Works matching DE "COWDEN syndrome"

Results: 205

Genetic Predisposition to Breast Cancer and Its Management.

Published in:

2021

By:

Srivastava, Anurag;
Jatoi, Ismail

Publication type:

Editorial

Gastrointestinal tract cancers: Genetics, heritability and germ line mutations (Review).

Published in:

Oncology Letters, 2017, v. 13, n. 3, p. 1499, doi. 10.3892/ol.2017.5629

By:

XIAO-PENG LV

Publication type:

Article

Dysplastic cerebellar gangliocytoma/Lhermitte-Duclos disease.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2018, v. 18, n. 11, p. 779, doi. 10.3969/j.issn.1672-6731.2018.11.015

By:

HAN Tong

Publication type:

Article

Dysplastic cerebellar gangliocytoma/Lhermitte-Duclos disease.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2018, v. 18, n. 11, p. 787, doi. 10.3969/j.issn.1672-6731.2018.11.016

By:

YAN Xiao-ling

Publication type:

Article

Cowden disease and multicystic dysplastic kidney: increased risk of renal cancer?

Published in:

Clinical Kidney Journal, 2012, v. 5, n. 5, p. 453, doi. 10.1093/ckj/sfs069

By:

Teixeira, Ana;
Edery, Patrick;
Cochat, Pierre

Publication type:

Article

Lack of chromosome 15q11-q13 region involvement in a family with Cowden disease/Bannayan-Zonana syndrome.

Published in:

1998

By:

Dasouki, Majed J.;
Marney, Annis;
Butler, Merlin G.;
Dasouki, M J;
Marney, A;
Butler, M G

Publication type:

commentary

Cowden syndrome (multiple hamartoma syndrome).

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 8, p. 957, doi. 10.1111/ced.12140

By:

Aslam, A.;
Coulson, I. H.

Publication type:

Article

Thyroid disease in children and adolescents with PTEN hamartoma tumor syndrome (PHTS).

Published in:

2018

By:

Plamper, Michaela;
Schreiner, Felix;
Gohlke, Bettina;
Kionke, Janina;
Korsch, Eckard;
Kirkpatrick, James;
Born, Mark;
Aretz, Stefan;
Woelfle, Joachim

Publication type:

journal article

Elevation of methylated DNA in KILLIN/PTEN in the plasma of patients with thyroid and/or breast cancer.

Published in:

OncoTargets & Therapy, 2014, v. 7, p. 2085, doi. 10.2147/OTT.S53597

By:

Ng, Enders K.;
Shin, Vivian Y.;
Leung, Candy P.;
Chan, Vivian W.;
Law, Fian B.;
Siu, Man T.;
Lang, Brian H.;
Ma, Edmond S.;
Kwong, Ava

Publication type:

Article

Genetic basis of Cowden syndrome and its implications for clinical practice and risk management.

Published in:

Application of Clinical Genetics, 2016, v. 9, p. 83, doi. 10.2147/TACG.S41947

By:

Gammon, Amanda;
Jasperson, Kory;
Champine, Marjan

Publication type:

Article

Cowden Syndrome: A Result of Mutation in the PTEN Tumour Suppressor Gene.

Published in:

Periodontal Practice Today, 2006, v. 3, n. 4, p. 269

By:

Patanwala, Alifya;
Chapple, Iain L. C.

Publication type:

Article

Hamartoma esplénico. Reporte de caso.

Published in:

2014

By:

Soto-Medina, Carlos Alberto;
Mier-Escurra, Erik Antonio;
Treviño-Garza, Francisco;
Ripa-Galván, Paola

Publication type:

Case Study

Cowden Syndrome Associated with Severe Periodontal Disease: A Short Literature Review and a Case Report.

Published in:

2018

By:

Perić, Marina;
Toma, Selena;
Lasserre, Jérôme Frédéric;
Brecx, Michel

Publication type:

journal article

Cowden syndrome with bronchial asthma.

Published in:

Turkish Journal of Pediatrics, 2010, v. 52, n. 3, p. 330

By:

Özsürekci, Yasemin;
Yavuz, Süleyman Tolga;
Alanay, Yasemin;
Ütine, Gülen Eda;
Kalaycı, Ömer

Publication type:

Article

Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes.

Published in:

2014

By:

Forte, Giovanna;
Grossi, Valentina;
Celestini, Valentina;
Lucisano, Giuseppe;
Scardapane, Marco;
Varvara, Dora;
Patruno, Margherita;
Bagnulo, Rosanna;
Loconte, Daria;
Giunti, Laura;
Petracca, Antonio;
Giglio, Sabrina;
Genuardi, Maurizio;
Pellegrini, Fabio;
Resta, Nicoletta;
Simone, Cristiano

Publication type:

journal article

Fibroma esclerótico. Comunicación de 16 casos. Estudio clínicopatológico y revisión del tema.

Published in:

Dermatología Revista Mexicana, 2013, v. 57, n. 2, p. 104

By:

Navarrete Franco, Gisela;
Ramos Garibay, José Alberto;
González González, Maribet;
Maya Aranda, Susana Esther;
López Zaragoza, Iliana;
Gaxiola Alvarez, Edna A.

Publication type:

Article

A rare cause of oral papillomatous lesions: Cowden syndrome.

Published in:

2012

By:

Balci, Didem Didar;
Çelik, M. Murat;
Çelik, Ebru;
Demir, Mehmet;
Yaldiz, Mehmet

Publication type:

Case Study

Porokeratotic eccrine ostial and dermal duct nevus: a unique case treated with CO<sub>2</sub> laser.

Published in:

Clinical Case Reports, 2017, v. 5, n. 5, p. 675, doi. 10.1002/ccr3.846

By:

Zade, John;
Jfri, Abdulhadi;
Nabatian, Adam;
Alajaji, Abdullah;
Geller, Lauren;
Khorasani, Hooman

Publication type:

Article

Hereditary Syndromes Manifesting as Endometrial Carcinoma: How Can Pathological Features Aid Risk Assessment?

Published in:

BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/219012

By:

Wong, Adele;
Ngeow, Joanne

Publication type:

Article

Frequency of Germline PTEN Mutations in Differentiated Thyroid Cancer.

Published in:

Thyroid, 2011, v. 21, n. 5, p. 505, doi. 10.1089/thy.2010.0365

By:

Nagy, Rebecca;
Ganapathi, Shireen;
Comeras, Ilene;
Peterson, Charissa;
Orloff, Mohammed;
Porter, Kyle;
Eng, Charis;
Ringel, Matthew D.;
Kloos, Richard T.

Publication type:

Article

Thyroid Pathology in PTEN-Hamartoma Tumor Syndrome: Characteristic Findings of a Distinct Entity.

Published in:

Thyroid, 2011, v. 21, n. 2, p. 135, doi. 10.1089/thy.2010.0226

By:

Anna Ray Laury;
Massimo Bongiovanni;
Jean-Christophe Tille;
Harry Kozakewich;
Vânia Nosé

Publication type:

Article

Clinical Features and Genetic Predisposition to Hereditary Nonmedullary Thyroid Cancer.

Published in:

Thyroid, 2009, v. 19, n. 12, p. 1343, doi. 10.1089/thy.2009.1607

By:

Menno R. Vriens;
Insoo Suh;
Willieford Moses;
Electron Kebebew

Publication type:

Article

Cowden's disease : A rare case.

Published in:

Pravara Medical Review, 2011, v. 3, n. 3, p. 28

By:

Yelikar, B. R.;
Maheshkumar, U.;
Vijayalaxmi, S. P.;
Raghunath, R.

Publication type:

Article

von Meyenburg complex (VMC) – A case report.

Published in:

Indian Journal of Medical Specialities, 2016, v. 7, n. 3, p. 132, doi. 10.1016/j.injms.2016.08.003

By:

Sharma, B.B.;
Sharma, Shweta;
Sharma, Shashi;
Sharma, Sandeep;
Ramchandran, Priya

Publication type:

Article

Cowden syndrome- Clinico-radiological illustration of a rare case.

Published in:

2013

By:

PATIL, PRASHANT B.;
SREENIVASAN, V.;
GOEL, SUMIT;
NAGARAJU, K.;
VASHISHTH, SHIRIN;
GUPTA, SWATI;
GARG, KANIKA

Publication type:

Case Study

Laparoscopic Excision of a Symptomatic Brunneroma.

Published in:

2011

By:

Carboni, Fabio;
Valle, Mario;
Garofalo, Alfredo;
Mariantonia, Carosi

Publication type:

Case Study

Inherited predisposition to endometrial cancer: Moving beyond Lynch syndrome.

Published in:

2015

By:

Stadler, Zsofia K.;
Robson, Mark E.

Publication type:

Editorial

Germline PTEN, SDHB-D, and KLLN alterations in endometrial cancer patients with Cowden and Cowden-like syndromes: An international, multicenter, prospective study.

Published in:

Cancer (0008543X), 2015, v. 121, n. 5, p. 688, doi. 10.1002/cncr.29106

By:

Mahdi, Haider;
Mester, Jessica L.;
Nizialek, Emily A.;
Ngeow, Joanne;
Michener, Chad;
Eng, Charis

Publication type:

Article

Intestinal bleeding from arteriovenous malformations of the small bowel in a patient with Cowden syndrome: report of a case.

Published in:

Surgery Today, 2013, v. 43, n. 5, p. 542, doi. 10.1007/s00595-012-0460-x

By:

Nakayama, Yoshifumi;
Segawa, Jun;
Sujita, Kazufumi;
Minagawa, Noritaka;
Torigoe, Takayuki;
Hisaoka, Masanori;
Yamaguchi, Koji

Publication type:

Article

Evaluation of breast involvement in relation to Cowden syndrome: a radiological and clinicopathological study of patients with PTEN germ-line mutations.

Published in:

2006

By:

Sabaté, Josep M.;
Gómez, Antonio;
Torrubia, Sofía;
Blancas, Carme;
Sánchez, Gloria;
Alonso, M. C.;
Lerma, E.;
Sabaté, Josep M;
Gómez, Antonio;
Torrubia, Sofía;
Sánchez, Gloria

Publication type:

journal article

Extradural temporopolar approach for parahypothalamic hypothalamic hamartoma and use of posterior communicating artery as resection margin pointer.

Published in:

Child's Nervous System, 2015, v. 31, n. 4, p. 603, doi. 10.1007/s00381-015-2631-8

By:

Udayakumaran, Suhas;
Ayiramuthu, Parasuraman;
Panikar, Dilip

Publication type:

Article

RE: Cowden Syndrome and PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria.

Published in:

2014

By:

PILARSKI, ROBERT;
BURT, RANDALL;
KOHLMAN, WENDY;
PHO, LANA;
SHANNON, KRISTEN M.;
SWISHER, ELIZABETH

Publication type:

Letter to the Editor

RE: Cowden Syndrome and PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria.

Published in:

2014

By:

MIN-HAN TAN;
CHARIS ENG

Publication type:

Letter to the Editor

Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: How to Define Rare Genetic Syndromes.

Published in:

JNCI: Journal of the National Cancer Institute, 2013, v. 105, n. 21, p. 1595, doi. 10.1093/jnci/djt290

By:

Lachlan, Katherine L.

Publication type:

Article

Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria.

Published in:

JNCI: Journal of the National Cancer Institute, 2013, v. 105, n. 21, p. 1607, doi. 10.1093/jnci/djt277

By:

Pilarski, Robert;
Burt, Randall;
Kohlman, Wendy;
Pho, Lana;
Shannon, Kristen M.;
Swisher, Elizabeth

Publication type:

Article

KILLIN Gene Discovery Stirs Up Research on Cowden Syndrome Cancers.

Published in:

JNCI: Journal of the National Cancer Institute, 2011, v. 103, n. 5, p. 362, doi. 10.1093/jnci/djr055

By:

Schmidt, Charlie

Publication type:

Article

StatBite Lifetime Risk of Selected Cancers for People With Cowden Syndrome.

Published in:: JNCI: Journal of the National Cancer Institute, 2011, v. 103, n. 5, p. 363, doi. 10.1093/jnci/djr065
Publication type:: Article

Acute-Onset Cerebellar Symptoms in Lhermitte-Duclos Disease: Case Report.

Published in:

Cerebellum, 2013, v. 12, n. 1, p. 127, doi. 10.1007/s12311-012-0394-2

By:

Hariri, Omid;
Khachekian, Arsineh;
Muilli, Dan;
Amin, Jenny;
Minassian, Tanya;
Berman, Blake;
Ritter, Yoav;
Siddiqi, Javed

Publication type:

Article

Breast Cancer in Cowden Syndrome: Manifestation of a Familial Cancer Syndrome.

Published in:

Clinical Journal of Oncology Nursing, 2010, v. 14, n. 1, p. 33, doi. 10.1188/10.CJON.33-35

By:

Erickson, Janetlynne;
Lyon, Debra E.

Publication type:

Article

Magnetic resonance characteristics of adult-onset Lhermitte-Duclos disease: An indicator for active cancer surveillance?

Published in:

Molecular & Clinical Oncology, 2014, v. 2, n. 3, p. 415, doi. 10.3892/mco.2014.258

By:

GUANGQUAN WEI;
WEI ZHANG;
QINLONG LI;
XIAOWEI KANG;
HAITAO ZHAO;
XIANPING LIU;
XING TANG;
YUANMING WU;
JUNTAO HAN;
HONG YIN

Publication type:

Article

Renal angiomyolipoma.

Published in:

BJU International, 2012, v. 110, p. 25, doi. 10.1111/j.1464-410X.2012.11618.x

By:

Lienert, Andrew R.;
Nicol, David

Publication type:

Article

Acral Plexiform Palisaded Encapsulated Neuromas as the Initial Cutaneous Manifestation of Cowden Syndrome.

Published in:

Pediatric Dermatology, 2017, v. 34, n. 4, p. e219, doi. 10.1111/pde.13161

By:

Harris, Elizabeth;
Mir, Adnan

Publication type:

Article

Unusual presentation of familial gingival fibromatosis among male siblings.

Published in:

Journal of Indian Society of Periodontology, 2017, v. 21, n. 2, p. 152, doi. 10.4103/jisp.jisp_207_16

By:

Manoj, Margabandhu;
Garg, Renu;
Babu, Kennedy

Publication type:

Article

A family with PTEN mutations with malignancy and an unusually high number of offspring with autism spectrum disorder: a case report.

Published in:

2018

By:

Gruhl, Sabrina L.;
Sharma, Pankaj;
Han, Thang S.

Publication type:

journal article

PTEN mosaicism with features of Cowden syndrome.

Published in:

Clinical Genetics, 2013, v. 84, n. 6, p. 593, doi. 10.1111/cge.12078

By:

Gammon, A;
Jasperson, K;
Pilarski, R;
Prior, TW;
Kuwada, S

Publication type:

Article

PTEN in colorectal cancer: a report on two Cowden syndrome patients.

Published in:

Clinical Genetics, 2012, v. 81, n. 6, p. 555, doi. 10.1111/j.1399-0004.2011.01639.x

By:

Kersseboom, R;
Dubbink, HJ;
Corver, WE;
van Tilburg, AJP;
Poley, JW;
van Leerdam, ME;
Atmodimedjo, PN;
van de Laar, IMBH;
Collée, JM;
Dinjens, WNM;
Morreau, H;
Wagner, A

Publication type:

Article

Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23.

Published in:

Clinical Genetics, 2012, v. 81, n. 2, p. 110, doi. 10.1111/j.1399-0004.2011.01763.x

By:

Dahdaleh, FS;
Carr, JC;
Calva, D;
Howe, JR

Publication type:

Article

Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients.

Published in:

2022

By:

Pena-Couso, Laura;
Ercibengoa, María;
Mercadillo, Fátima;
Gómez-Sánchez, David;
Inglada-Pérez, Lucía;
Santos, María;
Lanillos, Javier;
Gutiérrez-Abad, David;
Hernández, Almudena;
Carbonell, Pablo;
Letón, Rocío;
Robledo, Mercedes;
Rodríguez-Antona, Cristina;
Perea, José;
Urioste, Miguel;
PHTS Working Group

Publication type:

journal article

Cowden syndrome and pituitary tumours.

Published in:

2018

By:

Srichomkwun, P;
Houngngam, N;
Boonchaya-Anant, P;
Chutinet, A;
Buranasupkajorn, P;
Snabboon, T

Publication type:

Case Study

Benign fibrous hamartoma of infancy: a case of MR imaging paralleling histologic findings.

Published in:

Skeletal Radiology, 2014, v. 43, n. 11, p. 1639, doi. 10.1007/s00256-014-1940-4

By:

Stensby, J.;
Conces, M.;
Nacey, N.

Publication type:

Article