日本発のHHT関連の論文

 
 

日本発のHHT関連の2011年以降の最近の論文をlist upします.


詳しくは、abstractへ ← click


Ozawa H, Ohki T, Kanaoka Y, Maeda K, Hagiwara S: Open arterial reconstruction of multiple hepatic artery aneurysms in a patient with hereditary hemorrhagic telangiectasia: A case report. Medicine (Baltimore) 95:e5430, 2016


Miyake R, Fujino T, Abe K, Hosokawa K, Ohtani K, Morisaki H, Yamada O, Higo T, Ide T:  Pulmonary arterial hypertension associated with hereditary hemorrhagic telangiectasia successfully treated with sildenafil. Int J Cardiol 214:275-276, 2016 (no abstract available)


Yoshioka Y, Nozawa H, Tanaka J, Nishikawa T, Tanaka T, Kiyomatsu T, Kawai K, Hata K, Kazama S, Yamaguchi H, Ishihara S, Sunami E, Kitayama J, Watanabe T: Small bowel adenocarcinoma arising in a patient with hereditary hemorrhagic telangiectasia: A case report. Oncol Lett 11:2137-2139, 2016


Minami K, Haji T: Intranasal topical estrogen in the management of epistaxis in hereditary hemorrhagic telangiectasia. Acta Otolaryngol 2016 Jan 25:1-4 (Epub ahead of print)


Ichimura K, Kikuchi H, Imayoshi D, Dias MS: Topical application of timolol decreases the severity and frequency of epistaxis in patients who have previously undergone nasal dermoplasty for hereditary hemorrhagic telangiectasia. Auris Nasus Larynx 2015 Dec 28, pii: S0385-8146(15)30001-8. doi: 10.1016/j.anl.2015.12.001. [Epub ahead of print]


Shimoda Y, Osanai T, Nakayama N, et al: De novo arteriovenous malformation in a patient with hereditary hemorrhagic telangiectasia. J Neurosurg Pediatr (Epub ahead of print)


Nishioka Y, Akamatsu N, Sugawara Y, et al: Hereditary hemorrhagic telangiectasia with hepatic vascular malformations. Cade Rep Med 2015; 2015:917818. doi: 10.1155/2015/917818. Epub 2015 May 21.


Komiyama M, et al: Neuroradiological manifestations of hereditary hemorrhagic telangiectasia in 139 Japanese patients. Neurol Med Chir (Tokyo) 55:479-486, 2015, doi:10.2176/nmc.oa.2015-0040


小宮山雅樹:遺伝性出血性毛細血管拡張症.脳卒中の外科 43:193-200, 2015


Saji N, Kawarai T, Miyamoto R, et al: Exome sequencing identifies a novel intronic mutation in ENG that causes recurrence of pulmonary arteriovenous malformations. J Neurol Sci 352:29-33, 2015 doi: 10.1016/j.jns.2015.02.007. Epub 2015 Apr 2.


小宮山雅樹:遺伝性出血性毛細血管拡張症.循環器内科 77:327-330, 2015


Kato Y, Maruyama H, Uchino A, Tanahashi N: Late-onset portosystemic encephalopathy in a patient with Rendu-Osler-Weber disease. Intern Med 53:2653-2654, 2014 (no abstract available)


Komaki Y, Kanmura S, Funakawa K, Komaki F, Hashimoto S, Taguchi H, Numata M, Fujita H, Uto H, Ido A, Tsubouchi H: A case of hereditary hemorrhagic telangiectasia with repeated hemobilia arrested by argon plasma coagulation under direct peroral cholangioscopy. Gastrointest Endosc 80:528-9, 2014 (no abstract available)


Nakamura Y, Shinkata F, Ryugo M, et al: Redo cardiac surgery for active prosthetic valve endocarditis associated with hereditary hemorrhagic telangiectasia: report of a case. Surg Today 44:2378-2381, 2014


Ishiwata T, Terada J, Tanabe N, et al: Pulmonary arterial hypertension as the first manifestation in a patient with hereditary hemorrhagic telangiectasia. Intern Med 53:2359-2363, 2014


山本慶子、須田 明、飯田智彦、他:胸腔内出血をきたした妊娠合併遺伝性出血性毛細血管拡張症の1例.日本呼吸器学会誌 2:782-787, 2013


   Fukushima H, Mitsuhashi T, Oto T, et al: Successful lung transplantation in a case with diffuse pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia. Am J Transplant 13:3278-3281, 2013. doi: 10.1111/ajt.12499. Epub 2013 Oct 24.


 Komiyama M, Ishiguro T, Yamada O, et al: Hereditary Hemorrhagic Telangiectasia in Japanese Patients. J Hum Genet, doi:10.1038/jhg.2013.113, 7 November 2013


 Komiyama M, Ishiguro T, Umaba, et al: Transcardiac, retrograde transvenous embolization of proximally occluded pulmonary arteriovenous malformation. CardioVasc Interv Radiol DOI 10.1007/s00270-013-0755-3, 23 October 2013


 住友靖彦、山下幸政、板井良輔、他:SMAD4の変異が証明された若年性ポリポーシス/遺伝性出血性末梢血管拡張症複合症候群の1例.日消誌 110:64-73, 2013


   Morita H, Kimura N,  Yuri K, et al: Bentall Operation for Prosthetic Valve Endocarditis with Hereditary Hemorrhagic Telangiectasia. Ann Thorac Cardiovasc Surg   http://dx.doi.org/10.5761/atcs.cr.12.01933


   NIshida T, Faughnan ME, Krings T, et al: Brain arteriovenous malformations associated with hereditary hemorrhagic telangiectasia: gene-phenotype correlations. Am J Med Genet A, 156A:2829-2834, 2012, DOI 10.1002/ajmg.a.35622


 瀬川正孝: 肺動静脈瘻を切除したRendu-Osler-Weber病. 胸部外科 65:862-865, 2012


 Sugiyama T, Nakayama N, Terasaka S, et al: Giant calcified thrombosed varices secondary to a pial arteriovenous fistula associated with hereditary hemorrhagic telangiectasia. Neurol Med Chir (Tokyo) 52:506-509, 2012


 Ishii D, Takechi A, Seyama G, et al: Ruptured large basilar artery aneurysm associated with an arteriovenous malformation in hereditary hemorrhagic telangiectasia. Neurol Med Chir (Tokyo) 52:502- 505, 2012


 Suzuki A, Nakashima D, Miyawaki Y, et al: A novel ENG mutation causing impaired co-translational processing of endoglin associated with hereditary hemorrhagic telangiectasia. Thromb Res 129:e200-208, doi: 10.1016/j.thromres.2011.12.030. Epub 2012 Mar 3.


 Ichimura K, Kikuchi H, Imayoshi S: A new method of nasal dermoplasty (MW grafting method) in patients with large septal perforation. Laryngoscope. 121:1715-1717, 2011


 Ichimura K, Kikuchi H, Imayoshi S, et al: Are patients with severe epistaxis caused by hereditary hemorrhagic telangiectasia satisfied with nostril closure surgery? Auris Nasus Larynx 39:59-64, 2012, doi: 10.1016/j.anl.2011.03.003. Epub 2011 May 17.


 Nakayama M, Nawa T, Chonan T et al: Prevalence of pulmonary arteriovenous malformations as estimated by low-dose thoracic CT screening. Intern Med 51:1677-1681, 2012


 竹田淳恵、藤堂謙一、山本司郎、山上 宏、川本未知、幸原伸夫:遺伝性出血性毛細血管拡張症にともなう肺動静脈瘻を介して奇異性脳塞栓症を発症した1例.臨床神経 52:161-165, 2012


 Kaneko M, Nozawa H, Kitayama J, Sunami E, Akahane M, Yamauchi N, Furukawa Y, Nagawa H: A case of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) with multiple polyps arising in the cecum and appendix. Acta Gastroenterol Belg 74:352–354, 2011



last update on 2016 5 12