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Differential
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achilles tendon, enlarged
Addison's disease
Adies pupil
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
algorithm
angiography, neurologic complications with
ankle reflex, absent
areflexia
artery of Adamkiewicz
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
behavioral disorder
bladder dysfunction
bone marrow transplantation
brainstem, atrophy
brainstem, lesion of
burning paresthesia
CAG repeats
cane
cardiomyopathy
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebral palsy
cerebrospinal fluid, lactic acid concentration
cerebrotendinous xanthomatosis
Charcot-Marie-Tooth
chenodeoxycholic acid
children
chromosomal abnormality
chromosome 2
chromosome 6
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
consanguinity
corpus callosum, thinning
cultured skin fibroblasts
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diet
differential diagnosis
distal muscle atrophy
distal muscle weakness
Dravet syndrome
drug induced neurologic disorders
dysarthria
dysmetria
dysmorphic
dysphagia
ears of the Lynx MR sign
electroencephalogram, inflammatory disease
encephalopathy
epicanthal folds
epidemiology of neurology
epileptic encephalopathy
exome sequencing
eye movement, disorders of
facial appearance, abnormal
failure to thrive
falling
familial
FARS2 deficiency
fatty acid, elevated plasma content
fever
fine motor function, impaired
finger nose finger test
foot deformity
foot drop
frataxin
Friedreich's ataxia
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
hammertoes
hand weakness
hearing loss
hepatomegaly
high arched feet
hyperreflexia
hypogonadism
hypomyelination
hypotonia
iatrogenic neurologic disorders
imbalance
impulsivity
inborn errors of metabolism
incoordination
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
Jewish
lactic acidemia
leg weakness, bilateral
Leigh's disease
leukodystrophy
liver disease
Lorenzo's oil
meningitis, CSF cell count-normal
mental retardation
microcephaly
microdontia
middle cerebellar peduncle
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
MRI
MRI, abnormal
myelin protein zero gene
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myoclonus, epilepsy
nerve conduction studies
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
next-generation sequencing
night blindness
numbness, extremity
nystagmus
nystagmus, rotary
ocular motility, disorders of
oculodentodigital dysplasia
optic ataxia
optic atrophy
orthostatic hypotension
pain, foot
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraplegia
paraplegia, acute
paraplegia, neonatal
paresthesias
past pointing
Pelizaeus Merzbacher
peroxisomal disease
personality change
pes cavus
polyglucosan body disease
polyneuropathy
pons, lesion of
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing, neurologic problems
psychomotor retardation
pupil
pupil, dilated and fixed, bilateral
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
release phenomena
review article
Romberg's sign
scissors gait
SCN1A gene
scoliosis
screening
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, tonic-clonic
skin, darkening of
sodium channel dysfunction
spastic ataxia
spastic diplegia
spastic paraplegia, type 11
spasticity
speech, loss of
spinal cord, infarction of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinocerebellar degeneration
status epilepticus
steppage gait
stiff legs
striatonigral degeneration
striatonigral degeneration, infantile
subcortical U fibers
symmetric brain lesions
syndactyly
teeth, abnormal
testicular atrophy
titubation
toe walking
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
umbilical artery catheterization
urinary incontinence
visual impairment
walking, difficulty with
weakness
weakness, progressive
wheelchair
white matter disease
xanthoma, tendon
Showing articles 150 to 200 of 1537 << Previous Next >>

A Case of Progressive Myelopathy in a Middle-Aged Woman
JAMA Neurol 76:1253-1254, Muccilli, A.,et al, 2019

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

Acute Paraplegia in a Healthy Child
BMJ 367:L6257, Haque, A.K.M.,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

Acute Maternal Confusion and Neonatal Seizure Postpartum
BMJ 364:k5399, Jakes, A.D.,et al, 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

Management of Stroke in Neonates and Children
Stroke 50:e51-e96, Ferriero, D.M.,et al, 2019

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

A 23-Year-Old Man with Headaches, Confusion, and Lower Extremity Weakness
Neurol 92:863-867, Patel, N.M.,et al, 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Clinical Features of Syphilitic Myelitis with Longitudinally Extensive Myelopathy on Spinal Magnetic Resonance Imaging
World J Clin Cases 7:1282-1290, Yuang,J-L.,et al, 2019

Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Neonatal Abstinence Syndrome
JAMA 319:1362-1374, Wachman, E.,et al, 2018

Varicella-Zoster Virus-Related Hemorrhagic Encephalomyelitis
Neurol 90:e1360-e1361, Ganesh, A.,et al, 2018

A 30-year-old man with acute paraplegia and left foot gangrene
Neurol 90:e1355-e1359, Paliwal, V.K.,et al, 2018

Long-Term Risk of Hemorrhagic Stroke In Young Patients with Congenital Heart Disease
Stroke 49:1155-1162, Giang, K.W.,et al, 2018

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
NEJM 379:282-289, Case 22-2018, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Distinctive Imaging in a Paucisymptomatic Child with Leukodystrophy
Neruol 91:e1368-e1369, Sharawat, I.K.,et al, 2018

Childhood Seizures After Phototherapy
Pediatrics 142:e20180648, Newman, T.B.,et al, 2018

Congenital Myasthenic Syndromes in Adult Neurology Clinic
Neurol 91:e1770-e1777, Kao, J.C.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 2018

Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
Front Neurol doi.10.3398/jneur.2017.00108, Piroth,T.,et al, 2017

Bipolar II Disorder as the Initial Presentation of CADASIL:An Underdiagnosed Manifestation
Neuropsych Dis Treat 13:2175-2179, Wang,J.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

Surgery for Drug-Resistant Epilepsy in Children
NEJM 377:1639-1647, Dwivedi, R.,et al, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

A 61-year-old woman with Lower Extremity Paralysis and Sensory Loss
Neurol 89:e257-e263, Manners, J.,et al, 2017

Population-based Study of Ischemic Stroke Risk after Trauma in Children and Young Adults
Neurol 89:2310-2316, Fox, C.K.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 45-year-old woman with Immobility and Incontinence
Neurol 88:e212-e218, Zhang, B.,et al, 2017

A 10-year-old boy with Bilateral Vision Loss
Neurol 88:e221-e224, Bulwa, Z.,et al, 2017

Buprenorphine for the Treatment of the Neonatal Abstinence Syndrome
NEJM 376:2341-2348, Kraft, W.K.,et al, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma Consistent with Neurolymphomatosis
NEJM 376:2471-2481, Case 19-2017, 2017



Showing articles 150 to 200 of 1537 << Previous Next >>