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abdominal contractions
Alexanders disease
Alexanders disease, adult onset
amyotrophic lateral sclerosis
aphonia
areflexia
astrogliopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
auditory evoked brainstem potentials
autoantibodies
autoimmune disease
autonomic dysfunction
Behcet's syndrome
botulinum toxin
brainstem, dysfunction, eye movement disorders with
brainstem, infarction of
brainstem, lesion of
Brueghel's syndrome
bulbar palsy
celiac disease, adult
cerebellar atrophy, primary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellum, disease of
cerebrovascular accident
clonazepam
complications
degenerative diseases of CNS
dementia
demyelinating disease
developmental retardation
dilantin
diplopia
dizziness
dysarthria
dysdiadochokinesia
dysmetria
ear, clicking of
electroencephalogram
electroencephalogram, abnormalities of
encephalopathy
epilepsia partialis continua
eye movement, disorders of
failure to thrive
familial
fine motor function, impaired
gait disorder
gene
gene mutation
genetic neurologic disorders
GFAP gene
glutamic acid decarboxylase, antibody
head nodding
heart sign
heralding manifestation
hyperreflexia
hypometric saccades
imbalance
inferior olivary nucleus
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal biopsy
lateropulsion
leukodystrophy
leukoencephalopathy, differential diagnosis
life expectancy
locked-in syndrome
macrocephaly
malabsorption syndrome
medulla oblongata
medulla oblongata, lesion of
meningitis
midbrain
midbrain, infarction of
misdiagnosis
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
multiple sclerosis
multiple sclerosis, misdiagnosis
myoclonus
myoclonus, abdominal
myoclonus, segmental
myoclonus, treatment of
neurologic disease
neuropathology
nystagmus
nystagmus, gaze-evoked
nystagmus, monocular
nystagmus, pendular
nystagmus, primary position of gaze
nystagmus, upbeating on upgaze
nystagmus, vertical
ocular dysmetria
ocular myoclonus
olivary degeneration, hypertrophic
optic atrophy
oscillopsia
palatal myoclonus
palatal myoclonus, essential
paraparesis
paraparesis, spastic
paroxysmal neurologic deficits
pontine hemorrhage
posterior inferior cerebellar artery syndrome
prognosis
progressive ataxia and palatal tremor
progressive neurologic disorder
Purkinje cell
remote effect of cancer on the nervous system
respiratory myoclonus
review article
Rosenthal fibers
seizure
seizure, clicking sound with
seizure, focal
sleep
sodium valproate
speech disorder
speech disorder, non aphasic
spinal cord, injury of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinopontine atrophy, dominant
stiff man syndrome
tandem gait, ataxic
transsynaptic degeneration
treatment of neurologic disorder
triangle of Guillain and Mollaret
tumor pseudoprogression
Wernekinck commissure syndrome
Whipple's disease
white matter disease
Showing articles 100 to 150 of 402 << Previous Next >>

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

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

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

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

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

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

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

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

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 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

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

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

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

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

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

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

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

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

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

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

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

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

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

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

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

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

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

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

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

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

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

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

Clinical Correlations of Mutations in the SCN1A Gene: From Febrile Seizures to Severe Myoclonic Epilepsy in Infancy
Pediatr Neurol 30:236-243, Ceulemans,B.P.G.M.,et al, 2004

The Acoustic Startle Reflex in Ischemic Stroke
Neurol 62:114-116, Jankelowitz,S.K. & Colebatch,J.G., 2004

B- and T-cell Markers in Opsoclonus-Myoclonus Syndrome
Neurol 62:1526-1532,1466, Pranzatelli,M.R.,et al, 2004

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004



Showing articles 100 to 150 of 402 << Previous Next >>