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Differential
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agraphia
akinesia
akinesia of eyelid function
alexia
alpha-fetoprotein
Alzheimer's disease, visual variant
aminoacidurias
ANA
anomic aphasia
anterior cerebral artery
anterior cerebral artery territory infarction
anterior cerebral artery, occlusion, language disorder with
aphasia
aphasia, children
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apraxia
apraxia of eye movements
apraxia of eyelid closure
apraxia of eyelid opening
apraxia, constructional
apraxia, speech
arthritis
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
attention deficit disorder with hyperactivity
autism
automobile accidents
Benedict's solution test
bifid uvula
blepharospasm
brain biopsy
bruxism
calcification, intracranial
carcinoembryonic antigen
carcinoma
carotid artery disease
carotid artery occlusion, bilateral
carotid artery occlusion, neck
carphology
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral arteries, territory of
cerebral cortical atrophy
cerebral infarction
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrovascular accident
cerebrovascular accident, bilateral
Charcot's sign
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cleft palate
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
confusion
cortical-basal ganglionic degeneration
degenerative diseases of CNS
dementia
dementia, childhood
dementia, frontotemporal
dementia, presenile
diabetes mellitus
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
drooling
dysarthria
dysphagia
dysplasia of C.N.S.
dystonia
ecchymoses
electroencephalogram
encephalitis
encephalitis, viral
executive dysfunction
extrapyramidal movement disorder, progressive
eye closure
eye movement, disorders of
familial
ferric chloride test
fever
frontal lobe, pathologic signs of
gag reflex, depressed
gait disorder
gait, apraxic
gaze palsy
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
growth retardation
handwriting
hearing problems in children
hemianopia, homonymous
hemiparesis
hypertension
hypotonia
immunodeficiency
immunosuppression
immunosuppressive agents
in situ hybridization
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intelligence quotient
jaw jerk, abnormal
karyotyping
klippel feil syndrome
language disorder in adults
language disorders in children
L-dopa
leukemia
lid
lid abnormalities
lobar atrophy
lymphoma
maple syrup urine disease
masked facies
memory, impairment of
mental retardation
microaneurysm, retinal
micrographia
midline defect in children
misdiagnosis
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, serial
multiple system atrophy
mutism
myelodysplasia
myoclonus
myoclonus, stimulus sensitive
nasal speech
neglect
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic examination, focal
neuropathology
neuropathology, brain
neuropathy
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
palatopharyngeal incompetence
Parkinson disease
Parkinsonism syndrome
pathology
personality change
phenylketonuria
Pick bodies
Pick's disease
pneumonia
polymerase chain reaction
posterior cortical atrophy
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
ptosis
pure akinesia
radiation hypersensitivity
release phenomena
respirations in CNS disease
retropulsion
Rett's syndrome
review article
rigidity
rocking
scoliosis
seizure
seizure, advice to parents and teachers regarding
seizure, psychosocial aspects of
seizure, treatment of
semantic dementia
simultanagnosia
single photon emission computed tomography
skin, lesions in neurologic disorders
somnolence
speech disorder
speech disorder, childhood
speech, loss of
spina bifida
spinal muscular atrophy
steroid therapy, CNS treatment and complications with
stuttering
systemic lupus erythematosus
tachycardia
tauopathy
telangiectases
temporal lobe, atrophy
thrombocytopenia
urinary incontinence
urine test for metabolic disorders
visual field defect
visuospatial disturbance
walking, difficulty with
wheelchair
white matter disease
word-finding difficulty
Showing articles 150 to 200 of 608 << Previous Next >>

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Legionella
Adams & Victors Principles of Neurology, Chp 32, pg 709, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Infantile Gaucher Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 982, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Alzheimer Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1063, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Parkinson Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1082, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1096, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Dystonia Musculorum Deformans
Adams & Victors Principles of Neurology, Chp 39, pg 1099, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Friedreich Ataxia
Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Cerebellar Degeneration
Adams & Victors Principles of Neurology, Chp 39, pg 1105, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

A Syndrome of Bilateral Symmetrical Basal Ganglia Lesions in Diabetic Dialysis Patients
Am J Kidney Dis 63: 286-288, Finelli, P.F. & Singh, J.U., 2014

Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease
Neurol 82:49-56, Graff-Radford, J.,et al, 2014

Progressive Cerebellar Ataxia and New-Onset Diabetes
Lancet 383:186, Kong, M.,et al, 2014

Progressive Visuospatial Problems in a 71-Year-Old Man
Neurol 83:e6-e10, Symmonds, M.,et al, 2014

Visuoperception Test Predicts Pathologic Diagnosis of Alzheimer Disease in Corticobasal Syndrome
Neurol 83:510-519, Boyd, C.D.,et al, 2014

Motor Neurone Disease
BMJ 349:g4052, Nageshwaran, S.,et al, 2014

A 32-year-old Woman with Right-Sided Numbness and Word-Finding Difficulties
Neurol 83:e98-e102, Busza, A.,et al, 2014

An Unusual Headache
BMJ 349:g5602, Graham, U.M.,et al, 2014

A Cause of Intractable Vomiting
Neurol 83:e141-e144, Yeo, L.L.L.,et al, 2014

A 75-year-old man with 3 years of Visual Difficulties
Neurol 83:e160-e165, Berkowitz, A.L.,et al, 2014

Primary Sjogren Syndrome Presenting as Isolated Lesion of Medulla Oblongata
Neurol 84:e5-e6, Chen, J.,et al, 2014

Juvenile Myasthenia Gravis: Recommendations for Diagnostic Approaches and Treatment
Neuropediatrics 45:75-83, Marina, A.D.,et al, 2014

Gait Freezing and Speech Disturbance in Parkinsons Disease
Neurol Sci 35:357-363, Park,H.K.,et al, 2014

A Creutzfeldt-Jakob Disease Case Presenting with Psychiatric Symptoms
JNBS doi:10.5455/JNBS.1386249156, Aslan,A.A.,et al, 2014

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

Extensive Striatal, Cortical, and White Matter Brain MRI Abnormalities in Wilson Disease
Neurol 81:1557, Trocello, J.M.,et al, 2013

A Welsh-Sparing Dysphasia
Lancet 382: 1608, Rice, S.P.,et al, 2013

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Limbic Encephalitis as the Presenting Feature of Sj�gren Syndrome
Neurol Clin Pract 3:165-167, Finelli, P. & Inoa, V., 2013

Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
MSJ 17:1107-1112, Kim, W.,et al, 2013

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Visuospatial deficits in posterior cortical atrophy: structural and functional correlates
JNNP 83:860-863,855, Andrade, K.,et al, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Clinicopathologic Conference, Acute Ischemic Stroke due to Basilar Artery Embolism. Patent Foramen Ovale
NEJM 367:1450-1460, Case 31-2012, 2012

Myasthenia Gravis
BMJ 345:e8497, Spillane, J.,et al, 2012

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

Folic Acid Supplements in Pregnancy and Severe Language Delay in Children
JAMA 36:1566-1573, Roth, C.,et al, 2011

A Strange Case of Waitress Headache
Lancet 378:1824, Libera, D.D.,et al, 2011

Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Clinical and Radiological Features of Rotavirus Cerebellitis
AJNR 31:1591-1595, Takanashi,J.,et al, 2010



Showing articles 150 to 200 of 608 << Previous Next >>