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Differential
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acquired immunodeficiency syndrome
acute ataxia of childhood
acute cerebellar ataxia
adverse drug reaction
alcohol, neurologic complications with
alcoholism
alien hand syndrome
alopecia
alternating rapid movement
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis-like syndrome
ankle reflex, absent
anterior horn cell disease
anterior tibial muscle weakness
anti citrullinated antibody
anti Yo antibody
anticholinergic drugs
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, mechanism of action of
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
antiviral agents
aphasia
apraxia
areflexia
arthralgia
arthropathy
arylsulfatase A
asterixis
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
attention deficit disorder with hyperactivity
autoantibodies
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
behavioral disorder
belching
benign essential tremor
benign essential tremor, refractory
benzodiazepine
beta adrenergic blocker
biologic markers
blindness
bradykinesia
brain atrophy
brain biopsy
CAG repeats
calcification, intracranial
carbamazepine
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
central nervous system, infection of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hemorrhage
cerebellar hypoplasia
cerebellar lesion
cerebellum, disease of
cerebral cortical atrophy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, enzymes in
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, red cells in
cerebrovascular accident
chest x-ray, abnormal
children
chills
chorea
chylomicron retention disease
cirrhosis
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cogwheel rigidty
Collier's sign
conduction block
confusion
consanguinity
conversion reaction
corpus callosum, lesion of
corpus callosum, thinning
cortical-basal ganglionic degeneration
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cyclophosphamide
deafness
decerebrate posture
degenerative diseases of CNS
dementia
dentate nuclei
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
differential diagnosis
difficulty going down stairs
dilantin
dilantin, factors influencing metabolism of
distal muscle weakness
doriden
drowsiness
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspnea
dystonia
dystonia, focal
dystonia, post traumatic
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, focal delta activity
electromyogram
encephalitis
entrapment neuropathy
enzyme, serum
erythema nodosum
exome sequencing
eye movement, disorders of
facial weakness
facial weakness, bilateral
failed medical management
falling
false positive VDRL
familial
fasciculation
fatigue
fever
fine motor function, impaired
finger nose finger test
fingerprint bodies
foot deformity
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
gait disorder
gamma amino butyric acid
gammaglobulin therapy, intravenous
gastrointestinal perforation
gaze palsy
gender
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
glucose tolerance test, abnormal
glycine
granular osmiphilic material
Guyon's canal
gynecomastia
hallucination
hammertoes
hand weakness
handwriting
head injury
head injury, delayed deterioration following
head nodding
headache
heavy metal intoxication
hemiplegia
hemochromatosis
hemochromatosis, primary
hepatic encephalopathy
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
hiccoughs
high arched feet
Huntington's chorea
hyperosmolality
hyperreflexia
hyperthyroidism
hypocalcemia
hypoparathyroidism
hyporeflexia
hypotonia
hypotonia, infants
imbalance
immunosuppressive agents
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
incoordination
infantile spasm
intellectual deficit
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Kernig's sign
Krabbe's disease
kuru plaques
lactic acidemia
lactic dehydrogenase(LDH)
laminectomy
laminectomy, lumbar
laughing, pathologic
leg weakness, bilateral
Leigh's disease
leukodystrophy
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
leukopenia
liver function enzymes
low back pain
lysosomal storage disease
memory, impairment of
meningeal enhancement
meningismus
meningitis, carcinomatous
meningoencephalitis
mental retardation
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
molecular genetics
mononeuropathy
mosquito
motor neuron disease
movement disorder
movement disorder, delayed onset
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, psychogenic
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, negative
multiple sclerosis
multiple sclerosis, treatment of
multiple system atrophy
muscle biopsy
muscle cramp
muscle stiffness
muscle weakness, proximal
myelinolysis, extrapontine
myelomalacia
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
mysoline
nausea and vomiting
negative
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuroaxonal leukodystrophy
neuroendocrinology
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuronal ceroid-lipofuscinosis
neuronal intranuclear inclusion disease
neuronopathy
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, peripheral
nursing home
nutritional deficiency
nystagmus
nystagmus, rotary
nystagmus, vertical
occupational neuropathies
oculogyric crisis
ophthalmoplegia
optic atrophy
optic neuropathy
optic neuropathy, bilateral
orthostatic hypotension
osmotic demyelination syndrome
pain, back
paraplegia
paresthesias
Parkinson disease
Parkinson disease, benign tremulous
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
past pointing
pericarditis
pes cavus
phlebotomy
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, neurologic problems with
polymerase chain reaction, false negative
polymyositis
pons, lesion of
postoperative neurologic complications
prevention of neurologic disorders
prognosis
progressive neurologic disorder
propranolol
prothrombin time, prolonged
psychosis
purpura
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rash
Raynaud's phenomenon
rectal biopsy
reflex sympathetic dystrophy
remote effect of cancer on the nervous system
respiratory myoclonus
respiratory tract infection
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rigidity
Sabin-Feldman dye test
saccadic eye movements, abnormal
sciatica
sedimentation rate, elevated
seizure
seizure, children
seizure, minor motor
seizure, petit mal
seizure, tonic-clonic
seizure, treatment of
serum glutamic oxaloacetic transaminase
skin, biopsy
skin, darkening of
sodium valproate
sodium valproate, toxicity
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
speech, loss of
spinocerebellar ataxia
spinocerebellar ataxia type 12
spinocerebellar ataxia type 3/Machado Joseph disease
splenomegaly
stage-fright
staggering
startle myoclonus
startle reaction
status epilepticus
stimulation, deep brain
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
stuttering
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
systemic lupus erythematosus, skin changes in
tandem gait, ataxic
tauopathy
terfenadine
tetany
thalamotomy
thalamus, focused ultrasound ablation
thrombocytopenia
thrombotic thrombocytopenia purpura
thyrotoxicosis
titubation
toe walking
tongue, fasciculations of
tonic foot response
torticollis, post traumatic
toxoplasma complement fixation test
toxoplasmosis, acquired
toxoplasmosis, CNS
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, classification
tremor, differential diagnosis of
tremor, intention
tremor, leg
tremor, orthostatic
tremor, physiologic
tremor, post traumatic
tremor, postural
tremor, psychogenic
tremor, resting
tremor, rubral
tremor, surgical treatment of
tremor, thalamic stimulation for suppression of
tremor, treatment of
tremor, voice
tremor, writing
trimethoprim-sulfamethoxazole
trinucleotide repeats
tripping
typing
ulnar nerve, compression of
ulnar neuropathy
urticaria
uveitis
vagus nerve stimulation
Venereal Disease Research Laboratory test
vertigo
viral infection
viral infection, CNS
visual loss
vitamin E deficiency
walking, delayed
walking, difficulty with
weakness
weight gain
weight loss
West Nile fever
wheelchair
white matter disease
wide based gait
workup
writers cramp
writing
X-linked bulbospinal neuronopathy
Showing articles 300 to 350 of 1263 << Previous Next >>

Long-Term Outcome of Bilateral Pallidal Deep Brain Stimulation for Primary Cervical Dystonia
Neurol 68:457-459, Hung,S.W.,et al, 2007

Comparison of Levetiracetam and Controlled-Release Carbamazepine in Newly Diagnosed Epilepsy
Neurol 68:402-408, Brodie,M.J.,et al, 2007

Clinical Update:Diagnosis and Treatment of Essential Tremor
Lancet 369:1152-1154, Benito-Leon,J&Louis,E.D., 2007

Pathological Gambling after Bilateral Subthalamic Nucleus Stimulation in Parkinson Disease
JNNP 78:517-519, Smeding,H.M.M.,et al, 2007

Orthostatic Myoclonus: A Contributor to Gait Decline in Selected Elderly
Neurol 68:1826-1830, Glass,G.A.,et al, 2007

A 46-Year-Old Woman With Severe Weakness Following Acute Respiratory Distress Syndrome
Neurol 68:1529-1535, Waclawik,A.J.,et al, 2007

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

Is DBS-STN Appropriate to Treat Severe Parkinson Disease in an Elderly Population?
Neurol 68:1345-1355, Derost,P.-P.,et al, 2007

Electromyographic Biofeedback for the Recovery of Motor Function After Stroke
Stroke 38:1999-2000, Woodford,H.J. &Price,C., 2007

Safety and Tolerability of Gene Therapy With an Adeno-Associated Virus (AAV) Borne GAD gene for Parkinsons Disease: An Open Label, Phase I Trial
Lancet 369:2097-2105,2056, Kaplitt,M.G.,et al, 2007

Treatment Options in the Modern Management of Parkinson Disease
Arch Neurol 64:1083-1088, Schapira,A.H.V., 2007

Deep Brain Stimulation
Neurologist 13:237-252, Kem,DS. &Kumar,R., 2007

Segmental Zoster Paresis of Limbs: Report of Three Cases and Review of Literature
Neurologist 13:313-317, Kawajiri,S.,et al, 2007

Acute Deep-Brain Stimulation of the Internal and External Globus Pallidus in Primary Dystonia: Functional Mapping of the Pallidum
Arch Neurol 64:1281-1286, Houeto,J.-L.,et al, 2007

A 75-Year-Old Man With Cognitive Impairment and Gait Changes, Lewy Body Disease
Neurol 69:1183-1189, Lippa,C.F.,et al, 2007

Kaleidoscopic Vision and a Jerking Leg on the Ski Slope
Lancet 370:1878, Kiechl,S.,et al, 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

HIV Infection Presenting with Motor Axonal Variant of Guillain-Barre Syndrome
J Clin Neuromusc Dis 9:303-305, Wagner, J.C. and Bromberg, M.B., 2007

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

The Clinical Spectrum of Neuralgic Amyotrophy in 246 cases
Brain 129:438-450, Alfen, N.V. & Baziel, G.M., 2006

What is the Risk of Developing Parkinsonism Following Neuroleptic Use?
Neurol 66:941-943, Noyes,K.,et al, 2006

Practice Parameter: Treatment of Parkinson Disease with Motor Fluctuations and Dyskinesia (An Evidence-Based Review)
Neurol 66:983-995, Pahwa,R.,et al, 2006

Phrenic Neuropathy Due to Neuralgic Amyotrophy
Neurol 66:1582-1584, Tsao,B.E.,et al, 2006

A Randomized Trial of Deep-Brain Stimulation for Parkinsons Disease
NEJM 355:896-908, Deuschl,G.,et al, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Fragile X Premutation With Atypical Symptoms at Onset
Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006

Common Misdiagnosis of a Common Neurological Disorder: How Are We Misdiagnosing Essential Tremor?
Arch Neurol 63:1100-1104, Jain,S.,et al, 2006

West Nile Virus Neuroinvasive Disease
Ann Neurol 60:286-300, Davis,L.E.,et al, 2006

Severe Botulism After Focal Injection of Botulinum Toxin
Neurol 67:1855-1856, Souayah,N.,et al, 2006

Case 35-2006: A Newborn Boy with Hypotonia
NEJM 355:2132-2142, Brown,R.H.,et al, 2006

Pallidal Deep-Brain Stimulation in Primary Generalized or Segmental Dystonia
NEJM 355:1978-1990, Kupsch,A.,et al, 2006

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Varicella Zoster Virus Cerebellitis in a 66-Year-Old Patient Without Herpes Zoster
Lancet 367:182, Ratzka,P.,et al, 2006

Suicide After Deep Brain Stimulation of the Internal Globus Pallidus for Dystonia
Neurol 66:142-143, Foncke,E.M.J.,et al, 2006

Cetirizine-Induced Dystonic Movements
Neurol 66:143-144, Rajput,A. &Baerg,K., 2006

Panic and Fear Induced by Deep Brain Stimulation
JNNP 77:410-412, Shapira,HN.A.,et al, 2006

Topiramate in Essential Tremor, A Double-Blind, Placebo-Controlled Trial
Neurol 66:672-677, Ondo,W.G.,et al, 2006

Etiological and Therapeutical Observations in a Case of Belly Dancers Dyskinesia
Movement Disorders 20:251-253, Linazasoro,G., et al, 2005

Cervical Radiculopathy
NEJM 353:392-399, Carette,S. &Fehlings,M.G., 2005

Initial Diagnoses Given to Persons with the Fragile X Associated Tremor/Ataxia Syndrome (FXTAS)
Neurol 65:299-301, Hall,D.A.,et al, 2005

Dysphagia as the Sole Manisfestation of Myasthenia Gravis
JNNP 76:1297-1300, Llabrs,M.,et al, 2005

Cluster Headache:Pathogenesis,Diagnosis, and Management
Lancet 366:843-855, May,A., 2005

Science and Ethics of Sham Surgery, A Survey of Parkinson Disease Clinical Researchers
Arch Neurol 62:1357-1360,1343, Kim,S.Y.H.,et al, 2005

Guillain-Barre Syndrome
Lancet 366:1653-1666, Hughes,R.C. &Comblath,D.R., 2005

Practice Parameter:Therapies for Essential Tremor
Neurol 64:2008-2020, Zesiewicz,T.A.,et al, 2005

Bi-Hemispheric Anterior Cerebral Artery with Drop Attacks and Limb Shaking TIAs
Neurol 65:174, Gerstner,E.,et al, 2005

A Variant in the HS1-BP3 Gene is Associated with Familial Essential Tremor
Neurol 64:417-421, Higgins, J.J., et al, 2005

Bilateral Deep-Brain Stimulation of the Globus Pallidus in Primary Generalized Dystonia
NEJM 352:5 459-467, 498, Vidailhet, M., et al, 2005

The Serotonin Syndrome
NEMJ 352:1112-20, Boyer, E.W. & Shannon, M., 2005

Chronic Inflammatory Demyelinating Polyneuropathy
NEJM 352:1343-1356, Koller,H.,et al, 2005



Showing articles 300 to 350 of 1263 << Previous Next >>