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Pubmed Id: 20694011

Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.

Ferreira RC, Pan-Hammarström Q, Graham RR, Gateva V, Fontán G, Lee AT, Ortmann W, Urcelay E, Fernández-Arquero M, Núñez C, Jorgensen G, Ludviksson BR, Koskinen S, Haimila K, Clark HF, Klareskog L, Gregersen PK, Behrens TW, Hammarström L

Nat Genet. 2010 Sep;42(9):777-80. Epub 2010 Aug 8

Pubmed Id: 20934598

Infant colitis--it's in the genes.

Glocker EO, Frede N, Perro M, Sebire N, Elawad M, Shah N, Grimbacher B

Lancet. 2010 Oct 9;376(9748):1272

Pubmed Id: 20676093

The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88.

He B, Santamaria R, Xu W, Cols M, Chen K, Puga I, Shan M, Xiong H, Bussel JB, Chiu A, Puel A, Reichenbach J, Marodi L, Döffinger R, Vasconcelos J, Issekutz A, Krause J, Davies G, Li X, Grimbacher B, Plebani A, Meffre E, Picard C, Cunningham-Rundles C, Casanova JL, Cerutti A

Nat Immunol. 2010 Sep;11(9):836-45. Epub 2010 Aug 1

Pubmed Id: 19668218

Recruitment of the cytoplasmic adaptor Grb2 to surface IgG and IgE provides antigen receptor-intrinsic costimulation to class-switched B cells.

Engels N, König LM, Heemann C, Lutz J, Tsubata T, Griep S, Schrader V, Wienands J.

Nat Immunol. 2009 Sep;10(9):1018-25. Epub 2009 Aug 9

Pubmed Id: 19909361

The B-lymphoid Grb2 interaction code.

Neumann K, Oellerich T, Urlaub H, Wienands J

Immunol Rev. 2009 Nov;232(1):135-49

Pubmed Id: 19290921

Bruton's tyrosine kinase (Btk): function, regulation, and transformation with special emphasis on the PH domain.

Mohamed AJ, Yu L, Bäckesjö CM, Vargas L, Faryal R, Aints A, Christensson B, Berglöf A, Vihinen M, Nore BF, Smith CI

Immunol Rev. 2009 Mar;228(1):58-73

Pubmed Id: 20926771

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.

Booth C, Gilmour KC, Veys P, Gennery AR, Slatter MA, Chapel H, Heath PT, Steward CG, Smith O, O'Meara A, Kerrigan H, Mahlaoui N, Cavazzana-Calvo M, Fischer A, Moshous D, Blanche S, Pachlopnik Schmid J, Latour S, de Saint-Basile G, Albert M, Notheis G, Rieber N, Strahm B, Ritterbusch H, Lankester A, Hartwig NG, Meyts I, Plebani A, Soresina A, Finocchi A, Pignata C, Cirillo E, Bonanomi S, Peters C, Kalwak K, Pasic S, Sedlacek P, Jazbec J, Kanegane H, Nichols KE, Hanson IC, Kapoor N, Haddad E, Cowan M, Choo S, Smart J, Arkwright PD, Gaspar HB

Blood. 2011 Jan 6;117(1):53-62. Epub 2010 Oct 6

Pubmed Id: 21119115

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).

Pachlopnik Schmid J, Canioni D, Moshous D, Touzot F, Mahlaoui N, Hauck F, Kanegane H, Lopez-Granados E, Mejstrikova E, Pellier I, Galicier L, Galambrun C, Barlogis V, Bordigoni P, Fourmaintraux A, Hamidou M, Dabadie A, Le Deist F, Haerynck F, Ouachée-Chardin M, Rohrlich P, Stephan JL, Lenoir C, Rigaud S, Lambert N, Milili M, Schiff C, Chapel H, Picard C, de Saint Basile G, Blanche S, Fischer A, Latour S

Blood. 2011 Feb 3;117(5):1522-9. Epub 2010 Nov 30

Pubmed Id: 21576700

T and B lymphocyte abnormalities in bone marrow biopsies of common variable immunodeficiency.

Ochtrop ML, Goldacker S, May AM, Rizzi M, Draeger R, Hauschke D, Stehfest C, Warnatz K, Goebel H, Technau-Ihling K, Werner M, Salzer U, Eibel H, Schlesier M, Peter HH

Blood. 2011 Jul 14;118(2):309-18. Epub 2011 May 16

Pubmed Id: 19666505

Circulating CD21low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells.

Rakhmanov M, Keller B, Gutenberger S, Foerster C, Hoenig M, Driessen G, van der Burg M, van Dongen JJ, Wiech E, Visentini M, Quinti I, Prasse A, Voelxen N, Salzer U, Goldacker S, Fisch P, Eibel H, Schwarz K, Peter HH, Warnatz K

Proc Natl Acad Sci U S A. 2009 Aug 11;106(32):13451-6. Epub 2009 Jul 29

Pubmed Id: 19666484

B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.

Warnatz K, Salzer U, Rizzi M, Fischer B, Gutenberger S, Böhm J, Kienzler AK, Pan-Hammarström Q, Hammarström L, Rakhmanov M, Schlesier M, Grimbacher B, Peter HH, Eibel H

Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13945-50. Epub 2009 Aug 6

Pubmed Id: 19004789

The transcriptional regulator PLZF induces the development of CD44 high memory phenotype T cells.

Raberger J, Schebesta A, Sakaguchi S, Boucheron N, Blomberg KE, Berglöf A, Kolbe T, Smith CI, Rülicke T, Ellmeier W

Proc Natl Acad Sci U S A. 2008 Nov 18;105(46):17919-24. Epub 2008 Nov 12

Pubmed Id: 21135220

Impaired induction of DNA lesions during immunoglobulin class-switch recombination in humans influences end-joining repair.

Kracker S, Imai K, Gardès P, Ochs HD, Fischer A, Durandy AH

Proc Natl Acad Sci U S A. 2010 Dec 21;107(51):22225-30. Epub 2010 Dec 6

Pubmed Id: 21376379

Pathogen-specific IgG antibody levels in immunodeficient patients receiving immunoglobulin replacement do not provide additional benefit to therapeutic management over total serum IgG.

Chua I, Lagos M, Charalambous BM, Workman S, Chee R, Grimbacher B

J Allergy Clin Immunol. 2011 Jun;127(6):1410-1. Epub 2011 Mar 3

Pubmed Id: 20159255

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome.

Woellner C, Gertz EM, Schäffer AA, Lagos M, Perro M, Glocker EO, Pietrogrande MC, Cossu F, Franco JL, Matamoros N, Pietrucha B, Heropolitańska-Pliszka E, Yeganeh M, Moin M, Español T, Ehl S, Gennery AR, Abinun M, Breborowicz A, Niehues T, Kilic SS, Junker A, Turvey SE, Plebani A, Sánchez B, Garty BZ, Pignata C, Cancrini C, Litzman J, Sanal O, Baumann U, Bacchetta R, Hsu AP, Davis JN, Hammarström L, Davies EG, Eren E, Arkwright PD, Moilanen JS, Viemann D, Khan S, Maródi L, Cant AJ, Freeman AF, Puck JM, Holland SM, Grimbacher B

J Allergy Clin Immunol. 2010 Feb;125(2):424-432.e8

Pubmed Id: 20004785

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

Engelhardt KR, McGhee S, Winkler S, Sassi A, Woellner C, Lopez-Herrera G, Chen A, Kim HS, Lloret MG, Schulze I, Ehl S, Thiel J, Pfeifer D, Veelken H, Niehues T, Siepermann K, Weinspach S, Reisli I, Keles S, Genel F, Kutukculer N, Camcioğlu Y, Somer A, Karakoc-Aydiner E, Barlan I, Gennery A, Metin A, Degerliyurt A, Pietrogrande MC, Yeganeh M, Baz Z, Al-Tamemi S, Klein C, Puck JM, Holland SM, McCabe ER, Grimbacher B, Chatila TA

J Allergy Clin Immunol. 2009 Dec;124(6):1289-302.e4

Pubmed Id: 20471071

Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.

Lucas M, Lee M, Lortan J, Lopez-Granados E, Misbah S, Chapel H

J Allergy Clin Immunol. 2010 Jun;125(6):1354-1360.e4. Epub 2010 May 14

Pubmed Id: 21458042

The C76R transmembrane activator and calcium modulator cyclophilin ligand interactor mutation disrupts antibody production and B-cell homeostasis in heterozygous and homozygous mice.

Bacchelli C, Buckland KF, Buckridge S, Salzer U, Schneider P, Thrasher AJ, Gaspar HB

J Allergy Clin Immunol. 2011 May;127(5):1253-9.e13. Epub 2011 Mar 31

Pubmed Id: 22035880

Genetic CD21 deficiency is associated with hypogammaglobulinemia.

Thiel J, Kimmig L, Salzer U, Grudzien M, Lebrecht D, Hagena T, Draeger R, Völxen N, Bergbreiter A, Jennings S, Gutenberger S, Aichem A, Illges H, Hannan JP, Kienzler AK, Rizzi M, Eibel H, Peter HH, Warnatz K, Grimbacher B, Rump JA, Schlesier M

J Allergy Clin Immunol. 2012 Mar;129(3):801-810.e6. Epub 2011 Oct 27

Pubmed Id: 19714644

Regression of systemic lupus erythematosus after development of an acquired toll-like receptor signaling defect and antibody deficiency.

Visentini M, Conti V, Cagliuso M, Tinti F, Siciliano G, Trombetta AC, Mitterhofer AP, Fiorilli M, Quinti I

Arthritis Rheum. 2009 Sep;60(9):2767-71

Pubmed Id: 19421184

From the fetal liver to spleen and gut: the highway to natural antibody.

Rosado MM, Aranburu A, Capolunghi F, Giorda E, Cascioli S, Cenci F, Petrini S, Miller E, Leanderson T, Bottazzo GF, Natali PG, Carsetti R

Mucosal Immunol. 2009 Jul;2(4):351-61. Epub 2009 May 6

Pubmed Id: 21622550

Lung MRI as a possible alternative to CT scan for patients with primary immune deficiencies and increased radiosensitivity.

Serra G, Milito C, Mitrevski M, Granata G, Martini H, Pesce AM, Sfika I, Bonanni L, Catalano C, Fraioli F, Quinti I

Chest. 2011 Dec;140(6):1581-9. Epub 2011 May 26

Pubmed Id: 21078901

TLR ligation triggers somatic hypermutation in transitional B cells inducing the generation of IgM memory B cells.

Aranburu A, Ceccarelli S, Giorda E, Lasorella R, Ballatore G, Carsetti R

J Immunol. 2010 Dec 15;185(12):7293-301. Epub 2010 Nov 15

Pubmed Id: 19008192

Immunoglobulin class switch recombination: study through human natural mutants.

Durandy A

Philos Trans R Soc Lond B Biol Sci. 2009 Mar 12;364(1517):577-82

Pubmed Id: 21287551

Telomere-dependent replicative senescence of B and T cells from patients with type 1a common variable immunodeficiency.

Visentini M, Cagliuso M, Conti V, Carbonari M, Mancaniello D, Cibati M, Siciliano G, Giorda E, Keller B, Warnatz K, Fiorilli M, Quinti I

Eur J Immunol. 2011 Mar;41(3):854-62. doi: 10.1002/eji.201040862. Epub 2011 Feb 2

Pubmed Id: 21469123

Switched memory B cells maintain specific memory independently of serum antibodies: the hepatitis B example.

Rosado MM, Scarsella M, Pandolfi E, Cascioli S, Giorda E, Chionne P, Madonne E, Gesualdo F, Romano M, Ausiello CM, Rapicetta M, Zanetti AR, Tozzi A, Carsetti R

Eur J Immunol. 2011 Jun;41(6):1800-8. doi: 10.1002/eji.201041187. Epub 2011 May 25

Pubmed Id: 20520773

Long-lived plasma cells and memory B cells produce pathogenic anti-GAD65 autoantibodies in Stiff Person Syndrome.

Rizzi M, Knoth R, Hampe CS, Lorenz P, Gougeon ML, Lemercier B, Venhoff N, Ferrera F, Salzer U, Thiesen HJ, Peter HH, Walker UA, Eibel H

PLoS One. 2010 May 26;5(5):e10838

Pubmed Id: 19494827

An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene.

Sazzini M, Zuntini R, Farjadian S, Quinti I, Ricci G, Romeo G, Ferrari S, Calafell F, Luiselli D

Genes Immun. 2009 Sep;10(6):566-78. Epub 2009 Jun 4

Pubmed Id: 19020530

The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency.

Haimila K, Einarsdottir E, de Kauwe A, Koskinen LL, Pan-Hammarström Q, Kaartinen T, Kurppa K, Ziberna F, Not T, Vatta S, Ventura A, Korponay-Szabo IR, Adány R, Pocsai Z, Széles G, Dukes E, Kaukinen K, Mäki M, Koskinen S, Partanen J, Hammarström L, Saavalainen P

Genes Immun. 2009 Mar;10(2):151-61. Epub 2008 Nov 20

Pubmed Id: 19450280

Transcriptional signatures of Itk-deficient CD3+, CD4+ and CD8+ T-cells.

Blomberg KE, Boucheron N, Lindvall JM, Yu L, Raberger J, Berglöf A, Ellmeier W, Smith CE

BMC Genomics. 2009 May 18;10:233

Pubmed Id: 20739362

Pharmacological inhibition of TLR9 activation blocks autoantibody production in human B cells from SLE patients.

Capolunghi F, Rosado MM, Cascioli S, Girolami E, Bordasco S, Vivarelli M, Ruggiero B, Cortis E, Insalaco A, Fantò N, Gallo G, Nucera E, Loiarro M, Sette C, De Santis R, Carsetti R, Ruggiero V

Rheumatology (Oxford). 2010 Dec;49(12):2281-9. Epub 2010 Aug 25

Pubmed Id: 20627700

Association of FcRn expression with lung abnormalities and IVIG catabolism in patients with common variable immunodeficiency.

Freiberger T, Grodecká L, Ravcuková B, Kurecová B, Postránecká V, Vlcek J, Jarkovský J, Thon V, Litzman J

Clin Immunol. 2010 Sep;136(3):419-25

Pubmed Id: 20864887

Common variable immunodeficiency at the end of a prospering decade: towards novel gene defects and beyond.

Eibel H, Salzer U, Warnatz K

Curr Opin Allergy Clin Immunol. 2010 Dec;10(6):526-33

Pubmed Id: 19629655

Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiency.

Mohammadi J, Liu C, Aghamohammadi A, Bergbreiter A, Du L, Lu J, Rezaei N, Amirzargar AA, Moin M, Salzer U, Pan-Hammarström Q, Hammarström L

J Clin Immunol. 2009 Nov;29(6):777-85. Epub 2009 Jul 23

Pubmed Id: 19834793

IgA deficiency and the MHC: assessment of relative risk and microheterogeneity within the HLA A1 B8, DR3 (8.1) haplotype.

Mohammadi J, Ramanujam R, Jarefors S, Rezaei N, Aghamohammadi A, Gregersen PK, Hammarström L

J Clin Immunol. 2010 Jan;30(1):138-43. Epub 2009 Oct 16

Pubmed Id: 21365217

Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study.

Quinti I, Soresina A, Guerra A, Rondelli R, Spadaro G, Agostini C, Milito C, Trombetta AC, Visentini M, Martini H, Plebani A, Fiorilli M; IPINet Investigators

J Clin Immunol. 2011 Jun;31(3):315-22. Epub 2011 Mar 2

Pubmed Id: 19883425

6th International Immunoglobulin Symposium: poster presentations.

Fernandez-Cruz E, Kaveri SV, Peter HH, Durandy A, Cantoni N, Quinti I, Sorensen R, Bussel JB, Danieli MG, Winkelmann A, Bayry J, Käsermann F, Späth P, Helbert M, Salama A, van Schaik IN, Yuki N

Clin Exp Immunol. 2009 Dec;158 Suppl 1:60-7

Pubmed Id: 19438597

Decrease in phenotypic regulatory T cells in subsets of patients with common variable immunodeficiency.

Horn J, Manguiat A, Berglund LJ, Knerr V, Tahami F, Grimbacher B, Fulcher DA

Clin Exp Immunol. 2009 Jun;156(3):446-54

Pubmed Id: 20538026

Fatal adult-onset antibody deficiency syndrome in a patient with cartilage hair hypoplasia.

Horn J, Schlesier M, Warnatz K, Prasse A, Superti-Furga A, Peter HH, Salzer U

Hum Immunol. 2010 Sep;71(9):916-9. Epub 2010 Jun 9

Pubmed Id: 21488866

Importance of B cell co-stimulation in CD4(+) T cell differentiation: X-linked agammaglobulinaemia, a human model.

Martini H, Enright V, Perro M, Workman S, Birmelin J, Giorda E, Quinti I, Lougaris V, Baronio M, Warnatz K, Grimbacher B

Clin Exp Immunol. 2011 Jun;164(3):381-7. doi: 10.1111/j.1365-2249.2011.04377.x. Epub 2011 Apr 13

Pubmed Id: 20646002

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders.

Packwood K, Drewe E, Staples E, Webster D, Witte T, Litzman J, Egner W, Sargur R, Sewell W, Lopez-Granados E, Seneviratne SL, Powell RJ, Ferry BL, Chapel HM

Clin Exp Immunol. 2010 Sep;161(3):536-41. doi: 10.1111/j.1365-2249.2010.04216.x

Pubmed Id: 21470209

Review of gastric cancer risk factors in patients with common variable immunodeficiency disorders, resulting in a proposal for a surveillance programme.

Dhalla F, da Silva SP, Lucas M, Travis S, Chapel H

Clin Exp Immunol. 2011 Jul;165(1):1-7. doi: 10.1111/j.1365-2249.2011.04384.x. Epub 2011 Apr 6

Pubmed Id: 20378010

B lymphocyte subsets and their functional activity in the early months of life.

Avanzini MA, Maccario R, Belloni C, Carrera G, Bertaina A, Cagliuso M, La Rocca M, Valsecchi C, Mantelli M, Castellazzi AM, Quinti I, De Silvestri A, Marconi M

Int J Immunopathol Pharmacol. 2010 Jan-Mar;23(1):247-54

Pubmed Id: 19161832

Phylogeny of Tec family kinases identification of a premetazoan origin of Btk, Bmx, Itk, Tec, Txk, and the Btk regulator SH3BP5.

Ortutay C, Nore BF, Vihinen M, Smith CI

Adv Genet. 2008;64:51-80

Pubmed Id: 20357490

Change in referral diagnoses and diagnostic delay in hypogammaglobulinaemic patients during 28 years in a single referral centre.

Litzman J, Stikarovska D, Pikulova Z, Pavlik T, Pesak S, Thon V, Kuklinek P, Lokaj J

Int Arch Allergy Immunol. 2010;153(1):95-101. Epub 2010 Apr 1

Pubmed Id: 20477064

Common variable immunodeficiency: a multifaceted and puzzling disorder.

Bergbreiter A, Salzer U

Expert Rev Clin Immunol. 2009 Mar;5(2):167-80

Pubmed Id: 20357490

Change in referral diagnoses and diagnostic delay in hypogammaglobulinaemic patients during 28 years in a single referral centre.

Litzman J, Stikarovska D, Pikulova Z, Pavlik T, Pesak S, Thon V, Kuklinek P, Lokaj J

Int Arch Allergy Immunol. 2010;153(1):95-101. Epub 2010 Apr 1

Pubmed Id: 20627700

Association of FcRn expression with lung abnormalities and IVIG catabolism in patients with common variable immunodeficiency.

Freiberger T, Grodecká L, Ravcuková B, Kurecová B, Postránecká V, Vlcek J, Jarkovský J, Thon V, Litzman J

Clin Immunol. 2010 Sep;136(3):419-25

Pubmed Id: 21930294

Outcome of allogeneic stem cell transplantation in adults with common variable immunodeficiency.

Rizzi M, Neumann C, Fielding AK, Marks R, Goldacker S, Thaventhiran J, Tarzi MD, Schlesier M, Salzer U, Eibel H, Warnatz K, Finke J, Grimbacher B, Peter HH

J Allergy Clin Immunol. 2011 Dec;128(6):1371-1374.e2. Epub 2011 Sep 17

Pubmed Id: 19850008

Phosphatidylinositol-3-kinase-dependent phosphorylation of SLP-76 by the lymphoma-associated ITK-SYK fusion-protein.

Hussain A, Faryal R, Nore BF, Mohamed AJ, Smith CI

Biochem Biophys Res Commun. 2009 Dec 18;390(3):892-6. Epub 2009 Oct 20

Pubmed Id: 21469132

Complex phosphorylation dynamics control the composition of the Syk interactome in B cells.

Bohnenberger H, Oellerich T, Engelke M, Hsiao HH, Urlaub H, Wienands J

Eur J Immunol. 2011 Jun;41(6):1550-62. doi: 10.1002/eji.201041326. Epub 2011 May 25

Pubmed Id: 21473955

Antibody forming cells and plasmablasts in peripheral blood in CVID patients after vaccination.

Chovancova Z, Vlkova M, Litzman J, Lokaj J, Thon V

Vaccine. 2011 May 31;29(24):4142-50. Epub 2011 Apr 5

Pubmed Id: 21705277

Efficacy and safety of Hizentra(®) in patients with primary immunodeficiency after a dose-equivalent switch from intravenous or subcutaneous replacement therapy.

Jolles S, Bernatowska E, de Gracia J, Borte M, Cristea V, Peter HH, Belohradsky BH, Wahn V, Neufang-Hüber J, Zenker O, Grimbacher B

Clin Immunol. 2011 Oct;141(1):90-102. Epub 2011 Jun 12

Pubmed Id: 21674136

Efficacy and safety of hizentra®, a new 20% immunoglobulin preparation for subcutaneous administration, in pediatric patients with primary immunodeficiency.

Borte M, Pac M, Serban M, Gonzalez-Quevedo T, Grimbacher B, Jolles S, Zenker O, Neufang-Hueber J, Belohradsky B

J Clin Immunol. 2011 Oct;31(5):752-61. Epub 2011 Jun 15

Pubmed Id: 21577231

Mucosal antifungal defence: IL-17 signalling takes centre stage.

Glocker EO, Grimbacher B

Immunol Cell Biol. 2011 Nov;89(8):823-5. doi: 10.1038/icb.2011.39. Epub 2011 May 17

Pubmed Id: 21457142

Serum trough IgG level and annual intravenous immunoglobulin dose are not related to body size in patients on regular replacement therapy.

Khan S, Grimbacher B, Boecking C, Chee R, Allgar V, Holding S, Wong G, Huissoon A, Herriot R, Doré P, Sewell W

Drug Metab Lett. 2011 Apr;5(2):132-6

Pubmed Id: 21543760

Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LG.

Rigaud S, Lopez-Granados E, Sibéril S, Gloire G, Lambert N, Lenoir C, Synaeve C, Stacey M, Fugger L, Stephan JL, Fischer A, Picard C, Durandy A, Chapel H, Latour S

Blood. 2011 Jul 14;118(2):252-61. Epub 2011 May 4

Pubmed Id: 21497890

Genome-wide association identifies diverse causes of common variable immunodeficiency.

Orange JS, Glessner JT, Resnick E, Sullivan KE, Lucas M, Ferry B, Kim CE, Hou C, Wang F, Chiavacci R, Kugathasan S, Sleasman JW, Baldassano R, Perez EE, Chapel H, Cunningham-Rundles C, Hakonarson H

J Allergy Clin Immunol. 2011 Jun;127(6):1360-7.e6. Epub 2011 Apr 17

Pubmed Id: 20387103

Immunomodulatory therapy to achieve maximum efficacy: doses, monitoring, compliance, and self-infusion at home.

Lucas M, Hugh-Jones K, Welby A, Misbah S, Spaeth P, Chapel H

J Clin Immunol. 2010 May;30 Suppl 1:S84-9

Pubmed Id: 20375545

Toll-like receptor responses in IRAK-4-deficient neutrophils.

van Bruggen R, Drewniak A, Tool AT, Jansen M, van Houdt M, Geissler J, van den Berg TK, Chapel H, Kuijpers TW

J Innate Immun. 2010;2(3):280-7. Epub 2009 Dec 16

Pubmed Id: 19811837

Complement receptor 3, not Dectin-1, is the major receptor on human neutrophils for beta-glucan-bearing particles.

van Bruggen R, Drewniak A, Jansen M, van Houdt M, Roos D, Chapel H, Verhoeven AJ, Kuijpers TW

Mol Immunol. 2009 Dec;47(2-3):575-81. Epub 2009 Oct 7

Pubmed Id: 19807274

Dissecting the group of common variable immunodeficiency disorders.

Aslam A, Chapel H

Clin Infect Dis. 2009 Nov 1;49(9):1339-40

Pubmed Id: 19344423

Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions.

Chapel H, Cunningham-Rundles C

Br J Haematol. 2009 Jun;145(6):709-27. Epub 2009 Mar 30

Pubmed Id: 21324660

The signaling tool box for tyrosine-based costimulation of lymphocytes.

Engels N, Wienands J

Curr Opin Immunol. 2011 Jun;23(3):324-9. Epub 2011 Feb 14

Pubmed Id: 21905497

Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency.

Tampella G, Baronio M, Vitali M, Soresina A, Badolato R, Giliani S, Plebani A, Lougaris V

J Investig Allergol Clin Immunol. 2011;21(5):348-53

Pubmed Id: 21822214

The B-cell antigen receptor signals through a preformed transducer module of SLP65 and CIN85.

Oellerich T, Bremes V, Neumann K, Bohnenberger H, Dittmann K, Hsiao HH, Engelke M, Schnyder T, Batista FD, Urlaub H, Wienands J

EMBO J. 2011 Aug 5;30(17):3620-34. doi: 10.1038/emboj.2011.251

Pubmed Id: 20696632

Home-based subcutaneous immunoglobulin G replacement therapy under real-life conditions in children and adults with antibody deficiency.

Hoffmann F, Grimbacher B, Thiel J, Peter HH, Belohradsky BH; Vivaglobin Study Group

Eur J Med Res. 2010 Jun 28;15(6):238-45

Pubmed Id:

Flow Based Enumeration of Plasmablasts in Peripheral Blood After Vaccination as a Novel Diagnostic Marker for Assessing Antibody Responses in Patients with Hypogammaglobulinaemia.

Vojtech Thon, Marcela Vlkova, Zita Chovancova, Jiri Litzman and Jindrich Lokaj

In: Clinical Flow Cytometry - Emerging Applications. Edited by Ingrid Schmid. InTech, Chapter 7, pp. 125-142

Pubmed Id:

Transmembrane Activator and Calcium-Modulator and Cyclophilin Ligand Interactor (TACI) Expression is Essential for Human B-cell Tolerance.

Romberg N, Saadoun D, Rachid R, Geha R, Grimbacher B, Cunningham-Rundles C, Meffre E

Clin Immunol. 2010; Suppl 135:S16. doi: 10.1016/j.clim.2010.03.053

Pubmed Id:

Health-Related Quality of Life of Patients with Primary Immunodeficiency Switching from Intravenous IgG to a New 20% Subcutaneous IgG.

Quevedo TG, Mannhardt-Laakmann W, Bernatowska E, Serban M, Jolles S, de Gracia J, Grimbacher B, Wang E, Borte M

Clin Immunol. 2010; Suppl 135:S87. doi: 10.1016/j.clim.2010.03.261

Pubmed Id:

Allogeneic stem cell transplantation in patients with common variable immunodeficiency.

Marks R, Rizzi M, Neumann C, Fielding A, Goldacker S, Salzer U, Eibel H, Warnatz K, Grimbacher B, Finke J, Peter HH

Bone Marrow Transplant 2011. 46: S163; doi:10.1038/bmt.2011.47

Pubmed Id:

Successful Allogeneic Hematopoietic Stem Cell Transplantation for Severe Inflammatory Bowel Disease – IL10 Receptor Deficiency May Serve as a Novel Therapeutic Paradigm.

Beier R, Kotlarz D, Boztug K, Glocker E, Pfister ED, Diestelhorst J, Murugan D, Baumann U, Koletzko S, Sauerbrey A, Bruderus S, Grimbacher B, Sauer MG, Sykora KW, Klein C

Blood (ASH Annual Meeting Abstracts) 2010 116: Abstract 2379

Pubmed Id:

Immunological principles of safety vaccination in children (Czech).

Thon V

Pediatrie pro praxi. ISSN 1213-0494, 2010, vol. 11, no. 6, pp. 354-357

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Necessity to postpone BCG vaccination - a lesson from complications and deaths in children with primary immunodeficiencies (Czech).

Thon V

Stud pneumol phthiseol. 2010, 70:1, s.30-34. ISSN: 1213-810X

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Angeborene immundefekte (German).

Schmidt RE

Forum Sanitas - Das informative Medizinmagazin. 2007(3):9-11