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Addison's disease
arylsulfatase A
arylsulfatase A pseudodeficiency
ataxia
ataxia, cerebellar
behavioral disorder
burning feet
carcinoma of pancreas
CAT scan, abnormal
cerebrospinal fluid, elevated protein of
cognition
complications
cultured skin fibroblasts
Cushing's syndrome
dementia
depression
differential diagnosis
dystonia
dystonia, focal
encephalitis
enzyme, defect
evoked potentials
falling
familial
frontal lobe, behavior with disease of
frontal lobe, lesion of
gait disorder
gene mutation
genetic neurologic disorders
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hallucination, auditory
hepatolenticular degeneration(Wilson's disease)
hyperadrenalism
hyperparathyroidism
hyperthyroidism
hypoglycemia
hypoparathyroidism
hypothyroidism
imbalance
intellectual deterioration
leg weakness, bilateral
leukodystrophy
leukoencephalopathy, differential diagnosis
lysosomal storage disease
memory, impairment of
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
MRI
MRI, abnormal
multiple sclerosis
multiple sclerosis, cognitive presenttion
multiple sclerosis, differential diagnosis of
neoplasm, intracranial
nerve biopsy
nerve conduction studies
neuroendocrinology
neurologic disease, diagnoses of
neuropathy
neuropathy, peripheral
neuropsychiatry
pain, abdominal
paraparesis
paraparesis, spastic
pernicious anemia
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
porphyria
progressive neurologic disorder
psychiatric manifestations of brain tumors
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, cause of
review article
schizophrenia
seizure
somatosensory evoked potentials
stem cell transplantation
syphilis, neurologic complications with
systemic lupus erythematosus
treatment of neurologic disorder
urinary sulfatidase excretion
visual evoked response
white matter disease
Showing articles 0 to 50 of 2382 Next >>

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
Neurol 67:859-863, Rauschka,H.,et al, 2006

Clinical Symptoms of Adult Metachromatic Leukodystrophy and Arylsulfatase A Pseudodeficiency
Arch Neurol 52:408-413, Hageman,A.T.M.,et al, 1995

Characteristics of the Dementia in Late-Onset Metachromatic Leukodystrophy
Neurol 44:662-665, Shapiro,E.G.,et al, 1994

Adult-Onset Metachromatic Leukodystrophy Presenting as Isolated Peripheral Neuropathy
Neurol 42:1396-1398, Fressinaud,C.,et al, 1992

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Adult Metachromatic Leukodystrophy, Value of Computed Tomographic Scanning & Magnetic Resonance Imaging of the Brain
Arch Neurol 44:225-227, Waltz,G.,et al, 1987

Metachromatic Leukodystrophy:Conduct Disorder Progressing to Dementia
JNNP 50:488-510, Fisher,N.R.,et al, 1987

Adult Metachromatic Leucodystrophy:An Underdiagnosed Disease
JNNP 50:1710-1712, Cerizza,M.,et al, 1987

Adult Metachromatic Leukodystrophy:Neurophysiologic Findings
Neurol 35:1776-1778, Wulff,C.H.&Trojaborg,W., 1985

Metachromatic Leukodystrophy Manifesting as a Schizophrenic Disorder:Computed Tomographic Correlation
Ann Neurol 18:94-95, Finelli,P.F., 1985

Computed Tomography in Late-Onset Metachromatic Leucodystrophy
Neuroradiology 26:39-44, Schipper,H.I.,et al, 1984

Metachromatic Leukodystrophy (MLD) , XV. Adult MLD with Focal Lesions by Computed Tomography
Arch Neurol 40:354-355, Skomer,C.,et al, 1983

Sulfatide Lipidosis:Metachromatic Leukodystrophy
in The Metabolic Basis of Inherited Disease, McGraw-Hill Co, 5th ed, 1983, Ch. 44., Kolodny,E.&Moser,H., 1983

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Organic Disease Presenting as a Psychiatric Syndrome
Postgrad Med 54:78, , 1973

Metachromatic Leukodystrophy
in Handbook of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , (Ed) , Vol 10, North-Holland Publ, o, Amsterdam, Peiffer, J., 1970

Studies on Adult Metachromatic Leukodystrophy
J Neurol Sci 9:567-584, Muller,D.,et al, 1969

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Bilateral Temporal Pole Involvement in Adult-Onset X-Linked Adrenoleukodystrophy
JAMA Neurol 78:367-368, Liu, M.,et al, 2021

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Spinal Cord Involvement in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
JAMA Neurol 77:1169-1170, Li, S.,et al, 2020

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease
Neurol 82:49-56, Graff-Radford, J.,et al, 2014

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Sporadic Adult-Onset Leukoencephalopathy with Neuroaxonal Spheroids Mimicking Cerebral MS
Neurol 70:1128-1133, Keegan,B.M.,et al, 2008

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

X-Linked Adrenoleukodystrophy:Adult Cerebral Variant
Neurol 43:1518-1522, Farrell,D.F.,et al, 1993

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Long-Term Effects of Antidarsagene Autotemcel for Metachromatic Leukodystrophy
NEJM 392:1609-1620, Fumagalli,F.,et al, 2025

Newborn Screening and Presymptomatic Treatment of Metachromatic Leukodystrophy
NEJM 391:1256-1258, Laugwitz,L.,et al, 2024

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Brain Calcification in a Young Woman With Seizures, Explore the Rare Differentials
Neurol 100:397-398, Menon,B.,et al, 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Lentiviral Haematopoietic stem-cell gene therapy for early-onset metachromatic leukodystrophy: long-term results from a non-randomised, open-label, phase 1/2 trial and expanded access
Lancet 399:372-383, Fumagalli, F.,et al, 2022

Clinicopathologic Conference, Seizure from Neurocysticercosis
NEJM 385:1894-1902, Case 34-2021, 2021

Antiseizure Medication Withdrawal in Seizure-Free Patients: Practice Advisory Update Summary
Neurol 97:1072-1081, Gloss, D.,et al, 2021

When Should a Brain MRI Be Performed in Children with New-Onset Seizures? Results of a Large Prospectice Trial
AJNR 42:1645-1701, Hourani, R.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Initial Management of Seizure in Adults
NEJM 385:251-263, Smith, P.E.M., 2021

Dissecting Aneurysm of the Anterior Temporal Artery:A Rare Case Report and Literature Review
J Neurol Surg A 82:285-288, Hou,K., et al, 2021

Epilepsy in Older People
Lancet 395:735-748, Sen, A.,et al, 2020

A Rare Case of Metachromatic Leukodystrophy with Multiple Bilateral Cranial Nerve Enhancement
Neurol 93:e1742-e1743, Sonowal, P.,et al, 2019



Showing articles 0 to 50 of 2382 Next >>