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Refinado por: Base de dados/Biblioteca: Oxford Journals remover tipo de recurso: Reports remover
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1
Sterile abscesses possibly stem from acantholytic folliculitis in comedonal Darier disease: a case report
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Report
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Sterile abscesses possibly stem from acantholytic folliculitis in comedonal Darier disease: a case report

Komatsu-Fujii, T ; Murata, T ; Adachi, E ; Kaku, Y ; Wada, T ; Nakagawa, N ; Kosugi, S ; Uehara, T ; Kosaki, K ; Kataoka, T ; Egawa, G ; Dainichi, T ; Kabashima, K

The British journal of dermatology, 2021, Vol.185 (3), p.667-669

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2
Dilated cardiomyopathy (DCM) associated with SSA antibody in primary Sjögren syndrome
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Dilated cardiomyopathy (DCM) associated with SSA antibody in primary Sjögren syndrome

Nishinarita, M. ; Nakagawa, M. ; Tanaka, E.

Modern Rheumatology, 2000, Vol.10 (2), p.114-116

Taylor & Francis

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3
Muir-Torre syndrome caused by partial duplication of MSH2 gene by Alu-mediated nonhomologous recombination
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Muir-Torre syndrome caused by partial duplication of MSH2 gene by Alu-mediated nonhomologous recombination

Yanaba, K. ; Nakagawa, H. ; Takeda, Y. ; Koyama, N. ; Sugano, K.

British Journal of Dermatology, 2008, Vol.158 (1), p.150-156

Oxford, UK: Blackwell Publishing Ltd

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4
Taxane-induced scleroderma
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Report
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Taxane-induced scleroderma

Itoh, M. ; Yanaba, K. ; Kobayashi, T. ; Nakagawa, H.

British Journal of Dermatology, 2007, Vol.156 (2), p.363-367

Oxford, UK: Blackwell Publishing Ltd

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5
Angioimmunoblastic lymphadenopathy-type peripheral T-cell lymphoma with cutaneous infiltration: report of a case and its gene expression profile
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Angioimmunoblastic lymphadenopathy-type peripheral T-cell lymphoma with cutaneous infiltration: report of a case and its gene expression profile

Murakami, T. ; Ohtsuki, M. ; Nakagawa, H.

British Journal of Dermatology, 2001, Vol.144 (4), p.878-884

Oxford, UK: Blackwell Science Ltd

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6
Mild phenotype of familial cylindromatosis associated with an R758X nonsense mutation in the CYLD tumour suppressor gene
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Report
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Mild phenotype of familial cylindromatosis associated with an R758X nonsense mutation in the CYLD tumour suppressor gene

Oiso, N. ; Mizuno, N. ; Fukai, K. ; Nakagawa, K. ; Ishii, M.

British Journal of Dermatology, 2004, Vol.151 (5), p.1084-1086

Oxford, UK: Blackwell Science Ltd

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7
Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromes
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Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromes

Bursztejn, A.-C. ; Briggs, T.A. ; del Toro Duany, Y. ; Anderson, B.H. ; O'Sullivan, J. ; Williams, S.G. ; Bodemer, C. ; Fraitag, S. ; Gebhard, F. ; Leheup, B. ; Lemelle, I. ; Oojageer, A. ; Raffo, E. ; Schmitt, E. ; Rice, G.I. ; Hur, S. ; Crow, Y.J.

British Journal of Dermatology, 2015, Vol.173 (6), p.1505-1513

Blackwell Publishing Ltd

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8
A tender red plaque on the elbow of a 93-year-old woman
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A tender red plaque on the elbow of a 93-year-old woman

Ladoyanni, E. ; Neil, D. A. H. ; Shah, F.

Clinical and Experimental Dermatology, 2007, Vol.32 (2), p.233-234

Oxford, UK: Blackwell Publishing Ltd

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9
Diffuse lentiginosis in a patient with Werner's syndrome-a possible association with incomplete leopard syndrome
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Diffuse lentiginosis in a patient with Werner's syndrome-a possible association with incomplete leopard syndrome

LAZAROV, A. ; FINKELSTEIN, E. ; AVINOACH, I. ; KACHKO, L. ; HALEVY, S.

Clinical and Experimental Dermatology, 1995, Vol.20 (1), p.46-50

Oxford, UK: Blackwell Publishing Ltd

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10
Glycosaminoglycan and versican deposits in taxane-induced sclerosis
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Glycosaminoglycan and versican deposits in taxane-induced sclerosis

Okada, K. ; Endo, Y. ; Miyachi, Y. ; Koike, Y. ; Kuwatsuka, Y. ; Utani, A.

British Journal of Dermatology, 2015, Vol.173 (4), p.1054-1058

Blackwell Publishing Ltd

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