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Differential
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abducens nerve paralysis
acetylcholine
acoustic nerve
advances in neurology
alcohol intolerance
alkylating agents
altered states of consciousness
Alzheimer's disease
anticholinesterase
antimetabolite
areflexia
asparginase
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
atonic bladder
auditory evoked brainstem potentials
autonomic dysfunction
Babinski sign
baclofen
blindness
blood dyscrasias, neurologic findings with
bradykinesia
brainstem, atrophy
CAG repeats
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
cerebrospinal fluid, pressure low
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chorea
chromosome 14
chromosome 6
Clinical Pathologic Conference(C.P.C.)
controversies in neurology
cranial neuropathy, multiple
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
depression
diplopia
down-beat nystagmus, primary position of gaze
dysarthria
encephalopathy
enzyme, defect
evoked potentials
excitotoxin
facial nerve palsy, bilateral
facial pain
familial
fever
fluorouracil
flush syndrome
foot drop
fragile-X syndrome
Friedreich's ataxia
gait disorder
gaze palsy, supranuclear
gene mutation
genetic neurologic disorders
genetic screening
genetic testing
glutamate dehydrogenase deficiency
glutamic acid
hallucination
headache
HLA
hot cross bun sign
huntingtin
Huntington's chorea
hydroxytryptophan L-5(L-5 HTP)
hyponatremia
hypoxia
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
incoordination
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
isoniazid
jaw pain
Korsakoff's psychosis
L-dopa
leukemia, neurologic findings assoc.with
leukoencephalopathy
life expectancy
macular degeneration
meningismus
meningoencephalopathy
methotrexate
methylhydrazine derivatives
molecular genetics
monoamine oxidase inhibitors
movement disorder, extrapyramidal
MRI
MRI, abnormal
multiple system atrophy
muscle pain
muscle weakness
myelomalacia
myoclonic jerks
myotonia dystrophica
nausea and vomiting
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neurotoxin
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nitrogen mustard
nystagmus
ocular motility, disorders of
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optic atrophy
orthostatic hypotension
pain
palatal myoclonus
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paresthesias
Parkinson disease
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
physostigmine
pleocytosis of cerebrospinal fluid
pons, atrophy
pontocerebellar atrophy
procarbazine
prognosis
pseudobulbar palsy
psychological testing
psychological testing, neurologic problems
ptosis
ptosis, bilateral
Purkinje cell
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
retinal degeneration
retinitis pigmentosa
review article
seizure
Shy-Drager syndrome
sleep apnea
sleep pathology and physiology
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinopontine atrophy, dominant
striatonigral degeneration
strokelike episodes
symmetric brain lesions
tinnitus
transient neurologic deficit
trazodone
treatment of neurologic disorder
trinucleotide repeats
vinblastine
vincristine neurotoxicity
vocal cord paralysis
white matter disease
wrist drop
X-linked bulbospinal neuronopathy
Showing articles 600 to 650 of 1306 << Previous Next >>

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 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

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Multiple Sclerosis in Children Under 6 Years of Age
Neurol 53:478-484, Ruggieri,M.,et al, 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Clinicopath Conf,Multifocal Inflammatory Leukoencephalopathy Related to Combination Chemo with Fluorouracil/levamisole
NEJM 341:512-519, Case 24-1999, 1999

Dancing Eyes-Dancing Feet
Lancet 354:390, Imtiaz,K.E.&Vora,J.P., 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

A Man with Progressive Weakness in His Legs
Lancet 354:830, van der Meulen,M.F.G.,et al, 1999

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

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

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

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

Opsoclonus as a Dominant Sign in Primary Sjogrens Syndrome
Neuro-Opthlhal 22:135-138, Lubec,D.,et al, 1999

Pseudochoreoathetosis in Four Patients with Hypesthetic Ataxic Hemiparesis in a Thalamic Lesion
J Neurol 246:1075-1079, Kim, J.W., et al, 1999

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Neurology and the Blood:Haematological Abnormalities in Ischaemic Stroke
JNNP 64:150-159, Markus,H.S.&Hambley,H., 1998

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

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Risk of Cerebral Sinus Thrombosis in Oral Contraceptive Users Who Are Carriers of Hered Prothrombotic Cond
BMJ 316:589-592, deBruijn,S.F.T.M.,et al, 1998

Characteristic Magnetic Resonance Imaging Findings in Machado-Joseph Disease
Arch Neurol 55:33-37, Murata,Y.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,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

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

Serum S-100 and Neuron-Specific Enolase for Prediction of Regaining Consciousness After Global Cerebral Ischemia
Stroke 29:2363-2366, Martens,P.,et al, 1998

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

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

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998



Showing articles 600 to 650 of 1306 << Previous Next >>