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Items: 1 to 20 of 136

1.

A case of hereditary hemorrhagic telangiectasia.

Lee HE, Sagong C, Yeo KY, Ko JY, Kim JS, Yu HJ.

Ann Dermatol. 2009 May;21(2):206-8. doi: 10.5021/ad.2009.21.2.206. Epub 2009 May 31.

2.

Hereditary hemorrhagic telangiectasia.

Kamath N, Bhatia S, Singh H, Shetty A, Shetty S.

N Am J Med Sci. 2015 Mar;7(3):125-8. doi: 10.4103/1947-2714.153928.

3.

[A case of Rendu-Osler-Weber disease with brain hemorrhages and portal-systemic encephalopathy].

Arakawa S, Tanaka Y, Nakamura K, Oita J, Yamaguchi T.

Rinsho Shinkeigaku. 1994 Aug;34(8):817-22. Japanese.

PMID:
7994990
4.

[Excision of the rectum due to carcinoma in patient with hereditary hemorrhagic teleangiectasia].

Gajda S, Szczepanik AM, Misiak A, Szczepanik AB.

Pol Merkur Lekarski. 2011 Jul;31(181):45-7. Polish.

PMID:
21870709
5.

A case of hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber's disease) with dystrophic calcinosis cutis and retinal lesions.

Takahama H, Noto S, Ito M, Nishimoto H, Tadokoro M.

J Dermatol. 2002 Aug;29(8):512-5.

PMID:
12227486
6.

[Ophthalmologic diagnosis of hereditary hemorrhagic telangiectasia or Rendu-Osler-Weber disease].

Pizzamiglio-Martín C, Gil-Cazorla R, Guzmán-Glázquez J.

Arch Soc Esp Oftalmol. 2008 Jun;83(6):381-4. Spanish.

7.

Hereditary hemorrhagic telangiectasias: a challenge for the clinician.

Bergler W, Götte K.

Eur Arch Otorhinolaryngol. 1999;256(1):10-5. Review.

PMID:
10065379
8.
9.

Syndrome in question.

Meireles SI, Andrade SM, Gomes MF, Castro FA, Tebcherani AJ.

An Bras Dermatol. 2014 Jul-Aug;89(4):679-80.

10.

Anesthetic management of a patient with hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Case report.

Goulart AP, Moro ET, Guasti VM, Colares RF.

Rev Bras Anestesiol. 2009 Jan-Feb;59(1):74-8. English, Portuguese.

11.

Rendu-Osler-Weber syndrome: dermatological approach.

Barbosa AB, Hans Filho G, Vicari CF, Medeiros MZ, Couto DV, Takita LC.

An Bras Dermatol. 2015 May-Jun;90(3 Suppl 1):226-8. doi: 10.1590/abd1806-4841.20152563.

12.

Successful treatment for ampullary submucosal bleeding-induced pancreatitis: a rare sequla of hereditary hemorrhagic telangiectasia.

Sakai N, Yoshidome H, Ito H, Kimura F, Shimizu H, Togawa A, Ohtsuka M, Kato A, Yamaguchi T, Yoshikawa M, Miyazaki M.

Hepatogastroenterology. 2005 Jan-Feb;52(61):270-3. Review.

PMID:
15783047
13.

[Epistaxis in Rendu-Osler-Weber disease treated with selective embolization--case report].

Jarzabek M, Trojanowski P, Szajner M, Pyra K, Sojka M, Szczerbo-Trojanowska M.

Przegl Lek. 2012;69(7):317-9. Polish.

PMID:
23276024
14.

Gastric predominant hereditary hemorrhagic telangiectasia.

Katsinelos P, Chatzimavroudis G, Zavos C, Kamperis E, Triantafillidis I, Pilpilidis I, Katsinelos T, Papaziogas B.

Vasa. 2006 Nov;35(4):258-61.

PMID:
17109371
15.

[Osler--Rendu Disease: an example of a family clustering in a genetic disorder].

Mitu F, Lovin S, Rusu C, Mitu M, Georgescu T, Pandele GI, Covic M.

Rev Med Chir Soc Med Nat Iasi. 2002 Oct-Dec;106(4):820-4. Romanian.

PMID:
14974237
16.

[Rendu-Osler-Weber disease].

Sys L, van den Hoogen FJ.

Ned Tijdschr Tandheelkd. 2005 Sep;112(9):336-9. Review. Dutch.

PMID:
16184912
17.

Osler-Weber-Rendu disease: a six generation family.

Cheng LH, Tsai WJ.

Gaoxiong Yi Xue Ke Xue Za Zhi. 1992 Sep;8(9):495-502.

PMID:
1294765
18.

Osler-Weber-Rendu disease presenting as recurrent portosystemic encephalopathy in a 75-year-old female patient.

Ha J, Son BK, Ahn SB, Jo YK, Kim SH, Jo YJ, Park YS, Jung YY.

Korean J Gastroenterol. 2015 Jan;65(1):57-61.

19.

Osler-Weber-Rendu syndrome--dental implications.

da Silva Santos PS, Fernandes KS, Magalhães MH.

J Can Dent Assoc. 2009 Sep;75(7):527-30.

20.

Correlation of severity of epistaxis with nasal telangiectasias in hereditary hemorrhagic telangiectasia (HHT) patients.

Pagella F, Colombo A, Matti E, Giourgos G, Tinelli C, Olivieri C, Danesino C.

Am J Rhinol Allergy. 2009 Jan-Feb;23(1):52-8. doi: 10.2500/ajra.2009.23.3263.

PMID:
19379613

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