Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Colombia's Universal Health Insurance SystemGiedion, Ursula ; Uribe, Manuela VillarHealth Affairs, 2009-05, Vol.28 (3), p.853-863 [Periódico revisado por pares]United States: Health AffairsTexto completo disponível |
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2 |
Material Type: Artigo
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MarketWatch: Colombia's Universal Health Insurance SystemGiedion, Ursula ; Uribe, Manuela VillarHealth affairs (Millwood, Va.), 2009-05, Vol.28 (3), p.853-863 [Periódico revisado por pares]Texto completo disponível |
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3 |
Material Type: Artigo
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111:oral Designing a health benefits package for Honduras: from theory to practiceGiedion, Ursula ; Gongora, Pamela ; Jorgensen, Natalia ; Muñoz, RodrigoBMJ global health, 2022-04, Vol.7 (Suppl 2), p.A39-A39 [Periódico revisado por pares]London: BMJ Publishing Group LtdTexto completo disponível |
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4 |
Material Type: Artigo
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COVID-19 vaccines pricing policy options for low-income and middle- income countriesGuzman, Javier ; Hafner, Tamara ; Maiga, Lalla Arkia ; Giedion, UrsulaBMJ global health, 2021-03, Vol.6 (3), p.e005347 [Periódico revisado por pares]England: BMJ Publishing Group LTDTexto completo disponível |
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5 |
Material Type: Artigo
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A recurrent R718W mutation in COMP results in multiple epiphyseal dysplasia with mild myopathy: clinical and pathogenetic overlap with collagen IX mutationsJakkula, E ; Lohiniva, J ; Capone, A ; Bonafe, L ; Marti, M ; Schuster, V ; Giedion, A ; Eich, G ; Boltshauser, E ; Ala-Kokko, L ; Superti-Furga, AJournal of medical genetics, 2003-12, Vol.40 (12), p.942-948 [Periódico revisado por pares]England: BMJ Publishing Group LtdTexto completo disponível |
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6 |
Material Type: Artigo
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Acrocapitofemoral dysplasia: an autosomal recessive skeletal dysplasia with cone shaped epiphyses in the hands and hipsMortier, G R ; Kramer, P P G ; Giedion, A ; Beemer, F AJournal of medical genetics, 2003-03, Vol.40 (3), p.201-207 [Periódico revisado por pares]England: BMJ Publishing Group LtdTexto completo disponível |
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7 |
Material Type: Artigo
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A recurrent r718w mutation in COMP results in multiple epiphyseal dysplasia with mild myopathy: clinical and pat oqenetic overlap with collagen IX mutationsJAKKULA, E ; LOHINIVA, J ; SUPERTI-FURGA, A ; CAPONE, A ; BONAFE, L ; MARTI, M ; SCHUSTER, V ; GIEDION, A ; EICH, G ; BOLTSHAUSER, E ; ALA-KOKKO, LJournal of medical genetics, 2003, Vol.40 (12), p.942-948 [Periódico revisado por pares]London: BMJTexto completo disponível |
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8 |
Material Type: Artigo
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Unknown syndrome: ischiadic hypoplasia, renal dysfunction, immunodeficiency, and a pattern of minor congenital anomaliesBraegger, C ; Bottani, A ; Hallé, F ; Giedion, A ; Leumann, E ; Seger, R ; Willi, U ; Schinzel, AJournal of medical genetics, 1991-01, Vol.28 (1), p.56-59 [Periódico revisado por pares]England: BMJ Publishing Group LtdTexto completo disponível |
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9 |
Material Type: Artigo
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Unknown syndrome : ischiadic hypoplasia, renal dysfunction, immunodeficiency, and a pattern of minor congential anomaliesBRAEGGER, C ; BOTTANI, A ; HALLE, F ; GIEDION, A ; LEUMANN, E ; SEGER, R ; WILLI, U ; SCHINZEL, AJournal of medical genetics, 1991, Vol.28 (1), p.56-59 [Periódico revisado por pares]London: BMJTexto completo disponível |
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10 |
Material Type: Artigo
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Unknown syndrome: ischiadic hypoplasia, renal dysfunction, immunodeficiency, and a pattern of minor congenital anomaliesBraegger, C ; Bottani, A ; Halle, F ; Giedion, Andres ; Leumann, E ; Seger, R ; Willi, U ; Schinzel, AlbertBMJ Publishing Group 1991-01Texto completo disponível |