6.
Heindl M, Handel N, Ngeow J, Kionke J, Wittekind C, Kamprad M
. Autoimmunity, intestinal lymphoid hyperplasia, and defects in mucosal B-cell homeostasis in patients with PTEN hamartoma tumor syndrome. Gastroenterology. 2012; 142(5):1093-1096.e6.
DOI: 10.1053/j.gastro.2012.01.011.
View
7.
Hendriks Y, Verhallen J, van der Smagt J, Kant S, Hilhorst Y, Hoefsloot L
. Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases. Fam Cancer. 2003; 2(2):79-85.
DOI: 10.1023/a:1025713815924.
View
8.
Arch E, Goodman B, Van Wesep R, Liaw D, Clarke K, Parsons R
. Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease. Am J Med Genet. 1997; 71(4):489-93.
View
9.
Nelen M, Padberg G, Peeters E, Lin A, van den Helm B, Frants R
. Localization of the gene for Cowden disease to chromosome 10q22-23. Nat Genet. 1996; 13(1):114-6.
DOI: 10.1038/ng0596-114.
View
10.
Zhou X, Marsh D, Morrison C, Chaudhury A, Maxwell M, Reifenberger G
. Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults. Am J Hum Genet. 2003; 73(5):1191-8.
PMC: 1180498.
DOI: 10.1086/379382.
View
11.
Zori R, Marsh D, Graham G, Marliss E, Eng C
. Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome. Am J Med Genet. 1998; 80(4):399-402.
View
12.
Sumilo D, Nichols L, Ryan R, Marshall T
. Incidence of indications for tonsillectomy and frequency of evidence-based surgery: a 12-year retrospective cohort study of primary care electronic records. Br J Gen Pract. 2018; 69(678):e33-e41.
PMC: 6301361.
DOI: 10.3399/bjgp18X699833.
View
13.
Kara C, Ergin H, Kocak G, Kilic I, Yurdakul M
. Prevalence of tonsillar hypertrophy and associated oropharyngeal symptoms in primary school children in Denizli, Turkey. Int J Pediatr Otorhinolaryngol. 2002; 66(2):175-9.
DOI: 10.1016/s0165-5876(02)00247-1.
View
14.
Liaw D, Marsh D, Li J, Dahia P, Wang S, Zheng Z
. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat Genet. 1997; 16(1):64-7.
DOI: 10.1038/ng0597-64.
View
15.
Piccione M, Fragapane T, Antona V, Giachino D, Cupido F, Corsello G
. PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol. Am J Med Genet A. 2013; 161A(11):2902-8.
DOI: 10.1002/ajmg.a.36266.
View
16.
Celebi J, Ping X, Zhang H, Remington T, Sulica V, Tsou H
. Germline PTEN mutations in three families with Cowden syndrome. Exp Dermatol. 2000; 9(2):152-6.
DOI: 10.1034/j.1600-0625.2000.009002152.x.
View
17.
Marsh D, Dahia P, Zheng Z, Liaw D, Parsons R, GORLIN R
. Germline mutations in PTEN are present in Bannayan-Zonana syndrome. Nat Genet. 1997; 16(4):333-4.
DOI: 10.1038/ng0897-333.
View
18.
Lachlan K, Lucassen A, Bunyan D, Temple I
. Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers. J Med Genet. 2007; 44(9):579-85.
PMC: 2597943.
DOI: 10.1136/jmg.2007.049981.
View