Prolonged indirect hyperbilirubinemia in a moderately preterm boy with Mediterranean glucose-6-phosphate dehydrogenase and glutathione S-transferase Mu 1 null mutations. | BMJ Case Rep;20172017 Jan 09. | MEDLINE

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Prolonged indirect hyperbilirubinemia in a moderately preterm boy with Mediterranean glucose-6-phosphate dehydrogenase and glutathione S-transferase Mu 1 null mutations.

Al-Abdi, Sameer Yaseen.

Affiliation

Al-Abdi SY; Department of Pediatrics, King Abdulaziz Hospital, MNGHA, Al-Ahsa, Saudi Arabia.

BMJ Case Rep ; 20172017 Jan 09.

Article in En | MEDLINE | ID: mdl-28069791

Subject(s)

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyperbilirubinemia, Neonatal / Glucosephosphate Dehydrogenase Deficiency / Glutathione Transferase / Mutation Type of study: Diagnostic_studies / Risk_factors_studies Limits: Humans / Male / Newborn Language: En Journal: BMJ Case Rep Year: 2017 Document type: Article Affiliation country: Country of publication:

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyperbilirubinemia, Neonatal / Glucosephosphate Dehydrogenase Deficiency / Glutathione Transferase / Mutation Type of study: Diagnostic_studies / Risk_factors_studies Limits: Humans / Male / Newborn Language: En Journal: BMJ Case Rep Year: 2017 Document type: Article Affiliation country: Country of publication: