Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Material Type: Artigo
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Clinical characterization of the HOXA1 syndrome BSAS variantBOSLEY, T. M ; SALIH, M. A ; ALORAINY, I. A ; OYSTRECK, D. T ; NESTER, M ; ABU-AMERO, K. K ; TISCHFIELD, M. A ; ENGLE, E. CNeurology, 2007-09, Vol.69 (12), p.1245-1253 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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Material Type: Artigo
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Alternative to fluorescence assays to monitor fusion between Acholeplasma laidlawii cells and liposomesAbu‐Amero, K.K. ; Halablab, M.A. ; Miles, R.J.Letters in applied microbiology, 2002-01, Vol.35 (6), p.528-532 [Periódico revisado por pares]Oxford, UK: Blackwell Science LtdTexto completo disponível |
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3 |
Material Type: Artigo
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Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C geneABU‐AMERO, K. K. ; OWAIDAH, T. M. ; AL‐MAHED, M.Journal of thrombosis and haemostasis, 2006-05, Vol.4 (5), p.1152-1153 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing IncTexto completo disponível |
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4 |
Material Type: Artigo
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Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3Bosley, T.M. ; Salih, M.A. ; Jen, J.C. ; Lin, D.D. ; Oystreck, D. ; Abu-Amero, K.K. ; MacDonald, D.B. ; al Zayed, Z. ; al Dhalaan, H. ; Kansu, T. ; Stigsby, B. ; Baloh, R.W.American journal of ophthalmology, 2005-08, Vol.140 (2), p.355-355 [Periódico revisado por pares]Chicago: Elsevier IncTexto completo disponível |
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5 |
Material Type: Capítulo de Livro
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Congenital Cranial Dysinnervation DisordersBosley, T.M. ; Oystreck, D.T. ; Abu-Amero, K.K.Reference Module in Neuroscience and Biobehavioral Psychology, 2017Elsevier IncTexto completo disponível |
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6 |
Material Type: Capítulo de Livro
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Congenital Cranial Dysinnervation DisordersBosley, T.M. ; Oystreck, D.T. ; Abu-Amero, K.K.Encyclopedia of the Eye, 2010, Vol.1, p.346-355Texto completo disponível |