A practical approach to diagnosing adult onset leukodystrophies

Neurological Outcome in Cerebrotendinous Xanthomatosis Treated With Chenodeoxycholic Acid

(2013) Gilad Yahalom et al.   CLINICAL NEUROPHARMACOLOGY

Application of the 2010 revised criteria for the diagnosis of multiple sclerosis to patients with clinically isolated syndromes

(2013) T. F. Runia et al.   EUROPEAN JOURNAL OF NEUROLOGY

Tumefactive demyelination: an approach to diagnosis and management

(2013) T. A. Hardy et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Validation of next-generation sequencing technologies in genetic diagnosis of dementia

(2013) John Beck et al.   NEUROBIOLOGY OF AGING

Adult polyglucosan body disease: Natural History and Key Magnetic Resonance Imaging Findings

(2012) Fanny Mochel et al.   ANNALS OF NEUROLOGY

Brain biopsy in benign neurological disease

(2012) C. E. Gilkes et al.   JOURNAL OF NEUROLOGY

Oligoclonal bands and cerebrospinal fluid markers in multiple sclerosis: associations with disease course and progression

(2012) Pedro Lourenco et al.   Multiple Sclerosis Journal

MRI characteristics and scoring in HDLS due to CSF1R gene mutations

(2012) C. Sundal et al.   NEUROLOGY

The minimum prevalence of CADASIL in northeast England

(2012) S. K. Narayan et al.   NEUROLOGY

Leukoencephalopathies in Adulthood

(2012) Jan-Mendelt Tillema et al.   SEMINARS IN NEUROLOGY

Mitochondrial Syndromes with Leukoencephalopathies

(2012) Lee-Jun Wong   SEMINARS IN NEUROLOGY

Clinical Approach to Leukoencephalopathies

(2012) Deborah Renaud   SEMINARS IN NEUROLOGY

A comprehensive description of the severity groups in Cockayne syndrome

(2011) Valerie Natale   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy

(2011) Caterina Garone et al.   BRAIN

Brain biopsy in cryptogenic neurological disease

(2011) Claire M. Rice et al.   BRITISH JOURNAL OF NEUROSURGERY

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia Can Present as Frontotemporal Dementia Syndrome

(2011) Janice C. Wong et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

Leukoencephalopathy with brainstem and spinal cord involvement caused by a novel mutation in the DARS2 gene

(2011) Charalampos Tzoulis et al.   JOURNAL OF NEUROLOGY

Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL): From Discovery to Gene Identification

(2011) Toshio Fukutake   Journal of Stroke & Cerebrovascular Diseases

Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): A misdiagnosed disease entity

(2011) Christina Sundal et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

(2011) Rosa Rademakers et al.   NATURE GENETICS

Brain biopsy in dementia: clinical indications and diagnostic approach

(2010) Jonathan M. Schott et al.   ACTA NEUROPATHOLOGICA

A neurological perspective on mitochondrial disease

(2010) Robert McFarland et al.   LANCET NEUROLOGY

Natural history of adult-onset eIF2B-related disorders: a multi-centric survey of 16 cases

(2009) P. Labauge et al.   BRAIN

Metachromatic Leukodystrophy: A Case of Triplets With the Late Infantile Variant and a Systematic Review of the Literature

(2009) Asif Mahmood et al.   JOURNAL OF CHILD NEUROLOGY

Diagnostic algorithm for the differentiation of leukodystrophies in early MS

(2009) Wolfgang Köhler   JOURNAL OF NEUROLOGY

CADASIL

(2009) Hugues Chabriat et al.   LANCET NEUROLOGY

Leukodystrophies

(2009) Daniel J. Costello et al.   NEUROLOGIST

Invited Article: An MRI-based approach to the diagnosis of white matter disorders

(2009) R. Schiffmann et al.   NEUROLOGY

Can MR Imaging Diagnose Adult-Onset Alexander Disease?

(2008) L. Farina et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature

(2008) D. Pareyson et al.   BRAIN

Leukoencephalopathies associated with inborn errors of metabolism in adults

(2008) F. Sedel et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Methylenetetrahydrofolate reductase deficiency (homocystinuria type II) as a rare cause of rapidly progressive tetraspasticity and psychosis in a previously healthy adult

(2008) T. Birnbaum et al.   JOURNAL OF NEUROLOGY

Prevalence of mitochondrial DNA disease in adults

(2007) Andrew M. Schaefer et al.   ANNALS OF NEUROLOGY