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Porphobilinogen
Hyperbilirubinemia
A High Urinary Urobilinogen / Serum Total Bilirubin Ratio Reported in Abdominal Pain Patients Can Indicate Acute Hepatic Porphyria
Carbon Monoxide Production Associated with Ineffective Erythropoiesis * PETER Whitef RONALD F
Biochemical Differentiation of the Porphyrias
Porphyrins and Bile Pigments: Metabolism and Disorders Dr
Intrinsic Fluorescence of Protoporphyrin IX from Blood Samples Can Yield Information on the Growth of Prostate Tumours
D-Aminolaevulinic Acid-Induced Photodynamic Therapy Inhibits
Erythrocyte Uroporphyrinogen I Synthase Activity As an Indicator of Acute Porphyria
The Marvels of Biosynthesis: Tracking Nature's Pathways
HMBS Gene Hydroxymethylbilane Synthase
Kent Academic Repository Full Text Document (Pdf)
Compendium of Urinalysis Urine Test Strips and Microscopy
ALAD Gene Aminolevulinate Dehydratase
Characterization of the Porphobilinogen Deaminase Deficiency in Acute Intermittent Porphyria: IMMUNOLOGIC EVIDENCE for HETEROGENEITY of the GENETIC DEFECT
Purification of Porphobilinogen Deaminase and the Sequencing and Expression of Thehemc Gene of Rhodobacter Capsulatus
Porphobilinogen (PBG) Test Kit
Porphyria (Acute) Testing Algorithm*
Phytoestrogen Suppresses Efflux of the Diagnostic Marker Protoporphyrin IX in Lung Carcinoma
Top View
Porphobilinogen (Urine) Porphobilinogen (PBG) Is a Water-Soluble, Monopyrrole Porphyrin Precursor and Part of the Haem Biosynthetic Pathway
The Hoesch Test: Bedside Screening for Urinary
Disease Characteristics of Patients with Acute Hepatic Porphyria Patients
Allosteric Inhibition of Human Lymphoblast and Purified Porphobilinogen Deaminase by Protoporphyrinogen and Coproporphyrinogen
PORPHOBILINOGEN* on Prolonged Standing at Room Temperatures, Or
1807 Ml/1982
ARTICLE ALAD Porphyria Is a Conformational Disease
Motor Neuropathy in Porphobilinogen Deaminase–Deficient Mice Imitates the Peripheral Neuropathy of Human Acute Porphyria
Ppix) in Lung Carcinoma
PUBLIC SUMMARY of POSITIVE OPINION for ORPHAN DESIGNATION of Recombinant Human Porphobilinogen Deaminase for the Treatment of Acute Intermittent Porphyria
Amino Acids, Peptides and Proteins-III
Lessons from Porphyria
Molecular Pathways and Pigments Underlying the Colors of the Pearl Oyster Pinctada Margaritifera Var.Cumingii
Tyrosinemia Type 1: an Overview of Nursing Care
Acute Intermittent Porphyria: Identification and Expression of Exonic Mutations in the Hydroxymethylbilane Synthase Gene
Human Hydroxymethylbilane Synthase: Molecular PNAS PLUS Dynamics of the Pyrrole Chain Elongation Identifies Step-Specific Residues That Cause AIP
The Porphyrias: a Review
Acute Hepatic Porphyria Random Urine Testing Guide
On the Enzymic Defects in Hereditary Tyrosinemia*
Enigmatic Evolutionary History of Porphobilinogen Deaminase in Eukaryotic Phototrophs
A Variant Hereditary Coproporphyria
Acute Intermittent Porphyria: Novel Missense Mutations in the Human Hydroxymethylbilane Synthase Gene 1 1 1 1 Risha B
Seven Steps to Diagnose Delta-Aminolevulinic Acid Deficiency Porphyria
Recommendations for Diagnosing Acute Porphyrias
Confirmation of Hereditary Tyrosinemia Type 1 In