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Differential
(Click to cross reference)
abducens nerve paralysis
acanthocytosis
acoustic nerve
acral sensory symptoms
Addison's disease
adrenoleukodystrophy
adrenomyeloneuropathy
adult polyglucosan body disease
adverse drug reaction
agitation
akinetic mute
alcohol intolerance
algorithm
alien hand syndrome
alkylating agents
altered states of consciousness
alternating rapid movement
amaurosis fugax
amphiphysin antibodies
amygdala
ANA
anemia
anemia, megaloblastic
aneurysm
angiography, spinal
anhidrosis
anorexia
antecedent illness
anterior choroidal artery
anti GQ1b IgG antibody
anti Hu antibody
anti Ma
anti Ri antibody
anti Yo antibody
antiamphiphysin
antibiotics
antibiotics, neurologic complications with
antiganglioside antibodies
antimetabolite
areflexia
arrhythmia, cardiac
arterial dissection, vertebral
arteritides
arthralgia
arthritis
ascending paralysis
asparginase
astereognosis
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic hemiparesis
athetosis
atonic bladder
atypical
auditory evoked brainstem potentials
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic neuropathy
axonal degeneration
axonopathy, distal
B 12 deficiency
B12
Babinski sign
basal ganglia
basal ganglia, lesion of
Bassen-Kornzweig syndrome
bedridden
behavioral disorder
Bell's phenomenon
bladder dysfunction
blood dyscrasias, neurologic findings with
bovine spongiform encephalopathy
bradykinesia
brainstem, hematoma
brainstem, hemorrhage, primary
brainstem, infarction of
brainstem, lesion of
brainstem, syndrome
burning feet
burning hands
burning paresthesia
CAG repeats
carcinoma
carcinoma of breast
carcinoma of cervix
carcinoma of lung
carcinoma of ovary
carcinoma of uterus
cardiomegaly
cardiomyopathy
carpal tunnel syndrome
case studies
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, false negative
cataracts
caudate nucleus, atrophy
cavernous hemangioma
central nervous system, infection of
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellar lesion
cerebellar peduncle
cerebellar vermis
cerebellum, disease of
cerebral cortical atrophy
cerebral infarction
cerebro hepato renal syndrome
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, pressure low
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, vascular territory involved
cervical myelopathy
Charcot-Marie-Tooth
Cheiro-oral syndrome
chemotherapy, CNS treatment and complications with
children
chills
chorea
chorein
choreoathetosis
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
cognition
collagen vascular disease
collapsin response mediator protein 5 IgG
concentration, impaired
conduction block
confusion
congestive heart failure
constipation
contactin associated protein like 2 antibodies
conus medullaris, lesion of
convergence, impaired
conversion reaction
copper deficiency
cortical-basal ganglionic degeneration
cough
cranial nerve palsies
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
deafness
deafness, unilateral
deep gray nuclei
delay in diagnosis
delirium
dementia
demyelinating disease
depression
dermatomyositis
dexterity, impaired
diagnostic criteria
diarrhea
diet
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
dissociated sensory loss
distal muscle weakness
dizziness
DNA probes
down-beat nystagmus
drug abuse
drug induced neurologic disorders
dural arteriovenous malformation
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dyskinesia, buccal lingual facial
dysmetria
dysphagia
dyspnea
dyspraxia
dystonia
dystrophic calcification
ejection fraction, abnormal
electrical sensation
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electroretinograph
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalomyelitis
encephalomyelitis, paraneoplastic
encephalopathy
enzyme, muscle disease
epidemiology of neurology
epistaxis
erythema migrans
evoked potentials
exercise
exercise-induced leg numbness
exercise-induced vascular symptoms
eye movement, disorders of
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
falling
familial
family planning
fatigue
fever
fibrillations
fine motor function, impaired
fish
fish poisoning
Fisher C.M.
Fisher's syndrome
fistula, arterio-venous, dural
fistula, arterio-venous, dural, spinal
flaccid paralysis
flu-like illness
fluorescent treponema antibody absorption(FTA-ABS)
fluorouracil
flush syndrome
food-borne infection
foot deformity
foot drop
foot numbness
Friedreich's ataxia
Friedreich's ataxia, late onset
fundus, abnormality of
gait disorder
gait, spastic
gammaglobulin therapy, intravenous
ganglionitis
gangliosides
gasserian ganglia
gastrectomy, neurologic complications following
gastric partitioning
gastroenteritis
gaze palsy
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
girdle sensation
gluten sensitivity
Guillain Barre syndrome
Guillain Barre syndrome, ataxic form
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, ophthalmoplegia in
Guillain Barre syndrome, prognosis of
Guillain Barre syndrome, sensory
Guillain Barre syndrome, variant forms of
Hallervorden Spatz disease
hallucination
hallucination, visual
hammertoes
hand numbness
hand weakness
headache
headache, severe
headache, sudden onset of
hearing loss
heel-knee-shin test
hemianopia, homonymous
hemiataxia
hemiparesis
hemisensory loss
hemisensory syndrome
hemorrhage, thalamic
hepatomegaly
herpes simplex virus
herpes virus
herpes virus infection
herpes, genital
hiccoughs
Hispanics
hoarseness
Hodgkin's disease
homocysteine, serum
Horner's syndrome
hot cross bun sign
human immunodeficiency virus type 1
hyperhomocysteinemia
hyperreflexia
hypersegmented polys
hypertension
hypertonia
hyponatremia
hypophosphatemia
hyporeflexia
iatrogenic neurologic disorders
idiopathic
imbalance
immune checkpoint inhibitors
immunologic disease
immunology and the nervous system
immunosuppressive agents
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inclusion bodies
incontinence, fecal
incoordination
intellectual deficit
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intracerebral hemorrhage
intracerebral hemorrhage, small
iridoplegia
irritability
isoniazid
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
jaundice
jaw pain
Jewish
Kearns-Sayre syndrome
Korsakoff's psychosis
kyphoscoliosis, neurologic causes of
kyphosis
lactic dehydrogenase(LDH)
lacunar infarction
lacunar infarction, differential diagnosis of
lateral medullary syndrome
lateropulsion
Laurence-Moon-Bardet-Biedl syndrome
leg numbness
leg weakness, bilateral
Leigh's disease
leucine rich glioma inactivated 1 antibodies
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
Lhermitte's sign
limbic encephalitis
lip, biting
listeria monocytogenes
listeriosis, CNS
liver disease
Lyme disease
lymph node biopsy
lymphadenopathy
lymphadenopathy, hilar
lymphoma
macular degeneration
Madonna facies
malabsorption
malformation, vascular
malignancy screen
malignancy, occult
mastoiditis
medial medullary syndrome
mediastinum, mass of
medulla oblongata, infarction of
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, chronic
meningoencephalopathy
meningomyelitis
mental retardation
mental status, abnormal
methotrexate
methylhydrazine derivatives
methylmalonic acid, serum
methylmalonic acidemia
metronidazole
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
Minamata disease
miosis
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
molecular genetics
monoamine oxidase inhibitors
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mononeuritis multiplex
mononeuropathy
mononeuropathy multiplex
mortality
motor dysfunction
movement disorder
movement disorder, psychogenic
MRI
MRI, abnormal
MRI, angiography
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, contrast enhanced, subependymal
MRI, disappearing lesion on
MRI, flow void, blood
MRI, mass effect on
MRI, negative
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRS
mucopolysaccharidoses
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
myasthenia gravis, paraneoplastic
myasthenic syndrome
myelitis
myelitis, longitudinal
myelomalacia
myeloneuropathy
myelopathy
myelopathy, ascending
myelopathy, chronic progressive
myoclonus
myopathy, mitochondrial
myopathy, proximal
myopia
nasal septum, perforation of
nasal speech
nausea and vomiting
nerve biopsy
nerve conduction studies
nerve conduction studies, sensory
nerve growth factor
nerve root enhancement
neuritis
neurofibromatosis 1
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic examination
neurologic signs
neurologic symptoms
neuromuscular junction
neuronal cell surface antigen
neuronal ceroid-lipofuscinosis
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, iatrogenic
neuropathy, motor, multifocal
neuropathy, onion bulb
neuropathy, painful
neuropathy, paraneoplastic
neuropathy, peripheral
neuropathy, recurrent
neuropathy, sensory
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neuropathy, toxic
neuropathy, vasculitic, systemic
neurosyphilis
neurotoxic
neurotoxin
neutropenia
next-generation sequencing
night blindness
night sweats
nitrogen mustard
nitrous oxide
NMDA antagonists
non-dominant hemisphere
numbness, ascending
numbness, extremity
numbness, generalized
nystagmus
nystagmus, dissociated
nystagmus, gaze-evoked
nystagmus, upbeating on upgaze
nystagmus, vertical
old age, neurology of
onconeural antibodies
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, progressive external
ophthalmoplegia, recurrent
ophthalmoplegia, total
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic nerve
optic neuropathy
orthostatic hypotension
otitis, neurologic complications with
ovarian tumor
overlap syndrome
pain
pain, abdominal
pain, back
pain, foot
pain, hemibody
pain, leg
pain, neuropathic
pain, testicular
pancytopenia
papilledema
papillitis
paraneoplastic brainstem encephalitis
paraneoplastic cerebellar degeneration
paraneoplastic ganglionopathy
paranoia
paraparesis
paraparesis, spastic
paraplegia
parenteral alimentation
paresthesias
paresthesias, feet
paresthesias, generalized
paresthesias, hands
Parkinson disease
Parkinsonism syndrome
pathologic reflex
penicillin
periarteritis nodosa
perineum, numbness of
perioral numbness
peripheral blood smear
peripheral blood smear, abnormal
peripheral nerve, lesion of
pernicious anemia
peroxisomal disease
personality change
pes cavus
photophobia
phytanic acid
pigmentary retinopathy
plasmapheresis
pleocytosis of cerebrospinal fluid
poison, mercury
POLG1 gene
polyclonal gammopathy
polyglucosan body
polyglucosan body disease
polyneuritis
polyneuritis, acute sensory
polyneuropathy
polyneuropathy, acute sensory
polyneuropathy, chronic idiopathic
polyneuropathy, chronic idiopathic, ataxic
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic inflammatory demyelinating, variant form
polyneuropathy, chronic inflammatory demyelinating-pure motor syn
polyneuropathy, chronic inflammatory demyelinating-sens atax var
polyneuropathy, chronic inflammatory demyelinating-variant forms
polyneuropathy, chronic relapsing
polyradiculoneuropathy
pons, infarction of
pons, lesion of
pontine hemorrhage
position sensation
position sensation, abnormal
positional head-hanging test
posterior column disease
posterior inferior cerebellar artery syndrome
postoperative neurologic complications
prion disease
procarbazine
prognosis
progressive neurologic disorder
proprioception
proprioception, abnormal
pruritus
pseudoathetosis
pseudochorea
psychiatric problems in neurologic disorders
psychological testing
psychosis
ptosis
ptosis, bilateral
pulmonary infiltrates
pupil
pupil, abnormality in neurologic disorders
pupil, dilated, bilateral
pupil, light reflex, abnormal
pure motor hemiplegia
pure sensory stroke
Purkinje cell
pyramidal
pyramidal tract
pyramidal tract dysfunction
pyridoxine
quadriparesis
quadriplegia
radicular pain
rash
Raynaud's phenomenon
reading disorder, acquired
real-time quaking-induced conversion
rectal sphincter tone, decreased
recurrent
Red flags
reflex, cutaneous
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
respiratory failure
respiratory tract infection
restiform body
retinal artery occlusion
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
reversible neurologic disorder
review article
RFC1 gene
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
rigidity
Riley-Day syndrome
risk factors
Romberg's sign
saccadic eye movements, abnormal
sarcoidosis
sarcoidosis, CNS
scleroderma
scleroderma, neurologic involvement with
scoliosis
scotoma
screening
sedimentation rate, elevated
seizure
seizure, hysterical
sensorimotor stroke
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
sensory level
sensory loss
sensory loss, asymmetric
sensory loss, band distribution
sensory loss, cortical
sensory loss, crossed pattern
sensory loss, cutaneous
sensory loss, leg
sensory loss, patchy
sensory loss, truncal
sensory nerve action potentials
sensory polyneuropathy
sensory symptoms
serologic testing
shell fish poisoning
shooting pain
Shy-Drager syndrome
sinusitis
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
small vessel disease
somatosensory evoked potentials
spastic ataxia
spasticity
speech disorder
speech disorder, non aphasic
spinal cord
spinal cord, biopsy
spinal cord, cervical
spinal cord, compression of
spinal cord, dorsal subpial enhancement
spinal cord, enlargement
spinal cord, lesion of
spinal cord, neoplasm, intramedullary
spinal cord, vascular malformation of
spinocerebellar ataxia
spinocerebellar ataxia type 6
spinocerebellar degeneration
spongy degeneration of brain
starvation, therapeutic
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
strabismus
strokelike episodes
sudden death
superior cerebellar artery syndrome
suspended sensory loss
swayback
symmetric brain lesions
syphilis, diagnosis and treatment
syphilis, meningomyelitis
syphilis, neurologic complications with
systemic illness
tachycardia
tandem gait, ataxic
tapetoretinal degeneration
tauopathy
testicular biopsy
thalamic ataxia syndrome
thalamic syndrome
thalamus, infarction of
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy
thrush
tick bite
tinnitus
tongue, biting
tongue, numbness of
tongue, smooth
tongue, swelling
tongue, weakness
toxic encephalopathy
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, thalamic
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
ulcers, fingertip
upgaze
upgaze, paralysis of
uremia
urinary frequency
urinary incontinence
urinary retention
urinary urgency
urine, dark
useless hand
Usher's syndrome
vertebral artery occlusion
vertebral artery stenosis
vertigo
vestibular areflexia
vestibulopathy
vibratory sensation
vibratory sensation, abnormal
vinblastine
vincristine neurotoxicity
viral infection
vision, blurred
visual cortex
visual evoked response
visual field defect
visual fields, constricted
visual loss
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin, multiple
vocal cord paralysis
vocalizations
voice, abnormality of
walking frame
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, functional
weakness, generalized
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
workup
wrist drop
writing
Showing articles 1200 to 1250 of 1775 << Previous Next >>

Pure Sensory Stroke Due to Midbrain Haemorrhage Limited to the Spinothalamic Pathway
JNNP 52:1427-1428, Azouvi,P.,et al, 1989

Isolated Midbrain Lesion Resulting From Closed Head Injury:A Unique Presentation of Ataxia Hemiparesis
Neurol 39:452-453, Hershkowitz,N.,et al, 1989

Primary Progressive Cerebellar Ataxia
Neuroradiology 31:16-18, Bradac,G.B.,et al, 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Central Nervous System Manifestations of Lyme Disease
Arch Neurol 46:790-795, Pachner,A.R.,et al, 1989

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Femoral Compression Neuropathy from a Mechanical Pressure Clamp
Neurol 39:1263, Massey,E.W.&Tim,R.W., 1989

Hysterical Gait Disorders:60 Cases
Neurol 39:586-589, Keane,J.R., 1989

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

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Trichloroethylene Cranial Neuropathy:Is It Really a Toxic Neuropathy or Does It Activate Latent Herpes Virus?
JNNP 52:297-303, Cavanaugh,J.B.&Buxton,P.H., 1989

Hereditary Sensory Neuropathy with Deafness:A Familial Multisystem Atrophy
Neurol 39:244-248, Horoupian,D.S., 1989

Taxol Produces a Predominantly Sensory Neuropathy
Neurol 39:368-373, Lipton,R.B.,et al, 1989

Cheiro-Oral Syndrome with Bilateral Oral Involvement:A Study of Pontine Lesions by High-Resolution MRI
JNNP 52:792-794, Matsumoto,S.,et al, 1989

Anterior Choroidal Artery Territory Infarction:A Small Vessel Disease
Stroke 20:616-619, Bruno,A.,et al, 1989

Sensory Tics in Tourette's Syndrome
Neurol 39:731-734, Kurlan,R.,et al, 1989

Risk Factors for Recurrent Nonsyncopal Falls, A Prospective Study
JAMA 261:2663-2668, Nevitt,M.C.,et al, 1989

Prevention of Falls Among the Elderly
NEJM 320:1055-1059, Tinetti,M.E.&Speechley,M., 1989

Radiation-Induced Dementia in Patients Cured of Brain Metastases
Neurol 39:789-796, DeAngelis,L.M.,et al, 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
Ann Neurol 25:419-420, Iwasaki,Y.,et al, 1989

Guillain-Barre Syndrome Presenting as High-Altitude Cerebral Edema
NEJM 321:545, Shlim,D.R.&Cohen,M.T., 1989

Syndrome of Cerebellar Ataxia and Hypogonadotrophic Hypogonadism:Evidence for Pituitary Gonadotrophin Deficiency
JNNP 52:407-409, Fox,A.C.K.,et al, 1989

The Olfactory and Cognitive Deficits of Parkinson's Disease:Evidence for Independence
Ann Neurol 25:166-171, Doty,R.L.,et al, 1989

Diabetic Truncal Neuropathy:Topography of the Sensory Deficit
Ann Neurol 25:233-238, Stewart,J.D., 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Clinicopath Conf
Primary (Granulomatous) Angiitis of Central Nervous System, Case Record 8-1989, NEJM 320:514-5249., , 1989

Peripheral Neuropathy in Primary Sjogren's Syndrome
Neurol 39:390-394, Mellgren,S.I.,et al, 1989

Opsoclonus-Myoclonus Syndrome:Correlation of Radiographic and Pathological Observations
Neuroradiology 31:250-252, Turchman,R.F.,et al, 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Brain White-Matter Changes in the Elderly Prone to Falling
Arch Neurol 46:1292-1296, Masdeu,J.C.,et al, 1989

Pure Sensory Stroke Due to a Pontine Lacune
Stroke 20:406-408, Hommel,M.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Variables Predicting Surgical Outcome in Symptomatic Hydrocephalus in the Elderly
Neurol 39:1601-1604, Graff-Radford,R.N.,et al, 1989

Symptomatic Congenital Hydrocephalus in the Elderly Simulating Normal Pressure Hydrocephalus
Neurol 39:1596-1600, Graff-Radford,N.R.&Godersky,J.C., 1989

Cerebral Palsy Diplegia:Improvements for Walking
BMJ 299:1115-1116, Patrick,J., 1989

The Radiologic Assessment of Trigeminal Neuropathy
AJR 153:1275-1282, Hutchins,L.G.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
Eur Neurol 29:61-66, Martinelli,P.,et al, 1989

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
Neurol 38:1056-1060, Zochodne,D.W.,et al, 1988

Cheiro-Oral Syndrome: Does It Have a Specific Localizing Value?
Eur Neurol 28:326-330, Holter,J.T. &Tijssen,C., 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988



Showing articles 1200 to 1250 of 1775 << Previous Next >>