Successful treatment of warts with a combination of maxacalcitol ointment and salicylic acid sticking plaster
スポンサーリンク
概要
- 論文の詳細を見る
- 2006-05-01
著者
-
TOMITA Yasushi
Department of Dermatology, Nagoya University Graduate School of Medicine
-
Inaba Hiroko
Department Of Dermatology Tokoname Municipal Hospital
-
Tomita Yasushi
Department Of Cardiology Nagoya Daini Red Cross Hospital
-
SUZUKI Tamio
Department of Dermatology, Nagoya University Graduate School of Medicine
-
Suzuki Tamio
Department Of Dermatology Nagoya University Graduate School Of Medicine
-
ADACHI Ayumi
Department of Dermatology, Nagoya University Graduate School of Medicine
-
Adachi Ayumi
Department Of Dermatology Nagoya University Graduate School Of Medicine
関連論文
- Genotyping of Candida albicans by Fragment Analysis of Microsatellites Combined with 25S rDNA and RPS-based Strategies
- Case of hypereosinophilic syndrome with cutaneous necrotizing vasculitis
- Molecular Cloning of cDNA Encoding a Novel Microphthalmia-Associated Transcription Factor Isoform with a Distinct Amino-Terminus
- Epidemiological study of Candida species in cutaneous candidiasis based on PCR using a primer mix specific for the DNA topoisomerase II gene
- PCR and PCR-RFLP techniques targeting the DNA topoisomerase II gene for rapid clinical diagnosis of the etiologic agent of dermatophytosis
- The effect of the long-term cultivation on telomere length and morphology of cultured epidermis
- Dyschromatosis symmetrica hereditaria associated with neurological disorders
- Dominant dystrophic epidermolysis bullosa caused by a novel G2037R mutation and by a known G2028R mutation in the type VII collagen gene (COL7A1)
- Primary cutaneous T-cell lymphoma of unspecified type with cytotoxic phenotype : Clinicopathological analysis of 27 patients
- Investigation of the IVS5 +5G → A splice site mutation of HPS1 gene found in Japanese patients with Hermansky-Pudlak syndrome
- Characterization of the human RAB38 and RAB7 genes : exclusion of new major pathological loci for Japanese OCA
- Genotype analysis of Candida albicans isolates obtained from different body locations of patients with superficial candidiasis using PCRs targeting 25S rDNA and ALT repeat sequences of the RPS
- Genotyping of Candida albicans on the basis of polymorphisms of ALT repeats in the repetitive sequence (RPS)
- EVALUATION OF CETIRIZINE HYDROCHLORIDE BASED FOR CHRONIC URTICARIA
- Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria
- Primary Cutaneous Ki-1^+ Anaplastic Large Cell Lymphoma : A Morphologic, Immunohistochemical and Genetic Study of an Indolent Case
- Successful topical hemotherapy with a new occlusive dressing for an intractable ulcer on the toe
- Effects of topical vehicles on growth of the lipophilic Malassezia species
- Antigenic components of Malassezia species for immunoglobulin E antibodies in sera of patients with atopic dermatitis
- Isolation and Characterization of a Major Antigenic Component of Malassezia globosa to IgE Antibodies in Sera of Patients with Atopic Dermatitis
- Two novel mutations detected in Japanese patients with oculocutaneous albinism
- Establishment of tyrosinase sequence database in normally pigmented Indians and Japanese for rapid determination of novel mutations
- Detection of various types of human papillomavirus DNA, mainly belonging to the cutaneous-group, more frequently in normal tissue than in squamous cell carcinomas of the lip
- A novel mutation of the tyrosinase gene causing oculocutaneous albinism type 1 (OCA1)
- Polymorphic sequences of the tyrosinase gene : allele analysis on 16 OCA1 patients in Japan indicate that three polymorphic sequences in the tyrosinase gene promoter could be powerful markers for indirect gene diagnosis
- Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9
- R278TER and P431L mutations of the tyrosinase gene exist in Japanese patients with tyrosinase-negative oculocutaneous albinism
- Dermoscopic evaluation of vascular structure of various skin tumors in Japanese patients
- Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria : Histological observation and comparison of genotypes and clinical phenotypes
- Mechanism of the Inhibitory Effect of Tranexamic Acid on Melanogenesis in Cultured Human Melanocytes in the Presence of Keratinocyte-conditioned Medium
- Establishment of a Screening System for Chemicals that Upregulate a Melanoma Antigen, Melan-A/MART-1
- Keratoacanthoma Centrifugum Marginatum Arising from a Scar after Skin Injury
- Successful treatment of warts with a combination of maxacalcitol ointment and salicylic acid sticking plaster
- Fixed Drug Eruption Due to Afloqualone : The First Reported Case
- Oculocutaneous Albinism and Analysis of Tyrosinase Gene in Japanese Patients
- Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4
- A novel MITF splice site mutation in a family with Waardenburg syndrome
- Linear immunoglobulin A bullous dermatosis associated with herpes simplex virus infection and Kawasaki disease
- Mutation analyses of patients with dyschromatosis symmetrica hereditaria : Five novel mutations of the ADAR1 gene
- A Case of Refractory Bullous Pemphigoid with Plasmapheresis-Associated Thrombopenia : Efficacy of Pulsed Intravenous Cyclophosphamide Therapy
- The Successful Use of Topical Tacrolimus Treatment for a Chronic Actinic Dermatitis Patient with Complications of Idiopathic Leukopenia
- Comparison of the melanogenesis in human black and light brown melanocytes
- Recurrent Dermatofibrosarcoma Protuberans with Myxoid and Fibrosarcomatous Changes Paralleled by Loss of CD34 Expression
- Dermoscopic features in a case of dyschromatosis symmetrica hereditaria
- Dystrophic epidermolysis bullosa pruriginosa of elderly onset
- Therapy-related myelodysplastic syndrome developed by dacarbazine, nimustine hydrochloride and vincristine sulfate (DAV) therapy for patient with malignant melanoma
- Microsatellite-based Genotyping of Candida albicans Isolated from Patients with Superficial Candidiasis
- Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain
- Oculocutaneous albinism type 3 : A Japanese girl with novel mutations in TYRP1 gene
- Prediction of additional lymph node positivity and clinical outcome of micrometastases in sentinel lymph nodes in cutaneous melanoma : A multi-institutional study of 450 patients in Japan
- Nephrogenic systemic fibrosis : A case report and review on Japanese patients