"Kr\u00E1l, Zden\u011Bk" . "P(NT11154), P(NT12130), P(NT12215), S, Z(MSM0021622434)" . "CZ - \u010Cesk\u00E1 republika" . "Szturz, Petr" . "Teleangiectasia hereditaria haemorrhagica \u2013 syndrom Osler-Weber-Rendu. Popis p\u0159\u00EDpadu a zku\u0161enost\u00ED s l\u00E9\u010Dbou"@cs . . . "6" . . "58" . . "173629" . . . "hereditary haemorrhagic telangiectasie; syndrom Osler-Weber-Rendu; haemangiomas; arteriovenous malformations; epistaxis; anaemia; estrogens; antiestrogens; raloxifen; thalidomide; bevacizumab; interferon alpha"@en . . . "Mayer, Ji\u0159\u00ED" . . "Adam, Zden\u011Bk" . "Teleangiectasia hereditaria haemorrhagica \u2013 syndrom Osler-Weber-Rendu. Popis p\u0159\u00EDpadu a zku\u0161enost\u00ED s l\u00E9\u010Dbou"@cs . . . "0042-773X" . . . "K\u00F6nig, Ji\u0159\u00ED" . . . . "Heredit\u00E1rn\u00ED hemoragick\u00E1 teleangiektazie je vrozen\u00E9 onemocn\u011Bn\u00ED s autozom\u00E1ln\u011B dominantn\u00EDm p\u0159enosem. Prvn\u00EDm p\u0159\u00EDznakem je krv\u00E1cen\u00ED z nosu, obvykle v 2. dek\u00E1d\u011B \u017Eivota. Teprve pozd\u011Bji, ve 3. \u010Di 4. dek\u00E1d\u011B, se vyvinou typick\u00E9 drobn\u00E9 c\u00E9vn\u00ED arterioven\u00F3zn\u00ED malformace velikosti \u0161pendl\u00EDkov\u00E9 hlavi\u010Dky (o pr\u016Fm\u011Bru 1\u20132 mm). B\u00FDvaj\u00ED na k\u016F\u017Ei a na sliznic\u00EDch dutiny \u00FAstn\u00ED a samoz\u0159ejm\u011B tak\u00E9 v \u017Ealudku a v tenk\u00E9m st\u0159ev\u011B. Krv\u00E1civ\u00E9 projevy nejen z oblasti nosu, ale tak\u00E9 z oblasti tr\u00E1vic\u00ED trubice zp\u016Fsobuj\u00ED v pokro\u010Dil\u00FDch p\u0159\u00EDpadech t\u011B\u017Ekou an\u00E9mii se z\u00E1vislost\u00ED na transfuz\u00EDch. Pokro\u010Dilej\u0161\u00ED formy heredit\u00E1rn\u00ED hemoragick\u00E9 teleangiektazie jsou prov\u00E1zeny rozvojem arterioven\u00F3zn\u00EDch c\u00E9vn\u00EDch malformac\u00ED v oblasti jater, plic a p\u0159\u00EDpadn\u011B v mozku. C\u00E9vn\u00ED arterioven\u00F3zn\u00ED malformace v oblasti jater zp\u016Fsobuj\u00ED hyperkinetick\u00FD ob\u011Bh, kter\u00FD m\u016F\u017Ee vy\u00FAstit do srde\u010Dn\u00EDho selh\u00E1n\u00ED. V arterioven\u00F3zn\u00EDch plicn\u00EDch malformac\u00EDch obch\u00E1z\u00ED krev filtraci plicn\u00EDm kapil\u00E1rn\u00EDm \u0159e\u010Di\u0161t\u011Bm, a tak se mohou infikovan\u00E9 mikrotromby dostal z oblasti doln\u00ED dut\u00E9 \u017E\u00EDly t\u0159eba do mozku." . . . . . "Chlupov\u00E1, Gabriela" . "RIV/00216224:14110/12:00060420!RIV13-MZ0-14110___" . "11"^^ . . . "14"^^ . "H\u00E1jek, Roman" . "Hereditary haemorrhagic telangiectasy is an inborn disease with autosomal dominant transmission. Nose bleeding usually occurs during the 2nd decade of life as the first sign of the disease. Later, during the 3rd or 4th decade of life, typical subtle, pinhead-sized (1\u20132 mm in diameter) vascular arteriovenous malformations occur. These are usually found on the oral mucosa and in the stomach and small intestine. During later stages of the disease, nose as well as gastrointestinal bleeding causes severe anaemia requiring transfusions. Advanced stages of hereditary hemorrhagic telangiectasy are associated with a development of ateriovenous vascular malformations in the liver, lungs and possibly the brain. Vascular ateriovenous malformations in the liver cause hyperkinetic circulation that may lead to heart failure."@en . "Vnit\u0159n\u00ED l\u00E9ka\u0159stv\u00ED" . "Teleangiectasia hereditaria haemorrhagica \u2013Osler-Weber-Rendu syndrome. Case study and treatment experience"@en . "Heredit\u00E1rn\u00ED hemoragick\u00E1 teleangiektazie je vrozen\u00E9 onemocn\u011Bn\u00ED s autozom\u00E1ln\u011B dominantn\u00EDm p\u0159enosem. Prvn\u00EDm p\u0159\u00EDznakem je krv\u00E1cen\u00ED z nosu, obvykle v 2. dek\u00E1d\u011B \u017Eivota. Teprve pozd\u011Bji, ve 3. \u010Di 4. dek\u00E1d\u011B, se vyvinou typick\u00E9 drobn\u00E9 c\u00E9vn\u00ED arterioven\u00F3zn\u00ED malformace velikosti \u0161pendl\u00EDkov\u00E9 hlavi\u010Dky (o pr\u016Fm\u011Bru 1\u20132 mm). B\u00FDvaj\u00ED na k\u016F\u017Ei a na sliznic\u00EDch dutiny \u00FAstn\u00ED a samoz\u0159ejm\u011B tak\u00E9 v \u017Ealudku a v tenk\u00E9m st\u0159ev\u011B. Krv\u00E1civ\u00E9 projevy nejen z oblasti nosu, ale tak\u00E9 z oblasti tr\u00E1vic\u00ED trubice zp\u016Fsobuj\u00ED v pokro\u010Dil\u00FDch p\u0159\u00EDpadech t\u011B\u017Ekou an\u00E9mii se z\u00E1vislost\u00ED na transfuz\u00EDch. Pokro\u010Dilej\u0161\u00ED formy heredit\u00E1rn\u00ED hemoragick\u00E9 teleangiektazie jsou prov\u00E1zeny rozvojem arterioven\u00F3zn\u00EDch c\u00E9vn\u00EDch malformac\u00ED v oblasti jater, plic a p\u0159\u00EDpadn\u011B v mozku. C\u00E9vn\u00ED arterioven\u00F3zn\u00ED malformace v oblasti jater zp\u016Fsobuj\u00ED hyperkinetick\u00FD ob\u011Bh, kter\u00FD m\u016F\u017Ee vy\u00FAstit do srde\u010Dn\u00EDho selh\u00E1n\u00ED. V arterioven\u00F3zn\u00EDch plicn\u00EDch malformac\u00EDch obch\u00E1z\u00ED krev filtraci plicn\u00EDm kapil\u00E1rn\u00EDm \u0159e\u010Di\u0161t\u011Bm, a tak se mohou infikovan\u00E9 mikrotromby dostal z oblasti doln\u00ED dut\u00E9 \u017E\u00EDly t\u0159eba do mozku."@cs . "Jakubcov\u00E1, Barbora" . . "13"^^ . "[D983F3B39ABA]" . "Krej\u010D\u00ED, Marta" . . . "Krupa, Petr" . . . . "RIV/00216224:14110/12:00060420" . "Teleangiectasia hereditaria haemorrhagica \u2013 syndrom Osler-Weber-Rendu. Popis p\u0159\u00EDpadu a zku\u0161enost\u00ED s l\u00E9\u010Dbou" . . "Teleangiectasia hereditaria haemorrhagica \u2013Osler-Weber-Rendu syndrome. Case study and treatment experience"@en . . . "14110" . "Adamov\u00E1, Zdenka" . "Pour, Lud\u011Bk" . . "Teleangiectasia hereditaria haemorrhagica \u2013 syndrom Osler-Weber-Rendu. Popis p\u0159\u00EDpadu a zku\u0161enost\u00ED s l\u00E9\u010Dbou" . . . . . . . "Neumann, Ale\u0161" . . "Simonides, Jan" . .