about
Seasonal palmar keratoderma in erythropoietic protoporphyria indicates autosomal recessive inheritance.Audit of the Use of Regular Haem Arginate Infusions in Patients with Acute Porphyria to Prevent Recurrent Symptoms.Best practice in primary care pathology: review 10.Biochemical diagnosis of phaeochromocytoma: two instructive case reports.Review of hepatocellular cancer, hypertension and renal impairment as late complications of acute porphyria and recommendations for patient follow-up.Direct measurement of the precursors of adrenocorticotropin in human plasma by two-site immunoradiometric assay.Are patients with familial hypercholesterolaemia well managed in lipid clinics? An audit of eleven clinics from the Department of Health Familial Hypercholesterolaemia Cascade Testing project.Pro-opiomelanocortin gene expression and peptide secretion in human small-cell lung cancer cell lines.Best practice guidelines on first-line laboratory testing for porphyria.Acute intermittent porphyria: fatal complications of treatment.Thyroid function tests in patients with familial dysalbuminaemic hyperthyroxinaemia (FDH)Biochemical investigation of unexplained diarrhoeaFatal isoniazid poisoningNon-classical congenital adrenal hyperplasia in association with porphyria cutanea tarda: co-incidence or trigger?Pseudoexon activation in the HMBS gene as a cause of the nonerythroid form of acute intermittent porphyria
P50
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P50
description
researcher
@en
wetenschapper
@nl
name
Mary Felicity Stewart
@en
Stewart MF
@ast
Stewart MF
@nl
type
label
Mary Felicity Stewart
@en
Stewart MF
@ast
Stewart MF
@nl
altLabel
Stewart MF
@en
prefLabel
Mary Felicity Stewart
@en
Stewart MF
@ast
Stewart MF
@nl
P106
P31
P496
0000-0002-2866-5384