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Differential
(Click to cross reference)
acute disseminated encephalomyelitis
akinetic mute
amnestic syndrome
amniocentesis
anatomy of
aqueduct of Sylvius, stenosis
aqueductal stenosis
ataxia, hereditary
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
blindness
calcarine artery
CAT scan
CAT scan, abnormal
cerebral venous infarction
cerebral venous thrombosis
cerebrovascular accident
cherry red spot
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
craniopharyngioma
deep gray nuclei
dementia
dementia, thalamic
developmental milestones, loss of
developmental retardation
differential diagnosis
drooling
dropped head syndrome
encephalitis
encephalitis, viral
encephalopathy
encephalopathy, neonatal
enzyme, defect
Fabry's disease
fundus, abnormality of
gangliosidosis GM2
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
glioma
hemangioma, cerebral
hemianopia, homonymous
hexosaminidase-A
hexosaminidase-A and B
Huntington's chorea
hypersomnia
hypomyelination
hypotonia
hypoxic encephalopathy
intracranial hypertension, benign
Jewish
Krabbe's disease
lacunar infarction
lenticular nucleus, lesion of, bilateral
leukodystrophy
level of consciousness, decreased
lipid storage disorder of CNS
lysosomal storage disease
metachromatic leukodystrophy
molecular genetics
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
MRI, hypointense signal foci on
multiple sclerosis
muscle spasm
muscular dystrophy
muscular dystrophy, Duchenne
myelinolysis, extrapontine
neurofibromatosis 1
neuropathology
optic atrophy
optic glioma
optic neuritis
optic neuritis, bilateral
papilledema
pediatric neurology
pituitary, adenoma
pons, lesion of
pontine glioma
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
psychomotor retardation
retrobulbar neuritis
review article
rigidity
Sandhoff's disease
Schilder's disease
screening
seizure
skin, biopsy
spasticity
startle reaction
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
symmetric brain lesions
Tay-Sachs disease
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
tone, muscle, increased
top of the basilar syndrome
vision, failure of in childhood
visual acuity, decreased
Wernicke's encephalopathy
white matter disease
Showing articles 350 to 400 of 2264 << Previous Next >>

A Case of Slowly Progressive Painful Paraparesis
Neurol 82:1476-1479, Corbetto, M.,et al, 2014

Stroke and NonStroke Brain Attacks in Children
Neurol 82:1434-1440, Mackay, M.T.,et al, 2014

Myasthenia in Pregnancy: Best Practice Guidelines from a UK Multispecialty Working Group
JNNP 85:538-543, Norwood, F.,et al, 2014

Familial Risk of Cerebral Palsy: Population Based Cohort Study
BMJ 349:g4294, g4514, Tollanes, M.C.,et al, 2014

Red Papules on the Tongue of a Patient with Hemiparesis
JAMA 312:741-742, Chiu, H.Y. & Lin, S.J., 2014

Somatic Mutations in Cerebral Cortical Malformations
NEJM 371:733-743, Jamuar, S.S.,et al, 2014

Controlled Trial of Transfusions for Silent Cerebral Infarcts in Sickle Cell Anemia
NEJM 371:699-710, DeBaun, M.R.,et al, 2014

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

Imaging Findings in MR Imaging-Guided Focused Ultrasound Treatment for Patients with Essential Tremor
AJNR 35:891-896, Wintermark, M.,et al, 2014

Deep-Brain Stimulation - Entering the Era of Human Neural-Network Modulation
NEJM 371:1369-1373, Okun, M.S., 2014

Distinctive Pattern of White Matter Injury in Neonates with Rotavirus Infection
Neurol 84:21-27,13, Yeom, J.S.,et al, 2014

Juvenile Myasthenia Gravis: Recommendations for Diagnostic Approaches and Treatment
Neuropediatrics 45:75-83, Marina, A.D.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
J Stroke Cerebrovasc Dis 23:441-443, Kuroki, T.,et al, 2014

Intracranial Lesions with High Signal Intensity on T1-weighted MR images - Review of Pathologies
Pol J Radiol 78:36-46, Zimmy, Anna.,et al, 2013

Febrile Infection-Related Epilepsy Syndrome: A Study of 12 Patients
Seizure 22:553-559, Caraballo, R.H.,et al, 2013

Autism and Mental Retardation among Offspring born after In Vitro Fertilization
JAMA 310:75-84, Sandin, S.,et al, 2013

A Pilot Study of Focused Ultrasound Thalamotomy for Essential Tremor
NEJM 369:640-648, Elias, W.J.,et al, 2013

Tourettes Syndrome
BMJ 347:f4964, Cavanna, A.E. & Seri, S., 2013

Evidence-Based Guideline Update: Vagus Nerve Stimulation for the Treatment of Epilepsy
Neurol 81:1453-1459, Morries, G.L.,et al, 2013

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

Pediatric Intracerebral Hemorrhage
JAMA Neurol 70:448-454,437, Beslow, L.et al, 2013

Longitudinally Extensive Transverse Myelitis in Neuro-Beh�et Disease
Neurol 80:e189-e190, Graham, D.,et al, 2013

Prenatal Valproate Exposure and Risk of Autism Spectrum Disorders and Childhood Autism
JAMA 309:1696-1703, Christensen, J.,et al, 2013

Association Between Childhood Migraine and History of Infantile Colic
JAMA 309:1607-1612,1636, Romanello, S.,et al, 2013

Efficacy and Safety of Everolimus for Subependymal Giant Cell Astrocytomas Associated with Tuberous Sclerosis Complex (EXIST-1): A Multicenter, Randomized, Placebo-Controlled Phase 3 Trial
Lancet 381:125-132, Franz, D.,et al, 2013

Association Between Maternal Use of Folic Acid Supplements and Risk of Autism Spectrum Disorders in Children
JAMA 309:570-577, Suren, P.,et al, 2013

Chediak-Higashi Syndrome: Pathognomonic Feature
Lancet 382:1514, Antunes, H.,et al, 2013

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

MRI and EEG as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy
Neurol 79:2349-2354, Morita, M.,et al, 2012

Efficacy and Safety of Ketamine in Refractory Status Epilepticus in Children
Neurol 79:2355-2358, Rosati, A.,et al, 2012

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

Intramuscular Versus Intravenous Therapy for Prehospital Status Epilepticus
NEJM 366:591-600,659, Silbergleit,R.,et al, 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

CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
Neurol 78:1150-1156, Deiva,K.,et al, 2012

Evidence-based Guideline: Intravenous Immunoglobulin in the Treatment of Neuromascular Disorders
Neurol 78:1009-1015, Patwa,H.S.,et al, 2012

Evidence-based Guideline Update: Medical Treatment of Infantile Spasms
Neurol 78:1974-1980, Go, C.Y.,et al, 2012

Restricted Diffusion in Vanishing White Matter
Arch Neurol 69:723-727, Van de Lei, H.D.W.,et al, 2012

Screening Patients with a Family History of Subarachnoid Haemorrhage for Intracranial Aneurysms: Screening Uptake, Patient Characteristics and Outcome
JNNP 83:86-88, Miller, T.D.,et al, 2012

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

Cerebral Amyloid Angiopathy
eMedicine, Jan, Menon, R.S., 2012

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

Stroke Recurrence in Children with Congenital Heart Disease
Ann Neurol 72:103-111, Rodan, L.,et al, 2012

Clinical Reasoning: A Case of Treatable Spastic Paraparesis
Neurol 79: e50-e53, McKinnon, J.H. & Bosch E.P., 2012

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,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

Clinical and Biomarker Changes in Dominantly Inherited Alzheimers Disease
NEJM 367:795-804,864, Bateman, R.J.,et al, 2012



Showing articles 350 to 400 of 2264 << Previous Next >>