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Differential
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acetylcholine receptor
acetylcholine receptor antibody
Africa
alternating rapid movement
amyotrophic lateral sclerosis
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
Arnold Chiari malformation
ataxia
ataxia, cerebellar
ataxia, sensory
ataxic gait
autoantibodies
autoimmune disease
Babinski sign
blindness
bone biopsy
BRAF protooncogene
brain biopsy
brainstem, lesion of
cane
cardiomyopathy
CAT scan
CAT scan, abdomen
CAT scan, abnormal
cataracts
cataracts, congenital
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, secondary
cerebellar hypoplasia
cerebellar lesion
cerebellum, disease of
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
Clinical Pathologic Conference(C.P.C.)
Coffin-Siris syndrome
congenital malformation
constipation
contractures, joint
cornea, opacity of
cough
coumarin
cyst, arachnoid
cyst, arachnoid, infant
Dandy Walker malformation
Dandy Walker malformation, adult
developmental abnormality of brain
developmental retardation
diarrhea
differential diagnosis
digits, abnormal
diplopia
disability, neurological
distal muscle weakness
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysmetria
dysmorphic
dysphagia
emergency room
encephalitis, brainstem
encephalocele
endemic area
Erdheim-Chester disease
eye movement, disorders of
falling
fetal alcohol syndrome
fingernails, abnormal
fingernails, hypoplastic
fontanel, bulging
gait disorder
gait, spastic
ganglionitis
gastrocnemius muscle weakness
gene
gene mutation
genetic neurologic disorders
geographic location
glabellar sign
glutamic acid decarboxylase, antibody
granulomatous disease
headache
health insurance
heel-knee-shin test
hemangioma
hemangioma, facial
hemangioma, skin
histiocytosis
human T-lymphotropic virus type I(HTLV-I)
hydrocephalus
hydrocephalus, acute
hydrocephalus, classification of
hydrocephalus, communicating
hydrocephalus, congenital
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hyperreflexia
hypertrichosis
hyporeflexia
hypotonia
imbalance
immunologic disease
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
incoordination
infection
interferon alpha
intracranial pressure, increased
intraventricular hemorrhage
joint hypermobility
leg weakness, bilateral
lissencephaly
long bone lesion
macrocephaly
Maghreb
malformation, CNS, congenital
Mary Walker phenomenon
memory, defect of recent
memory, impairment of
meningeal enhancement
microcephaly
micropthalmia
midbrain, atrophy
misdiagnosis
mobility
mobility aids
mortality
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, contrast enhanced, high dose
MRI, disappearing lesion on
MRI, nodular enhancement
MRI, optic nerve
MRI, spinal cord
muscle biopsy
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, neonatal
myasthenia gravis, neuromuscular junction in
myasthenia gravis, passive transfer of
myasthenia gravis, receptor site in
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myelomalacia
myelopathy
myelopathy, chronic progressive
myopathy
neck pain
neck weakness
nerve conduction studies
neurocutaneous disease
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
nystagmus, gaze-evoked
nystagmus, upbeating on upgaze
old age, neurology of
optic nerve, enhancement
oscillopsia
pain, leg
papilledema
paraparesis, spastic
paraspinal muscle
perivascular enhancement
physical therapy
plasmapheresis
pleocytosis of cerebrospinal fluid
pons, lesion of
position sensation
positional head-hanging test
posterior column disease
posterior fossa
posterior fossa, lesion of
prognosis
progressive neurologic disorder
proprioception
pseudoathetosis
psychomotor retardation
reading disorder, acquired
release phenomena
retinal detachment
retinal dysplasia
retroperitoneal fibrosis
retroperitoneal mass
reversible neurologic disorder
review article
Romberg's sign
saccadic eye movements, abnormal
sclerosis, bone
scooters
screening
sensory loss
sensory loss, patchy
sensory nerve action potentials
shunt procedure, ventricular
snout reflex
spasticity
speech disorder
speech disorder, non aphasic
steroid therapy, CNS treatment and complications with
stiff legs
stiff man syndrome
tandem gait, ataxic
tauopathy
teratogenic drugs
thymus and neuromuscular function
tone, muscle, increased
treatment of neurologic disorder
tremor
ulnar nerve, compression of
ulnar nerve, deep palmar branch of
ulnar neuropathy
ultrasonography
urinary urgency
Vemurafenib
vestibulopathy
vibratory sensation, abnormal
vision, blurred
visual loss
voice, abnormality of
Walker-Warburg syndrome
walking frame
walking, difficulty with
weakness
weakness, progressive
wheelchair
white matter disease
wide based gait
Showing articles 0 to 20 of 20

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

A 52-year-old Man with Diplopia and Ataxia
Neurol 87:e140-e143, Bradshaw, M.J.,et al, 2016

A 73-year-old Man with Diplopia and Ataxia
Neurol 85:e96-e100, Gupta, H.V.,et al, 2015

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Hydrocephalus
Adams & Victors Principles of Neurology, Chp 30, pg 622, Ropper, A.H.,et al, 2014

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Congenital Muscular Dystrophy
eMedicine (Jan), Lopate,G., 2007

Disease Progression in Sporadic Inclusion Body Myositis: Observations in 78 Patients
Neurol 55:296-198, Peng,A. et al, 2000

A 44-Year-Old Woman with Difficulty Walking
JAMA 284:2632-2639, Iezzoni,L.I., 2000

The Clinical Spectrum of Anti-GAD Antibody-Positive Patients with Stiff-Person Syndrome
Neurol 55:1531-1535, Dalakas,M.C.,et al, 2000

Association of Facial Hemangiomas with Dandy-Walker and Other Posterior Fossa Malformations
J Pediatr 122:379-384, Reese,V.,et al, 1993

The Dandy-Walker Syndrome
In Handbk of Clin Neurology, Elsevier Publ, Amsterdam, 50:32387., Epstein,M.H.&Johanson,C.E., 1987

Coffin-Siris Syndrome, Neuropathologic Findings
Arch Neurol 42:350-353, DeBassio,W.A.,et al, 1985

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

Ulnar Nerve Palsy & Walking Frames
BMJ 285:778, Reid,R.I.,et al, 1982

Myasthenia Gravis
NEJM 298:136, Drachman,D.B., 1978

Adult Onset of the Dandy-Walker Syndrome
Arch Neurol 35:672-674, Lipton,H.L.,et al, 1978



Showing articles 0 to 20 of 20