Thyroid hormone transport in developing brain

Current Opinion in Endocrinology, Diabetes and Obesity

Volumn 18, Issue 5, 2011, Pages 295-299

  Bernal, Juan ^a,b  

^a CSIC   (Spain)

^b CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

Author keywords

Allan Herndon Dudley syndrome; brain development; deiodinases; leukoencephalopathy; thyroid gland; thyroid hormones; X chromosome

Indexed keywords

LIOTHYRONINE; THYROID HORMONE; THYROXINE;

BLOOD BRAIN BARRIER; BRAIN DEVELOPMENT; DEIODINATION; GENE; GENE MUTATION; HORMONE TRANSPORT; LEUKOENCEPHALOPATHY; MCT8 GENE; MYELINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; REVIEW; THYROID HORMONE CELL TRANSPORT DEFECT; THYROID HORMONE RELEASE; X CHROMOSOME LINKED DISORDER;

ANIMALS; BIOLOGICAL TRANSPORT; BRAIN; HUMANS; MENTAL RETARDATION, X-LINKED; MONOCARBOXYLIC ACID TRANSPORTERS; MUSCLE HYPOTONIA; MUSCULAR ATROPHY; THYROID HORMONES; THYROXINE; TRIIODOTHYRONINE;

EID: 80052434018     PISSN: 1752296X     EISSN: 17522978     Source Type: Journal    
DOI: 10.1097/MED.0b013e32834a78b3     Document Type: Review

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