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Differential
(Click to cross reference)
abdominal distention
abducens nerve paralysis
abducens nerve paralysis, bilateral
abiotrophy
acanthocytosis
acetylcholine receptor
acetylcholine receptor antibody
acquired immunodeficiency syndrome
adrenoleukodystrophy
advances in neurology
adverse drug reaction
agammaglobulinemia
akinesia of eyelid function
algorithm
alpha-fetoprotein
aminoacidopathies
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
ANA
anterior tibial muscle weakness
anti GQ1b IgG antibody
anti Hu antibody
anti Ma
anti Ri antibody
anti Yo antibody
antitoxin
antiviral agents
aphasia
aphonia
applause sign
apraxia of eye movements
apraxia of eyelid opening
areflexia
arm swing, reduced
arrhythmia, cardiac
arteritis, temporal
aspergillosis
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atlanto axial dislocation, congenital
atrial fibrillation
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic dysfunction, acute
autonomic neuropathy
azathioprine
azidodeoxythymidine
basal ganglia, calcification of
basal ganglia, lesion, bilateral
basilar artery stenosis
Bassen-Kornzweig syndrome
blepharospasm
blindness
blindness, sudden
botulism
botulism antitoxin
brainstem, dysfunction
brainstem, lesion of
brainstem, tuberculoma of
bulbar dysfunction
bulbar palsy
bulbar palsy, acute
cachexia
calcification, intracranial
carcinoembryonic antigen
carcinoma
carcinoma of bladder
carcinoma of lung
carcinoma of ovary
carcinoma of testis
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, dense artery sign
CAT scan, disappearing lesion on
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, muscle
cataracts
cataracts, congenital
cause of death
cavernous sinus
cavernous sinus, lesion of
cavernous sinus, syndrome
celiac disease, childhood
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral glucose metabolism
cerebral infarction
cerebritis
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
Charcot's sign
chemosis
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 14
chronic progressive external ophthalmoplegia
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
coenzyme Q10 deficiency
cognition
cogwheel rigidty
collagen vascular disease
coma
comorbidities
confusion
congenital myopathy
congestive heart failure
conjunctival biopsy
conjunctival injection
consanguinity
cornea, abnormal
corpus callosum, lesion of
cortical blindness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
critical care unit
cyst, parenchymal
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, rapidly progressive
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
difficulty climbing stairs
digitalis intoxication
diplopia
disorientation
distal muscle atrophy
distal muscle weakness
dizziness
DNA probes
downward gaze
drooling
drug induced neurologic disorders
dwarfism
dysarthria
dysdiadochokinesia
dysphagia
dyspnea
dyspraxia
dysthyroid ocularmyopathy
dystonia
dystrophin
edema, periorbital
electrical sensation
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
emtricitabine
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalocele
encephalopathy
encephalopathy, progressive
enzyme, muscle disease
epidemiology of neurology
epilepsia partialis continua
exercise intolerance
extraocular muscle atrophy
extraocular muscle enlargement
extraocular muscle lesion
extrapyramidal movement disorder, progressive
eye closure
eye movement, disorders of
eye, pain in
face, elongated
face, numbness of
facial appearance, abnormal
facial nerve
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
familial
fasciculation
fatigue
fever
fibrillations
fine motor function, impaired
Fisher C.M.
Fisher's syndrome
fistula, arterio-venous, carotid-cavernous
foot drop
Friedreich's ataxia
fundus, abnormality of
gait disorder
gait, apraxic
gammaglobulin therapy, intravenous
gangliosides
gangliosidosis GM1
gangliosidosis, generalized
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
glaucoma
gonadal dysgenesis
granulomatosis with polyangiitis
Graves ophthalmopathy
growth retardation
Guillain Barre syndrome, ophthalmoplegia in
Hallervorden Spatz disease
Hallgren's syndrome
headache
headache, chronic
headache, progressive
headache, sudden onset of
hearing loss
heart block
heart murmur
hemangioma
hemianopia
hemianopia, homonymous
hemianopia, transient
hemiparesis
hepatic failure
hepatomegaly
heralding manifestation
hippus
Hispanics
histochemistry of muscle
HLA
Horner's syndrome
human immunodeficiency virus type 1
Hurler's syndrome
hypersomnia
hyperthyroidism
hypocalcemia
hypoglycorrhachia
hypogonadism
hypomagnesemia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypophonia
hyporeflexia
hypothyroidism
hypotonia
iatrogenic neurologic disorders
ideomotor apraxia
idiopathic inflammatory orbital disease
imbalance
immunocompetent
immunodeficiency
immunohistochemistry
immunosuppression
immunosuppressive agents
impulsivity
inattention
inclusion body myositis
infantile tremor syndrome
intellectual deficit
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal pseudoobstruction
intracerebral hemorrhage
iridoplegia
ischemic exercise test
jaw jerk, abnormal
Kearns-Sayre syndrome
kelch-like protein 11 antibodies
keratoconus
lactic acidemia
Lafora's disease
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
leukemia
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lid closure, weakness of
life expectancy
lipoprotein receptor-related protein 4
locked-in syndrome
lordosis
lymphadenopathy, hilar
lymphoma
macular degeneration
malabsorption
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malignancy screen
malignancy, occult
masked facies
medial rectus palsy
medulla oblongata, lesion of
MELAS syndrome
Melkersson's syndrome
memory, defect of recent
memory, impairment of
meningeal biopsy
meningeal enhancement
meningitis
meningitis, leukemic
meningitis, TB
mental retardation
mental status, abnormal
MERRF syndrome
metabolic acidosis
metachromatic leukodystrophy
midbrain
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitral valve lesion
mitral valve prolapse
MNGIE syndrome
molecular genetics
monoclonal antibodies
mononeuropathy multiplex
mortality
motor neuron disease
motor neuron disease, juvenile form
movement disorder
movement disorder, extrapyramidal
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, extraocular muscle enhancement
MRI, muscle
MRI, negative
mucopolysaccharidoses
multicore myopathy
multiple sclerosis
multiple sclerosis, acute
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
MuSK antibodies
myasthenia gravis
myasthenia gravis, classification
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, receptor site in
myasthenia gravis, seronegative
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenia gravis, variants
myasthenic crisis
myasthenic syndrome
myelopathy
myocarditis
myoclonus
myoclonus, epilepsy
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopathy, proximal
myopathy, toxic
myopia
myositis
myositis, ocular
myotonia
myotonia dystrophica
nasal stuffiness
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
nerve conduction studies
neuritis
neuroaxonal dystrophy
neurocutaneous disease
neuroendocrinology
neurogenic vs.myopathic atrophy
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuromyelitis optica (Devic's disease)
neuronal ceroid-lipofuscinosis
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, recurrent
neuropathy, sensory
neuropathy, vasculitic, systemic
neurotoxin
Niemann-Pick disease
night blindness
nonverbal
normal
nystagmus
nystagmus, dissociated
nystagmus, primary position of gaze
nystagmus, rotary
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
oculocephalic reflex
oculopharyngeal muscular dystrophy
old age, neurology of
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, painful
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
ophthalmoplegia, recurrent
ophthalmoplegia, total
ophthalmoplegia, unilateral
optic atrophy
optic disc edema
optic nerve
optic nerve, lesion of
optic neuritis
optic neuropathy
orbicularis oculi muscle
orbit
orbit, inflammation in
orbit, lesions of
orbital apex
orbital apex syndrome
oscillopsia
osteomyelitis
ovarian tumor
overlap syndrome
pachymeningitis, cranial
pain
pain, abdominal
pancytopenia
papilledema
papillitis
paraneoplastic brainstem encephalitis
paraneoplastic cerebellar degeneration
paraparesis
paraparesis, spastic
parasellar syndrome
Parkinson disease, axial symptoms
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathology
penguin silhouette sign
periarteritis nodosa
periodic paralysis
periodic paralysis, thyrotoxic
peroxisomal disease
personality change
photophobia
photophobia, central
pigmentary retinopathy
plasmapheresis
pleocytosis of cerebrospinal fluid
POLG1 gene
polydactyly
polymerase chain reaction
polymyalgia rheumatica
polymyositis
polyneuropathy
polyneuropathy, chronic relapsing
pons, lesion of
practice guidelines
pregnancy, neurologic complications in
progeria
prognosis
progressive infantile poliodystrophy
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
proptosis
proptosis, bilateral
proptosis, unilateral
prostigmine
proteinuria
proximal muscle atrophy
pseudobulbar palsy
pseudomyasthenia
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
ptosis, familial
ptosis, unilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated and fixed, unilateral
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
quality of life
radiation hypersensitivity
radiculopathy
ragged-red fibers
rapidly progressing neurologic illness
Raynaud's phenomenon
recurrent
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
renal failure
renal tubular acidosis
repetitive nerve stimulation
respiratory failure
reticular activating system
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
retrocollis
retropulsion
review article
rhabdomyolysis
rhomboencephalopathy
rigidity
rigidity, axial
rituximab
saccadic eye movements, abnormal
scannig speech
schizophrenia
scintillations
scleroderma
scleroderma, neurologic involvement with
scoliosis
scotoma
screening
sedimentation rate
sedimentation rate, elevated
seizure
seminoma
sensorineural hearing loss
sequencing difficulty
serologic testing
seronegative
short stature
sinemet
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
skin, tight
Southern immunoblot test
spasticity
Spielmeyer Vogt syndrome
spina bifida
spinal muscular atrophy
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spongy degeneration of brain
squamous cell carcinoma of head and neck
standing difficulty
startle reaction
Stephens syndrome
steroid
steroid therapy, CNS treatment and complications with
strabismus
strokelike episodes
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subarachnoid hemorrhage
succinate dehydrogenase deficiency
sudden death
symmetric brain lesions
systemic illness
tandem gait, ataxic
tapetoretinal degeneration
tau protein
telangiectases
temporal lobe, lesion
tetany
thalamus, lesion of-bilateral
thymectomy
thymic hyperplasia
thymoma
thyroiditis
Tolosa Hunt syndrome
tongue, fasciculations of
transverse smile
treatment of neurologic disorder
tremor
trigeminal nerve
trigeminal nerve, lesion of
trinucleotide repeats
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
ulcerative colitis
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
uremia
Usher's syndrome
vasculitides
vertigo
vestibulopathy
vision, blurred
visual acuity, decreased
visual acuity, decreased, monocular
visual field defect
visual fields, constricted
visual loss
visual loss, slow-unilateral
visual symptoms
vitamin deficiency
vitamin E
vitamin E deficiency
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
web sites
weight loss
wheelchair
whistle, inability to
white matter disease
white matter disease, pattern
wide based gait
winging of scapula
xanthopsia
Showing articles 1200 to 1250 of 6077 << Previous Next >>

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

Lacunar Strokes & Infarcts:A Review
Neurol 32:871-876, Fisher,C.M., 1982

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Meningitis, In Clinical Neurology
Harper & Row Publishers, 1981, p. 1-55., Sahs,A.L.,et al, 1981

Neurological Complications of Ethylene Glycol Intoxication
Arch Neurol 38:724-726, Berger,J.R.,et al, 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

Pituitary Apoplexy:Its Incidence & Clinical Significance
J Neurosurg 55:187-193, Wakai,S.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Pituitary Metastasis:Incidence in Cancer Patients & Clinical Differentiation from Pituitary Adenoma
Neurol 31:998-1002, Max,M.B.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

The Hot Bath Test in the Diagnosis of Multiple Sclerosis
JAMA 246:1113-1114, Malhotra,A.S.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Abnormalities of Gaze in Cerebrovascular Disease
Stroke 12:251-254, Pedersen,R.A.,et al, 1981

Paralysis of Cranial Nerves III, IV & VI
Arch Ophthalmol 99:76-79, Rush,J.A.,et al, 1981

Transient Oculomotor Paralysis in Pseudotumor Cerebri
Neurol 31:182-184, McCammon,A.,et al, 1981

Clin. Path. Conference
Malignant Lymphoma Involving Brainstem, Case 31-1981, NEJM 305:270-277981., , 1981

Transient Ophthalmoparesis with Doxepin Overdosage
Ann Neurol 9:618, LeWitt,P.A., 1981

Familial Spastic Paraplg, Peroneal Neuropathy, & Crural Hypopig, A New Neurocut Synd
Neurol 31:754-757, Stewart,R.M.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Neurological Disease In Ex-Far-East Prisoners Of War
Lancet 2:135-137, Gibberd,F.B.,et al, 1980

Clin. Path. Conference
Type B Botulism, Unclassified Form, Case Record 48-1980, NEJM 303:1347-135580., , 1980

Ocular Defects in Children with Cerebral Palsy
BMJ 281:487-488, Black,P.D., 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Multiple Vertebral Hemangiomas Resembling Metastases with Spinal Cord Compression
Arch Neurol 37:247-248, Zito,G.,et al, 1980

Clinical Aspects of CNS Cysticercosis
Arch Int Med 140:1309-1313, Shanley,J.D.,et al, 1980

Use of Adrenal Biopsy in Diagnosing Adreno-leukomyeloneuropathy
Arch Neurol 37:634-636, Weiss,G.M.,et al, 1980

Metastatic Infiltration of Nerves in the Cavernous Sinus
Arch Neurol 37:59-61, Unsold,R.,et al, 1980

Ophthalmoplegia, Ptosis, & Miosis in Temporal Arteritis
Neurol 30:1054-1058, Dimant,J.,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

Midline Granuloma
Topel J. L. in Vinken P. J. & Bruyn, G. N. (Eds) Handbook of Clin Neurol, Vol 39, North-Holland Publ, Co, Amsterda, 1980

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Ophthalmoplegia & Bulbar Palsy in Variant Form of Maple Syrup Urine Disease
Ann Neurol 6:71-72, Chhabria,S.,et al, 1979

Chronic Progressive Myelopathy:Investigation with CSF Electrophoresis, Evoked Potentials, & CT Scan
Ann Neurol 6:419-424, Patty,D.W.,et al, 1979

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

Tolosa-Hunt Syndrome with Sellar Erosion
Ann Neurol 6:129-131, Polsky,M.,et al, 1979

Primary Aberrant Oculomotor Regeneration due to Intracranial Aneurysm
Arch Neurol 36:570-571, Cox,T.A.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Superior Branch Palsy of Oculomotor Nerve & Pupillary Constriction Caused by Intracranial Carotid Artery Aneurysm
Ann Neurol 5:493-495, Feder,R.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Midbrain Asterixis
Ann Neurol 6:362-364, Bril,V.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Abnormalties In Cultured Muscle & Periphral Nerve Of A Patient With Adrenomyeloneuropathy
NEJM 301:588-590, Askanas,V.,et al, 1979

Correlation of Computed Tomographic, Angiographic, & Neuropathological Changes in Giant Cerebral Aneurysms
Radiology 132:85-92, Pinto,R.S.,et al, 1979



Showing articles 1200 to 1250 of 6077 << Previous Next >>