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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 500 to 550 of 1208 << Previous Next >>

JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
Eur Neurol 59:205-207, Shin,H.-W.,et al, 2008

Practice Parameter: Assessing Patients in a Neurology Practice for Risk of Falls (An Evidence-Based Review)
Neurol 70:473-479, Thurman,D.J.,et al, 2008

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Opsoclonus-Myoclonus Syndrome Asssociated with Benign Ovarian Teratoma
Neurol 70:1292-1293, Fitzpatrick,A.S.,et al, 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Association of Gait and Balance Disorders With Age-Related White Matter Changes: The LADIS Study
Neurol 70:935-942, Baezner,H.,et al, 2008

A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
NEJM 358:1009-1017, Stepens,A.,et al, 2008

Reversible Parkinsonism and Ataxia Associated With High-Dose Octreotide
Neurol 70:2345-2346, Espay,A.J., 2008

Second Consensus Statement on the Diagnosis of Multiple System Atrophy
Neurol 71:670-676, Gilman,S.,et al., 2008

Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease
AJNR 29:1519-1524, Meissner,B.,et al., 2008

Curable Cause of Paraplegia: Spinal Dural Arteriovenous Fistulae
Stroke 39:2756-2759, Aghakhani,N.,et al, 2008

Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
Brain 131:2553-2563, Saiz,A., et al, 2008

Opsoclonus-Myoclonus-Ataxia Syndrome with Autoantibodies to Glutamic Acid Decarboxylase
Clin Neurol Neurosurg 110:619-621, Markakis,I.,et al, 2008

Auto-Immune Cerebellar Ataxia with Anti-GAD Antibodies Accompanied by De Novo Late-Onset Type 1 Diabetes Mellitus
Diabetes Metab 34:386-388, Bayreuther,C.,et al, 2008

Bilateral Basal Ganglia Lesions in Patients with End-Stage Diabetic Nephropathy
Nephrology 13:68-72, Li, J.,et al, 2008

Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
J Neuro-Ophthalmol 28:58-68, Ko,M.W.,et al, 2008

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
J Neurol 254:1609-1611, Collison,K. and Rees,J., 2007

"Salt and Pepper" in the Eye and Face: A Prelude to Brainstem Ischemia
Am J Ophthalmol 144:322-325, Conforto, A.B.,et al, 2007

Superficial Siderosis
Arch Neurol 64:491-496, Kumar,J, 2007

Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
NEJM 356:612-620, Case 4-2007, 2007

Neuroimaging of Bilateral Caudate Infarction Manifesting as Parkinsonian Gait Disorder
Conn Med 71:149-150, Finelli,P.F., et al, 2007

Wernicke Encephalopathy After Obesity Surgery: A Systematic Review
Neurol 68:807-811, Singh,S. &Kumar,A., 2007

Clinicopath Conf,Lyme Disease of the Nervous System
NEJM 356:1561-1570, Case Record 11-2007, 2007

Improvement of Gait by Chronic, High Doses of Methylphenidate in Patients with Advanced Parkinsons Disease
JNNP 78:470-475, Devos,D.,et al, 2007

Orthostatic Myoclonus: A Contributor to Gait Decline in Selected Elderly
Neurol 68:1826-1830, Glass,G.A.,et al, 2007

Causative Factors and Epidemiology of Bilateral Vestibulopathy in 255 Patients
Ann Neurol 61:524-532, Zingler,V.C.,et al, 2007

Ataxic vs Painful Form of Paraneoplastic Neuropathy
Neurol 69:564-572, Oki,Y.,et al, 2007

Angelman Syndrome Revisited
Neurologist 13:305-312, Paprocka,J.,et al, 2007

Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
Ann Neurol 62:347-355, Bonthius,D.J.,et al, 2007

Stroke Among Patients with Dizziness, Vertigo and Imbalance in the Emergency Department, A Population-Based Study
Stroke 37:2484-2487, Kerber,K.A.,et al, 2006

Clinicopath Conf., Degoss Disease
NEJM 355:2575-2584, Case 38-2006, 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Upside Down Reversal of Vision Due to an Isolated Acute Cerebellar Ischemic Infarction
J Neurol 253:953-954, Hern�ndez,A.H.,et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Isolated Abducens Nerve Palsy as a Regional Variant of Guillain-Barre Syndrome
JNS 243:35-38, Tatsumoto, M.,et al, 2006

Spinal dural arteriovenous fistulas: a congestive myelopathy that initially mimics a peripheral nerve disorder
Brain 129:3150-3164, Jellema, K., et al, 2006

Early Clinical Signs and Imaging Findings in Gerstmann-Straussler-Scheinker Syndrome (Pro102Leu)
Neurol 66:1672-1678, Arata,H.,et al, 2006

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

Opsoclonus Persisting During Sleep in West Nile Encephalitis
Arch Neurol 63:1324-1326, Alshekhlee,A.,et al, 2006

Peripheral Neuropathies in Waldenstroms Macroglobulinaemia
JNNP 77:224-228, Levine,T.,et al, 2006

First Symptom in Sporadic Creutzfeldt-Jakob Disease
Neurol 66:286-287, Rabinovici,G.D.,et al, 2006

Varicella Zoster Virus Cerebellitis in a 66-Year-Old Patient Without Herpes Zoster
Lancet 367:182, Ratzka,P.,et al, 2006

Cerebellar Infarction int he Territory of the Medial Branch of the Superior Cerebellar Artery
Neurol 66:115-117, Sohn,S.-I.,et al, 2006

Lyme Neuroborreliosis Presenting as the Syndrome of Inappropriate Antidiutetic Hormone Secretion
MedGenMed 8:71, Perkins, M.P.,et al, 2006



Showing articles 500 to 550 of 1208 << Previous Next >>