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acetazolamide
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
akinetic mute
alternating rapid movement
alternating rapid movement, impaired
amyotrophic lateral sclerosis
anorexia
areflexia
arm swing, reduced
arrhythmia, cardiac
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic hemiparesis
atrial fibrillation
attention deficit disorder with hyperactivity
attention span
Babinski sign
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
biologic markers
bone marrow transplantation
bradykinesia
brain atrophy
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
brainstem, syndrome
cardiomyopathy
CAT scan
CAT scan, abnormal
cataplexy
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral palsy
cerebral palsy, associated problems with
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congestive heart failure
consanguinity
corona radiata
cortical-basal ganglionic degeneration
cough
cranial neuropathy
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, rapidly progressive
depression
developmental milestones, loss of
dexterity, impaired
diabetes mellitus
diarrhea
diplopia
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drooling
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
electroencephalogram, abnormalities of
electromyogram
electrophoretic pattern, CSF
embolism
encephalitis
encephalopathy
epileptic encephalopathy
exome sequencing
eye movement, disorders of
failure to thrive
falling
familial
familial periodic ataxia
FARS2 deficiency
fatigue
fine motor function, impaired
finger nose finger test
finger numbness
foam cells
foot drop
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
glabellar sign
granular osmiphilic material
hammertoes
handwriting
head nodding
headache
hearing loss
heel-knee-shin test
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
heralding manifestation
hormone replacement
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hypertonia
hypogonadism
hypogonadism, hypogonadotropic
hypometric saccades
hypotonia
iatrogenic neurologic disorders
imbalance
immunohistochemistry
inattention
incoordination
inferior olivary nucleus
insomnia
intellectual deficit
intellectual deterioration
intelligence quotient
internal capsule
introverted
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
jaundice
Kayser-Fleischer ring
lacunar infarction
lacunar infarction, differential diagnosis of
lateropulsion
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
Lorenzo's oil
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
medulla oblongata, neoplasm of
memory, defect of recent
memory, impairment of
meningitis, CSF cell count-normal
microcephaly
midbrain, atrophy
misdiagnosis
mitochondrial disease
molecular genetics
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, negative
MRI, spinal cord
MRI, spine
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
myelomalacia
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
nausea and vomiting
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve conduction studies
neurofibrillary degeneration
neurofibromatosis 1
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, sensory
next-generation sequencing
Niemann-Pick disease
numb clumsy hands syndrome
nystagmus
ocular motility, disorders of
olivary degeneration, hypertrophic
optic atrophy
ovarian dysgenesis
palatal myoclonus
paraparesis
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
Perrault syndrome
personality change
pes cavus
pons, infarction of
pontine hemorrhage
positional head-hanging test
prevention of neurologic disorders
prion disease
prion protein gene
prognosis
progressive ataxia and palatal tremor
progressive myoclonic epilepsy
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychosis
pure dysarthria
pure motor hemiplegia
pursuit eye movements, abnormal
pyramidal tract dysfunction
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
release phenomena
retropulsion
review article
rigidity
risk factors
Romberg's sign
rubella encephalitis
rubella encephalitis, progressive
rubella virus
saccadic eye movements, abnormal
scoliosis
seizure
seizure, children
sensorimotor stroke
sensorineural hearing loss
sensory loss
serologic testing
serologic testing of cerebrospinal fluid
slit lamp examination
slurred speech
spastic ataxia
spastic diplegia
spasticity
speech disorder
speech disorder, non aphasic
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
splenomegaly
spontaneous remission
square wave jerks
staggering
strokelike episodes
suck reflex
superior cerebellar artery infarction
superior cerebellar artery syndrome
symmetric brain lesions
tandem gait, ataxic
tau protein
tauopathy
thalamus, lesion of-bilateral
titubation
toe walking
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
upgaze, paralysis of
vertigo
vertigo, episodic
very long chain fatty acids
vestibulopathy
vibratory sensation, abnormal
viral infection, CNS
vision, blurred
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, progressive
weight loss
white matter disease
wide based gait
workup
Showing articles 50 to 100 of 1064 << Previous Next >>

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

The Useless Hand of Oppenheim
Pract Neurol 17:464-468, Wiblin, L. & Guadagno, J., 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

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

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Uremic Encephalopathy
Adams & Victors Principles of Neurology Chp 40, pg 1145, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Mercury
Adams & Victors Principles of Neurology Chp 43, pg 1223, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
Adams & Victors Principles of Neurology, Chp 37, pg 968, 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

A Man with Tingling Fingers
BMJ 346:f1443, Larkman, M.,et al, 2013

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

Early Child Development and Exposure to Antiepileptic Drugs Prenatally and Through Breastfeeding
JAMA Neurol 70:1367-1374, Veiby, G.,et al, 2013

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Validation of the Coin Rotation Test: A Simple, Inexpensive, and Convenient Screening Tool for Impaired Psychomotor Processing Speed
Neurologist 16:249-253, Hill,B.D., et al, 2010

Parkinsons Disease
Lancet 373:2055-2066, Lees,A.J.,et al, 2009

Motor Development in Very Preterm and Very Low-Birth-Weight Children From Birth to Adolescence: A Meta-Analysis
JAMA 302:2235-2242, 2257, De Kieviet,J.,et al, 2009

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Clinicopath Conf., Severe Microangiopathy of Diabetic Vasculopathy with Multiple Cerebral Infarcts
NEJM 357:164-173, Case Study 21-2007, 2007

Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
J Neurol 254:1609-1611, Collison,K. and Rees,J., 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Reversible Corpus Callosum Lesion in Legionnaires Disease
JNNP 75:651-654, Morgan, J.C.,et al, 2004

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

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

Clumsiness, Confusion, Coma, and Valproate
Lancet 353:1408, Ellaway,C.J.,et al, 1999

Bilateral Thalamic Stimulation for the Treatment of Essential Tremor
Neurol 53:1447-1450, Pahwa,R.,et al, 1999

Metabolic Abnormalities in Development Dyslexia Detected by 1H Magnetic Resonance Spectroscopy
Lancet 351:1849-1852, Rae,C.,et al, 1998

Incoordination in Patients with Overuse Syndrome
Neurol 51:512-519, Fry,H.J.H.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

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

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Neuroimaging Findings in Patients on Immunosuppressive Therapy:Experience with Tacrolimus Toxicity
AJR 166:683-688, Appignani,B.A.,et al, 1996

Midcervical Central Cord Syndrome:Numb & Clumsy Hands Due to Midline Cervical Disc Protrusion at C3-4 Intervert Level
JNNP 58:607-613, Nakajima,M.&Hirayama,K., 1995

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

'Anesthesia Paresthetica':Nitrous Oxide-Induced Cobalamin Deficiency
Neurol 45:1608-1610, 14351995., Kinsella,L.J.&Green,R., 1995

Initial and Follow-up Brain MRI Findings and Correlation with the Clinical Course in Wilson's Disease
Neurol 44:1064-1068, Roh,J.K.,et al, 1994



Showing articles 50 to 100 of 1064 << Previous Next >>