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Article

Bone marrow suppression in the setting of normal thiopurine methyltransferase phenotype testing.

Clinical pediatrics - 1 Sept 2010

Best Chad, Sudel Boris

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Share to Anti-Inflammatory Agents, Non-Steroidal
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Purine-Pyrimidine Metabolism, Inborn Errors

Source

Identifiers

PMID: 19420179
DOI: 10.1177/0009922809335739

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Bone marrow suppression in the setting of normal thiopurine methyltransferase phenotype testing.PMID 19420179Read ↗

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Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severitiesSemantic proximity Read ↗

Reducing risk in thiopurine therapy.Semantic proximity Read ↗

Systematic review of thiopurine methyltransferase genotype and enzymatic testing strategies.Semantic proximity Read ↗

Thiopurine methyltransferase: should it be measured before commencing thiopurine drug therapy?Semantic proximity Read ↗

Pulmonary fibrosis, bone marrow failure, and telomerase mutation.Semantic proximity Read ↗

Implementation of TPMT testing.Semantic proximity Read ↗

Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance.Semantic proximity Read ↗

Heterozygosity for the thiopurine methyltransferase *3A allele in an acute non-lymphoblastic leukaemia patient with delayed marrow regeneration following H-DAT chemotherapy.Semantic proximity Read ↗

Identification of rare defective allelic variants in cases of thiopurine S-methyltransferase deficient activity.Semantic proximity Read ↗

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