Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
agitation
akinetic mute
apraxia of eyelid opening
ataxia
athetosis
basal ganglia, lesion of
behavioral disorder
bilirubin encephalopathy
biologic markers
blinking, reduced
bradykinesia
bradyphrenia
breast feeding
catalepsy
cataplexy
cerebellar degeneration
cerebral cortical atrophy
children
choreoathetosis
Clinical Pathologic Conference(C.P.C.)
compulsivity
cortical-basal ganglionic degeneration
cry, abnormal
cry, high-pitched
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontotemporal
dementia, presenile
depression
developmental retardation
diagnostic criteria
differential diagnosis
disability, neurological
disease modifying agents
dizziness
dysarthria
dysphagia
dystonia
encephalopathy
executive dysfunction
exome sequencing
eye movement, disorders of
falling
fever
fracture, long bone
frontal lobe, pathologic signs of
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
hallucination
hallucination, visual
head injury
hearing loss
hepatomegaly
hepatosplenomegaly
heralding manifestation
hummingbird sign
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
imbalance
imbalance, postural
inattention
incoordination
intellectual deficit
intellectual deterioration
jaundice
kernicterus
life expectancy
lipid storage disorder of CNS
lysosomal storage disease
masked facies
memory, impairment of
mental retardation
midbrain
midbrain, atrophy
miglustat
mimics
misdiagnosis
moro reflex
mortality
movement disorder
MRI
MRI, abnormal
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, negative
multiple system atrophy
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuroophthalmology
neuropathology
neuropathology, brain
Niemann-Pick disease
nystagmus
obsessive-compulsive disorder
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, neonatal
ophthalmoplegia, total
opisthotonus
organomegaly
paranoia
Parkinson disease, atypical
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
personality change
preclinical
premature infant
prognosis
progressive neurologic disorder
progressive supranuclear palsy
progressive supranuclear palsy, natural history
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychotic behavior
rapidly progressing neurologic illness
reading disorder, acquired
reading problem, causes of
release phenomena
review article
rigidity, axial
saccadic eye movements
saccadic eye movements, abnormal
salivation, excessive
schizophrenia
screening
seizure
seizure, laughing as manifestation
sensorineural hearing loss
setting sun phenomena
speech disorder
splenomegaly
suck, poor
synucleinopathy
systemic illness
tau protein
tauopathy
treatment of neurologic disorder
upgaze, paralysis of
vertical gaze
walking, difficulty with
whole genome sequencing
Showing articles 50 to 100 of 9150 << Previous Next >>

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Complete Ophthalmoplegia After Zoster Ophthalmicus
J Neuro-Ophthalmol 17:262-265, Chang-Godinich,A.,et al, 1997

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Prolonged Paralysis Due to Nondepolarizing Neuromuscular Blocking Agents and Corticosteroids
Muscle & Nerve 17:647-654994., Barohn,R.J.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Isolated Horizontal Supranuclear Gaze Palsy as a Marker of Severe Systemic Involvement in Gaucher's Disease
Neurol 43:1993-1997, Patterson,M.C.,et al, 1993

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

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

Dysphagia in Patients with the Post-Polio Syndrome
NEJM 324:1162-1167, 1206-12071991., Sonies,B.C.&Dalakas,M.C., 1991

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.R.,et al, 1990

Risk Factors for Progressive Supranuclear Palsy
Neurol 38:1546-1552, Davis,P.H.,et al, 1988

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Sino-Orbital Aspergillosis Associated with Total Ophthalmoplegia
Laryngoscope 95:190-192, Yumoto,E.,et al, 1985

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

Conjugate Gaze Paresis in Stroke Patients With Unilateral Damage
Arch Neurol 39:482-486, DeRenzi,E.,et al, 1982

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

The Carotid-Cavernous Fistula:Spontaneous & Traumatic, In Clinical Neuro-Ophthalmology
3rd Ed, Williams & Wilkins, Baltimore, p. 1714, Walsh,F.B.&Hoyt,W.F., 1969

Mucormycosis
NEJM 394:684-698, Kontoyiannia,D.P. & Walsh, T.J., 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

Melas Syndrome
Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025

Adult-Onset Coats Plus, A Case of Leukoencephalopathy with Calcifications, a Tumefactive Brain Lesion, and a Presumed Autoimmune Disease
Neurol 105:e214124, Gerrao,C.,et al, 2025

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

Acromegaly
NEJM 393:1926-1939, Giustina,A. & Colao,A.,, 2025

Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2243-2253, 2264, Johnson,M.D.,& Williams, M.A., 2025

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

Clinical Presentation, Investigation Findings, and Outcomes of IgG4-Related Pachymeningitis,A Systematic Review
JAMA Neurol 82:193-199, Terrim,S.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,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

Pan-Neurofascin Nodo-Paranodopathy Presenting as Fulminant Guillain-Barre Syndrome
Neurol 105:e213848, Cabral,A.,et al, 2025

Risdiplam in Presymptomatic Spinal Muscular Atrophy
NEJM 393:671-682, Finkel,R.S.,et al, 2025

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

Primary Central Nervous System Vasculitis
NEJM 391:1028-1037, Salvarani,C.,et al, 2024

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

Mortality and Causes of Death in Children with Cerebral Palsy with Scoliosis Treated with and without Surgery
Neurol 101:e1787-e1792, Ahonen,M.,et al, 2023

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

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

Characteristics of Progressive Multifocal Leukoencephalopathy Associated with Sarcoidosis without Therapeutic Immune Suppression
JAMA Neurol 80:624-633, McEntire,C.R.S.,et al, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

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

Clinical Features and Diagnosis of Intramedullary Spinal Cord Abscess in Adults, A Systematic Review
Neurol 101:e836-e844, Harrold,G.K.,et al, 2023

A 67-YEar-Old Man with Multiple Intracranial Lesions
Neurol 101:e845-e851, Ngo,A.,et al, 2023

Neurobrucellosis:The Great Mimicker
Rev Soc Bras Med Trop 55:e0567-e2012, Soares,C.N.,et al, 2022

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022



Showing articles 50 to 100 of 9150 << Previous Next >>