Works matching Multiple endocrine neoplasia type 2 (MEN 2)

Results: 88

Ganglioneuromatous polyposis associated with type 2 B multiple endocrine neoplasia (MEN 2B) - case report.

Published in:

Annals of Agricultural & Environmental Medicine, 2024, v. 31, n. 2, p. 302, doi. 10.26444/aaem/171736

By:

Rycyk-Bojarzyńska, Anna;
Kasztelan-Szczerbińska, Beata;
Cichoż-Lach, Halina;
Jargieło, Anna

Publication type:

Article

The Gene Causing Multiple Endocrine Neoplasia Type 2 (MEN 2).

Published in:

Annals of Medicine, 1994, v. 26, n. 3, p. 199, doi. 10.3109/07853899409147890

By:

Ponder, B. A. J.

Publication type:

Article

Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypes.

Published in:

European Journal of Endocrinology, 2010, v. 163, n. 2, p. 301, doi. 10.1530/EJE-10-0333

By:

Cristina Romei

Publication type:

Article

DNA Testing for More Sophisticated Clinical Management of Multiple Endocrine Neoplasia Type 2 (Men 2).

Published in:

Japanese Journal of Clinical Oncology, 1998, v. 28, n. 10, p. 588, doi. 10.1093/jjco/28.10.588

By:

Futami, Hitoyasu

Publication type:

Article

Evaluation of potential mechanisms underlying genotype–phenotype correlations in multiple endocrine neoplasia type 2.

Published in:

Oncogene, 2006, v. 25, n. 50, p. 6637, doi. 10.1038/sj.onc.1209669

By:

Miše, N.;
Drosten, M.;
Racek, T.;
Tannapfel, A.;
Pützer, B. M.

Publication type:

Article

Elevated Calcitonin Levels in a Patient With a Pheochromocytoma: A Case Report.

Published in:

American Surgeon, 2023, v. 89, n. 12, p. 6227, doi. 10.1177/00031348221117035

By:

Shihabi, Areej;
Issa, Peter P.;
Cironi, Katherine;
Omar, Mahmoud;
Abdelgawad, Mohamed;
Kandil, Emad

Publication type:

Article

Transcription Association of VHL and SDH Mutations Link Hypoxia and Oxidoreductase Signals in Pheochromocytomas.

Published in:

Annals of the New York Academy of Sciences, 2006, v. 1073, n. 1, p. 208, doi. 10.1196/annals.1353.023

By:

DAHIA, PATRICIA L. M.

Publication type:

Article

Very early detection of RET proto-oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children: presence of C-cell malignant disease in asymptomatic carriers.

Published in:

2002

By:

Sanso, Gabriela E.;
Domene, Horacio M.;
Garcia Rudaz, Maria C.;
Pusiol, Eduardo;
de Mondino, Ana K.;
Roque, Maria;
Ring, Alejandro;
Perinetti, Hector;
Elsner, Boris;
Iorcansky, Sonia;
Barontini, Marta;
Garcia, RudazMariaC;
de, MondinoAnaK

Publication type:

journal article

Prophylactic thyroidectomy in multiple endocrine neoplasia type 2.

Published in:

Expert Review of Endocrinology & Metabolism, 2010, v. 5, n. 6, p. 867, doi. 10.1586/EEM.10.58

By:

Raue, Friedhelm;
Frank-Raue, Karin

Publication type:

Article

Multiple endocrine neoplasia type 2.

Published in:

Expert Review of Endocrinology & Metabolism, 2009, v. 4, n. 5, p. 443, doi. 10.1586/EEM.09.33

By:

Lips, Cornelis J. M.;
Veelen, Wendy van;
Links, Thera P.;
Höppener, Jo W. M.

Publication type:

Article

Thyroid Malignancy and Cutaneous Lichen Amyloidosis: Key Points Amid RET Pathogenic Variants in Medullary Thyroid Cancer/Multiple Endocrine Neoplasia Type 2 (MEN2).

Published in:

International Journal of Molecular Sciences, 2024, v. 25, n. 18, p. 9765, doi. 10.3390/ijms25189765

By:

Stanescu, Laura-Semonia;
Ghemigian, Adina;
Ciobica, Mihai-Lucian;
Nistor, Claudiu;
Ciuche, Adrian;
Radu, Andreea-Maria;
Sandru, Florica;
Carsote, Mara

Publication type:

Article

The minisequencing method: a simple strategy for genetic screening of MEN 2 families.

Published in:

BMC Genetics, 2002, v. 3, p. 8, doi. 10.1186/1471-2156-3-8

By:

Bugalho, Maria João;
Domingues, Rita;
Sobrinho, Luís

Publication type:

Article

Analysis of Mutations of the RET Proto-oncogene in Patients with Medullary Thyroid Carcinoma.

Published in:

Russian Journal of Genetics, 2003, v. 39, n. 6, p. 706, doi. 10.1023/A:1024474314212

By:

Amosenko, F.A.;
Brzhezovskiy, V. Zh.;
Lyubchenko, L.N.;
Shabanov, M.A.;
Kozlova, V.M.;
Vanushko, V.E.;
Kazubskaya, T.P.;
Garkavtseva, R.F.;
Kalinin, V.N.

Publication type:

Article

Prophylactic thyroidectomy in multiple endocrine neoplasia: the impact of molecular mechanisms of RET proto-oncogene.

Published in:

Langenbeck's Archives of Surgery, 2003, v. 388, n. 1, p. 17, doi. 10.1007/s00423-003-0368-4

By:

Frilling, Andrea;
Weber, Frank;
Tecklenborg, Carsten;
Broelsch, Christoph Erich

Publication type:

Article

No correlation between RET immunostaining and the codon 918 mutation in sporadic medullary thyroid carcinoma.

Published in:

Langenbeck's Archives of Surgery, 1999, v. 384, n. 1, p. 60, doi. 10.1007/s004230050175

By:

Bockhorn, M.;
Frilling, A.;
Kalinin, V.;
Schröder, S.;
Broelsch, C. E.

Publication type:

Article

Laparoscopic bilateral cortical-sparing adrenalectomy for pheochromocytoma.

Published in:

2016

By:

Biteman, Benjamin;
Randall, James;
Brody, Fred;
Biteman, Benjamin R;
Randall, James A

Publication type:

journal article

The mouse soluble GFRα4 receptor activates RET independently of its ligand persephin.

Published in:

Oncogene, 2007, v. 26, n. 26, p. 3892, doi. 10.1038/sj.onc.1210161

By:

Yang, J.;
Runeberg-Roos, P.;
Leppänen, V.-M.;
Saarma, M.

Publication type:

Article

A model for GFRa4 function and a potential modifying role in multiple endocrine neoplasia 2.

Published in:

Oncogene, 2005, v. 24, n. 6, p. 1091, doi. 10.1038/sj.onc.1207826

By:

Vanhorne, Judith B.;
Andrew, Scott D.;
Harrison, Karen J.;
Taylor, Sherryl A. M.;
Thomas, Bradley;
McDonald, Thomas J.;
Ainsworth, Peter J.;
Mulligan, Lois M.

Publication type:

Article

The pressure rises: update on the genetics of phaeochromocytoma.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2347, doi. 10.1093/hmg/11.20.2347

By:

Maher, Eamonn R.;
Eng, Charis

Publication type:

Article

Genetic Predisposition to Phaeochromocytoma: Analysis of Candidate Genes GDNF, RET and VHL.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 7, p. 1051, doi. 10.1093/hmg/6.7.1051

By:

Woodward, Emma R.;
Eng, Charis;
McMahon, Rob;
Voutilainen, Raimo;
Affara, Nabeel A.;
Ponder, Bruce A. J.;
Maher, Eamonn R.

Publication type:

Article

Haplotype analysis of MEN 2 mutations.

Published in:

Human Molecular Genetics, 1994, v. 3, n. 10, p. 1771

By:

Gardner, Emily;
Mulligan, Lois M.;
Eng, Charis;
Healey, Catherine S.;
Kwok, John B.J.;
Ponder, Margaret A.;
Ponder, Bruce A.J.

Publication type:

Article

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.

Published in:

Human Molecular Genetics, 1994, v. 3, n. 2, p. 237

By:

Eng, Charis;
SmIth, Darrin P.;
MullIgan, Lois M.;
Nagal, Maria A.;
Healey, Catherine S.;
Ponder, Margaret A.;
Gardner, Emily;
Scheumann, Georg F.W.;
Jackson, CharIes E.;
Tunnacllffe, Alan;
Ponder, Bruce A.J.

Publication type:

Article

Phaeochromocytoma associated with a de novo VHL mutation as form fruste of von Hippel-Lindau disease.

Published in:

2001

By:

Frenzel, Sabine;
Apel, Thomas W.;
Heidemann, Peter H.;
Zerres, Klaus;
Neumann, Hartmut P. H.;
Dörr, Helmuth G.;
Frenzel, S;
Apel, T W;
Heidemann, P H;
Zerres, K;
Neumann, H P;
Dörr, H G

Publication type:

journal article

Survival at 20 Years of a Medullary Thyroid Carcinoma with Bone and Pulmonary Metastases.

Published in:

Pan Arab Journal of Oncology, 2016, v. 9, n. 2, p. 30

By:

Messad, F.;
Bensalem, A.

Publication type:

Article

Poster Presentations on Adrenal, Pituitary, and Other Endocrine Glands, Parathyroid Gland, Thyroid Gland.

Published in:: 2016
Publication type:: Case Study

High prevalence of exon 8 G533 C mutation in apparently sporadic medullary thyroid carcinoma in Greece.

Published in:

Clinical Endocrinology, 2012, v. 77, n. 6, p. 857, doi. 10.1111/j.1365-2265.2012.04462.x

By:

Sarika, H. L.;
Papathoma, A.;
Garofalaki, M.;
Vasileiou, V.;
Vlassopoulou, B.;
Anastasiou, E.;
Alevizaki, M.

Publication type:

Article

Phaeochromocytoma, new genes and screening strategies.

Published in:

2006

By:

Gimenez-Roqueplo, Anne-Paule;
Lehnert, Hendrik;
Mannelli, Massimo;
Neumann, Hartmut;
Opocher, Giuseppe;
Maher, Eamonn R.;
Plouin, Pierre-François

Publication type:

Other

RET codon 804 mutations in multiple endocrine neoplasia 2: genotype-phenotype correlations and implications in clinical management.

Published in:

Clinical Genetics, 2011, v. 79, n. 1, p. 1, doi. 10.1111/j.1399-0004.2010.01453.x

By:

Mukherjee, S.;
Zakalik, D.

Publication type:

Article

RET is expressed but not mutated in extra-adrenal paragangliomas.

Published in:

Journal of Pathology, 2000, v. 191, n. 3, p. 264, doi. 10.1002/1096-9896(2000)9999:9999<::AID-PATH638>3.0.CO;2-I

By:

Krijger, Ronald R. de;
Harst, Erwin van der;
Muletta-Feurer, Seraina;
Bruining, Hajo A.;
Lamberts, Steven W. J.;
Dinjens, Winand N. M.;
Roth, Jürgen;
Heitz, Philipp U.;
Komminoth, Paul

Publication type:

Article

Anesthetic Management of Clinically Silent Familial Pheochromocytoma with MEN 2A: A Report of Four Cases.

Published in:

Indian Journal of Surgery, 2016, v. 78, n. 5, p. 414, doi. 10.1007/s12262-016-1539-1

By:

Aggarwal, Shipra;
Talwar, Vandana;
Virmani, Pooja;
Kale, Suniti

Publication type:

Article

Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET.

Published in:

2008

By:

Moore, S. W.;
Zaahl, M. G.

Publication type:

journal article

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and...

Published in:

Nature, 1994, v. 367, n. 6461, p. 375, doi. 10.1038/367375a0

By:

Hofstra, Robert M.W.;
Landsvater, Rudy M.

Publication type:

Article

Dermal Hyperneury and Multiple Sclerotic Fibromas in Multiple Endocrine Neoplasia Type 2A Syndrome.

Published in:

2017

By:

Alegría-Landa, Victoria;
Jo-Velasco, Margarita;
Robledo, Mercedes;
Requena, Luis

Publication type:

journal article

Genotype—Phenotype Correlation of Patients with Multiple Endocrine Neoplasia Type 2 in Japan.

Published in:

Japanese Journal of Clinical Oncology, 1998, v. 28, n. 10, p. 590, doi. 10.1093/jjco/28.10.590

By:

Egawa, Shin-ichi;
Futami, Hitoyasu;
Takasaki, Kayo;
Iihara, Masatoshi;
Okamoto, Takahiro;
Kanbe, Masako;
Ohi, Toshitaka;
Saio, Yukie;
Miyauchi, Akira;
Takiyama, Yumi;
Koga, Masafumi;
Miyanaga, Ken;
Inoue, Ken-ichi;
Mitsuyama, Shoshu;
Nomura, Yoshio;
Takei, Hiroyuki;
Mugiya, Soichi;
Ishida, Osamu;
Zeze, Fujio;
Shakutsui, Shiro

Publication type:

Article

A Nationwide Clinical Survey of Patients With Multiple Endocrine Neoplasia Type 2 and Familial Medullary Thyroid Carcinoma in Japan.

Published in:

Japanese Journal of Clinical Oncology, 1997, v. 27, n. 3, p. 128

By:

lihara, Masatoshi;
Yamashita, Tomoyuki;
Okamoto, Takahiro;
Kanbe, Masako;
Yamazaki, Kiyomi;
Egawa, Shin-ichi;
Yamaguchi, Ken;
Obara, Takao

Publication type:

Article

Germ Line Mutation in the RET Proto-oncogene Associated with Familial Multiple Endocrine Neoplasia Type 2B: A Case Report.

Published in:

Japanese Journal of Clinical Oncology, 1995, v. 25, n. 3, p. 104

By:

Ishida, Osamu;
Zeki, Kazuya;
Morimoto, Isao;
Yamamoto, Shigeki;
Fujihira, Takashi;
Eto, Sumiya

Publication type:

Article

Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 8, p. 457, doi. 10.1038/sj.ejhg.5200829

By:

A. Cascon;
Ruiz-Llorente, S.

Publication type:

Article

Genetic diagnosis of endocrine disorders in Cyprus through the Cyprus Institute of Neurology and Genetics: an ENDO-ERN Reference Center.

Published in:

Orphanet Journal of Rare Diseases, 2024, v. 19, p. 1, doi. 10.1186/s13023-024-03171-4

By:

Neocleous, Vassos;
Fanis, Pavlos;
Toumba, Meropi;
Skordis, Nicos;
Phylactou, Leonidas A.

Publication type:

Article

Medullary thyroid carcinoma identified within the first year of life in children with hereditary multiple endocrine neoplasia type 2A (codon 634) and 2B.

Published in:

European Journal of Endocrinology, 2009, v. 160, n. 5, p. 807, doi. 10.1530/EJE-08-0854

By:

Zenaty, D

Publication type:

Article

Different expression of catecholamine transporters in phaeochromocytomas from patients with von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2.

Published in:

European Journal of Endocrinology, 2005, v. 153, n. 4, p. 551, doi. 10.1530/eje.1.01987

By:

Thanh-Truc Huynh

Publication type:

Article

Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma.

Published in:

Oncogene, 2002, v. 21, n. 3, p. 479, doi. 10.1038/sj.onc.1205133

By:

Koch, Christian A.;
Huang, Steve C.;
Zhengping Zhuang;
Stolle, Catherine;
Azumi, Norio;
Chrousos, George P.;
Vortmeyer, Alexander O.;
Pacak, Karel

Publication type:

Article

Allelic imbalance of the mutant and wild-type RET allele in MEN 2A-associated medullary thyroid carcinoma.

Published in:

Oncogene, 2001, v. 20, n. 53, p. 7809, doi. 10.1038/sj.onc.1204991

By:

Koch, Christian A;
Huang, Steve C;
Moley, Jeffrey F;
Azumi, Norio;
Chrousos, George P;
Gagel, Robert F;
Zhuang, Zhengping;
Pacak, Karel;
Vortmeyer, Alexander O

Publication type:

Article

Medullary Thyroid Carcinoma in a Patient with MEN 1 Syndrome. Case Report and Literature Review.

Published in:

OncoTargets & Therapy, 2020, v. 13, p. 7599, doi. 10.2147/OTT.S259656

By:

Friziero, Alberto;
Dalt, Gianfranco Da;
Piotto, Andrea;
Serafini, Simone;
Grego, Andrea;
Galuppini, Francesca;
Pennelli, Gianmaria;
Sperti, Cosimo

Publication type:

Article

CR56 Metastatic thyroid cancer after thyroidectomy in patient with MEN2A syndrome: a case report.

Published in:

Lijecnicki Vjesnik, 2023, v. 145, p. 74, doi. 10.26800/LV-145-supl2-CR56

By:

Čala, Ana;
Dušek, Tina

Publication type:

Article

Single-incision port robot-assisted surgery for thymic carcinoid tumor resection.

Published in:

2022

By:

Shidei, Hiroaki;
Mitsuboshi, Shota;
Yamamoto, Tomoko;
Kanzaki, Masato

Publication type:

journal article

Medullary thyroid carcinoma: surgical treatment advances.

Published in:

Expert Review of Anticancer Therapy, 2007, v. 7, n. 6, p. 877, doi. 10.1586/14737140.7.6.877

By:

Dionigi, Gianlorenzo;
Bianchi, Veronica;
Rovera, Francesca;
Boni, Luigi;
Piantanida, Eliana;
Tanda, Maria Laura;
Dionigi, Renzo;
Bartalena, Luigi

Publication type:

Article

Multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma: an update.

Published in:

2013

By:

Wells Jr, Samuel A;
Pacini, Furio;
Robinson, Bruce G;
Santoro, Massimo;
Wells, Samuel A Jr

Publication type:

journal article

The Clinical Spectrum of Multiple Endocrine Neoplasia Type 2a Caused by the Rare Intracellular RET Mutation S891A.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 9, p. E92, doi. 10.1210/jc.2010-0375

By:

Schulte, Klaus-Martin;
Machens, Andreas;
Fugazzola, Laura;
McGregor, Alan;
Diaz-Cano, Salvador;
Izatt, Louise;
Aylwin, Simon;
Talat, Nadia;
Beck-Peccoz, Paolo;
Dralle, Henning

Publication type:

Article

High Penetrance of Pheochromocytoma Associated with the Novel C634Y/Y791F Double Germline Mutation in the RET Protooncogene.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 1, p. 1318, doi. 10.1210/jc.2009-1355

By:

Toledo, Rodrigo A.;
Wagner, Simona M.;
Coutinho, Flavia L.;
Lourenço, Delmar M.;
Azevedo, Juliana A.;
Longuini, Viviane C.;
Reis, Mariana T. A.;
Reis, Sheila A. C.;
Siqueira, Sheila A. C.;
Lucon, Antonio M;
Tavares, Marcos R.;
Fragoso, Maria C. B. V.;
Pereira, Adelaide A.;
Dahia, Patricia L. M.;
Mulligan, Lois M.;
Toledo, Sergio P. A.

Publication type:

Article

Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.

Published in:

2010

By:

Erlic, Zoran;
Hoffmann, Michael M;
Sullivan, Maren;
Franke, Gerlind;
Peczkowska, Mariola;
Harsch, Igor;
Schott, Matthias;
Gabbert, Helmut E;
Valimäki, Matti;
Preuss, Simon F;
Hasse-Lazar, Kornelia;
Waligorski, Dariusz;
Robledo, Mercedes;
Januszewicz, Andrzej;
Eng, Charis;
Neumann, Hartmut P H

Publication type:

journal article