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Differential
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aminoacidurias
ammonia
anatomy of
anorexia
Arnold Chiari malformation
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
Behcet's syndrome
beriberi
beriberi, infantile
blood dyscrasias, neurologic findings with
brain atrophy
brainstem
brainstem, lesion of
bulimia
calcification, intracranial
Canavan's disease
carbon monoxide poisoning
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, false negative
cataracts
caudate nucleus
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar atrophy, secondary
cerebellar lesion
cerebral cortex
cerebral infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, nonvascular territory
cerebrovascular accident, young adult
children
chorea
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
cognition
color vision, impaired
crying
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deafness, congenital
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
differential diagnosis
dizziness
dysarthria
dystonia
electron microscopy
encephalitis
encephalitis, Japanese
encephalitis, viral
encephalopathy
encephalopathy, neonatal
enkephalins
enzyme, defect
eye movement, disorders of
Fabry's disease
Fahr disease
failure to thrive
familial
flavivirus
fontanel, bulging
Friedreich's ataxia
gadolinium
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
glioma
glutaric acidemia
gyrus, abnormal
head injury
head lag
headache
hearing loss
heart block
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hiccoughs
histochemistry
histochemistry of muscle
hyperglycemia
hyperphagia
hyperreflexia
hypoglycemia
hyponatremia
hypothermia
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
inborn errors of metabolism
infant and newborn with distress, neurologic prognosis in
infant, evaluation of
intellectual deterioration
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intestinal pseudoobstruction
intraventricular hemorrhage
iron, brain
irritability
Jakob-Creutzfeldt disease
Kearns-Sayre syndrome
lactic acidemia
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
magnetic susceptibility
maple syrup urine disease
Marinesco-Sjogren syndrome
MELAS syndrome
mental retardation
MERRF syndrome
metabolic disorder, primary
metabolic disorder, primary-screening tests
metronidazole
microhemorrhage, intracerebral
midbrain, lesion of
mitochondrial disease
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, diffusion weighted
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
MRI, target sign
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle pain
myelitis, longitudinal
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
neoplasm, primary of CNS
neurofibromatosis 1
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, peripheral
neurotoxin
nutritional deficiency
nystagmus
nystagmus, rotary
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic neuropathy
osmotic demyelination syndrome
overlap syndrome
owl's eye sign of spinal cord
pancytopenia
paraparesis, spastic
Parkinson disease
pes cavus
pigmentary retinopathy
POLG1 gene
polyneuropathy
pons, lesion of
progressive infantile poliodystrophy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
remote effect of cancer on the nervous system
respiratory failure
restless leg syndrome
retinopathy
review article
Romberg's sign
seizure
seizure, children
sensorineural hearing loss
sensory loss
short stature
spasticity
speech, loss of
spinal cord
spinal cord, lesion of
spinocerebellar degeneration
spongy degeneration of brain
status epilepticus
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
substantia nigra
suck, poor
symmetric brain lesions
term infant
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
titubation
tonic spasms
treatment of neurologic disorder
tremor
tremor, intention
urine test for metabolic disorders
visual acuity, decreased
vitamin deficiency
Von Hippel Lindau
weakness
weakness, progressive
weight loss
Wernicke's encephalopathy
white matter disease
white matter disease, periventricular
wide based gait
workup
Showing articles 150 to 200 of 751 << Previous Next >>

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

Aspergillus Meningitis: A Rare Clinical Manifestation of Central Nervous System Aspergillosis
J Infect 66:218-238, Antinori, S.,et al, 2013

Sporadic Creutzfeldt-Jakob Disease with Focal Findings: Caveats to Current Diagnostic Criteria
Neurol Internat 5:1-5, Mader, E.C.,et al, 2013

Brain MRI Findings in Neurologically Asymptomatic patients with Infective Endocarditis
ANJR 34:1579-1584, Hess,A.,et al, 2013

Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
AJNR 33:1945-1950, Lee,H.,et al, 2012

A Comparison of Tau and 14-3-3 Protein in the Diagosis of Creutzfeldt-Jakob Disease
Neurol 79:547-552, Hamlin, C.,et al, 2012

Evidence-based Guideline: Diagnostic accuracy of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease
Neurol 79:1499-1506, Muayqil, T.,et al, 2012

Differential Diagnosis of Jakob-Creutzfeldt Disease
Arch Neurol 69:1578-1582,1554, Paterson, R.,et al, 2012

Complications and Outcome of Infective Endocarditis
UpToDate January, Spelman, D. & Sexton, D., 2012

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

Infective Endocarditis at Autopsy
Medicine 91:152-164, Fernandez Guerrero,M.L.,et al, 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

Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
Neurol 76:1711-1719, Vitali, P.,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

Anticoagulation in Patients with Stroke With Infective Edocarditis Is Safe
Stroke 42:1795-1796,1799, Rasmussen, R.V., 2011

Anticoagulation Should Not Be Used in Most Patients With Stroke With Infective Endocarditis
Stroke 42:1797-1798,1799, Sila, C., 2011

Encephalitis and antibodies to synaptic and neuronal cell surface proteins
Neurol 77:179-189, Lancaster, E.,et al, 2011

Rapidly Progressive Alzheimer Disease
Arch Neurol 68:1124-1130, Schmidt, C.,et al, 2011

Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
Ann Neurol 70:437-444, Chitravas, N.,et al, 2011

Neuropathy in Parkinson Disease
Neurol 77:1947-1950, e132, Rajabally, Y.A. and Martey, J., 2011

Epstein-Barr Virus Infections of the Nervous System
www.medlink.com, Nov, Amlie-Lefond,C., 2011

The Evaluation of Rapidly Progressive Dementia
The Neurologist 17:67-74, Rosenbloom,M.H. &Atri,A., 2011

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Vitamin B12-Responsive Severe Leukoencephalopathy and Autonomic Dysfunction in a Patient With "Normal" Serum B12 Levels
JNNP 81:1369-1371, Graber,J.J.,et al, 2010

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Copper Deficiency as a Treatable Cause of Poor Balance
BMJ 340:864-866, Khaleeli,Z., et al, 2010

Pneumonias Link With the Head and Neck
Lancet 376:388, Mariotti,P., et al, 2010

Open Biopsy in Patients With Acute Progressive Neurologic Decline and Absence of Mass Lesion
Neurol 75:419-424, Schuette,A.J., et al, 2010

Sporadic Creutzfeldt-Jakob Disease Mimicking Nonconvulsive Status Epilepticus
Neurol 74:1995-1999, Lapergue,B., et al, 2010

Isolated Acute Nontraumatic Cortical Subarachnoid Hemorrhage
AJNR 31:1355-1362, Cuvinciuc,V.,et al, 2010

Serum vitamin B12 and Folate Status in Patients with Inflammaotry Bowel Diseases
Eur J Med 21:320-323, Yakut, M.,et al, 2010

Recommendations for the Practice of Echocardiography in Infective Endocarditis
Eur J Echocard 11:202-207, Habib, G.,et al, 2010

Active Infective Endocarditis after Mitral Valve Repair
Gen Thorac Cardiovasc Surg 58:49-52, Miura, T.,et al, 2010

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

Small Fiber Neuropathy: A Burning Problem
Cleve Clin J Med 76:297-305, Tavee, J. & Zhou, L., 2009

Non-Infectious Endocarditis in a Patient with cANCA-associated Small Vessel Vasculitis
Rheumatology 48:592-594, Horino, T.,et al, 2009

MRI Lesion Profiles in Sporadic Creutzfeldt-Jakob Disease
Neurol 72:1994-2001, Meissner,B.,et al, 2009

Cerebral Microbleeds Are Frequent in Infective Endocarditis; A Case-Control Study
Stroke 40:3461-3465, Klein,I.,et al, 2009

Practice Parameter: Evaluation of Distal Symmetric Polyneuropathy: Role of Laboratory and Genetic Testing (An Evidence-Based Review)
Nuerol 72:185-192, England,J.D.,et al, 2009

Rapidly Progressive Neurodegenerative Dementias
Arch Neurol 66:201-207, Josephs,K.A.,et al, 2009

Pathologic Correlates of Diffusion MRI Changes in Creutzfeldt-Jakob Disease
Neurol 72:1425-1431, Manners,D.N.,et al, 2009

Persistent Neutrophilic Meningitis
JNNP 80:697-698, Pinto, V.L.,et al, 2009

Inverted V Sign in Subacute Combined Degeneration of Spinal Cord
Neurol 72:e3, Kumar,A.&Singh,A.K., 2009

Vitamin B12 Deficiency and Severe Weight Loss in an Elderly Patient
Tenn Med 101:35-36, Gupta,N.K. & Powers,J.S., 2008

Sporadic Creutzfeldt-Jakob Disease in Two Adolescents
JNNP 79:14-18, Murray,K.,et al, 2008

Systematic Review of Therapeutic Intervention in Human Prion Disease
Neurol 70:1272-1281, Stewart,L.A.,et al, 2008

Transmissible Spongiform Encephalopathy in the 21st Century: Neuroscience for the Clinical Neurologist
Neurol 70:713-722, Brown,P., 2008

Rapidly Progressive Dementia
Ann Neurol 64:97-108, Geschwind,M.D.,et al., 2008

Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease
AJNR 29:1519-1524, Meissner,B.,et al., 2008

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



Showing articles 150 to 200 of 751 << Previous Next >>