Works matching Sipple syndrome

Results: 102

Sipple Syndrome: From Diagnosis to Management - A Case Report.

Published in:

Middle East Journal of Cancer, 2024, v. 15, n. 1, p. 72, doi. 10.30476/mejc.2023.95092.1754

By:

Mira, Ruwaida;
Mira, Ranim;
Sherad, Moftah O.;
Rohuma, Mohamed

Publication type:

Article

Sipple syndrome with pregnancy: Anesthetic and obstetrical implications.

Published in:

2014

By:

Bajwa, Sukhminder Jit Singh

Publication type:

Editorial

Vaginal delivery in a patient with pheochromocytoma, medullary thyroid cancer, and primary hyperparathyroidism (multiple endocrine neoplasia type 2A, Sipple's syndrome).

Published in:

2014

By:

Muzannara, Muhammad Anas;
Tawfeeq, Nasser;
Nasir, Mahmood;
Al Harbi, Mohammed Khulaif;
Geldhof, Georges;
Dimitriou, Vassilios

Publication type:

Case Study

Analysis of Eight Sipple's Syndrome Patients and Review of Eighty-two Cases from the Japanese Literature.

Published in:

Japanese Journal of Clinical Oncology, 1990, v. 20, n. 4, p. 392

By:

Oishi, Seiichi;
Sasaki, Masato;
Yamauchi, Jouji;
Umeda, Teruhisa;
Sato, Tatsuo

Publication type:

Article

Sipple's Syndrome with a Malignant Pheochromocytoma Presenting as a Pericardial Effusion.

Published in:

Cardiology, 1978, v. 63, n. 5, p. 305, doi. 10.1159/000169909

By:

Westfried, Morris;
Mandel, Donald;
Alderete, Martha N.;
Groopman, Jacob;
Minkowitz, Stanley

Publication type:

Article

Sipple's Syndrome: Medullary Thyroid Carcinoma, Pheochromocytoma, and Parathyroid Disease.

Published in:

Annals of Internal Medicine, 1973, v. 78, n. 4, p. 561, doi. 10.7326/0003-4819-78-4-561

By:

Keiser, Harry R.;
Beaven, Michael A.;
Doppman, John;
Wells, Sam;
Buja, L. Maximilian

Publication type:

Article

Sipple syndrome: marked variability of the disease within a family and implications for management.

Published in:

1981

By:

Stevenson, J. C.;
Hillyard, C. J.;
Spanos, E.;
MacIntyre, I.;
Ackroyd, N.;
Lynn, J.;
Brown, M. J.;
Stevenson, B. M.

Publication type:

journal article

Quality of Life and Coping in Multiple Endocrine Neoplasia Type 2.

Published in:

Journal of the Endocrine Society, 2019, v. 3, n. 6, p. 1167, doi. 10.1210/js.2018-00371

By:

Correa, Fernanda A;
Farias, Evelin C;
Castroneves, Luciana A;
Lourenço, Delmar M;
Hoff, Ana O

Publication type:

Article

Preimplantation Genetic Diagnosis of Multiple Endocrine Neoplasia Type 2A Using Informative Markers Identified by Targeted Sequencing.

Published in:

Thyroid, 2018, v. 28, n. 3, p. 281, doi. 10.1089/thy.2017.0200

By:

Songchang Chen;
Shuyuan Li;
Junyu Zhang;
Lanlan Zhang;
Yiyao Chen;
Li Wang;
Li Jin;
Yuting Hu;
Xiaoping Qi;
Hefeng Huang;
Chenming Xu

Publication type:

Article

Founder Effect of the RET<sup>C611Y</sup> Mutation in Multiple Endocrine Neoplasia 2A in Denmark: A Nationwide Study.

Published in:

Thyroid, 2017, v. 27, n. 12, p. 1505, doi. 10.1089/thy.2017.0404

By:

Mathiesen, Jes Sloth;
Kroustrup, Jens Peter;
Vestergaard, Peter;
Stochholm, Kirstine;
Poulsen, Per Løgstrup;
Rasmussen, Åse Krogh;
Feldt-Rasmussen, Ulla;
Gaustadnes, Mette;
Ørntoft, Torben Falck;
Rossing, Maria;
Nielsen, Finn Cilius;
Albrechtsen, Anders;
Brixen, Kim;
Godballe, Christian;
Frederiksen, Anja Lisbeth

Publication type:

Article

Clinical Features of a Family with Multiple Endocrine Neoplasia Type 2A Caused by the D631Y RET Mutation.

Published in:

Thyroid, 2017, v. 27, n. 10, p. 1332, doi. 10.1089/thy.2016.0536

By:

Ospina, Naykky Singh;
Maraka, Spyridoula;
Donegan, Diane;
Morris, John C.

Publication type:

Article

RET C611Y Germline Variant in Multiple Endocrine Neoplasia Type 2A in Denmark 1930–2021: A Nationwide Study.

Published in:

Cancers, 2025, v. 17, n. 3, p. 374, doi. 10.3390/cancers17030374

By:

Hansen, Anders Würgler;
Vestergaard, Peter;
Poulsen, Morten Møller;
Rasmussen, Åse Krogh;
Feldt-Rasmussen, Ulla;
Madsen, Mette;
Næraa, Rune Weis;
Hansen, Dorte;
Main, Katharina;
Pedersen, Henrik Baymler;
Londero, Stefano Christian;
Rolighed, Lars;
Hahn, Christoffer Holst;
Rask, Klara Bay;
Maare, Christian;
Nielsen, Heidi Hvid;
Gaustadnes, Mette;
Rossing, Maria;
Hermann, Pernille;
Mathiesen, Jes Sloth

Publication type:

Article

Does Genotype-Specific Phenotype in Patients with Multiple Endocrine Neoplasia Type 2 Occur as Current Guidelines Predict?

Published in:

Cancers, 2024, v. 16, n. 3, p. 494, doi. 10.3390/cancers16030494

By:

Binter, Teresa;
Baumgartner-Parzer, Sabina;
Schernthaner-Reiter, Marie Helene;
Arikan, Melisa;
Hargitai, Lindsay;
Niederle, Martin Bruno;
Niederle, Bruno;
Scheuba, Christian;
Riss, Philipp

Publication type:

Article

Primary Hyperparathyroidism in Multiple Endocrine Neoplasia Type 2A in Denmark: A Nationwide Population-Based Retrospective Study in Denmark 1930–2021.

Published in:

Cancers, 2023, v. 15, n. 7, p. 2125, doi. 10.3390/cancers15072125

By:

Holm, Magnus;
Vestergaard, Peter;
Poulsen, Morten Møller;
Rasmussen, Åse Krogh;
Feldt-Rasmussen, Ulla;
Bay, Mette;
Rolighed, Lars;
Londero, Stefano;
Pedersen, Henrik Baymler;
Hahn, Christoffer Holst;
Rask, Klara Bay;
Nielsen, Heidi Hvid;
Gaustadnes, Mette;
Rossing, Maria Caroline;
Hermann, Anne Pernille;
Godballe, Christian;
Mathiesen, Jes Sloth

Publication type:

Article

Familial Occurrence of Parathyroid Adenomas, Pheochromocytoma, and Medullary Carcinoma of the Thyroid with Amyloid Stroma (Sipple's Syndrome).

Published in:

Annals of Internal Medicine, 1968, v. 68, n. 6, p. 1305, doi. 10.7326/0003-4819-68-6-1305

By:

Sarosi, George;
Doe, Richard P.

Publication type:

Article

Gran Ronda d Medicina Interna y Especialidades del Hospital Nacional Cayetano Heredia.

Published in:

Revista Medica Herediana, 2013, v. 24, n. 3, p. 242

By:

Vásquez, Sergio;
Barrios, Miguel;
Villena, Jaime;
Tejada, Hermes

Publication type:

Article

Pentavalent Technetium-99m (V)-DMSA Uptake in a Pheochromocytoma in a Patient with Sipple's Syndrome.

Published in:

Journal of Nuclear Medicine, 1990, v. 31, n. 1, p. 105

By:

Adams, Bruce K.;
Fataar, Abdulbassier;
Byrne, Michael J.;
Levitt, Naomi S.;
Matley, Philip J.

Publication type:

Article

Sipple's Syndrome with Liver Tumors Examined by Iodine-131 MIBG and Technetium-99m(V)-DMSA.

Published in:

Journal of Nuclear Medicine, 1988, v. 29, n. 6, p. 1130

By:

Ohta, Hitoya;
Endo, Keigo;
Fujita, Toru;
Koizumi, Mitsuru;
Konishi, Junji;
Maki, Atsuhiko;
Mori, Keiichirou;
Ozawa, Kazue;
Inoue, Gen;
Nakano, Yutaka

Publication type:

Article

A FAMILIAL CASE OF MEN2A: EVERYTHING STARTED FROM HYPERTENSIVE EPISODES.

Published in:

Acta Marisiensis. Seria Medica, 2024, v. 70, p. 217

By:

Chiper, Ştefania;
Bulgariu, Georgiana-Loredana;
Lencu, Codruţa Gherman

Publication type:

Article

DIAGNOSTIC AND MANAGEMENT CHALLENGES OF MEDULLARY THYROID CARCINOMA IN PEDIATRIC PATIENTS WITH INHERITED MEN2A SYNDROMES.

Published in:

Acta Marisiensis. Seria Medica, 2024, v. 70, p. 187

By:

Szentgyörgyi, Anna;
Suciu, Delia-Ioana;
Usatiuc, Lia-Oxana

Publication type:

Article

Multiple endocrine neoplasia similar to human subtype 2A in a dog: Medullary thyroid carcinoma, bilateral pheochromocytoma and parathyroid adenoma.

Published in:

2016

By:

Soler Arias, E. A.;
Castillo, V. A.;
Trigo, R. H.;
Aristarain, M. E. Caneda

Publication type:

Case Study

HEREDITARY LOCALIZED PRURITUS IN AFFECTED MEMBERS OF A KINDRED WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A (SIPPLE'S SYNDROME).

Published in:

Clinical Endocrinology, 1989, v. 30, n. 1, p. 57, doi. 10.1111/j.1365-2265.1989.tb03727.x

By:

NUNZIATA, V.;
GIANNATTASIO, R.;
GIOVANNI, G.;
D'ARMIENTO, M. R.;
MANCINI, M.

Publication type:

Article

SIPPLE'S SYNDROME ASSOCIATED WITH A LARGE PROLACTINOMA.

Published in:

Clinical Endocrinology, 1987, v. 27, n. 5, p. 607, doi. 10.1111/j.1365-2265.1987.tb01191.x

By:

BERTRAND, J.-H.;
RITZ, P.;
REZNIK, Y.;
GROLLIER, G.;
POTIER, J.-C.;
EVRAD, C.;
MAHOUDEAU, J. A.

Publication type:

Article

Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience.

Published in:

Clinical Medicine Insights: Endocrinology & Diabetes, 2017, n. 10, p. 1, doi. 10.1177/1179551417705122

By:

Chutintorn Sriphrapradang;
Kitjapong Choopun;
Atchara Tunteeratum;
Thanyachai Sura

Publication type:

Article

A new concept of unopposed beta-adrenergic overstimulation in a patient with pheochromocytoma.

Published in:

2005

By:

Kantorovich, Vitaly;
Pacak, Karel

Publication type:

Case Study

Management of hyperparathyroidism (PHP) in MEN2 syndromes in Europe.

Published in:

Thyroid Research, 2013, v. 6, n. S1, p. 1, doi. 10.1186/1756-6614-6-S1-S10

By:

Alevizaki, Maria

Publication type:

Article

Thrombotic Microangiopathy After Spontaneous Pheochromocytoma Rupture: A Rare MEN 2A Case.

Published in:

Turkish Journal of Endocrinology & Metabolism, 2020, v. 24, n. 3, p. 247, doi. 10.25179/tjem.2020-74367

By:

ÇORDAN, İlker;
KOCABAŞ, Muhammet;
YILMAZ, Seda;
CAN, Mustafa;
KARAKÖSE, Melia;
ÇALIŞKAN BURGUCU, Hatice;
KULAKSIZOĞLU, Mustafa;
KARAKURT, Feridun

Publication type:

Article

Utilization of Genetic Testing for RET Mutations in Patients with Medullary Thyroid Carcinoma: a Single-Center Experience.

Published in:

Journal of Genetic Counseling, 2018, v. 27, n. 6, p. 1411, doi. 10.1007/s10897-018-0273-1

By:

Parkhurst, Emily;
Calonico, Elise;
Abboy, Sridevi

Publication type:

Article

Medullary Thyroid Carcinoma in MEN2A: ATA Moderate- or High-Risk RET Mutations Do Not Predict Disease Aggressiveness.

Published in:

2017

By:

Voss, Rachel K;
Feng, Lei;
Lee, Jeffrey E;
Perrier, Nancy D;
Graham, Paul H;
Hyde, Samual M;
Nieves-Munoz, Frances;
Cabanillas, Maria E;
Waguespack, Steven G;
Cote, Gilbert J.;
Gagel, Robert F;
Grubbs, Elizabeth G;
Hyde, Samuel M

Publication type:

journal 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

Results of Surgical Therapy in Patients with Medullary Thyroid Carcinoma.

Published in:

Indian Journal of Surgery, 2016, v. 78, n. 4, p. 309, doi. 10.1007/s12262-015-1386-5

By:

Vlad, Mihaela;
Zosin, Ioana;
Timar, Bogdan;
Lazar, Fulger;
Vlad, Adrian;
Timar, Romulus;
Cornianu, Marioara

Publication type:

Article

Synchronous bilateral endoscopic adrenalectomy: experiences after 18 operations.

Published in:

2004

By:

Jäger, F;
Jäger, E;
Heintz, A;
Junginger, T

Publication type:

journal article

What is New in Multiple Endocrine Neoplasia Type 2?

Published in:

Endocrinology Research & Practice, 2025, v. 29, n. 1, p. 59, doi. 10.5152/erp.2025.24477

By:

Çakır, Mehtap

Publication type:

Article

Recurrence of phaeochromocytoma in pregnancy in a patient with multiple endocrine neoplasia 2A: a case report and review of literature.

Published in:

2016

By:

Tingi, Efterpi;
Kyriacou, Angelos;
Verghese, Lynda

Publication type:

Case Study

The Changing Face of Multiple Endocrine Neoplasia 2A: From Symptom-Based to Preventative Medicine.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 9, p. e734, doi. 10.1210/clinem/dgad156

By:

Machens, Andreas;
Lorenz, Kerstin;
Brandenburg, Tim;
Führer-Sakel, Dagmar;
Weber, Frank;
Dralle, Henning

Publication type:

Article

Similar Stage-dependent Survival and Outcome in Sporadic and Hereditary Medullary Thyroid Carcinoma.

Published in:

2021

By:

Raue, Friedhelm;
Bruckner, Thomas;
Frank-Raue, Karin

Publication type:

journal article

C Cell and Follicular Epithelial Cell Precursor Lesions of the Thyroid.

Published in:

Archives of Pathology & Laboratory Medicine, 2017, v. 141, n. 12, p. 1646, doi. 10.5858/arpa.2016-0399-RA

By:

Scognamiglio, Theresa

Publication type:

Article

Genetic diagnosis of a Chinese multiple endocrine neoplasia type 2A family through whole genome sequencing.

Published in:

Journal of Biosciences, 2017, v. 42, n. 2, p. 209, doi. 10.1007/s12038-017-9686-5

By:

Du, Zhen-Fang;
Li, Peng-Fei;
Zhao, Jian-Qiang;
Cao, Zhi-Lie;
Li, Feng;
Ma, Ju-Ming;
Qi, Xiao-Ping

Publication type:

Article

Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation.

Published in:

Indian Journal of Medical Research, 2014, v. 139, n. 5, p. 779

By:

Birla, Shweta;
Singla, Rajiv;
Sharma, Arundhati;
Tandon, Nikhil

Publication type:

Article

MEDULLARY CARCINOMA OF THE THYROID, MULTIPLE PHAEOCHROMOCYTOMAS, MUCOSAL NEUROMAS, MARFANOID HABITUS AND OTHER ABNORMALITIES (SIPPLE'S SYNDROME).

Published in:

Medical Journal of Australia, 1976, v. 2, n. 5, p. 173, doi. 10.5694/j.1326-5377.1976.tb134453.x

By:

Bartley, Paul C.;
Lloyd, H. M.;
Aitken, R. E.

Publication type:

Article

28. Multiple Endocrine Neoplasia Type 2A, 2B (Sipple Syndrome), and Familial Medullary Thyroid Cancer.

Published in:: JNCI: Journal of the National Cancer Institute, 2008, n. 38, p. 58
Publication type:: Article

Role of MEN2A-derived RET in maintenance and proliferation of medullary thyroid carcinoma.

Published in:

2004

By:

Drosten, Matthias;
Hilken, Gero;
Böckmann, Miriam;
Rödicker, Florian;
Mise, Nikica;
Cranston, Aaron N.;
Dahmen, Uta;
Ponder, Bruce A. J.;
Pützer, Brigitte M.;
Böckmann, Miriam;
Rödicker, Florian;
Pützer, Brigitte M

Publication type:

journal article

A large Chinese pedigree of multiple endocrine neoplasia type 2A with a novel C634Y/D707E germline mutation in RET exon 11.

Published in:

Oncology Letters, 2017, v. 14, n. 3, p. 3552, doi. 10.3892/ol.2017.6583

By:

Fanqian Lu;
Xiaohong Chen;
Yunlong Bai;
Yaru Feng;
Jian Wu

Publication type:

Article

Genetic analysis and clinical investigation of a pedigree with multiple endocrine neoplasia type 2A: A case report.

Published in:

Oncology Letters, 2016, v. 12, n. 4, p. 2657, doi. 10.3892/ol.2016.5028

By:

HONG-JIN ZOU;
YU-SHU LI;
ZHONG-YAN SHAN

Publication type:

Article

Notalgia Paresthetica and Multiple Endocrine Neoplasia Syndrome 2A: A Case Report.

Published in:

Pediatric Dermatology, 2016, v. 33, n. 5, p. e303, doi. 10.1111/pde.12907

By:

Alcántara, Francisco;
Feito, Marta;
Albizuri, Fátima;
Beato, María;
De Lucas, Raúl

Publication type:

Article

Distribution of RET Mutations and Evaluation of Treatment Approaches in Hereditary Medullary Thyroid Carcinoma in Turkey.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, n. 1, p. 13, doi. 10.4274/jcrpe.2219

By:

Aydoğan, Berna İmge;
Yüksel, Bağdagül;
Tuna, Mazhar Müslüm;
Başaran, Mehtap Navdar;
Kocaeli, Ayşen Akkurt;
Ertörer, Melek Eda;
Aydın, Kadriye;
Güldiken, Sibel;
Şimşek, Yasin;
Karaca, Züleyha Cihan;
Yılmaz, Merve;
Aktürk, Müjde;
Anaforoğlu, İnan;
Kebapçı, Nur;
Duran, Cevdet;
Taşlıpınar, Abdullah;
Kulaksızoğlu, Mustafa;
Gürsoy, Alptekin;
Dağdelen, Selçuk;
Erdoğan, Murat Faik

Publication type:

Article

A Family with Multiple Endocrine Neoplasia Type 2A: Importance of Early Prophylactic Thyroidectomy.

Published in:

2015

By:

Çatlı, Gönül;
Koçyiğit, Cemil;
Can, Şule;
Dündar, Bumin Nuri

Publication type:

Abstract

RET gene mutations (genotype and phenotype) of multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma.

Published in:

Cancer (0008543X), 2014, v. 120, n. 13, p. 1920, doi. 10.1002/cncr.28661

By:

Krampitz, Geoffrey W.;
Norton, Jeffrey A.

Publication type:

Article

An Extended Family with Familial Medullary Thyroid Carcinoma and Hirschsprung's Disease.

Published in:

Journal of Nippon Medical School, 2014, v. 81, n. 2, p. 64, doi. 10.1272/jnms.81.64

By:

Takehito Igarashi;
Ritsuko Okamura;
Tomoo Jikuzono;
Shinya Uchino;
Iwao Sugitani;
Kazuo Shimizu

Publication type:

Article

Functional analysis of RET with multiple endocrine neoplasia type 2.

Published in:

2017

By:

Zhang, Meihua;
Liu, Yao;
Fu, Jie;
Hu, Ying;
Sun, Zheng

Publication type:

journal article