派博傳思國際中心

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

作者: 粗野的整個    時間: 2025-3-21 17:52
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)學科排名




書目名稱Epidermolysis Bullosa網絡公開度




書目名稱Epidermolysis Bullosa網絡公開度學科排名




書目名稱Epidermolysis Bullosa被引頻次




書目名稱Epidermolysis Bullosa被引頻次學科排名




書目名稱Epidermolysis Bullosa年度引用




書目名稱Epidermolysis Bullosa年度引用學科排名




書目名稱Epidermolysis Bullosa讀者反饋




書目名稱Epidermolysis Bullosa讀者反饋學科排名





作者: characteristic    時間: 2025-3-21 21:42

作者: 領帶    時間: 2025-3-22 03:16

作者: Felicitous    時間: 2025-3-22 05:19

作者: FILLY    時間: 2025-3-22 10:28
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
作者: SIT    時間: 2025-3-22 15:11

作者: SIT    時間: 2025-3-22 17:56
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
作者: 增長    時間: 2025-3-22 21:18
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
作者: FRONT    時間: 2025-3-23 02:09
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
作者: arthroscopy    時間: 2025-3-23 08:30
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.
作者: 不自然    時間: 2025-3-23 11:50
Gastrointestinal Aspects of Epidermolysis Bullosational problems and growth retardation of these patients. The most severe problems are related to involvement of the proximal gut, oropharynx, and esophagus. However, anal lesions and altered colonic function lead to frequent difficulties with bowel function. In one study of 101 EB patients represen
作者: Contend    時間: 2025-3-23 14:51

作者: 弄污    時間: 2025-3-23 22:03

作者: 全等    時間: 2025-3-23 23:28
Dental Aspects of Epidermolysis Bullosaillustrated in epidermolysis bullosa (EB), a heterogeneous group of genetic disorders in which blistering of the skin and mucosa occur as a result of minor trauma.. In many patients, chewing and eating may cause formation of painful oral blisters that severely compromise nutritional intake. In addit
作者: cuticle    時間: 2025-3-24 06:21
Otorhinolaryngologic Aspects of Epidermolysis Bullosanvolved.. This is well illustrated by cases in which blisters occur in the larynx. Except for the true vocal cords and parts of the epiglottis, the larynx is covered with pseudo-stratified columnar epithelium containing goblet cells. And yet, blister formation has been noted in almost all parts of t
作者: 軟膏    時間: 2025-3-24 06:43

作者: 存心    時間: 2025-3-24 11:32
Discounted Cash Flow in the Standard Caseisters and erosions in the skin, and sometimes the mucous membranes, after mild trauma. These hereditary disorders should be distinguished from other genetic and acquired diseases (see below) and should not be confused with epidermolysis bullosa acquisita.
作者: vanquish    時間: 2025-3-24 17:23
John Eatwell,Murray Milgate,Peter Newmanseparated into one of three broad groups—simplex, junctional, and dystrophic EB—based on shared pathologic features. These specific ultrastructural findings are in some forms of EB accompanied by selective defects in expression of basement membrane or epidermal cell surface antigens or epitopes.
作者: seduce    時間: 2025-3-24 19:08

作者: 終點    時間: 2025-3-25 02:18

作者: 肌肉    時間: 2025-3-25 04:32
Current Perspectives and Differential Diagnosis in Epidermolysis Bullosaisters and erosions in the skin, and sometimes the mucous membranes, after mild trauma. These hereditary disorders should be distinguished from other genetic and acquired diseases (see below) and should not be confused with epidermolysis bullosa acquisita.
作者: 是限制    時間: 2025-3-25 09:21
Pathology and Pathogenesis of Epidermolysis Bullosaseparated into one of three broad groups—simplex, junctional, and dystrophic EB—based on shared pathologic features. These specific ultrastructural findings are in some forms of EB accompanied by selective defects in expression of basement membrane or epidermal cell surface antigens or epitopes.
作者: 名字的誤用    時間: 2025-3-25 15:14

作者: 芳香一點    時間: 2025-3-25 18:29
Hematologic Problems in Epidermolysis Bullosape of EB. In some cases, the anemia associated with EB can be refractory to therapy. Other hematologic disorders reported in EB include coagulation abnormalities in a small number of patients, and immunological alterations.
作者: 向宇宙    時間: 2025-3-25 22:56
978-1-4612-7717-0Springer-Verlag New York, Inc. 1992
作者: Ferritin    時間: 2025-3-26 01:58
https://doi.org/10.1007/978-1-4612-2914-8anesthesia; differential diagnosis; management; nursing; nutrition; pathology; prenatal diagnosis; reconstr
作者: 莎草    時間: 2025-3-26 06:08
Discounted Cash Flow in the Standard Caseisters and erosions in the skin, and sometimes the mucous membranes, after mild trauma. These hereditary disorders should be distinguished from other genetic and acquired diseases (see below) and should not be confused with epidermolysis bullosa acquisita.
作者: Blood-Vessels    時間: 2025-3-26 09:51

作者: 按等級    時間: 2025-3-26 16:13
John Eatwell,Murray Milgate,Peter Newmanseparated into one of three broad groups—simplex, junctional, and dystrophic EB—based on shared pathologic features. These specific ultrastructural findings are in some forms of EB accompanied by selective defects in expression of basement membrane or epidermal cell surface antigens or epitopes.
作者: 糾纏    時間: 2025-3-26 18:13

作者: 整理    時間: 2025-3-26 20:57
Design der empirischen Untersuchung,nalysis 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
作者: creditor    時間: 2025-3-27 01:34
Allokationsbedingungen im Arbeitsmarkts given the name “epidermolysis bullosa” because the clinical features of the disease were reminiscent of hereditary dystrophic epidermolysis bullosa. The early published cases. were diagnosed by the clinical appearance of the disease, and it is likely that at least some of these cases were not bona
作者: anaerobic    時間: 2025-3-27 05:47

作者: 里程碑    時間: 2025-3-27 09:47
Nicholas E. Grossoehme,David P. Giedroct 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
作者: Pillory    時間: 2025-3-27 14:19

作者: 細胞膜    時間: 2025-3-27 20:36
https://doi.org/10.1007/978-981-19-1562-8e. 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.
作者: 異端邪說2    時間: 2025-3-27 22:48

作者: 創(chuàng)作    時間: 2025-3-28 04:21

作者: TEM    時間: 2025-3-28 09:05

作者: 高度贊揚    時間: 2025-3-28 12:27

作者: 破裂    時間: 2025-3-28 16:13
https://doi.org/10.1007/978-3-531-91949-2nvolved.. This is well illustrated by cases in which blisters occur in the larynx. Except for the true vocal cords and parts of the epiglottis, the larynx is covered with pseudo-stratified columnar epithelium containing goblet cells. And yet, blister formation has been noted in almost all parts of t
作者: 牌帶來    時間: 2025-3-28 21:40

作者: GEON    時間: 2025-3-28 22:54

作者: 策略    時間: 2025-3-29 03:18
Otorhinolaryngologic Aspects of Epidermolysis Bullosageal involvement is rare, and a search of the English literature revealed only 10 cases, including one we had managed ourselves.. We are aware of an additional case managed by others (Scott Schaeffer, M.D., personal communication). In this chapter, we review these cases and discuss guidelines in pro
作者: Optic-Disk    時間: 2025-3-29 11:17

作者: 作嘔    時間: 2025-3-29 15:09
https://doi.org/10.1007/978-3-662-39567-7ance patterns being either autosomal dominant or autosomal recessive. It is traditional to classify dystrophic EB into recessive and dominant types. A clear-cut inheritance pattern can be recognized in many families by the presence of multiple affected siblings in a family with normal parents. Histo
作者: Prologue    時間: 2025-3-29 15:53
https://doi.org/10.1007/978-3-531-91949-2geal involvement is rare, and a search of the English literature revealed only 10 cases, including one we had managed ourselves.. We are aware of an additional case managed by others (Scott Schaeffer, M.D., personal communication). In this chapter, we review these cases and discuss guidelines in pro
作者: Fabric    時間: 2025-3-29 21:59

作者: 錢財    時間: 2025-3-30 03:35
ent. 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 d978-1-4612-7717-0978-1-4612-2914-8
作者: 強制令    時間: 2025-3-30 05:42
nosis 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.
作者: ingenue    時間: 2025-3-30 09:36





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