ENDO 2009 (6/10/09)
 
Expert Commentary: Review of Treatments for Short Stature
Expert Commentary: Review of Treatments for Short Stature
Mitchell Geffner, MD
Kurt Midyett, MD
 
Expert Comentary: Clinical Trial Update <br> First-Year Height Velocities with Once-Daily and Twice-Daily Dosing of rhIGF-1 in Prepubertal Children with Primary IGF-1 Deficiency
Expert Comentary: Clinical Trial Update
First-Year Height Velocities with Once-Daily and Twice-Daily Dosing of rhIGF-1 in Prepubertal Children with Primary IGF-1 Deficiency
Kurt Midyett, MD
Alan Rogol, MD
 
Emerging Cardiovascular Data from the KEEPS Trial
Emerging Cardiovascular Data from the KEEPS Trial
Virginia Miller, MD
 
Symposium Highlights: Partial Growth Hormone Deficiency
Symposium Highlights: Partial Growth Hormone Deficiency
Alan D. Rogol, MD
 
High-Dose Octreotide LAR Is Effective and Safe in Patients with Acromegaly Inadequately Controlled by Conventional Somatostatin Analog Therapy: A Randomized, Controlled Trial
High-Dose Octreotide LAR Is Effective and Safe in Patients with Acromegaly Inadequately Controlled by Conventional Somatostatin Analog Therapy: A Randomized, Controlled Trial
Gherardo Mazziotti, MD
 
Craniofacial and Extremity Growth Evaluation in Patients with Turner Syndrome during Growth Hormone Therapy
Craniofacial and Extremity Growth Evaluation in Patients with Turner Syndrome during Growth Hormone Therapy
Maria Estela Justamante de Faria, MD
 
Genetic Polymorphisms Associated with Changes in Serum IGF-I in Prepubertal Children with Growth Hormone Deficiency (GHD) or Turner Syndrome (TS) after One Month of Growth Hormone (GH) Therapy: The PREDICT Study Introducing Pharmacogenomics into Clini
Genetic Polymorphisms Associated with Changes in Serum IGF-I in Prepubertal Children with Growth Hormone Deficiency (GHD) or Turner Syndrome (TS) after One Month of Growth Hormone (GH) Therapy: The PREDICT Study Introducing Pharmacogenomics into Clini
PE Clayton, P Chatelain, V Peterkova, A Belgorosky, D Veimo, A Ferrandez, M Tuefferd, J Dauvillier, L Tato, and PREDICT Investigators
 
Four Year Efficacy and Safety Data of Treatment with Omnitrope® 5 mg/ml Lyophilized Formulation in Children with Growth Failure Due to Growth Hormone Deficiency
Four Year Efficacy and Safety Data of Treatment with Omnitrope® 5 mg/ml Lyophilized Formulation in Children with Growth Failure Due to Growth Hormone Deficiency
F Peter, T Romer, B Koehler, E Solyom, M Walczak, A Muzsnai, A Rudzka-Kocjan, E Kaluza-Guzikowska, E Petriczko, and PH Saenger
 
Growth Hormone Administration Reduces Visceral Adiposity and HsCRP in Patients with Growth Hormone Deficiency Following Cure of Acromegaly: A Randomized, Placebo-Controlled Study
Growth Hormone Administration Reduces Visceral Adiposity and HsCRP in Patients with Growth Hormone Deficiency Following Cure of Acromegaly: A Randomized, Placebo-Controlled Study
Karen K. Miller, MD