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Biomolecules / Metabolism / Photosynthesis / Porphyrin / Heme / PPOX / Hereditary coproporphyria / Coproporphyrinogen III / Uroporphyrinogen III decarboxylase / Chemistry / Tetrapyrroles / Porphyrias


21 THE PORPHYRIAS PETER N. MEISSNER RICHARD J. HIFT RALPH E. KIRSCH
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Document Date: 2009-04-15 10:28:45

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City

Cape Town / /

Company

Peripheral Side / /

Continent

Europe / /

Country

Netherlands / Sweden / South Africa / Finland / /

Currency

pence / /

Facility

University of Cape Town / Groote Schuur Hospital / University of Cape Town Liver Research Centre / /

IndustryTerm

acetate / active site / 5amino / mammalian systems / keto / metal ion / protein products / expression systems / metal ions / avian systems / cytochrome-dependent energy production / amino-methyl / enzyme active site / redox reactive metal centers / gene product / propionate side chain / catalytic site / metal binding sites / divalent metal ion / polyadenylation site / termination site / chemical structure / tetrapyrrole product / /

MedicalCondition

Pseudomonas / photosensitive skin disease / neuronal injury / hydrops fetalis / amino acid The Porphyrias / III Cosynthetase Deficiency / Porphobilinogen Deaminase Deficiency The clinical syndrome / hereditary coproporphyria / Barré syndrome / acute intermittent porphyria / Thereafter clinical disorders / severe axonal necrosis / erythropoietic porphyria / intermittent porphyria / Protoporphyrinogen Oxidase Deficiency / porphyrias / disorder / demyelination / severe flaccid quadriparesis / tachycardia / Severe UROS deficiency / clinical syndrome / functional heme deficiency / metabolic disorders / constipation / profound anemia / Porphobilinogen Deaminase Deficiency / nonacute porphyrias / porphyria / dehydratase deficiency / Porphyrias ALA / lead poisoning / abdominal pain / hereditary tyrisonemia / physiologic disorders / paralysis / Ferrochelatase Deficiency / Hereditary / hypertension / respiratory failure / Uroporphyrinogen Decarboxylase Deficiency / direct intraneuronal heme deficiency / notably severe abdominal pain / hereditary ALA dehydratase deficiency / human porphyria / Acid Dehydratase Deficiency / characteristic clinical disorders / Variegate porphyria / ileus / seizure / skin disease / Doss porphyria / cosynthase Uroporphyrinogen decarboxylase Coproporphyrinogen oxidase Protoporphyrinogen oxidase Ferrochelatase Disorder ALA / acute neurologic syndrome / vomiting / acute porphyrias / experimental porphyria / predominately neurologic syndrome / Erythropoietic protoporphyria / deficiency / SPECIFIC SYNDROMES OF PORPHYRIA / OF PORPHYRIA / vomiting progressing / heme deficiency / Coproporphyrinogen Oxidase Deficiency / anemia / syndrome / Disorders / rare autosomal-recessive disorder / /

Organization

Cape Town Liver Research Centre / Heme Administration Heme administration / University of Cape Town / Medical Research Council / Department of Medicine / Groote Schuur Hospital / AR AD / Assembly of the Tetrapyrrolic / /

Position

VP / messenger / /

Product

glycine / /

ProvinceOrState

Alabama / /

Technology

drug metabolism / x-ray / hybridization / polymerization / directed mutagenesis / Cloning / human genome / Cloning technology / crystallization / condensation / genotype / recombinant DNA / /

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