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Differential
(Click to cross reference)
acetylcholine receptor
acetylcholine receptor antibody
Africa
alternating rapid movement
alternating rapid movement, impaired
amyotrophic lateral sclerosis
ANA
anticardiolipin antibodies
antiphospholipid antibody syndrome
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
Arnold Chiari malformation
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxic gait
atypical
autoantibodies
autoimmune disease
automobile accidents
B cell lymphoma
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
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, three territory involvement
chemotherapy, CNS treatment and complications with
children
chorea
chromosomal abnormality
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
Clinical Pathologic Conference(C.P.C.)
Coffin-Siris syndrome
cognition
cognition, slowed
confusion
congenital malformation
constipation
contractures, joint
conversion reaction
cornea, opacity of
cough
coumarin
Creutzfeldt-Jakob disease, genetic
cyst, arachnoid
cyst, arachnoid, infant
Dandy Walker malformation
Dandy Walker malformation, adult
dementia, familial
depression
developmental abnormality of brain
developmental retardation
diarrhea
differential diagnosis
difficulty climbing stairs
digits, abnormal
diplopia
disability, neurological
disorientation
distal muscle weakness
diurnal variation
dizziness
dopa responsive dystonia
dysarthria
dysdiadochokinesia
DYSF gene
dysferlin
dysferlinopathy
dyskinesia, buccal lingual facial
dysmetria
dysmorphic
dysphagia
dystonia
emergency room
encephalitis, brainstem
encephalocele
endemic area
Erdheim-Chester disease
eye movement, disorders of
falling
familial
fetal alcohol syndrome
finger nose finger test
fingernails, abnormal
fingernails, hypoplastic
fontanel, bulging
foot deformity
gait disorder
gait, spastic
ganglionitis
gastrocnemius muscle weakness
gene
gene mutation
genetic neurologic disorders
geographic location
glabellar sign
glutamic acid decarboxylase, antibody
granulomatous disease
handwriting
headache
health insurance
heel-knee-shin test
hemangioma
hemangioma, facial
hemangioma, skin
hemianopia
hemiparesis
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
hypocomplementemia
hyporeflexia
hypotonia
imbalance
immunologic disease
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
incoordination
infection
intellectual deterioration
interferon alpha
intracranial pressure, increased
intraventricular hemorrhage
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
joint hypermobility
L-dopa
leg weakness, bilateral
leg weakness, unilateral
lissencephaly
long bone lesion
lymphoma
lymphoma, primary of CNS
macrocephaly
Maghreb
malformation, CNS, congenital
Mary Walker phenomenon
memory, defect of recent
memory, impairment of
meningeal enhancement
mental status, abnormal
microcephaly
micropthalmia
midbrain, atrophy
misdiagnosis
mobility
mobility aids
mortality
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, contrast enhanced, high dose
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, nodular enhancement
MRI, optic nerve
MRI, punctate pattern
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 examination, focal
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
psychiatric problems in neurologic disorders
psychomotor retardation
reading disorder, acquired
real-time quaking-induced conversion
Red flags
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
startle myoclonus
steroid therapy, CNS treatment and complications with
stiff legs
stiff man syndrome
tandem gait, ataxic
tauopathy
teratogenic drugs
Three territory sign
thrombophlebitis
thymus and neuromuscular function
toe walking
tone, muscle, increased
treatment of neurologic disorder
tremor
tripping
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
walking frame
walking, difficulty with
weakness
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
workup
Showing articles 0 to 24 of 24

Clinicopathologic Conference, Antiphospholipid Syndrome due to SLE with Hypocomplimentemia
NEJM 389: 2277-2285, Case 38-2023, 2023

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

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

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 24 of 24