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hereditary hemorrhagic telangiectasia (29) 29
humans (26) 26
index medicus (25) 25
epistaxis (18) 18
osler-rendu-weber disease (18) 18
female (16) 16
male (14) 14
rendu-osler-weber disease (14) 14
adult (13) 13
aged (13) 13
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osler-rendu-weber syndrome (13) 13
telangiectasia, hereditary hemorrhagic - complications (12) 12
rendu-osler-weber病 (11) 11
web (11) 11
pulmonary arteriovenous fistula (10) 10
静脈 (10) 10
telangiectasia, hereditary hemorrhagic - genetics (8) 8
hht (7) 7
pulmonary artery - abnormalities (7) 7
肺動静脈瘻 (7) 7
otorhinolaryngology (6) 6
pulmonary arteriovenous malformation (6) 6
telangiectasia, hereditary hemorrhagic - diagnosis (6) 6
adolescent (5) 5
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epistaxis - etiology (5) 5
medicine & public health (5) 5
osler-rendu disease (5) 5
osler–rendu–weber disease (5) 5
pulmonary veins - abnormalities (5) 5
surgery (5) 5
telangiectasis (5) 5
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aged, 80 and over (4) 4
disease (4) 4
genetics (4) 4
genetics & heredity (4) 4
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pulmonary arteriovenous malformations (4) 4
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telangiectasia (4) 4
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antigens, cd - genetics (3) 3
arteriovenous malformations (3) 3
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arteriovenous malformations - diagnosis (3) 3
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phenotype (3) 3
pulmonary arterial hypertension (3) 3
receptors, cell surface - genetics (3) 3
rendu-osler-weber syndrome (3) 3
respiratory system (3) 3
retrospective studies (3) 3
telangiectasia, hereditary hemorrhagic (3) 3
telangiectasia, hereditary hemorrhagic - drug therapy (3) 3
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abridged index medicus (2) 2
activin receptors, type ii (2) 2
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antifibrinolytic agents - therapeutic use (2) 2
argon plasma coagulation (2) 2
arteriovenous malformations - therapy (2) 2
bevacizumab (2) 2
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Journal Article
HNO, ISSN 0017-6192, 05/2018, Volume 66, Issue 5, pp. 405 - 414
Journal Article
Oral Diseases, ISSN 1354-523X, 01/2011, Volume 17, Issue 1, pp. 125 - 127
Journal Article
Actas Dermo-Sifiliográficas (English Edition), ISSN 1578-2190, 09/2019, Volume 110, Issue 7, pp. 526 - 532
Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder with an estimated worldwide prevalence... 
Epistaxis | Osler-Weber-Rendu | Osler-Rendu-Weber disease | Telangiectasia
Journal Article
Clinical and Experimental Otorhinolaryngology, ISSN 1976-8710, 06/2017, Volume 10, Issue 2, pp. 153 - 157
Journal Article
Clinical Genetics, ISSN 0009-9163, 07/2016, Volume 90, Issue 1, pp. 55 - 62
Patients with germline mutations in SMAD4 can present symptoms of both juvenile polyposis syndrome ( JPS ) and hereditary hemorrhagic telangiectasia ( HHT ):... 
juvenile polyposis syndrome | melena | Smad4‐related juvenile polyposis | Osler–Rendu disease | hereditary hemorrhagic telangiectasia | Smad4 protein | epistaxis | Epistaxis | Melena | Juvenile polyposis syndrome | Osler-Rendu disease | Hereditary hemorrhagic telangiectasia | Smad4-related juvenile polyposis | MANAGEMENT | RISK | PULMONARY ARTERIOVENOUS-MALFORMATIONS | PREVALENCE | AORTOPATHY | COLORECTAL-CANCER | GENETICS & HEREDITY | UPDATE | BMPR1A | Humans | Middle Aged | Male | Neoplastic Syndromes, Hereditary - surgery | Intestinal Polyposis - diagnosis | Telangiectasia, Hereditary Hemorrhagic - genetics | Aorta - metabolism | Intestinal Polyposis - congenital | Telangiectasia, Hereditary Hemorrhagic - diagnosis | Telangiectasia, Hereditary Hemorrhagic - surgery | Smad4 Protein - genetics | Adult | Female | Registries | Neoplastic Syndromes, Hereditary - genetics | Retrospective Studies | Telangiectasia, Hereditary Hemorrhagic - complications | Gene Expression | Intestinal Polyposis - genetics | Neoplastic Syndromes, Hereditary - diagnosis | Aorta - pathology | Phenotype | Intestinal Polyposis - complications | Adolescent | Denmark | Neoplastic Syndromes, Hereditary - complications | Heterozygote | Aged | Mutation | Intestinal Polyposis - surgery | Genetic research | Genetic aspects | Genotype & phenotype | Genetic disorders | Index Medicus
Journal Article
Journal of Plastic, Reconstructive & Aesthetic Surgery, ISSN 1748-6815, 2006, Volume 59, Issue 5, pp. 537 - 540
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脳卒中の外科, ISSN 0914-5508, 2015, Volume 43, Issue 3, pp. 193 - 200
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Rendu-Weber disease, is an autosomal dominant disorder that results from multi-system vascular... 
hepatic arteriovenous malformation | brain arteriovenous malformation | pulmonary arteriovenous malformation | hereditary hemorrhagic telangiectasia | Osler-Rendu-Weber disease
Journal Article
HNO, ISSN 0017-6192, 3/1998, Volume 46, Issue 3, pp. 228 - 232
Bei der hereditären hämorrhagischen Teleangiektasie (Morbus Osler-Rendu-Weber) stellt die rezidivierende Epistaxis für den Patienten eine große Belastung und... 
Epistaxis | Argon-Plasma- Koagulation | Schlüsselwörter Morbus Osler | Argon plasma coagualtion | Nasenschleimhaut | Osler-Rendu-Weber disease | Nasal mucosa | Argon plasma coagulation
Journal Article
Der Chirurg, ISSN 0009-4722, 6/1998, Volume 69, Issue 6, pp. 639 - 641
Hepatic involvement in hereditary hemorrhagic telangiectasia (HHT) is rare. Among local pathologic alterations like fibrosis and cirrhosis, arteriovenous... 
Rendu-Osler-Weber disease | Hepatic artery | Expanderprothese | Banding | Morbus Osler-Rendu-Weber | Leberarterie | Schlüsselwörter: Heriditäre hämorrhagische Teleangiektasie | Hereditary hemorrhagic telangiectasia | Expander prosthesis
Journal Article
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