- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1824-7288
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Hemolytic crisis in a G6PD-deficient infant after ingestion of pumpkin ; volume:40 ; number:1 ; day:21 ; month:7 ; year:2014 ; pages:1-3 ; date:12.2014
The Italian journal of pediatrics ; 40, Heft 1 (21.7.2014), 1-3, 12.2014
- Urheber
-
Zuccotti, Gian Vincenzo
- Beteiligte Personen und Organisationen
-
Redaelli, Francesca
Gualdi, Valentina
Rizzi, Valeria
Mameli, Chiara
Dilillo, Dario
Fabiano, Valentina
SpringerLink (Online service)
- DOI
-
10.1186/1824-7288-40-71
- URN
-
urn:nbn:de:1111-2016032344520
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:47 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Zuccotti, Gian Vincenzo
- Redaelli, Francesca
- Gualdi, Valentina
- Rizzi, Valeria
- Mameli, Chiara
- Dilillo, Dario
- Fabiano, Valentina
- SpringerLink (Online service)
Ähnliche Objekte (12)
Hemolytic Anemia and Hypoxic Brain Injury following Mothball Ingestion in a G6PD Nondeficient Infant: A Case Report
A vegetable-induced hemolytic crisis in a G6PD deficient person: a case report
Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
Telomerase prevents accelerated senescence in glucose-6-phosphate dehydrogenase (G6PD)-deficient human fibroblasts
Erratum to: Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
Castleman disease and SLE in a G6PD-deficient Marfan patient: a case report and literature review
Charakterisierung und Vergleich von "Mittelmeer"- ähnlichen und (A-)- ähnlichen G6PD- Varianten, Charakterisierung einer G6PD- Variante einer G6PD- defekten Maus und Einsatz der Mikroimmunoaffinitätschromatografie zur Isolierung der G6PD
Acute hemolytic crisis complicated with ischemic cardiac injury and methemoglobinaemia following ingestion of naphthalene: a case report
Molekulargenetische G6PD-Genotypisierung und Bestimmung er Genfrequenzen polymorpher G6PD-Varianten in Südwest-Nigeria
Norovirus: a novel etiologic agent in hemolytic uremic syndrome in an infant
The friendly use of chloroquine in the COVID-19 disease: a warning for the G6PD -deficient males and for the unaware carriers of pathogenic alterations of the G6PD gene
A Case Report of a Teaspoon Portion of Fava Beans Caused Severe Hemolysis in G6PD-Deficient Baby: Time to Include G6PD Enzyme Testing in the Premarital Screening Program and Newborns
Hemolytic Anemia and Hypoxic Brain Injury following Mothball Ingestion in a G6PD Nondeficient Infant: A Case Report
A vegetable-induced hemolytic crisis in a G6PD deficient person: a case report
Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
Telomerase prevents accelerated senescence in glucose-6-phosphate dehydrogenase (G6PD)-deficient human fibroblasts
Erratum to: Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
Castleman disease and SLE in a G6PD-deficient Marfan patient: a case report and literature review
Charakterisierung und Vergleich von "Mittelmeer"- ähnlichen und (A-)- ähnlichen G6PD- Varianten, Charakterisierung einer G6PD- Variante einer G6PD- defekten Maus und Einsatz der Mikroimmunoaffinitätschromatografie zur Isolierung der G6PD
Acute hemolytic crisis complicated with ischemic cardiac injury and methemoglobinaemia following ingestion of naphthalene: a case report
Molekulargenetische G6PD-Genotypisierung und Bestimmung er Genfrequenzen polymorpher G6PD-Varianten in Südwest-Nigeria
Norovirus: a novel etiologic agent in hemolytic uremic syndrome in an infant
The friendly use of chloroquine in the COVID-19 disease: a warning for the G6PD -deficient males and for the unaware carriers of pathogenic alterations of the G6PD gene
A Case Report of a Teaspoon Portion of Fava Beans Caused Severe Hemolysis in G6PD-Deficient Baby: Time to Include G6PD Enzyme Testing in the Premarital Screening Program and Newborns
Hemolytic Anemia and Hypoxic Brain Injury following Mothball Ingestion in a G6PD Nondeficient Infant: A Case Report
A vegetable-induced hemolytic crisis in a G6PD deficient person: a case report
Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
Telomerase prevents accelerated senescence in glucose-6-phosphate dehydrogenase (G6PD)-deficient human fibroblasts
Erratum to: Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
Castleman disease and SLE in a G6PD-deficient Marfan patient: a case report and literature review
Charakterisierung und Vergleich von "Mittelmeer"- ähnlichen und (A-)- ähnlichen G6PD- Varianten, Charakterisierung einer G6PD- Variante einer G6PD- defekten Maus und Einsatz der Mikroimmunoaffinitätschromatografie zur Isolierung der G6PD
Acute hemolytic crisis complicated with ischemic cardiac injury and methemoglobinaemia following ingestion of naphthalene: a case report
Molekulargenetische G6PD-Genotypisierung und Bestimmung er Genfrequenzen polymorpher G6PD-Varianten in Südwest-Nigeria
Norovirus: a novel etiologic agent in hemolytic uremic syndrome in an infant
The friendly use of chloroquine in the COVID-19 disease: a warning for the G6PD -deficient males and for the unaware carriers of pathogenic alterations of the G6PD gene