Research & Literature

Hereditary hemorrhagic telangiectasia.

Chung MG

Handbook of clinical neurology 2015; (132()):185-97.

Nasal closure for the treatment of epistaxis secondary to hereditary hemorrhagic telangiectasia.

Sena Esteves S, Cardoso C, Silva A, et al.

Acta otorrinolaringologica espanola 2016; (67(6)):345-348 doi:10.1016/j.otorri.2015.12.002.

Review of diagnostic uses of shunt fraction quantification with technetium-99m macroaggregated albumin perfusion scan as illustrated by a case of Osler-Weber-Rendu syndrome.

Chokkappan K, Kannivelu A, Srinivasan S, Babut SB

Annals of thoracic medicine 2016; (11(2)):155-60 doi:10.4103/1817-1737.180020.

[Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): clinical manifestations and multidisciplinary management].

Frigerio C, Aebischer N, Baud D, et al.

Revue medicale suisse 2016; (12(517)):896-901.

Prevalence and characteristics of brain arteriovenous malformations in hereditary hemorrhagic telangiectasia: a systematic review and meta-analysis.

Brinjikji W, Iyer VN, Wood CP, Lanzino G

Journal of neurosurgery 2017; (127(2)):302-310 doi:10.3171/2016.7.JNS16847.

Abdominal vascular syndromes: characteristic imaging findings.

Cardarelli-Leite L, Velloni FG, Salvadori PS, et al.

Radiologia brasileira 2016; (49(4)):257-263 doi:10.1590/0100-3984.2015.0136.

Liver Findings in Patients with Hereditary Hemorrhagic Telangiectasia.

Song W, Zhao D, Li H, et al.

Iranian journal of radiology : a quarterly journal published by the Iranian Radiological Society 2016; (13(4)):e31116 doi:10.5812/iranjradiol.31116.

Hereditary Hemorrhagic Telangiectasia and Myocardial Infarction.

Martínez-Quintana E, Rodríguez-González F, Gopar-Gopar S

The International journal of angiology : official publication of the International College of Angiology, Inc 2016; (25(5)):e81-e83 doi:10.1055/s-0035-1551795.

Bevacizumab and gastrointestinal bleeding in hereditary hemorrhagic telangiectasia.

Ou G, Galorport C, Enns R

World journal of gastrointestinal surgery 2016; (8(12)):792-795 doi:10.4240/wjgs.v8.i12.792.

High-Output Heart Failure Contributing to Recurrent Epistaxis Kiesselbach Area Syndrome in a Patient With Hereditary Hemorrhagic Telangiectasia.

Bhattad VB, Bowman JN, Panchal HB, Paul TK

Journal of investigative medicine high impact case reports 2017; (5(1)):2324709617692833 doi:10.1177/2324709617692833.

Gastrointestinal Manifestations of Hereditary Hemorrhagic Telangiectasia (HHT): A Systematic Review of the Literature.

Jackson SB, Villano NP, Benhammou JN, et al.

Digestive diseases and sciences 2017; (62(10)):2623-2630 doi:10.1007/s10620-017-4719-3.

Hereditary hemorrhagic telangiectasia with bilateral pulmonary vascular malformations: A case report.

Vojnosanitetski pregled 2016; (73(10)):956-60 doi:10.2298/VSP150515094L.

Anesthesia management of a patient with a femoral neck fracture and hered-itary hemorrhagic telangiectasia.

Tsoleridis T, Galanou L, Tsoleridis S

Hippokratia 2016; (20(4)):303-305.

Congestive cirrhosis in Osler-Weber-Rendu syndrome: A rare case report.

Leitão P, Carvalho A, Guerra C, et al.

Radiology case reports 2018; (13(1)):51-54 doi:10.1016/j.radcr.2017.10.011.

Bevacizumab for Refractory Gastrointestinal Bleeding in Rendu-Osler-Weber Disease.

Bernardes C, Santos S, Loureiro R, et al.

GE Portuguese journal of gastroenterology 2018; (25(2)):91-95 doi:10.1159/000481289.

Hereditary hemorrhagic telangiectasia: diagnosis and management from the hematologist's perspective.

Kritharis A, Al-Samkari H, Kuter DJ

Haematologica 2018; (103(9)):1433-1443 doi:10.3324/haematol.2018.193003.

SMAD4 Prevents Flow Induced Arteriovenous Malformations by Inhibiting Casein Kinase 2.

Ola R, Künzel SH, Zhang F, et al.

Circulation 2018; (138(21)):2379-2394 doi:10.1161/CIRCULATIONAHA.118.033842.

Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations: clinical aspects.

Meier NM, Foster ML, Battaile JT

Cardiovascular diagnosis and therapy 2018; (8(3)):316-324 doi:10.21037/cdt.2017.12.07.

Osler-Weber-Rendu Syndrome in Relation to Dermatology.

Orizaga-Y-Quiroga TL, Villarreal-Martínez A, Jaramillo-Moreno G, Ocampo-Candiani J

Actas dermo-sifiliograficas 2019; (110(7)):526-532 doi:10.1016/j.ad.2018.11.007.

Hereditary Hemorrhagic Telangiectasia: A Rare Cause of Anemia.

Jan W, Tameez Ud Din A, Chaudhary FMD, et al.

Cureus 2019; (11(8)):e5349 doi:10.7759/cureus.5349.

Hereditary hemorrhagic telangiectasia of liver: Pathophysiology with role of radiology in diagnosis and treatment.

Viyannan M, Balalakshmoji D, Leelakrishnan V

The Indian journal of radiology & imaging 2020; (30(1)):98-101 doi:10.4103/ijri.IJRI_367_19.

Management of Gastrointestinal Bleeding in Rendu-Osler Disease.

Tortora A, Marmo C, Gasbarrini A, et al.

Reviews on recent clinical trials 2020; (15(4)):321-327 doi:10.2174/1574887115666200603160033.

Pulmonary arteriovenous malformation in a pediatric patient with epistaxis and hypoxemia.

England RW, Weiss CR

Radiology case reports 2020; (15(10)):1759-1763 doi:10.1016/j.radcr.2020.07.026.

Differential Expression of Circulating Plasma miRNA-370 and miRNA-10a from Patients with Hereditary Hemorrhagic Telangiectasia.

Ruiz-Llorente L, Albiñana V, Botella LM, Bernabeu C

Journal of clinical medicine 2020; (9(9)) doi:10.3390/jcm9092855.

[Diagnostic Criteria and Treatment of Hereditary Hemorrhagic Telangiectasia].

Seebauer CT, Kuehnel T, Uller W, et al.

Laryngo- rhino- otologie 2020; (99(10)):682-693 doi:10.1055/a-1220-7045.

[Pulmonary arteriovenous shunt - a rare cause of recurrent stroke due to paradoxical embolism].

Belopasova AV, Dobrynina LA, Kalashnikova LA, et al.

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2020; (120(9)):107-113 doi:10.17116/jnevro2020120091107.

Hereditary Hemorrhagic Telangiectasia in a Sudanese Patient.

Elawad OAMA, Albashir AAD, Mirghani Ahmed MM, et al.

Case reports in medicine 2020; (2020()):6395629 doi:10.1155/2020/6395629.

Pulmonary Vascular Complications in Hereditary Hemorrhagic Telangiectasia and the Underlying Pathophysiology.

Bofarid S, Hosman AE, Mager JJ, et al.

International journal of molecular sciences 2021; (22(7)) doi:10.3390/ijms22073471.

Traumatic Pulmonary Arteriovenous Malformation Presenting as Spontaneous Hemothorax.

Azimi-Ghomi O, Ramirez M, Brummund D, et al.

Cureus 2021; (13(6)):e16072 doi:10.7759/cureus.16072.

[Epistaxis-overview and current aspects].

Thangavelu K, Köhnlein S, Eivazi B, et al.

HNO 2021; (69(11)):931-942 doi:10.1007/s00106-021-01110-4.

A Rare Case of Upper Gastrointestinal Bleeding: Osler-Weber-Rendu Syndrome.

Jargielo A, Rycyk A, Kasztelan-Szczerbinska B, Cichoz-Lach H

Medicina (Kaunas, Lithuania) 2022; (58(3)) doi:10.3390/medicina58030333.

Hereditary hemorrhagic telangiectasia (OslerWeberRendu syndrome) - Part II. Pharmacological therapy and international guidelines for the therapy 2020.

Adam Z, Brančiková D, Romanová G, et al.

Vnitrni lekarstvi 2021; (67(7)):419-424.

Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) Part I. Pathophysiology, clinical symptoms and recommend screening for vascular malformations.

Adam Z, Brančiková D, Romanová G, et al.

Vnitrni lekarstvi 2021; (67(6)):339-344.

A Rare Case of Hereditary Hemorrhagic Telangiectasia: A Case Report.

Khan AR, Waqar S, Wazir MH, Arif A

Cureus 2022; (14(4)):e24517 doi:10.7759/cureus.24517.

Rendú Osler Weber Syndrome; case report.

García Córdova OM, Pérez Morales TC, Barón Hernández VADP, Cuéllar JSS

Radiology case reports 2022; (17(9)):3025-3030 doi:10.1016/j.radcr.2022.05.088.

Not Your Typical Nosebleed: A Case Report and Personal Account of a Patient With Osler-Weber-Rendu Syndrome.

Zhitnitsky M, Gilde J

The Permanente journal 2022; (26(2)):138-143 doi:10.7812/TPP/21.137.

Hepatic involvement in hereditary hemorrhagic telangiectasia mimicking focal nodular hyperplasia.

Alvarenga Fernandes D, de Fátima Ferreira Santana Boin I, Batista Araújo Filho JA, et al.

Revista espanola de enfermedades digestivas 2023; (115(3)):152-154 doi:10.17235/reed.2022.9069/2022.

Case report: Diagnosis of hereditary hemorrhagic telangiectasia (Osler Weber Rendu Syndrome) in a 23-year-old male presented with anemia and thrombocytopenia and its response to bevacizumab.

Yunus H, Amin S, Haq FU, et al.

Frontiers in medicine 2022; (9()):1001695 doi:10.3389/fmed.2022.1001695.

Hereditary Hemorrhagic Telangiectasia-A Case Series Experience from a Liver Transplant Center in Romania.

Pavel C, Cabel T, Dinuță D, et al.

Diagnostics (Basel, Switzerland) 2022; (12(12)) doi:10.3390/diagnostics12122959.

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

Alkhalid Y, Darji Z, Shenkar R, et al.

Vascular medicine (London, England) 2023; (28(2)):153-165 doi:10.1177/1358863X231151731.

[Hereditary hemorrhagic telangiectasia].

Parrot A, Barral M, Amiot X, et al.

Revue des maladies respiratoires 2023; (40(5)):391-405 doi:10.1016/j.rmr.2023.02.007.

Pulmonary Arteriovenous Malformation in a Patient with Suspected Hereditary Hemorrhagic Telangiectasia: A Case Report.

Zuabi N, Thompson SR, Lucas A, Wray A

Journal of education & teaching in emergency medicine 2021; (6(1)):V9-V11 doi:10.21980/J8M353.

ROTH SPOTS IN A RENDU-OSLER-WEBER SYNDROME.

Ferreira de Moura T, Servettaz A, Henry A, et al.

Retinal cases & brief reports 2024; (18(6)):712-714 doi:10.1097/ICB.0000000000001479.

Post-Partum Hemorrhage (PPH) as Implicated by Osler-Weber-Rendu Syndrome.

Powers P, Combs S

Cureus 2023; (15(8)):e43388 doi:10.7759/cureus.43388.

Pulmonary Hypertension Due to High-Output Heart Failure: Hereditary Hemorrhagic Telangiectasia.

Kılıçkıran Avcı B, Soysal AU, Cerme E, et al.

Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2023; (51(7)):493-497 doi:10.5543/tkda.2023.13614.

Genome sequencing identify chromosome 9 inversions disrupting ENG in 2 unrelated HHT families.

Tusseau M, Eyries M, Chatron N, et al.

European journal of medical genetics 2024; (68()):104919 doi:10.1016/j.ejmg.2024.104919.

Hereditary Hemorrhagic Telangiectasia (Osler's Disease): Systemic, Interdisciplinary, Relatively Common—and Often Missed.

Geisthoff UW, Mahnken AH, Denzer UW, et al.

Deutsches Arzteblatt international 2024; (121(18)):601-607.

Osler-Weber-Rendu Syndrome as a Rare Cause of Liver Cirrhosis.

Tuna C, Frazão T, Garcês Soares S, et al.

Cureus 2024; (16(9)):e69869 doi:10.7759/cureus.69869.

A case of fatal cerebral air embolism in a patient with Osler-Weber-Rendu Disease.

Mahaux A, Scrivener M, Ferrão-Santos S, et al.

Acta neurologica Belgica 2025; (125(3)):865-867 doi:10.1007/s13760-025-02726-x.

Updates on the Pathogenesis and Therapeutic Approaches for Hereditary Hemorrhagic Telangiectasia.

Yadav A, Shabani Z, Dhaliwal JK, et al.

Current vascular pharmacology 2025; (23(5)):339-351 doi:10.2174/0115701611346772250122111526.

Combined Fascia Iliaca and Sacral Erector Spinae Plane Blocks for Hip Surgery in Hereditary Hemorrhagic Telangiectasia: A Case Report.

Marrone F, Paventi S, Tomei M, et al.

A&A practice 2025; (19(3)):e01950 doi:10.1213/XAA.0000000000001950.

Hereditary haemorrhagic telangiectasia in skin of colour: a dermoscopic, histopathological and radiological approach.

Singh S, Choudhary S, Srivastava A, et al.

BMJ case reports 2025; (18(5)) doi:10.1136/bcr-2025-265940.

Osler-Weber-Rendu Syndrome: A Case Report and Brief Literature Review.

Schild L, Boden E

South Dakota medicine : the journal of the South Dakota State Medical Association 2025; (78(4)):166-168.

Complications of liver vascular malformations in hereditary hemorrhagic telangiectasia during pregnancy.

Lucà M, Cerrone A, Tosetti G, et al.

European journal of obstetrics, gynecology, and reproductive biology 2025; (315()):114733 doi:10.1016/j.ejogrb.2025.114733.

Hereditary Hemorrhagic telangiectasia: a rare familial case with delayed diagnosis despite decades of recurrent bleeding.

Rahi AV, Kumar A, Singh J, et al.

Oxford medical case reports 2025; (2025(9)):omaf189 doi:10.1093/omcr/omaf189.

Epistaxis Prevention, Treatment, and Future Perspectives for Hereditary Hemorrhagic Telangiectasia.

Ficany A, Del Alamo M, Bernabeu C, et al.

Journal of clinical medicine 2025; (14(21)) doi:10.3390/jcm14217724.

Unusual Onset of Hereditary Hemorrhagic Telangiectasia Due to Somatic Mutational Mosaicism: Case Report and Review of the Literature.

Mirra V, Rosa M, Fontanella C, et al.

Children (Basel, Switzerland) 2025; (12(12)) doi:10.3390/children12121701.

A CASE OF REFRACTORY IRON DEFICIENCY ANEMIA REVEALING HEREDITARY HEMORRHAGIC TELANGIECTASIA.

Elshweikh S, Almutairi A, Al Musaiteer T, et al.

Georgian medical news 2025; 6-11.