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Pediatric Endocrinology

Contributing journals to this collection:
Journal of Clinical Endocrinology & Metabolism, Molecular Endocrinology, Endocrinology, Endocrine Reviews, and Endocrine Society Journals

Citations 41-50 of 803 total displayed.

Past content

J. Clin. Endocrinol. Metab.
Endocrine Care
Duplications of the Functional CYP21A2 Gene Are Primarily Restricted to Q318X Alleles: Evidence for a Founder Effect
S. Kleinle, R. Lang, G. F. Fischer, H. Vierhapper, F. Waldhauser, M. Födinger, and S. M. Baumgartner-Parzer
J. Clin. Endocrinol. Metab. 94: 3954 -3958; published online before print as doi:10.1210/jc.2009-0487 [Abstract] [Full text]  

J. Clin. Endocrinol. Metab.
Endocrine Care
Acanthosis Nigricans and Insulin Sensitivity in Patients with Achondroplasia and Hypochodroplasia due to FGFR3 Mutations
Kyriaki S. Alatzoglou, Peter C. Hindmarsh, Caroline Brain, John Torpiano, and Mehul T. Dattani
J. Clin. Endocrinol. Metab. 94: 3959 -3963; published online before print as doi:10.1210/jc.2009-0322 [Abstract] [Full text]  

J. Clin. Endocrinol. Metab.
Endocrine Research
Association of Thyroid Gland Volume, Serum Insulin-Like Growth Factor-I, and Anthropometric Variables in Euthyroid Prepubertal Children
Malene Boas, Laszlo Hegedüs, Ulla Feldt-Rasmussen, Niels E. Skakkebæk, Linda Hilsted, and Katharina M. Main
J. Clin. Endocrinol. Metab. 94: 4031 -4035; published online before print as doi:10.1210/jc.2009-0939 [Abstract] [Full text]  

J. Clin. Endocrinol. Metab.
Endocrine Research
X-Linked Congenital Adrenal Hypoplasia with Hypogonadotropic Hypogonadism Caused by an Inversion Disrupting a Conserved Noncoding Element Upstream of the NR0B1 (DAX1) Gene
Beate Skinningsrud, Eystein S. Husebye, Gregor D. Gilfillan, Eirik Frengen, Aage Erichsen, Kristina Gervin, Eli Ormerod, Thore Egeland, and Dag E. Undlien
J. Clin. Endocrinol. Metab. 94: 4086 -4093; published online before print as doi:10.1210/jc.2009-0923 [Abstract] [Full text]  

J. Clin. Endocrinol. Metab.
Endocrine Research
HHEX-IDE Polymorphism Is Associated with Low Birth Weight in Offspring with a Family History of Type 1 Diabetes
Christiane Winkler, Thomas Illig, Kerstin Koczwara, Ezio Bonifacio, and Anette-Gabriele Ziegler
J. Clin. Endocrinol. Metab. 94: 4113 -4115; published online before print as doi:10.1210/jc.2009-0970 [Abstract] [Full text]  

J. Clin. Endocrinol. Metab.
Article
Identification and Functional Studies of Two New Dual-Oxidase 2 (DUOX2) Mutations in a Child with Congenital Hypothyroidism and a Eutopic Normal-Size Thyroid Gland
Massimo Tonacchera, Giuseppina De Marco, Patrizia Agretti, Lucia Montanelli, Caterina Di Cosmo, Andrea Claudia Freitas Ferreira, Antonio Dimida, Eleonora Ferrarini, Helton Estrela Ramos, Claudia Ceccarelli, Federica Brozzi, Aldo Pinchera, and Paolo Vitti
J. Clin. Endocrinol. Metab. published September 29, 2009, doi:10.1210/jc.2009-0426 [Abstract]  

J. Clin. Endocrinol. Metab.
Article
Body Composition and Bone Mineral Density in Children with Premature Adrenarche and the Association of LRP5 Gene Polymorphisms with Bone Mineral Density
Pauliina Utriainen, Jarmo Jääskeläinen, Anne Saarinen, Esko Vanninen, Outi Mäkitie, and Raimo Voutilainen
J. Clin. Endocrinol. Metab. published September 29, 2009, doi:10.1210/jc.2009-0315 [Abstract]  

J. Clin. Endocrinol. Metab.
Article
A Novel Loss-of-Function Mutation, Gln459Arg, of the Calcium-Sensing Receptor Gene Associated with Apparent Autosomal Recessive Inheritance of Familial Hypocalciuric Hypercalcemia
Steven A. Lietman, Yardena Tenenbaum-Rakover, Tjin Shing Jap, Wu Yi-Chi, Yang De-Ming, Changlin Ding, Najat Kussiny, and Michael A. Levine
J. Clin. Endocrinol. Metab. published September 29, 2009, doi:10.1210/jc.2008-2484 [Abstract]  

J. Clin. Endocrinol. Metab.
Article
Recombinant Thyrotropin Use in Children and Adolescents with Differentiated Thyroid Cancer: A Multicenter Retrospective Study
Markus Luster, Daria Handkiewicz-Junak, Armando Grossi, Margaret Zacharin, David Taïeb, Ofelia Cruz, Anne Hitzel, Juan Antonio Vallejo Casas, Uwe Mäder, Massimo E. Dottorini for the Pediatric rhTSH Investigators Group
J. Clin. Endocrinol. Metab. published September 22, 2009, doi:10.1210/jc.2009-0593 [Abstract]  

J. Clin. Endocrinol. Metab.
Article
X-Linked Congenital Adrenal Hypoplasia with Hypogonadotropic Hypogonadism Caused by an Inversion Disrupting a Conserved Noncoding Element Upstream of the NR0B1 (DAX1) Gene
Beate Skinningsrud, Eystein S. Husebye, Gregor D. Gilfillan, Eirik Frengen, Aage Erichsen, Kristina Gervin, Eli Ormerod, Thore Egeland, and Dag E. Undlien
J. Clin. Endocrinol. Metab. published September 22, 2009, doi:10.1210/jc.2009-0923 [Abstract]  

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