Journal of dermatological case reports最新文献

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Dermatofibrosarcoma protuberans in a 10-year-old child. 10岁儿童隆突性皮肤纤维肉瘤。
Journal of dermatological case reports Pub Date : 2013-12-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1160
Uwe Wollina
{"title":"Dermatofibrosarcoma protuberans in a 10-year-old child.","authors":"Uwe Wollina","doi":"10.3315/jdcr.2013.1160","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1160","url":null,"abstract":"<p><strong>Background: </strong>Dermatofibrosarcoma protuberans is a rare mesenchymal malignancy in childhood and adolescence. The tumor is characterized by dermal spindle cell proliferation with infiltration of subcutaneous tissue, expression of CD34, and a specific fusion of the platelet-derived growth factor beta with the collagen type 1alpha1 gene.</p><p><strong>Main observation: </strong>We observed a 10-year-old girl with a medaillon-like, asymptomatic plaque on the chest that was diagnosed as DSFP. The tumor was completely removed by delayed Mohs surgery. Follow-up so far has shown a complete response.</p><p><strong>Conclusions: </strong>The prognosis of dermatofibrosarcoma protuberans in children is excellent as long as early diagnosis is followed by complete excision with Mohs surgery as a golden standard.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 4","pages":"121-4"},"PeriodicalIF":0.0,"publicationDate":"2013-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2013.1160","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32025679","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Prevalence of skin diseases in a dermatology outpatient clinic in Turkey. A cross-sectional, retrospective study. 皮肤病的流行病学门诊诊所在土耳其。横断面、回顾性研究。
Journal of dermatological case reports Pub Date : 2013-12-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1156
Memet Ersan Bilgili, Hamza Yildiz, Gulben Sarici
{"title":"Prevalence of skin diseases in a dermatology outpatient clinic in Turkey. A cross-sectional, retrospective study.","authors":"Memet Ersan Bilgili,&nbsp;Hamza Yildiz,&nbsp;Gulben Sarici","doi":"10.3315/jdcr.2013.1156","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1156","url":null,"abstract":"<p><strong>Background: </strong>Dermatologic diseases vary widely as a result of geographic location, climate, socioeconomic status, and personal habits, and internal factors, such as age, gender, and heredity.</p><p><strong>Objective: </strong>The aim of the study was to determine the main causes for outpatient visits in a dermatology outpatient clinic in Turkey.</p><p><strong>Materials and methods: </strong>The outpatient clinic records of the Dermatology Department of Eskisehir Yunus Emre Government Hospital, dated between 1 January 2011 and 1 January 2012, were retrospectively assessed. Patients were grouped according to age, gender and clinical diagnosis.</p><p><strong>Results: </strong>A total of 11,040 new patients with 12,174 skin problems were included in the study. The study group was 55.7% female and 44.3% male. The age range was between 1 and 99 years. The most commonly encountered diseases were: acne (13.1% of patients), fungal infections (8.5%), contact dermatitis (8.5%), urticaria (8.3%), psoriasis (5.5%), viral warts (4.1%), lichen simplex chronicus (3.0%), callus, atopic dermatitis, and seborrheic dermatitis (2.2% each).</p><p><strong>Conclusions: </strong>It appears that certain skin diseases acne, fungal infections, contact dermatitis and urticarial cause serious health problems. Public health policies should be implemented in order to manage these problems rationally.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 4","pages":"108-12"},"PeriodicalIF":0.0,"publicationDate":"2013-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2013.1156","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32025677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 43
Photoletter to the editor: Diffuse cocaine-related purpura. 给编辑的照片信:弥漫性可卡因相关紫癜。
Journal of dermatological case reports Pub Date : 2013-12-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1159
Debjeet Sarkar, Hussein A Kammona, Leonard N Lamsen, Bradley A McAbee, Christopher T Clark, Solomon S Lee, Shane E Kelley
{"title":"Photoletter to the editor: Diffuse cocaine-related purpura.","authors":"Debjeet Sarkar,&nbsp;Hussein A Kammona,&nbsp;Leonard N Lamsen,&nbsp;Bradley A McAbee,&nbsp;Christopher T Clark,&nbsp;Solomon S Lee,&nbsp;Shane E Kelley","doi":"10.3315/jdcr.2013.1159","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1159","url":null,"abstract":"<p><p>Diffuse purpura is an uncommon skin manifestation found in platelet and coagulation disorders, meningococcemia, vasculitides and cocaine use. Reports of cocaine-related purpura predominantly involve adulteration with the anti-helminthic, levamisole. Levamisole enhances the effects of cocaine and is known to cause vasculitis. Recently, the CDC also released an advisory of oxymorphone being used intravenously causing thrombogenic thrombocytopenic purpura (TTP). We report the case of a patient with diffuse purpura ultimately diagnosed with cocaine-related thrombogenic vasculopathy. In the current environment of adulterated cocaine usage and increased prescription narcotic abuse, it is crucial to investigate substance abuse as a cause of diffuse purpura. </p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 4","pages":"132-3"},"PeriodicalIF":0.0,"publicationDate":"2013-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2013.1159","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32025682","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Coexistence of aplasia cutis congenita, faun tail nevus and fetus papyraceus. 先天性皮肤发育不全、羊尾痣和胎儿纸莎草痣共存。
Journal of dermatological case reports Pub Date : 2013-09-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1148
Pelin Ustüner, Nursel Dilek, Yunus Saral, Işık Ustüner
{"title":"Coexistence of aplasia cutis congenita, faun tail nevus and fetus papyraceus.","authors":"Pelin Ustüner,&nbsp;Nursel Dilek,&nbsp;Yunus Saral,&nbsp;Işık Ustüner","doi":"10.3315/jdcr.2013.1148","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1148","url":null,"abstract":"<p><strong>Background: </strong>Aplasia cutis congenita is a disorder of the skin embryonic development characterized by a defect of localized or widespread areas of skin at birth. The lesions are mostly oval, 1-3 cm in diameter, with localization on the parietal part of scalp (60%) and rarely on the face and extremities.</p><p><strong>Main observations: </strong>Herein, we reported a case of aplasia cutis congenita termly born at 39 weeks of gestation to a 30-year-old mother with bronchial asthma attacks. She was referred for 3 punched-out punctate depressed defective lesions in 0.4 cm's diameter on the vertex covered with necrotic and hemorrhagic crusts. There was a hypertrichotic area consisting of tufts of terminal hair on the lumbosacral area over a sinus tract. Maternal perinatal drugs included aerosol salbutamol sulfate, ipratropium bromide and oral montelukast sodium for bronchial asthma. The pregnancy was firstly started as a di-chorionic, di-amniotic twin gestation, but deteriorated after the fetal resorption of the co-twin in the 20th gestational week resulting in fetus papyraceus.</p><p><strong>Conclusion: </strong>In multi-gestational pregnancies, the presence of the fetus papyraceus or the death of the co-twins should make the neonatologists and dermatologists be aware of the possible cutaneous defects like aplasia cutis congenita. We emphasize that the possibility of this rare entity should be kept in mind in the presence of fetus papyraceus, perinatal drug use, maternal cigarette smoke, or maternal diseases like bronchial asthma in multiple gestations.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 3","pages":"93-6"},"PeriodicalIF":0.0,"publicationDate":"2013-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797017/pdf/jdcr-07-093.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31814394","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 12
A lesion suspected of melanoma by dermoscopy: we must trust this diagnostic tool. 皮肤镜检查怀疑为黑色素瘤的病变:我们必须相信这个诊断工具。
Journal of dermatological case reports Pub Date : 2013-09-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1151
Paula Cabral de Menezes Gurfinkel, Gabriella Campos-do-Carmo, Cleide Eiko Ishida, Juan Piñeiro-Maceira, Paulo Marcos Valiante, Marcia Ramos-E-Silva
{"title":"A lesion suspected of melanoma by dermoscopy: we must trust this diagnostic tool.","authors":"Paula Cabral de Menezes Gurfinkel,&nbsp;Gabriella Campos-do-Carmo,&nbsp;Cleide Eiko Ishida,&nbsp;Juan Piñeiro-Maceira,&nbsp;Paulo Marcos Valiante,&nbsp;Marcia Ramos-E-Silva","doi":"10.3315/jdcr.2013.1151","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1151","url":null,"abstract":"<p><strong>Background: </strong>The incidence of cutaneous melanoma is increasing worldwide and early diagnosis is essential since the prognosis is poor in advanced stages of disease. Dermoscopy emerged as an additional and important diagnostic procedure for the early diagnosis of cutaneous melanoma.</p><p><strong>Main observation: </strong>We report a case of a 52-year-old man, who developed a pigmented lesion in the right pretibial region. Dermoscopy highly suggestive of melanoma. The initial histopathological evaluation suggested a benign lesion. Since dermoscopy was very suspicious, a more extensive histopathological study of the excised skin fragment was performed. This led to a change of diagnosis to a melanoma with partial regression.</p><p><strong>Conclusions: </strong>The present case shows that occasionally dermoscopy may be more informative for diagnosis of melanoma than an initial histopathology result.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 3","pages":"88-92"},"PeriodicalIF":0.0,"publicationDate":"2013-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797016/pdf/jdcr-07-088.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31814393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
A Unique Case of Classic Kaposi's sarcoma restricted to the toes. 一例局限于脚趾的经典卡波西肉瘤。
Journal of dermatological case reports Pub Date : 2013-09-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1146
Anne S Renteria, Vickie A Marshall, Yanyu Sun, Porselvi Chockalingam, Jay S Cooper, Yiwu Huang, Denise Whitby
{"title":"A Unique Case of Classic Kaposi's sarcoma restricted to the toes.","authors":"Anne S Renteria,&nbsp;Vickie A Marshall,&nbsp;Yanyu Sun,&nbsp;Porselvi Chockalingam,&nbsp;Jay S Cooper,&nbsp;Yiwu Huang,&nbsp;Denise Whitby","doi":"10.3315/jdcr.2013.1146","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1146","url":null,"abstract":"<p><strong>Background: </strong>Kaposi's sarcoma associated-herpesvirus causes all forms of Kaposi's sarcoma, and six major subtypes have been described based on the amino acid sequences of the open reading frame K1.</p><p><strong>Main observation: </strong>A 71-year-old man from China, HIV negative, presented with nodules on the dorsal aspect of his toes. Biopsy confirmed the diagnosis of Kaposi's sarcoma and virology studies of his blood and saliva confirmed the presence of Kaposi's sarcoma associated-herpesvirus infection. Viral genotyping was consistent with subtype C3. Intervention has been deferred as our patient has remained clinically asymptomatic and without evident growth of his lesions over a 2-year follow up.</p><p><strong>Conclusions: </strong>We herein report the first known case of Kaposi's sarcoma restricted to the toes caused by the viral subtype C3 in an HIV-negative patient from Harbin, China.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 3","pages":"97-100"},"PeriodicalIF":0.0,"publicationDate":"2013-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797018/pdf/jdcr-07-097.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31814395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Photoletter to the editor: Dermatitis herpetiformis co-localised with vitiligo in a patient with autoimmune polyglandular syndrome. 致编辑的信:自身免疫性多腺综合征患者疱疹样皮炎与白癜风共发。
Journal of dermatological case reports Pub Date : 2013-09-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1153
Abby E Macbeth, Kevin Y C Lee, Nick J Levell, Laszlo Igali, George W M Millington
{"title":"Photoletter to the editor: Dermatitis herpetiformis co-localised with vitiligo in a patient with autoimmune polyglandular syndrome.","authors":"Abby E Macbeth,&nbsp;Kevin Y C Lee,&nbsp;Nick J Levell,&nbsp;Laszlo Igali,&nbsp;George W M Millington","doi":"10.3315/jdcr.2013.1153","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1153","url":null,"abstract":"<p><p>We report a case of dermatitis herpetiformis co-localised with segmental vitiligo in a 37-year-old woman with a background history of autoimmune polyglandular syndrome type 2. We propose genetic mosaicism as a possible mechanism. There has only been one previous case report in which dermatitis hepetiformis co-localised in close proximity but not exclusively within vilitigo in a patient with autoimmune thyroiditis. To our knowledge, this is the first case report of dermatitis herpetiformis co-localised exclusively to segmental vitiligo in the presence of autoimmune polyglandular syndrome. </p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 3","pages":"101-2"},"PeriodicalIF":0.0,"publicationDate":"2013-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797019/pdf/jdcr-07-101.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31814396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Photoletter to the editor: Squamous cell carcinoma associated with and masquerading as molluscum contagiosum. 给编辑的照相信:鳞状细胞癌与传染性软疣相关并伪装成传染性软疣。
Journal of dermatological case reports Pub Date : 2013-09-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1152
Manikoth Payyanadan Binitha, Sasidharan Pillai Sarita, Mohan Manju
{"title":"Photoletter to the editor: Squamous cell carcinoma associated with and masquerading as molluscum contagiosum.","authors":"Manikoth Payyanadan Binitha,&nbsp;Sasidharan Pillai Sarita,&nbsp;Mohan Manju","doi":"10.3315/jdcr.2013.1152","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1152","url":null,"abstract":"<p><p>Squamous cell carcinoma is a non-melanoma skin cancer with a significant risk of mortality if not diagnosed promptly. A high index of suspicion is required, since it may mimic many benign conditions. Molluscum contagiosum is an innocuous viral infection which can also mimic a wide variety of other conditions. We report a case of squamous cell carcinoma on the anterior chest wall resembling a giant molluscum contagiosum, where the patient also had molluscum contagiosum at other sites. In addition, he developed herpes zoster of the left fifth thoracic dermatome. After surgical removal of the cancer, there was prompt subsidence of the molluscum contagiosum lesions without any specific treatment. This report highlights the importance of early biopsy in the diagnosis of squamous cell carcinoma. As the patient had no other conditions or therapy that could account for the immunosuppression, we hypothesize that the occurrance of molluscum contagiosum and zoster along with the squamous cell carcinoma indicates possible immunosuppression due to the carcinoma, though no metastatic spread could be detected. </p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 3","pages":"103-5"},"PeriodicalIF":0.0,"publicationDate":"2013-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797020/pdf/jdcr-07-103.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31814397","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Letter to the editor: Temporary renal insufficiency associated with topical tacrolimus treatment of multilocal pyoderma gangrenosum. 致编辑:局部他克莫司治疗多局部坏疽性脓皮病的暂时性肾功能不全。
Journal of dermatological case reports Pub Date : 2013-09-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1154
Uwe Wollina
{"title":"Letter to the editor: Temporary renal insufficiency associated with topical tacrolimus treatment of multilocal pyoderma gangrenosum.","authors":"Uwe Wollina","doi":"10.3315/jdcr.2013.1154","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1154","url":null,"abstract":"Prof. Dr. U. Wollina, Department of Dematology and Allergology, Academic Teaching Hospital Dresden-Friedrichstadt,Freidrichstrasse 41, 01067 Dresden, Germany. E-mail: wollina-uw@khdf.deIn renal transplant patients maintenance therapy with lowdose tacrolimus and mycophenolate mofetil in combinationis used to prevent renal injury and graft rejection.","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 3","pages":"106-7"},"PeriodicalIF":0.0,"publicationDate":"2013-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797021/pdf/jdcr-07-106.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31814398","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Pentoxifylline-induced drug rash with eosinophilia and systemic symptoms (DRESS) in a patient with caffeine intolerance. 咖啡因不耐受患者的己酮可可碱引起的药物皮疹伴嗜酸性粒细胞增多和全身症状(DRESS)。
Journal of dermatological case reports Pub Date : 2013-09-30 eCollection Date: 2013-01-01 DOI: 10.3315/jdcr.2013.1150
Rebecca B Saunderson, Roger Garsia, Alexander P Headley, Geoffrey W McCaughan, Sandra O'Toole, Simone I Strasser
{"title":"Pentoxifylline-induced drug rash with eosinophilia and systemic symptoms (DRESS) in a patient with caffeine intolerance.","authors":"Rebecca B Saunderson,&nbsp;Roger Garsia,&nbsp;Alexander P Headley,&nbsp;Geoffrey W McCaughan,&nbsp;Sandra O'Toole,&nbsp;Simone I Strasser","doi":"10.3315/jdcr.2013.1150","DOIUrl":"https://doi.org/10.3315/jdcr.2013.1150","url":null,"abstract":"<p><strong>Background: </strong>Drug rash with eosinophilia and systemic symptoms (DRESS) is a severe drug reaction characterised by rash, eosinophilia and systemic involvement.</p><p><strong>Main observations: </strong>We report a case of DRESS induced by pentoxifylline used for the treatment of severe alcoholic hepatitis, in a patient with longstanding caffeine intolerance. A history of intolerance to caffeine and other methylxanthines is listed as a contraindication to the use of pentoxifylline, yet this precaution is not mentioned in alcoholic hepatitis treatment guidelines.</p><p><strong>Conclusions: </strong>Prescribers should always seek a history of intolerance to caffeine and related compounds prior to use of pentoxifylline, as severe life threatening reactions can occur.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"7 3","pages":"77-81"},"PeriodicalIF":0.0,"publicationDate":"2013-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797013/pdf/jdcr-07-077.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31814390","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
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