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Differential
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abducens nerve paralysis
abducens nerve paralysis, bilateral
acetazolamide
achilles tendon, enlarged
acoustic nerve
Adies pupil
adverse drug reaction
aggression
alcohol
alcohol, neurologic complications with
Alexanders disease
Alexanders disease, adult onset
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
alternating rapid movement, impaired
AMPA receptor antibodies
amyloid plaques
anergy
aneurysm, berry
anisocoria
anorexia
anti GQ1b IgG antibody
anti IgLON5
anti Ma
anti Ri antibody
anti Yo antibody
anxiety
aphasia
aphonia
apraxia of eye movements
areflexia
Arnold Chiari malformation
arterial dissection
arterial dissection, vertebral
arthralgia
arthritis
astrogliopathy
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic hemiparesis
ataxic-dystonia syndromes
ataxin
ataxin-2
ATP1A3 gene
atypical
autoantibodies
autoimmune disease
autoimmune encephalopathy
autonomic dysfunction
autonomic neuropathy
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery stenosis
behavioral disorder, acute
benign positional vertigo
biologic markers
blindness
brain biopsy
brainstem, atrophy
brainstem, dysfunction
brainstem, dysfunction, eye movement disorders with
brainstem, glioma
brainstem, hemorrhage, primary
brainstem, hypoplasia
brainstem, infarction of
brainstem, lesion of
brainstem, malformation
brainstem, neoplasms of
bulbar palsy
burning skin
cafe au lait spots
CAG repeats
canalolithiasis
carcinoembryonic antigen
carcinoma
carcinoma of breast
carcinoma of ovary
carcinoma of testis
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, pelvis
cataracts
celiac disease, adult
central hypoventilation
central nervous system, infection of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hemorrhage
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar peduncle
cerebellar vermis
cerebellitis
cerebellitis, autoimmune
cerebellum
cerebellum, disease of
cerebral edema
cerebral infarction
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, mimics
chenodeoxycholic acid
chest x-ray, abnormal
children
chlorpromazine
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 19
chromosome 6
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel pursuit movements
collagen vascular disease
Collier's sign
coma
cone-rod dystrophy
confusion
congenital malformation
conjugate gaze, forced
conjunctivitis
consanguinity
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
cranio-cervical junction
creatine phosphokinase(CPK)elevated
Cuba
cyst
cyst, parenchymal
cyst, subcortical
cystic fibrosis, neurologic complications with
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, familial
dementia, rapidly progressive
dentate nuclei, lesion of
depression
developmental abnormality of brain
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
diplopia
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
downward gaze, paralysis of
DPPX
DPPX, antibodies, encephalitis
drooling
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
ejection fraction, abnormal
electrocardiogram, abnormal
electromyogram
electroretinograph
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, focal
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, parainfectious
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
episodic neurologic deficits
erythema migrans
exercise intolerance
exome sequencing
eye movement, disorders of
eye, pain in
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial weakness, bilateral
failure to thrive
falling
false negative
familial
familial hemiplegic migraine
fasciculation
fatigue
fever
fine motor function, impaired
finger nose finger test
finger numbness
Fisher's syndrome
flu-like illness
fourth ventricle, enlargement of
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gangliosides
gaze deviation
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
GFAP gene
GluD2
glutamic acid decarboxylase, antibody
granulomatous disease
gray hair
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, ophthalmoplegia in
Guillain Barre syndrome, variant forms of
hand flapping
handwriting
head injury
head nodding
headache
hearing loss
heart sign
heel-knee-shin test
hemifacial spasm
hemiplegia
hepatomegaly
hepatosplenomegaly
HGPPS
HLA
hoarseness
hydrocephalus
hypercalcemia
hyperesthesia
hyperhidrosis
hyperreflexia
hypersomnia
hypocalcemia
hypogonadism
hypohidrosis
hypometric saccades
hypoparathyroidism
hypoparathyroidism, idiopathic
hyposmia
hypothalamus, disturbance of
hypothermia
hypothyroidism
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunodeficiency
immunohistochemistry
immunosuppression
immunotherapy
impotence
impulsivity
incoordination
inferior olivary nucleus
insomnia
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal biopsy
intracranial pressure, increased
iridoplegia
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Joubert syndrome
Kearns-Sayre syndrome
kelch-like protein 11 antibodies
labyrinthitis
labyrinthitis, acute
lactic acidemia
lateral medullary syndrome
lateropulsion
lateropulsion, ocular
Leigh's disease
leukemia
leukocytosis
leukoencephalopathy
level of consciousness, decreased
light-near dissociation, causes of
liver disease
Lyme disease
lymphadenopathy
lymphadenopathy, hilar
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
macrocephaly
malabsorption syndrome
malformation, CNS, congenital
malignancy, occult
mammillary bodies
medulla oblongata
medulla oblongata, infarction of
medulla oblongata, lesion of
medulla oblongata, malformation
medulla oblongata, neoplasm of
MELAS syndrome
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, chronic
meningitis, meningococcal
meningitis, prevention
meningitis, prophylaxis against
meningoencephalitis
mental retardation
mental status, abnormal
metabolic disorder, primary
metabolic disorder, primary-screening tests
microcephaly
midbrain
midbrain, atrophy
midbrain, infarction of
midbrain, lesion of
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
mononeuritis multiplex
mortality
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, negative
MRI, pelvis
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle cramp
muscle pain
muscle spasm, face
muscle weakness, proximal
myelitis
myelomalacia
myelopathy
myocarditis
myoclonic jerks
myoclonus
myoclonus, segmental
myopathy
myopathy, mitochondrial
myopia
myotonia
nausea and vomiting
neisseria meningitis
nerve conduction studies
neuritis
neuroblastoma
neurocutaneous disease
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuronopathy
neuroophthalmology
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, peripheral
neuropathy, sensory
neurosyphilis
neurotoxin
night sweats
nystagmus
nystagmus, cerebellar
nystagmus, direction changing
nystagmus, dissociated
nystagmus, gaze-paretic
nystagmus, monocular
nystagmus, pendular
nystagmus, periodic alternating
nystagmus, positional
nystagmus, primary position of gaze
nystagmus, retractorius
nystagmus, rotary
nystagmus, upbeating on upgaze
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
ocular dyskinesia
ocular dysmetria
ocular flutter
ocular motility, disorders of
oculogyric crisis
olivary degeneration, hypertrophic
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, progressive external
ophthalmoplegia, total
opsoclonus
opsoclonus, differential diagnosis of
opsoclonus-myoclonus syndrome
optic atrophy
optic neuropathy
optical coherence tomography
oscillopsia
ovarian tumor
ovary, enlarged
overlap syndrome
palatal myoclonus
panic attacks
papilledema
papillitis
paraneoplastic cerebellar degeneration
paraparesis
paraparesis, spastic
parasomnia
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
pathology
pelvic mass
periaqueductal lesion
pericarditis
periodic alternating gaze
peripheral nerve, lesion of
perphenazine
personality change
phenothiazine
pituitary, lesion of
pleocytosis of cerebrospinal fluid
pleurisy
pneumoencephalogram(PEG)
pneumonia
polymyositis
polyradiculoneuropathy
pons, hypoplasia
pons, lesion of
pontine glioma
Poretti-Boltshauser syndrome
positional head-hanging test
posterior inferior cerebellar artery syndrome
precipitating factors
pretectal syndrome
prion disease
progeria
prognosis
progressive ataxia and palatal tremor
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proteinuria
pseudoabducens palsy
pseudointernuclear ophthalmoplegia
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
pulmonary edema
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated, bilateral
pupil, ectopic-acquired
pupil, light reflex, abnormal
pupil, tonic
pure motor hemiplegia
Purkinje cell
Purkinje cell surface antibody
purpura
pursuit eye movements, abnormal
pyramidal tract dysfunction
pyramidal tract, uncrossed
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
radiation hypersensitivity
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
recurrent
reflex, brainstem
remote effect of cancer on the nervous system
renal failure
renal stones
respirations in CNS disease
respiratory tract infection
retina, abnormal
retinal degeneration
retropulsion
review article
rhomboencephalopathy
rigidity
Romberg's sign
saccadic eye movements, abnormal
salivation, excessive
sarcoidosis
sarcoidosis, CNS
scannig speech
scoliosis
scoliosis, neurologic association with
sedimentation rate, elevated
seizure
seizure, children
seminoma
sensorineural hearing loss
serologic testing
short stature
sicca syndrome
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skew deviation
skew deviation, alternating
skin, lesions in neurologic disorders
skull x-ray
skull x-ray, abnormal
sleep apnea, obstructive
sleep pathology and physiology
slurred speech
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, delayed development of
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 28
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
spontaneous remission
sports medicine, neurology of
square wave jerks
staggering
status epilepticus
steroid therapy, CNS treatment and complications with
strabismus
strokelike episodes
sweating
sweating, abnormality of
swimming
symmetric brain lesions
syphilis, neurologic complications with
tandem gait, ataxic
tau protein
tauopathy
telangiectases
temporal lobe, lesion
teratoma
teratoma, ovarian
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine
thiamine deficiency
third nerve
third nerve lesions, nuclear
third nerve palsy
third nerve palsy, partial
third ventricle, wall
thyrotropin-releasing hormone
tick bite
tilting
tinnitus
titubation
tonsillar herniation of cerebellum
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremor, jaw
tremulousness
triangle of Guillain and Mollaret
trigeminal neuralgia
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
ultrasonography
uncal herniation
unconsciousness
upgaze
upgaze, paralysis of
uveitis
vertigo
vertigo, episodic
vertigo, positional
vertigo, treatment of
vestibular function, tests of
vestibular neuritis
vestibulopathy
vibratory sensation, abnormal
viral infection
vision, blurred
visual loss
visual loss, progressive
visual loss, slow
vitamin deficiency
vitamin E
vitamin E deficiency
vitiligo
vitreous opacities
vocal cord paralysis
voice, abnormality of
walking frame
walking, difficulty with
weakness
weight loss
Wernekinck commissure syndrome
Wernicke's encephalopathy
West Nile fever
wheelchair
Whipple's disease
white matter disease
wide based gait
workup
xanthoma, tendon
xerophthalmia
xerostomia
 		Showing articles 50 to 100 of 18280 << Previous Next >>

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Alternating Skew on Lateral Gaze (Bilateral Abducting Hypertropia)
Ann Neurol 23:190-192, Moster,M.L.,et al, 1988

Vitamin E Deficiency & Neurologic Disease in Adults with Cystic Fibrosis
Ann Int Med 107:51-54, Sitrin,M.D.,et al, 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Eye-Movement Disorders in Brain-Stem & Cerebellar Stroke
Arch Neurol 44:141-148, Bogousslavsky,J.&Meienberg,O., 1987

Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
Arch Neurol 43:1050-1053, Farris,B.K.,et al, 1986

Wernicke's Encephalopathy
NEJM 312:1035-1039, Reuler,J.B.,et al, 1985

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Effect Of Thyrotropin-Releasing Hormone On Ataxia Of Spinocerebellar Degeneration
Lancet 1:418-419, Sobue,I.,et al, 1981

Opsoclonic Cerebellopathy, A Paraneoplastic Syndrome Responsive to Thiamine
Arch Neurol 38:780-781, Nausieda,P.A.,et al, 1981

Eye Movements in Patients with Wallenberg's Syndrome
Ann NY Acad Sci 374:600-613, Baloh,R.W.,et al, 1981

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

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

Periodic Alternating Gaze
Neurol 29:222-224, Stewart,J.D.,et al, 1979

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

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

Primary position upbeat nystagmus:a Clinicopathologic Study
Neurol 27:294, Gilman,N.,et al, 1977

Neurologic Manifestations in Sarcoidosis
Ann Int Med 87:336, Delaney,P., 1977

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

Ocular Motor Abnormalities in Hereditary Cerebellar Ataxia
Brain 99:207-234, Zee,D.S.,et al, 1976

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

Oculogyric Crisis
In Ocular Differential Diagnosis, Lea & Febiger, Phila. 1975 p. 133, Roy,F.H., 1975

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

Acquired Pendular Nystagmus with Oscillopsia in Multiple Sclerosis:A Sign of Cerebellar Nuclei Disease
JNNP 37:570, Aschoff,J.C.,et al, 1974

Ocular Dyskinesia in Cerebellar Disease
Brain 95:685, Ellenberger,C.,et al, 1972

Ocular Motor Manifestations of Brainstem & Cerebellar Dysfunction
Chap 9, p 104 Neuro-Ophthalmol ed J. L. Smith., Daroff,R.B., 1850

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

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

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

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

A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
Neurol 105:e214183, Costa,R., et al, 2025

A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
Neurol 105:e214233, Bu,S.,et al, 2025

A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
Neurol 105:e214381, Gomez,A.C.et al, 2025

A 66-Year-Old Man with Chronic Orthostatic Hypotension
Neurol 105:e214294, Lenka,A. & Vernino,S, 2025

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Ocular Myasthenia Gravis, Central Ocular Motor Signs and Unilateral Visual Loss Caused by the Great Neuro-Ophthalmologic Impersonator
Neurol 102:e209260, Young,A. & Johnston,J.L., 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

Wall-Eyed Bilateral Internuclear Ophthalmoplegia Variant Syndrome Caused by Isolated Left Thalamic Infarction
Neurol 102:e209475, Wu,B.P.,et al, 2024

The "Chameleon Eyes Sign" in Myasthenia Gravis
Neurol 103:e209756, Zara,P.,et al, 2024

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
www.UptoDate.com, Sept, Flanagan,E.P. & Tillema,J-M, 2023

MR Imaging Patterns and Prognosis in Powassan Virus Encephalitis
Neurologist doi.10.1097/NRI.0000000000000533, Finelli,P.F., 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A 25-Year-Old Woman With Eye Swelling and HEadache
Neurol 100:879-883, Hehir,A.,et al, 2023

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
Neurol 98:251-255, Decker, J. & Singh, M., 2022

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

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



Showing articles 50 to 100 of 18280 << Previous Next >>