Neurologic Disease in a Child With Hepatoerythropoietic Porphyria
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.1994.tb00589.x/fullpdf
Reference21 articles.
1. THE PORPHYRIAS AND ERYTHROPOIETIC PROTOPORPHYRIA: AN UNUSUAL CASE
2. Hepatoerythropoietic porphyria: A variant of childhood-onset porphyria cutanea tarda
3. Uroporphyrinogen decarboxylase deficiency in hepatoerythropoietic porphyria: further evidence for genetic heterogeneity
4. Hepatoerythropoietic porphyria in a woman with short stature and deformed hands
5. Hepatoerythropoietic porphyria
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2. Porphyria Diagnostics—Part 1: A Brief Overview of the Porphyrias;Current Protocols in Human Genetics;2015-07
3. Neurologic Disorders Associated with Gastrointestinal Diseases and Nutritional Deficiencies;Swaiman's Pediatric Neurology;2012
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5. THE VERY FIRST DESCRIPTION OF A PATIENT WITH HEPATOERYTHROPOIETIC PORPHYRIA IN ARGENTINA. BIOCHEMICAL AND MOLECULAR STUDIES;CELL MOL BIOL;2009
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