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Differential
(Click to cross reference)
abscess, intracerebral
acanthosis nigricans
alpha-fetoprotein
anemia
apraxia of eye movements
areflexia
Arnold Chiari malformation
arteriovenous malformation
arteriovenous malformation, pulmonary
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
athetosis
autoimmune disease
biologic markers
blood dyscrasias, neurologic findings with
brain biopsy
brain biopsy, stereotaxic
cafe au lait spots
carcinoembryonic antigen
carcinoma
carcinoma of breast
CAT scan
CAT scan, abnormal
CAT scan, chest
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
cerebral palsy
cerebrospinal fluid, xanthochromia of
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cisterna magna
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
C-reactive protein, elevated
degenerative diseases of CNS
dental procedure, neurologic complications with
diabetes mellitus
DiGeorge syndrome
drooling
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dystonia
electromyogram
electronystagmography
electrophoretic pattern, serum
epistaxis
Epstein-Barr virus
eye movement, disorders of
familial
fistula, arterio-venous, pulmonary
fourth ventricle, enlargement of
Friedreich's ataxia
gait disorder
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glioma
gray hair
growth retardation
head injury
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
hereditary hemorrhagic telangiectasia(HHT)
hyperglycemia
hypogonadism
hypotonia
imbalance
immunodeficiency
immunoelectrophoresis, serum
immunologic disease
immunosuppression
incoordination
infection
insulin resistance
Leigh's disease
leukemia
leukemia, neurologic findings assoc.with
leukocytosis
leukoencephalopathy
lipid storage disorder of CNS
liver disease
lymphadenopathy
lymphoma
Marinesco-Sjogren syndrome
masked facies
meningismus
mental retardation
microhemorrhage, intracerebral
misdiagnosis
mitral valve prolapse
molecular genetics
mongolism
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, hypointense signal foci on
MRI, negative
MRI, perfusion
MRS
multiple sclerosis
multiple system atrophy
myelomalacia
neoplasm, primary intracerebral
nerve biopsy
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination, focal
neuropathology
neuropathy
nystagmus
ocular motility, disorders of
ophthalmoplegia
optokinetic nystagmus(O.K.N.)
papilledema
pathology
pneumonia
poliomyelitis
poliomyelitis vaccine
polyneuropathy
progeria
prognosis
progressive neurologic disorder
pulmonary infection
pulmonary infiltrates
radiation hypersensitivity
remote effect of cancer on the nervous system
review article
risk factors
saccadic eye movements
saccadic eye movements, abnormal
scannig speech
skin, darkening of
skin, lesions in neurologic disorders
slurred speech
spinal muscular atrophy
spinocerebellar degeneration
staggering
tandem gait, ataxic
telangiectases
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
vaccination, neurologic complications with
vaccine
vertigo
viral infection
viral infection, CNS
vitamin E deficiency
vitiligo
Von Hippel Lindau
walking, difficulty with
weight loss
wheelchair
white matter disease
workup
Showing articles 550 to 600 of 1080 << Previous Next >>

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

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

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Development of Wernicke-Korsakoff Syndrome After Long Intervals Following Gastrectomy
Arch Neurol 55:1242-1245, Shimomura,T.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

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

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

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

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

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

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

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

A Case-Control and Nerve Biopsy Study of CREST Mutliple Mononeuropathy
Neurol 49:1641-1645, Dyck,P.J.B.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 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

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,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

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Perimesencephalic Nonaneurysmal Subarachnoid Hemorrhage:First Hint of a Cause
Neurol 49:634-636, Wijdicks,E.F.M.&Schievink,W.I., 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

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

Balance in the Healthy Elderly
Arch Neurol 54:976-981, Camicioli,R.,et al, 1997

Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
Neurol 49:1131-1133, Chinnery,P.F.,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

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

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

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

An Emotional 13-Year Old Girl
Lancet 348:1000, Kanabar,D.J.,et al, 1996

Total Alopecia, Diabetes Mellitus, and Falls
Lancet 348:1420, Mueller-Schoop,J.W., 1996

Cytomegalovirus Encephalitis
Ann Int Med 125:577-578, Arribas,J.R.,et al, 1996

Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996

Clinicopath Conf
Q Fever, Acute (with Cerebellar and Meningeal Involvement) , Case 38-1996, NEJM 335:1829-1834., , 1996

Exceptional Multiplicity of Cerebral AVMs Assoc with Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
AJNR 17:1733-1742, Putman,C.M.,et al, 1996



Showing articles 550 to 600 of 1080 << Previous Next >>