ESPE Abstracts

ESPE Abstracts

Published by BioScientifica
Volume 82 | ESPE2014 | Next issue

53rd Annual ESPE (ESPE 2014)

Dublin, Ireland
18 Sept 2014 - 20 Sept 2014

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Dublin, Ireland; 18-20 September 2014. Further information

Poster Category 3

Growth (1)

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Growth
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Growth (2)

hrp0082p3-d2-823 | Growth (1)

Correlation Between Initial Treatment Effect of Recombinant Human GH and Exon 3 Polymorphism of GH Receptor in Chinese GH Deficiency Children

hrp0082p3-d2-824 | Growth (1)

GH Deficiency in a Case with Neurofibromatosis-Noonan Syndrome

hrp0082p3-d2-825 | Growth (1)

Monitoring of GH Treatment by the Electronic Auto-Injection Device Easypod™ Allows to Improve the Outcome and Maximize Adherence in Patients with Generally High Adherence Rates

hrp0082p3-d2-826 | Growth (1)

Usability and Safety of FlexPro® PenMate® in Patients, Caregivers and Healthcare Professionals (HCPs)

hrp0082p3-d2-827 | Growth (1)

Impairment of Glucose Metabolism in GH Deficient Children Under GH Replacement

hrp0082p3-d2-828 | Growth (1)

Growth Response After 1 Year of GH Treatment in Children Born Small for Gestational (SGA) Without GH Deficiency: our Experience

hrp0082p3-d2-829 | Growth (1)

Cross-Sectional and Prospective Study of the Effects of GH Therapy on Metabolic Panel in Children with GH Deficiency

hrp0082p3-d2-830 | Growth (1)

Prader–Willi Syndrome and GH Therapy: valuable Effects and Adverse Events

hrp0082p3-d2-831 | Growth (1)

Recovery of Central Fever After GH Therapy in a Patient with GH Deficiency Secondary to Posttraumatic Brain Injury

hrp0082p3-d2-832 | Growth (1)

The Impact of GH Replacement Therapy in Children Born Small-for-Gestational-Age: growth Response and Safety Profile

hrp0082p3-d2-833 | Growth (1)

GH Treatment in 50 Child with Short Stature: Lebanese Experience

hrp0082p3-d2-834 | Growth (1)

Effectiveness of GH Therapy in Children with Short Stature and Decreased GH Peak in Stimulating Tests is Independent from GH Secretion After Falling Asleep

hrp0082p3-d2-835 | Growth (1)

An Unusual Case of a Child with GH Deficiency and Arnold-Chiari Malformation Type I

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