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Results 1 to 25 of 41845

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Subcutaneous Immunoglobulin for Primary and Secondary Immunodeficiencies: an Evidence-Based ReviewLINGMAN-FRAMME, Jenny; FASTH, Anders.Drugs (Basel). 2013, Vol 73, Num 12, pp 1307-1319, issn 0012-6667, 13 p.Article

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, Jana; CANIONI, Danielle; GALICIER, Lionel et al.Blood. 2011, Vol 117, Num 5, pp 1522-1529, issn 0006-4971, 8 p.Article

Deficient alternative complement pathway activation due to factor D deficiency by 2 novel mutations in the complement factor D gene in a family with meningococcal infectionsSPRONG, Tom; ROOS, Dirk; WEEMAES, Corry et al.Blood. 2006, Vol 107, Num 12, pp 4865-4870, issn 0006-4971, 6 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

Mutations in neutrophil elastase causing congenital neutropenia lead to cytoplasmic protein accumulation and induction of the unfolded protein responseKÖLLNER, Inga; SODEIK, Beate; BEGER, Carmela et al.Blood. 2006, Vol 108, Num 2, pp 493-500, issn 0006-4971, 8 p.Article

Pulmonary fungal infection : Imaging findings in immunocompetent and immunocompromised patientsCHONG, Semin; KYUNG SOO LEE; YI, Chin A et al.European journal of radiology. 2006, Vol 59, Num 3, pp 371-383, issn 0720-048X, 13 p.Article

Bronchial hyper-responsiveness in selective IgA deficiencyPAPADOPOULOU, Athina; MERMIRI, Despina; TAOUSANI, Sofia et al.Pediatric allergy and immunology. 2005, Vol 16, Num 6, pp 495-500, issn 0905-6157, 6 p.Article

Practice parameter for the diagnosis and management of primary immunodeficiencyBONILLA, Francisco A; BERNSTEIN, I. Leonard; ORANGE, Jordan S et al.Annals of allergy, asthma, & immunology. 2005, Vol 94, Num 5, pp S1-S63, issn 1081-1206, SUP1Article

Tracé plat = Common variable immunodeficiencyBERNARD, Philippe; LEYRAL, Gwenaelle; GISSEROT, Olivier et al.Concours médical (Paris). 2004, Vol 126, Num 6, pp 337-339, issn 0010-5309, 3 p.Article

Defective B-cell-negative selection and terminal differentiation in the ICF syndromeBLANCO-BETANCOURT, Carla E; MONCLA, Anne; MILILI, Michèle et al.Blood. 2004, Vol 103, Num 7, pp 2683-2690, issn 0006-4971, 8 p.Article

Female agammaglobulinemia due to the Bruton tyrosine kinase deficiency caused by extremely skewed X-chromosome inactivationTAKADA, Hidetoshi; KANEGANE, Hirokazu; NOMURA, Akihiko et al.Blood. 2004, Vol 103, Num 1, pp 185-187, issn 0006-4971, 3 p.Article

Janus kinase 3 (JAK3) deficiency: clinical, immunologic, and molecular analyses of 10 patients and outcomes of stem cell transplantationROBERTS, Joseph L; LENGI, Andrea; BROWN, Stephanie M et al.Blood. 2004, Vol 103, Num 6, pp 2009-2018, issn 0006-4971, 10 p.Article

LAD-III, a leukocyte adhesion deficiency syndrome associated with defective rap 1 activation and impaired stabilization of integrin bondsKINASHI, Tatsuo; AKER, Memet; SOKOLOVSKY-EISENBERG, Maya et al.Blood. 2004, Vol 103, Num 3, pp 1033-1036, issn 0006-4971, 4 p.Article

Naturally occurring anti-IFN-γ autoantibody and severe infections with Mycobacterium cheloneae and Burkholderia cocovenenansHÖFLICH, Conny; SABAT, Robert; VOLK, Hans-Dieter et al.Blood. 2004, Vol 103, Num 2, pp 673-675, issn 0006-4971, 3 p.Article

Cytokine imbalance in hyper-IgE syndrome: reduced expression of transforming growth factor β and interferon γ genes in circulating activated T cellsOHGA, Shouichi; NOMURA, Akihiko; IHARA, Kenji et al.British journal of haematology. 2003, Vol 121, Num 2, pp 324-331, issn 0007-1048, 8 p.Article

Early manifestation and recognition of C2 complement deficiency in the form of pyogenic infection in infancyLITZMAN, J; FREIBERGER, T; BARTONKOVA, D et al.Journal of paediatrics and child health. 2003, Vol 39, Num 4, pp 274-277, issn 1034-4810, 4 p.Article

B lymphocytes from individuals with common variable immunodeficiency respond to B lymphocyte stimulator (BLyS protein) in vitroSTEWART, Donn M; MCAVOY, Michael J; HILBERT, David M et al.Clinical immunology (Orlando, Fla. Print). 2003, Vol 109, Num 2, pp 137-143, issn 1521-6616, 7 p.Article

Complement component C7 deficiency in a Spanish familyVAZQUEZ-BERMUDEZ, M. F; BARROSO, S; DE INMUNOLOGIA, Servicio et al.Clinical and experimental immunology (Print). 2003, Vol 133, Num 2, pp 240-246, issn 0009-9104, 7 p.Article

HIV/AIDS in Central Africa: Pathogenesis, immunological and médical issuesSIBANDA, Elopy Nimele; STANCZUK, Grazyna; KASOLO, Francis et al.International archives of allergy and immunology. 2003, Vol 132, Num 3, pp 183-195, issn 1018-2438, 13 p.Article

Hyper-IgM syndrome with putative dominant negative mutation in activation-induced cytidine deaminaseKASAHARA, Yukiko; KANEKO, Hideo; FUKAO, Toshiyuki et al.Journal of allergy and clinical immunology. 2003, Vol 112, Num 4, pp 755-760, issn 0091-6749, 6 p.Article

Severe T- and B-cell immune deficiency associated with malignant thymomaYEL, Leman; LIAO, Otto; LIN, Fritz et al.Annals of allergy, asthma, & immunology. 2003, Vol 91, Num 5, pp 501-505, issn 1081-1206, 5 p.Article

Granulomatose septique chronique révélée par une ostéomyélite multifocale = Multifocal osteomyelitis as the first manifestation of chronic granulomatous diseaseLAUNAY, F; SOBLER, J.-M; KONE-PAUT, I et al.Revue de chirurgie orthopédique et réparatrice de l'appareil moteur. 2003, Vol 89, Num 6, pp 544-548, issn 0035-1040, 5 p.Article

Primary immunodeficiency diseasesBONILLA, Francisco A; GEHA, Raif S.Journal of allergy and clinical immunology. 2003, Vol 111, Num 2, pp S571-S581, issn 0091-6749, SUPArticle

Infectious disease risk in the elderlyBENDER, Bradley S.Immunology and allergy clinics of North America. 2003, Vol 23, Num 1, issn 0889-8561, vi, 57-64 [9 p.]Article

Familial chronic nail candidiasis with ICAM-1 deficiency: a new form of chronic mucocutaneous candidiasisZUCCARELLO, D; SALPIETRO, D. C; GANGEMI, S et al.Journal of medical genetics. 2002, Vol 39, Num 9, pp 671-675, issn 0022-2593Article

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