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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 50 to 100 of 18777 << Previous Next >>

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
NEJM 358:1009-1017, Stepens,A.,et al, 2008

Tau Forms in CSF as a Reliable Biomarker for Progressive Supranuclear Palsy
Neurol 71:1796-1803, Borroni,B.,et al, 2008

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Paraneoplastic Chorea Associated with CRMP-5 Neuronal Antibody and Lung Carcinoma
Ann Neurol 51:625-630, Vernino,S.,et al, 2002

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

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

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

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

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

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

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

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

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

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

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

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

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

Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
NEJM 394:282-294, Case 202026, 2026

An 83-Year-Old Female Patient with a Pupil Involving Oculomotor Nerve Palsy
Neurol 105:e214383, Riegel,D.C.,et al, 2025

Recurrent Ischemic Strokes Due to Os Odontoideum
Ann Neurol 98:1315-1317, Wang,J.,et al, 2025

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

A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
Neurol 105:e214183, Costa,R., 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

Unveiling the Clinical and Imaging Signatures of Intravascular Lymphoma of the Central Nervous System:A Multicentric Cohort Study
Ann Neurol 97:435-448, Berthet,E.,et al, 2025

Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
Neurol 104: e213682, Hayakawa,I.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025



Showing articles 50 to 100 of 18777 << Previous Next >>