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Canavan disease
Report of the 2014 ELA Families / Scientists Meeting
Pediatric Multiple Sclerosis
Canavan Disease: a Neurometabolic Disease Caused by Aspartoacylase Deficiency
WO 2014/031901 Al 27 February 2014 (27.02.2014) P O P C T
Pathologic Classification of White Matter Disorders • Demyelinating
New Diagnostic Criteria for Infantile Nystagmus. an Upgraded
Acetate Supplementation Reduces Disease Progression, Alters Cns
Leukodystrophies by Raphael Schiffmann MD (Dr
Advanced Imaging
Pediatric Versus Adult MS: Similar Or Different? Angelo Ghezzi1*, Damiano Baroncini1, Mauro Zaffaroni1 and Giancarlo Comi2
Anaesthetic Considerations for the Child with Leukodystrophy
State of the Art &&&&&&&&&&&&&& Neuroimaging and the Timing of Fetal and Neonatal Brain Injury
A Clinical Approach to the Diagnosis of Patients with Leukodystrophies and Genetic Leukoencephelopathies
Epidermal Growth Factor (Egf) and Variants Thereof for Medical Uses in Neuro-De/Regeneration
Contents Overview of the Project
Metabolomic Profiling in Neuromyelitis Optica Spectrum Disorder
IV. Acute Disseminated Encephalomyelitis (ADEM)
Emerald Health Pharmaceuticals Important Notice
Top View
Health Evidence Review Commission's Genetics Advisory Panel
PDCO Agenda of the 26-29 January 2021 Meeting
The Neuropathology of Myelin Diseases
Canavan Disease
Lab Code Test Name Cpt4 Code
Genetic Testing of Leukodystrophies Unraveling Extensive Heterogeneity
Canavan Disease
Canavan Disease
Jemds.Com Original Research Article
CNS DEMYELINATION (GENERAL) Dem3 (1)
A Practical Approach to White Matter Disease
Canavan Disease: CT and MR Imaging of the Brain
White Matter Diseases
Magnetic Stimulation in Clinical Neurophysiology. 2Nd
Leukodystrophy: Noun / Leu·Ko·Dys·Tro·Phy (Lōō'kō-Dĭs'trə-Fē) Leuko (White), Dys (Lack Of) and Troph (Growth)
Demyelinating Disorders of Central Nervous System
PDCO Minutes of the 26-29 January 2021 Meeting
Lysosomes, Peroxisomes and Mitochondria: Function and Disorder
VU Research Portal
Lab Code Test Name
Clinical and Genetic Characteristics of Leukodystrophies in Africa Mutaz Amin, Liena Elsayed, Ammar Eltahir Ahmed1
Leukodystrophy Fact Sheet
Canavan Disease Testing
White Matter Diseases
United States Patent ( 10) Patent No
An Essential Role for Sphingosine 1-Phosphate in Oligodendrocyte Survival and Remyelination
Annexes to the Annual Report of the European Medicines Agency 2020
A Practical Approach to Adult-Onset White Matter Diseases, with Illustrative Cases
Canavan Disease (Aspartoacylase Deficiency): Report of the First Case
Diagnostic Brain Biopsy - 15 Year Experience at NIMHANS
Imaging Pediatric Leukodystrophies