About: Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new cases

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scientific article published on 01 May 1974

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 1974 (uk) im Mai 1974 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en mayu de 1974 (ast) scientific article published on 01 May 1974 (en)
publication date	wds:Q67284384-389C1F61-B63D-40BB-B5EA-4C0775C96858
publication date	1974-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q67284384-4746FFAE-6DF1-43EB-B4D3-F1CE172EDA91
language of work or name	English
cites work	wds:Q67284384-52A91486-9FD3-4DF1-9CD4-46C497B146B3 wds:Q67284384-636FB376-8ED3-44B7-B7E2-DBD350F8D5F9 wds:Q67284384-7CF0776A-DC14-4A8F-8A95-5B5F6DD294B4 wds:Q67284384-C68523F4-7F4F-4A06-9383-FCB3A68281EB wds:Q67284384-C6C0AFF9-05BA-4C58-BC89-0ED046658A7E wds:Q67284384-EFB58C30-BE31-4C7D-B39D-D6A6D3DADAD8 wds:Q67284384-F21944DE-6CC6-4C40-AD6D-BDFFFB27245D
cites work	Fucosidosis. Human alpha-L-fucosidases The abnormalities of lysosomal enzymes in mucopolysacc- haridoses. Fucosidosis. Mucopolysaccharidosis by absence of alpha-fucosidase Deficiency of α-L-Fucosidase The use of white cells as a source of diagnostic material for lipid storage diseases
author name string	wds:Q67284384-11628F95-C026-4C30-A847-62CC0229B8E9 wds:Q67284384-1BA64A12-D993-43DB-B0A5-EC53DAD45F7D wds:Q67284384-B0095071-EDA8-42F8-9C52-DB30BE26A210 wds:Q67284384-D10C83E6-26B1-414E-AB08-DBC50D994280
author name string	R Gatti P Durand C Borrone X Trias
rdfs:label	Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new cases (en) Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new cases (nl)
skos:prefLabel	Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new cases (en) Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new cases (nl)
name	Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new cases (en) Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new cases (nl)
title	wds:Q67284384-1D634718-249A-49FF-B992-EF034FF4C9DD
title	Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new cases (en)
page(s)	wds:Q67284384-DDA31116-F4A4-4281-A358-84B050DA8F46
page(s)	727-730
instance of	wds:Q67284384-ACD2991E-343D-4910-8DC0-393A69A5BD27
instance of	scholarly article
main subject	wds:Q67284384-25843321-2758-4F69-AD33-7793154E9FA3
main subject	fucosidosis
PubMed ID	wds:Q67284384-35D850BF-9E64-4510-A347-A0897FF42D3E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/4206842
PubMed ID	4206842
published in	wds:Q67284384-9882D313-71E9-475A-8715-2AB7A00E73ED
published in	The Journal of Pediatrics
issue	wds:Q67284384-9661309B-21B4-45D6-87C7-88BCBE321849
volume	wds:Q67284384-3F8FE5E1-9AEB-4A60-AD31-FF09239E1388
issue	5
volume	84
DOI	wds:Q67284384-904DC960-7B7F-4E54-B299-433490C70F95
DOI	http://dx.doi.org/10.1016/S0022-3476(74)80019-3
DOI	10.1016/S0022-3476(74)80019-3
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q67284384
is cites work of	Mucopolysaccharidoses and mucolipidoses Urinary Abnormalities in Fucosidosis. Characterization of a Disaccharide and Two Glycoasparagines Four year follow-up of a case of fucosidosis treated with unrelated donor bone marrow transplantation Angiokeratoma corporis diffusum with features of a mucopolysaccharidosis. Ultrastructural studies of type II fucosidosis Genetic polymorphism of α-L-fucosidase in brittany (France) Silent allele as genetic basis of fucosidosis Fucosidosis: Detection of the carrier state in peripheral blood leukocytes Biochemical and genetic studies of plasma and leukocyte alpha-L-fucosidase Fucosidosis in a native-born Briton Fucosidosis in Calabria: founder effect or high gene frequency Detection of carriers and prenatal diagnosis for fucosidosis in Calabria A sensitive fluorometric assay for alpha-kl-fucosidase Vacuolated lymphocytes in type II glycogenosis ?A diagnostic approach? Ocular findings in a case of fucosidosis Paediatric Fabry disease: prognostic significance of ocular changes for disease severity Absence of alpha-fucosidase activity in two sisters showing a different phenotype Radiographic features of fucosidosis Lumbar kyphosis in Hunter's disease (MPS II) Vascular disorders. Letter: On genetic variants in fucosidosis Brain abnormalities in fucosidosis: transplantation or supportive therapy? Ocular findings in a patient with fucosidosis. Fucosidosis: How many cases undetected? Letter:Acute haemolytic anaemia due to IgM and IgA penicillin antibody α-L-fucosidase in cultured bone marrow fibroblasts from fucosidosis patients
is cites work of	wds:Q34302974-C676286D-9F12-410F-8136-11EA98705A2B wds:Q36657783-0F37689F-1AB3-4499-B77F-C60B2768ADD8 wds:Q59085290-34BE77D7-0151-41DC-9628-FFEEC805E3C8 wds:Q66972923-1C2438DB-5271-4A8A-A81A-B8DE5096734F wds:Q36194571-9DD49A87-0A0C-4D39-AEAA-DE3826BF59FE wds:Q67326435-09CBC3F2-F365-4851-AAFB-F5E188444DA7 wds:Q40305580-DDE0FC83-7639-46F8-A3AF-AACBA4FE6C3E wds:Q43613031-1FB1A6AB-747F-43BC-82E3-684D8C494E2B wds:Q48291919-30EBDB2F-5C3C-454D-B321-2D0437B86497 wds:Q39725099-466EAAFA-A30C-4460-BDC2-21F04B167CED wds:Q40517878-39FF4B46-F425-481E-A41A-A4F0E9E51BF9 wds:Q33667637-2B74D02C-90B0-46B3-A5F7-A481D77B0131 wds:Q36607370-4F654DC9-1C97-45A6-B026-227743A69A5C wds:Q39343064-5E77BF23-49D4-416D-9F92-26D55ADFD5C3 wds:Q39343071-B49722FD-4A74-467B-876B-BC8FA198B62D

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