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Titlebook: Epidermolysis Bullosa; Basic and Clinical A Andrew N. Lin,D. Martin Carter Book 1992 Springer-Verlag New York, Inc. 1992 anesthesia.differe

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書目名稱Epidermolysis Bullosa
副標(biāo)題Basic and Clinical A
編輯Andrew N. Lin,D. Martin Carter
視頻videohttp://file.papertrans.cn/314/313206/313206.mp4
圖書封面Titlebook: Epidermolysis Bullosa; Basic and Clinical A Andrew N. Lin,D. Martin Carter Book 1992 Springer-Verlag New York, Inc. 1992 anesthesia.differe
描述Because skin blisters are the initial manifestation of epidermolysis bullosa (EB), patients invariably present to the dermatologist for diagnosis and treatment. However, EB is a systemic disease whose management requires input from clinicians in virtually all fields of medicine, including pediatri- cians, surgeons, dentists, gastroenterologists, hematologists, otorhinolaryn- gologists, dietitians, and physical therapists, to name a few. Because EB is a rare disease, few clinicians are familiar with it, and many recoil at the pros- pect of caring for individuals covered with blisters caused by a disease they know little about. For patients, insult is thus added to injury and they feel abandoned, neglected, and frustrated. One way to remedy this deplorable situation is to provide clinicians with a compact source of information de- tailing the principles of EB diagnosis and treatment. This text seeks to fulfill this role. From 1986-1991, The Rockefeller University Hospital has been the co- ordinating center of the National EB Registry. Supported by The National Institutes of Health, this Registry consists of four university centers* commit- ted to collecting clinical data concerning d
出版日期Book 1992
關(guān)鍵詞anesthesia; differential diagnosis; management; nursing; nutrition; pathology; prenatal diagnosis; reconstr
版次1
doihttps://doi.org/10.1007/978-1-4612-2914-8
isbn_softcover978-1-4612-7717-0
isbn_ebook978-1-4612-2914-8
copyrightSpringer-Verlag New York, Inc. 1992
The information of publication is updating

書目名稱Epidermolysis Bullosa影響因子(影響力)




書目名稱Epidermolysis Bullosa影響因子(影響力)學(xué)科排名




書目名稱Epidermolysis Bullosa網(wǎng)絡(luò)公開度




書目名稱Epidermolysis Bullosa網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Epidermolysis Bullosa被引頻次




書目名稱Epidermolysis Bullosa被引頻次學(xué)科排名




書目名稱Epidermolysis Bullosa年度引用




書目名稱Epidermolysis Bullosa年度引用學(xué)科排名




書目名稱Epidermolysis Bullosa讀者反饋




書目名稱Epidermolysis Bullosa讀者反饋學(xué)科排名




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Linkage Studies in Epidermolysis Bullosanalysis of the skin of patients. Although many detailed analyses have been performed, thus far they have not demonstrated convincingly what primary genetic abnormality underlies the skin disease. Despite remarkable insights into a few diseases (e.g., mutant hemoglobins in sickle cell disease, decrea
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Epidermolysis Bullosa Simplex: A Clinical Overviewlisters generally heal without scarring unless lesions become infected, and milia generally do not occur. Mucosal involvement is usually restricted to the mouth, and estimates of the incidence of oral blistering range from 2%. to 30%.. Nails and teeth are usually normal. Corneal involvement. has bee
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Junctional Epidermolysis Bullosa: A Clinical Overviewt zone located between the basal cell plasma membrane and the lamina densa (Fig. 8.1). Like other forms of epidermolysis bullosa (EB), several subtypes are recognized (Table 8.1). These are differentiated mainly on the basis of clinical manifestations, and it is unclear if they represent varying exp
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Recessive Dystrophic Epidermolysis Bullosa: A Clinical Overviewmbrane zone deep to the lamina densa) and recessive inheritance. Ultimately, the diagnosis depends on confirmation of the level of separation by ultrastructural examination (Fig. 9.1), antigen mapping, or preferably both.. This disorder has also been called dermolytic EB to emphasize the importance
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Dominant Dystrophic Epidermolysis Bullosa: A Clinical Overviewe. Patients often present with trauma-induced blisters at birth or shortly thereafter. In contrast to epidermolysis bullosa simplex (EBS), blisters heal with scarring (Fig. 10.1), but the severe mittenlike scars of the hands and feet so characteristic of recessive dystrophic EB do not occur in DDEB.
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