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Publication Date:
August 2010
ISSN:
2191-0251

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Editor-in-Chief: Zadik, Zvi

Editorial Board Member: Cassorla, Fernando / Cutfield, Wayne / de Muinck Keizer-Schrama, Sabine M.P.F. / Fideleff, Hugo L. / LaFranch, Stephen H. / Lanes M. D., Roberto / Levitsky, Lynne / Lippe, Barbara / Pfäffle, Roland / Root, Allen W. / Rosenfeld, Ron G. / Werther, George / Kiess, Wieland

12 Issues per year

IMPACT FACTOR 2011: 0.875
5-year IMPACT FACTOR: 1.026

VolumeIssuePage

Issues

Issue 8 (Aug 2010), pp. 741 - 850

Association of Serum Adiponectin Levels with Artherosclerosis and the Metabolic Syndrome in Obese Children

Liu, Yun-Ling / Liang, Hong-Ri / Liu, Hao-Tian / Li, Shu-Ying / Zhou, Ye-ying / Cheng, Hui-Ling / Zhou, Liao-Sheng

Page 743

Septo-optic Dysplasia

Choh, Naseer A. / Choh, Suhil A. / Khanday, Rahil Y. / Jehangir, Majid

Page 753

Hyperandrogenism among Elite Adolescent Female Athletes

Eliakim, A. / Marom, N. / Galitskaya, L. / Nemet, D.

Page 755

Confirmation of Neonatal Screening: Reference Intervals and Evaluation of Methodological Changes in TSH Measurement

Fideleff, Gabriel / Suárez, Martha G. / Sobrado, Patricia G. V. / Celadilla, María L. / Mardyks, Mario / Rodriguez, Carmen C. / Jelen, Ana / Boquete, Hugo R. / Fideleff, Hugo L.

Page 759

Antihyperlipidemic Agents Cause a Decrease in von Willebrand Factor Levels in Pediatric Patients with Familial Hyperlipidemia

Yalçin, S. Songül / Güneş, Bülent / Ünal, Şule / Gümrük, Fatma / Coşkun, Turgay

Page 765

GHR and VDR Genes do not Contribute to the Growth Hormone (GH) Response in GH Deficient and Turner Syndrome Patients

Álvarez-Nava, Francisco / Marcano, Henry / Pardo, Tatiana / Paoli, Mariela / Gunczler, Peter / Soto, Marisol / Villalobos, Joalice / Lanes, Roberto

Page 773

Is BaF3 Bioassay Useful to Identify Patients with Bioinactive Growth Hormone?

Pagani, Sara / Chaler, Eduardo A. / Meazza, Cristina / Maceiras, Mercedes / Gonzalez, Maria Eugenia / Rivarola, Marco A. / Cantoni, Francesca / Travaglino, Paola / Della Croce, Lucia / Laarej, Kamilia / Bozzola, Mauro / Belgorosky, Alicia

Page 783

Congenital Hypothyroidism: Etiology

Dias, V. M. A. / Campos, A. P. C. B. / Chagas, A. J. / Silva, R. M.

Page 815

Familial Hyperinsulinism-Hyperammonemia Syndrome in a Family with Seizures: Case Report

de las Heras, Javier / Garin, Intza / de Nanclares, Guiomar Perez / Aguayo, Anibal / Rica, Itxaso / Castaño, Luis / Vela, Amaia

Page 827

Genital Sanguineous Discharge in Prepuberty: A Case of Mullerian Papilloma of Vagina in a 9 Year-Old Girl

Tumini, Stefano / Carinci, Silvia / Anzellotti, Maria Teresa / Lelli Chiesa, Pier Luigi / Rossi, Carlo / Stuppia, Liborio / Bertelloni, Silvano / Chiarelli, Francesco

Page 831

Glycogen Storage Disease Type III with Hypoketosis

Clemente, María / Gussinyer, Miquel / Arranz, José Antonio / Riudor, Encarnació / Yeste, Diego / Albisu, Marian / Carrascosa, Antonio

Page 833

McCune-Albright Syndrome (MAS): Early and Extensive Bone Fibrous Dysplasia Involvement and “Mistaken Identity” Oophorectomy

Gucev, Zoran / Tasic, Velibor / Jancevska, Aleksandra / Krstevska-Konstantinova, Marina / Pop-Jordanova, Nada

Page 837

Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene

Forghani, Nikta / Lum, Catherine / Krishnan, Sowmya / Wang, Jining / Wilson, Darrel M. / Blackett, Piers R. / Malloy, Peter J. / Feldman, David

Page 843

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