A Case of Hereditary Multiple Telangiectases
نویسندگان
چکیده
منابع مشابه
Myocardial telangiectases in hereditary hemorrhagic telangiectasia.
472 Communications to the Editor 1 Glauser FL, Fairman RP The uncertain role of the neutrophil in increased permeability pulmonary edema. Chest 1985; 88:601-07 2 Dyer EL, Brigham KL, Snapper JR. Circulating granulocytes are not essential for lung mechanics changes produced by phorbol myristate acetate. Am Rev Respir Dis 1984; 129:A350 3 Dyer EL, Snapper JR. The role of circulating granulocytes ...
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in this Institute by serial transplantations in Sprague-Dawley rats for almost 2 years, because they proved to be useful in the study of various problems related to neoplastic growth (6, 8). Origi nally, these tumors were rather polymorph in their histologie appearance and contained islets of chondrosarcomatous and osteosarcomatous tissue ; but gradually they have assumed a purely fibrosarcomat...
متن کاملA syndrome of multiple telangiectases produced by a transplantable fibrosarcoma.
in this Institute by serial transplantations in Sprague-Dawley rats for almost 2 years, because they proved to be useful in the study of various problems related to neoplastic growth (6, 8). Origi nally, these tumors were rather polymorph in their histologie appearance and contained islets of chondrosarcomatous and osteosarcomatous tissue ; but gradually they have assumed a purely fibrosarcomat...
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در این تحقیق دانش زبانشناسی و کاربردشناسی زبان آموزان ایرانی در سطح بالای متوسط مقایسه شد. 50 دانش آموز با سابقه آموزشی مشابه از شش آموزشگاه زبان مختلف در دو آزمون دانش زبانشناسی و آزمون دانش گفتار شناسی زبان انگلیسی شرکت کردند که سوالات هر دو تست توسط محقق تهیه شده بود. همچنین در این تحقیق کارایی کتابهای آموزشی زبان در فراهم آوردن درون داد کافی برای زبان آموزان ایرانی به عنوان هدف جانبی تحقیق ...
15 صفحه اولMultiple Hereditary Osteochondromatosis: A Case Report
OBJECTIVES Common carious lesions owing to vomiting are not widespread in children. In this case, we aimed to report an 11-years-old male patient with common carious lesions due to repeated vomitings, chewing and eating difficulty and retarded growth with Multiple Hereditary Osteochondromatosis (MHO). CASE REPORT An 11-years-old boy was referred to Department of Pediatric Dentistry in Faculty...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1910
ISSN: 0035-9157
DOI: 10.1177/003591571000300256