Neurogenetics

April 2005, Volume 11, Issue 2
BROWSE ISSUES

Neurogenetics

April 2005, Vol.11, No.2

Guest Editor:

Henry L. Paulson, MD, PhD

ISSN: 1080-2371

Online ISSN: 1538-6899

Faculty: PDF Only
FACULTY
CONTINUUM: Lifelong Learning in Neurology
April 2005 - Volume 11 - Issue 2, Neurogenetics
doi: 10.1212/01.CON.0000293691.70098.8c
Editor's Preface
Articles
Key Points
Abbreviations
Appendix
Issue Overview

LIST OF ABBREVIATIONS

CONTINUUM: Lifelong Learning in Neurology April 2005 - Volume 11 - Issue 2, Neurogenetics - [no page #] doi: 10.1212/01.CON.0000293690.70098.c5
  • AD Alzheimer's disease; autosomal dominant
  • ADM Adductor digiti minimi
  • ADNFLE Autosomal dominant nocturnal frontal lobe epilepsy
  • ALS Amyotrophic lateral sclerosis
  • AOA Ataxia with oculomotor apraxia
  • AOA1 Ataxia with oculomotor apraxia type 1
  • Apo E Apolipoprotein E
  • AR Androgen receptor
  • ARSACS Autosomal recessive spastic ataxia of Charlevoix-Saguenay
  • AT Ataxia telangiectasia
  • ATLD Ataxia telangiectasia-like disorder
  • ATM Ataxia telangiectasia mutated
  • AVED Ataxia with isolated vitamin E deficiency
  • CDC Central core disease
  • CFTD Congenital fiber-type disproportion
  • CH Congenital hypomyelination
  • CK Creatine kinase
  • CLIA Clinical Laboratory Improvement Amendments
  • CMAP Compound motor action potential
  • CMD Congenital muscular dystrophy
  • CMT Charcot-Marie-Tooth disease
  • D/BMD Duchenne-Becker muscular dystrophy
  • dHMN Distal hereditary motor neuropathy
  • DM Myotonic dystrophy
  • DM1 Myotonic dystrophy type 1
  • DM2 Myotonic dystrophy type 2
  • DNA Deoxyribonucleic acid
  • DRPLA Dentatorubral-pallidoluysian atrophy
  • DSN Dejerine-Sottas neuropathy
  • EA Episodic ataxia
  • EDMD Emery-Dreifuss muscular dystrophy
  • EEG Electroencephalogram
  • EHL Extensor hallucis longus
  • EPM1 Progressive myoclonus epilepsy type 1
  • FA Friedreich ataxia
  • FDI First dorsal interosseus
  • FISH Fluorescent in situ hybridization
  • FKRP Fukutin-related protein
  • FSHD Facioscapulohumeral muscular dystrophy
  • FXTAS Fragile X-associated tremor ataxia syndrome
  • GABA γ-Aminobutyric acid
  • GABAA γ-Aminobutyric acid subtype A
  • GABAB γ-Aminobutyric acid subtype B
  • GDAP1 Ganglioside-induced differentiation-associated protein-1
  • GEFS+ Generalized epilepsy with febrile seizures plus
  • GPCR G-protein couples receptor
  • HD Huntington's disease
  • HIPAA Health Insurance Portability and Accountability Act
  • HIV Human immunodeficiency virus
  • HMN Hereditary motor neuropathy
  • HMN-V Hereditary motor neuropathy type V
  • HMSN Hereditary motor and sensory neuropathy
  • HMSN-I Hereditary motor and sensory neuropathy type I
  • HMSN-R Hereditary motor and sensory neuropathy-Russe
  • HNPP Hereditary neuropathy with liability to pressure palsies
  • HSAN Hereditary sensory and autonomic neuropathy
  • IOSCA Infantile-onset spinocerebellar ataxia
  • JME Juvenile myoclonic epilepsy
  • KSS Kearns-Sayre syndrome
  • LGMD Limb-girdle muscular dystrophy
  • MD Muscular dystrophy
  • MDS Miller-Dieker syndrome
  • MELAS Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes
  • MERRF Myoclonic epilepsy with ragged red fibers
  • MJD Machado-Joseph disease
  • MRI Magnetic resonance imaging
  • mRNA Messenger ribonucleic acid
  • mtDNA Mitochondrial DNA
  • MTP Microsomal triglyceride transfer protein
  • NARP Neuropathy, ataxia, retinitis pigmentosa
  • NCV Nerve conduction velocity
  • NF1 Neurofibromatosis type 1
  • OPMD Oculopharyngeal muscular dystrophy
  • PDC Pyruvate dehydrogenase complex
  • PNS Peripheral nervous system
  • RNA Ribonucleic acid
  • SBMA Spinobulbar muscular atrophy
  • SCA Spinocerebellar ataxia
  • SCA1 Spinocerebellar ataxia type 1
  • SCABD Spinocerebellar ataxia with blindness, deafness
  • SCAN 1 Spinocerebellar ataxia with axonal neuropathy type 1
  • sHSP Small heat shock protein
  • SMA Spinal muscular atrophy
  • SMEI Severe myoclonic epilepsy of infancy
  • SNAP Sensory nerve action potential
  • TDP Tyrosyl 1-phosphodiesterase
  • TSC Tuberous sclerosis complex
  • αTTP α-Tocopherol transfer protein
© 2005 American Academy of Neurology