| For: | Vorselaars VM, Velthuis S, Snijder RJ, Vos JA, Mager JJ, Post MC. Pulmonary hypertension in hereditary haemorrhagic telangiectasia. World J Cardiol 2015; 7(5): 230-237 [PMID: 26015855 DOI: 10.4330/wjc.v7.i5.230] |
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| URL: | https://www.wjgnet.com/1949-8462/full/v7/i5/230.htm |
| Number | Citing Articles |
| 1 |
Grace Arndt, Ronald Wai, Hilary Stiel. Subcutaneous Tranexamic Acid at the End of Life in a Patient With Hereditary Hemorrhagic Telangiectasia. Journal of Palliative Medicine 2024; 27(6) doi: 10.1089/jpm.2023.0379
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| 2 |
Sophie Dupuis-Girod, Vincent Cottin, C.L. Shovlin. The Lung in Hereditary Hemorrhagic Telangiectasia. Respiration 2017; 94(4) doi: 10.1159/000479632
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| 3 |
Sala Bofarid, Anna E. Hosman, Johannes J. Mager, Repke J. Snijder, Marco C. Post. Pulmonary Vascular Complications in Hereditary Hemorrhagic Telangiectasia and the Underlying Pathophysiology. International Journal of Molecular Sciences 2021; 22(7) doi: 10.3390/ijms22073471
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| 4 |
Claudie Fogang D, Gallice Martin, Françoise Boehlen, Georges L Savoldelli. Anaesthetic management for caesarean section in a patient with hereditary haemorrhagic telangiectasia and severe epistaxis during pregnancy. BMJ Case Reports 2023; 16(10) doi: 10.1136/bcr-2023-255530
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| 5 |
Nicolás Ariza Ordoñez, Antonia Pino Marín, Juan Sebastián Bonilla Crespo, Alberto Navarro Navajas, Gabriel Antonio Oliver, Hector M. Medina, Julián F. Forero. An Unusual Cause of Right Heart Dysfunction and High Output Heart Failure in a Young Woman. Journal of Cardiovascular Development and Disease 2022; 9(12) doi: 10.3390/jcdd9120418
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| 6 |
Wen Li, Chang‐ming Xiong, Qing Gu, Xiao‐tong Wang, Xiao‐ling Cheng, Li Huang, Tao Yang, Qin Luo, Zhi‐hui Zhao, Xin‐hai Ni, Zhi‐hong Liu, Jian‐guo He. The clinical characteristics and long‐term prognosis of pulmonary arterial hypertension associated with hereditary hemorrhagic telangiectasia. Pulmonary Circulation 2018; 8(2) doi: 10.1177/2045894018759918
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| 7 |
Yasunori Inoguchi, Bunji Kaku, Naotaka Kitagawa, Shoji Katsuda. Hereditary Hemorrhagic Telangiectasia with SMAD4 Mutations Is Associated with Fatty Degeneration of the Left Ventricle, Coronary Artery Aneurysm, and Abdominal Aortic Aneurysm. Internal Medicine 2019; 58(3) doi: 10.2169/internalmedicine.1287-18
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| 8 |
Eileen M. Harder, Wassim H. Fares. Hospitalizations with hereditary hemorrhagic telangiectasia and pulmonary hypertension in the United States from 2000 to 2014. Respiratory Medicine 2019; 147 doi: 10.1016/j.rmed.2018.12.013
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| 9 |
Patricia P. Bloom, Josanna Rodriguez-Lopez, Alison S. Witkin, Hanny Al-Samkari, David J. Kuter, Amirkasra Mojtahed, Jay Luther. Ammonia Predicts Hepatic Involvement and Pulmonary Hypertension in Patients With Hereditary Hemorrhagic Telangiectasia. Clinical and Translational Gastroenterology 2020; 11(1) doi: 10.14309/ctg.0000000000000118
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| 10 |
Brittany M. Scarpato, Jamie McDonald, Pinar Bayrak-Toydemir, C. Gregory Elliott, Barbara C. Cahill, Lyska L. Emerson, Lynn M. Keenan. The Shunt of It. Chest 2023; 163(5) doi: 10.1016/j.chest.2023.01.020
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| 11 |
Katie L. Mowers, Lynne Sekarski, Andrew J. White, R. Mark Grady. Pulmonary arteriovenous malformations in children with hereditary hemorrhagic telangiectasia: a longitudinal study. Pulmonary Circulation 2018; 8(3) doi: 10.1177/2045894018786696
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| 12 |
Aymen Mirza, Bibek Bista, Vidhya Annavajjhala, Chinyere O’Connor. Refractory Hypoxemia in an Asymptomatic 6-Year-Old: It is not Always the Heart. Clinical Pediatrics 2025; 64(12) doi: 10.1177/00099228251356184
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| 13 |
Takahiro Arano, Takuro Imamoto, Rika Suda, Hajime Kasai, Toshihiko Sugiura, Ayako Shigeta, Keiko Yamamoto, Jun Nagata, Seiichiro Sakao, Nobuhiro Tanabe, Koichiro Tatsumi. Heritable pulmonary arterial hypertension complicated by multiple pulmonary arteriovenous malformations. Respiratory Medicine Case Reports 2021; 32 doi: 10.1016/j.rmcr.2021.101352
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| 14 |
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| 15 |
Freya Droege, Kruthika Thangavelu, Boris A Stuck, Andreas Stang, Stephan Lang, Urban Geisthoff. Life expectancy and comorbidities in patients with hereditary hemorrhagic telangiectasia. Vascular Medicine 2018; 23(4) doi: 10.1177/1358863X18767761
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| 16 |
Batool Alsheikh, Othman Aljohani, Nicole G. Coufal. Paediatric pulmonary hypertension caused by an ACVRL1 mutation presenting as Ortner syndrome. Cardiology in the Young 2018; 28(12) doi: 10.1017/S1047951118001531
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| 17 |
Peiran Yang, Paul B. Yu. Bone Morphogenetic Proteins: Systems Biology Regulators. 2017; doi: 10.1007/978-3-319-47507-3_13
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| 18 |
Veronique M. M. Vorselaars, Anna E. Hosman, Cornelis J. J. Westermann, Repke J. Snijder, Johannes J. Mager, Marie-Jose Goumans, Marco C. Post. Pulmonary Arterial Hypertension and Hereditary Haemorrhagic Telangiectasia. International Journal of Molecular Sciences 2018; 19(10) doi: 10.3390/ijms19103203
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| 19 |
Anna M. Kasparova, Zarina S. Valieva, Tamila V. Martynyuk. A rare clinical case of the patient with pulmonary hypertension associated with hereditary hemorrhagic telangiectasia. Case report. Terapevticheskii arkhiv 2022; 94(4) doi: 10.26442/00403660.2022.04.201453
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| 20 |
Masako Harada, Kyohei Kondo, Hiroyuki Nunoi, Osamu Yamada. The Effect of Upfront Combination Therapy for Pulmonary Arterial Hypertension Associated with Hereditary Hemorrhagic Telangiectasia Type-1: A Girl with a Novel Mutation in the Endoglin Gene. Pediatric Cardiology and Cardiac Surgery 2017; 33(3) doi: 10.9794/jspccs.33.221
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| 21 |
Luca Ielasi, Matteo Tonnini, Fabio Piscaglia, Ilaria Serio. Current guidelines for diagnosis and management of hepatic involvement in hereditary hemorrhagic teleangiectasia. World Journal of Hepatology 2023; 15(5): 675-687 doi: 10.4254/wjh.v15.i5.675
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| 22 |
Tristan Sinnatamby, Jennifer LaBranche, Maxine Farr-Jones, Tiana Fenske, Dilini Vethanayagam, Mehmet Baysal. Obstructive airway disorders affecting individuals with hereditary hemorrhagic telangiectasia: A database review. PLOS One 2025; 20(9) doi: 10.1371/journal.pone.0331690
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| 23 |
Toshihiko Sugiura, Koichiro Tatsumi. Clinical Relevance of Genetic Factors in Pulmonary Diseases. Respiratory Disease Series: Diagnostic Tools and Disease Managements 2018; doi: 10.1007/978-981-10-8144-6_9
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| 24 |
David Montani, Pierre Thoré, Étienne-Marie Jutant, Marc Humbert. Orphan Lung Diseases. 2023; doi: 10.1007/978-3-031-12950-6_41
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| 25 |
Samuel B. Jackson, Nicholas P. Villano, Jihane N. Benhammou, Michael Lewis, Joseph R. Pisegna, David Padua. Gastrointestinal Manifestations of Hereditary Hemorrhagic Telangiectasia (HHT): A Systematic Review of the Literature. Digestive Diseases and Sciences 2017; 62(10) doi: 10.1007/s10620-017-4719-3
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| 26 |
Po‐Yang Tsou, Melisa Ruiz‐Gutierrez, Ahmad Alomari, Pei‐Lun Kuo, Timothy Klouda. Epidemiology of complications among hospitalized children with hereditary hemorrhagic telangiectasia: A kids' inpatient database study. Pediatric Pulmonology 2024; 59(5) doi: 10.1002/ppul.26922
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| 27 |
Thomas Kühnel, Kornelia Wirsching, Walter Wohlgemuth, Ajay Chavan, Katja Evert, Veronika Vielsmeier. Hereditary Hemorrhagic Telangiectasia. Otolaryngologic Clinics of North America 2018; 51(1) doi: 10.1016/j.otc.2017.09.017
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| 28 |
Vincent Avecilla. Effect of Transcriptional Regulator ID3 on Pulmonary Arterial Hypertension and Hereditary Hemorrhagic Telangiectasia. International Journal of Vascular Medicine 2019; 2019 doi: 10.1155/2019/2123906
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| 29 |
Laura Lopes, Pedro Gonçalo Ferreira. Hereditary haemorrhagic telangiectasia as a cause of exertional dyspnoea. BMJ Case Reports 2026; 19(5) doi: 10.1136/bcr-2026-273656
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| 30 |
Joshua Hodgson, Lidia Ruiz‐Llorente, Jamie McDonald, Oliver Quarrell, Kelechi Ugonna, James Bentham, Rebecca Mason, Jennifer Martin, David Moore, Katie Bergstrom, Pinar Bayrak‐Toydemir, Whitney Wooderchak‐Donahue, Nicholas W. Morrell, Robin Condliffe, Carmelo Bernabeu, Paul D. Upton. 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. Molecular Genetics & Genomic Medicine 2021; 9(12) doi: 10.1002/mgg3.1685
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| 31 |
Bipneet Singh, Jahnavi Ethakota, Palak Grover, Gurleen Kaur. Catch me if you can- Hereditary hemorrhagic telangiectasia presenting as gastrointestinal bleed!. Medical Reports 2025; 13 doi: 10.1016/j.hmedic.2025.100289
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| 32 |
William Salibe-Filho, Bruna Mamprim Piloto, Ellen Pierre de Oliveira, Marcela Araújo Castro, Breno Boueri Affonso, Joaquim Maurício da Motta-Leal-Filho, Edgar Bortolini, Mário Terra-Filho. Pulmonary arteriovenous malformations: diagnostic and treatment characteristics. Jornal Brasileiro de Pneumologia 2019; 45(4) doi: 10.1590/1806-3713/e20180137
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| 33 |
Claire L Shovlin, Robin Condliffe, James W Donaldson, David G Kiely, Stephen J Wort. British Thoracic Society Clinical Statement on Pulmonary Arteriovenous Malformations. Thorax 2017; 72(12) doi: 10.1136/thoraxjnl-2017-210764
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| 34 |
Beth L. Roman, Andrew P. Hinck. ALK1 signaling in development and disease: new paradigms. Cellular and Molecular Life Sciences 2017; 74(24) doi: 10.1007/s00018-017-2636-4
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| 35 |
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| 36 |
Inga Duerig, Ekaterina Pylaeva, Irem Ozel, Sami Wainwright, Ilona Thiel, Sharareh Bordbari, Maksim Domnich, Elena Siakaeva, Antonia Lakomek, Felicia Toppe, Carolin Schleupner, Urban Geisthoff, Stephan Lang, Freya Droege, Jadwiga Jablonska. Nonfunctional TGF-β/ALK1/ENG signaling pathway supports neutrophil proangiogenic activity in hereditary hemorrhagic telangiectasia. Journal of Leukocyte Biology 2023; 114(6) doi: 10.1093/jleuko/qiad090
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| 37 |
Sihan Wang, Ping Yang, Hongmin Xi, Xiangyun Yin, Lili Ma, Liangliang Li, Xianghong Li. Case Report: Shared manifestation, distinct etiologies: severe pulmonary hypertension in both mother and neonate. Frontiers in Pediatrics 2025; 13 doi: 10.3389/fped.2025.1612410
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| 38 |
Shanglei Ning, Yunfei Xu, Weida Lu, Yuxin Chen. Laparoscopic Double Hepatic Artery Banding/Ligation for Patients With Hepatic Hereditary Haemorrhagic Telangiectasia (HHHT). EJVES Vascular Forum 2023; 60 doi: 10.1016/j.ejvsvf.2023.09.007
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| 39 |
Yumiko Ikubo, Hajime Kasai, Toshihiko Sugiura, Takahiko Saito, Hiroki Shoji, Seiichiro Sakao, Yasunori Kasahara, Nobuhiro Tanabe, Koichiro Tatsumi. Pulmonary Hypertension that Developed During Treatment for Hepatopulmonary Syndrome and Pulmonary Arteriovenous Malformation. Internal Medicine 2019; 58(12) doi: 10.2169/internalmedicine.1993-18
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| 40 |
Maryam Ranjbar, Ahmad Amin, Ali Amin, Hamidreza Pouraliakbar, Arezoo Mohamadifar. High Cardiac Output State Due to Pelvic Arterio-Venous Shunt: A Case Report and Review of the Literature. ESC Heart Failure 2023; 10(4) doi: 10.1002/ehf2.14396
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