Results 121 to 130 of about 75,403 (287)
Thyroglobulin-like Antigens in a Goiter with Impaired Thyroglobulin Biosynthesis
A human congenital goiter has been shown to contain minute amounts of TG-like immunoreactive material (1). The subcellular distribution of the TG-like antigens after differential centrifugation of the homogenate and digitonin solubilization of the particulate fractions has been studied by means of a RIA of TG: 61% of the antigens were found in the ...
Bernal, Juan, Obregón, María Jesús
openaire +3 more sources
Free thyroxine (FT4) median (interquartile range) and percentage FT4 within reference range for patients pre‐ and post‐levothyroxine (LT4) treatment versus untreated individuals. ABSTRACT Introduction This retrospective study aimed to investigate how free thyroxine (FT4) and thyroid‐stimulating hormone (TSH) levels change in the years pre‐ and post ...
Michael Stedman +10 more
wiley +1 more source
Hürthle cell carcinoma: current perspectives. [PDF]
Hürthle cell carcinoma (HCC) can present either as a minimally invasive or as a widely invasive tumor. HCC generally has a more aggressive clinical behavior compared with the other differentiated thyroid cancers, and it is associated with a higher rate ...
Ahmadi, Sara +3 more
core +1 more source
This article describes the unusual cytology features of a DICER1‐mutated thyroid nodule. Fine needle aspiration revealed predominantly cell debris/degenerated cells and rare viable follicular cells with mild cytologic atypia. Surgical resection revealed a nodule with nearly complete infarction, which is one specific feature of DICER1‐mutated thyroid ...
Wenli Dai +3 more
wiley +1 more source
Trace amine-associated receptor 1 (Taar1) has been suggested as putative receptor of thyronamines. These are aminergic messengers with potential metabolic and neurological effects countering their contingent precursors, the thyroid hormones (THs ...
Maria Qatato +5 more
doaj +1 more source
Apeced in Turkey: a case report and insights on genetic and phenotypic variability [PDF]
APECED is a rare monogenic recessive disorder caused by mutations in the AIRE gene. In this manuscript, we report a male Turkish patient with APECED syndrome who presented with chronic mucocutaneous candidiasis associated with other autoimmune ...
Alessandra Fierabraccia +4 more
core +1 more source
Abstract A 61‐year‐old man visited our hospital with a sudden onset of polydipsia and polyuria occurring 5 days prior, accompanied by a 5‐kg weight loss. A month prior, his glycated hemoglobin level was 6.2%. Precisely 8 days before the first visit, he had a fever, and hyperglycemic symptoms began shortly thereafter.
Megumi Sato +6 more
wiley +1 more source
What Is Your Diagnosis? Superficial Cervical Lymph Node Cytology
Veterinary Clinical Pathology, EarlyView.
Vinicius N. Hirata +4 more
wiley +1 more source
ObjectiveTo investigate the predictive value of preoperative serum thyroglobulin (Tg) and anti-thyroglobulin antibodies (TgAb) for central compartment lymph node metastasis (CLNM) in patients with clinically node-negative (cN0) papillary thyroid ...
Xi Lin +3 more
doaj +1 more source
This case highlights a novel genotype–phenotype correlation in the field of endocrinology. Specific endocrine and imaging assessment, in addition to next-generation sequencing (NGS), was performed on the Illumina MiSeq platform, using a TruSight One ...
Mara Carsote +9 more
doaj +1 more source

