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Differential
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alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
aminoacidurias
anti MAG antibodies
anti Yo antibody
aphasia
aphasia, children
apraxia, speech
aspiration
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
ataxic hemiparesis
attention deficit disorder with hyperactivity
attention span
autism
autoantibodies
Babinski sign
basal ganglia, degeneration
basilar artery stenosis
behavioral disorder
Benedict's solution test
bifid uvula
bradykinesia
brainstem, atrophy
brainstem, lesion of
calcification, intracranial
carcinoma
carcinoma of breast
carcinoma of ovary
CAT scan, emission, abnormal
catalepsy
cataplexy
cerebellar ataxia, children
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
chairbound
chemotherapy, CNS treatment and complications with
children
chorea
choreoathetosis
cleft palate
Clinical Pathologic Conference(C.P.C.)
cognition
complications
confusion
consanguinity
cortical-basal ganglionic degeneration
cranial nerve palsies
cranial nerve palsies, bilateral
cranial neuropathy, multiple
crying, pathologic
cryptococcal antigen
cryptococcal meningitis
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, presenile
demyelinating disease
developmental milestones, loss of
diagnostic criteria
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
diplopia
disability, neurological
disease modifying agents
dizziness
drooling
drowsiness
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphonia
dysplasia of C.N.S.
dyspraxia
dystonia
electroencephalogram
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, acute
epileptic encephalopathy
exome sequencing
eye movement, disorders of
facial nerve palsy
failure to thrive
falling
familial
FARS2 deficiency
ferric chloride test
fine motor function, impaired
foam cells
fungal infection
fungal infection, CNS
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
head nodding
headache
headache, intractable
hearing loss
hearing problems in children
heel-knee-shin test
hemiplegia
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
hyperreflexia
hypoglycorrhachia
hypotonia
iatrogenic neurologic disorders
imbalance
immunocompetent
immunodeficiency
immunomodulation
immunotherapy
inattention
incontinence, fecal
incoordination
infection
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
jaundice
karyotyping
Kayser-Fleischer ring
klippel feil syndrome
language disorders in children
laughing, pathologic
lethargy
leukemia
lipid storage disorder of CNS
liver disease
locked-in syndrome
lysosomal storage disease
maple syrup urine disease
masked facies
memory, impairment of
meningeal enhancement
meningeal enhancement, nodular
meningitis
meningitis, CSF cell count-normal
meningitis, fungal
meningitis, neutrophilic
meningitis, neutrophilic, persistent
mental retardation
mental status, abnormal
methotrexate
microcephaly
midbrain
midbrain, infarction of
midline defect in children
mimics
misdiagnosis
mitochondrial disease
monoclonal antibodies
monoparesis
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, negative
MRI, nodular enhancement
multiple system atrophy
mutism
myelodysplasia
nasal speech
nausea and vomiting
negative
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neuropathology
neuropathy
neurotoxic
neurotoxicity, acute
Niemann-Pick disease
ocular motility, disorders of
palatopharyngeal incompetence
paraneoplastic cerebellar degeneration
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
personality change
phenylketonuria
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
pneumonia
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychosis
psychosis, childhood
psychosocial aspects
ptosis
ptosis, unilateral
pulmonary infection
pure motor hemiplegia
pursuit eye movements, abnormal
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
recurrent
release phenomena
remote effect of cancer on the nervous system
review article
rigidity
saccadic eye movements, abnormal
salivation, excessive
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, psychosocial aspects of
seizure, treatment of
single photon emission computed tomography
skin, lesions in neurologic disorders
slit lamp examination
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spina bifida
splenomegaly
stare
stuttering
suck reflex
telangiectases
third nerve palsy
third nerve palsy, bilateral
third nerve palsy, partial
toe walking
tongue, impaired movements of
transient neurologic deficit
treatment of neurologic disorder
tremor
upgaze
upgaze, paralysis of
urinary incontinence
urine test for metabolic disorders
vertigo
walking, difficulty with
weight loss
wheelchair
wide based gait
Showing articles 0 to 50 of 15263 Next >>

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

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

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
Ann Clin Trans Neurol 3:655-663, Venkatraman,A. & Opal,P., 2016

Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
NEJM 356:612-620, Case 4-2007, 2007

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Pure Midbrain Infarction:Clinical Syndromes, MRI, and Etiologic Patterns
Neurol 44:2032-2040, Bogousslavsky,J.,et al, 1994

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Wilson's Disease:The Problem of Delayed Diagnosis
JNNP 55:692-696, Walshe,J.M.&Yealland,M., 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Pediatric Neurology
Psych Annals 2:1, , 1972

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
Neurol 105:e214099, Mizutani,H.,et al, 2025

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

Clinicopathological Conference, Systemic Lupus Erythematosus with Antiphospholipid Syndrome
NEJM 386:1560-1570, Case 12-2022, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

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

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

An 81-year-old Woman with Decreased Consciousness and Fluctuating Right Facial Droop
Neurol 94:843-848, Van Ommeren, R.,et al, 2020

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

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

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

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

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

Neuro-Sweet Disease Presenting as Ischemic Stroke and Aseptic Meningitis
Neurol 91:e2197-e2199, Das, A.S.,et al, 2018

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

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

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

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

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

Infratentorial Dural Arteriovenous Fistula Resulting in Brainstem Edema and Enhancement
Neurol 88:503-504, Emmer, B.J.,et al, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017



Showing articles 0 to 50 of 15263 Next >>