164 related articles for article (PubMed ID: 31166879)
1. Sclerosing Pneumocytoma of the Lungs Arising in a Child With PTEN Mutation.
Nasr Y; Bettoli M; El Demellawy D; Sekhon H; de Nanassy J
Pediatr Dev Pathol; 2019; 22(6):579-583. PubMed ID: 31166879
[TBL] [Abstract][Full Text] [Related]
2. Association of multiple vertebral hemangiomas and severe paraparesis in a patient with a PTEN hamartoma tumor syndrome. Case report.
Jenny B; Radovanovic I; Haenggeli CA; Delavelle J; Rüfenacht D; Kaelin A; Blouin JL; Bottani A; Rilliet B
J Neurosurg; 2007 Oct; 107(4 Suppl):307-13. PubMed ID: 17941496
[TBL] [Abstract][Full Text] [Related]
3. Pulmonary sclerosing pneumocytoma masquerading adenocarcinoma with co-existing BRAF V600E and PTEN mutation.
Dantis K; Gupta AK; Kashyap NK; Kashyap Y; Ranganath TG; Pati SK; Kumar M; Thakur S; Ravina M
Cancer Treat Res Commun; 2021; 28():100429. PubMed ID: 34246179
[TBL] [Abstract][Full Text] [Related]
4. Storiform collagenoma as a clue for Cowden disease or PTEN hamartoma tumour syndrome.
Al-Daraji WI; Ramsay HM; Ali RB
J Clin Pathol; 2007 Jul; 60(7):840-2. PubMed ID: 17513505
[No Abstract] [Full Text] [Related]
5. Large pulmonary sclerosing pneumocytoma in a young female: A rare lung tumor.
Kang DK; Kang MK; Heo W; Hwang YH; Kim JY
Thorac Cancer; 2021 Jun; 12(12):1909-1911. PubMed ID: 33951309
[TBL] [Abstract][Full Text] [Related]
6. Primary lung adenocarcinoma occurring in a PTEN related syndrome (Cowden's disease): routine EGFR sequencing also highlights two rare somatic mutations S768I and V769L.
Boespflug A; Couraud S; Bringuier PP; Isaac S; Gérinière L; Perrot E; Edery P; Durieu I; Souquet PJ
Lung Cancer; 2013 Mar; 79(3):318-20. PubMed ID: 23261230
[TBL] [Abstract][Full Text] [Related]
7. PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.
Kurek KC; Howard E; Tennant LB; Upton J; Alomari AI; Burrows PE; Chalache K; Harris DJ; Trenor CC; Eng C; Fishman SJ; Mulliken JB; Perez-Atayde AR; Kozakewich HP
Am J Surg Pathol; 2012 May; 36(5):671-87. PubMed ID: 22446940
[TBL] [Abstract][Full Text] [Related]
8. Novel PTEN mutation in Cowden syndrome: case report with late diagnosis and non-malignant course.
Martínez-Doménech A; García-Legaz Martínez M; Magdaleno-Tapial J; Pérez-Pastor G; Rodríguez-López R; Pérez-Ferriols A
Dermatol Online J; 2019 May; 25(5):. PubMed ID: 31220904
[TBL] [Abstract][Full Text] [Related]
9. VATS approach for pulmonary sclerosing pneumocytoma: a case report.
Solari L; Agrafiotis AC; Lardinois I
Acta Chir Belg; 2022 Apr; 122(2):123-126. PubMed ID: 32397805
[TBL] [Abstract][Full Text] [Related]
10. [Oncology image. Patient with Cowdenovym Syndrome caused by PTEN mutation].
Puchmajerova A; Vasovcak P; Polacek V
Klin Onkol; 2014; 27(4):303. PubMed ID: 25185272
[No Abstract] [Full Text] [Related]
11. Sclerosing pneumocytoma mixed with a typical carcinoid tumor: A case report and review of literature.
Wang Z; Yang MQ; Huang WJ; Zhang D; Xu HT
Medicine (Baltimore); 2019 Feb; 98(5):e14315. PubMed ID: 30702609
[TBL] [Abstract][Full Text] [Related]
12. Pulmonary sclerosing pneumocytoma: clinical features and prognosis.
Zheng Q; Zhou J; Li G; Man S; Lin Z; Wang T; Chen B; Lin F
World J Surg Oncol; 2022 Apr; 20(1):140. PubMed ID: 35490241
[TBL] [Abstract][Full Text] [Related]
13. Biomarker May Predict Cancer Versus Autism Risk in Pten Hamartoma Tumor Syndrome: Decreased levels of fumarate were more strongly associated with autism than cancer in persons with PTEN mutations.
Am J Med Genet A; 2020 Jan; 182(1):7-8. PubMed ID: 31825175
[No Abstract] [Full Text] [Related]
14. Estimate of de novo mutation frequency in probands with PTEN hamartoma tumor syndrome.
Mester J; Eng C
Genet Med; 2012 Sep; 14(9):819-22. PubMed ID: 22595938
[TBL] [Abstract][Full Text] [Related]
15. Multiple, recurrent, refractory vascular malformations as the primary presenting feature of a PTEN mutation.
Sharabi SE; Koshy JC; Hollier LH
Pediatr Dermatol; 2011; 28(4):466-7. PubMed ID: 21793891
[TBL] [Abstract][Full Text] [Related]
16. How to recognize Cowden syndrome: A novel PTEN mutation description.
Delannoy P; Debray FG; Verloes A; Beckers A; Valdes-Socin H
Ann Endocrinol (Paris); 2017 Jul; 78(3):188-190. PubMed ID: 28262255
[No Abstract] [Full Text] [Related]
17. PTEN mutation in a Japanese boy with autonomously functioning thyroid nodule.
Nyuzuki H; Kogai T; Hishinuma A; Ogawa Y; Saitoh A; Nagasaki K
Pediatr Int; 2017 Nov; 59(11):1223-1224. PubMed ID: 29359449
[No Abstract] [Full Text] [Related]
18. Identification of a novel pathogenic deep intronic variant in PTEN resulting in pseudoexon inclusion in a patient with juvenile polyps.
Jelsig AM; Rønlund K; Gede LB; Frederiksen JH; Karstensen JG; Birkedal U; van Overeem Hansen T
J Hum Genet; 2023 Oct; 68(10):721-724. PubMed ID: 37336910
[TBL] [Abstract][Full Text] [Related]
19. PTEN mosaicism with features of Cowden syndrome.
Gammon A; Jasperson K; Pilarski R; Prior T; Kuwada S
Clin Genet; 2013 Dec; 84(6):593-5. PubMed ID: 23240978
[TBL] [Abstract][Full Text] [Related]
20. Catch them if you are aware: PTEN postzygotic mosaicism in clinically suspicious patients with PTEN Hamartoma Tumour Syndrome and literature review.
Hendricks LAJ; Schuurs-Hoeijmakers J; Spier I; Haadsma ML; Eijkelenboom A; Cremer K; Mensenkamp AR; Aretz S; Vos JR; Hoogerbrugge N
Eur J Med Genet; 2022 Jul; 65(7):104533. PubMed ID: 35640862
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
