ライフサイエンスコーパス: erythroderma

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1 patients with atopic dermatitis with severe erythroderma.

2 m classical bullous congenital ichthyosiform erythroderma.

3 yndrome is characterized by neonatal scaling erythroderma, a bamboolike hair defect, a substantial sk

4 ve skin disorder characterized by congenital erythroderma, a specific hair-shaft abnormality, and ato

5 th cases of bullous congenital ichthyosiform erythroderma also due to keratin 1 mutations, which show

6 Subjects with erythroderma and active plaque phenotypes displayed elev

7 nct from those of patients with inflammatory erythroderma and from healthy volunteers.

8 listering and erythroderma in infancy and by erythroderma and ichthyosis thereafter.

9 congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD syndrome), hydrops-

10 Congenital Hemidysplasia with Ichthyosiform erythroderma and Limb Defects (CHILD) syndrome, an X-lin

11 congenital hemidysplasia with ichthyosiform erythroderma and limb defects.

12 m abnormalities and a pruritic ichthyosiform erythroderma, are together diagnostic of NLSDI.

13 ne pole and classic congenital ichthyosiform erythroderma at the other.

14 Bullous congenital ichthyosiform erythroderma (BCIE) is characterized by blistering and e

15 y using biopsy samples of psoriasis, AD, and erythroderma belonging to the surgical pathology files o

16 kin disease bullous congenital ichthyosiform erythroderma by gene targeting.

17 n termed nonbullous congenital ichthyosiform erythroderma (CIE).

18 ease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manife

19 er characterized by congenital ichthyosiform erythroderma, hair shaft defects and atopy, caused by mu

20 ified in a child with congenital exfoliative erythroderma, hypotrichosis, severe nail dystrophy and f

21 ified in a child with congenital exfoliative erythroderma, hypotrichosis, severe nail dystrophy and f

22 ma (BCIE) is characterized by blistering and erythroderma in infancy and by erythroderma and ichthyos

23 igated the pathogenesis of the ichthyosiform erythroderma in patients from three unrelated kindreds w

24 Congenital erythroderma is a rare and often life-threatening condit

25 is a severe immunodeficiency associated with erythroderma, lymphoproliferation, elevated IgE, and hyp

26 ts with ichthyosis (congenital ichthyosiform erythroderma, n = 6; lamellar ichthyosis, n = 7; epiderm

27 Nonbullous congenital ichthyosiform erythroderma (NCIE) is a nonsyndromic form of autosomal

28 with little evidence of blood involvement to erythroderma often in association with frank leukemia, a

29 cell lymphoma, including 31 with exfoliative erythroderma or Sezary syndrome and 11 with mycosis fung

30 of the pathophysiological characteristics of erythroderma, psoriasis, and AD and may influence therap

31 equently diagnosed as psoriasis (n = 7), and erythroderma subsequently diagnosed as AD (n = 5).

32 nic psoriasis (n = 20), chronic AD (n = 20), erythroderma subsequently diagnosed as psoriasis (n = 7)

33 at least moderately severe symptoms (diffuse erythroderma, tachycardia, chest tightness, wheezing, fa

34 variant of bullous congenital ichthyosiform erythroderma that has recently been described in two sep

35 The clinical features of erythroderma, trichorrhexis invaginata, and atopic manif

36 tients with CTCL especially individuals with erythroderma where they could exacerbate and/or perpetua

37 howed skin abnormalities, such as congenital erythroderma with a shiny, translucent skin.

38 s, mycosis fungoides (MF), or as exfoliative erythroderma with circulating atypical cells, Sezary syn

39 ls (PBMCs) from patients with advanced CTCL (erythroderma with circulating malignant T cells) and hea

40 Tg-KLK5 mice developed an exfoliative erythroderma with scaling, growth delay, and hair abnorm

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