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Demyelinating neuropathy in genetically confirmed acute intermittent porphyria

  • Published:2015-07-02 Issue:5 Volume:52 Page:916-917
  • ISSN:0148-639X
  • Container-title:Muscle & Nerve
  • language:en
  • Short-container-title:Muscle Nerve

Author:

Younger David S.1,Tanji Kurenai2

Affiliation:

1. Department of Neurology; New York University School of Medicine; and the Global Institute of Public Health; New York University; New York

2. Department of Pathology & Cell Biology; Division of Neuropathology; Columbia University Medical Center; New York

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference10 articles.

1. Clinical presentation and electrophysiological findings of porphyric neuropathies: a follow-up study;Wu;Muscle Nerve,2015

2. Acute porphyria: necropsy studies in nine cases;Ten Eyck;Proc Staff Meet Mayo Clin,1961

3. Changes in the nervous system in acute porphyria;Denny Brown;Brain,1945

4. The neuropathology of acute porphyria;Gibson;J Pathol Bacteriol,1956

5. Acute intermittent porphyria. A clinical and biochemical study of 46 patients;Stein;Medicine,1970

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1. Sensorimotor problem: Genetic neuropathies;Neurogenetics for the Practitioner;2024

2. Critical illness–associated weakness and related motor disorders;Motor System Disorders, Part I: Normal Physiology and Function and Neuromuscular Disorders;2023

3. Neurogenetic motor disorders;Motor System Disorders, Part I: Normal Physiology and Function and Neuromuscular Disorders;2023

4. Characterisation of a common hotspot variant in acute intermittent porphyria sheds light on the mechanism of hydroxymethylbilane synthase function;FEBS Open Bio;2022-09-26

5. Acute porphyrias – A neurological perspective;Brain and Behavior;2021-10-17
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