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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 1229 << Previous Next >>

3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
Neurol 75:1079-1083, Wortmann,S.B.,et al, 2010

Sensory Ganglionopathy Due to Gluten Sensitivity
Neurol 75:1003-1008, Hadjivassiliou,M.,et al, 2010

Opsoclonus-Myoclonus Syndrome in Anti-N-Methyl-D-Aspartate Receptor Encephalitis
Arch Neurol 67:118-121, Kurian,M.,et al, 2010

Subclinical Hypothyroidism Presenting with Gait Abnormality
The Neurologist 16:115-116, Edvardsson,B. &Persson,S., 2010

Assessment: Symptomatic Treatment for Muscle Cramps (an Evidence-Based Review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 74:691-696, Katzberg,H.D.,et al, 2010

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

Primary Central Nervous System Post-Transplantation Lymphoproliferative Disorder
CANCER 16:863-870, Cavaliere, R.,et al, 2010

MR Imaging Findings in 56 Patients with Wernicke Encephalopathy: Nonalcoholics May Differ from Alcoholics
AJNR 30:171-176, Zuccoli,Z.,et al, 2009

Neurosarcoidosis: A Study of 30 New Cases
JNNP 80:297-304, Joseph,F.G. &Scolding,N.J., 2009

Slurred Speech and Spirochaetes
Lancet 373:978, Thukral,A.,et al, 2009

High Doses of Deferiprone May Be Associated with Cerebellar Syndrome
BMJ 338:653, Beau-Salinas,F.,et al, 2009

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations
NEJM 360:1960-1970, Bockenhauer,D.,et al, 2009

Frequency, Characteristics, and Risk Factors for Amiodarone Neurotoxicity
Arch Neurol 66:865-869, Orr,C.F. &Ahlskog,E., 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

A 54-Year-Old Woman with Progressive Gait Disturbance and MRI Abnormalities
Neurol 73:466-474, Hochberg,F.H.,et al, 2009

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Paraneoplastic Syndromes Affecting Brain and Cranial Nerves
UpToDate May 2009, Dalmau,J. &Rosenfeld,M., 2009

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



Showing articles 500 to 550 of 1229 << Previous Next >>