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Differential
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alcohol, neurologic complications with
alcoholism
alien hand syndrome
alpha-fetoprotein
ANA
anergy
anticardiolipin antibodies
antiphospholipid antibody syndrome
aphasia
aphasia, progressive, primary
apraxia
apraxia of eye movements
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
autoantibodies
autoimmune encephalopathy
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bradykinesia
brain atrophy
brainstem, lesion of
cachexia
carcinoembryonic antigen
carcinoma
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellitis, autoimmune
cerebellum, disease of
cerebrospinal fluid, abnormal
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, three territory involvement
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cirrhosis
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
confusion
consanguinity
contractures, joint
corpus callosum, thinning
cortical-basal ganglionic degeneration
cranial neuropathy, multiple
degenerative diseases of CNS
dementia
developmental milestones, loss of
diabetes insipidus
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
disorientation
dopa responsive dystonia
DPPX
DPPX, antibodies, encephalitis
drooling
dysarthria
dysdiadochokinesia
dyskinesia, buccal lingual facial
dysphagia
dystonia
dystonia, children
encephalitis, autoimmune
encephalopathy
encephalopathy, progressive
enzyme, defect
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial nerve palsy
falling
familial
frontal behavioral spatial syndrome
gait disorder
galactorrhea
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
granulomatous disease
growth retardation
Hallervorden Spatz disease
headache
hemiparesis
hepatic failure
hepatolenticular degeneration, non-Wilsonian
hepatosplenomegaly
hydrocephalus
hyperammonemic encephalopathy
hypercalcemia
hyperesthesia
hyperreflexia
hypertonia
hypocomplementemia
hypophonia
hyporeflexia
hypothalamus, disturbance of
hypotonia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
intellectual deficit
intellectual deterioration
iron, brain
L-dopa
lenticular nucleus, lesion of, bilateral
leukemia
liver disease
lymphadenopathy, hilar
lymphoma
manganese intoxication
marche a petits pas
memory, impairment of
meningitis
meningitis, aseptic
mental retardation
mental status, abnormal
Mini Mental Status Examination
misdiagnosis
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, high signal intensity of basal ganglia
MRI, paramagnetic effect
MRI, T1 weighted high signal foci
multiple system atrophy
myelopathy
myelopathy, hepatic
myopathy
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic disease, tempo
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
ocular motility, disorders of
optic atrophy
orthostatic hypotension
PANK2 mutation
papilledema
paraparesis, spastic
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
pathology
peripheral nerve, lesion of
personality change
pituitary, lesion of
portal caval shunt
postural abnormality
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
pyramidal tract
pyramidal tract dysfunction
radiation hypersensitivity
renal stones
retinitis pigmentosa
review article
rigidity
Romberg's sign
sarcoidosis
sarcoidosis, CNS
scoliosis
sea-blue histiocytes
seizure
skin, lesions in neurologic disorders
skull x-ray
skull x-ray, abnormal
spasticity
speech disorder
speech disorder, childhood
spinal cord, lesion of
spinal muscular atrophy
stare
steroid therapy, CNS treatment and complications with
substantia nigra
synucleinopathy
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tandem gait, ataxic
tau protein
tauopathy
telangiectases
Three territory sign
thrombophlebitis
titubation
transient ischemic attack
treatment of neurologic disorder
tremor
tyrosine hydroxylase deficiency
uveitis
visual evoked response
visual impairment
walking frame
walking, difficulty with
weight loss
wheelchair
wide based gait
workup
Showing articles 0 to 50 of 18777 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Clinicopathologic Conference, Antiphospholipid Syndrome due to SLE with Hypocomplimentemia
NEJM 389: 2277-2285, Case 38-2023, 2023

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

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

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

Acquired Hepatocerebral Degeneration
Neurol 87:e144, Bateman, J.R. & Roque, D.A., 2016

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Neurologic Manifestations in Sarcoidosis
Ann Int Med 87:336, Delaney,P., 1977

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

Bobble-Head Doll Syndrome in a Child
Neurol 104: e213694, Chityala,A.,et al, 2025

A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
Neurol 105:e214233, Bu,S.,et al, 2025

A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
Neurol 105:e214381, Gomez,A.C.et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
Neurol 105:e214297, Chen,Z., et al, 2025

A 62-Year-Old Man with Progressive Limb Weakness, Involuntary Movements, and HyperCKemia
JAMA Neurol 82L:1286-1287, Liu,Y.,et al, 2025

Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
NEJM 389:1416-1423, Case 31-2023, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

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

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

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,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 Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
Ann Neurol 88:637-638, Wu, H.,et al, 2020

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

Chronic Dengue Virus Panencephalitis in a Patient with Progressive Dementia with Extrapyramidal Features
Ann Neurol 86:695-703, Johnson, T.P.,et al, 2019

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

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

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

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

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

Wilson Disease
NIDDK Oct2018, , 2018

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

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

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

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

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013

Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
NEJM 369:2021-2030, Watchko, J.F.,et al, 2013

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



Showing articles 0 to 50 of 18777 Next >>