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acoustic nerve
adolescent medicine
advances in neurology
alien hand syndrome
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
AMPA receptor antibodies
anosmia
anti GQ1b IgG antibody
anti IgLON5
anticholinergic drugs
anxiety
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
areflexia
arm swing, reduced
aspiration
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic-dystonia syndromes
athetosis
ATP1A3 gene
attention span
autoantibodies
autoimmune basal ganglia encephalitis
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basilar impression
behavioral disorder
biologic markers
biopterin deficiency
bladder dysfunction
blepharospasm
bradykinesia
brainstem, atrophy
brainstem, lesion of
bruxism
bulbar palsy
calcitonin
carbamazepine
carcinoembryonic antigen
carcinoma
cardiomyopathy
cataplexy
cataracts
central hypoventilation
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebrovascular accident
cerebrovascular accident, young adult
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 20
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
comorbidities
compression fracture
conjugate gaze, forced
conversion reaction
cortical-basal ganglionic degeneration
cranial neuropathy, multiple
crying, pathologic
cultured skin fibroblasts
degenerative diseases of CNS
delay in diagnosis
dementia
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
diurnal variation
dopa responsive dystonia
downward gaze
drooling
dysarthria
dysarthria-clumsy hand syndrome
dyskinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, focal
dystonia, psychogenic
dystonia, treatment of
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalopathy
enzyme, defect
equinovarus
exercise
exercise-induced neurologic dysfunction
exome sequencing
exophthalmus
eye movement, disorders of
facial nerve palsy
falling
familial
fine motor function, impaired
foam cells
foot deformity
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gangliosidosis GM1
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamic acid decarboxylase, antibody
grasp reflex
grimacing
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hand weakness
hands, fisted
head circumference
headache
hearing loss
heart block
hemidystonia
hemifacial spasm
hemiplegia
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
HLA
hoarseness
Hodgkin's disease
hydrocephalus
hyperreflexia
hypometric saccades
hypophonia
hyposmia
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
immunotherapy
inattention
inclusion bodies, intranuclear
incontinence, fecal
incoordination
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
iron, brain
Jakob-Creutzfeldt disease
jaundice
Kayser-Fleischer ring
Kearns-Sayre syndrome
laughing, pathologic
L-dopa
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
leucine rich glioma inactivated 1 antibodies
leukemia
limbic encephalitis
lipid storage disorder of CNS
liver disease
low back pain
lymphoma
macular degeneration
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, carcinomatous
mental retardation
mental status, abnormal
MERRF syndrome
microcephaly
midbrain
midbrain, atrophy
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoclonal antibodies
mortality
motor dysfunction
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, spine
multiple system atrophy
muscle spasm, face
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neurologic symptoms, unexplained
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathy
Niemann-Pick disease
NMDA antagonists
numb clumsy hands syndrome
nystagmus
nystagmus, monocular
ocular motility, disorders of
opened mouth
ophelia syndrome
ophthalmoplegia
optic atrophy
optic atrophy, unilateral
optic neuropathy
optokinetic nystagmus, abnormal
Paget's disease
Paget's disease, psychosis in
Paget's disease, spinal cord problem in
pain
palilalia
pancytopenia
PANK2 mutation
paraparesis
parasomnia
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penguin silhouette sign
personality change
personality disorder
pigmentary retinopathy
pitfalls
pleocytosis of cerebrospinal fluid
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
PRKN gene
procyclidine
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
pull test
radiation hypersensitivity
radiculopathy
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Red flags
release phenomena
respirations in CNS disease
retinal artery occlusion
retinal hemorrhages
retinopathy
retrocollis
Rett's syndrome
reversible neurologic disorder
review article
rigidity
rigidity, axial
risk factors
rituximab
root lesion, nerve
running
saccadic eye movements, abnormal
salivation, excessive
screening
seizure
sensorineural hearing loss
sensory loss, cortical
sequencing difficulty
serologic testing
serologic testing, false negative
seronegative
short stature
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
speech disorder
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
stare
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
striatal encephalitis
suck reflex
superior orbital fissure syndrome
swallow evaluation
tau protein
tauopathy
telangiectases
tetrahydrobiopterin
toe walking
tonic foot response
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, postural
tremor, psychogenic
trigeminal neuralgia
tripping
upgaze
upgaze, paralysis of
urinary incontinence
vertebral-basilar insufficiency
vision, blurred
visual symptoms
vocal cord paralysis
walking
walking frame
walking, difficulty with
weight loss
wheelchair
wide based gait
Wolfram syndrome
Showing articles 650 to 700 of 8642 << Previous Next >>

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

Progressive & Treatable Cerebellar Ataxia in Macroglobulinemia
Neurol 30:536-538, Spencer,S.S.,et al, 1980

Nervous System Toxicity of Chemo Agents
Young, DF, in Vinken PJ, Bruyn GW, Handbook of Clin Neurol, North-Holland Publ Co, Amster, Vol 39, 1, 80, p 104, 1980

Hysterical Gaits
In the Neurologic Examination, Ed. Russell N. DeJong, 4th Edition, Harper & Row, Publ, Hagerstown, p, 426, 1979

Neurologic Abnormalities of Lyme Disease
Medicine 58:281-294, Reik,L.,et al, 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Meige's Disease, A Clinical Form of Facial Convulsion, Bilateral & Medial
Arch Neurol 36:635-637, Tolosa,E.S.,et al, 1979

Meige Disease:Striatal Dopaminergic Preponderance
Neurol 29:1126-1130, Tolosa,E.S.,et al, 1979

Hydrocephalic Dementia in Pagets Disease of the Skull:Treatment by Ventriculoatrial Shunt
Neurol 29:513-516, Goldhammer,Y.,et al, 1979

Optic Neuropathy & Ophthalmoplegia in Herpes Zoster Oticus
Neurol 29:726-729, Carroll,W.M.,et al, 1979

Self-Limited Granulomatous Angiitis of the Cerebellum
Ann Neurol 5:490-492, Beresford,H.R.,et al, 1979

Helper & Suppressor T-Lymphocyte Leukemia In Ataxia Telangiectasia
NEJM 300:700-704, Saxon,A.,et al, 1979

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Ataxic Hemiparesis
Arch Neurol 35:126, Fisher,C.M., 1978

Aggravation of Tardive Dyskinesia by Phenytoin
NEJM 298:457, DeVeaugh-Geiss,J., 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Ataxia Telangiectasia
Arch Neurol 35:553-554, Teplitz,R.L., 1978

Eye Movements in Ataxia-telangiectasia
Neurol 28:1099-1104, Baloh,R.W.,et al, 1978

Cerebrovascular diseases
In Harrison's Principles of Internal Medicine, 1977. McGraw-Hill Book Co. , p1., , 1977

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

DiGeorge Syndrome Associated with Glioma & Two Kinds of Viral Infection
NEJM 296"1235, Asamoto,H., 1977

Fisher's Syndrome:A Pharmacological Study of the Pupils
Ann Neurol 2:63, Okajima,T.,et al, 1977

Effects of Learning on Visceral Functions-Biofeedback
NEJM 296:1274, Miller,N.E.,et al, 1977

A Syndrome of Early Recognition of Occult Hydrocephalus & Cerebral Atrophy
Quart J Med 183:365, Botez,M.I.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Tonic Pupils with Acute Ophthalmoplegic Polyneuritis
Ann Neurol 2:393, Keane,J.R., 1977

The Central Nervous System in a Case of Neurolathyrism
Neurol 27:1176, Striefler,M.,et al, 1977

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Blepharospasm-oromandibular Dystonia Dyndrome (Brueghel's syndrome) :A Variant of Adult-onset Torsion Dystonia
JNNP 39:1204, Marsden,C.D., 1976

Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

Hypophosphatemia Mimicking Acute Guillain-Barre-Strohl Syndrome
JAMA 235:1040-1041, Weintraub,M.I., 1976

MGH-CPC-Ataxic Telangiectasia & Left Frontal Lobe Glioma
NEJM 292:1231, , 1975

Progressive Rubella Encephalitis
NEJM 292:990-993, 994-998, 1023-1024975., Townsend,J.J., 1975

Oral Facial Dyskinesia Assoc. with Prolonged use of Antihistamine Decongestants
NEJM 293:486, Thach,B.T.,et al, 1975

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

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

Progressive Rubella Panencephalitis
NEJM 292:990-993,1023, Townsend,J.,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

Pseudointernuclear Ophthalmoplegia in Acute Idiopathic Polyneuritis (Fisher's Syndrome)
Am J Ophthalmol 77:725, Swick,H.M., 1974

Neurologic Syndrome Associated with Antipsychotic Drug Use
NEJM 289:20, 1973, 290:110974., , 1974

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974



Showing articles 650 to 700 of 8642 << Previous Next >>