Works about HEREDITARY hemorrhagic telangiectasia

Results: 751

Hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber syndrome) and atrial fibrillation – is it ever too late to do something?!

Published in:

2025

By:

Juren, Ivana Petrović;
Čikara, Marija Ivić;
Grizelj, Danijela;
Pavlović, Nikola;
Prša, Sandra;
Križić, Kristina Milevoj;
Podravec, Vlasta Soukup;
ČlekovićKovačić, Andreja;
Lukaš, Matea;
Ladić, Iva;
Lipošćak, Gabriela

Publication type:

Abstract

Good obstetric outcome after embolisation of pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasia: Planned pregnancy may also be important in this condition.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2014, v. 54, n. 2, p. 191, doi. 10.1111/ajo.12154

By:

Takahashi, Hironori;
Matsubara, Shigeki;
Saito, Koyomi;
Bando, Masashi

Publication type:

Article

Hepatic artery embolization for treatment of patients with hereditary hemorrhagic telangiectasia and symptomatic hepatic vascular malformations.

Published in:

2004

By:

Chavan, Ajay;
Caselitz, Martin;
Gratz, Karl-Friedrich;
Lotz, Joachim;
Kirchhoff, Timm;
Piso, Plinio;
Wagner, Siegfried;
Manns, Michael;
Galanski, Michael

Publication type:

journal article

Intrahepatic porto-hepatic venous shunts in Rendu-Osler-Weber disease: imaging demonstration.

Published in:

2004

By:

Matsumoto, Shunro;
Mori, Hiromu;
Yamada, Yasunari;
Hayashida, Tomoko;
Hori, Yuzo;
Kiyosue, Hiro

Publication type:

journal article

Atypical venous drainage system and distinct vascular characteristics in pediatric intracerebral hemorrhage caused by multiple micro arteriovenous malformations.

Published in:

2024

By:

Saito, Katsuya;
Ikeda, Go;
Akutsu, Yoshimitsu;
Kano, Hideyuki;
Akutsu, Hiroyoshi

Publication type:

Case Study

Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia.

Published in:

Child's Nervous System, 2024, v. 40, n. 7, p. 2101, doi. 10.1007/s00381-024-06366-z

By:

Beslow, Lauren A.;
Vossough, Arastoo;
Kim, Helen;
Nelson, Jeffrey;
Lawton, Michael T.;
Pollak, Jeffrey;
Lin, Doris D. M.;
Ratjen, Felix;
Hammill, Adrienne M.;
Hetts, Steven W.;
Gossage, James R.;
Whitehead, Kevin J.;
Faughnan, Marie E.;
Krings, Timo;
Brain Vascular Malformation Consortium HHT Investigator Group;
Atherton, Mary E.;
Chakinala, Murali M.;
Clancy, Marianne S.;
Henderson, Katharine;
Hetts, Steven

Publication type:

Article

Giant, symptomatic mixed vascular malformation containing a cavernoma, developmental venous anomaly, and capillary telangiectasia in a 19-month-old infant.

Published in:

Child's Nervous System, 2022, v. 38, n. 5, p. 1005, doi. 10.1007/s00381-021-05358-7

By:

Gaztanaga, Wendy;
Luther, Evan;
McCarthy, David;
Chamyan, Gabriel;
Wang, Shelly;
Ragheb, John

Publication type:

Article

Introduction to phacomatoses (neurocutaneous disorders) in childhood.

Published in:

Child's Nervous System, 2020, v. 36, n. 10, p. 2229, doi. 10.1007/s00381-020-04758-5

By:

Ruggieri, Martino;
Polizzi, Agata;
Marceca, Gioacchino Paolo;
Catanzaro, Stefano;
Praticò, Andrea D.;
Di Rocco, Concezio

Publication type:

Article

Ischemic stroke due to sporadic and genetic pulmonary arteriovenous malformations: Case report.

Published in:

Brain Circulation, 2022, v. 8, n. 1, p. 57, doi. 10.4103/bc.bc_66_21

By:

Tagliapietra, Matteo;
Turri, Giulia;
Bortolotti, Federica;
Mansueto, Giancarlo;
Monaco, Salvatore

Publication type:

Article

Percutaneous embolization of pulmonary arteriovenous malformations in adult patient with Rendu–Osler–Weber: a case report.

Published in:

European Heart Journal Case Reports, 2023, v. 7, n. 11, p. 1, doi. 10.1093/ehjcr/ytad533

By:

Schutyser, Wouter;
Budts, Werner;
Verhamme, Peter

Publication type:

Article

Rhinoscleroma in a 9-year old boy: Rare case report.

Published in:

Global Pediatric Health, 2023, p. 1, doi. 10.1177/2333794X231210673

By:

Kabila, Badr;
Zhim, Meriem;
Naggar, Amine;
Hadad, Siham el;
Allali, Nazik;
Chat, Latifa;
Elouazzani, Hafsa;
Cherradi, Nadia

Publication type:

Article

A case of hereditary hemorrhagic telangiectasia treated with cryotherapy.

Published in:

2024

By:

Wen, Su‐Ying;
Huang, Ya‐Yun

Publication type:

Case Study

Dermoscopy as an efficient aid to diagnose pigmentary and vascular component of periorbital melanosis: A cross‐sectional study.

Published in:

Journal of Cosmetic Dermatology, 2022, v. 21, n. 11, p. 5880, doi. 10.1111/jocd.15141

By:

Chhabra, Namrata;
Khare, Soumil;
Sachdev, Divya

Publication type:

Article

Massive Hemothorax by Ruptured Arteriovenous Malformation.

Published in:

Medicina Moderna, 2024, v. 31, n. 3, p. 267, doi. 10.31689/rmm.2024.31.3.267

By:

CADAR, Genoveva;
RADU, Otilia

Publication type:

Article

Hereditary hemorrhagic telangiectasia and health-related quality of life: a qualitative investigation.

Published in:

2020

By:

Martinent, Guillaume;
Carrot, Manon;
Chirac, Anne;
Dupuis-Girod, Sophie;
Fargeton, Anne-Emmanuelle;
Blois Da Conceição, Stéphanie;
Fourdrinoy, Sylvie

Publication type:

journal article

Allogeneic hematopoietic stem cell transplantation for acute lymphoblastic leukemia with accompanying hereditary hemorrhagic telangiectasia.

Published in:

2024

By:

Habraszka, Daniel;
Gawęda, Szymon;
Spałek, Adrianna;
Helbig, Grzegorz

Publication type:

Case Study

Application of contrast-enhanced ultrasound in hemothorax of hereditary hemorrhagic telangiectasia: A case report and literature review.

Published in:

2023

By:

Chen, Jie;
Zhang, Bo

Publication type:

Case Study

TIMolol nasal spray as a treatment for epistaxis in hereditary hemorrhagic telangiectasia (HHT) – Study protocol of the prospective, randomized, double-blind, controlled cross-over TIM-HHT trial.

Published in:

Clinical Hemorheology & Microcirculation, 2022, v. 80, n. 3, p. 307, doi. 10.3233/CH-211253

By:

Andorfer, K.E.C.;
Seebauer, C.T.;
Koller, M.;
Zeman, F.;
Berneburg, M.;
Fischer, R.;
Vielsmeier, V.;
Bohr, C.;
Kühnel, T.S.

Publication type:

Article

High Rates of Bleeding Complications among Hospitalized Patients with Hereditary Hemorrhagic Telangiectasia in the United States.

Published in:

2016

By:

Brinjikji, Waleed;
Wood, Christopher P.;
Lanzino, Giuseppe;
Cloft, Harry J.;
Misra, Sanjay;
Kallmes, David F.;
Kamath, Patrick;
Pruthi, Rajiv K.;
Krowka, Michael J.;
Swanson, Karen L.;
Iyer, Vivek N.

Publication type:

journal article

Hereditary hemorrhagic telangiectasia: First demonstration of a founder effect in Italy; the ACVRL1 c.289_294del variant originated in the country of Bergamo 200 years ago.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 8, p. 1, doi. 10.1002/mgg3.1972

By:

Sbalchiero, Anna;
Abu Hweij, Yasmin;
Mazza, Tommaso;
Buscarini, Elisabetta;
Scotti, Claudia;
Pagella, Fabio;
Manfredi, Guido;
Matti, Elina;
Spinozzi, Giuseppe;
Olivieri, Carla

Publication type:

Article

Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an "HHT‐like" syndrome in children.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 12, p. 1, doi. 10.1002/mgg3.1685

By:

Hodgson, Joshua;
Ruiz‐Llorente, Lidia;
McDonald, Jamie;
Quarrell, Oliver;
Ugonna, Kelechi;
Bentham, James;
Mason, Rebecca;
Martin, Jennifer;
Moore, David;
Bergstrom, Katie;
Bayrak‐Toydemir, Pinar;
Wooderchak‐Donahue, Whitney;
Morrell, Nicholas W.;
Condliffe, Robin;
Bernabeu, Carmelo;
Upton, Paul D.

Publication type:

Article

Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 11, p. 1, doi. 10.1002/mgg3.1498

By:

Aagaard, Katrine S.;
Brusgaard, Klaus;
Miceikaite, Ieva;
Larsen, Martin J.;
Kjeldsen, Anette D.;
Lester, Emilie B.;
Ousager, Lilian B.;
Tørring, Pernille M.

Publication type:

Article

Variant analysis in Chinese families with hereditary hemorrhagic telangiectasia.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.893

By:

Zhao, Yali;
Zhang, Yuan;
Wang, Xiangdong;
Zhang, Luo

Publication type:

Article

Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia.

Published in:

Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 3, p. 350, doi. 10.1002/mgg3.377

By:

Pawlikowska, Ludmila;
Nelson, Jeffrey;
Guo, Diana E.;
McCulloch, Charles E.;
Lawton, Michael T.;
Kim, Helen;
Faughnan, Marie E.

Publication type:

Article

<italic>ENG</italic> mutational mosaicism in a family with hereditary hemorrhagic telangiectasia.

Published in:

Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 1, p. 121, doi. 10.1002/mgg3.361

By:

Tørring, Pernille M.;
Kjeldsen, Anette D.;
Ousager, Lilian Bomme;
Brusgaard, Klaus

Publication type:

Article

EP10.10: Large fetal pulmonary arteriovenous malformation with severe cardiomegaly and favourable postnatal outcome.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 237, doi. 10.1002/uog.19939

By:

Guerra, F.A.;
Vogt, S.;
Garcia‐Huidobro, T.;
Olate, A.;
Solis, N.;
Vega, A.;
Ferrand, P.;
Gajardo, M.;
Rodriguez, J.G.

Publication type:

Article

Loss-of-Function in SMAD4 Might Not Be Critical for Human Natural Killer Cell Responsiveness to TGF-β.

Published in:

Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00904

By:

Healy, Lachlan P.;
Rossi, Gustavo R.;
Rautela, Jai;
Slade, Charlotte A.;
Huntington, Nicholas D.;
Winship, Ingrid M.;
Souza-Fonseca-Guimaraes, Fernando

Publication type:

Article

Unusual Cause of Persistent Epistaxis with Severe Anemia in a Child.

Published in:

2022

By:

Zemene, Yilkal;
Hailu, Tadele;
Wiedermann, Josh

Publication type:

Case Study

A Novel SMAD4 Mutation Causing Severe Juvenile Polyposis Syndrome with Protein Losing Enteropathy, Immunodeficiency, and Hereditary Haemorrhagic Telangiectasia.

Published in:

Case Reports in Gastrointestinal Medicine, 2015, v. 2015, p. 1, doi. 10.1155/2015/140616

By:

Johansson, Joel;
Sahin, Christofer;
Pestoff, Rebecka;
Ignatova, Simone;
Forsberg, Pia;
Edsjö, Anders;
Ekstedt, Mattias;
Stenmark Askmalm, Marie

Publication type:

Article

Medical Imaging Quiz - Case 73.

Published in:

Archives of Hellenic Medicine / Arheia Ellenikes Iatrikes, 2023, v. 40, n. 3, p. 281

By:

Botsa, E.;
Thanou, I.;
Bompou, M.;
Thanos, L.

Publication type:

Article

Medical Imaging Quiz – Case 73.

Published in:

Archives of Hellenic Medicine / Arheia Ellenikes Iatrikes, 2023, v. 40, n. 2, p. 281

By:

Botsa, E.;
Thanou, I.;
Bompou, M.;
Thanos, L.

Publication type:

Article

Medical Imaging Quiz – Case 56.

Published in:

Archives of Hellenic Medicine / Arheia Ellenikes Iatrikes, 2019, v. 36, n. 5, p. 711

By:

Botsa, E.;
Thanou, I.;
Barmpouti, E.;
Antoniadi, K.;
Thanos, L.

Publication type:

Article

Ασυνήθεις αγγειακές παθήσεις του ήπατος.

Published in:

Archives of Hellenic Medicine / Arheia Ellenikes Iatrikes, 2018, v. 35, n. 6, p. 729

By:

Μάνη, H.;
Βασίλιεβα, Λ.;
Ντουράκης, Σ. Π.

Publication type:

Article

V‐Y advancement flap for the repair of localized cutaneous defects following nasal closure in severe hereditary hemorrhagic telangiectasia.

Published in:

International Forum of Allergy & Rhinology, 2024, v. 14, n. 12, p. 1961, doi. 10.1002/alr.23415

By:

Jama, Guled M.;
Gane, Simon

Publication type:

Article

Reply to: "Intralesional cidofovir injections for the treatment of multifocal exophytic sinonasal papilloma": The utility of topical cidofovir.

Published in:

International Forum of Allergy & Rhinology, 2024, v. 14, n. 9, p. 1543, doi. 10.1002/alr.23436

By:

Chatelet, Florian;
Vinciguerra, Alessandro;
Marc, Morgane;
Verillaud, Benjamin;
Herman, Philippe

Publication type:

Article

Severe epistaxis after posterior nasal nerve ablation requiring surgical intervention: A multi‐center case series.

Published in:

International Forum of Allergy & Rhinology, 2024, v. 14, n. 7, p. 1269, doi. 10.1002/alr.23339

By:

Khan, Najm S.;
Yoshiyasu, Yuki;
Wang, Brian S.;
Khoudari, Antoine;
Clerico, Dean M.;
King, Jackson M.;
Steele, Toby O.;
Dhanda, Aatin K.;
Takashima, Masayoshi;
Ahmed, Omar G.

Publication type:

Article

Severe unilateral refractory epistaxis arising from the septal branch of the anterior ethmoid artery.

Published in:

International Forum of Allergy & Rhinology, 2024, v. 14, n. 6, p. 1135, doi. 10.1002/alr.23330

By:

Nguyen, Theodore V.;
Bitner, Benjamin F.;
Hong, Ellen M.;
Pang, Jonathan C.;
Meller, Leo Li Tang;
Nguyen, Cecilia;
Kuan, Edward C.

Publication type:

Article

Exploring effects of atmospheric conditions in hereditary hemorrhagic telangiectasia.

Published in:

International Forum of Allergy & Rhinology, 2023, v. 13, n. 12, p. 2172, doi. 10.1002/alr.23183

By:

Yusuf, Hamzah M.;
Rasheed, Amna;
Hetts, Steven;
Kim, Helen;
Loftus, Patricia;
Conrad, Miles

Publication type:

Article

Injection of cyanoacrylate glue for hereditary hemorrhagic telangiectasia.

Published in:

International Forum of Allergy & Rhinology, 2022, v. 12, n. 11, p. 1439, doi. 10.1002/alr.23017

By:

Anciaux, Maeva;
Lebreton, Jean‐Pascal;
Tonnerre, Denis;
Leclerc, Justine;
Dufour, Xavier;
Carsuzaa, Florent

Publication type:

Article

Randomized, controlled, double‐blinded clinical trial of effect of bevacizumab injection in management of epistaxis in hereditary hemorrhagic telangiectasia patients undergoing surgical cauterization.

Published in:

International Forum of Allergy & Rhinology, 2022, v. 12, n. 8, p. 1034, doi. 10.1002/alr.22961

By:

Khanwalkar, Ashoke R.;
Rathor, Aakanksha;
Read, Amelia K.;
Paknezhad, Hassan;
Ma, Yifei;
Hwang, Peter H.

Publication type:

Article

Epistaxis grading in Osler's disease: comparison of comprehensive scores with detailed bleeding diaries.

Published in:

International Forum of Allergy & Rhinology, 2017, v. 7, n. 3, p. 293, doi. 10.1002/alr.21867

By:

Parzefall, Thomas;
Wolf, Axel;
Frei, Klemens;
Kaider, Alexandra;
Riss, Dominik

Publication type:

Article

Fluorescein-guided intraoperative endoscopy in patients with hereditary hemorrhagic telangiectasia: first impressions.

Published in:

International Forum of Allergy & Rhinology, 2017, v. 7, n. 3, p. 300, doi. 10.1002/alr.21880

By:

Pagella, Fabio;
Pusateri, Alessandro;
Zaccari, Dario;
Bongetta, Daniele;
Zoia, Cesare;
Spinozzi, Giuseppe;
Olivieri, Carla;
Matti, Elina

Publication type:

Article

Treatment of severe refractory epistaxis in hereditary hemorrhagic telangiectasia using a two-flap nasal closure method.

Published in:

International Forum of Allergy & Rhinology, 2016, v. 6, n. 5, p. 544, doi. 10.1002/alr.21703

By:

Timmins, Benjamin H.;
Hunter, Benjamin N.;
Wilson, Kevin F.;
Ward, P. Daniel

Publication type:

Article

Intravenous bevacizumab for complications of hereditary hemorrhagic telangiectasia: a review of the literature.

Published in:

International Forum of Allergy & Rhinology, 2015, v. 5, n. 11, p. 1042, doi. 10.1002/alr.21587

By:

Arizmendez, Natalia P.;
Rudmik, Luke;
Poetker, David M.

Publication type:

Article

The effects of epistaxis on health-related quality of life in patients with hereditary hemorrhagic telangiectasia.

Published in:

International Forum of Allergy & Rhinology, 2014, v. 4, n. 11, p. 921, doi. 10.1002/alr.21374

By:

Merlo, Christian A.;
Yin, Linda X.;
Hoag, Jeffrey B.;
Mitchell, Sally E.;
Reh, Douglas D.

Publication type:

Article

Editorial.

Published in:

2014

By:

Ferguson, BJ

Publication type:

Editorial

Familial skin lesions and bleeding presenting with anaemia in an elderly female.

Published in:

2013

By:

Rao, K. Satyanarayana;
Rao, D. Srinivasa;
Seshaiah, K. V.;
Deepak, Yadlapalli C.

Publication type:

Journal Article

Family History of Headache and Epistaxis Associated with Ischemic Stroke.

Published in:

Turkish Journal of Neurology / Turk Noroloji Dergisi, 2020, v. 26, n. 4, p. 334, doi. 10.4274/tnd.2020.48902

By:

Eu Jene Choi;
Dong Goo Lee;
Do-Hyung Kim;
Sang Hyun Jang

Publication type:

Article

Diagnosis and management of gastrointestinal bleeding.

Published in:

1969

By:

Gordon, H. Earl;
Clarke, James S.;
Goldstein, Howard;
Kadell, Barbara;
Ozeran, Robert S.;
Passaro Jr., Edward P.;
Schwabe, Arthur D.;
Gordon, H E;
Clarke, J S;
Goldstein, H;
Kadell, B;
Ozeran, R S;
Passaro, E P Jr;
Schwabe, A D

Publication type:

journal article

Intraretinal and subretinal fluid in exudative nonproliferative macular telangiectasia type 2.

Published in:

2022

By:

Manayath, George J.;
Ninan, Rohan Suresh;
Verghese, Shishir;
Narendran, Venkatapathy

Publication type:

Case Study