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acrocyanosis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
Africa
Aicardi-Goutieres syndrome
algorithm
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ataxia
ataxia, progressive
atypical
Babinski sign
basal ganglia, calcification of
bladder dysfunction
bone marrow transplantation
brain atrophy
bulbar palsy
calcification, intracranial
camptocormia
cane
CAT scan, abnormal
cerebellar atrophy, primary
cerebrospinal fluid, abnormal
chilbran skin lesions
children
constipation
corpus callosum
corpus callosum, atrophy of
corpus callosum, thinning
cultured skin fibroblasts
degenerative diseases of CNS
dementia, childhood
demyelinating disease
dentate nuclei, lesion of
diagnostic criteria
diet
differential diagnosis
distal muscle weakness
dysarthria
dysphagia
dystonia
dystonia, children
ears of the Lynx MR sign
ELISA
emergency room
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epidemiology of neurology
familial
fasciculation
fatty acid, elevated plasma content
feeding disorder
fever
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gait, spastic
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gene therapy
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genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
geographic location
hand weakness
head lag
hemiparesis
high arched feet
human T-lymphotropic virus type I(HTLV-I)
hyperpyrexia, CNS disorder causing
hyperreflexia
hypogonadism
hypotonia
intellectual deficit
interferon alpha
intrauterine
intrinsic hand muscles, wasting of
irritability
jaw jerk, abnormal
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
Lorenzo's oil
Maghreb
microcephaly
Mills syndrome
misdiagnosis
motor neuron disease
movement disorder
MRI, abnormal
MRI, emergent
multiple sclerosis, misdiagnosis
muscle cramp
myelopathy
myelopathy, chronic progressive
neck weakness
neurologic disease, diagnoses of
neurologic signs
neuropathology
next-generation sequencing
pain, leg
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
peroxisomal disease
pleocytosis of cerebrospinal fluid
polymerase chain reaction
prenatal
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive neurologic disorder
psychomotor retardation
pyramidal tract dysfunction
review article
screening
seizure
skin, darkening of
skin, lesions in neurologic disorders
spastic ataxia
spastic paraplegia, type 11
spastic paraplegia, type 15
spasticity
spastin
speech disorder, childhood
startle reaction
stiff legs
testicular atrophy
toe walking
treatment of neurologic disorder
urinary urgency
walking frame
walking, difficulty with
weakness
weakness, progressive
wheelchair
white matter disease
Showing articles 50 to 100 of 3736 << Previous Next >>

The Hereditary Spastic Paraplegias
Arch Neurol 60:1045-1049, Fink,J.K., 2003

Recurrent Reversible Paraplegia
Lancet 357:1092, Haran,M. & Ni,S., 2001

Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
JNNP 71:795-797, Kasim,S.,et al, 2001

Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Hereditary Spastic Paraparesis: A Review of New Developments
JNNP 69:150-160, McDermott,C.J. et al, 2000

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

Granulomatous Compressive Thoracic Myelopathy as the Initial Manifestation of Wegener's Granulomatosis
Neurol 51:1769-1770, Kelly,P.J.,et al, 1998

Transdural Spinal Cord Herniation:Imaging and Clinical Spectra
AJNR 19:1337-1344, 11851998., Watters,M.R.,et al, 1998

Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,et al, 1997

Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997

HTLV-Associated Myelopathy in a Cohort of HTLV-I and HTLV-II Infected Blood Donors
neurol 48:315-320, Murphy,E.L.,et al, 1997

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
Ann Neurol 40:675-678, Edwin,D.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Progressive Deterioration of Intellect and Motor Function Occurring Several Decades after Cranial Irradiation
ARch Neurol 53:814-818, Duffey,P.,et al, 1996

Human T-Cell Lymphotropic Virus Type 1-Associated Myelopathy, Sjogren Syndrome, and Lymphocytic Pneumonitis
Arch Neurol 53:940-942, Kompoliti,A.,et al, 1996

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

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Chronic Myelopathy Associated with Human Herpesvirus-6
Neurol 45:2015-2017, Mackenzie,I.R.A.,et al, 1995

Clinicopathologic Correlations of HIV-1-Associated Vacuolar Myelopathy:An Autopsy-Based Case-Control Study
Neurol 44:2159-2164, DalPan,G.J.,et al, 1994

Progressive Spastic Paraparesis Revealing Primary Hyperparathyroidism
Neurol 44:178-179, Thomas,P.&Lebrun,C., 1994

Brief Report:Relief of Spinal Cord Compression from Vertebral Hemangioma by Intralesional Injection of Absolute Ethanol
NEJM 331:508-511, Heiss,J.D.,et al, 1994

Werner's Syndrome Associated with Spastic Paraparesis and Peripheral Neuropathy
Neurol 43:1252-1254, Umehara,F.,et al, 1993

Spastic Ataxia Associated with Human T-Cell Lymphotropic Virus Type II Infection
Ann Neurol 33:411-414, Harrington,W.J.,et al, 1993

Isolation of HTLV-II from Pt with Chronic, Prog Neurol Dis Clin Indistinguish from HAM/Tropical Spastic Paraparesis
Ann Neurol 33:392-396, Jacobson,S.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
Neurol 43:333-337, Junger,s.S.,et al, 1993

Human T Lymphotropic Virus Type I-Assoc Myelopathy, A Rpt of 10 Pts Born in US
Arch Neurol 49:1113-1118, Sheremata,W.A.,et al, 1992

Chronic Myelopathy Associated with Human T-Lymphotropic Virus Type I (HTLV-I)
Ann Int Med 117:933-946, Gessain,A.&Gout,O., 1992

Intramedullary Cavernous Angiomas of the Spinal Cord:Clinical, Path, & Surgical Manag
Neurosurgery 31:219-230, Ogilvy,C.S.,et al, 1992

Isolated Granulomatous Angiitis of the Spinal Cord
Ann Neurol 32:580-582, Caccamo,D.V.&Garcia,J.H., 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

Presence of HTLV-I Proviral DNA in Central Nervous System of Patients with HTLV-I-Associated Myelopathy
Ann Neurol 31:39-45, Kira,J.,et al, 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Diagnosis and Treatment of Ossification of the Posterior Longitudinal Ligament of the Spine:8 Cases and Lit Review
Am J Med 92:296-306, Trojan,D.A.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

HTLV-I-Associated Myelopathy Associated with Blood Transfusion in the US:Epidemiologic & Molecular Evidence
Neurol 41:192-197, Kaplan,J.E.,et al, 1991

Syphilitic Meningomyelitis
Neurol 41:325-326, Strom,T.&Schneck,S.A., 1991



Showing articles 50 to 100 of 3736 << Previous Next >>