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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 650 to 700 of 1234 << Previous Next >>

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

MR Findings in Listerial Rhombencephalitis
AJNR 17:593-596, Alper,G.,et al, 1996

Lyme Neuroborreliosis Disguised as Normal Pressure Hydrocephalus
Neurol 46:1743-1745, Danek,A.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Falls and Urinary Incontinence in a 66-Year Old Woman
Lancet 347:1738, Yusuf,S.W.,et al, 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

Clinical Correlates of White Matter Findings on Cranial Magnetic Resonance Imaging of 3301 Elderly People
Stroke 27:1274-1282, 12691996., Longstreth,W.T.,et al, 1996

Treatment of Advanced Parkinson's Disease by Posterior GPi Pallidotomy:1-Year Results of a Pilot Study
Ann Neurol 40:355-366, 3411996., Baron,M.S.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Ataxic Hemiparesis and Hemiageusia from an Isolated Post-Traumatic Midbrain Lesion
Neurol 47:1348-1349, Johnson,T.M., 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

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996

Age on Onset, Sex, & Cardiomyopathy as Predictors of Disability and Survival in Friedreich's Disease
Neurol 47:1260-1264, DeMichele,G.,et al, 1996

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

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Neuroradiologic Aspects of Chester-Erdheim Disease
AJNR 16:735-740, Caparros-Lefebvre,D.,et al, 1995

Erdheim-Chester Disease and Slowly Progressive Cerebellar Dysfunction
JNNP 58:238-240, Fukazawa,T.,et al, 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Leukoencephalopathy with Swelling & A Discrepantly Mild Clinical Course in Eight Children
Ann Neurol 37:324-334, van der Knaap,M.S.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 1995

Improvement of Paraneoplastic Opsoclonus-Myoclonus After Protein A Column Therapy
NEJM 332:192, Nitschke,M.,et al, 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Syndromes of Pontine Base Infarction:A Clinical-Radiological Correlation Study
Stroke 26:950-955, Kim,J.S.,et al, 1995

Clinical and Topographical Range of Callosal Infarction:A Clinical and Radiological Correlation Study
JNNP 59:238-242, Giroud,M.&Duman,R., 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Neurotox of Antimicrob & Antimalarial Agents
In Intox of Nervous System, Part II, Handbk Clin Neurol, Elsevier Science 21 (65) :471., Moorhouse,D.F.,et al, 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Neuroblastoma-Associated Opsoclonus-Myoclonus Treated with IVIgG
J Pediatr 127:328-329, Petruzzi,M.J.&deAlarcon,P.A., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995



Showing articles 650 to 700 of 1234 << Previous Next >>