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Differential
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acanthocytosis
Aicardi-Goutieres syndrome
algorithm
amyotrophic chorea-acanthocytosis
areflexia
ataxic gait
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, hemorrhage
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bicaudate index
biotin
blepharospasm
blood dyscrasias, neurologic findings with
brain atrophy
brainstem, lesion of
calcification, intracranial
calcification, intracranial, rim
cardiac arrest
cardiac arrest and resuscitation
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus
caudate nucleus, atrophy
caudate nucleus, hemorrhage of
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral glucose metabolism
cerebrospinal fluid, oligoclonal IgG in
children
chorea
chorea, familial
chorein
choreoathetosis
chromosomal abnormality
chromosome 19
cognition
coma
cortical infarction
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cyanide poison
cyst
cyst, parenchymal
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei, lesion of
differential diagnosis
disability rating scale, neurological
disability, neurological
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dystonia
dystonic reaction, acute
electroencephalogram, focal delta activity
electromyogram
encephalitis, focal
encephalitis, Rasmussen's
encephalopathy
encephalopathy, anoxic
encephalopathy, post anoxic
enzyme, defect
failure to thrive
familial
gait disorder
gene
gene mutation
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutaric acidemia
glutaric aciduria
gray matter
Huntington's chorea
Huntington's chorea, presymptomatic detection of
Huntington's disease, children
hydrocephalus
hyperreflexia
hyporeflexia
hypotension, systemic
hypotonia
hypoxia
hypoxic encephalopathy
inborn errors of metabolism
infantile bilateral striatal necrosis
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
iron, brain
lacunar infarction
laminar necrosis, cortical
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
Lesch-Nyhan syndrome
leukoencephalopathy
level of consciousness, decreased
lip, biting
lobar atrophy
mammillary bodies
McLeod syndrome
memory, impairment of
methanol intoxication
midbrain, lesion of
movement disorder
MRI
MRI, abnormal
MRI, gradient-echo
MRI, serial
MRI, susceptibility weighted
MRI, volumetry
multiple sclerosis
multiple sclerosis, plaque
myoclonus
myopathy
neurologic disease, diagnoses of
neuropathology
neuropathy
neurotoxin
nutritional deficiency
nystagmus
optic atrophy
optic nerve, lesion of
optic neuropathy
optic neuropathy, toxic
Parkinson disease, arteriosclerotic
Parkinsonism syndrome
periaqueductal lesion
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
putamen, lesion of
putamen, lesion of, bilateral
rigidity
screening
seizure
seizure, focal
seizure, intractable
self-mutilation
sensory nerve action potentials
single photon emission computed tomography
spasticity
striatum, lesion of
striatum, lesion of, bilateral
symmetric brain lesions
thalamus, lesion of
thalamus, lesion of-bilateral
third ventricle, wall
tic
tongue, biting
treatment of neurologic disorder
trinucleotide repeats
ventriculostomy
vocalizations
Wernicke's encephalopathy
white matter disease
white matter disease, periventricular
Showing articles 1300 to 1350 of 2428 << Previous Next >>

Reversal of Subacute Paraneoplastic Cerebellar Syndrome with Intravenous Immunoglobulin
Neurol 44:1184-1185, Counsell,C.E.,et al, 1994

Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutations in Multiple Sclerosis
Ann Neurol 36:109-112, Kellar-Wood,H.,et al, 1994

Mitochondrial DNA mutations in an Outbreak of Optic Neuropathy in Cuba
Neurol 44:843-845, Hirano,M.,et al, 1994

Eye Movements in Parkinsonian Syndromes:Vidailhet
M. , et al, Neurol 35:420-42694., , 1994

Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
JNNP 57:278-284, Burn,D.J.,et al, 1994

Charact of Medial Temporal Lobe Epilepsy:Interictal & Ictal EEG, Neuropsych Test, Imaging, Surg Results & Path
Ann Neurol 34:781-787, Williamson,P.D.,et al, 1993

Hippocampal Sclerosis in Epilepsy and Childhood Febrile Seizures
Lancet 342:1391-1394, Kuks,J.B.M.,et al, 1993

Hippocampal Sclerosis in Children with Intractable Temporal Lobe Epilepsy:Detection with MR Imaging
AJR 161:1045-1048, Grattan-Smith,J.D.,et al, 1993

Diagnosis of Medial Temporal Lobe Seizure Onset:Relative Specificity and Sensitivity of Quantitative MRI
Neurol 43:2117-2124, Spencer,S.S.,et al, 1993

X-Chromosome Effects on Female Brain:A Magnetic Resonance Imaging Study of Turner's Syndrome
Lancet 342:1197-1200, Murphy,D.G.M.,et al, 1993

Functional and Magnetic Resonance Imaging Correlates of Callosal Involvement in Multiple Sclerosis
Arch Neurol 50:1077-1082, Pelletier,J.,et al, 1993

Hallervorden-Spatz Disease with Bilat Invol of Globus Pallidus & Substantia Nigra:MR Demonstra
J Comput Assist Tomogr 17:961-963, Porter-Grenn,L.,et al, 1993

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Conjugal Amyotrophic Lateral Sclerosis:Report of a Young Married Couple
Neurol 43:2378-2380, Cornblath,D.R.,et al, 1993

MRI Pallidal Hyperintensity & Brain Atrophy in Cirrhotic Pts:2 Different MRI Patterns of Clin Deterior?
Neurol 43:2570-2573, Kulisevsky,J.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

MRI Abnormalities in Creutzfeldt-Jakob Disease
Neuroradiology 35:584-585, DiRocco,A.,et al, 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

Mycoplasma Pneumoniae Infection May Cause Striatal Lesions Leading to Acute Neurologic Dysfunction
Neurol 43:2150-2151, Saitoh,S.,et al, 1993

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Hemibody Tremor Related to Stroke
Stroke 24:2094-2096, Dethy,S.,et al, 1993

Choroid Plexus Infection in Cerebral Toxoplasmosis in AIDS Patients
Neurol 43:2035-2040, Falangola,M.F.&Petito,C.K., 1993

Neurosurgical Management of the Acquired Immunodeficiency Syndrome
West J Med 158:249-253, Andrews,B.T.&Kenefick,T.P., 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Spinal Cord MRI Using Multi-Array Coils and Fast Spin Echo, II. Findings in Multiple Sclerosis
Neurol 43:2632-2637, Kidd,D.,et al, 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Communicating Hydrocephalus, Basilar Invagination, and Other Neurologic Features in Osteogenesis Imperfecta
Neurol 43:2603-2608, Charnas,L.R.&Marini,J.C., 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Leber's Hereditary Optic Neuropathy, New Genetic Considerations
Arch Neurol 50:540-548, Newman,N.J., 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Embolic Cerebral Infarction:MR Findings in the First 3 Hours AFter Onset
AJR 160:1077-1082, Shimosegawa,E.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

The Natural History of Amyotrophic Lateral Sclerosis
Neurol 43:1316-1322, Ringel,S.P.,et al, 1993

MRI in Acute Transverse Myelopathy
Neuroradiology 35:221-226, Holtas,S.,et al, 1993

Facial Asymmetry, Hippocampal Pathology, & Remote Symptomatic Seizures:A Temporal Lobe Epileptic Syndrome
Neurol 43:725-727, Cascino,G.D.,et al, 1993

Update on Surgical Treatment of the Epilepsies, Second Intern Palm Desert Conf on Surgical Trtm of Epilepsies (1992)
Neurol 43:1612-1617, Engel,J.Jr., 1993

Early Childhood Prolonged Febrile Convulsions, Atrophy & Sclerosis of Mesial Struc & Temporal Lobe Epilepsy:An MRI Study
Neurol 43:1083-1087, Cendes,F.,et al, 1993

Magnetic Resonance Imaging in Childhood Intractable Partial Epilepsies:Pathologic Correlations
Neurol 43:681-687, Kuzniecky,R.,et al, 1993



Showing articles 1300 to 1350 of 2428 << Previous Next >>