Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Inmunodeficiencia mixta")

Document Type [dt]

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

Publication Year[py]

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

Discipline (document) [di]

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

Language

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 833

  • Page / 34
Export

Selection :

  • and

Cutaneous granulomas in children with combined immunodeficiencySIEGFRIED, E. C; PROSE, N. S; FRIEDMAN, N. J et al.Journal of the American Academy of Dermatology. 1991, Vol 25, Num 5, pp 761-766, issn 0190-9622, 1Article

Síndrome de Omenn (inmunodeficiencia combinada con eosinofilia) = Syndrome de Omenn (immunodéficit associé à une hyperéosinophile) = Omenn's syndrome (immune deficiency associated with a hypereosinophily)DAUDEN TELLO, E; MANZANARES LOPEZ-MANZANARES, J; PASCUAL RUIZ, V et al.Actas dermo-sifiliográficas (Ed. impresa). 1987, Vol 78, Num 2, pp 71-77, issn 0001-7310Article

Severe Combined ImmunodeficiencyPUNNOOSE, Ann R; LYNM, Cassio; GOLUB, Robert M et al.JAMA, the journal of the American Medical Association. 2013, Vol 309, Num 1, issn 0098-7484, p. 98Article

In vitro functional correction of the mutation responsible for murine severe combined immune deficiency by small fragment homologous replacementZAYED, Hatem; MCIVOR, R. Scott; WIEST, David L et al.Human gene therapy. 2006, Vol 17, Num 2, pp 158-166, issn 1043-0342, 9 p.Article

Severe combined immunodeficiency-molecular pathogenesis and diagnosisGASPAR, H. B; GILMOUR, K. C; JONES, A. M et al.Archives of disease in childhood. 2001, Vol 84, Num 2, pp 169-173, issn 0003-9888Article

Progressive multifocal leucoencephalopathy, sclerosing cholangitis, bronchiectasis and disseminated warts in a patient with primary combined immune deficiencyMISBAH, S. A; SPICKETT, G. P; ZEMAN, A et al.Journal of clinical pathology. 1992, Vol 45, Num 7, pp 624-627, issn 0021-9746Article

A SCID patient reconstituted with HLA-incompatible fetal stem cells as a model for studying transplantation tolerance. CommentaryRONCAROLO, M.-G; BACCHETTA, R; BIGLER, M et al.Blood cells. 1991, Vol 17, Num 2, pp 391-406, issn 0340-4684Conference Paper

Correction of SCID-X1 Using an Enhancerless Vav PromoterALMARZA, E; ZHANG, F; SANTILLI, G et al.Human gene therapy. 2011, Vol 22, Num 3, pp 263-270, issn 1043-0342, 8 p.Article

Accessibility of chromosomal recombination breaks in nuclei of wild-type and DNA-PKcs-deficient cellsFRANCO, Daniel; YUNG CHANG.DNA repair. 2009, Vol 8, Num 7, pp 813-821, issn 1568-7864, 9 p.Article

Late-Onset Combined Immune Deficiency: A Subset of Common Variable Immunodeficiency with Severe T Cell DefectMALPHETTES, Marion; GERARD, Laurence; VIALLARD, Jean-François et al.Clinical infectious diseases. 2009, Vol 49, Num 9, pp 1329-1338, issn 1058-4838, 10 p.Article

Severe combined immunodeficiency. A model disease for molecular immunology and therapyFISCHER, Alain; LE DEIST, Francoise; HACEIN-BEY-ABINA, Salima et al.Immunological reviews. 2005, Vol 203, pp 98-109, issn 0105-2896, 12 p.Article

Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disordersWADA, T; TAKEI, K; YACHIE, A et al.Clinical and experimental immunology (Print). 2000, Vol 119, Num 1, pp 148-155, issn 0009-9104Article

Mutation analysis of IL2RG in human X-linked severe combined immunodeficiencyPUCK, J. M; PEPPER, A. E; BUCKLEY, R. H et al.Blood. 1997, Vol 89, Num 6, pp 1968-1977, issn 0006-4971Article

Major histocompatibility complex Class II deficiency : a clinical reviewELHASID, R; ETZIONI, A.Blood reviews. 1996, Vol 10, Num 4, pp 242-248, issn 0268-960XConference Paper

Long-term human hematopoiesis in SCID-hu mice bearing transplanted fragments of adult bone and bone marrow cellsHEIKE, Y; OHIRA, T; TAKAHASHI, M et al.Blood. 1995, Vol 86, Num 2, pp 524-530, issn 0006-4971Article

Relationship between patterns of engraftment in peripheral blood and immune reconstitution after allogeneic bone marrow transplantation for (severe) combined immunodeficiencyVAN LEEUWEN, J. E. M; VAN TOL, M. J. D; HARALDSSON, A et al.Blood. 1994, Vol 84, Num 11, pp 3936-3947, issn 0006-4971Article

IgG antibody response to polyethylene glycol-modified adenosine deaminase in patients with adenosine deaminase deficiencyCHAFFEE, S; MARY, A; STIEHM, E. R et al.The Journal of clinical investigation. 1992, Vol 89, Num 5, pp 1643-1651, issn 0021-9738Article

Tolerance of engrafted donor T cells following bone marrow transplantation for severe combined immunodeficiencyKEEVER, C. A; FLOMENBERG, N; BROCHSTEIN, J et al.Clinical immunology and immunopathology (Print). 1988, Vol 48, Num 3, pp 261-276, issn 0090-1229Article

Cancer in families with severe combined immune deficiencyMORRELL, D; CHASE, C. L; SWIFT, M et al.Journal of the National Cancer Institute. 1987, Vol 78, Num 3, pp 455-458, issn 0027-8874Article

Identification of a deletion in the adenosine deaminase gene in a child with severe combined immunodeficiencyMARKERT, M. L; HERSHFIELD, M. S; WIGINTON, D. A et al.The Journal of immunology (1950). 1987, Vol 138, Num 10, pp 3203-3206, issn 0022-1767Article

Fatal combined immunodeficiency associated with heterozygous mutation in STAT1SHARFE, Nigel; NAHUM, Amit; NEWELL, Andrea et al.Journal of allergy and clinical immunology. 2014, Vol 133, Num 3, pp 807-817, issn 0091-6749, 11 p.Article

Neurocognitive Function of Patients with Severe Combined ImmunodeficiencySHAH, Ami J; KOHN, Donald B.Immunology and allergy clinics of North America. 2010, Vol 30, Num 1, issn 0889-8561, 143-151, ix [10 p.]Article

Severe combined immunodeficiency with abnormalities in expression of the common leucocyte antigen, CD45CALE, C. M; KLEIN, N. J; NOVELLI, V et al.Archives of disease in childhood. 1997, Vol 76, Num 2, pp 163-164, issn 0003-9888Article

The molecular basis of X-linked severe combined immunodeficiency : Defective cytokine receptor signalingLEONARD, W. J.Annual review of medicine. 1996, Vol 47, pp 229-239, issn 0066-4219Article

Adenosine deaminase deficiency due to heterozygous abnormality consisting of a deletion of exon 7 and the absence of enzyme mRNAKASHII, S; ITO, K; MONDEN, S et al.Journal of cellular biochemistry. 1991, Vol 47, Num 1, pp 49-53, issn 0730-2312Article

  • Page / 34