(Q37106302)

18 August 2017

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title

Approach to the patient with recurrent infections (English)

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18 August 2017

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Mark Ballow

1

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18 August 2017

publication date

1 April 2008

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Clinical Reviews in Allergy & Immunology

18 August 2017

published in

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18 August 2017

volume

34

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18 August 2017

issue

2

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18 August 2017

page(s)

129-140

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Familial hemolytic-uremic syndrome and homozygous factor H deficiency

18 August 2017

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FS12016-007-8041-2

New perspectives on the immunology of chronic mucocutaneous candidiasis

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12016-007-8041-2

Clinical, molecular, and cell biological aspects of Chediak-Higashi syndrome

21 January 2018

1 reference

12 December 2020

IgG subclass distribution of antibodies to bacterial and viral antigens

1 reference

12 December 2020

IgG subclass distribution of antibody induced by immunization with the isolated and protein-conjugated polysaccharide of H. influenzae b and G2m(n) distribution of serum IgG2 in man

1 reference

12 December 2020

Clinical spectrum of X-linked hyper-IgM syndrome

1 reference

12 December 2020

Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: Further evidence for an X-linked lethal syndrome.

1 reference

12 December 2020

ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome

1 reference

12 December 2020

Ataxia-Telangiectasia: A Multisystem Hereditary Disease with Immunodeficiency, Impaired Organ Maturation, X-Ray Hypersensitivity, and a High Incidence of Neoplasia

1 reference

12 December 2020

Inherited interleukin 12 deficiency in a child with bacille Calmette-Guérin and Salmonella enteritidis disseminated infection

1 reference

12 December 2020

Serum levels of immune globulins in health and disease: a survey

1 reference

12 December 2020

X-linked agammaglobulinemia: an analysis of 96 patients

1 reference

12 December 2020

Chronic mucocutaneous candidiasis

1 reference

12 December 2020

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

1 reference

12 December 2020

Human interferon-gamma-mediated immunity is a genetically controlled continuous trait that determines the outcome of mycobacterial invasion

1 reference

12 December 2020

Impaired interferon gamma-mediated immunity and susceptibility to mycobacterial infection in childhood

1 reference

12 December 2020

IgG subclass deficiency: a personal viewpoint.

1 reference

12 December 2020

Phagocyte immunodeficiencies and their infections

1 reference

12 December 2020

Cutaneous manifestations of ataxia-telangiectasia

1 reference

12 December 2020

Partial albinism with immunodeficiency: Griscelli syndrome: report of a case and review of the literature

1 reference

12 December 2020

Common variable immunodeficiency: clinical and immunological features of 248 patients.

1 reference

12 December 2020

Leukocyte adhesion deficiency syndromes: adhesion and tethering defects involving beta 2 integrins and selectin ligands

1 reference

12 December 2020

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

1 reference

12 December 2020

Clinical and immunologic analyses of 103 patients with common variable immunodeficiency

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12 December 2020

Role of TBX1 in human del22q11.2 syndrome

1 reference

12 December 2020

Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients.

1 reference

12 December 2020

Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).

1 reference

12 December 2020

Chédiak-Higashi syndrome: presentation of seven cases.

1 reference

12 December 2020

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12 December 2020

Absent specific viral antibodies in patients with transient hypogammaglobulinemia of infancy

1 reference

12 December 2020

WHIM syndrome, an autosomal dominant disorder: clinical, hematological, and molecular studies

1 reference

12 December 2020

Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

1 reference

12 December 2020

A multiinstitutional survey of the Wiskott-Aldrich syndrome.

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12 December 2020

Practice parameter for the diagnosis and management of primary immunodeficiency

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12 December 2020

Patient-centred screening for primary immunodeficiency: a multi-stage diagnostic protocol designed for non-immunologists.

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12 December 2020

Clinical and immunologic studies of common variable immunodeficiency.

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12 December 2020

Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity

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12 December 2020

Idiopathic late-onset immunoglobulin deficiency. Clinical observations in 50 patients

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12 December 2020

Primary immunodeficiency disorders: antibody deficiency

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12 December 2020

Anaphylactic reactions after gamma globulin administration in patients with hypogammaglobulinemia. Detection of IgE antibodies to IgA

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12 December 2020

Recent advances in understanding of the molecular basis of anhidrotic ectodermal dysplasia: discovery of a ligand, ectodysplasin A and its two receptors.

1 reference

12 December 2020

DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion

1 reference

12 December 2020

Influence of age on the response to Streptococcus pneumoniae vaccine in patients with recurrent infections and normal immunoglobulin concentrations

1 reference

12 December 2020

Autoimmune lymphoproliferative syndrome

1 reference

12 December 2020

Autoimmune lymphoproliferative syndrome. A human disorder of abnormal lymphocyte survival

1 reference

12 December 2020

The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis

1 reference

12 December 2020

Congenital neutropenia: advances in diagnosis and treatment

1 reference

12 December 2020

Clinical and laboratory evaluation of complement deficiency

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12 December 2020

Genetic, biochemical, and clinical features of chronic granulomatous disease.

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12 December 2020

Prediction of persistent immunodeficiency in the DiGeorge anomaly

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12 December 2020

Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease

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12 December 2020

Environmental tobacco smoke: a hazard to children. American Academy of Pediatrics Committee on Environmental Health

1 reference

12 December 2020

Clincal, immunologic, and genetic features of an autoimmune lymphoproliferative syndrome associated with abnormal lymphocyte apoptosis

1 reference

12 December 2020

An X-linked syndrome of diarrhea, polyendocrinopathy, and fatal infection in infancy.

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12 December 2020

Immunodeficiency and infections in ataxia-telangiectasia.

1 reference

12 December 2020

Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome. Report of two new patients and review of the literature

1 reference

12 December 2020

Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency

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12 December 2020

Cross-talk between CD40 and CD40L: lessons from primary immune deficiencies

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12 December 2020

Complement deficiencies

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12 December 2020

Prenatal diagnosis and genetic analysis of X-linked immunodeficiency disorders

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12 December 2020

Lytic granules, secretory lysosomes and disease

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12 December 2020

Structure and function of the gastrointestinal tract in primary immunodeficiency syndromes. A study of 39 patients

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12 December 2020

Leukocyte adhesion deficiency II-from A to almost Z.

1 reference

12 December 2020

Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: a model of immune dysregulation

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12 December 2020

Familial Reticuloendotheliosis with Eosinophilia

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12 December 2020

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

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12 December 2020

Vaccine-associated poliomyelitis in a child with sex-linked agammaglobulinemia

1 reference

12 December 2020

10.1007/S12016-007-8041-2

Identifiers

DOI

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18 August 2017

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