín-Frías; Milagros Alonso B; Yoko Oyakawa B; M.
10.3252/pso.eu.54espe - European Society for Paediatric ...abstracts.eurospe.org/hrp/0084/eposters/hrp0084p3-972_eposter.pdf · born small for gestational age and with Ullrich-Turner
10.3252/pso.eu.54espeabstracts.eurospe.org/hrp/0084/eposters/hrp0084p3-1216_eposter.pdf · AFTNs thyroid carcinoma was identified in about 10% [3]. Case presentation An 17-years-old
Somatotropic pituitary insufficiency in Kearns-Sayre ...abstracts.eurospe.org/hrp/0084/eposters/hrp0084p3-957_eposter.pdf · BMC Pediatr. 2013; 13(27): 1 -9. (1) KSS is usually detected