Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID).

PubWeight™: 2.04‹?› | Rank: Top 2%

🔗 View Article (PMC 1905641)

Published in Clin Exp Immunol on May 01, 2000

Authors

L Hammarström1, I Vorechovsky, D Webster

Author Affiliations

1: Division of Clinical Immunology, Huddinge University Hospital, Huddinge, Sweden. Lennart.Hammarstrom@csb.ki.se

Articles citing this

Long-term follow-up and outcome of a large cohort of patients with common variable immunodeficiency. J Clin Immunol (2007) 2.43

Selective IgA deficiency. J Clin Immunol (2010) 2.02

Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: clinical and immunologic outcomes in heterozygotes. J Allergy Clin Immunol (2007) 1.62

Physiology of IgA and IgA deficiency. J Clin Immunol (2001) 1.61

Genome-Wide Analyses Suggest Mechanisms Involving Early B-Cell Development in Canine IgA Deficiency. PLoS One (2015) 1.41

Pathogenesis, diagnosis, and management of primary antibody deficiencies and infections. Clin Microbiol Rev (2009) 1.38

Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. Nat Genet (2010) 1.32

IgA deficiency: correlation between clinical and immunological phenotypes. J Clin Immunol (2008) 1.30

Pathogenesis and treatment of gastrointestinal disease in antibody deficiency syndromes. J Allergy Clin Immunol (2009) 1.30

Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency. Am J Hum Genet (2013) 1.23

Gastrointestinal manifestations in patients with common variable immunodeficiency. Dig Dis Sci (2007) 1.20

Functional flexibility of intestinal IgA - broadening the fine line. Front Immunol (2012) 1.13

International Consensus Document (ICON): Common Variable Immunodeficiency Disorders. J Allergy Clin Immunol Pract (2015) 1.11

Retracted The European internet-based patient and research database for primary immunodeficiencies: update 2011. Clin Exp Immunol (2012) 1.11

Diagnosis and treatment of gastrointestinal disorders in patients with primary immunodeficiency. Clin Gastroenterol Hepatol (2013) 1.09

High serum levels of BAFF, APRIL, and TACI in common variable immunodeficiency. Clin Immunol (2007) 1.08

Clinical and immunological features of 65 Iranian patients with common variable immunodeficiency. Clin Diagn Lab Immunol (2005) 1.01

Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency. Am J Hum Genet (2015) 1.00

High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency. PLoS Genet (2012) 0.94

IgA production requires B cell interaction with subepithelial dendritic cells in Peyer's patches. Science (2016) 0.93

Primary immunodeficiency disorders in the Republic of Ireland: first report of the national registry in children and adults. J Clin Immunol (2005) 0.93

Immunity to microbes: lessons from primary immunodeficiencies. Infect Immun (2007) 0.93

Immunodeficiency associated with DNA repair defects. Clin Exp Immunol (2000) 0.91

Defective maturation of dendritic cells in common variable immunodeficiency. Clin Exp Immunol (2006) 0.89

Screening of functional and positional candidate genes in families with common variable immunodeficiency. BMC Immunol (2008) 0.89

Intracellular cytokine production by Th1/Th2 lymphocytes and monocytes of children with symptomatic transient hypogammaglobulinaemia of infancy (THI) and selective IgA deficiency (SIgAD). Clin Exp Immunol (2002) 0.88

Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q. Hum Genet (2005) 0.88

Clinical immunology review series: An approach to the management of pulmonary disease in primary antibody deficiency. Clin Exp Immunol (2009) 0.88

Incomplete penetrance of susceptibility genes for MHC-determined immunoglobulin deficiencies in monozygotic twins discordant for type 1 diabetes. J Autoimmun (2006) 0.86

Placental transfer of maternally-derived IgA precludes the use of guthrie card eluates as a screening tool for primary immunodeficiency diseases. PLoS One (2012) 0.86

Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders. Clin Immunol (2015) 0.86

B-cell subpopulations in children: National reference values. Immun Inflamm Dis (2014) 0.86

Chronic immune activation in common variable immunodeficiency (CVID) is associated with elevated serum levels of soluble CD14 and CD25 but not endotoxaemia. Clin Exp Immunol (2012) 0.85

Serum bactericidal antibody responses to meningococcal polysaccharide vaccination as a basis for clinical classification of common variable immunodeficiency. Clin Vaccine Immunol (2008) 0.84

Detection of anti-IgA antibodies using the particle gel immunoassay: a rapid test for increased patient safety. Blood Transfus (2014) 0.84

Antibody deficiency in chronic rhinosinusitis: epidemiology and burden of illness. Am J Rhinol Allergy (2013) 0.83

Increased serum levels of soluble CD30 in patients with common variable immunodeficiency and its clinical implications. J Clin Immunol (2007) 0.83

Frequent false positive beta human chorionic gonadotropin tests in immunoglobulin A deficiency. Clin Exp Immunol (2005) 0.83

RAG1 deficiency may present clinically as selective IgA deficiency. J Clin Immunol (2015) 0.83

Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneity. Hum Genet (2003) 0.82

Increased apoptosis of CD20+ IgA + B cells is the basis for IgA deficiency: the molecular mechanism for correction in vitro by IL-10 and CD40L. J Clin Immunol (2006) 0.82

The gastrointestinal frontier: IgA and viruses. Front Immunol (2013) 0.82

Pulmonary and sinus diseases in primary humoral immunodeficiencies with chronic productive cough. Arch Dis Child (2003) 0.82

Circulating phenotypic B-1 cells are decreased in common variable immunodeficiency and correlate with immunoglobulin M levels. Clin Exp Immunol (2013) 0.82

T and B lymphocyte subpopulations and activation/differentiation markers in patients with selective IgA deficiency. Clin Exp Immunol (2007) 0.81

Altered serum cytokine signature in common variable immunodeficiency. J Clin Immunol (2014) 0.81

The Microbiome, Timing, and Barrier Function in the Context of Allergic Disease. Immunity (2016) 0.80

Clinical significance of anti-HEV IgA in diagnosis of acute genotype 4 hepatitis E virus infection negative for anti-HEV IgM. Dig Dis Sci (2009) 0.80

Decreased IgA+ plasma cells and IgA expression in acute liver necrosis mice. World J Gastroenterol (2010) 0.80

Decreased production of immunoglobulin M and A in autoimmune pancreatitis. J Gastroenterol (2009) 0.80

Expression of Fc gamma and complement receptors in monocytes of X-linked agammaglobulinaemia and common variable immunodeficiency patients. Clin Exp Immunol (2007) 0.79

Common variable immune deficiency in children--clinical characteristics varies depending on defect in peripheral B cell maturation. J Clin Immunol (2013) 0.79

Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8. BMC Med Genet (2009) 0.78

Monozygotic twins discordant for common variable immunodeficiency reveal impaired DNA demethylation during naïve-to-memory B-cell transition. Nat Commun (2015) 0.78

Oxcarbazepine-induced immunoglobulin deficiency. Clin Diagn Lab Immunol (2005) 0.78

Common variable immunodeficiency: etiological and treatment issues. Int Arch Allergy Immunol (2009) 0.77

Characterization of Herpesvirus saimiri-transformed T lymphocytes from common variable immunodeficiency patients. Clin Exp Immunol (2002) 0.77

Peyer's patches: organizing B-cell responses at the intestinal frontier. Immunol Rev (2016) 0.76

Infliximab therapy for Crohn's-like disease in common variable immunodeficiency complicated by massive intestinal hemorrhage: a case report. BMC Res Notes (2014) 0.75

An unsual case of persistent inguinal swelling - beware immunodeficiency. JRSM Short Rep (2011) 0.75

Role of B cells in common variable immune deficiency. Expert Rev Clin Immunol (2009) 0.75

Association of HLA-DRB1, DQA1 and DQB1 Alleles and Haplotypes with Common Variable Immunodeficiency in Iranian Patients. Avicenna J Med Biotechnol (2012) 0.75

A case of primary immune deficiency presenting with nephrotic syndrome. NDT Plus (2010) 0.75

Bilateral lung transplantation in a patient with humoral immune deficiency: a case report with review of the literature. Case Reports Immunol (2014) 0.75

Microbiota-specific Th17 Cells: Yin and Yang in Regulation of Inflammatory Bowel Disease. Inflamm Bowel Dis (2016) 0.75

Silencing the alarm: insights into the interaction between host and pathogen. Conference on Microbial Pathogenesis: Mechanisms of Infectious Disease. EMBO Rep (2007) 0.75

Prevalence and pattern of humoral immunodeficiency in chronic refractory sinusitis. Eur Arch Otorhinolaryngol (2016) 0.75

[Common variable immunodeficiency: a clinical challenge]. Z Rheumatol (2013) 0.75

Crohn's-like colitis in a patient with immunodeficiency associated with a defect in expression of inducible costimulator. Dig Dis Sci (2006) 0.75

How to Assess, Control, and Manage Uncontrolled CRS/Nasal Polyp Patients. Curr Allergy Asthma Rep (2017) 0.75

Large cell lymphoma presenting as a flare of colitis in a patient with common variable immune deficiency. Dig Dis Sci (2007) 0.75

Reversal of Immunoglobulin A Deficiency in Children. J Clin Immunol (2014) 0.75

Articles cited by this

Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin Immunol (1999) 7.25

Primary hypogammaglobulinaemia: a survey of clinical manifestations and complications. Q J Med (1993) 4.58

Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta-deficient mice. Immunity (1997) 3.99

Lymphotoxin-alpha-deficient mice. Effects on secondary lymphoid organ development and humoral immune responsiveness. J Immunol (1995) 3.69

Sulfasalazine: a potent and specific inhibitor of nuclear factor kappa B. J Clin Invest (1998) 2.90

NF-kappa B RelA-deficient lymphocytes: normal development of T cells and B cells, impaired production of IgA and IgG1 and reduced proliferative responses. J Exp Med (1997) 2.66

B cells from p50/NF-kappa B knockout mice have selective defects in proliferation, differentiation, germ-line CH transcription, and Ig class switching. J Immunol (1996) 2.53

Subcutaneous immunoglobulin replacement in patients with primary antibody deficiencies: safety and costs. Lancet (1995) 2.43

IgG subclasses in selective IgA deficiency: importance of IgG2-IgA deficiency. N Engl J Med (1981) 2.18

Prospective study of cancer in patients with hypogammaglobulinaemia. Lancet (1985) 2.03

CD40 ligand expression is defective in a subset of patients with common variable immunodeficiency. Proc Natl Acad Sci U S A (1994) 1.94

Primary hypogammaglobulinaemia: impaired lung function and body growth with delayed diagnosis and inadequate treatment. Eur J Respir Dis (1984) 1.77

Development of a common variable immunodeficiency in IgA-deficient patients. Clin Immunol Immunopathol (1996) 1.68

Switch transcripts in immunoglobulin class switching. Science (1995) 1.62

Targeted deletion of the IgA constant region in mice leads to IgA deficiency with alterations in expression of other Ig isotypes. J Immunol (1999) 1.61

Interleukin 10 and immune restoration in common variable immunodeficiency. Lancet (1993) 1.60

Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome. Proc Natl Acad Sci U S A (1998) 1.51

Common variable immunodeficiency: how many diseases? Immunol Today (1997) 1.48

Antibody-independent protective mucosal immunity to gastric helicobacter infection in mice. Cell Immunol (1999) 1.43

TNF and lymphotoxin-alpha polymorphisms associated with common variable immunodeficiency: role in the pathogenesis of granulomatous disease. J Immunol (1997) 1.42

Progressive immunodeficiency in a patient with IgA deficiency. Ann Allergy Asthma Immunol (1997) 1.41

IgA deficiency. Adv Immunol (1997) 1.33

Increased susceptibility to Mycoplasma infection in patients with hypogammaglobulinemia. Am J Med (1986) 1.31

Persistent activation of the tumor necrosis factor system in a subgroup of patients with common variable immunodeficiency--possible immunologic and clinical consequences. Blood (1996) 1.30

Immunoglobulin replacement therapy by self-infusion at home. Clin Exp Immunol (1988) 1.30

Mucosal immunity to influenza without IgA: an IgA knockout mouse model. J Immunol (1999) 1.29

Encephalomyelitis in primary hypogammaglobulinaemia. Brain (1996) 1.25

Altered hepatic transport of immunoglobulin A in mice lacking the J chain. J Exp Med (1995) 1.24

Intracellular cytokine production by human CD4+ and CD8+ T cells from normal and immunodeficient donors using directly conjugated anti-cytokine antibodies and three-colour flow cytometry. Clin Exp Immunol (1996) 1.24

Lymphoproliferative lesions in patients with common variable immunodeficiency syndrome. Am J Surg Pathol (1992) 1.21

Lack of specific antibody response in common variable immunodeficiency (CVID) associated with failure in production of antigen-specific memory T cells. MRC Immunodeficiency Group. Clin Exp Immunol (1997) 1.19

IgA class switch in I alpha exon-deficient mice. Role of germline transcription in class switch recombination. J Clin Invest (1996) 1.17

Interleukin 10 induces B lymphocytes from IgA-deficient patients to secrete IgA. J Clin Invest (1994) 1.16

Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition. Am J Hum Genet (1999) 1.15

Studies on the enteropathy associated with primary hypogammaglobulinaemia. Gut (1994) 1.14

Lack of association of secretory component with IgA in J chain-deficient mice. J Immunol (1996) 1.13

IL-4 plus CD40 monoclonal antibody induces human B cells gamma subclass-specific isotype switch: switching to gamma 1, gamma 3, and gamma 4, but not gamma 2. J Immunol (1995) 1.13

Primary defect in CD8+ lymphocytes in the antibody deficiency disease (common variable immunodeficiency): abnormalities in intracellular production of interferon-gamma (IFN-gamma) in CD28+ ('cytotoxic') and CD28- ('suppressor') CD8+ subsets. Clin Exp Immunol (1998) 1.12

Sarcoidosis and primary hypogammaglobulinaemia: a report of two cases and a review of the literature. Sarcoidosis (1985) 1.12

Deficiency of IL-5 receptor alpha-chain selectively influences the development of the common mucosal immune system independent IgA-producing B-1 cell in mucosa-associated tissues. J Immunol (1999) 1.08

Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency. J Immunol (1994) 1.06

Age-related changes in serum immunoglobulins in patients with familial IgA deficiency and common variable immunodeficiency (CVID). Clin Exp Immunol (1997) 1.04

Immunoglobulin subclass distribution of human anti-carbohydrate antibodies: aberrant pattern in IgA-deficient donors. Immunology (1985) 1.03

Autoimmune blood dyscrasias in five patients with hypogammaglobulinemia: response of neutropenia to vincristine. J Clin Immunol (1981) 1.02

X-linked immunodeficiency with hyper-IgM (XHIM). Clin Exp Immunol (2000) 1.02

Mycoplasmal arthritis in patients with primary immunoglobulin deficiency: clinical features and outcome in 18 patients. Br J Rheumatol (1997) 0.98

Long-term outcome of chronic hepatitis C virus infection in primary hypogammaglobulinaemia. QJM (1999) 0.97

Chromosomal radiosensitivity in common variable immune deficiency. Mutat Res (1993) 0.96

IgA deficiency in one of identical twins. Br Med J (1976) 0.96

Immunodeficiencies associated with sulphasalazine therapy in inflammatory arthritis. Br J Rheumatol (1991) 0.95

Development of hypogammaglobulinaemia in a patient with common variable immunodeficiency. Eur J Pediatr (1989) 0.95

Activation via the antigen receptor is impaired in T cells, but not in B cells from patients with common variable immunodeficiency. Eur J Immunol (1996) 0.94

Abnormal CD40-mediated activation pathway in B lymphocytes from patients with hyper-IgM syndrome and normal CD40 ligand expression. J Immunol (1997) 0.93

Recovery of antibody production after HIV infection in 'common' variable hypogammaglobulinaemia. Clin Exp Immunol (1989) 0.93

CD95 expression and function on lymphocyte subpopulations in common variable immunodeficiency (CVID); related to increased apoptosis. Clin Exp Immunol (1999) 0.92

In vivo expression of human immunoglobulin germ-line mRNA in normal and in immunodeficient individuals. Clin Exp Immunol (1994) 0.92

Subclass distribution of antigen-specific IgA antibodies in normal donors and individuals with homozygous C alpha 1 or C alpha 2 gene deletions. J Immunol (1990) 0.91

Diagnosis of enterovirus brain disease in hypogammaglobulinemic patients by polymerase chain reaction. Clin Infect Dis (1993) 0.91

Enhanced generation of reactive oxygen species in monocytes from patients with common variable immunodeficiency. Clin Exp Immunol (1994) 0.88

Transfer of IgA deficiency to a bone-marrow-grafted patient with aplastic anaemia. Lancet (1985) 0.88

Survey of serum IgA, IgG, and IgM concentrations in a large beagle population in which IgA deficiency had been identified. Am J Vet Res (1988) 0.87

Changes in serum immunoglobulin patterns in adults with common variable immunodeficiency. Clin Exp Immunol (1991) 0.86

Discordance between IgA switching at the DNA level and IgA expression at the mRNA level in IgA-deficient patients. Clin Immunol (1999) 0.85

Genetics of IgA deficiency. APMIS (1995) 0.84

Prophylactic therapy for selective IgA deficiency. Lancet (1997) 0.84

The significance of IgG subclasses and mannan-binding lectin (MBL) for susceptibility to infection in apparently healthy adults with IgA deficiency. Clin Exp Immunol (1999) 0.84

Orthotopic liver transplantation for chronic hepatitis in two patients with common variable immunodeficiency. Gastroenterology (1995) 0.84

Characterization of Haemophilus influenzae isolates from the respiratory tract of patients with primary antibody deficiencies: evidence for persistent colonizations. Scand J Infect Dis (1995) 0.83

Lack of IgG in a healthy adult: a rare case of dysgammaglobulinemia with undetectable serum IgG, IgA2, and IgE. Clin Immunol Immunopathol (1984) 0.83

IgA deficiency in shar-pei dogs. Vet Immunol Immunopathol (1986) 0.83

Selective IgA deficiency in the dog. Clin Immunol Immunopathol (1985) 0.82

IgA and IgG2 deficiency associated with zonisamide therapy: a case report. Epilepsia (1997) 0.81

Detection of IgA heavy chain constant region genes in IgA deficient donors: evidence against gene deletions. Clin Exp Immunol (1985) 0.81

A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: evidence from meiotic mapping of 83 multiple-case families. J Immunol (1999) 0.80

IL-10-driven immunoglobulin production by B lymphocytes from IgA-deficient individuals correlates to infection proneness. Clin Exp Immunol (1996) 0.79

Cyclosporine A induced colitis and acquired selective IgA deficiency in a patient with juvenile chronic arthritis. J Rheumatol (1993) 0.79

IgA2 allotypes determined by restriction fragment length polymorphism in IgA deficiency. Re-expression of the silent A2m(2) allotype in the children of IgA-deficient patients. J Immunogenet (1988) 0.79

Captopril-induced IgA deficiency. Lancet (1991) 0.77

Case report: immunoglobulin A deficiency in patients with juvenile rheumatoid arthritis treated with aspirin. Biotherapy (1993) 0.77

Failure in IgA secretion by surface IgA-positive B cells in common variable immunodeficiency (CVID). Clin Exp Immunol (1994) 0.77

Selective IgA deficiency in chickens with spontaneous autoimmune thyroiditis. Nature (1976) 0.77

Incidental correction of severe IgA deficiency by displacement bone marrow transplantation. Bone Marrow Transplant (1991) 0.77

Articles by these authors

(truncated to the top 100)

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell (1996) 7.86

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene. Nat Genet (1998) 3.94

X-linked ichthyosis due to steroid-sulphatase deficiency. Lancet (1978) 3.00

High prevalence of thymic tissue in adults with human immunodeficiency virus-1 infection. J Clin Invest (1998) 2.47

Low frequency of alterations of the alpha (PPP2R1A) and beta (PPP2R1B) isoforms of the subunit A of the serine-threonine phosphatase 2A in human neoplasms. Oncogene (2000) 2.08

Randomized trial of a specialist genetic assessment service for familial breast cancer. J Natl Cancer Inst (2000) 1.92

Vitamin D-binding protein contributes to COPD by activation of alveolar macrophages. Thorax (2011) 1.89

The FHIT gene at 3p14.2 is abnormal in breast carcinomas. Cancer Res (1996) 1.75

N-methyl-D-aspartate antagonists limit aminoglycoside antibiotic-induced hearing loss. Nat Med (1996) 1.69

Milk allergy: clinical picture and familial incidence. Can Med Assoc J (1967) 1.66

Posthumous diagnosis of long QT syndrome from neonatal screening cards. Heart Rhythm (2010) 1.65

Re-evaluation of the tympanic thermometer in the emergency department. Ann Emerg Med (1992) 1.59

Phosphonomethyl analogues of hexose phosphates. Biochem J (1976) 1.49

Absence of a newly described cytochrome b from neutrophils of patients with chronic granulomatous disease. Lancet (1978) 1.45

A mammalian patched homolog is expressed in target tissues of sonic hedgehog and maps to a region associated with developmental abnormalities. J Biol Chem (1996) 1.44

Interaction of campylobacter species with antibody, complement and phagocytes. Gut (1989) 1.37

Osteomalacia in elderly patients with fracture of the femoral neck. A clinico-pathological study. J Bone Joint Surg Br (1973) 1.36

Impaired antibody affinity maturation process characterizes a subset of patients with common variable immunodeficiency. J Immunol (2000) 1.35

Comparison of the rate of sequence variation in the hypervariable region of E2/NS1 region of hepatitis C virus in normal and hypogammaglobulinemic patients. Hepatology (1998) 1.33

Refinement of the LOH region 1 at 11q23.1 deleted in human breast carcinomas and sublocalization of 11 expressed sequence tags within the refined region. Oncogene (1999) 1.28

Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation. Cancer Res (1996) 1.25

Viruses in febrile convulsions. Lancet (1980) 1.22

An arsenical analogue of adenosine diphosphate. Biochem J (1978) 1.21

Detection of human immunodeficiency virus by reverse transcriptase assay, antigen capture assay, and radioimmunoassay. J Clin Microbiol (1987) 1.21

Circulating levels of cobalt and chromium from metal-on-metal hip replacement are associated with CD8+ T-cell lymphopenia. J Bone Joint Surg Br (2009) 1.21

Immature B cells in fetal development and immunodeficiency: studies of IgM, IgG, IgA and IgD production in vitro using Epstein-Barr virus activation. Eur J Immunol (1982) 1.21

An assessment of the suitability of bromocresol green for the determination of serum albumin. Clin Chim Acta (1974) 1.17

Anti-tumour necrosis factor-alpha therapy for severe enteropathy in patients with common variable immunodeficiency (CVID). Clin Exp Immunol (2007) 1.17

FT Raman microscopy of untreated natural plant fibres. Spectrochim Acta A Mol Biomol Spectrosc (1997) 1.14

A second activation peptide from bovine cationic trypsinogen. Biochem J (1977) 1.14

Does 77C-->G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus? Nat Genet (2001) 1.11

Risk factors for low BMD in healthy men age 50 years or older: a systematic review. Osteoporos Int (2008) 1.11

How to quantify coughing: correlations with quality of life in chronic cough. Eur Respir J (2008) 1.07

Molecular cloning and characterization of LOH11CR2A, a new gene within a refined minimal region of LOH at 11q23. Genomics (1997) 1.05

Low frequency of E-cadherin alterations in familial breast cancer. Breast Cancer Res (2001) 1.04

An ecological model for school-based mental health services for urban low-income aggressive children. J Behav Health Serv Res (1998) 1.03

A study of the interaction of bromocresol green with isolated serum globulin fractions. Clin Chim Acta (1974) 1.03

Compartmental bone morphometry in the mouse femur: reproducibility and resolution dependence of microtomographic measurements. Calcif Tissue Int (2005) 1.03

Hematopoietic potential of cryopreserved and ex vivo manipulated umbilical cord blood progenitor cells evaluated in vitro and in vivo. Blood (1996) 1.02

Newborn screening for congenital adrenal hyperplasia in New Zealand. J Pediatr (1995) 0.98

Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia. J Clin Endocrinol Metab (1999) 0.97

The role of alcohol use in intimate partner femicide. Am J Addict (2001) 0.95

Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia. Leukemia (2004) 0.94

The modification and removal of the N-terminal residue of trypsin by transamination. Biochem J (1972) 0.91

Thyrocalcitonin and its role in calcium homeostasis. J Endocrinol (1967) 0.90

Sustained retroviral gene marking and expression in lymphoid and myeloid cells derived from transduced hematopoietic progenitor cells. Gene Ther (1996) 0.90

Failure of influenza vaccine to prevent two successive outbreaks of influenza A H1N1 in a school community. Br J Gen Pract (1990) 0.90

Maternal hydrocephalus in pregnancy and delivery: a report of two cases. West Indian Med J (2007) 0.90

Complicated head trauma from machete wounds: the experience from a tertiary referral hospital in Jamaica. Int J Inj Contr Saf Promot (2011) 0.90

Identification of Btk mutations in 20 unrelated patients with X-linked agammaglobulinaemia (XLA). Hum Mol Genet (1995) 0.89

Treatment of resistant mycoplasma infection in immunocompromised patients with a new pleuromutilin antibiotic. J Infect (2001) 0.89

Molecular diagnosis of X-linked agammaglobulinaemia. Lancet (1993) 0.89

BTKbase, mutation database for X-linked agammaglobulinemia (XLA) Nucleic Acids Res (1997) 0.88

The immediate reaction between bromcresol green and serum as a measure of albumin content. Clin Chem (1977) 0.87

Preimplantation human blastocysts release factors that differentially alter human endometrial epithelial cell adhesion and gene expression relative to IVF success. Hum Reprod (2013) 0.87

Genital prolapse amongst the Pokot. East Afr Med J (1975) 0.87

Molecular cloning of a proteolytic antibody light chain. J Biol Chem (1994) 0.87

Mycoplasma amphoriforme sp. nov., isolated from a patient with chronic bronchopneumonia. Int J Syst Evol Microbiol (2005) 0.86

Oxymetholone in the treatment of anaemia in chronic renal failure. Br J Urol (1972) 0.85

Dietary practices in pyridoxine non-responsive homocystinuria: a European survey. Mol Genet Metab (2013) 0.84

Molecular cloning and characterization of ZNF202: a new gene at 11q23.3 encoding testis-specific zinc finger proteins. Genomics (1998) 0.83

Missense mutations at ATM gene and cancer risk. Lancet (1999) 0.83

Interim estimates of 2013/14 influenza clinical severity and vaccine effectiveness in the prevention of laboratory-confirmed influenza-related hospitalisation, Canada, February 2014. Euro Surveill (2014) 0.83

Plant-derived measles virus hemagglutinin protein induces neutralizing antibodies in mice. Vaccine (2001) 0.83

Uncoupling agents: arsenical analogues of pyrophosphate and their compounds. Biochem Soc Trans (1977) 0.83

Information and consent for newborn screening: practices and attitudes of service providers. J Med Ethics (2008) 0.82

UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients. Oncogene (2000) 0.82

Assessment of responses of normal human B lymphocytes to different isolates of human immunodeficiency virus: role of normal donor and of cell line used to prepare viral isolate. AIDS Res Hum Retroviruses (1989) 0.82

Dietary management of urea cycle disorders: European practice. Mol Genet Metab (2013) 0.82

Brain abscess at the University Hospital of the West Indies. West Indian Med J (2000) 0.81

Using wound fluid analyses to identify trace element requirements for efficient healing. J Wound Care (2001) 0.81

The effects of auditory deprivation on morphological maturation of the ventral cochlear nucleus. Arch Otorhinolaryngol (1989) 0.81

Tuberculosis outbreak associated with a mosque: challenges of large scale contact tracing. Euro Surveill (2008) 0.81

Recurrent ATM mutations in T-PLL on diverse haplotypes: no support for their germline origin. Blood (2001) 0.80

Neonatal screening in New Zealand. BMJ (1996) 0.80

Absence of xid mutation in X-linked agammaglobulinaemia. Lancet (1993) 0.79

Organo-selenium-containing dental sealant inhibits bacterial biofilm. J Dent Res (2013) 0.78

Serum protein studies in myocardial infarction. Gerontol Clin (Basel) (1966) 0.78

The Ætiology of Retinitis Pigmentosa, with cases. Trans Am Ophthalmol Soc (1878) 0.78

Why do we see JAK2 exon 12 mutations in myeloproliferative neoplasms? Leukemia (2013) 0.78

Orbital psuedotumour with intracranial extension. A case report. West Indian Med J (1998) 0.78

Mycophenolic acid and some antioxidants induce differentiation of monocytic lineage cells and augment production of the IL-1 receptor antagonist. Ann N Y Acad Sci (1993) 0.78

Successful treatment of autoimmune lymphoproliferative syndrome and refractory autoimmune thrombocytopenic purpura with a reduced intensity conditioning stem cell transplantation followed by donor lymphocyte infusion. Bone Marrow Transplant (2007) 0.78

Comparisons of magnitude estimation scaling of rock music by children, young adults, and older people. Percept Mot Skills (1999) 0.78

Comparing patients' and nurses' views of interstitial cystitis: a pilot study. Urol Nurs (1990) 0.78

Baroreceptor involvement in the immobility reflex. Behav Biol (1978) 0.77

Adhesives in larynx repair. Laryngoscope (1989) 0.77

The effect of protracted tetracycline treatment on bone growth and maturation. Clin Orthop Relat Res (1983) 0.77

Dietary management of urea cycle disorders: UK practice. J Hum Nutr Diet (2012) 0.77

Determination of HDL-cholesterol using 2,4,6-tribromo-3-hydroxybenzoic acid with a commercial CHOD-PAP reagent. Ann Clin Biochem (1984) 0.77

Malaria kills one child every 30 seconds. J Public Health Policy (2001) 0.77

Cochlear implantation of a patient with a previously undescribed mitochondrial DNA defect. J Laryngol Otol (2001) 0.77

First ISNS Reference Preparation for Neonatal Screening for thyrotropin, phenylalanine and 17alpha-hydroxyprogesterone in blood spots. J Inherit Metab Dis (2007) 0.77

Pregnancy in a drug-abusing population. Am J Drug Alcohol Abuse (1986) 0.76

Quality evaluation of newborn screening programs. Acta Paediatr Suppl (1999) 0.76

Allelic imbalance on chromosomes 13 and 17 and mutation analysis of BRCA1 and BRCA2 genes in monozygotic twins concordant for breast cancer. Carcinogenesis (2001) 0.76

Meningococcal meningitis in two patients with primary antibody deficiency treated with replacement intravenous immunoglobulin. J Clin Pathol (2006) 0.76

Removal by transamination and scission of residues from the peptide representing the copper-transport site of serum albumin. Biochem J (1978) 0.75

High dose frusemide in the treatment of hypertension in chronic renal insufficiency and of terminal renal failure. Postgrad Med J (1971) 0.75

Further assessment of the normal cholecystogram. Br Med J (1977) 0.75