Physician
Gastroenterology
Dr. Neville R. Pimstone, MD
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Doctor Neville R. Pimstone, MD is an expert in the field of Gastroenterology. Dr. Neville R. Pimstone is a published doctor as well. He has 57 publications published. The latest was: Early hepatitis C virus-RNA responses predict interferon treatment outcomes in chronic hepatitis C. The Consensus Interferon Study Group.
Publications
- Proactive Case Finding to Concurrently Improve Curative and Palliative Care in Patients with End-Stage Liver Disease.
- Roles and pitfalls of transplantation in human porphyria.
- Recommendations for the diagnosis and treatment of the acute porphyrias.
- "Wait-and-see": an alternative approach to managing acute Hepatitis C with high-dose interferon-alpha monotherapy.
- Acute pancreatitis associated with interferon and ribavirin therapy in patients with chronic Hepatitis C.
- A STUDY OF THE STARCH-IODINE COMPLEX: A MODIFIED COLORIMETRIC MICRO DETERMINATION OF AMYLASE IN BIOLOGIC FLUIDS.
- Paraparesis, hypermanganesaemia, and polycythaemia: a novel presentation of Cirrhosis.
- Utility of Hepatitis C virus serotypes in predicting response to treatment of chronic Hepatitis C. Consensus Interferon Study Group.
- Biochemical and viral response to consensus interferon (CIFN) therapy in chronic Hepatitis C patients: effect of baseline viral concentration. Consensus Interferon Stu...
- Early Hepatitis C virus-RNA responses predict interferon treatment outcomes in chronic Hepatitis C. The Consensus Interferon Study Group.
- Porphyria cutanea tarda, Hepatitis C, and HFE gene mutations in North America.
- Acute renal failure associated with nonfulminant Hepatitis A viral infection.
- Diagnostic performance of a receptor-binding radiopharmacokinetic model.
- Evaluation of hepatocellular function by way of receptor-mediated uptake of a technetium-99m-labeled asialoglycoprotein analog.
- Congenital erythropoietic porphyria, diminished activity of uroporphyrinogen decarboxylase and dyserythropoiesis.
- Current status of medical treatment of Gallstones.
- Tumour localization of uroporphyrin isomers I and III and their correlation to albumin and serum protein binding.
- Dual mechanism of inhibition of rat liver uroporphyrinogen decarboxylase activity by ferrous iron: its potential role in the genesis of porphyria cutanea tarda.
- Splenic embolization monitored by the video dilution technique.
- Fibrolamellar hepatocarcinoma: radiology, management, and pathology.
- Optimal photodynamic band of red light in hematoporphyrin derivative (HPD) photoradiation therapy of cancer.
- A comparative study of 28 porphyrins and their abilities to localize in mammary mouse carcinoma: uroporphyrin I superior to hematoporphyrin derivative.
- Porphyrin:protoporphyrin:plasma protein interaction--the metabolic basis for the tumor localization of hematoporphyrin derivative--a preliminary report.
- The incorporation of glycine-2-14C into urinary uric acid in normal and porphyric human subjects.
- Clinical Response to long-term propranolol therapy in hyperthyroidism.
- Enzymatic defects in hepatic porphyria. Preliminary observations in patients with porphyria cutanea tarda and variegate porphyria.
- The formation of cerebrospinal fluid xanthochromia after subarachnoid hemorrhage. Enzymatic conversion of hemoglobin to bilirubin by the arachnoid and choroid plexus.
- Renal degradation of hemoglobin.
- Enzymatic degradation of heme. Oxygenative cleavage requiring cytochrome P-450.
- Inducible heme oxygenase in the kidney: a model for the homeostatic control of hemoglobin catabolism.
- The enzymatic degradation of hemoglobin to bile pigments by macrophages.
- Repetitive ventricular tachycardia--Response to cardioversion, potassium and digitalis.
- Beta-adrenergic blockade in thyrotoxic myopathy.
- Further studies of microsomal haem oxygenase: mechanism for stimulation of enzyme activity and cellular localization.
- Biochemical diagnosis and monitoring therapeutic modulation of Disease activity in an unusual case of congenital erythropoietic porphyria.
- A potential biochemical explanation for the genesis of porphyria cutanea tarda. Studies on the inherent biochemical defect in highly purified human erythrocyte uroporp...
- Reduced substrate affinity for human erythrocyte uroporphyrinogen decarboxylase constitutes the inherent biochemical defect in porphyria cutanea tarda.
- In vitro studies of the mechanism of inhibition of rat liver uroporphyrinogen decarboxylase activity by ferrous iron under anaerobic conditions.
- Hematologic and hepatic manifestations of the cutaneous porphyrias.
- The interaction of tumour-localizing porphyrins with collagen, elastin, gelatin, fibrin and fibrinogen.
- Evidence for two uroporphyrinogen decarboxylase isoenzymes in human erythrocytes.
- Histopathology of early and late human allograft rejection.
- Defective human erythrocyte uroporphyrinogen decarboxylase in familial porphyria cutanea tarda: the metabolic lesion or the result of endogenous porphyrinemia?
- Utility of porphyrins and light in the diagnosis and treatment of malignancy.
- Therapeutic efficacy of oral charcoal in congenital erythropoietic porphyria.
- Selective in vivo tumor localization of uroporphyrin isomer I in mouse mammary carcinoma: superiority over other porphyrins in a comparative study.
- Free radical mechanism of oxidation of uroporphyrinogen in the presence of ferrous iron.
- Uroporphyrinogen decarboxylases from human erythrocytes: purification, complete separation and partial characterization of two isoenzymes.
- The hepato-renal syndrome--a review.
- The hepatic lesion in protoporphyria (PP): preliminary studies of haem metabolism, liver structure and ultrastructure.
- Hepatic haem metabolism in porphyria cutanea tarda (PCT): enzymatic studies and their relation to liver ultrastructure.
- The diagnostic value of blood plasma porphyrin methyl ester profiles produced by quantitative TLC.
- The nature of hepatic cytochrone P-450 induced in hexachlorobenzene-fed rats.
- Erythrohepatic protoporphyria (EHP) in South Africa.
- Activation of uroporphyrinogen decarboxylase by ferrous iron in porphyria cutanea tarda.
- Familial symptomatic porphyria in South Africa.
Procedures Preformed
- Colonoscopy, Proctosigmoidoscopy, and Sigmoidoscopy
Conditions Treated
- Anemia
- Cholecystitis and Gallstones
- Cirrhosis
- Crohn's Disease (Regional Enteritis)
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Doctors Specialties
- Gastroenterology
Accepted Insurances
Education
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UCSF -
University of Cape Town Faculty of Medicine
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