Works matching Sipple syndrome

Results: 105

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

Рецидив синдрому Сіппла.

Published in:

International Journal of Endocrinology / Mìžnarodnij Endokrinologìčnij Žurnal, 2025, v. 21, n. 3, p. 336, doi. 10.22141/2224-0721.21.3.2025.1547

By:

О. В., Сафонова;
Ю. О., Маркевич;
А. М., Урбанович;
М.-Ю. Ю., Маркевич;
А. C., Сафонов

Publication type:

Article

The Challenges of Estimating Medullary Thyroid Cancer Risk in Variant Carriers—Reevaluating RET.

Published in:

2025

By:

Felsky, Daniel;
Narod, Steven A.

Publication type:

Opinion

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

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

Clinical significance of RET mutation screening in a pedigree of multiple endocrine neoplasia type 2A.

Published in:

Molecular Medicine Reports, 2016, v. 14, n. 2, p. 1413, doi. 10.3892/mmr.2016.5371

By:

RONGBIAO YING;
JUN FENG

Publication type:

Article

RMRP, RMST, FTX and IPW: novel potential long non-coding RNAs in medullary thyroid cancer.

Published in:

2021

By:

Luzón-Toro, Berta;
Villalba-Benito, Leticia;
Fernández, Raquel María;
Torroglosa, Ana;
Antiñolo, Guillermo;
Borrego, Salud

Publication type:

Letter

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

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

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

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

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

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

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

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

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

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

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

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

Screening for medullary carcinoma of the thyroid in families with Sipple's syndrome: evaluation of new stimulation tests.

Published in:

European Journal of Clinical Investigation, 1977, v. 7, n. 1, p. 7, doi. 10.1111/j.1365-2362.1977.tb01563.x

By:

TELENIUS-BERG, MARGARETA;
ALMQVIST, SVEN;
BERG, BERTEL;
HEDNER, PAVO;
INGEMANSSON, STIG;
TIBBLIN, STEN;
WÄSTHED, BIRGITTA

Publication type:

Article

"Genetic tumor syndromes of the head and neck: Update in the genomic era".

Published in:

Neuroradiology Journal, 2025, v. 38, n. 3, p. 277, doi. 10.1177/19714009241269462

By:

Brahmbhatt, Sneh;
Agarwal, Amit;
Shetty, Dhruv;
Desai, Amit;
Bhatt, Alok A

Publication type:

Article

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

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

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

F-DOPA PET/CT revealed synchronous neuroendocrine tumors in two sisters with MEN2A syndrome.

Published in:

Endocrine (1355008X), 2013, v. 43, n. 2, p. 458, doi. 10.1007/s12020-012-9854-1

By:

Treglia, Giorgio;
Castaldi, Paola;
Rufini, Vittoria

Publication type:

Article

Mutation screening of RET proto-oncogene in a family with medullary thyroid carcinoma, marfanoid habitus and pheochromocytoma; from clinically MEN2B to genetically MEN2A syndrome.

Published in:

2012

By:

Hasani-Ranjbar, Shirin;
Amoli, Mahsa

Publication type:

Letter

Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family.

Published in:

Endocrine (1355008X), 2011, v. 40, n. 3, p. 481, doi. 10.1007/s12020-011-9501-2

By:

Mastroianno, Sandra;
Torlontano, Massimo;
Scillitani, Alfredo;
D'Aloiso, Leonardo;
Verrienti, Antonella;
Bonfitto, Nazario;
De Bonis, Antonio;
D'Agruma, Leonardo;
Muscarella, Lucia;
Guarnieri, Vito;
Dicembrino, Franca;
Maranghi, Marianna;
Durante, Cosimo;
Filetti, Sebastiano

Publication type:

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

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

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

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

A 6-Base Pair in Frame Germline Deletion in Exon 7 Of RET Leads to Increased RET Phosphorylation, ERK Activation, and MEN2A.

Published in:

2016

By:

Latteyer, S;
Klein-Hitpass, L;
Khandanpour, C;
Zwanziger, D;
Poeppel, T D;
Schmid, K W;
Führer, D;
Moeller, L C

Publication type:

journal article

The approach to the patient with paraganglioma.

Published in:

2009

By:

Neumann, Hartmut P H;
Eng, Charis

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

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

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