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 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

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

Multiple endocrine neoplasia type IIA (Sipple's syndrome) presenting in pregnancy.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2000, v. 40, n. 4, p. 473, doi. 10.1111/j.1479-828X.2000.tb01188.x

By:

Joseph, Jean V;
Harrison, Robert;
Davis, Robert S

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

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

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

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

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

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

A Brief Review on The Molecular Basis of Medullary Thyroid Carcinoma.

Published in:

Cell Journal (Yakhteh), 2017, v. 18, n. 4, p. 485

By:

Mohammadi, Masoumeh;
Hedayati, Mehdi

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

Lesiones quísticas múltiples adrenales como expresión morfológica de feocromocitoma quístico bilateral en el contexto de síndrome de Sipple (neoplasia endocrina múltiple tipo 2a): presentación de un caso.

Published in:

Anales de Radiologia, Mexico, 2019, v. 18, n. 3, p. 193, doi. 10.24875/ARM.19000084

By:

Gómez-Castro, Iván I.;
Ibarra-Vivas, Pilar A.;
Barreda-Escalante, Raúl;
Piña-Moneda, Loudwin O.;
Granados-Sandoval, Enrique

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

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

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

Spectrum of Germline RET variants identified by targeted sequencing and associated Multiple Endocrine Neoplasia type 2 susceptibility in China.

Published in:

2021

By:

Qi, Xiao-Ping;
Zhao, Jian-Qiang;
Fang, Xu-Dong;
Lian, Bi-Jun;
Li, Feng;
Wang, Hui-Hong;
Cao, Zhi-Lie;
Zheng, Wei-Hui;
Cao, Juan;
Chen, Yu

Publication type:

journal 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

The Role of Adrenal Cortex-Sparing Surgery for Bilateral Masses in Three Cases.

Published in:

Üroonkoloji Bülteni, 2020, v. 19, n. 1, p. 42, doi. 10.4274/uob.galenos.2019.1237

By:

Kan, Elif Kılıç;
Özden, Ender;
Atmaca, Ayşegül;
Çolak, Ramis

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

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

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

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

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

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

Detection of hepatic metastasis from medullary thyroid cancer with Tc-99m-MIBI scintigraphy in a patient with Sipple's syndrome.

Published in:

2001

By:

Sato, Shuhei;
Okumura, Yoshihiro;
Tamizu, Atsuko;
Maki, Kumi;
Akaki, Shiro;
Takeda, Yoshihiro;
Kanazawa, Susumu;
Hiraki, Yoshio;
Sato, S;
Okumura, Y;
Tamizu, A;
Maki, K;
Akaki, S;
Takeda, Y;
Kanazawa, S;
Hiraki, Y

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

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

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

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

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 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

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

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

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

Sipple's Syndrome (Multiple Endocrine Neoplasia) in Pregnancy ... Case Report.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 1982, v. 22, n. 4, p. 243, doi. 10.1111/j.1479-828X.1982.tb01455.x

By:

Chodankar, Cussuma M.;
Abhyankar, Shashikala C.;
Deodhar, Kamlakar P.;
Shanbhag, Anant M.

Publication type:

Article

Prospective Genetic Screening in Multiple Endocrine Neoplasia Syndromes.

Published in:

Children, 2024, v. 11, n. 8, p. 1012, doi. 10.3390/children11081012

By:

Paun, Diana;
Tilici, Dana;
Paun, Sorin;
Mirica, Alexandra

Publication type:

Article

Psychosocial Characteristics and Experiences in Patients with Multiple Endocrine Neoplasia Type 2 (MEN2) and Medullary Thyroid Carcinoma (MTC).

Published in:

Children, 2022, v. 9, n. 6, p. 774, doi. 10.3390/children9060774

By:

Lockridge, Robin;
Bedoya, Sima;
Allen, Taryn;
Widemann, Brigitte C.;
Akshintala, Srivandana;
Glod, John;
Wiener, Lori

Publication type:

Article