Results 311 to 320 of about 150,574 (342)
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Molecular genotyping of the non‐invasive encapsulated follicular variant of papillary thyroid carcinoma

Histopathology, 2018
The non‐invasive encapsulated follicular variant of papillary thyroid carcinoma (FVPTC) has been managed as a low‐risk malignancy. Recently, a proposal was made to reclassify this tumour type as a premalignant lesion and rename it non‐invasive follicular
T. Kim   +15 more
semanticscholar   +1 more source

Identification and Application of an Aptamer Targeting Papillary Thyroid Carcinoma Using Tissue-SELEX.

Analytical Chemistry, 2019
Aptamers, short DNA or RNA oligonucleotides, which evolved from systematic evolution of ligands by exponential enrichment (SELEX), can perform specific target recognition.
Wen Zhong   +11 more
semanticscholar   +1 more source

Papillary and Follicular Thyroid Carcinoma

New England Journal of Medicine, 1998
Papillary and follicular carcinomas of the thyroid are differentiated carcinomas developed from the follicular epithelium, that keep some of its morphological and functional characteristics. Their increased incidence is related to an improved screening. Thyroid carcinoma usually presents as a thyroid nodule.
openaire   +4 more sources

Noninvasive Follicular Variant of Papillary Thyroid Carcinoma and the Afirma Gene-Expression Classifier.

Thyroid, 2016
BACKGROUND It is now recognized that noninvasive follicular variant of papillary thyroid carcinoma (NFVPTC) is a distinct subset of FVPTC with an exceedingly indolent clinical course.
Kristine S Wong   +6 more
semanticscholar   +1 more source

Papillary Thyroid Carcinoma

2008
A computerized PubMed search of MEDLINE 1966–May 2006 was performed. The terms “thyroid,” “papillary,” and “thyroidectomy” were exploded and the resulting articles were cross-referenced, yielding 2203 trials. An additional search was performed to identify those that mapped to the medical subject headings “thyroid neoplasms” and “thyroidectomy,” as well
Gregory W. Randolph, Cristian M. Slough
openaire   +2 more sources

Papillary and follicular thyroid carcinoma

Best Practice & Research Clinical Endocrinology & Metabolism, 2000
Papillary and follicular thyroid carcinomas are among the most curable of all cancers. However, some patients are at high risk of recurrence or even death from their cancer. Most of these patients can be identified at the time of diagnosis using well-established prognostic indicators.
Massimo Torlantano, Martin Schlumberger
openaire   +3 more sources

Oxyphilic Papillary Thyroid Carcinomas

American Journal of Clinical Pathology, 1995
Oxyphilic papillary carcinomas of the thyroid have not been extensively studied because they are rare. The morphology and behavior of 34 cases were described. The average age was 44.1 years, the female-to-male ratio was 3.9:1, and the average diameter of the tumors was 2.3 cm. All had papillary structures present.
Marie E. Beckner   +2 more
openaire   +3 more sources

Occult Papillary Carcinoma of the Thyroid

Archives of Surgery, 1980
Retrospective review was undertaken of 137 patients with occult papillary carcinoma of the thyroid (lesions less than or equal to 1.5 cm in diameter) who were operated on at the Mayo Clinic, Rochester, Minn, between 1926 and 1955. Mean follow-up period was 25.3 years. Operations were conservative. No patient underwent bilateral total lobectomy.
Oliver H. Beahrs   +4 more
openaire   +3 more sources

Risk factors for recurrence in patients with papillary thyroid carcinoma undergoing modified radical neck dissection

British Journal of Surgery, 2016
This study evaluated the impact of lymph node‐related factors on the risk of and site of recurrence in patients who had papillary thyroid carcinoma with lymph node metastasis in the lateral compartment (classified as pN1b).
Young Mok Lee   +5 more
semanticscholar   +1 more source

Familial Papillary Thyroid Carcinoma

2006
Over the last decade, several lines of evidence have been accumulated that support the existence of fPTC susceptibility genes. Preliminary clinical characteristics of fPTC have been identified, and linkage studies have identified the chromosomal locations of putative fPTC susceptibility genes. A logical clinical approach to fPTC is emerging.
Diana M. Malchoff, Carl D. Malchoff
openaire   +3 more sources

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