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1 ose naltrexone is an effective treatment for Hailey-Hailey disease.
2 role of low-dose naltrexone for treatment of Hailey-Hailey disease.
3 ure of the mutation and clinical features of Hailey-Hailey disease.
4 ansport ATPase, were recently found to cause Hailey-Hailey disease.
5 (SPCA1a) is implicated in breast cancer and Hailey-Hailey disease.
6 s low-dose naltrexone as a novel therapy for Hailey-Hailey disease.
7 a(2+) transporter ATP2C1 have been linked to Hailey-Hailey disease.
9 the apparently normal skin of a patient with Hailey-Hailey disease and studied a biopsy of this lesio
10 f the human gene, hSPCA1, has been linked to Hailey-Hailey disease, characterized by skin ulceration
11 eplicated in vivo, because clinically normal Hailey-Hailey disease epidermis contained lower Ca2+ sto
12 reen all 28 translated exons of ATP2C1 in 24 Hailey-Hailey disease families and three sporadic cases
15 recently identified as the defective gene in Hailey-Hailey disease (HHD), an autosomal dominant skin
19 appeared normal and exhibited no evidence of Hailey-Hailey disease; however, aged heterozygotes had a
23 levels comparable to other epithelial cells, Hailey-Hailey disease keratinocyte Golgi Ca2+ refill is
25 und that the abnormal Ca2+ signaling seen in Hailey-Hailey disease keratinocytes correlates with decr
26 mbly of intercellular junctions, we cultured Hailey-Hailey disease keratinocytes in medium containing
29 outpatient clinic of 3 patients with severe Hailey-Hailey disease recalcitrant to at least 4 therapi
30 esent herein 3 cases of patients with severe Hailey-Hailey disease treated with low-dose naltrexone w
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