Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("GRIMBACHER, Bodo")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 29

  • Page / 2
Export

Selection :

  • and

Mendelian traits causing susceptibility to mucocutaneous fungal infections in human subjectsENGELHARDT, Karin R; GRIMBACHER, Bodo.Journal of allergy and clinical immunology. 2012, Vol 129, Num 2, pp 294-305, issn 0091-6749, 12 p.Article

Hyper-IgE syndromesGRIMBACHER, Bodo; HOLLAND, Steven M; PUCK, Jennifer M et al.Immunological reviews. 2005, Vol 203, pp 244-250, issn 0105-2896, 7 p.Article

Therapeutic Management of Primary Immunodeficiency in Older PatientsVERMA, Nisha; THAVENTHIRAN, Anthony; GATHMANN, Benjamin et al.Drugs & aging. 2013, Vol 30, Num 7, pp 503-512, issn 1170-229X, 10 p.Article

Common variable immunodeficiency is associated with a functional deficiency of invariant natural killer T cellsYIFANG GAO; WORKMAN, Sarita; GADOLA, Stephan et al.Journal of allergy and clinical immunology. 2014, Vol 133, Num 5, pp 1420-1428, issn 0091-6749, 9 p.Article

Infant colitis—it's in the genesGLOCKER, Erik-Oliver; FREDE, Natalie; PERRO, Mario et al.Lancet (British edition). 2010, Vol 376, Num 9748, issn 0140-6736, p. 1272Article

Analysis of families with common variable immunodeficiency (VID) and IgA deficiency suggests linkage of CVID to chromosome 16qSCHÄFFER, Alejandro A; PFANNSTIEL, Jessica; WEBSTER, A. David B et al.Human genetics. 2006, Vol 118, Num 6, pp 725-729, issn 0340-6717, 5 p.Article

Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associationsGERMESHAUSEN, Manuela; GRUDZIEN, Magda; ZEIDLER, Cornelia et al.Blood. 2008, Vol 111, Num 10, pp 4954-4957, issn 0006-4971, 4 p.Article

Anti-IgA antibodies in Common Variable Immunodeficiency (CVIC) : Diagnostic workup and therapeutic strategyHORN, Julia; THON, Vojtech; BARTONKOVA, Dana et al.Clinical immunology (Orlando, Fla. Print). 2007, Vol 122, Num 2, pp 156-162, issn 1521-6616, 7 p.Article

Mitochondrial DNA and sperm quality in patients under antiretroviral therapyDIEHL, Susanne; VERNAZZA, Pietro; TREIN, Andreas et al.AIDS (London). 2003, Vol 17, Num 3, pp 450-451, issn 0269-9370, 2 p.Article

Community acquired Staphylococcus aureus meningitis and cerebral abscesses in a patient with a Hyper-IgE and a Dubowitz-like syndromeBEITZKE, Markus; ENZINGER, Christian; WINDPASSINGER, Christian et al.Journal of the neurological sciences. 2011, Vol 309, Num 1-2, pp 12-15, issn 0022-510X, 4 p.Article

Common Variable Immunodeficiency : An Update on Etiology and ManagementYONG, Patrick F. K; TARZI, Michael; CHUA, Ignatius et al.Immunology and allergy clinics of North America. 2008, Vol 28, Num 2, issn 0889-8561, ix-x, 367-386 [22 p.]Article

Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjectsSTEPENSKY, Polina; KELLER, Baerbel; FUCHS, Ilka et al.Journal of allergy and clinical immunology. 2013, Vol 131, Num 2, pp 477-485, issn 0091-6749, 9 p.Article

A Homozygous CARD9 Mutation in a Family with Susceptibility to Fungal InfectionsGLOCKER, Erik-Oliver; HENNIGS, Andre; JAMAL, Sarah et al.The New England journal of medicine. 2009, Vol 361, Num 18, pp 1727-1735, issn 0028-4793, 9 p.Article

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCKS) in the autosomal-recessive form of hyper-IgE syndromeENGELHARDT, Karin R; MCGHEE, Sean; EHL, Stephan et al.Journal of allergy and clinical immunology. 2009, Vol 124, Num 6, pp 1289-1302, issn 0091-6749, 14 p.Article

An antibody-deficiency syndrome due to mutations in the CD19 geneVAN ZELM, Menno C; REISLI, Ismail; FRANCO, José L et al.The New England journal of medicine. 2006, Vol 354, Num 18, pp 1901-1912, issn 0028-4793, 12 p.Article

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)KLEIN, Christoph; GRUDZIEN, Magda; BOHN, Georg et al.Nature genetics. 2007, Vol 39, Num 1, pp 86-92, issn 1061-4036, 7 p.Article

Differential efficacy of human recombinant interferon-α2a on ocular and extraocular manifestations of Behçet disease: Results of an open 4-center trialKÖTTER, Ina; VONTHEIN, Reinhard; ZIERHUT, Manfred et al.Seminars in arthritis and rheumatism. 2004, Vol 33, Num 5, pp 311-319, issn 0049-0172, 9 p.Article

ICOS deficiency in patients with common variable immunodeficiencySALZER, Ulrich; MAUL-PAVICIC, Andrea; SKRABL, Andrea et al.Clinical immunology (Orlando, Fla. Print). 2004, Vol 113, Num 3, pp 234-240, issn 1521-6616, 7 p.Article

Deep Dermatophytosis and Inherited CARD9 DeficiencyLANTERNIER, Fanny; PATHAN, Saad; GUELLIL, Boumediene et al.The New England journal of medicine. 2013, Vol 369, Num 18, pp 1704-1714, issn 0028-4793, 11 p.Article

Genetic CD21 deficiency is associated with hypogammaglobulinemiaTHIEL, Jens; KIMMIG, Lucas; GUTENBERGER, Sylvia et al.Journal of allergy and clinical immunology. 2012, Vol 129, Num 3, pp 801-810, issn 0091-6749, 10 p.Article

Outcome of allogeneic stem cell transplantation in adults with common variable immunodeficiencyRIZZI, Marta; NEUMANN, Carla; WARNATZ, Klaus et al.Journal of allergy and clinical immunology. 2011, Vol 128, Num 6, pp 1371-1374, issn 0091-6749, 4 p.Article

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndromeWOELLNER, Cristina; GERTZ, E. Michael; PIETRUCHA, Barbara et al.Journal of allergy and clinical immunology. 2010, Vol 125, Num 2, pp 424-432, issn 0091-6749, 9 p.Article

A Syndrome with Congenital Neutropenia and Mutations in G6PC3BOZTUG, Kaan; APPASWAMY, Giridharan; GATZKE, Anna-Katherina et al.The New England journal of medicine. 2009, Vol 360, Num 1, pp 32-43, issn 0028-4793, 12 p.Article

Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiencyWARNATZ, Klaus; BOSSALLER, Lukas; DRAEGER, Ruth et al.Blood. 2006, Vol 107, Num 8, pp 3045-3052, issn 0006-4971, 8 p.Article

Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and AutoimmunityLOPEZ-HERRERA, Gabriela; TAMPELLA, Giacomo; SRUGO, Izhak et al.American journal of human genetics. 2012, Vol 90, Num 6, pp 986-1001, issn 0002-9297, 16 p.Article

  • Page / 2