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Differential
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adverse drug reaction
alopecia
alternating rapid movement
anti IgLON5
anticholinergic drugs
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, mechanism of action of
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
anxiety
apnea
apraxia
ataxia
ataxia, truncal
ataxic gait
athetosis
autoantibodies
autoimmune disease
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, lesion of
behavioral disorder
behavioral disorder, acute
belching
bradykinesia
brain biopsy
brain scan
bulbar palsy
carbamazepine
cardiac arrest
cardiac arrest and resuscitation
CAT scan, abnormal
cerebellar atrophy, primary
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid
cerebrospinal fluid, hydroxyindoleacetic acid, 5(5-HIAA)
cerebrospinal fluid, lactic acid concentration
children
chorea
chromosomal abnormality
chromosome 7
Clinical Pathologic Conference(C.P.C.)
clonazepam
clonus
cognition
cogwheel rigidty
coma
coma, episodic
confusion
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, reversible
dementia, treatment of
developmental milestones
developmental milestones, loss of
disability, neurological
drug induced neurologic disorders
drug overdose
dysmetria
dysphagia
dyspnea
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, anoxic
encephalopathy, delayed
encephalopathy, Hashimoto's
encephalopathy, post anoxic
episodic disorders
episodic neurologic deficits
episodic unconsciousness
epsilon sarcoglycan gene
extrapyramidal
falling
familial
fasciculation
fine motor function, impaired
fingerprint bodies
Fisher C.M.
gait disorder
gamma amino butyric acid
gammaglobulin therapy, intravenous
gene
gene mutation
genetic neurologic disorders
glutamic acid decarboxylase, antibody
glycine
granular osmiphilic material
handwriting
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hiccoughs
hoarseness
Huntington's chorea
hyperreflexia
hypersomnia
hypertonia
hypophonia
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunotherapy
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinence, fecal
infantile spasm
intellectual deficit
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
kuru plaques
lactic acidemia
leg spasms, painful
Leigh's disease
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
life support, withdrawal of
lithium
memory, impairment of
mental status, abnormal
misdiagnosis
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, treatment of
MRI
MRI, abnormal
MRI, disappearing lesion on
muscle spasm
muscle twitching
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, epilepsy
myoclonus, post anoxic
myoclonus, sleep
myoclonus, stimulus sensitive
myoclonus, treatment of
negative
neuroaxonal leukodystrophy
neuromuscular disease, electrodiagnosis of
neuronal ceroid-lipofuscinosis
neuropathology
neurotoxic
nystagmus
nystagmus, rotary
old age, neurology of
optic atrophy
orthostatic hypotension
Parkinson disease
Parkinsonism syndrome
paroxysmal neurologic disorder
PAS positive
PAS positive material in the brain
personality change
pheneturide
piracetam
prognosis
progressive encephalomyelitis with rigidity syndrome
progressive neurologic disorder
psychiatric problems in neurologic disorders
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
REM sleep behavior disorder
respiratory failure
respiratory myoclonus
rigidity
Romberg's sign
seizure
seizure, children
seizure, minor motor
seizure, petit mal
seizure, tonic-clonic
seizure, treatment of
sleep pathology and physiology
sodium valproate
sodium valproate, toxicity
spastic dysphonia
spasticity
speech disorder
speech, loss of
startle myoclonus
startle reaction
status epilepticus
status epilepticus, myoclonic
stiripentol
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
stuttering
tandem gait, ataxic
thalamus
titubation
treatment of neurologic disorder
tremor
tremor, intention
tremor, writing
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
urinary retention
viral infection, CNS
vocalizations
walking, difficulty with
wheelchair
writers cramp
writing
Showing articles 200 to 250 of 816 << Previous Next >>

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Essential Palatal Myoclonus
NEJM 362:e64, Scozzafava,J. &Yager,J., 2010

Predictors of Neurologic Outcome in Hypothermia After Cardiac Arrest
Ann Neurol 68:907-914, Fugate,J.E.,et al, 2010

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Paraneoplastic Syndromes Affecting Brain and Cranial Nerves
UpToDate May 2009, Dalmau,J. &Rosenfeld,M., 2009

A Fisherman Who Could Not Row
Lancet 373:432, Das,A.,et al, 2009

Diagnosis and New Treatment in Muscle Channelopathies
JNNP 80:360-365, Meola,G.,et al, 2009

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Opsoclonus-Myoclonus Syndrome Asssociated with Benign Ovarian Teratoma
Neurol 70:1292-1293, Fitzpatrick,A.S.,et al, 2008

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
Arch Neurol 65:1341-1346, Geschwind,M.D.,et al, 2008

Statin Induced Myopathy
BMJ 337:1159-1162, Sathasivam,S. &Lecky,B., 2008

Opsoclonus-Myoclonus-Ataxia Syndrome with Autoantibodies to Glutamic Acid Decarboxylase
Clin Neurol Neurosurg 110:619-621, Markakis,I.,et al, 2008

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

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

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

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

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

Tiagabine-Induced Myoclonic Status Epilepticus in a Nonepileptic Patient
Neurol 68:310, Vollmar,C. &Noachtar,S., 2007

CNS Lupus: A Study of 41 Patients
Neurol 69:644-654, Joseph,F.G.,et al, 2007

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

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 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

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Benign Tremulous Parkinsonism
Arch Neurol 63:354-357,321, Josephs,K.A.,et al, 2006

Adult Onset Subacute Sclerosing Panencephalitis: Clinical Profile of 39 Patients From a Tertiary Care Centre
JNNP 77:630-633, Prashanth,L.K.,et al, 2006

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

Opsoclonus Persisting During Sleep in West Nile Encephalitis
Arch Neurol 63:1324-1326, Alshekhlee,A.,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

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

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

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Febrile Myoclonus
Neurol 64:169-170, Narula,S. &Goraya,J.S., 2005

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

West Nile Virus Presenting as Opsoclonus-myoclonus Cerebellar Ataxia
Neurol 64: 1095-1096, Khosla,J.S., et al, 2005

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

Does This Patient Have Myasthenia Gravis?
JAMA 293:1906-1914, Scherer,K.,et al, 2005

Neurologic Manifestations in Welders with Pallidal MRI T1 Hyperintensity
Neurol 64:2033-2039,2001, Josephs,K.A.,et al, 2005

Vagal Nerve Stimulation Effect on Cerebellar Tremor in Multiple Sclerosis
Neurol 65:499, Marrosu,F.,et al, 2005

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

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

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

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



Showing articles 200 to 250 of 816 << Previous Next >>