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■ Abbreviation / Long Form : CID / combined immunodeficiency

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Total Number of Papers: 54
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Abbreviation:   CID  (>> Co-occurring Abbreviation)
Long Form:   combined immunodeficiency
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No. Year Title Co-occurring Abbreviation
2019 Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation. GOF, GVHD, HSCT, IFN-gamma, IL-17, STAT1
2019 Primary immune regulatory disorders for the pediatric hematologist and oncologist: A case-based review. ALPS, CVID, IPEX
2018 Acquired and Innate Immunity Impairment and Severe Disseminated Mycobacterium genavense Infection in a Patient With a NF-kappaB1 Deficiency. cTfh
2018 ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome. ADA, aHSCT, ERT, HSCGT
2018 Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11). CARD11
2018 Diagnosis of DOCK8 deficiency using Flow cytometry Biomarkers: an Egyptian Center experience. ---
2018 DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile. HSCT
2018 ORAI1 mutations abolishing store-operated Ca2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency. STIM, Treg
2018 T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency. TCR
10  2017 Human NF-kappaB1 Haploinsufficiency and Epstein-Barr Virus-Induced Disease-Molecular Mechanisms and Consequences. CVIDs, EBV, NF-kappaB1
11  2017 Loss of NHEJ1 Protein Due to a Novel Splice Site Mutation in a Family Presenting with Combined Immunodeficiency, Microcephaly, and Growth Retardation and Literature Review. bp, NGS, NHEJ1
12  2017 Novel compound heterozygous mutations in ZAP70 in a Chinese patient with leaky severe combined immunodeficiency disorder. IBD, TCR
13  2017 Novel Mutation of ZAP-70-related Combined Immunodeficiency: First Case from the National Iranian Registry and Review of the Literature. ---
14  2017 Novel nonsense gain-of-function NFKB2 mutations associated with a combined immunodeficiency phenotype. CVID, GOF
15  2016 Activating PI3Kdelta mutations in a cohort of 669 patients with primary immunodeficiency. CVID, PI3Kdelta
16  2016 Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations. BCR
17  2016 Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1. CMV, GOF, IFN, STAT1
18  2015 DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients. HSCT
19  2015 Identification of patients with RAG mutations previously diagnosed with common variable immunodeficiency disorders. CVID, PIDD
20  2015 SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling. ---
21  2015 The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency. AR, DOCK8, HIES, STAT3
22  2014 Retrospective TREC testing of newborns with Severe Combined Immunodeficiency and other primary immunodeficiency diseases. PID, SCID, TREC
23  2014 TTC7A mutations disrupt intestinal epithelial apicobasal polarity. MIA, TTC7A
24  2013 A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiency. MALT1
25  2013 Mismatched related hematopoietic stem cell transplantation in primary immunodeficiency. GVHD, HIGM, HLA, HSCT, PBSC, PIDs, SCID
26  2013 The many faces of Artemis-deficient combined immunodeficiency - Two patients with DCLRE1C mutations and a systematic literature review of genotype-phenotype correlation. DSB
27  2013 The role of hematopoietic stem cell transplantation in SP110 associated veno-occlusive disease with immunodeficiency syndrome. HSCT, SCID, VODI
28  2012 Defining combined immunodeficiency. CD40L, FoxP3, IL10RA, IL2RG, PNP, SCID, TD, TREC, ZAP70
29  2011 Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients. CI, HSCT, MHC
30  2010 Autoimmunity, autoinflammation and lymphoma in combined immunodeficiency (CID). ---
31  2010 Hematopoietic stem cell transplantation for profound T-cell deficiency (combined immunodeficiency). HSCT, PTD
32  2006 Radiation-induced delayed cell death in a hypomorphic Artemis cell line. DSBs
33  2006 Successful umbilical cord blood stem cell transplantation in a patient with Rothmund-Thomson syndrome and combined immunodeficiency. UCB
34  2002 Restriction in T-cell receptor repertoire in a patient affected by trichothiodystrophy and CD4+ lymphopenia. TCR, TCRBV, TTD
35  2001 Defective dendritic cell maturation in a child with nucleotide excision repair deficiency and CD4 lymphopenia. APCs, DCs, NER, TFIIH, TTD, UV
36  2000 Malakoplakia of the colon in an infant with severe combined immunodeficiency (SCID) and charge association. SCID
37  1998 Early emergence of ganciclovir-resistant human cytomegalovirus strains in children with primary combined immunodeficiency. HCMV
38  1997 In vitro T cell depletion using Campath 1M for mismatched BMT for severe combined immunodeficiency (SCID). GMCFU, SCID
39  1996 Genetic evidence for a new type of major histocompatibility complex class II combined immunodeficiency characterized by a dyscoordinate regulation of HLA-D alpha and beta chains. MHC
40  1994 Pathology of the pancreas in severe combined immunodeficiency and DiGeorge syndrome: acute graft-versus-host disease and unusual viral infections. GVHD, SCID
41  1994 Serum hypoxanthine and xanthine concentrations in horses heterozygous for combined immunodeficiency. ---
42  1993 Combined immunodeficiency (CID) with oligoclonal gammopathy. ---
43  1990 Evidence that appearance of thymulin in plasma follows lymphoid chimerism and precedes development of immunity in patients with lethal combined immunodeficiency transplanted with T cell-depleted haploidentical marrow. CIDTP, SCID
44  1987 Immunologic reconstitution of foals with combined immunodeficiency. ELA
45  1986 Treatment of congenital immune deficiencies with a thymic hormone--thymic humoral factor. THF
46  1980 Combined immunodeficiency of Arabian horses: confirmation of autosomal recessive mode of inheritance. ---
47  1980 Total plasma corticosteroid concentrations in horses with combined immunodeficiency. ---
48  1979 In vitro of adenosine on lymphocytes and erythrocytes from horses with combined immunodeficiency. ATP, EHNA, PBL, PHA
49  1978 Maintenance of foals with combined immunodeficiency: causes and control of secondary infections. ---
50  1978 Short stature, absent thumbs, flat facies, anosmia and combined immune deficiency (CID). ---
51  1977 Combined immunodeficiency in foals in Arabian breeding: evaluation of mode of inheritance and estimation of prevalence of affected foals and carrier mares and stallions. ---
52  1976 Alterations of the thymus and other lymphoid tissue in young horses with combined immunodeficiency. ---
53  1976 Combined immunodeficiency with failure of colostral immunoglobulins transfer in foals. FPT
54  1975 Combined immunodeficiency disease: an inborn error of purine metabolism. ADA