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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 100 to 150 of 18777 << Previous Next >>

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

A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025

Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

Clinicopathologic Conference, Cryptococcal Meningoencephalitis
NEJM 391:2361-2369, Case 40-2024, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

Rabbit Syndrome
Neurol102:e209275, Huynh,T.U., & Beckley, E.H., 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Paraneoplastic Calmodulin Kinase-Like Vesicle-Associated Protein (CAMKV) Autoimmune Encephalitis
Ann Neurol 96:21-33, Gilligan,M.,et al, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

Progressive Peripheral Neuropathy in a 66-Year-Old Woman with Sezary Syndrome
Neurol 103:e209983, Fanouraki,S.,et al, 2024

Isolated Primary Central Nervous System Lymphoma of the Optic Nerve, A Case Report and Review of the Literature
Neurologist 29:351-355, Keertana,J.,et al, 2024

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

Neurologic Manifestations of Hyperthyroidism and Graves Disease
www.UptoDate.com, Oct 28, Rubin,D.I., 2024

A Woman With Multifocal Ischemic Strokes and Progressive Cognitive Impairment Due to Intravascular Lymphoma
Stroke 54:e488-e451, Stamm,B., et al, 2023

Manganese Accumulation in the Brain
NEJM 389:1320, Sherman,S.V., 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

Clinicopathologic Conference, Factitious Disorder
NEJM 388:1609-1615, Case 13-2023, 2023

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

A 66-Year-Old Woman With Progressive Encephalopathy and Bilateral Hearing Loss
Neurol 100:254-258, Rivers,D.,et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

Torticollis in a Child with Otalgia
BMJ 378:e070608, Sarathi, C.I.P.,et al, 2022

Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
Neurol 99:e1957-e1967, Corp, D.T.,et al, 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

Reversible Symmetric Basal Ganglia Lesions in a Patient with Diabetes Undergoing Dialysis
Neurol 98:773-774, Quigley, S., 2022

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

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

Inconsistency and Incongruence: The Two Diagnostic Pillars of Functional Movement Disorder
Lancet 400:328, Hess, C.H.,et al, 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
Neurol 98:e95-e102, Wang, T.,et al, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

A 55-Year-Odd Man with Old Behavior and Abnormal Movements
Neurol 97:1090-1093, McIntosh, P. & Scott, B., 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

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

A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
Neurol 97:95-98, Dessy, A.,et al, 2021

A 64-Year-Old Man with Multiple Cranial Neuropathies
Neurol 97:e215-e221, Lefland, A.,et al, 2021

Focal Cerebral Arteriopathy of Childhood, Clinical and Imaging Correlates
Stroke 52:2258-2265, Oesch,G.,et al, 2021



Showing articles 100 to 150 of 18777 << Previous Next >>