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Results: 1 to 20 of 116

Similar articles for PubMed (Select 17526801)

1.

The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management.

Tan WH, Baris HN, Burrows PE, Robson CD, Alomari AI, Mulliken JB, Fishman SJ, Irons MB.

J Med Genet. 2007 Sep;44(9):594-602. Epub 2007 May 25.

2.

Increased Prevalence of Developmental Venous Anomalies in Children with Intracranial Neoplasms.

Jones BV, Linscott L, Koberlein G, Hummel TR, Leach JL.

AJNR Am J Neuroradiol. 2015 May 28. [Epub ahead of print]

PMID:
26021620
3.

Overgrowth Syndromes With Vascular Anomalies.

Blei F.

Curr Probl Pediatr Adolesc Health Care. 2015 Apr;45(4):118-131. doi: 10.1016/j.cppeds.2015.03.002. Epub 2015 Apr 27. Review.

PMID:
25937473
4.

Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome.

Busa T, Milh M, Degardin N, Girard N, Sigaudy S, Longy M, Olshchwang S, Sobol H, Chabrol B, Philip N.

Eur J Paediatr Neurol. 2015 Mar;19(2):188-92. doi: 10.1016/j.ejpn.2014.11.012. Epub 2014 Dec 16.

PMID:
25549896
5.

PTEN hamartoma tumour syndrome: early tumour development in children.

Smpokou P, Fox VL, Tan WH.

Arch Dis Child. 2015 Jan;100(1):34-7. doi: 10.1136/archdischild-2014-305997. Epub 2014 Aug 11.

PMID:
25114091
6.

Vascular anomalies.

Lee EI.

Semin Plast Surg. 2014 May;28(2):47-8. doi: 10.1055/s-0034-1376258. No abstract available.

7.

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. doi: 10.12809/hkmj133863.

8.

Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screening.

Marchese M, Conti V, Valvo G, Moro F, Muratori F, Tancredi R, Santorelli FM, Guerrini R, Sicca F.

BMC Med Genet. 2014 Feb 27;15:26. doi: 10.1186/1471-2350-15-26.

9.

Bannayan-Riley-Ruvalcaba syndrome with deforming lipomatous hamartomas in infant--case report.

Gontijo GM, Pinto CA, Rogatto SR, Cunha IW, Aguiar S Jr, Alves CA.

An Bras Dermatol. 2013 Nov-Dec;88(6):982-5. doi: 10.1590/abd1806-4841.20132730.

10.
11.

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

Peiretti V, Mussa A, Feyles F, Tuli G, Santanera A, Molinatto C, Ferrero GB, Corrias A.

J Clin Res Pediatr Endocrinol. 2013;5(4):261-5. doi: 10.4274/Jcrpe.984.

12.

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. doi: 10.1002/ajmg.a.36309. Epub 2013 Dec 20.

PMID:
24375884
13.

Increased prevalence of eosinophilic gastrointestinal disorders in pediatric PTEN hamartoma tumor syndromes.

Henderson CJ, Ngeow J, Collins MH, Martin LJ, Putnam PE, Abonia JP, Marsolo K, Eng C, Rothenberg ME.

J Pediatr Gastroenterol Nutr. 2014 May;58(5):553-60. doi: 10.1097/MPG.0000000000000253.

14.

Fibro-adipose vascular anomaly: clinical-radiologic-pathologic features of a newly delineated disorder of the extremity.

Alomari AI, Spencer SA, Arnold RW, Chaudry G, Kasser JR, Burrows PE, Govender P, Padua HM, Dillon B, Upton J, Taghinia AH, Fishman SJ, Mulliken JB, Fevurly RD, Greene AK, Landrigan-Ossar M, Paltiel HJ, Trenor CC 3rd, Kozakewich HP.

J Pediatr Orthop. 2014 Jan;34(1):109-17. doi: 10.1097/BPO.0b013e3182a1f0b8.

PMID:
24322574
15.

Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria.

Pilarski R, Burt R, Kohlman W, Pho L, Shannon KM, Swisher E.

J Natl Cancer Inst. 2013 Nov 6;105(21):1607-16. doi: 10.1093/jnci/djt277. Epub 2013 Oct 17. Review.

16.

PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol.

Piccione M, Fragapane T, Antona V, Giachino D, Cupido F, Corsello G.

Am J Med Genet A. 2013 Nov;161A(11):2902-8. doi: 10.1002/ajmg.a.36266. Epub 2013 Oct 7.

PMID:
24123798
17.

Muscle hemangiomatosis presenting as a severe feature in a patient with the pten mutation: expanding the phenotype of vascular malformations in bannayan-riley-ruvalcaba syndrome.

Soysal Y, Acun T, Lourenço C, Marques W Jr, Yakıcıer M.

Balkan J Med Genet. 2012 Jun;15(1):45-50. doi: 10.2478/v10034-012-0007-x.

18.

Bannayan-Riley-Ruvalcaba syndrome: MRI neuroimaging features in a series of 7 patients.

Bhargava R, Au Yong KJ, Leonard N.

AJNR Am J Neuroradiol. 2014 Feb;35(2):402-6. doi: 10.3174/ajnr.A3680. Epub 2013 Aug 1.

19.

Conjunctival hamartoma with eosinophilia--a novel lesion in a child with PTEN hamartoma syndrome.

Mudhar HS, Rogers NK.

Graefes Arch Clin Exp Ophthalmol. 2013 Aug;251(8):2077-9. doi: 10.1007/s00417-013-2406-4. Epub 2013 Jul 3. No abstract available.

PMID:
23821119
20.

Biochemical screening and PTEN mutation analysis in individuals with autism spectrum disorders and macrocephaly.

Hobert JA, Embacher R, Mester JL, Frazier TW 2nd, Eng C.

Eur J Hum Genet. 2014 Feb;22(2):273-6. doi: 10.1038/ejhg.2013.114. Epub 2013 May 22.

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