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- Reviews in Medicine, Alan Sugar, Editor
- DIFFERENTIAL DIAGNOSIS of PEDIATRIC NEURODISORDERS Ped7 (1)
- (12) Patent Application Publication (10) Pub. No.: US 2007/0135335 A1 Collier Et Al
- Infantile Refsum Disease Associated with Hypobetalipoproteinemia Muneaki Matsuo1*, Tsugio Akutsu2, Naomi Kanazawa2 and Nobuyuki Shimozawa3
- Peroxisome Biogenesis Disorders in the Zellweger Spectrum: an Overview of Current Diagnosis, Clinical Manifestations, and Treatment Guidelines
- Classification of Mulibrey Nanism As a New Peroxisomal
- Application of the International Classification of Diseases to Neurology \ Second Edition
- Cone Rod Dystrophy Precision Panel Overview Indications Clinical Utility
- Frequently Asked Questions About Peroxisomal Biogenesis Disorders (PBD)
- Zellweger Spectrum Disorders
- Orphanet Report Series 180 160 Collection 140 Rare Diseases
- Source: State: 12.06.2018 ORPHA68367 10507
- Leukodystrophy Fact Sheet
- Cals (O) (5) (O) - (E)------O O Ocs) Iningas
- ABMGG Biochemical Genetics Blueprint and Content Codes (Effective August 2019)
- Leukodystrophy Overview Genereview Table 8 Authors: Vanderver A, Tonduti D, Schiffmann R, Schmidt J, Van Der Knaap M Date: February 2014
- Baby Boy with Elevated VLCFA and No Mutation
- Infantile Refsum Disease Commentary
- Long Chain Fatty Acids and Peroxisomal Disorders
- The Clinical Spectrum of Inherited Diseases Involved in the Synthesis and Remodeling of Complex Lipids. a Tentative Overview
- EGL Test Description
- Child Neurology: Zellweger Syndrome Paul R