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Drug reaction with eosinophilia and systemic symptoms/drug-induced hypersensitivity syndrome: clinical features of 27 patients
Drug reaction with eosinophilia and systemic symptoms/drug-induced hypersensitivity syndrome: clinical features of 27 patients
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Drug reaction with eosinophilia and systemic symptoms/drug-induced hypersensitivity syndrome: clinical features of 27 patients

Avancini, J. ; Maragno, L. ; Santi, C. G. ; Criado, P. R.

Clinical and experimental dermatology, 2015-12, Vol.40 (8), p.851-859 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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2
Longitudinal melanonychia due to voriconazole therapy during treatment of chromoblastomycosis
Longitudinal melanonychia due to voriconazole therapy during treatment of chromoblastomycosis
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Longitudinal melanonychia due to voriconazole therapy during treatment of chromoblastomycosis

Criado, P. R. ; Cosenza, F. D. ; Junior, W. B. ; Ferreira, P. S.

Clinical and experimental dermatology, 2018-01, Vol.43 (1), p.75-76 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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3
Direct immunofluorescence findings and thrombophilic factors in livedoid vasculopathy: how do they correlate?
Direct immunofluorescence findings and thrombophilic factors in livedoid vasculopathy: how do they correlate?
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Direct immunofluorescence findings and thrombophilic factors in livedoid vasculopathy: how do they correlate?

Criado, P. R. ; Di Giacomo, T. H. B. ; Souza, D. P. G. ; Santos, D. V. ; Aoki, V.

Clinical and experimental dermatology, 2014-01, Vol.39 (1), p.66-68 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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4
Monocyte-derived dendritic cells from patients with severe forms of chromoblastomycosis induce CD4⁺ T cell activation in vitro
Monocyte-derived dendritic cells from patients with severe forms of chromoblastomycosis induce CD4⁺ T cell activation in vitro
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Monocyte-derived dendritic cells from patients with severe forms of chromoblastomycosis induce CD4⁺ T cell activation in vitro

Sousa, M. Glória ; Ghosn, E. Eid Bou ; Nascimento, R. Ciciro ; Bomfim, G. Facchioli ; Noal, V ; Santiago, K ; de Maria Pedrozo e Silva Azevedo, C ; Marques, S. Garcia ; Gonçalves, A. Guedes ; de Castro Lima Santos, D. Wagner ; Criado, P. Ricardo ; Costa Martins, J. Eduardo ; Almeida, S. Rogerio

Clinical and experimental immunology, 2009-04, Vol.156 (1), p.117-125 [Periódico revisado por pares]

Oxford, UK: Oxford, UK : Blackwell Publishing Ltd

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5
Blisters on the legs
Blisters on the legs
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Blisters on the legs

Fernandes, J. D. ; Gabbi, T. V. B. ; Vilela, M. A. C. ; Sotto, M. N. ; Criado, P. R. ; Romiti, R.

Clinical and experimental dermatology, 2008-01, Vol.33 (1), p.81-82 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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6
An unusual association between scalp psoriasis and ophiasic alopecia areata: the Renbök phenomenon
An unusual association between scalp psoriasis and ophiasic alopecia areata: the Renbök phenomenon
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An unusual association between scalp psoriasis and ophiasic alopecia areata: the Renbök phenomenon

Criado, P. R. ; Valente, NeusA. Y. S. ; Michalany, N. S. ; Martins, J. E. C. ; Romiti, R. ; Aoki, V. ; Vasconcellos, C.

Clinical and experimental dermatology, 2007-05, Vol.32 (3), p.320-321 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
Necrobiotic xanthogranuloma with lambda paraproteinemia: case report of successful treatment with melphalan and prednisone
Necrobiotic xanthogranuloma with lambda paraproteinemia: case report of successful treatment with melphalan and prednisone
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Necrobiotic xanthogranuloma with lambda paraproteinemia: case report of successful treatment with melphalan and prednisone

Criado, PR ; Vasconcellos, C ; Pegas, JR ; Lopes, LF ; Ramos, CF ; Tebcherani, AJ ; Valente, NYS

The Journal of dermatological treatment, 2002, Vol.13 (2), p.87-89 [Periódico revisado por pares]

Oslo: Informa UK Ltd

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8
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
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Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder

Frints, Suzanna G M ; Ozanturk, Aysegul ; Rodríguez Criado, Germán ; Grasshoff, Ute ; de Hoon, Bas ; Field, Michael ; Manouvrier-Hanu, Sylvie ; E Hickey, Scott ; Kammoun, Molka ; Gripp, Karen W ; Bauer, Claudia ; Schroeder, Christopher ; Toutain, Annick ; Mihalic Mosher, Theresa ; Kelly, Benjamin J ; White, Peter ; Dufke, Andreas ; Rentmeester, Eveline ; Moon, Sungjin ; Koboldt, Daniel C ; van Roozendaal, Kees E P ; Hu, Hao ; Haas, Stefan A ; Ropers, Hans-Hilger ; Murray, Lucinda ; Haan, Eric ; Shaw, Marie ; Carroll, Renee ; Friend, Kathryn ; Liebelt, Jan ; Hobson, Lynne ; De Rademaeker, Marjan ; Geraedts, Joep ; Fryns, Jean-Pierre ; Vermeesch, Joris ; Raynaud, Martine ; Riess, Olaf ; Gribnau, Joost ; Katsanis, Nicholas ; Devriendt, Koen ; Bauer, Peter ; Gecz, Jozef ; Golzio, Christelle ; Gontan, Cristina ; Kalscheuer, Vera M

Molecular psychiatry, 2019-11, Vol.24 (11), p.1748-1768 [Periódico revisado por pares]

England: Nature Publishing Group

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9
Critical study of the isoconversional methods of kinetic analysis
Critical study of the isoconversional methods of kinetic analysis
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Critical study of the isoconversional methods of kinetic analysis

Criado, J. M. ; Sánchez-Jiménez, P. E. ; Pérez-Maqueda, L. A.

Journal of thermal analysis and calorimetry, 2008-04, Vol.92 (1), p.199-203 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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10
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Hu, H ; Haas, S A ; Chelly, J ; Van Esch, H ; Raynaud, M ; de Brouwer, A P M ; Weinert, S ; Froyen, G ; Frints, S G M ; Laumonnier, F ; Zemojtel, T ; Love, M I ; Richard, H ; Emde, A-K ; Bienek, M ; Jensen, C ; Hambrock, M ; Fischer, U ; Langnick, C ; Feldkamp, M ; Wissink-Lindhout, W ; Lebrun, N ; Castelnau, L ; Rucci, J ; Montjean, R ; Dorseuil, O ; Billuart, P ; Stuhlmann, T ; Shaw, M ; Corbett, M A ; Gardner, A ; Willis-Owen, S ; Tan, C ; Friend, K L ; Belet, S ; van Roozendaal, K E P ; Jimenez-Pocquet, M ; Moizard, M-P ; Ronce, N ; Sun, R ; O'Keeffe, S ; Chenna, R ; van Bömmel, A ; Göke, J ; Hackett, A ; Field, M ; Christie, L ; Boyle, J ; Haan, E ; Nelson, J ; Turner, G ; Baynam, G ; Gillessen-Kaesbach, G ; Müller, U ; Steinberger, D ; Budny, B ; Badura-Stronka, M ; Latos-Bieleńska, A ; Ousager, L B ; Wieacker, P ; Rodríguez Criado, G ; Bondeson, M-L ; Annerén, G ; Dufke, A ; Cohen, M ; Van Maldergem, L ; Vincent-Delorme, C ; Echenne, B ; Simon-Bouy, B ; Kleefstra, T ; Willemsen, M ; Fryns, J-P ; Devriendt, K ; Ullmann, R ; Vingron, M ; Wrogemann, K ; Wienker, T F ; Tzschach, A ; van Bokhoven, H ; Gecz, J ; Jentsch, T J ; Chen, W ; Ropers, H-H ; Kalscheuer, V M

Molecular psychiatry, 2016-01, Vol.21 (1), p.133-148 [Periódico revisado por pares]

England: Nature Publishing Group

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