Hemolytic crisis after excessive ingestion of fava beans in a male infant with G6PD Canton.

No abstract is available for this paper.

• Publication year

  1999

• Venue

  International journal of hematology

• Publication date

  1999-12-01

• Fields of study

  Medicine

• Identifiers
  PMID 10643148
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Neonatal jaundice and molecular mutations in glucose‐6‐phosphate dehydrogenase deficient newborn infants

  1996cited by this paper
• Hematologically important mutations: glucose-6-phosphate dehydrogenase.

  1996cited by this paper
• Haptoglobin therapy for acute favism: a Japanese boy with glucose‐6‐phosphate dehydrogenase Guadalajara

  1995cited by this paper
• Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by nonradioisotopic single-strand conformation polymorphism analysis.

  1994cited by this paper
• Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: five mutations account for most G6PD deficiency cases in Taiwan.

  1992cited by this paper
• Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan.

  1992cited by this paper
• G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg----Leu mutation.

  1990cited by this paper
• Frequency of glucose 6-phosphate dehydrogenase (G6PD) deficiency in Tokyo and a new variant: G6PD Musashino.

  1987cited by this paper
• Incidence and characteristics of glucose-6-phosphate dehydrogenase variants in Japan

  1979cited by this paper
• The removal of leukocytes and platelets from whole blood.

  1976cited by this paper

• Genotypic and phenotypic landscapes of 51 pharmacogenes derived from whole-genome sequencing in a Thai population

  2022cites this paper
• PharmGKB summary: very important pharmacogene information for G6PD

  2012cites this paper
• A case of glucose-6-phosphate dehydrogenase deficiency with hemolysis caused by mandibular third molar pericoronitis

  2012cites this paper
• Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi

  2011cites this paper
• Pro-oxidative effects of Chinese herbal medicine on G6PD-deficient erythrocytes in vitro.

  2008cites this paper
• Abdomen agudo como primera manifestación de crisis hemolítica

  2007cites this paper
• [Icterus, anemia, favism].

  2006cites this paper
• Ictericia, anemia, favismo

  2006cites this paper
• Glucose-6-Phosphate Dehydrogenase Variants Associated with Favism in Thai Children

  2006cites this paper
• Pro-oxidative effects of tea and polyphenols, epigallocatechin-3-gallate and epigallocatechin, on G6PD-deficient erythrocytes in vitro.

  2006cites this paper
• Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency.

  2001cites this paper