Works matching DE "SIPPLE syndrome"

Results: 76

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

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

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

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

Integrated DNA-based/biochemical screening for early diagnosis of multiple endocrine neoplasia type 2A (MEN2A).

Published in:

2013

By:

Qin Cui;
Wen Wang;
Zhenzhen Fu;
Xin Shao;
Zhihong Zhang;
Mei Zhang;
Xianxia Ju;
Kunlin Wang;
Jiawei Chen;
Hongwen Zhou

Publication type:

Case Study

Determination of RET Sequence Variation in an MEN2 Unaffected Cohort Using Multiple-Sample Pooling and Next-Generation Sequencing.

Published in:

Journal of Thyroid Research, 2012, p. 1, doi. 10.1155/2012/318232

By:

Margraf, R. L.;
Durtschi, J. D.;
Stephens, J. E.;
Perez, M.;
Voelkerding, K. V.

Publication type:

Article

Syncronous medullar thyroid cancer and primary hyperparathyroidism on a female within the sixth decade of life with positive family history for type 2A MEN syndrome.

Published in:

Romanian Journal of Medical Practice, 2016, v. 11, n. 4, p. 368, doi. 10.37897/rjmp.2016.4.13

By:

VALEA, Ana;
RADU, Otilia;
MORAR, Andra;
GHEMIGIAN, Adina;
CARSOTE, Mara

Publication type:

Article

The approach to the patient with paraganglioma.

Published in:

2009

By:

Neumann, Hartmut P H;
Eng, Charis

Publication type:

journal article

Mutations of the ret protooncogene in German multiple endocrine neoplasia families: relation between genotype and phenotype. German Medullary Thyroid Carcinoma Study Group.

Published in:

1996

By:

Frank-Raue, K;
Höppner, W;
Frilling, A;
Kotzerke, J;
Dralle, H;
Haase, R;
Mann, K;
Seif, F;
Kirchner, R;
Rendl, J;
Deckart, H F;
Ritter, M M;
Hampel, R;
Klempa, J;
Scholz, G H;
Raue, F

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

Diversity of mutations in the RET proto-oncogene and its oncogenic mechanism in medullary thyroid cancer.

Published in:

Critical Reviews in Clinical Laboratory Sciences, 2016, v. 53, n. 4, p. 217, doi. 10.3109/10408363.2015.1129529

By:

Hedayati, Mehdi;
Zarif Yeganeh, Marjan;
Sheikholeslami, Sara;
Afsari, Farinaz

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

Determination of the risk for familial disease in RET mutation-negative patients with medullary thyroid cancer.

Published in:

1998

By:

Tang;
Yeung;
Cockram;
Pang;
Tang, Nelson L.S.;
Tang, N L;
Yeung, V T;
Cockram, C S;
Pang, C P

Publication type:

Letter

Molecular mechanisms of development of multiple endocrine neoplasia 2 by RET mutations.

Published in:

1998

By:

Takahashi;
Asai;
Iwashita;
Murakami;
Ito;
Takahashi, Masahide;
Takahashi, M;
Asai, N;
Iwashita, T;
Murakami, H;
Ito, S

Publication type:

journal article

Local recurrence of pheochromocytoma in multiple endocrine neoplasia type 2A: a diagnostic and therapeutic challenge.

Published in:

Clinical Case Reports, 2016, v. 4, n. 3, p. 298, doi. 10.1002/ccr3.498

By:

Tramunt, Blandine;
Buffet, Alexandre;
Grunenwald, Solange;
Vezzosi, Delphine;
Bennet, Antoine;
Huyghe, Eric;
Zerdoud, Slimane;
Caron, Philippe

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

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

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

THE GORDON WILSON LECTURE EVOLUTION OF CLINICAL CANCER GENETICS.

Published in:

Transactions of the American Clinical & Climatological Association, 2016, v. 127, p. 127

By:

GARBER, JUDY E.

Publication type:

Article

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

Pheochromocytomas are diagnosed incidentally and at older age in neurofibromatosis type 1.

Published in:

Clinical Endocrinology, 2017, v. 86, n. 3, p. 332, doi. 10.1111/cen.13265

By:

Moramarco, Jessica;
El Ghorayeb, Nada;
Dumas, Nadine;
Nolet, Serge;
Boulanger, Luce;
Burnichon, Nelly;
Lacroix, André;
Elhaffaf, Zaki;
Gimenez Roqueplo, Anne‐Paule;
Hamet, Pavel;
Bourdeau, Isabelle

Publication type:

Article

Confusing genes: a patient with MEN2A and Cushing's disease.

Published in:

Clinical Endocrinology, 2013, v. 78, n. 6, p. 966, doi. 10.1111/cen.12072

By:

Naziat, Auditi;
Karavitaki, Niki;
Thakker, Rajesh;
Ansorge, Olaf;
Sadler, Greg;
Gleeson, Fergus;
Cranston, Treena;
McCormack, Ann;
Grossman, Ashley B;
Shine, Brian

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

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

Clinical spectrum of MEN2A in a large family caused by the infrequent RET mutation Cys609Phe.

Published in:

Clinical Genetics, 2013, v. 83, n. 4, p. 384, doi. 10.1111/j.1399-0004.2012.01921.x

By:

Oriola, J;
Biarnes, J;
Hernandez, C;
Simó, R

Publication type:

Article

Elevated basal serum levels of calcitonin and simultaneous surgery of MEN2A-specific tumors.

Published in:

Neoplasma, 2021, v. 68, n. 5, p. 1098, doi. 10.4149/neo_2021_210330N419

By:

Hai-Xiao TANG;
Hao YANG;
Feng LI;
Zhi-Lie CAO;
Yun-Teng HUANG;
Xiao-Ping QI

Publication type:

Article

RET oncogene in MEN2, MEN2B, MTC and other forms of thyroid cancer.

Published in:

2008

By:

Lodish, Maya B.;
Stratakis, Constantine A.

Publication type:

journal article

Germline founder variant c.1998delinsTTCT in the RET oncogene: a cohort study in 15 Belgian families.

Published in:

European Journal of Endocrinology, 2023, v. 189, n. 3, p. 402, doi. 10.1093/ejendo/lvad126

By:

Vuylsteke, Axelle;
Hannes, Laurens;
Brems, Hilde;
Devis, Koen;
Renard, Marleen;
Uyttebroeck, Anne;
Legius, Eric;
Decallonne, Brigitte

Publication type:

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

Challenging Perioperative Management of a MEN2A Syndrome Patient Complicated by Eisenmenger Syndrome Challenging Perioperative Management of a MEN2A Syndrome Patient Complicated by Eisenmenger Syndrome.

Published in:

Turkish Journal of Anaesthesiology & Reanimation, 2025, v. 53, n. 2, p. 82, doi. 10.4274/TJAR.2025.241768

By:

Rastogi, Amit;
Agarwal, Gaurav;
Sachan, Sumit;
Kapoor, Aditya;
Dabadghao, Preeti

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

Are the Pathological Characteristics of Prostate Cancer More Aggressive or More Indolent Depending upon the Patient Age?

Published in:

BioMed Research International, 2017, v. 2017, p. 1, doi. 10.1155/2017/1438027

By:

Ji, Guangjie;
Huang, Cong;
Song, Gang;
Xiong, Gengyan;
Fang, Dong;
Wang, He;
Hao, Han;
Cai, Lin;
He, Qun;
He, Zhisong;
Zhou, Liqun

Publication type:

Article

Painful Hip Leading to the Diagnosis of MEN 2B Syndrome.

Published in:

Case Reports in Endocrinology, 2012, p. 1, doi. 10.1155/2012/567060

By:

Ahmad, Mehtab;
Rizvi, Imran;
Jain, Amit;
Zaidi, Noorin

Publication type:

Article

Bilateral pheochromocytoma with ganglioneuroma component associated with multiple neuroendocrine neoplasia type 2A: a case report.

Published in:

2017

By:

Efared, Boubacar;
Atsame-Ebang, Gabrielle;
Tahirou, Soufiane;
Mazaz, Khalid;
Hammas, Nawal;
El Fatemi, Hinde;
Chbani, Laila

Publication type:

Case Study

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

Diagnosis and surgical treatment of multiple endocrine neoplasia type 2A.

Published in:

World Journal of Surgical Oncology, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1477-7819-12-8

By:

Kun-Long Tang;
Yi Lin;
Li-Ming Li

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

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

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

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

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

Clinical utility gene card for: multiple endocrine neoplasia type 2.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 1, p. -1, doi. 10.1038/ejhg.2011.142

By:

Raue, Friedhelm;
Rondot, Susanne;
Schulze, Egbert;
Szpak-Ulczok, Sylwia;
Jarzab, Barbara;
Frank-Raue, Karin

Publication type:

Article

MEN-2A syndrome and pulmonary metastasis.

Published in:

2002

By:

Alfaro, J J;
Lomos, C;
Estrado, J;
Lucas, T;
Lamas, C;
Estrada, J

Publication type:

journal article