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Differential
(Click to cross reference)
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 150 to 200 of 816 << Previous Next >>

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Lithium
Adams & Victors Principles of Neurology Chp 43, pg 1212, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Cocaine
Adams & Victors Principles of Neurology Chp 43, pg 1213, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Encephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 748, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Subacute Sclerosing Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Encephalitis Lethargica (non Economo Disease, sleeping sickness)
Adams & Victors Principles of Neurology, Chp 33, pg 768, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
Adams & Victors Principles of Neurology, Chp 33, pg 769, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
Adams & Victors Principles of Neurology, Chp 32, pg 710, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuronal Ceroid Lipofuscinosis (Batten Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 973, 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, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1116, Ropper, A.H.,et al, 2014

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

Serotonin Syndrome
BMJ 348:g1626, Buckley, N.A.,et al, 2014

Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
NEJM 370:792-794, McMinn, P.C., 2014

Drug Treatment of Epilepsy in Adults
BMJ 348:g2546, Schmidt, D. & Schachter, S.C., 2014

ICU-Acquired Weakness and Recovery from Critical Illness
NEJM 370:1626-1635, Kress, J.P. & Hall, J.B., 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

Mycoplasma Pneumoniae Infection: Neurologic Complications
www.MedLink.com, Oct, Greenlee, J.E., 2013

Clinicopathologic Conference, West Nile Virus Infection, Case 15-2013
NEJM 368:1919-1927, Vyas, J.,et al, 2013

Summary of Evidence-Based Guideline: Periprocedural Management of Antithrombic Medications in Patients with Ischemic Cerebrovascular Disease
Neurol 80:2065-2069, Armstrong, M.,et al, 2013

Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
Neurol 80:e220-e222, Morgan-Followell,B.& de los Reyes,E., 2013

The Eye of the Beholder: Inter-rater Agreement among Experts on Psychogenic Jerky Movement Disorders
JNNP 84:742-747, Van de Salm, S.,et al, 2013

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

Clinicopathologic Conference, Inflammatory Myopathy and Myasthenia Gravis Assoc. with Thymoma
NEJM 369:764-773, Case 26-2013, 2013

Mystery Case: A Young Boy with Myoclonic Jerks
Neurol 81:e130-e134, Musleh, C.,et al, 2013

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

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

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Dancing Eyes and Uvula after Brain Tumour Extirpation-A Sign of Tumour Progression?
Lancet 379:1983, Kipfer, S.,et al, 2012

Hashimoto Encephalopathy
Neurol 78:e134, Afshari, M.,et al, 2012

Progressive Gait Deterioration in Adolescents with Dravet Syndrome
Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012

Comorbidity of Migraine in Children Presenting with Epilepsy to a Tertiary Care Center
Neurol 79:468-473, Kelly, S.A.,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

Adult-Onset Opsoclonus-Myoclonus Syndrome
Arch Neurol 69:1598-1607, Klaas, J.,et al, 2012

Acquired Neurosyphilis Presenting as Movement Disorders
Mov Disord 27:690-695, Shah, B.B. & Lang, A.E., 2012

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.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

Pediatric Sciatic Neuropathies: A 30-year Prospective Study
Neurol 76:976-979, Srinivasan,J.,et al, 2011

Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
JNNP 82:646-651, Heath, C.A.,et al, 2011

Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
Arch Neurol 68:719-724, Robottom, B.J.,et al, 2011

N-methyl-D-aspartate Receptor Autoimmune Encephalitis Presenting With Opsoclonus-Myoclonus
Arch Neurol 68:1069-1072, Smith, J.H.,et al, 2011

Progressive Encephalomyelitis with Rigidity and Myoclonus Gycine and NMDA Receptor Antibodies
Neurol 77:439-443,414, Turner, M.R.,et al, 2011

Opsoclonus and Multiple Cranial Neuropathy as a Manifestation of Neuroborreliosis
Neurol 77:1013-1014, Sabien Van Erp, W.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Chronic Inflammatory Demyelinating Polyneuropathy: Etiology, Clinical Features, and Diagnosis
UpToDate, Sept, Lewis, R., 2010

Diagnosis and Management of Lumbar Spine Stenosis
JAMA 303:71-72, Haig,A. &Tomkins,C., 2010

Opsoclonus-Myoclonus Syndrome in Anti-N-Methyl-D-Aspartate Receptor Encephalitis
Arch Neurol 67:118-121, Kurian,M.,et al, 2010



Showing articles 150 to 200 of 816 << Previous Next >>