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Apr 16, 2015 (publication date) through Jun 2, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Dittus C, Streiff M, Ansell J. Bleeding and clotting in hereditary hemorrhagic telangiectasia. World J Clin Cases 2015; 3(4): 330-337 [PMID: 25879004 DOI: 10.12998/wjcc.v3.i4.330] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v3/i4/330.htm |
| Number | Citing Articles |
| 1 |
Urban W. Geisthoff, Ha‐Long Nguyen, Alexander Röth, Ulrich Seyfert. How to manage patients with hereditary haemorrhagic telangiectasia. British Journal of Haematology 2015; 171(4): 443 doi: 10.1111/bjh.13606
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| 2 |
P. Constant Dit Beaufils, S. De Gaalon, O. Espitia, G. Ploton, S. Mercier, R. Liberge, J. Connault. Une télangiectasie hémorragique héréditaire révélée tardivement par une thrombose veineuse cérébrale : à propos d'un cas. La Revue de Médecine Interne 2020; 41(9): 628 doi: 10.1016/j.revmed.2020.03.013
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| 3 |
A.V. Belopasova, L.A. Dobrynina, L.A. Kalashnikova, A.O. Chechetkin, A.R. Karshieva, S.A. Abugov, G.V. Mardanyan, M.B. Puretsky, A.B. Shteklein. Pulmonary arteriovenous shunt — a rare cause of recurrent stroke due to paradoxical embolism. Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova 2020; 120(9): 107 doi: 10.17116/jnevro2020120091107
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| 4 |
Suman Rao, Alisha Khan, Dana Aiello. Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia: A Case Report and Review of Literature. Cureus 2021; doi: 10.7759/cureus.15219
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| 5 |
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): 387 doi: 10.2169/internalmedicine.1287-18
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| 6 |
Anna Jargielo, Anna Rycyk, Beata Kasztelan-Szczerbinska, Halina Cichoz-Lach. A Rare Case of Upper Gastrointestinal Bleeding: Osler-Weber-Rendu Syndrome. Medicina 2022; 58(3): 333 doi: 10.3390/medicina58030333
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| 7 |
Bai-Guo Xu, Jing Liang, Ke-Feng Jia, Tao Han. Liver cirrhosis in a patient with hepatic hereditary hemorrhagic telangiectasia and Budd–Chiari syndrome: a case report. BMC Gastroenterology 2020; 20(1) doi: 10.1186/s12876-020-01311-1
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| 8 |
Jo SASAME, Yasunori TAKEMOTO, Izumi KOZANO, Takafumi KAWASAKI, Yoshihiro NUMAGAMI, Yasuhiko MOCHIMATSU, Nobuyuki SHIMIZU, Hidetoshi MURATA, Tetsuya YAMAMOTO. A Case of Head Trauma with Multiple Arteriovenous Shunts Complicated by a Pseudoaneurysm of the Middle Meningeal Artery. Surgery for Cerebral Stroke 2018; 46(5): 374 doi: 10.2335/scs.46.374
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| 9 |
Sen Li, Shu-Jie Wang, Yong-Qiang Zhao. Clinical features and treatment of hereditary hemorrhagic telangiectasia. Medicine 2018; 97(31): e11687 doi: 10.1097/MD.0000000000011687
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| 10 |
Neena Baby, SabuGeorge Kunnathuparambil, Prasanth Varghese, AneeshMangalasseril Kuriakose. Paradoxical Embolism in a Case of Hereditary Hemorrhagic Telangiectasia: Case Report with Literature Review. Neurology India 2020; 68(3): 665 doi: 10.4103/0028-3886.288990
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| 11 |
Yves Schild, Jonah Bosserhoff, Freya Droege, Elisabeth Littwitz-Salomon, Joachim Fandrey, Anna Wrobeln. Hypoxia-Inducible Factor–Prolyl Hydroxylase Inhibitor Improves Leukocyte Energy Metabolism in Hereditary Hemorrhagic Telangiectasia. Life 2023; 13(8): 1708 doi: 10.3390/life13081708
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| 12 |
Kunal Amin, Douglas Mckay. A Case Report of Hereditary Hemorrhagic Telangiectasia Diagnosed in a Podiatric Medical Patient. Journal of the American Podiatric Medical Association 2017; 107(2): 155 doi: 10.7547/15-144
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| 13 |
Julia Niklasson, Anders Rönnblom, Adnan Lidian, Andreas Thor. Oral manifestations and dental considerations of patients with hereditary hemorrhagic telangiectasia: a scoping review. Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 2023; 136(6): 691 doi: 10.1016/j.oooo.2023.08.001
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| 14 |
Antoni Riera-Mestre, José María Mora-Luján, Javier Trujillo-Santos, Jorge Del Toro, José Antonio Nieto, José María Pedrajas, Raquel López-Reyes, Silvia Soler, Aitor Ballaz, Pau Cerdà, Manel Monreal. Natural history of patients with venous thromboembolism and hereditary hemorrhagic telangiectasia. Findings from the RIETE registry. Orphanet Journal of Rare Diseases 2019; 14(1) doi: 10.1186/s13023-019-1172-8
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