Results 1 to 10 of about 119,065 (157)

Polyendocrine Disorders and Endocrine Neoplastic Syndromes [PDF]

open access: yesEndocrinology, 2021
This comprehensive reference book is meant to support clinicians in the diagnosis and treatment of polyendocrine diseases and endocrine neoplastic syndromes. Although a large majority of endocrine diseases present as sporadic cases, an increasing proportion can be identified as part of a polyendocrine or systemic syndrome.
Annamaria, Colao   +2 more
exaly   +5 more sources

Use of family history taking for hereditary neoplastic syndromes screening in primary health care: A systematic review protocol. [PDF]

open access: yesPLoS ONE, 2022
BackgroundAlthough most neoplasms result from complex interactions between the individual's genome and the environment, a percentage of cases is particularly due to inherited alterations that confer a greater predisposition to the development of tumors ...
Raphael Manhães Pessanha   +3 more
doaj   +4 more sources

Neoplastic Masquerade Syndromes in Patients With Uveitis [PDF]

open access: yesAmerican Journal of Ophthalmology, 2014
To identify the demographic and clinical characteristics, along with the frequency, of neoplastic masquerade syndromes in a tertiary uveitis clinic.A retrospective observational cohort.Demographic and clinical data on all patients presenting to the National Eye Institute (NEI) with uveitis between 2004 and 2012 were used to compare neoplastic ...
Chi-Chao Chan   +2 more
exaly   +3 more sources

Diagnostics of hereditary cancer syndromes by ngs. A database creation experience [PDF]

open access: yesКлиническая практика, 2021
Background: More than 500 thousand new cases of malignant neoplasms are registered annually in the Russian Federation, of which more than 50 thousand new cases are due to hereditary forms.
Ivan S. Abramov   +8 more
doaj   +1 more source

The importance of MIR-4328 gene mutations in Acute Promyelocytic Leukemia [PDF]

open access: yesDocumenta Haematologica, 2023
Introduction: miRNAs are involved in the pathogenesis of neoplastic syndromes by silencing target genes. As previously shown, hsa-mir-4328 is downregulated in Acute Promyelocytic Leukemia (APL).
Onda-Tabita CALUGARU   +5 more
doaj   +1 more source

Lynch-like Syndrome and its Molecular Approaches: A Brief Report and Literature Review [PDF]

open access: yesMiddle East Journal of Cancer, 2023
Lynch syndrome (LS) predisposes individuals to early-onset colorectal and other Lynch-associated cancer. This disorder is an autosomal dominant genetic disturbance caused by germline mutations in one of the mismatch repair genes.
Zeinab Abdollahi   +3 more
doaj   +1 more source

BRAF p.V600E associated poly-neoplastic syndrome [PDF]

open access: yesRare Tumors, 2021
We report a male patient who developed eight different cancers between ages 57 and 64. BRAF p.V600E mutation was detected in Langerhans cell histiocytosis, chronic lymphocytic leukemia, histiocytic sarcoma, melanoma, and adenocarcinoma of the lung. It was not detected in multiple myeloma, basal cell carcinoma, and papillary thyroid cancer. BRAF p.V600E
Muhamad Alhaj Moustafa   +6 more
openaire   +3 more sources

Prognostic role of neoplastic markers in Takotsubo syndrome [PDF]

open access: yesScientific Reports, 2021
AbstractTakotsubo syndrome (TTS) is an acute heart failure syndrome with significant rates of in and out-of-hospital mayor cardiac adverse events (MACE). To evaluate the possible role of neoplastic biomarkers [CA-15.3, CA-19.9 and Carcinoembryonic Antigen (CEA)] as prognostic marker at short- and long-term follow-up in subjects with TTS.
Santoro, Francesco   +12 more
openaire   +5 more sources

SDHB exon 1 deletion: A recurrent germline mutation in Colombian patients with pheochromocytomas and paragangliomas

open access: yesFrontiers in Genetics, 2023
Pheochromocytomas (PCCs) and paragangliomas (PGLs) (known as PPGL in combination) are rare neuroendocrine tumors of the adrenal medulla and extra-adrenal ganglia. About 40% of the patients with PPGL have a hereditary predisposition.
María Carolina Manotas   +15 more
doaj   +1 more source

Metastatic follicular thyroid cancer in a patient with Birt‐Hogg‐Dubé syndrome

open access: yesClinical Case Reports, 2021
Birt‐Hogg‐Dubé syndrome (BHDS) is an extremely rare genetic condition that predisposes to renal cell carcinoma. This case describes a novel case of a patient with BHDS who also develops follicular thyroid cancer.
Elisa K. Bongetti   +3 more
doaj   +1 more source

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