TY  - JOUR
AU  - Vázquez-Román, V
AU  - Cameselle-Teijeiro, J M
AU  - Fernández-Santos, J M
AU  - Ríos-Moreno, M J
AU  - Loidi, L
AU  - Ortiz, T
AU  - Martín-Lacave, I
PY  - 2022
DO  - 10.1007/s12022-022-09732-2
UR  - http://hdl.handle.net/10668/20964
T2  - Endocrine pathology
AB  - Pendred syndrome (PDS) is an autosomal recessive disorder caused by mutations in the gene that encodes pendrin. Pendred thyroid tissue is supposedly altered by the absence of functional pendrin, but it is still unknown whether other iodide exchangers...
LA  - en
KW  - Ciliogenesis
KW  - Follicular cells
KW  - Immunohistochemistry
KW  - Iodide channels
KW  - Pendred syndrome
KW  - Primary cilia
KW  - Humans
KW  - Iodides
KW  - Goiter, Nodular
KW  - Hearing Loss, Sensorineural
KW  - Carrier Proteins
KW  - Sulfate Transporters
KW  - Thyroid Diseases
KW  - Adenoma
TI  - Histopathological Features of Pendred Syndrome Thyroids Align with Differences in the Expression of Thyroid-Specific Markers, Apical Iodide Transporters, and Ciliogenesis Process.
TY  - research article
VL  - 33
ER  -