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acanthocytosis
acetylcholine
acoustic neurinoma, bilateral
adrenoleukodystrophy
advances in neurology
adverse drug reaction
albinism
alcohol intolerance
alcohol, neurologic complications with
algorithm
alpha-fetoprotein
alternating rapid movement
Alzheimer's disease
amantadine
aminoacidopathies
amyotrophic lateral sclerosis
anemia
antibodies to voltage-gated calcium channels
anticholinesterase
anticonvulsants
anticonvulsants, selection of
antioxidant
apraxia of eye movements
areflexia
Arnold Chiari malformation
arrhythmia, cardiac
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic-dystonia syndromes
ataxin
ataxin-2
atypical
auditory evoked brainstem potentials
autonomic dysfunction
Babinski sign
baclofen
bacterial infection
basal ganglia, degeneration
Bassen-Kornzweig syndrome
benign essential tremor
biologic markers
blindness
blood dyscrasias, neurologic findings with
bradykinesia
brain atrophy
brainstem, atrophy
brainstem, lesion of
CAG repeats
calcium channel dysfunction
carcinoembryonic antigen
carcinoma
carcinoma of lung
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
celiac disease, adult
central core disease
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 cortical atrophy
cerebral glucose metabolism
cerebro hepato renal syndrome
cerebrovascular accident
Chediak-Higashi syndrome
cherry red spot-myoclonus syndrome
children
chloride channel dysfunction
choking
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 12
chromosome 14
chromosome 6
chromosome 9
cigarette smoking
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Cockayne's syndrome
cognition
Collier's sign
cone-rod dystrophy
congestive heart failure
consanguinity
controversies in neurology
conversion reaction
copper deficiency
cornea, abnormal
cranio-cervical junction
creatine phosphokinase(CPK)elevated
Cuba
cystic fibrosis, neurologic complications with
deafmute
deafness
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dementia
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
dexterity, impaired
diabetes mellitus
diabetes mellitus, chemical
dilantin
diplopia
disability, neurological
distal muscle atrophy
DNA probes
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drooling
drug induced neurologic disorders
dwarfism
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
dyspraxia
dystonia
echocardiogram
echocardiogram, LVH
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electronystagmography, abnormal
electroretinograph
endocardial fibrosis
enzyme, defect
epidemiology of neurology
episodic neurologic deficits
ethics in neurology
evoked potentials
excitotoxin
exome sequencing
eye movement, disorders of
falling
familial
familial hemiplegic migraine
family planning
fasciculation
fatigue
fever
finger nose finger test
foot numbness
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
fundus, abnormality of
gait disorder
gangliosidosis GM2
gargoylism
gastrectomy, neurologic complications following
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
globus pallidus, lesion of
glutamate dehydrogenase deficiency
glutamic acid
glycogen storage disease
growth retardation
Guillain Barre syndrome
Hallervorden Spatz disease
Hallgren's syndrome
hammertoes
handwriting
head injury
head nodding
hearing loss
heart block
heel-knee-shin test
hepatolenticular degeneration(Wilson's disease)
hexosaminidase-A and B
HLA
hot cross bun sign
huntingtin
Huntington's chorea
Hurler's syndrome
hydroxytryptophan L-5(L-5 HTP)
hyperreflexia
hypertonia
hypokalemic periodic paralysis
hyposmia
hypotonia
hypoxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, ubiquitin
incoordination
intellectual deficit
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal lymphangiectasia
jaw jerk, abnormal
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
kyphosis
Lafora's disease
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
lecithin
leg weakness, bilateral
Leigh's disease
leukemia
leukocyte peroxidase
leukodystrophy
leukoencephalopathy
life expectancy
lipid storage disorder of CNS
lipid storage myopathy
liver disease
low back pain
lymphoma
macular degeneration
malabsorption
malabsorption syndrome
malformation, CNS, congenital
malignant hyperpyrexia
malondialdehyde
Marinesco-Sjogren syndrome
memory, impairment of
mental retardation
MERRF syndrome
metabolic disorder, primary
Mexican
middle cerebellar peduncle
middle cerebellar peduncle, lesion
migraine
migraine, hemiplegic
mimics
mirror writing
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, FLAIR
MRI, negative
MRI, spinal cord
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myasthenic syndrome
myelogram
myelomalacia
myeloneuropathy
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
myopia
myotonia congenita
myotonia dystrophica
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
neuritis
neurocutaneous disease
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuronopathy
neuroophthalmology
neuropathology
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
neurotoxin
neurotransmitter
neutropenia
nicotine
night blindness
numbness, extremity
nystagmus
nystagmus, primary position of gaze
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
obesity
ocular motility, disorders of
ocular myopathy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic nerve
optic neuropathy
optical coherence tomography
orbit, tomograms of
orthostatic hypotension
pain
pain, management of chronic
palatal myoclonus
pancytopenia
paramyotonia congenita
paraparesis, familial spastic
Parkinson disease
Parkinson disease, familial
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal neurologic deficits
pathologic reflex
pathology
periodic paralysis
peroxisomal disease
pes cavus
photophobia
physostigmine
pigmentary retinopathy
polydactyly
polymerase chain reaction
polymyositis
polyneuropathy
pons, atrophy
pontocerebellar atrophy
posterior column disease
potassium channel antibodies
potassium channel dysfunction
prevention of neurologic disorders
progeria
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
proprioception, abnormal
pseudobulbar palsy
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
Purkinje cell
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
radiation hypersensitivity
Red flags
refractive errors
Refsum's disease
remission
remote effect of cancer on the nervous system
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
risk factors
Romberg's sign
saccadic eye movements, abnormal
schizophrenia
scoliosis
seizure
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
sensory loss
Shy-Drager syndrome
sinemet
skew deviation
skew deviation, alternating
skin, biopsy
skin, lesions in neurologic disorders
sleep apnea
sleep pathology and physiology
sodium channel dysfunction
spastic ataxia
spasticity
sphingolipodoses
Spielmeyer Vogt syndrome
spinal cord, cervical
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, intramedullary
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 10
spinocerebellar ataxia type 12
spinocerebellar ataxia type 14
spinocerebellar ataxia type 16
spinocerebellar ataxia type 17
spinocerebellar ataxia type 2
spinocerebellar ataxia type 28
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 5
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
spinocerebellar degeneration
spinopontine atrophy, dominant
staggering
steatorrhea
striatonigral degeneration
syphilis, neurologic complications with
tandem gait, ataxic
tapetoretinal degeneration
telangiectases
thalamus
thyrotropin-releasing hormone
tinnitus
trazodone
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trimethoprim-sulfamethoxazole
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
Usher's syndrome
vertigo
vertigo, episodic
vestibulopathy
vibratory sensation
vibratory sensation, abnormal
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
visual loss, slow
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin supplementation
Von Hippel Lindau
walking, difficulty with
wheelchair
white matter disease
wide based gait
workup
X-linked bulbospinal neuronopathy
Showing articles 900 to 950 of 1208 << Previous Next >>

Clinicopath Conf
Primary (Granulomatous) Angiitis of Central Nervous System, Case Record 8-1989, NEJM 320:514-5249., , 1989

Syndrome of Cerebellar Ataxia and Hypogonadotrophic Hypogonadism:Evidence for Pituitary Gonadotrophin Deficiency
JNNP 52:407-409, Fox,A.C.K.,et al, 1989

Brain White-Matter Changes in the Elderly Prone to Falling
Arch Neurol 46:1292-1296, Masdeu,J.C.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Subacute Combined Degeneration of the Spinal Cord
In Rowland's, Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 691, Mancall,E.L., 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
Neurol 38:1056-1060, Zochodne,D.W.,et al, 1988

Clinicopath Conf
Paraneoplastic Encephalitis (Limbic and Brain-Stem Encephalitis) , Case Record 39-1988, NEJM 319:849, 860,, 1988

Pontine Lesion in Opsoclonus-Myoclonus Syndrome Shown by MRI
JNNP 51:1572-1575, Hattori,T.,et al, 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Sensory Form of Acute Polyneuritis
Neurol 38:1728-1731, Dawson,D.M.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Hyperthyroidism Presenting as Pyramidal Tract Disease
BMJ 297:1395-1396, Shaw,P.J.,et al, 1988

Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or Macrocytosis
NEJM 318:1720-1728, 1752-17541988., Lindenbaum,J.,et al, 1988

Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood
NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988

Thalamic Astasia:Inability to Stand After Unilateral Thalamic Lesions
Ann Neurol 23:596-603, Masdeu,J.C.&Gorelick,P.B., 1988

Creutzfeldt-Jakob Disease Following Pituitary-Derived Human Growth Hormone Therapy:A New American Case
Neurol 38:1131-1133, Marzewski,D.J.,et al, 1988

The Minor Symptoms of Increased Intracranial Pressure:101 Pts with Benign Intracranial Hypertension
Neurol 38:1461-1464, Round,R.&Keane,J.R., 1988

Opsoclunus, Myoclonus, Ataxia & Encephalopathy in Adults with Cancer:A Distinct Paraneoplastic Syndrome
Medicine 67:100-109, Anderson,N.E.,et al, 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Clinicopath Conf
Infiltrating Carcinoma of Breast (Paraneoplastic Opsoclonus Syndrome & SIADH) Case 9-1988, NEJM 318:, 63-578., 1988

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

Ataxic Hemiparesis:Three Different Locations of Lesions Studied by MRI
Neurol 38:1322-1324, Helweg-Larsen,S.,et al, 1988

Cerebellar Stroke
Editorial, Lancet 1:1031-10321988., , 1988

The Clinical and Computed Tomographic Features of Cerebellar Peduncular Hemorrhage
Neurol 38:1485-1487, Wizer,B.,et al, 1988

Dissection of the Intracranial Vertebral Artery
Neurol 38:868-877, Caplan,L.R.,et al, 1988

Risk Factors for Falls Among Elderly Persons Living in the Community
NEJM 319:1701-1707, Tinetti,M.E.,et al, 1988

Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
Arch Neurol 45:547-549, Vighetto,A.,et al, 1988

Vitamin E Deficiency & Neurologic Disease in Adults with Cystic Fibrosis
Ann Int Med 107:51-54, Sitrin,M.D.,et al, 1987

Rett's Syndrome, Correlation of Electroencephalogram Characteristics with Clinical Staging
Arch Neurol 44:1053-1056, Glaze,D.G.,et al, 1987

Ataxia After Severe Head Injury:The Pathological Substrate
Ann Neurol 22:77-79, Chester,C.S.&Reznick,B.R., 1987

Somatosensory Evoked Potentials in Lacunar Syndromes of Pure Motor & Ataxic Hemiparesis
Stroke 18:1093-1097, Kelly,M.A.,et al, 1987

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

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

Idiopathic Hypoparathyroidism with Extensive Brain Calcification & Persistent Neurologic Dysfunction
Neurol 37:307-309, Friedman,J.H.,et al, 1987

Long Term Exposure to Hydrogen Sulphide Producing Subacute Encephalopathy in a Child
BMJ 294:614, Gaitonde,U.B.&Sellar,R.J., 1987

Clinical & Magnetic Resonance Features of Primary Intracranial Arachnoid Cysts
Ann Neurol 21:342-348, Gandy,S.E.&Heier,L.A., 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



Showing articles 900 to 950 of 1208 << Previous Next >>