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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
neurotransmitter
nitrogen mustard
nystagmus
ocular motility, disorders of
ophthalmoplegia
optic atrophy
orthostatic hypotension
pain
palatal myoclonus
paraparesis
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 500 to 550 of 1285 << Previous Next >>

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Autoantibodies to Glutamic Acid Decarboxylase in Downbeat Nystagmus
JNNP 74:998-999, Antonini,G.,et al, 2003

Silent Infarcts Demonstrated by Diffusion-Weighted MRI in CADASIL
Eur Neurol 49: 178-180, Moon,S.Y.,et al, 2003

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

Does This Patient Have Parkinson Disease?
JAMA 289:347-353, Rao,G.,et al, 2003

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

Cerebellar Ataxia and Coenzyme Q10 Deficiency
Neurol 60:1206-1208, Lamperti,C.,et al, 2003

Prevalence of Antigliadin Antibodies in Ataxia Patients
Neurol 60:1674-1675,1566, Abele,M.,et al, 2003

Neurologic Manifestations of Vitamin B12 Deficiency
NEJM 348:2208, Scherer,K., 2003

Pernicious Anemia with Neuropsychiatric Dysfunction in a Patient with Sickle Cell Anemia Treated with Folate Supplementation
NEJM 348:2204-2207, Dhar,M.,et al, 2003

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

Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
Medicine 82:216-223, Rojas-Marcos,I.,et al, 2003

Mitochondrial Respiratory-Chain Diseases
NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003

A Longitudinal Study of Gait and Balance Dysfunction in Normal Older People
Arch Neurol 60:835-839, Baloh,R.W.,et al, 2003

Clinicopath Conf., Giant-Cell Arteritis
NEJM 349:170-180, Case 21-2003, 2003

Clinical Manifestations of Sarin Nerve Gas Exposure
JAMA 290:659-662, Lee,E.C., 2003

Biochemical And Clinical Aspects of Methotrexate Neurotoxicity
Chemotherapy 49:92-104, Vezmar,S.,et al, 2003

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

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

Paraneoplastic Syndromes Involving the Nervous System
NEJM 349:1543-1554, Darnell,R.B. &Posner,J.B., 2003

Spinal Dural Arteriovenous Fistulas: Clinical Features in 80 Patients
JNNP 74:1438-1440, Jellema,K.,et al, 2003

Symmetric Deep Cerebellar Lesions After Smoking Heroin
Arch Neurol 60:1605-1606, Ropper,A.H. &Blair,R., 2003

Reversible Metronidazole-Induced Lesions of the Cerebellar Dentate Nuclei
NEJM 346:68-69, Woodruff,B.K.,et al, 2002

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

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Friedreich Ataxia
Arch Neurol 59:743-747, Lynch,D.R.,et al, 2002

Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002

Opsoclonus-myoclonus Syndrome Following Epstein-Barr Virus Infection
Neurol 58:1131-1132, Verma,A. &Brozman,B., 2002

Nanging
Lancet 360:384, Ng, J. &Frith, R., 2002

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

Mycoplasma Pneumoniae Encephalitis in Childhood
J Microbiol Immunol Infect 35:173-178, Lin,W.-C., et al, 2002

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Legionella Infection
emedicine.com, Mobeen,R., 2002

Clinicopath Conf., Acute Disseminated Encephalomyelitis
NEJM 347:1433-1440, Case 34-2002, 2002

Abnormality of Gait as a Predictor of Non-Alzheimer's Dementia
NEJM 347:1761-1768, Verghese,J.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Neurological Complications of Coeliac Disease
Postgrad Med J 78:393-398, Tengah, D.S.N.A.,et al, 2002

Neurology of Ciguatera
JNNP 70:4-8, Pearn,J., 2001

Clinicopath Conf, Lymphocytic Meningitis and Lymphocytic Encephalomyelitis, Sensory Neuronopathy, Gangliositis, Small-Cell Carcinoma of Lung
NEJM 345:1758-1765, Case 38-2001, 2001

Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
Ann Neurol 50:812-815, Shan,D.,et al, 2001

Bilateral Abducens Nerve Paresis Associated with Anti-GQ1b IgG Antibody
Am J Ophthalmol 131:816-818, Sato, K. and Yoshikawa, H., 2001

Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
JNNP 71:81-87, Selim, M. and Drachman, D.A., 2001

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

Effects of Bilateral Subthalamic Nucleus Stimulation on Parkinsonian Gait
Neurol 57:144-146, Stolze,H.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
Neurol 56:385-388, Hadjivassiliou,M.,et al, 2001

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001



Showing articles 500 to 550 of 1285 << Previous Next >>