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Differential
(Click to cross reference)
adrenal mass
aggression
Aicardi-Goutieres syndrome
akinetic mute
Angelman syndrome
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
attention span
basal ganglia, calcification of
behavior, combative
behavioral disorder
benign essential tremor
brachycephaly
brainstem, lesion of
Brugada syndrome
calcification, intracranial
carcinoma
cardiac arrest
carotid artery occlusion, neck
CAT scan, abdomen
CAT scan, abnormal
catecholamine
cerebellar atrophy, primary
cerebellar hemangioma
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
children
chromosomal abnormality
chromosome 15
chromosome 19
chromosome 20
chromosome 20 ring
chromosome 3
Clinical Pathologic Conference(C.P.C.)
confidentiality
cyst
cyst, peritumoral
cyst, neoplastic cerebellum
cyst, parenchymal
deep gray nuclei
dementia
dementia, rapidly progressive
developmental milestones, loss of
developmental retardation
dexterity, impaired
drooling
dysarthria
dysmorphic
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
encephalopathy
endolymphatic sac tumors
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
familial
feeding disorder
fever
fish
fluorescene in situ hybridization
fundus, abnormality of
gait disorder
gene
gene mutation
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
headache
hearing loss
hearing loss, sudden, unilateral
hemangioblastoma
heralding manifestation
hydrocephalus
hyperactivity
hypertension
hypopigmentation of skin
hypotonia
interferon alpha
laughing, pathologic
leukoencephalopathy
macrognathia
medulla oblongata, lesion of
medulla oblongata, neoplasm of
mental retardation
microcephaly
molecular genetics
mortality
MRI
MRI, abdomen
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
muscular dystrophy
muscular dystrophy, classification
myopathy
myopathy, proximal
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neurocardiology
neurologic disease, diagnoses of
pancreatic cyst
pheochromocytoma
pleocytosis of cerebrospinal fluid
postural abnormality
prion disease
prion protein gene
prognathism
prognosis
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
proximal myotonic myopathy
radiation therapy, stereotactic
renal cell carcinoma
renal cyst
retinal hemangioma
retinal lesion
review article
seizure
skin, lesions in neurologic disorders
smiling
speech disorder
speech disorder, childhood
speech, delayed development of
spinal cord, lesion of
spinal cord, neoplasm
sudden death
syncope
syncope, recurrent
tandem gait, ataxic
teeth, wide-spaced
tinnitus
tongue, protrusion of
treatment of neurologic disorder
tremor
trinucleotide repeats
tumor suppressor gene
ventricular tachycardia
vertigo
Von Hippel Lindau
Von Hippel Lindau, screening protocol for
von Hippel-Lindau, screening
white matter disease
Showing articles 550 to 600 of 1417 << Previous Next >>

Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
BJR 73:256-265, Coulthard, A.,et al, 2000

Microscopic Polyangiitis: Clinical and Laboratory Findings in Eighty-five Patients
Arthritis Rheum 42:421--430, Guillevin, L.,et al, 1999

Diagnosis and Treatment of Wilson's Disease
Semin Neurol 19:261-270, Brewer,G.J.,et al, 1999

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

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

A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
Ann Neurol 46:671-678, Peiffer,A.,et al, 1999

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999

Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24
Neurol 53:1180-1183, Plaster,N.M.,et al, 1999

Treatment of Attention-Deficit-Hyperactivity Disorder
NEJM 340:780-788, Elia,J.,et al, 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

Clinicopath Conf,Wegener's Granulomatosis with Pachymeningeal Granulomatous Inflammation, Case 9-1999
NEJM 340:945-953, , 1999

Churg-Strauss Syndrome, Clinical Study and Long-Term Follow-Up of 96 Patients
Medicine 78:26-37, Guillevin,L.,et al, 1999

What Level of Care for the Neurofibromatoses?
Lancet 353:1114-1116, Huson,S.M., 1999

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999

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

Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
Neurol 53:629-631, Weil,S.,et al, 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Importance of Dural Ectasia in Phenotypic Assessment of Marfan's Syndrome
Lancet 354:910-913, 878, Fattori,R.,et al, 1999

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

New Developments in the Neurobiology of the Tuberous Sclerosis Complex
Neurol 53:1384-1390, Crino,P.B.&Henske,E.P., 1999

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,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

Difficult Asthma or Churg-Strauss Syndrome? Steroids May be Masking Undiagnosed Cases of Churg-Strauss Syndrome
BMJ 318:475-476, D'Cruz,D.P.,et al, 1999

Parkinson Disease in Twins,An Etiologic Study
JAMA 281:341-346,376, Tanner,C.M.,et al, 1999

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

Is There a Familial Carpal Tunnel Syndrome? An Evaluation and Literature Review
Muscle & Nerve 21:1533-1536, Gossett,J.G.&Change,P.F., 1998

Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
Circulation 97:2043-2048, Benson,D.W.,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

Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
Lancet 352:1892-1897, Labauge,P.,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

Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
Stroke 29:2507-2510, Ludemann,P.,et al, 1998

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,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

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Consumption of Fruit and Wine and the Decline in Cerebrovascular Disease Mortality in Spain (1975-1993)
Stroke 29:1556-1561, Artalejo,F.R.,et al, 1998

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

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

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

Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
JAMA 280:619-622, 6521998., Wu,W.S.,et al, 1998

Evidence for an Alzheimer Disease Susceptability Locus on Chromosome 12 and for Further Locus Heterogeneity
JAMA 280:614-618, 6521998., Rogaeva,E.,et al, 1998

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,et al, 1998

Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
Lancet 351:1081-1085, Van Duijn,C.M.,et al, 1998

Inclusion Body Myositis in Twins
Neurol 51:598-600, Amato,A.A.&Shebert,R.T., 1998

Effects of Prenatal & Postnatal Methylmercury Exposure from Fish Consump on Neurodevelop; Outcomes at 66 Months
JAMA 280:701-707, 7371998., Davidson,P.W.,et al, 1998

Learning & Memory Diff After Environ Exp to Waterways Cont Toxin-Producing Pfiesteria/Pfiesteria-Like Dinoflagellates
Lancet 352:532-539, Grattan,L.M.,et al, 1998

Hereditary Form of Parkinsonism-Dementia
Ann Neurol 43:768-781, Muenter,M.D.,et al, 1998

Facial Nerve is Liable to Pressure Palsy
Neurol 51:320-322, Foloni,T.E.,et al, 1998



Showing articles 550 to 600 of 1417 << Previous Next >>