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Differential
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alcohol, neurologic complications with
alcoholism
alien hand syndrome
ANA
anergy
anticardiolipin antibodies
antiphospholipid antibody syndrome
aphasia
aphasia, progressive, primary
apraxia
ataxia
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
cerebellar degeneration
cerebellitis, autoimmune
cerebellum, disease of
cerebrospinal fluid, abnormal
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, three territory involvement
children
chorea
choreoathetosis
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
diagnostic criteria
differential diagnosis
diplopia
disorientation
dopa responsive dystonia
DPPX
DPPX, antibodies, encephalitis
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 mutation
genetic neurologic disorders
genetic testing
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
granulomatous disease
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
imbalance
imbalance, postural
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
intellectual deficit
intellectual deterioration
iron, brain
L-dopa
lenticular nucleus, lesion of, bilateral
liver disease
lymphadenopathy, hilar
manganese intoxication
marche a petits pas
memory, impairment of
meningitis
meningitis, aseptic
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
neurologic disease, diagnoses of
neurologic disease, tempo
neuropathology
neuropathology, brain
neuropathy, peripheral
optic atrophy
orthostatic hypotension
PANK2 mutation
papilledema
paraparesis, spastic
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
peripheral nerve, lesion of
personality change
pituitary, lesion of
portal caval shunt
postural abnormality
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
pyramidal tract
pyramidal tract dysfunction
renal stones
retinitis pigmentosa
review article
rigidity
Romberg's sign
sarcoidosis
sarcoidosis, CNS
scoliosis
sea-blue histiocytes
seizure
skull x-ray
skull x-ray, abnormal
spasticity
speech disorder
speech disorder, childhood
spinal cord, lesion of
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
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 50 to 100 of 18462 << Previous Next >>

Progressive Multifocal Leukoencephalopathy Presenting with an Isolated Focal Movement Disorder
Movement Disorder 15:1006-1009, Stockhammer,G.,et al, 2000

Review of 23 Patients Affected by the Stiff Man Syndrome:Clinical Subdivision into Stiff Trunk (man) Syndrome,Stiff Limb Syndrome,and Progressive Encephalopmyelitis with Rigidity
JNNP 65:633-640, Barker,R.A.et al, 1998

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Extrapyramidal Symptoms in a BMT Recipient with Hyperintense Basal Ganglia and Elevated Manganese
Bone Marrow Transplantation 15:989-992, Fredstrom,S.,et al, 1995

Isolated Motor Control Dysfunction Related to Progressive Multifocal Leukoencephalopathy During AIDS with Normal MRI
Neurol 44:2352-2355, deToffol,B.,et al, 1994

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Clinical Use of Botulinum Toxin
National Institutes of Health Consensus Develop Conf Stmt, Nov 12-14, 1990, Arch Neurol 48:1294-1298, 199, 1991

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

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

New Uses and Old for Carbamazepine
Patient Care 24:48-81, Browne,T.R.,et al, 1990

Hypoxic-Ischemic Damage of the Basal Ganglia
Mov Disord 5:219-224, Hawker, K. & Lang, A.E., 1990

Acquired Hepatocerebral Degeneration:MR Similarity with Wilson Disease
J Comput Assist Tomogr 12:1076-1077, Hanner,J.S.,et al, 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Clinicopath. Conference
Pick's Disease of Brain, with Frontal Lobar Atrophy, Degen of Basal Ganglia, Case 16-1986, NEJM 314:, 101-,1986., 1986

"Apraxia"of Eyelid Opening:An Involuntary Levator Inhibition
Neurol 35:423-427, Lepore,F.E.,et al, 1985

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
NEJM 292:994-998,1023, Weil, M.L.,et al, 1975

Neurologic Manifestations of SLE 1972
Nebraska State Journ Med, Oct 1972, pp 395., Aita,J., 1972

Thromboangiitis Obliterans Cerebri
Edited by, Vinken, E. , Handbook Clinical Neurol 12:3842., Bernsmeier,A.&Held,K., 1972

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

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

An 81-Year-Old Man with Imbalance and Memory Impairment
, Golbe,L.I.,et al,

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,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

Addressing Systemic Complications of Acute Stroke: A Scientific Statement From the American Heart Association
Stroke 56:e15-e29, Kumar,S.,et al, 2025

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

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

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

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

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

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

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

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



Showing articles 50 to 100 of 18462 << Previous Next >>