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acanthocytosis
advances in neurology
akathisia
alcohol
alcohol, neurologic complications with
algorithm
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
Alzheimer's disease
Alzheimer's disease, familial
aminoacidopathies
aminoacidurias
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
anemia
anemia, hemolytic
anxiety
aphonia
apraxia
apraxia of eye movements
areflexia
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
athetosis, causes of
ATP1A3 gene
autonomic dysfunction
Babinski sign
baclofen
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
bicaudate index
biotin
blindness
blood dyscrasias, neurologic findings with
brain atrophy
brainstem, atrophy
brainstem, lesion of
CAG repeats
calcification, intracranial
carbamazepine
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
catalepsy
cataracts
caudate nucleus
caudate nucleus, atrophy
caudate nucleus, lesion of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortical atrophy
cerebrovascular accident
ceruloplasmin, serum
chewing movements
children
chorea
chorea, causes of
chorea, familial
chorea, familial benign
chorea, senile
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 12
chromosome 19
chromosome 2
cirrhosis
cirrhosis, causes of childhood
Clinical Pathologic Conference(C.P.C.)
clonazepam
cognition
confabulation
consanguinity
contractures, joint
copper metabolism, abnormal
cortical blindness
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dementia, rapidly progressive
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental disability
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
disease modifying agents
distal muscle atrophy
DNA probes
drooling
dying
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphasia
dyssynergia cerebellaris myoclonica
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, paroxysmal
dystonia, treatment of
dystonic reaction, acute
electroencephalogram, abnormalities of
electromyogram
electron microscopy
emotional lability
employment
encephalopathy
enzyme, defect
epileptic encephalopathy
episodic neurologic deficits
equinovarus
ethics in neurology
exercise intolerance
exome sequencing
eye movement, disorders of
failure to thrive
falling
familial
fasciculation
fatal familial insomnia
fever
flunarizine
fragile-X syndrome
Friedreich's ataxia
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
gliosis
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutaric acidemia
glutaric aciduria
grimacing
growth retardation
Hallervorden Spatz disease
hammertoes
handwriting
health insurance
hearing loss
hemiplegia
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
huntingtin
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, late onset
Huntington's chorea, membrane abnormality
Huntington's chorea, misdiagnosis of
Huntington's chorea, presymptomatic detection of
Huntington's chorea, sporadic form
Huntington's disease, children
hyperekplexia
hyperreflexia
hypertonia
hyporeflexia
hypotonia
imbalance
immunodeficiency
immunosuppression
impulsivity
inattention
inborn errors of metabolism
incoordination
infantile bilateral striatal necrosis
insight, loss
insomnia
intellectual deficit
intellectual deterioration
internet
iron, brain
Jakob-Creutzfeldt disease
jaundice
karyotyping
Kayser-Fleischer ring
lactic acidemia
lenticular nucleus, lesion of, bilateral
Lesch-Nyhan syndrome
leukemia
leukodystrophy
lip, biting
lipid storage disorder of CNS
liver disease
liver function enzymes
liver transplantation
lymphocyte capping, diminished
lymphoma
lysosomal storage disease
manic-depressive
McLeod syndrome
memory, defect of recent
memory, impairment of
meningitis, carcinomatous
mental retardation
mental status, abnormal
metabolic disorder, primary
microcephaly
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
Minamata disease
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, paroxysmal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, eye of tiger sign
MRI, FLAIR
MRI, gradient-echo
MRI, paramagnetic effect
MRI, susceptibility weighted
multiple system atrophy
muscle stiffness
muscle weakness
muscular dystrophy
muscular dystrophy, Duchenne
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myotonia dystrophica
neoplasm, primary intracranial
neoplasm, primary of CNS
neurocutaneous disease
neurodegeneration with brain iron accumulation
neuroendocrinology
neurofibromatosis 1
neurofibromatosis 2
neurologic disease
neurologic disease, diagnoses of
neurologic history
neurologic testing
neuronal migration disorder
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, peripheral
neurotoxin
neurotransmitter
next-generation sequencing
Niemann-Pick disease
nystagmus
nystagmus, gaze-evoked
nystagmus, monocular
ocular motility, disorders of
old age, neurology of
opened mouth
ophthalmoplegia
optic atrophy
optokinetic nystagmus, abnormal
palilalia
pancytopenia
PANK2 mutation
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal hemiplegia
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
pathology
penicillamine
peroxisomal disease
personality change
photosensitivity, skin
poison, mercury
poison, neurologic problems with
POLG1 gene
polymerase chain reaction
pons, atrophy
pontocerebellar atrophy
precipitating factors
prevention of neurologic disorders
prion disease
progeria
prognosis
progressive neurologic disorder
progressive pallidum atrophy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
putamen, lesion of
pyramidal tract
pyramidal tract dysfunction
quadriplegia
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recombinant DNA
recurrent
retinitis pigmentosa
review article
RFLPs
rigidity
salivation, excessive
schizophrenia
screening
sea-blue histiocytes
seizure
seizure, stimulus sensitive
self-mutilation
sensorineural hearing loss
short stature
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
spasticity
speech disorder
speech disorder, childhood
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 16
spinocerebellar degeneration
splenomegaly
startle reaction
status epilepticus
stereotypy
striatum, lesion of
striatum, lesion of, bilateral
striopallidodentate calcifications, familial idiopathic
substantia nigra
suicide
tardive dyskinesia
Tay-Sachs disease
telangiectases
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
tic
tongue, biting
torticollis
toxins, nervous system
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, wing beating
trinucleotide repeats
urea-cycle enzymopathies
uric acid, low
visual evoked response
walking, difficulty with
weight loss
wheelchair
white matter disease
wide based gait
workup
writers cramp
xeroderma pigmentosa
X-linked bulbospinal neuronopathy
Showing articles 550 to 600 of 2019 << Previous Next >>

Recurrent Acroparaesthesia During Febrile Infections
Lancet 363:1698, Bodamer,O.A.,et al, 2004

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004

Unilateral Putaminal CT, MR, and Diffusion Abonromalities Secondary to Nonketotic Hyperglycemia in the Setting of Acute Neurologic Symptoms Mimicking Stroke
AJNR 25:975-976, Wintermark,M.,et al, 2004

Hereditary Spastic Paraplegia
Arch Neurol 61:849-855,830, Orlacchio,A.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Neurological Sequelae in Twins Born After Assisted Conception: Controlled National Cohort Study
BMJ 329:311-314, Pinborg,A.,et al, 2004

Pathogenetic Mechanisms of Parkin in Parkinson's Disease
Lancet 364:722-724, Hattori,N. &Mizuno,Y., 2004

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004

The Occurence of Guillain-Barre Syndrome Within Families
Neurol 63:1747-1750, Geleijns,K.,et al, 2004

Natural History of Nonketotic Hyperglycinemia in 65 Patients
Neurol 63:1847-1853, Hoover-Fong,J.E.,et al, 2004

Clinical and Molecular Findings in Patients with Giant Axonal Neuropathy (GAN)
Neurol 62:13-16, Bruno,C.,et al, 2004

Clinical Spectrum of Episodic Ataxia Type 2
Neurol 62:17-22, Jen,J.,et al, 2004

Transmissible Spongiform Encephalopathies
Lancet 363:51-61, Collins,S.J.,et al, 2004

Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
Stroke 35:1790-1794, Cantu,C.,et al, 2004

Familial Leptomeningeal Amyloidosis With a Transthyretin Variant Asp18Gly Representing Repeated Subarachnoid Haemorrhages With Superficial Siderosis
JNNP 75:1463-1466, Jin,K.,et al, 2004

Repeated Screening for Intracranial Aneurysms in Familial Subarachnoid Hemorrhage
Stroke 34:2788-2791, Wermer,M.J.H.,et al, 2003

Long-Term Follow-Up of Thalamic Deep Brain Stimulation for Essential and Parkinsonian Tremor
Neurol 61:1601-1604, Kumar,R.,et al, 2003

The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease
Neurol 61:1475-1478, Taylor,R.A.,et al, 2003

Paraneoplastic Limbic Encephalitis (PLE) and Chorea Associated with CRMP-5 Neuronal Antibody
Neurol 61:1623-1624, Kinirons,P.,et al, 2003

Prevalence and Clinical Features of HTLV Neurologic Disease in the HTLV Outcomes Study
Neurol 61:1588-1594, Orland,J.R.,et al, 2003

Hereditary Neuropathy With Liability to Pressure Palsies Mimicking Hypoglossal Nerve Injuries
Neurol 61:1457-1458, Corwin,H.M. &Girardet,R.E., 2003

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Hereditary Infantile Hemiparesis, Retinal Arteriolar Tortuosity, and Leukoencephalopathy
Neurol 60:57-63,8, Vahedi,K.,et al, 2003

Encephalitis lethargica syndrome:20 new cases and evidence of basal ganglia autoimmunity
Brain 127, 21-33, Dale, R.C., et al, 2003

Post-Streptococcal Autoimmune Disorders of the Central Nervous System
Curr Opin Neurol 16:359-365, Snider,L. &Swedo,S., 2003

Treatment of Sporadic Hemiplegic Migraine with Calcium-Channel Blocker Verapamil
Neurol 60:120-121, Yu,W. &Horowitz,S.H., 2003

Primary Brain Tumours in Adults
Lancet 361:323-331, Behin,A.,et al, 2003

Prenatal Diagnosis Requests for Huntington's Disease when the Father is at Risk, and Does Not Want to Know His Genetic Status: Clinical, Legal, and Ethical Viewpoints
BMJ 326:331-333, Tassicker,R.,et al, 2003

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Neuropsychological and Quality of Life Outcomes 12 Months After Unilateral Thalamic Stimulation for Essential Tremor
JNNP 74:305-311, Fields,J.A.,et al, 2003

Rest Tremor in Patients with Essential Tremor
Arch Neurol 60:405-410, Cohen,O.,et al, 2003

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Predictors of Nursing Home Placement in Huntington Disease
Neurol 60:998-1001, Wheelock,V.L.,et al, 2003

Alzheimer's Disease and Parkinson's Disease
NEJM 348:1356-1364, Nussbaum,R.L. &Ellis,C.E., 2003

Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
BMJ 326:1078-1079, Plunkett,A.,et al, 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

von Hippel-Lindau Disease
Lancet 361:2059-2067, Lonser,R.R.,et al, 2003

Autosomal Dominant Acute Necrotizing Encephalopathy
Neurol 61:226-230, Neilson,D.E.,et al, 2003

Mental Retardation
Neurol 61:156-157, Patterson,M.C. &Zoghbi,H.Y., 2003

The Hereditary Spastic Paraplegias
Arch Neurol 60:1045-1049, Fink,J.K., 2003

Learning Disability
Lancet 362:811-821, Gillberg,C.&Soderstrom,H., 2003

Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
Ann Neurol 43:367-375, Rolfs,A.,et al, 2003

Hypoglossal Neuropathy in Hereditary Neuropathy with Liability to Pressure Palsy
Neurol 61:1154-1155, Winter,W.C. &Juel,V.C., 2003

Can We Prevent Cerebral Palsy?
NEJM 349:1765-1769, Nelson,K.B., 2003

Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
Arch Neurol 60:1541-1544,1521, Tedde,A.,et al, 2003

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002

Therapies for Movement Disorders
Arch Neurol 59:699-702, Goetz,C.G &Hinson,V.K., 2002

Familial Temporal Lobe Epilepsy with Febrile Seizures
Neurol 58:1429-1433, Depondt,C.,et al, 2002

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002



Showing articles 550 to 600 of 2019 << Previous Next >>