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*  Primary Immunodeficiencies - American Family Physician
Primary immunodeficiencies generally are considered to be relatively uncommon. There may be as many as 500,000 cases in the ... Common primary immunodeficiencies include disorders of humoral immunity (affecting B-cell differentiation or antibody ... Early recognition and diagnosis can alter the course of primary immunodeficiencies significantly and have a positive effect on ... Primary immunodeficiencies include a variety of disorders that render patients more susceptible to infections. If left ...
https://www.aafp.org/afp/2003/1115/p2001.html
*  A delayed diagnosis of X-linked hyper IgM syndrome complicated with toxoplasmic encephalitis in a child: A case report and...
... is an uncommon primary combined immunodeficiency disease caused by CD40L gene mutations. A delayed or missed diagnosis of XHIGM ... The X-linked hyper-immunoglobulin M syndrome (XHIGM) ... X-linked hyper-IgM syndrome with CD40LG mutation: two case ... Hyper-IgM Immunodeficiency Syndrome, Type 1/*complications/*diagnosis/physiopathology MH - Male MH - Toxoplasmosis, Cerebral/* ... The X-linked hyper-immunoglobulin M syndrome (XHIGM) is an uncommon primary combined immunodeficiency disease caused by CD40L ...
http://pubtransformer.com/Pubmed?pmid=29245273
*  Primary immunodeficiency - Wikipedia
Normal numbers of B cells with decreased IgG and IgA and increased IgM: Hyper-IgM syndromes Normal numbers of B cells with ... Pudlak syndrome type 2 Hyper-IgE syndrome Chronic mucocutaneous candidiasis Hepatic venoocclusive disease with immunodeficiency ... Hyper-IgD syndrome (HIDS) CIAS1-related diseases: Muckle-Wells syndrome Familial cold autoinflammatory syndrome Neonatal onset ... ataxia-like syndrome, Nijmegen breakage syndrome, Bloom syndrome DiGeorge syndrome (when associated with thymic defects) ...
https://en.wikipedia.org/wiki/Primary_immunodeficiency
*  Global Primary Immunodeficiency Diseases Market to Rise to US$7.5 bn by 2023; Antibody Deficiency to be Leading Disease Segment
Global Primary Immunodeficiency Diseases Market was recorded at US$4.4 bn in 2014, it is expected to exhibit a CAGR of 6.10% ... Cellular Immunodeficiency *Ataxia Telangiectasia. *Hyper IgM Syndromes. *Wiskott-Aldrich Syndrome. *DiGeorge Syndrome ... Key segments of the Global Primary Immunodeficiency Diseases Market. Global Primary Immunodeficiency Diseases Market, by ... Browse the full Primary Immunodeficiency Diseases Market (By Disease: Antibody Deficiency, Cellular Immunodeficiency and Innate ...
https://www.transparencymarketresearch.com/pressrelease/global-primary-immunodeficiency-disease-market.htm
*  Hyper Ige Syndrome (job's Syndrome): Diseases and Conditions | Pediatric Oncall
... is also known as Job's syndrome. It is a primary immunodeficiency where recurrent skin boils, eczema and pneumonia are seen. ... Hyper IGE Syndrome (Job's Syndrome) - Patient Education What is Hyper IgE syndrome? Hyper IgE syndrome (HIES) is also known as ... Ira Shah Hyper Ige Syndrome (Job's Syndrome) Hyper Ige Syndrome (Job's Syndrome) 8/1/2015 8/1/2015 ... Common Variable Immunodeficiency (CVID) Complement Deficiencies Digeorge Syndrome Hyper Igm Syndrome View all from ...
https://www.pediatriconcall.com/articles/immunodeficiencies/hyper-ige-syndrome-jobs-syndrome/hyper-ige-syndrome-jobs-syndrome-patient-education
*  The hyperimmunoglobulin E syndrome - clinical manifestation diversity in primary immune deficiency | Orphanet Journal of Rare...
The hyper-IgE syndromes are rare, complex primary immunodeficiencies characterized by clinical manifestation diversity, by ... In contrast to the latter syndrome, DOCK8 deficiency is associated with low IgM concentrations and impaired generation of a ... Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from ... classical hyper-IgE syndrome which is inherited in an autosomal dominant pattern and the autosomal recessive hyper-IgE syndrome ...
https://ojrd.biomedcentral.com/articles/10.1186/1750-1172-6-76
*  Type 1 Hyper-IgM Immunodeficiency Syndrome Summary Report | CureHunter
An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND. ... Hyper-IgM Immunodeficiency, X-Linked; Hyper-IgM Syndrome 1; HIGM1 Syndromes; Hyper IgM Immunodeficiency Syndrome, Type 1; Hyper ... Immunodeficiencies, X-Linked Hyper-IgM; Immunodeficiency, X-Linked Hyper-IgM; Syndrome 1, Hyper-IgM; Syndrome, HIGM1; Syndromes ... Type 1 Hyper-IgM Immunodeficiency Syndrome. Subscribe to New Research on Type 1 Hyper-IgM Immunodeficiency Syndrome ...
http://www.curehunter.com/public/keywordSummaryD053307-Type-1-Hyper-IgM-Immunodeficiency-Syndrome.do
*  106P- Common Variable Immunodeficiency, Isolated IgA Deficiency, Hyper-IgM and DiGeorge Syndrome
Common Variable Immunodeficiency is a heterogeneous group of disorders characterized by hypogammaglobulinemia, impaired ... 106P- Common Variable Immunodeficiency, Isolated IgA Deficiency, Hyper-IgM and DiGeorge Syndrome. ... Patients with the hyper-IgM syndrome produce normal (or even supranormal) levels of IgM antibodies to antigens but lack the ... This gene is located on the X chromosome; consequently, in approximately 70% of the cases, hyper-IgM syndrome is X-linked. In ...
http://www.4doctors.net/watch.php?vid=631425026
*  Study of Immune Responses and Safety of Recombinant Human CD40 Ligand in Patients With X-Linked Hyper-IgM Syndrome
X-linked HyperIgM Syndrome. *Immunoproliferative Disorders. *Hyper-IgM Immunodeficiency Syndrome. *Hyper-IgM Immunodeficiency ... hyper IgM syndrome (XHIM). XHIM is a rare genetic disease caused by mutations in the gene. encoding CD40 ligand (CD154) and is ... Study of Immune Responses and Safety of Recombinant CD40 Ligand in Patients With X-Linked Hyper IgM Syndrome. Trial Phase:. ... All patients must have a diagnosis of X-linked hyper IgM syndrome confirmed either by. molecular analysis of the CD40L gene or ...
http://www.knowcancer.com/cancer-trials/NCT00001145/
*  Skin Diseases in Primary Immunodeficiencies | SpringerLink
... with at least 120 distinct primary immunodeficiencies described in the literature. They can generally be... ... Primary immunodeficiencies are estimated to affect about 255,000 people in the United States, ... Mucocutaneous manifestations of the hyper-IgM immunodeficiency syndrome. J Am Acad Dermatol. 1998;38(2 Pt 1):191-6.CrossRef ... The hyper IgM syndrome-an evolving story. Pediatr Res. 2004;56(4):519-25.CrossRefPubMedGoogle Scholar ...
https://link.springer.com/chapter/10.1007/978-3-319-68790-2_2
*  Immunodeficiency with hyper IgM type 1 | Genetic and Rare Diseases Information Center (GARD) - an NCATS Program
... resources and questions answered by our Genetic and Rare Diseases Information Specialists for Immunodeficiency with hyper IgM ... Hyper IgM syndrome; X-linked hyper IgM syndrome; Hyper IgM immunodeficiency, x-linked; Hyper IgM syndrome; Hyper IgM syndrome 1 ... Immunodeficiency with hyper IgM type 1 Title Other Names:. X-linked hyper IgM syndrome; Hyper IgM immunodeficiency, x-linked; ... Hyper IgM syndrome. is a type of primary immunodeficiency. syndrome. Primary immunodeficiency occurs when part of a person's ...
https://rarediseases.info.nih.gov/diseases/73/immunodeficiency-with-hyper-igm-type-1
*  Prostate cancer cells hyper-activate CXCR6 signaling by cleaving CXCL16 to overcome effect of docetaxel.
Mutations of the gene for CD40 antigen result in HYPER-IGM IMMUNODEFICIENCY SYNDROME, TYPE 3. Signaling of the receptor occurs ... Mutations in the CD40 antigen gene result in HYPER-IGM IMMUNODEFICIENCY SYNDROME, TYPE 3. Signaling of the receptor occurs ... Prostate cancer cells hyper-activate CXCR6 signaling by cleaving CXCL16 to overcome effect of docetaxel.. 08:00 EDT 8th April ... Home » Topics » Gleason Score » Research » Prostate cancer cells hyper-activate CXCR6 signaling by cleaving CXCL16 to overcome ...
https://www.bioportfolio.com/resources/pmarticle/2342179/Prostate-cancer-cells-hyper-activate-CXCR6-signaling-by-cleaving-CXCL16-to-overcome.html
*  Recombinant human CD40 protein (Fc Chimera Active) (ab83917)
Defects in CD40 are the cause of hyper-IgM immunodeficiency syndrome type 3 (HIGM3) [MIM:606843]; also known as hyper-IgM ... syndrome 3. HIGM3 is an autosomal recessive disorder which includes an inability of B cells to undergo isotype switching, one ...
http://www.abcam.com/recombinant-human-cd40-protein-fc-chimera-active-ab83917.html
*  anti-AICDA Primary Antibodies
Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). ... deficiency with an autosomal recessive Hyper-immunoglobulin M syndrome by phenotype and genotype, with a novel mutation in ...
https://www.antikoerper-online.de/cellular-response-to-molecule-of-bacterial-origin-pathway-55/aicda-antibody-1823/
*  Product - GeneTex
Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). [provided by ...
https://www.genetex.com/Product/Detail/AICDA-antibody-N-term/GTX88708
*  AICDA rabbit monoclonal antibody - (H00057379-K) - Products - Abnova
Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). [provided by ...
http://www.abnova.com/products/products_detail.asp?catalog_id=H00057379-K
*  SelfDecode | Genome Analysis
Hyper-Igm Immunodeficiency Syndrome AICDA,CD40. Carcinoma, Transitional Cell CDKN1A,TP53. Melanoma, Experimental CALR. ... Immunodeficiency Without Anhidrotic Ectodermal Dysplasia IKBKG. Inclusion Body Myopathy With Early-Onset Paget Disease And ... Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant NFKBIA. Ectodermal Dysplasia, Hypohidrotic, ... Ectodermal Dysplasia, Anhidrotic, With Immunodeficiency, Osteopetrosis, And Lymphedema IKBKG. ...
https://www.selfdecode.com/molecular-function/GO:0031625/
*  CD154 - Wikipedia
GeneReviews/NCBI/NIH/UW entry on X-Linked Hyper IgM Syndrome or Immunodeficiency with Hyper-IgM, Type 1 ... Subauste CS (February 2002). "CD154 and type-1 cytokine response: from hyper IgM syndrome to human immunodeficiency virus ... Bhushan A, Covey LR (2002). "CD40:CD40L interactions in X-linked and non-X-linked hyper-IgM syndromes". Immunologic Research. ... hyper-IgM syndrome)".. *^ Lederman S, Yellin MJ, Krichevsky A, Belko J, Lee JJ, Chess L (April 1992). "Identification of a ...
https://en.wikipedia.org/wiki/CD154
*  A Study to Find Out How Safe and Effective Gammaplex® is in Young People With Primary Immunodeficiency - Full Text View -...
Common Variable Immunodeficiency. Agammaglobulinemia. Hyper-IgM Immunodeficiency Syndrome. Hyper-IgM Immunodeficiency Syndrome ... Common Variable Immunodeficiency. X-linked agammaglobulinemia. Hyper-IgM syndrome. Wiskott-Aldrich Syndrome. Immunoglobulins. ... Primary Immune Deficiency Disorders Common Variable Immunodeficiency X-linked Agammaglobulinemia Hyper-IgM Syndrome Wiskott- ... X-linked hyper IgM syndrome X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Common ...
https://clinicaltrials.gov/ct2/show/NCT01289847?term=Immunodeficiency+NOT+AIDS&recr=Open&rank=9
*  Hyper-IgM Syndrome - Immunology; Allergic Disorders - Merck Manuals Professional Edition
... treatment of Immunodeficiency Disorders from the Professional Version of the Merck Manuals. ... Autosomal recessive hyper-IgM syndrome. In autosomal recessive hyper-IgM syndrome with CD40 mutation, manifestations are ... Hyper-IgM syndrome is a primary immunodeficiency disorder that involves combined humoral and cellular immunity deficiencies. It ... Hyper-IgM syndrome is an immunoglobulin (Ig) deficiency characterized by normal or elevated serum IgM levels and decreased ...
http://www.merckmanuals.com/en-ca/professional/immunology-allergic-disorders/immunodeficiency-disorders/hyper-igm-syndrome
*  Coverage criteria policies
B-cell deficiencies including: common variable immune deficiency, X-linked immunodeficiency, and Hyper-IgM syndromes ... Secondary immunodeficiencies including:. * Acquired hypogammagloulin conditions including B-cell chronic lymphocytic leukemia ...
https://www.healthpartners.com/public/coverage-criteria/policy.html?contentid=AENTRY_046004
*  Recombinant E. coli UNG protein (ab171506) | Abcam
Defects in UNG are a cause of immunodeficiency with hyper-IgM type 5 syndrome (HIGM5) [MIM:608106]. Hyper-IgM syndrome is a ... condition characterized by normal or increased serum IgM concentrations associated with low or absent serum IgG, IgA, and IgE ...
https://www.abcam.com/recombinant-e-coli-ung-protein-ab171506.html
*  SelfDecode | Genome Analysis
Hyper-Igm Immunodeficiency Syndrome CD40. Hyper-Igm Immunodeficiency Syndrome, Type 1 CD40LG. ...
https://www.selfdecode.com/molecular-function/GO:0071356/
*  SWAP70 - Wikipedia
2002). "Analysis of SWAP-70 as a candidate gene for non-X-linked hyper IgM syndrome and common variable immunodeficiency". Clin ...
https://en.wikipedia.org/wiki/SWAP70
*  CD40抗体|Abcam中国|Anti-CD40抗体(ab10959)
Defects in CD40 are the cause of hyper-IgM immunodeficiency syndrome type 3 (HIGM3) [MIM:606843]; also known as hyper-IgM ... syndrome 3. HIGM3 is an autosomal recessive disorder which includes an inability of B cells to undergo isotype switching, one ...
http://www.abcam.cn/cd40-antibody-ab10959.html