Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Simon J. Raphael"'
Publikováno v:
Endocrine pathology. 3(3)
A 45-year-old woman presented with clinical symptoms of hypoglycemia of 4 months duration. Laboratory testing confirmed hyperinsulinemia; mild hypercalcemia and hypergastrine-mia were also documented. At the time of operation, 3 pancreatic endocrine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe4d809ee267e4313a68458a42714c1d
https://pubmed.ncbi.nlm.nih.gov/32138396
https://pubmed.ncbi.nlm.nih.gov/32138396
Autor:
Judit Zubovits, Wedad Hanna, Fang-I Lu, Elzbieta Slodkowska, Simon J. Raphael, Sharon Nofech-Mozes, Bin Xu, Carlos Parra-Herran
Publikováno v:
Modern Pathology. 31:1073-1084
Mammary fibroepithelial lesions encompass a wide spectrum of tumors ranging from an indolent fibroadenoma to potentially fatal malignant phyllodes tumor. The criteria used for their classification based on morphological assessment are often challengi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99389213bbea145b7fe114f7046acf67
https://doi.org/10.1038/s41379-018-0032-8
https://doi.org/10.1038/s41379-018-0032-8
Autor:
Raewyn M. Seaberg, David E. C. Cole, Geoffrey N. Hendy, Alfredo Scillitani, Simon J. Raphael, Andrew Y. Shuen, M. Jean Davidson, Vito Guarnieri, Catherine M. Kelly, Filomena Baorda, Orazio Palumbo
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-9 (2017)
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-9 (2017)
Background Inactivating mutations of CDC73 cause Hyperparathyroidism-Jaw Tumour syndrome (HPT-JT), Familial Isolated Hyperparathyroidism (FIHP) and sporadic parathyroid carcinoma. We conducted CDC73 mutation analysis in an HPT-JT family and confirm c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99d828063225e1d2dce48fe57ca9c871
https://pubmed.ncbi.nlm.nih.gov/28903740
https://pubmed.ncbi.nlm.nih.gov/28903740
Publikováno v:
Endocrine Pathology. 22:222-225
Ovarian thecal metaplasia is a rare tumor-like mesenchymal lesion of the adrenal gland that has been reported mainly in postmenopausal women and rarely in men. It was originally described as a wedge-shaped lesion composed of ovarian-like stroma resem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee237291c1754f3b31cc03a31055c640
https://doi.org/10.1007/s12022-011-9175-6
https://doi.org/10.1007/s12022-011-9175-6
Publikováno v:
American Journal of Clinical Pathology. 135:831-838
Merkel cell carcinoma (MCC) is an uncommon tumor with indistinct clinical features. The differential diagnosis includes small cell lung carcinoma (SCLC). We characterized the expression of terminal deoxynucleotidyl transferase (TdT) and a panel of im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a75a556e743b3fa0fc779f4d8a8f36
https://doi.org/10.1309/ajcplcb2q9qxdzaa
https://doi.org/10.1309/ajcplcb2q9qxdzaa
Publikováno v:
Annals of Diagnostic Pathology. 12:67-71
Medullary thyroid carcinoma (MTC) is an uncommon thyroid cancer comprising 5% to 8% of thyroid neoplasms. In contrast to common thyroid tumors, this tumor originates from the calcitonin-producing C cells. Regional metastases to cervical lymph nodes o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5f3c5ceab5488e2073060ba2db78033
https://doi.org/10.1016/j.anndiagpath.2006.08.004
https://doi.org/10.1016/j.anndiagpath.2006.08.004
Autor:
David E. C. Cole, Geoffrey N. Hendy, Raewyn M. Seaberg, Simon J. Raphael, Vito Guarnieri, Alfredo Scillitani, Catherine M. Kelly, Andrew Y. Shuen, Filomena Baorda, M. Jean Davidson, Orazio Palumbo
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-1 (2017)
BMC Medical Genetics
BMC Medical Genetics
Background Inactivating mutations of CDC73 cause Hyperparathyroidism-Jaw Tumour syndrome (HPT-JT), Familial Isolated Hyperparathyroidism (FIHP) and sporadic parathyroid carcinoma. We conducted CDC73 mutation analysis in an HPT-JT family and confirm c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a929593eaa3dd0bac684e36fbb7ebaf
http://link.springer.com/article/10.1186/s12881-017-0459-7
http://link.springer.com/article/10.1186/s12881-017-0459-7
Autor:
Sylvia L. Asa, Simon J. Raphael
Publikováno v:
Endocrine Pathology. 3:182-187
Positive immunohistochemical staining for three metal binding proteins, ceruloplasmin, lactoferrin, and transferrin, has been suggested to be a reliable diagnostic marker of malignant but not benign thyroid neoplasms. We tested this hypothesis on a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1740ee625bf9efbe89bc31600befd0a1
https://doi.org/10.1007/bf02921360
https://doi.org/10.1007/bf02921360
Autor:
Simon J. Raphael, Hagen Klieb
Context Oral verrucous carcinoma (OVC) and oral verrucous hyperplasia (OVH) may be clinically and histologically similar. Problems separating these lesions are compounded by poorly oriented tissue sections and biopsies failing to demonstrate lesional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3d98be381ce843ce827e206a30c6bef
https://europepmc.org/articles/PMC2807515/
https://europepmc.org/articles/PMC2807515/
Autor:
Simon J. Raphael
Publikováno v:
Endocrine pathology. 13(4)
This review article primarily discusses immunohistochemical markers used to aid the diagnosis of thyroid neoplasia. The review concentrates on high molecular weight cytokeratins, cytokertain 19, HBME-1, and galectin-3. Diagnostic uses of proliferatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c3dac4957f4f326807cb52a05ef925b
https://pubmed.ncbi.nlm.nih.gov/12665648
https://pubmed.ncbi.nlm.nih.gov/12665648