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acanthocytosis
acetylcholine
advances in neurology
algorithm
Alzheimer's disease
amantadine
amyotrophic lateral sclerosis
anticholinesterase
antioxidant
areflexia
Arnold Chiari malformation
arrhythmia, cardiac
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
Babinski sign
Bassen-Kornzweig syndrome
biologic markers
blindness
blood dyscrasias, neurologic findings with
brainstem, atrophy
CAG repeats
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar vermis
cerebral glucose metabolism
cerebrovascular accident
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
congestive heart failure
consanguinity
controversies in neurology
cornea, abnormal
deafmute
deafness
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dentatorubral-pallidoluysian atrophy
dexterity, impaired
diabetes mellitus
disability, neurological
dwarfism
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
echocardiogram
echocardiogram, LVH
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electronystagmography, abnormal
endocardial fibrosis
ethics in neurology
eye movement, disorders of
falling
familial
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gargoylism
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
Guillain Barre syndrome
Hallgren's syndrome
hammertoes
head injury
hearing loss
heart block
hepatolenticular degeneration(Wilson's disease)
Huntington's chorea
Hurler's syndrome
hydroxytryptophan L-5(L-5 HTP)
hyperreflexia
hypertonia
hypotonia
imbalance
incoordination
jaw jerk, abnormal
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
kyphosis
Laurence-Moon-Bardet-Biedl syndrome
lecithin
leg weakness, bilateral
Leigh's disease
leukoencephalopathy
life expectancy
lipid storage disorder of CNS
malformation, CNS, congenital
malondialdehyde
Marinesco-Sjogren syndrome
mental retardation
metabolic disorder, primary
misdiagnosis
mitochondrial disease
molecular genetics
MRI
MRI, abnormal
MRI, negative
MRI, spinal cord
mucopolysaccharidoses
multiple sclerosis
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myelomalacia
myopathy
myopia
myotonia dystrophica
nerve conduction studies
neuritis
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, amyloid
nystagmus
obesity
ocular motility, disorders of
ocular myopathy
optic atrophy
paraparesis, familial spastic
Parkinson disease
pathologic reflex
pes cavus
physostigmine
polydactyly
polyneuropathy
prognosis
progressive neurologic disorder
proprioception, abnormal
pseudoretinitis pigmentosa
psychiatric disorder
remote effect of cancer on the nervous system
retinitis pigmentosa
retinopathy
review article
Romberg's sign
saccadic eye movements, abnormal
schizophrenia
scoliosis
seizure
sensory loss
spastic ataxia
spasticity
Spielmeyer Vogt syndrome
spinal cord, cervical
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
staggering
tandem gait, ataxic
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
Usher's syndrome
vibratory sensation
vibratory sensation, abnormal
visual evoked response
visual field defect
visual fields, constricted
vitamin deficiency
vitamin E
vitamin E deficiency
Von Hippel Lindau
walking, difficulty with
wheelchair
white matter disease
wide based gait
workup
Showing articles 950 to 1000 of 1254 << Previous Next >>

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Breast & Other Cancers in Families with Ataxia-Telangiectasia
NEJM 316:1289-1294, Swift,M.,et al, 1987

The Neurologic Examination in Patients with Probable Alzheimer's Disease
Arch Neurol 44:929-932, Huff,F.J.,et al, 1987

Ataxic Hemiparesis with Contralateral Trigeminal Nerve Impairment Due to Pontine Hemorrhage
Stroke 18:244-245, Ambrosetto,P., 1987

Pontine Ataxic Hemiparesis Studied by a High Resolution Magnetic Resonance Imaging System
Ann Neurol 21:204-207, Nabatame,H.,et al, 1987

Urinary & Gait Disturbances as Markers for Early Multi-Infarct Dementia
Stroke 18:138-141, Kotsoris,H.,et al, 1987

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Neurologic Aspects of Boxing
Arch Neurol 44:453-459, Jordan,B.D., 1987

The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986

Normal-Pressure Hydrocephalus
Arch Neurol 43:940-942, Graff-Radford,N.R.&Godersky,J.C., 1986

Chronic Idiopathic Ataxic Neuropathy
Ann Neurol 19:545-554, Dalakas,M.C., 1986

Clinicopathological Conference
Scurvy, Wernicke-Korsakoff Syndrome, Case 33-1986, NEJM 315:503-50886., , 1986

Clinicopath. Conference
Malignant Lymphoma, Diffuse Small Cleaved-Cell Type, of Spinal Epidural Space ( & Orbit) , Case 47-1, 86, NEJM1-1409,1986., 1986

Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
Arch Neurol 43:1050-1053, Farris,B.K.,et al, 1986

The Leaking Labyrinth
BMJ 293:220-221, O'Donoghue,G.M.&Colman,B.H., 1986

Vitamin E Deficiency
Editorial, Lancet 1:423-4241986., , 1986

Tobacco Intolerance in Multiple System Atrophy
Neurol 36:986-988, Johnsen,J.A.,et al, 1986

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Neurologic Sequelae of Chronic Solvent Vapor Abuse
Neurol 36:698-702, Hormes,J.T.,et al, 1986

Vitamin E-Deficient Spinocerebellar Syndrome Due to Intestinal Lymphangiectasia
Neurol 36:554-556, Gutmann,L.,et al, 1986

The Spectrium of Neurologic Disorder From Vitamin E Deficiency
Neurol 36:917-921, Satya-Murti,S.,et al, 1986

Paraneoplastic Opsoclonus-Myoclonus, Associated with Medullary Thyroid Carcinoma & Review of the Literature
Arch Neurol 43:410-415, Dropcho,E.&Payne,R., 1986

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Clinicopath Conf (Juvenile) Periarteritis Nodosa (Kawasaki Syndrome)
with Involvement of Subcutaneous ( & Cerebral) Arteries, Case 43-1986, NEJM 315:1143-1154, , 1986

Hyponatraemia as a Cause of Reversible Ataxia
et al BMJ 293:1346, Kelsey,S.M., 1986

Cogan's Syndrome:18 Cases & a Review of the Literature
Mayo Clin Proc 61:344-361, Vollertsen,R.S.,et al, 1986

Clinical Signs in the Wernicke-Korsakoff Complex:A Retrospective Analysis of 131 Cases Diagnosed at Necropsy
JNNP 49:341-345, Harper,C.G.,et al, 1986

Clinicopath. Conference
Amyloid Polyneuropathy, Case Record 26-1986, NEJM 315:45-55986., , 1986

Hypesthetic-Ataxic-Hemiparesis in Thalamic Hemorrhage
Stroke 17:49-51, Verma,A.K.&Maheshwari,M.C., 1986

Partial Dorsal Mesencephalic Hemorrhages:Report of Three Cases
Neurol 36:529-533, Sand,J.J.,et al, 1986

The Clinical Features & Natural History of the Steele-Richardson-Olszewski Syndrome (Prog Supranuclear Palsy)
Neurol 36:1005-1006, Maher,E.R.,et al, 1986

Multiple Sclerosis, The Problem of Incorrect Diagnosis
Arch Neurol 43:578-583, Rudick,R.A.,et al, 1986

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Sudden Death Due to Massive Intraventricular Hemorrhage into an Unsuspected Ependymoma
Surg Neurol 24:63-66, Poon,T.P.&Solis,O.G., 1985

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Neurologic Signs in Senescence
Arch Neurol 42:1154-1157, Jenkyn,L.R.,et al, 1985

Atypical Alzheimer's Disease with Spastic Paresis & Ataxia
Ann Neurol 17:297-300, Aikawa,H.,et al, 1985

Blind Loop Syndrome, Vitamin E Malabsorption, & Spinocerebellar Degeneration
Neurol 35:338-342, Brin,M.F.,et al, 1985

Ataxic Creutzfeldt-Jakob Disease:Diagnostic Techniques & Neuropathologic Observations in Early Disease
Neurol 35:254-257, Jones,H.R.,et al, 1985

Wernicke's Encephalopathy
NEJM 312:1035-1039, Reuler,J.B.,et al, 1985

Cerebellar Infarction in the Superior Cerebellar Artery Distribution
Neurol 35:705-711, Kase,C.S.,et al, 1985

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

Subcortical Arteriosclerotic Encephalopathy, (Binswanger's Disease)
Arch Neurol 42:951-959, Kinkel,W.R.,et al, 1985

Lacunar Syndrome Due to Intracerebral Hemorrhage
Stroke 16:454-459, Mori,E.,et al, 1985

The Gait Abnormality of Huntington's Disease
Neurol 35:1450-1454, Koller,W.C.&Trimble,J., 1985

Atypical Presentation of Progressive Supranuclear Palsy
Ann Neurol 17:334-343, Davis,P.H.,et al, 1985

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

Spinocerebellar Degeneration Associated with a Selective Defect of Vitamin E Absorption
NEJM 313:32-35, Harding,A.E.,et al, 1985

Celiac Disease & Spinocerebellar Degeneration with Normal Vitamin E Status
Neurol 35:1199-1201, Ward,M.E.,et al, 1985

Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
NEJM 312:874-879, Petito,C.K.,et al, 1985



Showing articles 950 to 1000 of 1254 << Previous Next >>