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abiotrophy
adult polyglucosan body disease
advance directives
advances in neurology
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amyotrophic lateral sclerosis, diagnosis of
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amyotrophic lateral sclerosis, epidemiology of
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amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
anti IgLON5
apnea
areflexia
arm weakness
aspiration
autoantibodies
autonomic dysfunction
axonal degeneration
Babinski sign
basal ganglia, lesion of
behavioral disorder
BiPAP
bladder dysfunction
botulinum toxin
brain atrophy
Brugada syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, childhood
bulbar palsy, progressive
C9orf72
CAG repeats
camptocormia
CAT scan, abnormal
CAT scan, emission, abnormal
cerebral cortex
cerebral cortical atrophy
chewing, impaired
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
coma, episodic
complications
creatine phosphokinase(CPK)elevated
crying, pathologic
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dentatorubral-pallidoluysian atrophy
diabetes mellitus
differential diagnosis
disability, neurological
distal muscle weakness
DNA probes
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
emotional lability
encephalitis
encephalitis, autoimmune
encephalomyelitis
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigable chewing
fatigue
fibrillations
fine motor function, impaired
flaccid paralysis
flail arm syndrome
foot drop
fragile-X syndrome
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gag reflex, depressed
gait disorder
gait, spastic
gastrostomy
gastrostomy, percutaneous endoscopic
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
gynecomastia
hand weakness
hearing loss
hemiparesis
heralding manifestation
hoarseness
hospice
huntingtin
Huntington's chorea
hyperreflexia
hypersomnia
hypertension
hypophonia
hyporeflexia
hypotension, systemic
imbalance
immunotherapy
inclusion bodies
intellectual deficit
intellectual deterioration
internal capsule
intrinsic hand muscles, wasting of
jaw clonus
jaw closure weakness
jaw jerk, abnormal
Jewish
Kugelberg-Welander syndrome
laughing
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
leukoencephalopathy
life expectancy
liver disease
lobar atrophy
locked-in syndrome
masseter muscle weakness
memory, defect of recent
memory, impairment of
Mills syndrome
mimics
misdiagnosis
molecular genetics
mortality
motor neuron disease
motor neuron disease, misdiagnosis
MRI
MRI, abnormal
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
mutism
myelomalacia
myeloneuropathy
myocardial injury
myoclonus
myocytolysis
myopathy
myotonia dystrophica
nasal speech
neck weakness
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurogenic bladder
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neuronal migration disorder
neuronopathy
neuropathology
neuropathology, brain
neuropathy
neuropathy, motor, multifocal
neuroprotective agents
optic atrophy
pain
pain, management of chronic
palliative care
paralysis, acute areflexic
paraparesis, spastic
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
practice guidelines
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
radiculopathy
REM sleep behavior disorder
repetitive nerve stimulation
respirator
respiratory failure
retinitis pigmentosa
review article
riluzole
risk factors
saccadic eye movements, abnormal
salivation, excessive
sensorineural hearing loss
sleep
sleep pathology and physiology
spasticity
speech disorder
speech, loss of
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
sudden death
tandem gait, ataxic
temporal lobe, atrophy
temporalis muscle wasting
testicular atrophy
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
vestibular function, tests of
vocalizations
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weight loss
West Nile fever
wheelchair
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 1250 to 1300 of 2707 << Previous Next >>

The Roussy-Levy Family:From the Original Description to the Gene
Ann Neurol 46:770-773, Plante-Bordeneuve,V.,et al, 1999

Cervical Root Stimulation in a Case of Classic Neurogenic Thoracic Outlet Syndrome
Muscle & Nerve 22:1287-1292, Felice,K.J.,et al, 1999

Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy
JNNP 67:685-687, Duarte,J.,et al, 1999

Fetal Surgery for Myelomeningocele, Promise, Progress, and Problems
JAMA 282:1873-1874,1819,1826, Simpson,J.L., 1999

MR Findings in AIDS-Associated Myelopathy
AJNR 20:1412-1416,1387, Chong,J.,et al, 1999

Incidental Detection of Hippocampal Sclerosis on MR Images:Is It Significant?
AJNR 20:1609-1612,1575, Moore,K.R.,et al, 1999

Dementia as the Most Common Presentation of Cortical-Basal Ganglionic Degeneration
Neurol 53:1969-1974, Grimes,D.A.,et al, 1999

Effect of Vitamin C on Frequency of Reflex Sympathetic Dystrophty in Wrist Fractures:A Randomised Trial
Lancet 354:2025-2028, Zollinger,P.E.,et al, 1999

Neurologic Manifestations of Compressive Radiculopathy of the First Thoracic Root
Neurol 53:1149-1151, Levin,K.H., 1999

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

A Case of Sporadic Pick Disease With Onset at 27 Years
Arch Neurol 56:1289-1291, Jacob,J.,et al, 1999

Antithrombotic Therapy to Prevent Stroke in Patients with Atrial Fibrillation:A Meta-Analysis
Ann Int Med 131:492-501,537, Hart,R.G.,et al, 1999

HTLV-I-Associated Myelopathy:Acute Progression and Atypical MR Findings
AJNR 20:1417-1421, Shakudo,M.,et al, 1999

Beneficial Effect of Siphoning in Treatment of Adult Hydrocephalus
Arch Neurol 56:1224-1229,1199, Bergsneider,M.,et al, 1999

Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999

Neurologic Complications Associated with Hepatitis C Virus Infection
Neurol 53:861-864, Tembl,J.I.,et al, 1999

Age and Cause of Death in Mitochondrial Diseases
Neurol 53:855-857, Klopstock,T.,et al, 1999

The Clinical Course of Neuromyelitis Optica (Devic's Syndrome)
Neurol 53:1107-1114, Wingerchuk,D.M.,et al, 1999

Computed Tomography and Magnetic Resonance Imaging in Mild to Moderate Head Injury:Early and late Imaging Related to Outcome
Ann Neurol 46:70-78, van der Naalt,J.,et al, 1999

Signs and Symptoms of Duchenne Muscular Dystrophny and Becker Muscular Dystrophy Among Carriers in the Netherlands: A Cohort Study
Lancet 353:2116-2119, Hoogerwaard,E.M.,et al, 1999

Serial Magnetic Resonance Imaging of Cerebral Atrophy in Preclinical Alzheimer's Disease
Lancet 353:2125, Fox,N.C.,et al, 1999

Prevalence of Progressive Supranuclear Palsy and Multiple System Atrophy:A Cross-Sectional Study
Lancet 354:1771-1775, Schrag,A.,et al, 1999

A Longitudinal Study of Brain Atrophy in Relapsing Multiple Sclerosis
Neurol 53:139-148, Simon,J.H.,et al, 1999

Hypertensive Brainstem Encephalopathy:Three Cases Presenting with Severe Brainstem Edema
Neurol 53:652-654, Chang,G.Y.&Keane,J.R., 1999

Distal Myasthenic Gravis
Neurol 52:632-634, Nations,S.P.,et al, 1999

Magnetic Resonance Imaging-Based Volumetry Differentiates Idiopathic Parkinson's Syndrome from Multiple System Atrophy and Progressive Supranuclear Palsy
Ann Neurol 45:65-74, Schulz,J.B.,et al, 1999

Getting a Grip on the Myotonic Dystrophies
Neurol 52:12-13, Thornton,C.A.&Ashizawa,T., 1999

Quantitative MRI in Patients with Clinically Isolated Syndromes Suggestive of Demyelination
Neurol 52:599-606, Sailer,M.,et al, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

The Clinical Spectrum of Sarcoglycanopathies
Neurol 52:176-179, Angelini,C.,et al, 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Brain Structure and Neurocognitive and Behavioural Function in Adolescents Who Were Born Very Preterm
Lancet 353:1653-1657, Stewart,A.L.,et al, 1999

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

Clinicopath Conf,Wegener's Granulomatosis with Pachymeningeal Granulomatous Inflammation, Case 9-1999
NEJM 340:945-953, , 1999

Quantitative MRI in CADASIL, Correlation with Disability and Cognitive Performance
Neurol 52:1361-1367, Dichgans,M.,et al, 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Clinicopath Conf:Multisystem Neurodegenerative Disease with Dementia Pugilistica
NEJM 340:1269-1277, Case 12-1999, 1999

MR Imaging of Acute Coccidioidal Meningitis
AJNR 20:509-514, Erly,W.K.,et al, 1999

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

A 10-Year Study of Mortality in a Cohort of Patients with Myotonic Dystrophy
Neurol 52:1658-1662, Mathieu,J.,et al, 1999

PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
Neurol 50:760-763, Young,P.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

Cardiac Involvement in Genetically Confirmed Facioscapulohumeral Muscular Dystrophy
Neurol 51:1454-1456, Laforet,P.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998



Showing articles 1250 to 1300 of 2707 << Previous Next >>