Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Report
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Chylopericardium in a child with impaired venous access following small bowel transplantationBhole, V. ; Gozzini, S. ; Stumper, O. ; Advani, S. ; Sullivan, P. B. ; Rodrigues, A. F. ; Gupte, G. L.Pediatric Transplantation, 2011, Vol.15 (3), p.e39-e41Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
2 |
Material Type: Report
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Abnormal disposition of a branch of the ulnar nerve in the flexor retinaculumOlave, E ; Del Sol, M ; Gabrielli, C ; Rodrigues, C FJournal of anatomy, 1999, Vol.194 ( Pt 3), p.473-474Texto completo disponível |
3 |
Material Type: Report
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Metastatic intraocular chondrosarcoma in a dogRodrigues Jr, Emilio F. ; Ribeiro, Alexandre P. ; Perlmann, Eduardo ; Brooks, Dennis E. ; Laus, José LuizVeterinary Ophthalmology, 2009, Vol.12 (4), p.254-258Malden, USA: Blackwell Publishing IncTexto completo disponível |
4 |
Material Type: Report
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The ulnar tunnel: a rare disposition of its contentsOlave, E ; Del Sol, M ; Gabrielli, C ; Prates, J C ; Rodrigues, C FJournal of anatomy, 1997, Vol.191 ( Pt 4), p.615-616Texto completo disponível |
5 |
Material Type: Report
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Description of a patient cohort with Hereditary Sensory Neuropathy type 1 without retinal disease Macular Telangiectasia type 2 - implications for retinal screening in HSN1Rodrigues, Filipa Gomes ; Pipis, Menelaos ; Heeren, Tjebo F C ; Fruttiger, Marcus ; Gantner, Mari ; Vermeirsch, Sandra ; Okada, Mali ; Friedlander, Martin ; Reilly, Mary M ; Egan, CatherineJournal of the peripheral nervous system : JPNS, 2022, Vol.27 (3), p.215-224Texto completo disponível |
6 |
Material Type: Report
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Progeria: case report and new drugs perspectivesGrana, A G ; Silva, A A ; Moura Filho, F R ; Rodrigues Ferreira Rocha de Alencar, R ; Chicre Bandeira de Melo, PJournal of the European Academy of Dermatology and Venereology : JEADV, 2018, Vol.32 (7), p.e293-e294Texto completo disponível |
7 |
Material Type: Report
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EDA mutation by exome sequencing in non-syndromic X-linked oligodontiaMartins, L ; Machado, R A ; Araujo, D S ; Giovani, P A ; Rebouças, P D ; Rodrigues, L P ; Mofatto, L S ; Ribeiro, M M ; Coutinho, L L ; Puppin-Rontani, R M ; Coletta, R D ; Nociti, F H ; Kantovitz, K RClinical genetics, 2017, Vol.92 (2), p.227-229Texto completo disponível |
8 |
Material Type: Report
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Erythema annulare centrifugum during rituximab treatment for autoimmune haemolytic anaemiaMendes-Bastos, P ; Coelho-Macias, V ; Moraes-Fontes, M F ; Milheiro, A ; Rodrigues, A M ; Cardoso, JJournal of the European Academy of Dermatology and Venereology : JEADV, 2014, Vol.28 (8), p.1125-1127Texto completo disponível |
9 |
Material Type: Report
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Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephaloceleMeloni, V A ; Moysés-Oliveira, M ; Melo, M C C ; Caneloi, T P ; Dantas, A G ; Soares, M F F ; Fock, R ; Rodrigues de Nicola, P D ; Dias-da-Silva, M R ; Melaragno, M IClinical genetics, 2015, Vol.88 (6), p.593-596Texto completo disponível |
10 |
Material Type: Report
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Axillary tumourMartins, A ; Serrão, V ; Fiadeiro, T ; Lopes, M P ; Campos, F ; Pereira, H ; Rodrigues, J CHistopathology, 2008, Vol.52 (5), p.654-655Texto completo disponível |