Works matching DE "HEREDITARY hemorrhagic telangiectasia"

Results: 756

Gastrointestinal Bleeding in Hereditary Hemorrhagic Telangiectasia Accompanied with Very Severe Thrombocytopenia.

Published in:

2025

By:

Yanbin Wei;
Chuyan Chen;
Peng Li;
Dayong Huang;
Xin Yao

Publication type:

Case Study

Pediatric Pulmonary Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia: Screening, Diagnosis, and Management.

Published in:

Journal of Clinical Medicine, 2025, v. 14, n. 11, p. 3739, doi. 10.3390/jcm14113739

By:

Kaufman, Claire S.;
Nguyen, Minh Anh;
Bezold, Amy;
Chesnutt, Mark S.

Publication type:

Article

Case Report: Multiple cerebral infarctions in a patient with hereditary hemorrhagic telangiectasia following a fall.

Published in:

2025

By:

Gu, Linting;
Chen, Sheng;
Li, Wenwei;
Ye, Fanlong

Publication type:

Case Study

Efficacy of bevacizumab in hereditary hemorrhagic telangiectasia: a systematic review and network meta-analysis.

Published in:

European Archives of Oto-Rhino-Laryngology, 2025, v. 282, n. 6, p. 2821, doi. 10.1007/s00405-024-09177-9

By:

Taha, Amira Mohamed;
Fareed, Areeba;
Elewa, Mandy;
Hasan, Mohammed Tarek;
Elboraay, Toka;
Abouelmagd, Khaled;
Abdeljawad, Marwa Muhammed

Publication type:

Article

Clinical Phenotypes of a Pediatric Cohort with GDF2 -Related Hereditary Hemorrhagic Telangiectasia.

Published in:

Journal of Clinical Medicine, 2025, v. 14, n. 10, p. 3359, doi. 10.3390/jcm14103359

By:

Oliver, Owen;
Britt, Allison D.;
Borst, Alexandra J.;
Goldmuntz, Elizabeth;
Bakeer, Nihal;
Lang, Shih-shan;
Fuller, Stephanie;
Vossough, Arastoo;
Beslow, Lauren A.

Publication type:

Article

Brain arteriovenous malformations.

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2019, v. 76, n. 12, p. 1274, doi. 10.2298/VSP171221014S

By:

Stojanović, Sanja;
Spasić, Aleksandar;
Basta Nikolić, Marijana;
Kostić, Dejan;
Karać, Mirjana;
Turkalj, Ivan

Publication type:

Article

Clinical characteristics of hereditary hemorrhagic telangiectasia - case series and review of the literature.

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2019, v. 76, n. 4, p. 452, doi. 10.2298/VSP170412121P

By:

Popović, Dragan;
Sokić-Milutinović, Aleksandra;
Djuranović, Srđan;
Alempijević, Tamara;
Zgradić, Sanja;
Matović, Vera;
Tončev, Ljubiša;
Lukić, Snežana

Publication type:

Article

Paradoxical Emboli to Artery of Percehron in Hereditary Haemorrhagic Telangiectasia.

Published in:

2021

By:

Aaron, Sanjith;
Mary, John;
Arthur, Anupriya;
Nidugala, Shyamkumar;
Mani, Sunithi;
Prabakhar, A;
Sivadasan, Ajith;
Mathew, Vivek;
Alexander, Mathew;
Nidugala, Shyamkumar Keshava;
Prabakhar, A T

Publication type:

Letter

Paradoxical Embolism in a Case of Hereditary Hemorrhagic Telangiectasia: Case Report with Literature Review.

Published in:

2020

By:

Baby, Neena;
Kunnathuparambil, Sabu;
Varghese, Prasanth;
Kuriakose, Aneesh;
Kunnathuparambil, Sabu George;
Kuriakose, Aneesh Mangalasseril

Publication type:

journal article

A case of delayed-onset hereditary hemorrhagic telangiectasia with a frameshift ENG mutation.

Published in:

2019

By:

Akagawa, Hiroyuki;
Onda, Hideaki;
Nomura, Shunsuke;
Shinohara, Toyoaki;
Kasuya, Hidetoshi

Publication type:

Case Study

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

Gastrointestinal Bleeding in Patients with Hereditary Hemorrhagic Telangiectasia: Risk Factors and Endoscopic Findings.

Published in:

Journal of Clinical Medicine, 2020, v. 9, n. 1, p. 82, doi. 10.3390/jcm9010082

By:

Mora-Luján, José María;
Iriarte, Adriana;
Alba, Esther;
Sánchez-Corral, Miguel Ángel;
Berrozpe, Ana;
Cerdà, Pau;
Cruellas, Francesc;
Ribas, Jesús;
Castellote, Jose;
Riera-Mestre, Antoni

Publication type:

Article

Endovascular Management of Massive Hemoptysis Secondary to Systemic Collaterals in Previously Treated Pulmonary Arteriovenous Malformation.

Published in:

Vascular & Endovascular Surgery, 2019, v. 53, n. 8, p. 674, doi. 10.1177/1538574419870433

By:

Gorsi, Ujjwal;
Bansal, Akash;
Jugpal, Tejeshwar Singh;
Chaluvashetty, Sreedhara Bettadahally;
Sandhu, Manavjit Singh

Publication type:

Article

Risk factors and management outcomes in epistaxis: a tertiary centre experience.

Published in:

ANZ Journal of Surgery, 2023, v. 93, n. 3, p. 555, doi. 10.1111/ans.18179

By:

Hughes, Jed M.;
Teh, Bing Mei;
Hart, Cameron J.;
Gibbs, Harry H.;
Aung, Ar Kar

Publication type:

Article

Improvement in epistaxis management: the experience of a dedicated hereditary haemorrhagic telangiectasia clinic.

Published in:

ANZ Journal of Surgery, 2022, v. 92, n. 3, p. 499, doi. 10.1111/ans.17322

By:

Anning, Rebecca;
Huang, Johnson;
Ronan, Anne;
de Malmanche, Jillian;
Asher, Rebecca;
Low, Tsu‐Hui

Publication type:

Article

Video‐assisted thorascopic lobectomy for pulmonary arteriovenous malformations to prevent cerebral abscess.

Published in:

ANZ Journal of Surgery, 2019, v. 89, n. 10, p. E466, doi. 10.1111/ans.14779

By:

Heitmann, Paul T.;
Chan, Justin C. Y.;
McDonald, Matthew J.;
Worthington, Michael G.

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

Progressive choreodystonia in X‐linked hyper‐IgM immunodeficiency: a rare but recurrent presentation.

Published in:

Annals of Clinical & Translational Neurology, 2022, v. 9, n. 4, p. 577, doi. 10.1002/acn3.51538

By:

Škorvánek, Matej;
Jech, Robert;
Winkelmann, Juliane;
Zech, Michael

Publication type:

Article

Long-term bevacizumab is safe and effective in managing small bowel angioectasias bleeding refractory to conventional treatments: a case report.

Published in:

Gastroenterology Report, 2024, v. 12, p. 1, doi. 10.1093/gastro/goae070

By:

Compare, Debora;
Sgamato, Costantino;
Rocco, Alba;
Minieri, Stefano;
Cinque, Sofia;
Giordano, Flaviana;
Nardone, Gerardo

Publication type:

Article

Small bowel adenocarcinoma arising in a patient with hereditary hemorrhagic telangiectasia: A case report.

Published in:

2016

By:

YUICHIRO YOSHIOKA;
HIROAKI NOZAWA;
JUNICHIRO TANAKA;
TAKESHI NISHIKAWA;
TOSHIAKI TANAKA;
TOMOMICHI KIYOMATSU;
KAZUSHIGE KAWAI;
KEISUKE HATA;
SHINSUKE KAZAMA;
HIRONORI YAMAGUCHI;
SOICHIRO ISHIHARA;
EIJI SUNAMI;
JOJI KITAYAMA;
TOSHIAKI WATANABE

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

Hypoxia-Inducible Factor–Prolyl Hydroxylase Inhibitor Improves Leukocyte Energy Metabolism in Hereditary Hemorrhagic Telangiectasia.

Published in:

Life (2075-1729), 2023, v. 13, n. 8, p. 1708, doi. 10.3390/life13081708

By:

Schild, Yves;
Bosserhoff, Jonah;
Droege, Freya;
Littwitz-Salomon, Elisabeth;
Fandrey, Joachim;
Wrobeln, Anna

Publication type:

Article

Cerebral hemorrhage caused by hereditary hemorrhagic telangiectasia with ACVRL1 gene mutation: one case report.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2022, v. 22, n. 10, p. 887, doi. 10.3969/j.issn.1672-6731.2022.10.009

By:

JIA Jun-li;
WANG Qin-zhou;
DAI Ting-jun;
CUI Yi;
XU Guang-run

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

Optimal management of hereditary hemorrhagic telangiectasia.

Published in:

Journal of Blood Medicine, 2014, v. 5, p. 191, doi. 10.2147/JBM.S45295

By:

Garg, Neetika;
Khunger, Monica;
Gupta, Arjun;
Kumar, Nilay

Publication type:

Article

Strange Case of a Sojourn in Saranac.

Published in:

2021

By:

Chorba, Terence

Publication type:

Obituary

Telangiectasia of the lower limbs in a 40-year-old man.

Published in:

Clinical & Experimental Dermatology, 2024, v. 49, n. 10, p. 1265, doi. 10.1093/ced/llae171

By:

Damani, Namiz;
Gunavardhan, Anu;
Waas, Rachel L V

Publication type:

Article

Can Hemorrhagic Stroke Genetics Help Forensic Diagnosis in Pediatric Age (<5 Years Old)?

Published in:

Genes, 2024, v. 15, n. 5, p. 618, doi. 10.3390/genes15050618

By:

Treves, Biancamaria;
Sonnini, Elena;
La Russa, Raffaele;
Del Duca, Fabio;
Ghamlouch, Alessandro;
De Matteis, Alessandra;
Trignano, Claudia;
Marchal, Juan Antonio;
Carrillo, Esmeralda;
Napoletano, Gabriele;
Maiese, Aniello

Publication type:

Article

The ENG/VEGFα Pathway Is Likely Affected by a Nonsense Variant of Endoglin (ENG)/CD105, Causing Hereditary Hemorrhagic Telangiectasia Type 1 (HHT1) in a Chinese Family.

Published in:

Genes, 2024, v. 15, n. 3, p. 304, doi. 10.3390/genes15030304

By:

Liu, Kemeng;
Fu, Jiewen;
Guo, Kan;
Maghsoudloo, Mazaher;
Cheng, Jingliang;
Fu, Junjiang

Publication type:

Article

Improving Hereditary Hemorrhagic Telangiectasia Molecular Diagnosis: A Referral Center Experience.

Published in:

Genes, 2023, v. 14, n. 3, p. 772, doi. 10.3390/genes14030772

By:

Aguilera, Cinthia;
Padró-Miquel, Ariadna;
Esteve-Garcia, Anna;
Cerdà, Pau;
Torres-Iglesias, Raquel;
Llecha, Núria;
Riera-Mestre, Antoni

Publication type:

Article

MicroRNA-132-3p, Downregulated in Myeloid Angiogenic Cells from Hereditary Hemorrhagic Telangiectasia Patients, Is Enriched in the TGFβ and PI3K/AKT Signalling Pathways.

Published in:

Genes, 2022, v. 13, n. 4, p. 665, doi. 10.3390/genes13040665

By:

Cannavicci, Anthony;
Zhang, Qiuwang;
Faughnan, Marie E.;
Kutryk, Michael J. B.

Publication type:

Article

Hereditary Hemorrhagic Telangiectasia in Pediatric Age: Focus on Genetics and Diagnosis.

Published in:

Pediatric Reports, 2023, v. 15, n. 1, p. 129, doi. 10.3390/pediatric15010011

By:

Danesino, Cesare;
Cantarini, Claudia;
Olivieri, Carla

Publication type:

Article

Hereditary Hemorrhagic Telangiectasia.

Published in:

2015

By:

Kamath, Nagesh;
Bhatia, Sumit;
Singh, Harneet;
Shetty, Anurag;
Shetty, Shiran

Publication type:

Case Study

Unilateral Nevoid Telangiectasia in a Healthy Man.

Published in:

Case Reports in Dermatology, 2021, v. 13, n. 2, p. 330, doi. 10.1159/000514941

By:

Küçük, Kirley;
Bourlond, Florence;
Votquenne, Nicolas;
Benhadou, Farida

Publication type:

Article

Nationwide Awareness Campaign and Call for Dental Screening for Hereditary Hemorrhagic Telangiectasia in Germany.

Published in:

International Journal of Dentistry, 2023, p. 1, doi. 10.1155/2023/8737727

By:

Geisthoff, Urban W.;
Hölzle, Frank;
Stuck, Boris A.;
Jackowski, Joachim;
Hand Goetz, Catherine;
Grabowski, Christina;
Droege, Freya

Publication type:

Article

Elective left pulmonary artery embolisation for pulmonary arteriovenous malformations secondary to cavopulmonary anastomoses not responsive to heart transplantation: a case report.

Published in:

2019

By:

Bebawy, Caroline M.;
Gordon, Brent M.;
Bock, Matthew J.

Publication type:

journal article

Multidisciplinary coordinated care of hereditary hemorrhagic telangiectasia (Osler–Weber–Rendu disease).

Published in:

Vascular Medicine, 2023, v. 28, n. 2, p. 153, doi. 10.1177/1358863X231151731

By:

Alkhalid, Yasmine;
Darji, Zeena;
Shenkar, Robert;
Clancy, Marianne;
Dyamenahalli, Umesh;
Awad, Issam A

Publication type:

Article

Screening for pulmonary and brain vascular malformations is the North American standard of care for patients with hereditary hemorrhagic telangiectasia (HHT): A survey of HHT Centers of Excellence.

Published in:

Vascular Medicine, 2021, v. 26, n. 1, p. 53, doi. 10.1177/1358863X20974452

By:

Kilian, Alexandra;
Clancy, Marianne S;
Olitsky, Scott;
Gossage, James R;
Faughnan, Marie E

Publication type:

Article

Prevalence and diagnostic value of nail fold capillary microscopy in hereditary hemorrhagic telangiectasia: A retrospective study.

Published in:

Vascular Medicine, 2020, v. 25, n. 4, p. 341, doi. 10.1177/1358863X20910479

By:

Kroon, Steven;
Vorselaars, Veronique MM;
Hosman, Anna E;
Post, Martijn C;
Snijder, Repke J;
Mager, Johannes J

Publication type:

Article

Cutaneous collagenous vasculopathy: Differential diagnosis of primary telangiectasia as generalized essential telangiectasia, hereditary hemorrhagic telangiectasia, and hereditary benign telangiectasia.

Published in:

2019

By:

Jaquinandi, Vincent;
Stivalet, Olivier;
Grabas, Marie

Publication type:

Case Study

Early Signs of Cardiovascular Senescence in a Patient with Hereditary Hemorrhagic Telangiectasia.

Published in:

International Journal of Gerontology, 2023, v. 17, n. 2, p. 141, doi. 10.6890/IJGE.202304_17(2).0012

By:

Yen-Yu Liu;
Ta-Chuan Hung;
Chun-Wei Lee;
Yih-JerWu

Publication type:

Article

Cerebrovascular Events Secondary to Pulmonary Arteriovenous Malformation Based on Genetic Heterogeneity.

Published in:

Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2017, v. 54, n. 3, p. 286, doi. 10.5152/npa.2016.16997

By:

ÇELİK, Güner;
YURDAKUL, Hüseyin;
YILDIRIM, Erkan

Publication type:

Article

Identification of two distinct hereditary hemorrhagic telangiectasia patient subsets with different hepatic perfusion properties by combination of contrast-enhanced ultrasound (CEUS) with perfusion imaging quantification.

Published in:

PLoS ONE, 2019, v. 14, n. 4, p. 1, doi. 10.1371/journal.pone.0215178

By:

Schelker, Roland C.;
Andorfer, Kornelia;
Putz, Franz;
Herr, Wolfgang;
Jung, Ernst-Michael

Publication type:

Article

Severe pulmonary arterial hypertension in a patient with hereditary hemorrhagic telangiectasia and multiple pulmonary and hepatic arteriovenous malformations.

Published in:

Annals of Pediatric Cardiology, 2022, v. 15, n. 1, p. 73, doi. 10.4103/apc.apc_256_20

By:

Aramalla, Sunitha;
Bhyravavajhala, Srinivas;
Vanaparty, Bharathi;
Narayanan, Ramakrishna;
Yerram, Sreekanth

Publication type:

Article

PREVALENCE OF HEREDITARY HEMORRHAGIC TELANGIECTASIA IN A MEDICAL CARE PROGRAM ORGANIZATION IN BUENOS AIRES, ARGENTINA.

Published in:

Medicina (Buenos Aires), 2024, v. 84, n. 2, p. 221

By:

Serra, Marcelo M.;
Papi, Melina;
Serrano, Candelaria

Publication type:

Article

Examining the Prevalence of Previously Recorded Phenotypically Related Diagnoses Among Fee-for-Service Medicare Enrollees Newly Diagnosed with Mendelian Conditions.

Published in:

2022

By:

Weeks, William B.;
Huynh, Grace;
Cao, Stacey Y.;
Smith, Jeremy;
Bangur, Chaitanya;
Weinstein, James N.

Publication type:

Letter

Embolic Stroke Caused by Hereditary Hemorrhagic Telangiectasia with Pulmonary Arteriovenous Malformation.

Published in:

JGIM: Journal of General Internal Medicine, 2020, v. 35, n. 12, p. 3707, doi. 10.1007/s11606-020-06126-0

By:

Sueda, Keishiro;
Horiuchi, Masao;
Funakoshi, Hiraku;
Hiraoka, Eiji

Publication type:

Article

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu syndrome).

Published in:

2017

By:

Santos, Michael;
Santos, Michael A

Publication type:

journal article

Hereditary Hemorrhagic Telangiectasia Management.

Published in:

Radiologic Technology, 2017, v. 88, n. 3, p. 277

By:

Peterson, Jeffrey

Publication type:

Article