Articles with "multiple endocrine" as a keyword



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Can We Do Even Better? Preoperative Imaging Overestimates the Tumor Size in Pancreatic Neuroendocrine Neoplasms Associated with Multiple Endocrine Neoplasia Type 1

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Published in 2017 at "World Journal of Surgery"

DOI: 10.1007/s00268-017-4376-x

Abstract: Dr. Polenta and her colleagues have provided our neuroendocrine surgical community with a very interesting and detailed assessment of the accuracy of preoperative imaging for pancreatic neuroendocrine neoplasms (pNEN) in patients with multiple endocrine neoplasia… read more here.

Keywords: multiple endocrine; pancreatic neuroendocrine; neuroendocrine neoplasms; endocrine neoplasia ... See more keywords
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Genetics of Multiple Endocrine Neoplasia Type 1/Multiple Endocrine Neoplasia Type 2 Syndromes.

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Published in 2017 at "Endocrinology and metabolism clinics of North America"

DOI: 10.1016/j.ecl.2017.01.011

Abstract: Multiple endocrine neoplasia syndromes types 1 and 2 represent well-characterized yet clinically heterogeneous hereditary conditions for which diagnostic and management recommendations exist; genetic testing for these inherited endocrinopathies is included in these guidelines and is… read more here.

Keywords: endocrine neoplasia; neoplasia type; multiple endocrine; genetics ... See more keywords
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MEN 2A syndrome – Multiple endocrine neoplasia with autosomal dominant transmission

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Published in 2020 at "International Journal of Surgery Case Reports"

DOI: 10.1016/j.ijscr.2020.07.015

Abstract: Highlights • Every case essential, because MEN 2A is reported in 500–1000 families worldwide.• This case reflects correct clinical steps in avoidance of possible complications.• It contributes to the existing limited literature reports.• MTC can… read more here.

Keywords: men syndrome; multiple endocrine; endocrine neoplasia; autosomal dominant ... See more keywords
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Generation of non-integrated induced pluripotent stem cells from a 23-year-old male with multiple endocrine neoplasia type 1 syndrome.

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Published in 2017 at "Stem cell research"

DOI: 10.1016/j.scr.2016.12.002

Abstract: Urine resource cells were collected from a 23-year-old male with multiple endocrine neoplasia type 1 syndrome (MEN1) for generating iPS cells with episomal plasmids. Two stable iPSC lines with free of episomal plasmid were established.… read more here.

Keywords: neoplasia type; multiple endocrine; male multiple; endocrine neoplasia ... See more keywords
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Perioperative outcomes of syndromic paraganglioma and pheochromocytoma resection in patients with von Hippel‐Lindau disease, multiple endocrine neoplasia type 2, or neurofibromatosis type 1

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Published in 2017 at "Surgery"

DOI: 10.1016/j.surg.2017.08.002

Abstract: Background. Pheochromocytoma and/or paraganglioma associated with neurofibromatosis type 1, multiple endocrine neoplasia type 2A, and von Hippel‐Lindau disease have different catecholamine biochemical phenotypes. We examined perioperative outcomes of pheochromocytoma/paraganglioma resection in 3 syndromic forms. Methods.… read more here.

Keywords: neoplasia type; multiple endocrine; von hippel; endocrine neoplasia ... See more keywords
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Diagnosis of multiple endocrine neoplasia type 2B and management of its ocular features

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Published in 2018 at "Ophthalmic Genetics"

DOI: 10.1080/13816810.2017.1408849

Abstract: ABSTRACT Background: To describe ocular and vascular findings in a patient with multiple endocrine neoplasia type 2B. Materials and methods: Case report of a 31-year-old male who was referred for ocular assessment following diagnosis of… read more here.

Keywords: endocrine neoplasia; neoplasia type; multiple endocrine;
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MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A IN A FAMILY WITH RET C.1901G>A AND NOVEL SLC12A3 MUTATIONS

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Published in 2022 at "Journal of Hypertension"

DOI: 10.1097/01.hjh.0000837464.81691.1f

Abstract: Objective: In recent years, there has been a lot of controversy about the factors affecting the penetrance of multiple endocrine neoplasia type 2A(MEN2A). Some studies considered it may be related to gene mutations. In the… read more here.

Keywords: men2a; ret 1901g; novel slc12a3; multiple endocrine ... See more keywords
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In Vivo Confocal Microscopy of Prominent Conjunctival and Corneal Nerves in Multiple Endocrine Neoplasia Type 2B.

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Published in 2019 at "Cornea"

DOI: 10.1097/ico.0000000000002028

Abstract: OBJECTIVE To report a case of a patient affected by multiple endocrine neoplasia type 2B (MEN 2B) with imaging of conjunctival neuromas by in vivo confocal microscopy (IVCM). METHODS Case report. RESULTS A 48-year-old patient… read more here.

Keywords: microscopy; endocrine neoplasia; multiple endocrine; corneal nerves ... See more keywords
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Regional Growth Velocity and Incidence of Pancreatic Neuroendocrine Neoplasias in Multiple Endocrine Neoplasia Type 1

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Published in 2022 at "Pancreas"

DOI: 10.1097/mpa.0000000000002191

Abstract: Objectives Pancreatic neuroendocrine neoplasias (pNENs) in multiple endocrine neoplasia type 1 are predominantly found in the dorsal anlage. Whether their growth velocity and incidence might be related to their location in the pancreas has not… read more here.

Keywords: growth; incidence; growth velocity; multiple endocrine ... See more keywords
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Fibroblast Activation Protein Inhibitor Imaging and Therapy in a Patient With Multiple Endocrine Neoplasia Type 2A Syndrome.

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Published in 2022 at "Clinical nuclear medicine"

DOI: 10.1097/rlu.0000000000004051

Abstract: ABSTRACT A patient with multiple endocrine neoplasia type 2A syndrome who had exhausted several surgeries and radiotherapy was referred to nuclear medicine department for theranostic approaches. [68Ga]-DOTATATE PET/CT and [131I]I-mIBG SPECT/CT were performed, but the… read more here.

Keywords: endocrine neoplasia; multiple endocrine; patient; patient multiple ... See more keywords
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68Ga-DOTANOC PET/CT in Multiple Endocrine Neoplasia 1 With Associated Adrenocortical Carcinoma.

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Published in 2022 at "Clinical nuclear medicine"

DOI: 10.1097/rlu.0000000000004102

Abstract: ABSTRACT Multiple endocrine neoplasia 1 (MEN1) syndrome is an autosomal dominant syndrome comprising a triad of pancreatic, pituitary, and parathyroid tumors. Adrenal cortical carcinoma occurs rarely in MEN1 syndrome. Here, we have presented a case… read more here.

Keywords: carcinoma; multiple endocrine; dotanoc pet; 68ga dotanoc ... See more keywords