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Refinado por: Base de dados/Biblioteca: EBSCO_MEDLINE Complete(医学期刊全文数据库) remover tipo de recurso: Anais de Congresso remover
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1
Omenn Syndrome Associated with a Functional Reversion Due to a Somatic Second-Site Mutation in CARD11 Deficiency
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Ata de Congresso
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Omenn Syndrome Associated with a Functional Reversion Due to a Somatic Second-Site Mutation in CARD11 Deficiency

Fuchs, S ; Rensing-Ehl, A ; Pannicke, U ; Lorenz, M ; Jeelall, Y ; Rohr, J ; Speckmann, C ; Vraetz, T ; Farmand, S ; Schmitt-Graeff, A ; Fisch, P ; Strahm, B ; Henneke, P ; Enders, A ; Horikawa, K ; Goodnow, C ; Schwarz, K ; Ehl, S

JOURNAL OF CLINICAL IMMUNOLOGY, 2014, Vol.34, p.S474 [Periódico revisado por pares]

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2
Autosomal-Recessive Agammaglobulinemia Due to Homozygous Mutations in Artemis: Do We Need a Modifier?
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Ata de Congresso
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Autosomal-Recessive Agammaglobulinemia Due to Homozygous Mutations in Artemis: Do We Need a Modifier?

Volk, T ; Reisli, I ; Bjorkman, A ; Pannicke, U ; Fisch, P ; Schaffer, AA ; Bulashevska, A ; Gruning, BA ; Pfeifer, D ; Guner, S ; Sayar, EH ; Hammarstrom, L ; Durandy, A ; Salzer, U ; Pan-Hammarstrom, Q ; Rizzi, M ; Schwarz, K ; Grimbacher, B

JOURNAL OF CLINICAL IMMUNOLOGY, 2014, Vol.34, p.S146 [Periódico revisado por pares]

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3
Brodalumab assessment of hazards: A multinational safety (brahms) study of a biological anti-psoriatic drug across six European countries
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Ata de Congresso
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Brodalumab assessment of hazards: A multinational safety (brahms) study of a biological anti-psoriatic drug across six European countries

Reilev, M ; Jensen, P ; Stovring, H ; Ranch, LS ; Gini, R ; Bartolini, CC ; Trifiro, G ; Kirchmayer, U ; Rosa, AC ; Belleudi, V ; Haug, U ; Schwarz, S ; Schaefer, W ; Herings, R ; Smits, E ; Overbeek, J ; Holthuis, E ; Furu, K ; Gembert, K ; Hagg, D ; Tari, M ; Ientile, V ; Ingrasciotta, Y ; Egeberg, A ; Hallas, J

PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2022, Vol.31, p.487 [Periódico revisado por pares]

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4
Solve-RD: the ITHACA perspective
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Ata de Congresso
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Solve-RD: the ITHACA perspective

Denomme-Pichon, AS ; de Boer, E ; Jackson, A ; Benetti, E ; Banka, S ; Casari, G ; Ciolfi, A ; Clayton-Smith, J ; Dallapiccola, B ; Ellwanger, K ; Faivre, L ; Gilissen, C ; Graessner, H ; Haack, TB ; Hammarsjo, A ; Havlovicova, M ; Hoischen, A ; Hugon, A ; Kleefstra, T ; Lindstrand, A ; Lopez-Martin, E ; Macek, M ; Matalonga, L ; Morleo, M ; Nigro, V ; Nordgren, A ; Pettersson, M ; Pinelli, M ; Pizzi, S ; Posada, M ; Radio, FC ; Renieri, A ; Rooryck, C ; Ryba, L ; Schwarz, M ; Tartaglia, M ; Thauvin, C ; Torella, A ; Trimouille, A ; Votypka, P ; Vyshka, K ; Zurek, B ; Verloes, A ; Vitobello, A ; Vissers, L

EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, Vol.30 (SUPPL 1), p.236 [Periódico revisado por pares]

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5
Working group on implant research of the German Society of Surgery
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Working group on implant research of the German Society of Surgery

Aubin, H ; Ellenrieder, M ; Junge, K ; Kühn, C ; Larena-Avellaneda, A ; Lehmann, W ; Lütjens, G ; Mittelmeier, W ; Pakos, P ; Radtke, C ; Schmitz-Rixen, T ; Schwarz, M ; Steiner, T ; Walles, T ; Wünsch, L ; Wilhelmi, M

Chirurg, 2015, Vol.86 (3), p.290-292

Germany

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