About: Hematopoietic stem cell transplantation for complete IFN-γ receptor 1 deficiency: A multi-institutional survey

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article by Joachim Roesler et al published December 2004 in The Journal of Pediatrics

Attributes	Values
rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) article scientifique publié en 2004 (fr) наукова стаття, опублікована в грудні 2004 (uk) im Dezember 2004 veröffentlichter wissenschaftlicher Artikel (de) article by Joachim Roesler et al published December 2004 in The Journal of Pediatrics (en)
publication date	wds:Q56941102-AAA310E2-BADA-4A27-9B01-076981F83FAC
publication date	2004-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56941102-EAE743C4-5382-4C68-815C-808191095FE9
language of work or name	English
author name string	wds:Q56941102-0722DDF0-E6E7-422E-B1D6-0C82B1F29E49 wds:Q56941102-23042FB6-6827-48D6-934D-311764E8A724 wds:Q56941102-26C4EFBD-E142-4EBD-AFB2-4FB5CC5B385B wds:Q56941102-5DBC21B5-DC93-49F1-81F7-B3D959D56294 wds:Q56941102-6C5C6185-B9A3-4D68-B84A-5EC568B5335F wds:Q56941102-7A7C02CF-B7CD-40E9-84AB-2396180C6F17 wds:Q56941102-7E020A8F-D59E-4DE1-8F2A-B459C5323090 wds:Q56941102-87B3869A-C5F6-42DB-B1E4-2415AB74F87E wds:Q56941102-961F18FB-876F-4DBE-95DE-6E13E07543EE wds:Q56941102-CE9DE8C8-8762-452C-BAEB-AACB9E902D7A wds:Q56941102-E53D1B19-51F2-448D-B8C0-22A688409682
author name string	Alain Fischer Graham Davies Ursula Reuter Ansgar Schulz Paul Veys Wilhelm Friedrich Pierre Bordigoni Ewa Koscielniak Steven M. Holland Mike Levin Mitchell E. Horwitz
rdfs:label	Hematopoietic stem cell transplantation for complete IFN-γ receptor 1 deficiency: A multi-institutional survey (en) Hematopoietic stem cell transplantation for complete IFN-γ receptor 1 deficiency: A multi-institutional survey (nl)
skos:prefLabel	Hematopoietic stem cell transplantation for complete IFN-γ receptor 1 deficiency: A multi-institutional survey (en) Hematopoietic stem cell transplantation for complete IFN-γ receptor 1 deficiency: A multi-institutional survey (nl)
name	Hematopoietic stem cell transplantation for complete IFN-γ receptor 1 deficiency: A multi-institutional survey (en) Hematopoietic stem cell transplantation for complete IFN-γ receptor 1 deficiency: A multi-institutional survey (nl)
author	wds:Q56941102-180526DC-474A-4DE8-A6C3-F8E09C197906 wds:Q56941102-19F3BD34-6146-41A3-9DE8-86725FF2B4FF wds:Q56941102-A6E1C0F0-D1C8-4ED7-A3F3-CCFF816F49A3 wds:Q56941102-FDDDFC78-8BE4-4B86-813C-625A67306B18 wds:Q56941102-FEA882CF-0F67-45BE-B3DC-4865DDA8C8E5
author	Jean-Laurent Casanova Capucine Picard Joachim Roesler Christian Thiede Thomas Klingebiel
title	wds:Q56941102-5549DB5F-4DAA-46C5-AD23-702E2F1212D1
title	Hematopoietic stem cell transplantation for complete IFN-γ receptor 1 deficiency: A multi-institutional survey (en)
page(s)	wds:Q56941102-2BBEAC95-CEEE-41EC-8626-D7501F8B776B
page(s)	806-812
instance of	wds:Q56941102-0B5A6755-F38F-498E-B5B5-FBA84E7C5285
instance of	scholarly article
main subject	wds:Q56941102-BD97C8B4-AB2D-48E2-B5D7-CD0AD1962EEB
main subject	stem cell transplantation
PubMed ID	wds:Q56941102-12167365-4D94-4E68-B72A-10BAD188C3BD
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15580206
PubMed ID	15580206
published in	wds:Q56941102-D8B11AA8-1873-429A-BD2F-DB33CE6595EA
published in	The Journal of Pediatrics
issue	wds:Q56941102-980F4A90-9B16-42F9-9008-52EEC68B6E5E
volume	wds:Q56941102-D4A56AAC-DA83-4BBF-BF1B-CEE24CB4CFF9
issue	6
volume	145
DOI	wds:Q56941102-A4C58F08-4D43-4BB1-8FB2-837F32BA7BA5
DOI	http://dx.doi.org/10.1016/J.JPEDS.2004.08.021
DOI	10.1016/J.JPEDS.2004.08.021
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56941102
is cites work of	Adjunctive treatment of disseminated Mycobacterium avium complex infection with interferon alpha-2b in a patient with complete interferon-gamma receptor R1 deficiency Inborn errors of human JAKs and STATs Clinical features of dominant and recessive interferon γ receptor 1 deficiencies Chinese patients with defective IL-12/23-interferon-gamma circuit in Taiwan: partial dominant interferon-gamma receptor 1 mutation presenting as cutaneous granuloma and IL-12 receptor beta1 mutation as pneumatocele. Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation Successful hematopoietic stem cell transplantation in a child with active disseminated Mycobacterium fortuitum infection and interferon-γ receptor 1 deficiency Interferon gamma, IL-12, IL-12R and STAT-1 immunodeficiency diseases: disorders of the interface of innate and adaptive immunity Cytokine immunomodulation for the treatment of infectious diseases: lessons from primary immunodeficiencies A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon IFN-gamma mediates the rejection of haematopoietic stem cells in IFN-gammaR1-deficient hosts Mendelian Susceptibility to Mycobacterial Disease due to IL-12Rβ1 Deficiency in Three Iranian Children Host susceptibility to non-tuberculous mycobacterial infections Mendelian Susceptibility to Mycobacterial Disease due to IL-12Rβ1 Deficiency in Three Iranian Children Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-gamma receptor 1 deficiency Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patients Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations Role of interferon-γ in immune-mediated graft failure after allogeneic hematopoietic stem cell transplantation Impaired IFNγ-Signaling and Mycobacterial Clearance in IFNγR1-Deficient Human iPSC-Derived Macrophages. Diagnostic and therapeutic challenges in a child with complete interferon-γ receptor 1 deficiency Susceptibility to mycobacterial infection in a young man with a hypoglossal nerve palsy: the hunt for an immunological defect. Non-tuberculous mycobacteria in children: muddying the waters of tuberculosis diagnosis. Disseminated nontuberculous mycobacterial infection in a child with interferon-γ receptor 1 deficiency [Genetic susceptibility to mycobacterial disease: Mendelian disorders of the interleukin-12 -interferon-gamma axis] Bacillus Calmette-Guérin vaccine related lymphadenitis in children: Management guidelines endorsed by the Saudi Pediatric Infectious Diseases Society (SPIDS) IFN-γR1 defects: Mutation update and description of the IFNGR1 variation database Patient iPSC-Derived Macrophages to Study Inborn Errors of the IFN-γ Responsive Pathway Human Lentiviral Gene Therapy Restores the Cellular Phenotype of Autosomal Recessive Complete IFN-γR1 Deficiency
is cites work of	wds:Q38216460-A01205A4-13F4-453D-8DF2-EAE91FA53A28

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