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advances in neurology
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
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amyotrophic lateral sclerosis, misdiagnosis
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amyotrophic lateral sclerosis-like syndrome
areflexia
arm weakness
aspiration
Babinski sign
basal ganglia, lesion of
behavioral disorder
BiPAP
botulinum toxin
brain atrophy
Brugada syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
C0ORF72
CAG repeats
camptocormia
CAT scan, abnormal
cerebral cortex
cerebral cortical atrophy
chewing, impaired
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
complications
creatine phosphokinase(CPK)elevated
crying, pathologic
degenerative diseases of CNS
dementia
dementia, frontal lobe type
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dementia, rapidly progressive
dentatorubral-pallidoluysian atrophy
diabetes mellitus
differential diagnosis
distal muscle weakness
DNA probes
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
emotional lability
epidemiology of neurology
familial
fasciculation
fatigable chewing
fatigue
fibrillations
flail arm syndrome
foot drop
fragile-X syndrome
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gag reflex, depressed
gait disorder
gastrostomy
gastrostomy, percutaneous endoscopic
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
gynecomastia
hand weakness
hemiparesis
heralding manifestation
hoarseness
hospice
huntingtin
Huntington's chorea
hyperreflexia
hypertension
hyporeflexia
intellectual deficit
internal capsule
intrinsic hand muscles, wasting of
jaw clonus
jaw closure weakness
jaw jerk, abnormal
Kugelberg-Welander syndrome
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
life expectancy
liver disease
lobar atrophy
masseter muscle weakness
Mills syndrome
mimics
misdiagnosis
molecular genetics
motor neuron disease
MRI
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
myocardial injury
myocytolysis
myopathy
myotonia dystrophica
nasal speech
neck weakness
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neuronal migration disorder
neuronopathy
neuropathology
neuropathology, brain
neuropathy
neuropathy, motor, multifocal
neuroprotective agents
pain
pain, management of chronic
palliative care
paraparesis, spastic
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 dysfunction
quality of life
repetitive nerve stimulation
respirator
respiratory failure
review article
riluzole
risk factors
salivation, excessive
sleep
sleep pathology and physiology
spasticity
speech disorder
spinal muscular atrophy
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
sudden death
temporal lobe, atrophy
temporalis muscle wasting
testicular atrophy
tongue, atrophy
tongue, fasciculations of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weight loss
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 1250 to 1300 of 2615 << Previous Next >>

More on Reflex Sympathetic Dystrophy Syndrome Following Air-Bag Inflation
NEJM 338:334-335, Quarino,H.A., 1998

Proton Spectroscopy in Myotonic Dystrophy, Correlations with CTG Repeats
Arch Neurol 55:305-311, 2911998., Chang,L.,et al, 1998

Alzheimers Disease with Asymmetric Parietal Lobe Atrophy: A Case Report
J Neurol Sci 160:96-99, Kaida,K.-I.,et al, 1998

Dural Arteriovenous Fistulas as a Cause of Intracranial Hypertension Due to Impairment of Cranial Venous Outflow
JNNP 65:308-316, Cognard,C.,et al, 1998

Chronic Neutrophilic Meningitis Caused by Candida Albicans
Neurologia 13:362-366, del Pozo, M.M.,et al, 1998

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Anesthetic and Surgical Complictions in 219 Cases of Myotonic Dystrophy
Neurol 49:1646-1650, Mathieu,J.,et al, 1997

Complete Ophthalmoplegia After Zoster Ophthalmicus
J Neuro-Ophthalmol 17:262-265, Chang-Godinich,A.,et al, 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Mononeuropathy of a Distal Branch of the Femoral Nerve in a Body Building Champion
JNNP 63:669-671, Padua,L.,et al, 1997

Dentate Nuclei Invol in AIDS Pts with CNS Cryptococcosis:Imaging Findings with Path Correl
J Comput Assist Tomogr 21:175-182, Ruiz,A.,et al, 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Hepatoerythropoietic Porphyria:Neuroimaging Findings
AJNR 18:1557-1560, Berenguer,J.,et al, 1997

Clinicopath Conf
Botulism, Case 22-1997, NEJM 337:184-190997., , 1997

Optic Atrophy and Cerebral Infarcts Caused by Methanol Intoxication:MRI
Neuroradiology 39:192-194, Hsu,H.H.,et al, 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

What is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy
Arch Neurol 54:937-944, Litvan,I.,et al, 1997

Neurological Signs and Frontal White Matter Lesions in Vascular Parkinsonism
Stroke 28:965-969, Yamanouchi,H.&Nagura,H., 1997

Distinction of Idiopathic Parkinson's Dis from Multi-Syst Atrophy by Stim of Growth-Hormone Release w Clonidine
Lancet 349:1877-1881, Kimber,J.R.,et al, 1997

Cordarone (Amiodarone)
Product Insert, Wyeth-Ayerst Laboratories, June 1997., , 1997

Multifocal Motor Neuropathy Presenting as Ophthalmoplegia
Muscle & Nerve 20:347-351997., Pringle,C.E.,et al, 1997

Anticedents of Cerebral Palsy in a Multicenter Trial of Indomethacin for Intraventricular Hemorrhage
Arch Pediatr Adolesc Med 151:580-585, Allan,W.C.,et al, 1997

Postoperative Cerebral Edema Occurring in Children with Slit Ventricles
Pediatrics 99:625-630, Eldredge,E.,et al, 1997

Preliminary Results of Linear Accelerator Radiosurgery for Acoustic Schwannomas
J Neurosurg 85:1013-1019, Mendenhall,W.M.,et al, 1997

Ischemic Lesion Volumes in Acute Stroke by Diffusion-Weighted MRI Correlate with Clinical Outcome
Ann Neurol 42:164-170, Lovblad,K-O.,et al, 1997

Clinical Characteristics of Patients with Motor Disability Due to Conversion Disorder:A Prospective Study
JNNP 63:83-88, Binzer,M.,et al, 1997

Etiology and Early Prognosis of Newly Diagnosed Partial Seizures in Adults
Neurol 49:753-757, Van Paesschen,W.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

CT and MR Findings of Neuroacanthocytosis
J Comput Assist Tomogr 21:221-222, Okamoto,K.,et al, 1997

Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
Arch Neurol 54:251-254, Spranger,M.,et al, 1997

What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
Neurol 49:62-69, Litvan,I.,et al, 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Cysticercosis, Clinical Classification Based on Imaging Studies
Arch Int Med 157:1991-1997, Salgado,P.,et al, 1997

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

CAG Repeat Number Governs the Development Rate of Pathology in Huntington's Disease
Ann Neurol 41:689-692, Penney,J.B.,et al, 1997

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Atypical MRI Features of Wilson's Disease:High Signal in Globus Pallidus on T1-Weighted Images
Neuroradiology 39:171-174, Mochizuki,H.,et al, 1997

Serial Neuropsychological Assess & Magnetic Resonance Imagingf Analysis in Multiple Sclerosis
Arch Neurol 54:1018-1025, Hohol,M.J.,et al, 1997

Corticobasal Degeneration:Neuropathologic and Clinical Heterogeneity
Neurol 48:959-969, Schneider,J.A.,et al, 1997

Midline Cerebral Morphometry Distinguishes Frontotemporal Dementia and Alzheimer's Disease
Neurol 48:978-985, Kaufer,D.I.,et al, 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Frontotemporal Dementia and Early Alzheimer Disease:Differentiation with Frontal Lobe H-1 MR Spectroscopy
Radiology 203:829-836, Ernst,T.,et al, 1997

Clinical and Radiologic Findings in Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
AJNR 18:751-757, Cory,R.C.,et al, 1997

A 44-Month Clinical-Brain MRI Follow-Up in a Patient with B12 Deficiency
Neurol 49:878-881, Stojsavljevic,N.,et al, 1997



Showing articles 1250 to 1300 of 2615 << Previous Next >>