检索结果 - André Reis

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  1. 1
    Coleção "Estudos Internacionais" da Editora da Universidade (UFRGS)

    Coleção "Estudos Internacionais" da Editora da Universidade (UFRGS) 由 Silva, André Reis da

    出版 2003
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  2. 2
    Spectrum of mutations and genotype–phenotype analysis in Currarino syndrome

    Spectrum of mutations and genotype–phenotype analysis in Currarino syndrome 由 Joachim Köchling, Mohsen Karbasiyan, André Reis

    出版 2001
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  3. 3
    International Relations Theory in Brazil: trends and challenges in teaching and research

    International Relations Theory in Brazil: trends and challenges in teaching and research 由 Barasuol, Fernanda, Silva, André Reis da

    出版 2016
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  4. 4
    Type and Level of RMRP Functional Impairment Predicts Phenotype in the Cartilage Hair Hypoplasia–Anauxetic Dysplasia Spectrum

    Type and Level of RMRP Functional Impairment Predicts Phenotype in the Cartilage Hair Hypoplasia–Anauxetic Dysplasia Spectrum 由 Christian T. Thiel, Geert Mortier, Ilkka Kaitila, André Reis, Anita Rauch

    出版 2007
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  5. 5
    Genotype/Phenotype Correlation in Autosomal Recessive Lamellar Ichthyosis

    Genotype/Phenotype Correlation in Autosomal Recessive Lamellar Ichthyosis 由 Hans Christian Hennies, Wolfgang Küster, Victor Wiebe, Alice Krebsová, André Reis

    出版 1998
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  6. 6
    A influência do intervalo entre séries no número de repetições e na sobrecarga do treinamento de força

    A influência do intervalo entre séries no número de repetições e na sobrecarga do treinamento de força 由 Rodrigo Sudatti Delevatti, Márcio André Reis Renz, Leonardo Mendonça Pilar Silveira

    出版 2019
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  7. 7
    Hereditary spastic paraplegia caused by mutations in the SPG4 gene

    Hereditary spastic paraplegia caused by mutations in the SPG4 gene 由 Joachim Bürger, Núria Fonknechten, Maria Hoeltzenbein, Luitgart Neumann, Elfriede Bratanoff, Jamïlé Hazan, André Reis

    出版 2000
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  8. 8
    Prevalência da INgestão de Álcool nos Adolescentes - Estudo PINGA

    Prevalência da INgestão de Álcool nos Adolescentes - Estudo PINGA 由 André Reis, J Suárez Barros, Cristina Fonseca, Luísa Parreira, Manuel Gomes, Ivo Figueiredo, Sandra Matapa

    出版 2011
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  9. 9
    Self-Healing Collodion Baby: a Dynamic Phenotype Explained by a Particular Transglutaminase-1 Mutation

    Self-Healing Collodion Baby: a Dynamic Phenotype Explained by a Particular Transglutaminase-1 Mutation 由 Michael Raghunath, Hans-Christian Hennies, Bijan Ahvazi, Melanie Vogel, André Reis, Peter M. Steinert, Heiko Traupe

    出版 2003
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  10. 10
    Transcription factor Tcf4 is the preferred heterodimerization partner for Olig2 in oligodendrocytes and required for differentiation

    Transcription factor Tcf4 is the preferred heterodimerization partner for Olig2 in oligodendrocytes and required for differentiation 由 Miriam Wedel, Franziska Fröb, Olga Elsesser, Marie‐Theres Wittmann, D. Chichung Lie, André Reis, Michael Wegner

    出版 2020
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  11. 11
    Homozygosity Mapping in Families with Joubert Syndrome Identifies a Locus on Chromosome 9q34.3 and Evidence for Genetic Heterogeneity

    Homozygosity Mapping in Families with Joubert Syndrome Identifies a Locus on Chromosome 9q34.3 and Evidence for Genetic Heterogeneity 由 Kathrin Saar, Lihadh Al‐Gazali, László Sztriha, Franz Rueschendorf, Mohammed Nur-E-Kamal, André Reis, Riad Bayoumi

    出版 1999
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  12. 12
    A unique form of autosomal dominant cataract explained by gene conversion between β-crystallin B2 and its pseudogene

    A unique form of autosomal dominant cataract explained by gene conversion between β-crystallin B2 and its pseudogene 由 Vanita, Virinder Kaur Sarhadi, André Reis, Martin Jung, Daljit Singh, Karl Sperling, Jai Rup Singh, Joachim Bürger

    出版 2001
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  13. 13
    SÍNDROME DE LEUCOENCEFALOPATIA POSTERIOR REVERSÍVEL E LÚPUS ERITEMATOSO SISTÊMICO: RELATO DE CASO

    SÍNDROME DE LEUCOENCEFALOPATIA POSTERIOR REVERSÍVEL E LÚPUS ERITEMATOSO SISTÊMICO: RELATO DE CASO 由 P.A. Veloso, Daniela Aparecida Freitas, André Reis, Shirley Prado, A Montandon, N.A. Silva, Jozélia Rêgo

    出版 2017
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  14. 14
    Exome Pool-Seq in neurodevelopmental disorders

    Exome Pool-Seq in neurodevelopmental disorders 由 Bernt Popp, Arif B. Ekici, Christian T. Thiel, Juliane Hoyer, Antje Wiesener, Cornelia Kraus, André Reis, Christiane Zweier

    出版 2017
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  15. 15
    PNEUMONIA POR HERPES SIMPLES EM PACIENTE COM GRANULOMATOSE COM POLIANGEÍTE – RELATO DE CASO

    PNEUMONIA POR HERPES SIMPLES EM PACIENTE COM GRANULOMATOSE COM POLIANGEÍTE – RELATO DE CASO 由 Daniela Aparecida Freitas, P.A. Veloso, André Reis, Suarez Prado, Clarissa Maria Cardoso Guimarães, Nathalia Silva, Jozélia Rêgo

    出版 2017
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  16. 16
    Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling

    Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling 由 Georgia Vasileiou, Arif B. Ekici, Steffen Uebe, Christiane Zweier, Juliane Hoyer, Hartmut Engels, Jürgen Behrens, André Reis, Michel V. Hadjihannas

    出版 2015
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  17. 17
    Gene Localization for an Autosomal Dominant Familial Periodic Fever to 12p13

    Gene Localization for an Autosomal Dominant Familial Periodic Fever to 12p13 由 John C. Mulley, Kathrin Saar, Gerry Hewitt, Franz Rüschendorf, Hilary A. Phillips, Alison Colley, David Sillence, André Reis, Meredith Wilson

    出版 1998
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  18. 18
    AMILOIDOSE NODULAR PULMONAR E SÍNDROME DE SJÖGREN PRIMÁRIA: RELATO DE CASO

    AMILOIDOSE NODULAR PULMONAR E SÍNDROME DE SJÖGREN PRIMÁRIA: RELATO DE CASO 由 André Reis, Silvio Costa Neto, D.A. Feitas, P.A. Veloso, Christiane Pinheiro Fagundes Guimarães, N.A. Silva, Jozélia Rêgo

    出版 2017
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  19. 19
    Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations

    Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations 由 Raymonda Varon, E Seemanová, Krystyńa Chrzańowska, Oleg Hnateyko, Dorota Piekutowska‐Abramczuk, Małgorzata Krajewska‐Walasek, Jolanta Sykut‐Cegielska, Karl Sperling, André Reis

    出版 2000
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  20. 20
    TNF polymorphisms in psoriasis: Association of psoriatic arthritis with the promoter polymorphism <i>TNF</i>*‐<i>857</i> independent of the <i>PSORS1</i> risk allele

    TNF polymorphisms in psoriasis: Association of psoriatic arthritis with the promoter polymorphism <i>TNF</i>*‐<i>857</i> independent of the <i>PSORS1</i> risk allele 由 Kristian Reich, Ulrike Hüffmeier, Inke R. König, Jesús Lascorz, Jörg Lohmann, Jörg Wendler, Heiko Traupe, Rotraut Mößner, André Reis, Harald Burkhardt

    出版 2007
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