About: Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia

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About: Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia Goto Sponge NotDistinct Permalink

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scientific article published on 01 March 1968

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1968 (uk) im März 1968 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en marzu de 1968 (ast) scientific article published on 01 March 1968 (en)
publication date	wds:Q70082995-35008264-07AC-48DF-9DD1-4F848BDBED5D
publication date	1968-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q70082995-49C947BA-FBF3-476A-9422-B6716C0ED26A
language of work or name	English
cites work	wds:Q70082995-0E350D96-8D03-4AF5-AFAA-47C606CCD48D wds:Q70082995-103780DD-8538-4C90-BE4E-FAF71AF1206C wds:Q70082995-13C1CEA2-5E00-4DB0-B975-93A4CFD2BD9F wds:Q70082995-21EC0FB9-1AD6-4815-97CB-C214126E92EA wds:Q70082995-3034096A-A5D1-4083-95EA-19E809CFEB3B wds:Q70082995-3F48B80F-692F-497A-8B8B-1D93FB0B7CA3 wds:Q70082995-46374A2E-8C2F-4119-9713-C863C6876903 wds:Q70082995-514757A1-7C4B-45BA-B82D-43FF4BE7D45A wds:Q70082995-52C7A839-5720-4262-B98D-75CAD9EFE180 wds:Q70082995-57AD1F90-EC5C-47CA-BAC5-F04EB4FB7C3D wds:Q70082995-5DF3A2E4-77C6-4B03-8E88-B4A7C252547E wds:Q70082995-5F16D7AA-FDA2-4972-804D-DA7D2458CBD1 wds:Q70082995-6442FE12-1A22-4B1E-9DA6-772338AE3C0F wds:Q70082995-69930A6B-4E3B-4919-8432-ED1EB7B99320 wds:Q70082995-909CF3E0-0223-464E-90BD-195E8C972E20 wds:Q70082995-99763B5A-4EEC-47A4-8F50-4A5802E53076 wds:Q70082995-9B0B7C78-2600-411F-AA52-EF5DB48B2396 wds:Q70082995-BE9B8AA2-D1C7-4C21-B311-3EB73F6B0D83 wds:Q70082995-D712620F-C4D5-41A2-B319-834169770C59 wds:Q70082995-D7B86F28-036B-4C0A-9D4D-430FAC29399F wds:Q70082995-E3446DBE-BDBD-4974-9842-1E978916E7F1 wds:Q70082995-E36E7318-B747-4849-B67E-98C7484AC43B wds:Q70082995-E70135AE-D058-4871-8C3A-5FB3C3917DED
cites work	CHARACTERISTICS OF AN IMMUNE SYSTEM COMMON TO CERTAIN EXTERNAL SECRETIONS FAMILIAL LYMPHOPENIA WITH AGAMMAGLOBULINEMIA: AN ATTEMPT AT TREATMENT BY IMPLANTATION OF FETAL THYMUS Spontaneous chromosome aberrations in familial panmyelopathy The mechanism of appearance of immunoglobulin A in nasal secretions in man CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN The IgA system. I. Studies of the transport and immunochemistry of IgA in the saliva Chromosomal breakage and acute leukemia in congenital telangiectatic erythema and stunted growth Lymphoid tissue abnormalities associated with ataxia-telangiectasia Fanconi's anemia. Inherited susceptibility to chromosome breakage in various tissues Fatal hepatic and bronchial necrosis in adenovirus infection with thymic alymphoplasia Graft-vs-Host Reaction Following a Single Blood Transfusion Nutrition of animal cells in tissue culture; initial studies on a synthetic medium VIRUSES AND MAMMALIAN CHROMOSOMES. I. LOCALIZATION OF CHROMOSOME ABERRATIONS AFTER INFECTION WITH HERPES SIMPLEX VIRUS. Immunoglobulin A production in ataxia telangiectasia Thymic dysplasia. A separable entity from "swiss agammaglobulinemia" Further observations on the Swiss type of agammaglobulinemia (alymphocytosis). The effect of syngeneic bone-marrow cells Chromosome Abnormalities in Constitutional Aplastic Anemia The proteins in nasal secretion: a longitudinal study of the gammaA-globulin, gammaG-globulin, albumin, siderophilin, and total protein concentrations in nasal washings from adult male volunteers Clinical studies of hemolytic complement and the 11S component In vitro synthesis of the first component of complement by guinea pig small intestine Sites of production of primate serum proteins associated with complement system. RELATIONSHIPS OF VIRUSES, CHROMOSOMES AND CARCINOGENESIS Complement-dependent biological functions in complement deficiency in man
author name string	wds:Q70082995-01728A33-64F1-483D-95CE-0C170DF33569 wds:Q70082995-42226E39-4155-4F8E-BE66-2343BE702E8B wds:Q70082995-79BB6DAF-B06F-464C-984C-74B0B7304FAE wds:Q70082995-8D482F6D-E76E-4BF1-93AE-38EBBB870EB3 wds:Q70082995-90BDFE01-E4D7-4381-B73E-446EFC840A64 wds:Q70082995-9A9A479F-B7BD-4194-9BAD-02D2423575F2 wds:Q70082995-D4234897-9855-429E-83CB-31B3CF21782A wds:Q70082995-DAC107B1-BBC8-4164-B3AD-26B1A83DE9A3 wds:Q70082995-E06EF0A1-0D1E-4C72-99DC-7FEFF9546963 wds:Q70082995-EFDF055B-80E6-4FA6-B5A8-0413096CB316
author name string	O J Miller R D Rossen J C Jacobs J H Morse W A Blanc A de Capoa W C Heird J N Schullinger R A Walzer E McGilvray
rdfs:label	Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia (en) Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia (nl)
skos:prefLabel	Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia (en) Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia (nl)
name	Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia (en) Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia (nl)
title	wds:Q70082995-AD84BAB0-05DB-4CE4-997A-2F08D4CA1AFF
title	Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia (en)
page(s)	wds:Q70082995-02CF64C1-EDC8-4A72-8B7A-05F4B7DD8485
page(s)	499-503
instance of	wds:Q70082995-DA0A58B6-EF88-424D-AF44-FD565F125C72
instance of	scholarly article
main subject	wds:Q70082995-8D3FD731-7758-4AD7-A3B4-8AF6CEEFE18A
main subject	complement deficiency
PubMed ID	wds:Q70082995-6ECF139E-6DB2-486C-8E71-5A68E3E70EB0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/4170833
PubMed ID	4170833
published in	wds:Q70082995-7B765392-FD2C-465E-8E97-6EFE96397F4E
published in	The Lancet
issue	wds:Q70082995-E84FACB2-0FDF-4C7C-9CEA-7AB11AED6AC0
volume	wds:Q70082995-378A6D82-1AE9-4A78-BF33-803071C06C8A
issue	7541
volume	1
DOI	wds:Q70082995-8B31098A-16CF-4EFB-8914-84985E7CE252

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