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1 virus could contribute to the origin of this dermatosis.
2 bromatosis (NF1), the most common geno-oculo-dermatosis.
3 erma manifesting an associated ichthyosiform dermatosis.
4 t antigen in intraepidermal neutrophilic IgA dermatosis.
5 tibodies in patients with linear IgA bullous dermatosis.
6 characterized histologically by neutrophilic dermatosis.
7 oclastic vasculitis (23 [36%]), neutrophilic dermatosis (22 [34%]), and perivascular dermatitis (19 [
8 syndrome (SS) is a prototypical neutrophilic dermatosis, a class of inflammatory diseases marked by e
9              Intraepidermal neutrophilic IgA dermatosis, a rare skin disease entity manifested with b
10 tosa (PP) was considered a rare inflammatory dermatosis affecting primarily Asian individuals.
11 a disorder characterized by a photosensitive dermatosis and hepatic siderosis.
12 iral infection of a preexisting inflammatory dermatosis and is associated with considerable morbidity
13 , bullous pemphigoid, transient acantholytic dermatosis, and mycosis fungoides, and should be conside
14         Bullous pemphigoid (BP) is a bullous dermatosis associated with autoantibodies directed again
15 ein that is the target of linear IgA bullous dermatosis autoantibodies.
16          Atopic dermatitis (AD) is a chronic dermatosis bearing clinical, histological, and immunolog
17 description of an acute febrile neutrophilic dermatosis by Dr Robert Douglas Sweet, the dermatosis re
18 se (HHD), is a rare and debilitating genetic dermatosis characterized by chronic, recurrent vesicles,
19 Atopic dermatitis (AD) is a chronic allergic dermatosis characterized by epidermal thickening and der
20          Psoriasis is a chronic inflammatory dermatosis characterized by hyperproliferative keratinoc
21  gangrenosum is an inflammatory neutrophilic dermatosis characterized by painful cutaneous ulceration
22 ribe 3 patients with an unusual neutrophilic dermatosis characterized by relapsing episodes of fever,
23 aris (PRP) is an inflammatory papulosquamous dermatosis, characterized by hyperkeratotic follicular p
24 CL cases and HTLV-I PCR analysis of non-CTCL dermatosis controls showed no evidence that positive PCR
25                             Erosive pustular dermatosis (EPD) is a rare condition that typically affe
26              The etiology of this ulcerative dermatosis has not been identified, although it has been
27 mmatory syndrome that resembles neutrophilic dermatosis in humans and is characterized by persistent
28 ory skin disease that resembles neutrophilic dermatosis in humans.
29 moted MyD88-dependent signaling and mediates dermatosis in Ptpn6(spin) mice.
30 emphigoid (BP), the most frequent blistering dermatosis in the elderly, is associated with increased
31                                     Ice-pack dermatosis is an uncommon cold-induced process that occu
32                           Linear IgA bullous dermatosis (LABD) is an acquired autoimmune subepidermal
33  the clinical spectrum of linear IgA bullous dermatosis (LABD) or a separate disease entity.
34 era of some patients with linear IgA bullous dermatosis (LABD) recognize a 97 kDa antigen (LABD97) lo
35 d its adult counter-part, linear IgA bullous dermatosis (LABD), are characterized by linear depositio
36 d by colobomas, heart defects, ichthyosiform dermatosis, mental retardation (intellectual disability)
37                             Erosive pustular dermatosis of the scalp (EPDS) is an inflammatory skin c
38  Pyoderma gangrenosum (PG) is a neutrophilic dermatosis of unclear etiology.
39 opsies failed to reveal an underlying vulvar dermatosis or autoimmune bullous disorder.
40 ssociated autoinflammation with neutrophilic dermatosis (PAAND) is a monogenic autoinflammatory disor
41 ssociated autoinflammation with neutrophilic dermatosis (PAAND).
42 ked to the development of pigmented purpuric dermatosis (PPD).
43 in paediatric patients suggest evaluation of dermatosis-related cardiac involvement in patients with
44 c dermatosis by Dr Robert Douglas Sweet, the dermatosis remains a fascinating condition with regard t
45                                         This dermatosis shares clinical features and pathogenesis wit
46                All patients had neutrophilic dermatosis skin lesions, including tender red or violace
47 mmune blistering disorder linear IgA bullous dermatosis specifically recognized bands of 120 and 97 k
48         BackgroundAcute febrile neutrophilic dermatosis (Sweet syndrome) is a potentially fatal multi
49 ity, resulting in the pruritic, inflammatory dermatosis that characterizes AD.
50           Atopic dermatitis (AD) is a common dermatosis that highly impairs a patient's quality of li
51 erma gangrenosum (PG) is a rare neutrophilic dermatosis that presents with rapidly developing, painfu
52  Lichen planus is an autoimmune inflammatory dermatosis that typically affects the skin but can also
53 ity syndrome seems to be a neutrophil-driven dermatosis; therefore, many overlapping features with Sw
54 enotype is characterized by a photosensitive dermatosis with hepatic accumulation and urinary excreti
55 eletal deformities, pigmented hypertrichotic dermatosis with insulin-dependent diabetes syndrome, cha
56 ctions in all H and pigmented hypertrichotic dermatosis with insulin-dependent diabetes syndromes due
57                Chronic Atypical Neutrophilic Dermatosis with Lipodystrophy and Elevated temperature (
58                Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (
59 latory disease chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (
60 enitis suppurativa is a chronic inflammatory dermatosis with presentations ranging from painful nodul
61 nitis suppurativa is a systemic neutrophilic dermatosis, with a specific molecular signature associat