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Differential
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acoustic nerve, vestibular division of
acoustic neurinoma
acoustic neurinoma, bilateral
adrenoleukodystrophy
advances in neurology
adverse drug reaction
algorithm
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
anticonvulsants
anticonvulsants, effectiveness
antiviral agents
apolipoprotein E
APP
APP gene
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
ataxin
ataxin-2
audiogram
auditory evoked brainstem potentials
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
brain biopsy
brain purpura
brainstem, infarction of
cafe au lait spots
CAG repeats
calcification, intracranial
CAT scan, abnormal
cataracts
CD4 counts
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral infarction, hemorrhagic
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, recurrent
children
chorea
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 1
chromosome 12
chromosome 14
chromosome 17
chromosome 19
chromosome 2
chromosome 20
chromosome 21
chromosome 22
chromosome 3
chromosome 4
Cockayne's syndrome
cognition
confidentiality
consanguinity
cranial nerve tumor
Cuba
deafness
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
dementia
developmental retardation
diabetes mellitus
DNA probes
Dravet syndrome
drug induced neurologic disorders
dysarthria
dysphagia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, paroxysmal
dystonia, symptomatic
dystonia, treatment of
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electronystagmography
electroretinograph
enzyme, defect
ependymoma
epidemiology of neurology
equinovarus
eye movement, disorders of
familial
fever
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
globus pallidus, stimulation
gyrate atrophy of choroid and retina
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hamartoma
hearing loss
hepatosplenomegaly
highly active antiretroviral therapy
hot cross bun sign
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hyperornithinemia
hyperreflexia
hypogammaglobulinemia
hyposmia
imbalance
imbalance, postural
immune reconstitution inflammatory syndrome
intellectual deficit
intellectual deterioration
iron, brain
Kearns-Sayre syndrome
lacunar infarction
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
lenticular nucleus, lesion of, bilateral
leucine-rich repeat kinase 2 gene
livedo reticularis
long bone lesion
macular degeneration
meningioma
mental retardation
merlin
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, eye of tiger sign
MRI, gradient-echo
MRI, paramagnetic effect
MRI, spine
MRI, susceptibility weighted
mucopolysaccharidoses
multiple system atrophy
muscle cramp
muscle stiffness
muscular dystrophy
muscular dystrophy, classification
muscular dystrophy, Duchenne
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy, mitochondrial
myopia
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neoplasm, intracranial
neoplasm, intracranial, multiple
neoplasm, peripheral nerve
neoplasm, primary of CNS
neoplasm, primary of CNS-multiple
nerve growth factor
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neurodegeneration with brain iron accumulation
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurofibromin
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuronopathy
neuropathy
neuropathy, hereditary peripheral
night blindness
optic atrophy
optic glioma
optic nerve
optic neuropathy
orbit, tomograms of
palilalia
PANK2 mutation
Parkinson disease
Parkinson disease, familial
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal neurologic deficits
patient information and support
peroxisomal disease
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
postural abnormality
practice guidelines
pregnancy, neurologic complications in
presenilin-1 gene
presenilin-2 gene
prognosis
progressive neurologic disorder
proximal myotonic myopathy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract
pyramidal tract dysfunction
recombinant DNA
recurrent
refractive errors
Refsum's disease
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
RFLPs
rigidity
risk factors
root lesion, nerve
saccadic eye movements, abnormal
schwannoma
SCN1A gene
sea-blue histiocytes
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, tonic-clonic
seizure, treatment of
sensorineural hearing loss
sinemet
skin, biopsy
skin, lesions in neurologic disorders
sodium channel dysfunction
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
spinal cord, neoplasm
spinal cord, neoplasm, intramedullary
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
spinocerebellar degeneration
status epilepticus
steroid
stimulation, deep brain
substantia nigra
symmetric brain lesions
systemic illness
tandem gait, ataxic
tapetoretinal degeneration
tinnitus
topiramate
treatment of neurologic disorder
tremor
trinucleotide repeats
tubular aggregates, muscle
type 2 muscle fiber
Usher's syndrome
vasculitides
vasculopathy
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual loss
wheelchair
Wood's light
workup
Showing articles 150 to 200 of 1938 << Previous Next >>

Genetics of Cluster Headache Takes a Leap
Ann Neurol 90:191-192, Palotie, A., 2021

A 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

Clinicopathologic conference, Cryptococcal meningoencephalitis and advanced HIV infection
NEJM 383:2572-2580, Case 40-2020, 2020

Trends of Tuberculosis Case Detection, Mortality and Co-Infection with HIV in Ghana: A Retrospective Cohort Study
PLOSONE 15:e0234878, Osel, E.,et al, 2020

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Morvan Syndrome and Diffuse Large B-Cell Lymphoma in the Central Nervous System
Neurologist 25:73-77, Jiang, C.,et al, 2020

CASPR2 Autoimmunity in Children Expanding to Mild Encephalopathy with Hypertension
Neurol 94:e2290-e2301,953, Syrbe, S.,et al, 2020

A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
Neurol 94:994-999, Wildman, J.,et al, 2020

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

A 10-Year-Old Girl with Muscle Stiffness
Neurol 95:e773-e778, Prior, D.E. & Ghosh, P.S., 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

Spinal Xanthomatosis
Neurol 95:e1615-e1616, Valencia-Sanchez, C.,et al, 2020

Muscle Stiffness, Gait Instability, and Liver Cirrhosis in Wilsons Disease
Lancet 396:990, Kronlage, C.,et al, 2020

Recurrent Cerebral Ischemia During Pregnancies
Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020

Mycobacterium Haemophilum Infection
eMedicine.medscape.com 22144, Mazumder,S.A. & Chandrasekar,P.H., 2020

Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
AJNR 41:167-173, Bhatia,K.D.,et al, 2020

Clinical Characteristics and Treatment Outcomes for Patients Infected with Mycobacterium haemophilum
Emerg Inf Dis 25:1648-1652, Nookeu,P.,et al, 2019

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

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

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

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Ehlers-Danlos Syndromes
BMJ 366:I4966, Ghali, N.,et al, 2019

Neurosyphilis
NEJM 381:1358-1363, Ropper, A.H.,et al, 2019

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

CRAO and Silent Brain Infarcts caused by Cardiac Myxomas in Carney Complex
Neurol 92:e286-e287, Huang, L-T.,et al, 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019



Showing articles 150 to 200 of 1938 << Previous Next >>