Works matching IS 16632818 AND DT 2016 AND VI 86 AND IP 2

Results: 10

A Novel Mutation (S54C) of the PAX8 Gene in a Family with Congenital Hypothyroidism and a High Proportion of Affected Individuals.

Published in:

Hormone Research in Paediatrics, 2016, v. 86, n. 2, p. 137, doi. 10.1159/000445891

By:

Srichomkwun, Panudda;
admoni, Osnat;
Refetoff, Samuel;
de Vries, Liat

Publication type:

Article

Late Presentation of Fulminant Necrotizing Enterocolitis in a Child with Hyperinsulinism on Octreotide Therapy.

Published in:

Hormone Research in Paediatrics, 2016, v. 86, n. 2, p. 131, doi. 10.1159/000443959

By:

Hawkes, Colin Patrick;
adzick, N. Scott;
Palladino, andrew a.;
De León, Diva D.

Publication type:

Article

Time Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic Case.

Published in:

2016

By:

Stecchini, Monica F.;
Macedo, Delanie B.;
Reis, ana Claudia S.;
abreu, ana Paula;
Moreira, ayrton C.;
Castro, Margaret;
Kaiser, Ursula B.;
Latronico, ana Claudia;
antonini, Sonir R.

Publication type:

Case Study

Progressive Decline in Height Standard Deviation Scores in the First 5 Years of Life Distinguished Idiopathic Growth Hormone Deficiency from Familial Short Stature and Constitutional Delay of Growth.

Published in:

Hormone Research in Paediatrics, 2016, v. 86, n. 2, p. 117, doi. 10.1159/000448283

By:

Rothermel, Juliane;
Lass, Nina;
Toschke, Christina;
Reinehr, Thomas

Publication type:

Article

Long-Term Outcomes, Genetics, and Pituitary Morphology in Patients with Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiencies: A Single-Centre Experience of Four Decades of Growth Hormone Replacement.

Published in:

Hormone Research in Paediatrics, 2016, v. 86, n. 2, p. 106, doi. 10.1159/000448098

By:

Rohayem, Julia;
Drechsel, Hendrik;
Tittel, Bettina;
Hahn, Gabriele;
Pfaeffle, Roland;
Huebner, angela

Publication type:

Article

Anti-Zinc Transporter Protein 8 Antibody Testing Is Not Informative in Routine Prediabetes Screening in Young Patients with Autoimmune Thyroiditis and Celiac Disease.

Published in:

Hormone Research in Paediatrics, 2016, v. 86, n. 2, p. 100, doi. 10.1159/000448003

By:

Larizza, Daniela;
De amici, Mara;
Klersy, Catherine;
albanesi, Michela;
albertini, Riccardo;
Badulli, Carla;
Torre, Cristina;
Calcaterra, Valeria

Publication type:

Article

Skeletal Fragility in Children with Chronic Disease.

Published in:

Hormone Research in Paediatrics, 2016, v. 86, n. 2, p. 71, doi. 10.1159/000447583

By:

Joseph, S.;
McCarrison, S.;
Wong, S.C.

Publication type:

Article

Splicing Defects in the AAAS Gene Leading to both Exon Skipping and Partial Intron Retention in a Tunisian Patient with Allgrove Syndrome.

Published in:

Hormone Research in Paediatrics, 2016, v. 86, n. 2, p. 90, doi. 10.1159/000446539

By:

Kallabi, Fakhri;
Ben Rhouma, Bochra;
Baklouti, Siwar;
Ghorbel, Rania;
Felhi, Rahma;
Keskes, Leila;
Kamoun, Hassen

Publication type:

Article

Establishing Normal Ranges of Basal and ACTH-Stimulated Serum Free Cortisol in Children.

Published in:

Hormone Research in Paediatrics, 2016, v. 86, n. 2, p. 94, doi. 10.1159/000447946

By:

Eyal, Ori;
Limor, Rona;
Oren, asaf;
Schachter-Davidov, anita;
Stern, Naftali;
Weintrob, Naomi

Publication type:

Article

Automatic Determination of the Greulich-Pyle Bone Age as an Alternative Approach for Chinese Children with Discordant Bone Age.

Published in:

Hormone Research in Paediatrics, 2016, v. 86, n. 2, p. 83, doi. 10.1159/000446434

By:

Zhang, Ji;
Lin, Fangqin;
Ding, Xiaoyi

Publication type:

Article