About: Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 February 1961

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1961 (uk) im Februar 1961 veröffentlichter wissenschaftlicher Artikel (de) 1961 թվականի փետրվարի 1-ին հրատարակված գիտական հոդված (hy) artikull shkencor i botuar më 01 shkurt 1961 (sq) artículu científicu espublizáu en febreru de 1961 (ast) scientific article published on 01 February 1961 (en)
publication date	wds:Q78925479-E5DE429E-4E48-427B-A198-39ED3510847D
publication date	1961-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q78925479-45AA64F0-38E5-417F-83B7-0232424F93AD
language of work or name	English
cites work	wds:Q78925479-1A2094D9-04EE-45AA-8842-C4E2EC0D1F7C wds:Q78925479-65100A90-107C-4812-9613-3269C888BEDF wds:Q78925479-9963AA9A-70BC-46D6-9B12-B80E36675D79 wds:Q78925479-9AA123FC-E9FE-4D3B-8429-512FF9F072AC wds:Q78925479-CFEA2B00-40D8-4E7A-A612-664841791AF7 wds:Q78925479-FFFBAEB2-C486-4822-A017-E8222295C583
cites work	An hereditary enzymatic defect in erythrocyte metabolism: glucose-6-phosphage dehydrogenase deficiency Enzymatic Deficiency in Primaquine-Sensitive Erythrocytes Metabolic abnormalities of erythrocytes from patients with congenital nonspherocytic hemolytic anemia Kernikterus not associated with haemolytic disease Biochemical and genetic aspects of primaquine-sensitive hemolytic anemia Hyperbilirubinaemia and kernicterus in premature and full-term Bantu newborn infants.
author name string	wds:Q78925479-15C46CE3-BE45-475F-A910-44D44B76EDCE wds:Q78925479-3AC41D46-4F43-47F7-90A2-B337ACA132E5 wds:Q78925479-8FFC2A91-5B0A-4487-AC62-DDACE6947BB0
author name string	S A DOXIADIS T VALAES P FESSAS
rdfs:label	Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (en) Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (nl) Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (sq)
skos:prefLabel	Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (en) Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (nl) Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (sq)
name	Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (en) Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (nl) Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (sq)
title	wds:Q78925479-72184A22-0A3C-4CAE-B725-A04D15FD8DE5
title	Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice (en)
page(s)	wds:Q78925479-1CE2EA0B-07E7-4CB6-938F-EA46A9B850EC
page(s)	297-301
instance of	wds:Q78925479-0275C9A6-B59A-4FB0-8B05-0D0FBCBBF13D
instance of	scholarly article
main subject	wds:Q78925479-302F39D1-2837-442C-86AC-89B1E84E0E2D wds:Q78925479-EF8FF06C-FEB1-4495-B00F-AEB83D429614
main subject	glucose-6-phosphate dehydrogenase deficiency neonatal jaundice
PubMed ID	wds:Q78925479-8A56F81D-3551-49FC-BAD9-4D3754D1E8E1
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13724172
PubMed ID	13724172
published in	wds:Q78925479-3CA0EDA5-3DBA-4DE9-A603-2B25134B142E
published in	The Lancet
issue	wds:Q78925479-D21733CC-E096-4272-8B97-D4219AB7870B
volume	wds:Q78925479-07D66C5F-7C4A-4B4A-8897-CF20D4477CB0
issue	7172
volume	1
DOI	wds:Q78925479-B6770A18-20CC-4B74-B822-22EDB28F0C56
DOI	http://dx.doi.org/10.1016/S0140-6736(61)91476-3
DOI	10.1016/S0140-6736(61)91476-3
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q78925479
is cites work of	Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia Glucose-6-phosphate dehydrogenase deficiency, the sickling trait, and malaria in Saudi Arab children Morbidity and mortality related to exchangetransfusions A DUAL HEREDITARY RED BLOOD CELL DEFECT IN ONE FAMILY: HYPOCATALASEMIA AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY MILD GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN GREEK MALES Erythrocyte Metabolism and Hemolysis in the Newborn Clinical applications of some recent studies of erythrocyte enzymes Epidemiologic surveys of deleterious genes in different population groups in Israel Factors influencing neonatal jaundice RED CELL GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY--A NEWLY RECOGNIZED CAUSE OF NEONATAL JAUNDICE AND KERNICTERUS IN CANADA Glucose-6-phosphate dehydrogenase deficiency and haemolytic disease of the newborn in Israel GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND NEONATAL JAUNDICE IN NIGERIA: THEIR RELATION TO THE USE OF PROPHYLACTIC VITAMIN K ACUTE HEMOLYSIS DUE TO NAPHTHALENE INHALATION HEREDITARY HEINZ-BODY ANAEMIA, THROMBOCYTOPENIA, AND HAEMOGLOBINOPATHY (HB KOELN) IN A GLASGOW FAMILY RISK OF SEVERE JAUNDICE IN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY OF THE NEWBORN. DIFFERENCES IN POPULATION GROUPS Neonatal Jaundice Associated with Familial G6PD Deficiency in Israel GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY AND NEONATAL JAUNDICE IN CHINESE MALE INFANTS IN HONG KONG Screening for glucose-6-phosphate dehydrogenase deficiency can prevent severe neonatal jaundice Bilirubin and red cell metabolism in relation to neonatal jaundice Hemolysis in the newborn infant resulting from deficiencies of red blood cell enzymes: Diagnosis and management Neonatal jaundice in glucose-6-phosphate-dehydrogenase-deficient infants. Severe neonatal hyperbilirubinemia. A potential complication of glucose-6-phosphate dehydrogenase deficiency Primaquine-induced haemolysis in females heterozygous for G6PD deficiency. Anaemia in pregnancy associated with "big spleen disease" Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Jaundice GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND NEONATAL JAUNDICE IN SOUTH AFRICAN BANTU INFANTS. Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Jaundice in Jamaica Neonatal jaundice in Ibadan. Incidence and etiologic factors in babies born in hospital DRUG-INDUCED HEMOYTIC ANEMIAS ASSOCIATED WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY: AGENETICALLY HETEROGENOUS TRAIT Glucose-6-phosphate Dehydrogenase Activity Levels in Enzyme-deficient Greek Individuals. Factors influencing jaundice in immigrant Greek infants Jaundice in infants of Greek parentage: the unknown factor may be environmental Glucose-6-phosphate dehydrogenase deficiency in immigrant greek infants Glucose-6-Phosphate Dehydrogenase Deficiency in Maltese Newborn Infants G6PD deficiency and favism in the island of Rhodes (Greece) THE CONTROL OF DAPSONE HEINZ-BODY ANAEMIA WITH ADRENAL CORTICOSTEROIDS Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysis Phenacetin-induced haemolytic anaemia

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 190 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software