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Differential
(Click to cross reference)
adrenoleukodystrophy
adverse drug reaction
alternating rapid movement
amniocentesis
amyotrophic lateral sclerosis, guamian type of
anticonvulsants
anticonvulsants, selection of
arm swing, reduced
ataxia
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
behavioral disorder
blindness
bradykinesia
brain atrophy
brain biopsy
CAT scan, abnormal
cataracts
cerebellar atrophy, primary
cerebellar degeneration
cerebral cortical atrophy
cerebro hepato renal syndrome
cherry red spot
cherry red spot-myoclonus syndrome
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
cogwheel rigidty
conjunctival biopsy
deep gray nuclei
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
developmental milestones, loss of
developmental retardation
diagnostic criteria
DNA probes
drug induced neurologic disorders
dysarthria
dysmetria
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
encephalopathy
eye movement, disorders of
falling
familial
fine motor function, impaired
fingerprint bodies
fundus, abnormality of
gait disorder
gangliosidosis GM1
gangliosidosis, generalized
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
granular osmiphilic material
Hallervorden Spatz disease
herpes virus infection
hyperreflexia
hypotonia
imbalance
immunofluorescence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
intellectual deficit
intellectual deterioration
introverted
Jakob-Creutzfeldt disease
Kearns-Sayre syndrome
lactic acidemia
Lafora's disease
Laurence-Moon-Bardet-Biedl syndrome
lead poisoning
leukocyte peroxidase
lymphocyte fingerprint profiles
lysosomal storage disease
macular degeneration
marche a petits pas
memory, impairment of
mental retardation
MERRF syndrome
metachromatic leukodystrophy
microcephaly
mimics
misdiagnosis
molecular genetics
mongolism
mortality
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, serial
mucopolysaccharidoses
muscle biopsy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy, mitochondrial
myopia
negative
neuroaxonal dystrophy
neurofibrillary degeneration
neuroichthyosis
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathy
neuropathy, hereditary peripheral
Niemann-Pick disease
night blindness
ophthalmoplegia, plus syndrome
optic atrophy
optic nerve
optic neuropathy
paraparesis, familial spastic
Parkinson disease, postencephalitic
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
peroxisomal disease
pigmentary retinopathy
prenatal diagnosis by amniocentesis
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
putamen, lesion of
putamen, lesion of, bilateral
refractive errors
Refsum's disease
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
schizophrenia
sea-blue histiocytes
seizure
seizure, children
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
skin, biopsy
skull x-ray, abnormal
slurred speech
spinocerebellar degeneration
storage disease of CNS
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
tapetoretinal degeneration
treatment of neurologic disorder
tremor
tremor, intention
tuberous sclerosis
Unverricht-Lundborg disease
Usher's syndrome
ventricular enlargement
viral infection, CNS
vision, failure of in childhood
visual acuity, decreased
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
visual loss, slow
walking, difficulty with
Werdnig-Hoffman disease
West disease
wheelchair
wide based gait
Showing articles 100 to 150 of 748 << Previous Next >>

Paraneoplastic Encephalomyelitis with Glutamic Acid Decarboxylase Antibodies Presenting as Longitudinal Pyramidal Tract Hyperintensity
JAMA Neurol 77:899-900, Miralles, C.,et al, 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Opsoclonus in Anti-Ma2 Brain-Stem Encephalitis
NEJM 383:e84, Sacks, C.A.,et al, 2020

An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
Neurol 95:e3153-e3159, Russ, J.B.,et al, 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Treatment Approaches for MOG-Ab-Associated Demyelination in Children
Curr Treat Options Neurol 21:2, Hacohen, Y. & Banweil, B., 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
JAMA Neurol 76:728-729, Kim, D.D.,et al, 2019

Kelch-Like Protein 11 Antibodies in Seminoma-Associated Paraneoplastic Encephalitis
NEJM 381:47-54, Mandel-Brehm, C.,et al, 2019

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

Aquaporin-4 and MOG Autoantibody Discovery in Idiopathic Transverse Myelitis Epidemiology
Neurol 93:e414-e420, Sechi, E.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

A Case of Muscle Twitching with Psoriasis
JAMA Neurol 76:1119-1120, Qian, M.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

Neurodegenerative Disease Mortality Among Former Professional Soccer Players
NEJM 381:1801-1808,1862, Mackay, D.F.,et al, 2019

Amphiphysin-IgG Autoimmune Neuropathy
Neurol 93:e1873-e1880, Dubey, D.,et al, 2019

GQ1b-Seronegative Miller Fisher Syndrome Associated with Pembrolizumab
J Neuro-Ophthal 39:394-396, Green, K.E.,et al, 2019

Diagnostic Tools for Immune Causes of Encephalitis
Clin Microbiol Infect 25:431-436, Lascano, A.M.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Nivolumab-Induced Autoimmune Encephalitis in Two Patients with Lung Adenocarcinoma
Case Rep Neurol Med 2018;doi:10.1155/2018/2548528, Shah, S.,et al, 2018

MOG Encephalomyelitis: International Recommendations on Diagnosis and Antibody Testing
J Neuroinflammation 15:134, Jarius, S.et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Unintended Consequences of Mayo Paraneoplastic Evaluations
Neurol 91:e2057-e2066, Ebright, M.J.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Evaluation of Idiopathic Transverse Myelitis Revealing Specific Myelopathy Diagnoses
Neurol 90:e96-102, Zalewski, N.L.,et al, 2018

Autoimmune CRMP5 Neuropathy Phenotype and Outcome Defined from 105 Cases
Neurol 90:e103-e110, Dubey, D.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease
JAMA Neurol 75:65-71, Hamid, S.H.M.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Encephalitis with mGluR5 antibodies
Neurol 90:e1964-e1972, Spatola, M.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
Neurol 91:98-101, Marques-Matos, C.,et al, 2018

Acute Onset of Diplopia in Pregnancy
Neurol 91:e180-e184, Munro, Z. & Fernandez, D., 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

A 75-year-old man with parkinsonism, mood depression, and weight loss
Neurol 90:572-575, Frattini, E.,et al, 2018

A 30-year-old man with headache and sleep disturbance
Neurol 90:e1535-e1540, English, S.W.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Brain MRI Characteristics of Patients with Anti-N-Methyl-D-Aspartate Receptor Encephalitis and Their Associations with 2-Year Clinical Outcome
AJNR 39:824-829, Zhang, T.,et al, 2018

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017



Showing articles 100 to 150 of 748 << Previous Next >>