201 related articles for article (PubMed ID: 24629685)
1. [Cowden syndrome diagnosed in patients with macrocephaly].
Skytte AB; Bojesen A; Bygum A
Ugeskr Laeger; 2014 Jan; 176(2):165-7. PubMed ID: 24629685
[TBL] [Abstract][Full Text] [Related]
2. [Cowden syndrome can be a challenging diagnosis].
Skytte AB; Gerdes AM; Bygum A
Ugeskr Laeger; 2014 Jan; 176(2):162-5. PubMed ID: 24629684
[TBL] [Abstract][Full Text] [Related]
3. Lhermitte-Duclos Disease in association with Cowden Syndrome.
Nielson C; Fischer T; Fischer R; Donald J; Rajpara A
Dermatol Online J; 2016 May; 22(5):. PubMed ID: 27617518
[TBL] [Abstract][Full Text] [Related]
4. Clinical and genetic diagnosis of Cowden syndrome: A case report of a rare PTEN germline variant and diverse clinical presentation.
Arai H; Akagi K; Nakagawa A; Onai Y; Utsu Y; Masuda S; Aotsuka N
Medicine (Baltimore); 2023 Jan; 102(1):e32572. PubMed ID: 36607858
[TBL] [Abstract][Full Text] [Related]
5. Skin abnormalities in individuals with macrocephaly: Cowden disease from a dermatologist's point of view.
van der Velden JJ; Vreeburg M; Smeets EE; Schrander-Stumpel CT; van Steensel MA
Int J Dermatol; 2008 Nov; 47 Suppl 1():45-8. PubMed ID: 18986487
[TBL] [Abstract][Full Text] [Related]
6. Novel PTEN germline mutation in a family with mild phenotype: difficulties in genetic counseling.
Busa T; Chabrol B; Perret O; Longy M; Philip N
Gene; 2013 Jan; 512(2):194-7. PubMed ID: 23124040
[TBL] [Abstract][Full Text] [Related]
7. Cowden syndrome: clinical case and a brief review.
Lopes S; Vide J; Moreira E; Azevedo F
Dermatol Online J; 2017 Aug; 23(8):. PubMed ID: 29469739
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Atypical focal cortical dysplasia in a patient with Cowden syndrome.
Cheung KM; Lam CW; Chan YK; Siu WK; Yong L
Hong Kong Med J; 2014 Apr; 20(2):165-7. PubMed ID: 24714173
[TBL] [Abstract][Full Text] [Related]
11. Bilateral and symmetrical palmoplantar punctate keratoses in childhood: a possible clinical clue for an early diagnosis of PTEN hamartoma-tumour syndrome.
Ferran M; Bussaglia E; Matias-Guiu X; Pujol RM
Clin Exp Dermatol; 2009 Jul; 34(5):e28-30. PubMed ID: 19508470
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Multiple sclerotic fibromas of the skin: an important clue for the diagnosis of Cowden syndrome.
Kieselova K; Santiago F; Henrique M; Cunha MF
BMJ Case Rep; 2017 Aug; 2017():. PubMed ID: 28847996
[TBL] [Abstract][Full Text] [Related]
14. Cutaneous lipomas and macrocephaly as early signs of PTEN hamartoma tumor syndrome.
Martin H; Bessis D; Bourrat E; Mazereeuw-Hautier J; Morice-Picard F; Balguerie X; Chiaverini C;
Pediatr Dermatol; 2020 Sep; 37(5):839-843. PubMed ID: 32657433
[TBL] [Abstract][Full Text] [Related]
15. Head circumference in the clinical detection of PTEN hamartoma tumor syndrome in a clinic population at high-risk of breast cancer.
Shiovitz S; Everett J; Huang SC; Orloff MS; Eng C; Gruber SB
Breast Cancer Res Treat; 2010 Nov; 124(2):459-65. PubMed ID: 20349131
[TBL] [Abstract][Full Text] [Related]
16. Characteristic brain magnetic resonance imaging pattern in patients with macrocephaly and PTEN mutations.
Vanderver A; Tonduti D; Kahn I; Schmidt J; Medne L; Vento J; Chapman KA; Lanpher B; Pearl P; Gropman A; Lourenco C; Bamforth JS; Sharpe C; Pineda M; Schallner J; Bodamer O; Orcesi S; Oberstein SA; Sistermans EA; Yntema HG; Bonnemann C; Waldman AT; van der Knaap MS
Am J Med Genet A; 2014 Mar; 164A(3):627-33. PubMed ID: 24375884
[TBL] [Abstract][Full Text] [Related]
17. Cowden syndrome.
Farooq A; Walker LJ; Bowling J; Audisio RA
Cancer Treat Rev; 2010 Dec; 36(8):577-83. PubMed ID: 20580873
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Cutaneous lipoma in children: 5 cases with Bannayan-Riley-Ruvalcaba syndrome.
Buisson P; Leclair MD; Jacquemont S; Podevin G; Camby C; David A; Heloury Y
J Pediatr Surg; 2006 Sep; 41(9):1601-3. PubMed ID: 16952599
[TBL] [Abstract][Full Text] [Related]
20. Cowden syndrome.
Oliveira MA; Medina JB; Xavier FC; Magalhães M; Ortega KL
Dermatol Online J; 2010 Jan; 16(1):7. PubMed ID: 20137749
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
