Immune deficiency: evaluation, diagnosis, and therapy. (Q39871622)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4139682 AND SRC:MED&resulttype=core&format=json

7 October 2019

review article

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title

Immune deficiency: evaluation, diagnosis, and therapy (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4139682 AND SRC:MED&resulttype=core&format=json

7 October 2019

author name string

E W Gelfand

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4139682 AND SRC:MED&resulttype=core&format=json

7 October 2019

W D Biggar

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4139682 AND SRC:MED&resulttype=core&format=json

7 October 2019

R P Orange

series ordinal

3

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7 October 2019

publication date

1 November 1974

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Pediatric Clinics of North America

7 October 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4139682 AND SRC:MED&resulttype=core&format=json

7 October 2019

volume

21

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7 October 2019

issue

4

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7 October 2019

page(s)

745-776

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Establishment of immunological competence in a child with congenital thymic aplasia by a graft of fetal thymus

7 October 2019

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Agammaglobulinaemia with B lymphocytes. Specific defect of plasma-cell differentiation

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C1r deficiency: an inborn error associated with cutaneous and renal disease

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A BIOCHEMICAL ABNORMALITY IN HEREDIATRY ANGIONEUROTIC EDEMA: ABSENCE OF SERUM INHIBITOR OF C' 1-ESTERASE.

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Familial lipochrome pigmentation of histiocytes with hyperglobulinemia, pulmonary infiltration, splenomegaly, arthritis and susceptibility to infection

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Hereditary lymphopenic agammaglobulinemia associated with a distinctive form of short-limbed dwarfism and ectodermal dysplasia

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Polyclonal gammopathy and lymphoproliferation after transfer factor in severe combined immunodeficiency disease.

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Adenosine-deaminase deficiency in two patients with severely impaired cellular immunity

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Fatal granulomatous disease of childhood. An inborn abnormality of phagocytic function

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An abnormality of the alternate pathway of complement activation in sickle-cell disease

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Hereditary deficiency of the second component of complement (C'2) in man.

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Complement-Immunoglobulin Relation: Deficiency of C′lq Associated with Impaired Immunoglobulin G Synthesis

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The syndrome of cellular immunodeficiency with immunoglobulins

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Receptors for complement of leukocytes

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Hereditary deficiency of the sixth component of complement in man. I. Immunochemical, biologic, and family studies

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Chronic neutropenia and abnormal cellular immunity in cartilage-hair hypoplasia.

7 January 2021

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The Complement System

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Receptors for human gamma G globulin on human neutrophils.

7 January 2021

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The thymus and the immune system

7 January 2021

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A Familial Deficiency of the Phagocytosis-Enhancing Activity of Serum Related to a Dysfunction of the Fifth Component of Complement (C5)

7 January 2021

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Lazy-leucocyte syndrome. A new disorder of neutrophil function

7 January 2021

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In vitro bactericidal capacity of human polymorphonuclear leukocytes: diminished activity in chronic granulomatous disease of childhood

7 January 2021

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The cellular basis of immunological responses. A synthesis of some current views

7 January 2021

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Abnormal bactericidal, metabolic, and lysosomal functions of Chediak-Higashi Syndrome leukocytes

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The complement system of man. I.

7 January 2021

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Selective gamma-g globulin deficiencies in patients with recurrent pyogenic infections

7 January 2021

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Heat labile opsonins to pneumococcus. I. Participation of complement

7 January 2021

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Defect of neutrophil motility in a child with recurrent bacterial infections and disseminated cytomegalovirus infection.

7 January 2021

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The Wiskott-Aldrich syndrome. Results of transfer factor therapy

7 January 2021

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An anomaly of neutrophil morphology with impaired function

7 January 2021

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Impaired lymphocyte transformation in intestinal lymphangiectasia: evidence for at least two functionally distinct lymphocyte populations in man

7 January 2021

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Opsonins: their function, identity, and clinical significance

7 January 2021

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Deficiency of pneumococcal serum opsonizing activity in sickle-cell disease

7 January 2021

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Rosette-Forming Cells, Immunologic Deficiency Diseases and Transfer Factor

7 January 2021

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Homozygous deficiency of C3 in a patient with repeated infections

7 January 2021

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inferred from DOI database lookup

7 January 2021

based on heuristic

Job's Syndrome. Recurrent, "cold", staphylococcal abscesses

1 reference

https://api.crossref.org/works/10.1016/S0031-3955(16)33060-7

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0031-3955(16)33060-7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4139682 AND SRC:MED&resulttype=core&format=json

7 October 2019

1 reference