Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland

The Severity of Congenital Hypothyroidism of Central Origin Should Not Be Underestimated

(2015) Nitash Zwaveling-Soonawala et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Recent advances in central congenital hypothyroidism

(2015) Nadia Schoenmakers et al.   JOURNAL OF ENDOCRINOLOGY

A Novel Deletion in the Thyrotropin Beta-Subunit Gene Identified by Array Comparative Genomic Hybridization Analysis Causes Central Congenital Hypothyroidism in a Boy Originating from Turkey

(2014) Pia Hermanns et al.   Hormone Research in Paediatrics

An Evo-Devo Approach to Thyroid Hormones in Cerebral and Cerebellar Cortical Development: Etiological Implications for Autism

(2014) Pere Berbel et al.   Frontiers in Endocrinology

Factors Associated With Hearing Impairment in Patients With Congenital Hypothyroidism Treated Since the Neonatal Period: A National Population-Based Study

(2013) Lydia Lichtenberger-Geslin et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Making sense with thyroid hormone—the role of T3 in auditory development

(2013) Lily Ng et al.   Nature Reviews Endocrinology

Mass screening of newborns for congenital hypothyroidism of central origin by free thyroxine measurement of blood samples on filter paper

(2012) M. Adachi et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Molecular Mechanism of Scanning and Start Codon Selection in Eukaryotes

(2011) A. G. Hinnebusch   MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS

SignalP 4.0: discriminating signal peptides from transmembrane regions

(2011) Thomas Nordahl Petersen et al.   NATURE METHODS

Two Novel Mutations of the TSH-β Subunit Gene Underlying Congenital Central Hypothyroidism Undetectable in Neonatal TSH Screening

(2010) María Sonia Baquedano et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM