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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
aphasia
aphonia
applause sign
apraxia of eye movements
apraxia of eyelid opening
areflexia
arm swing, reduced
arrhythmia, cardiac
arteritis, temporal
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
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
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
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
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, 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
ideomotor apraxia
idiopathic inflammatory orbital disease
imbalance
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 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, 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
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
ovarian tumor
overlap syndrome
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
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
seizure
seminoma
sensorineural hearing loss
sequencing difficulty
serologic testing
seronegative
short stature
sinemet
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 50 to 100 of 5792 << Previous Next >>

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
Lancet 337:508-510, Arnaudo,E.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
Ann Neurol 29:606-614, Mhiri,C.,et al, 1991

Kearns-Sayre Syndrome Presenting as Renal Tubular Acidosis
Neurol 40:1761-1763, Eviatar,L.,et al, 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Kearns-Sayre Syndrome and Dilated Cardiomyopathy
Neurol 40:553-554, Tveskov,C.&Angelo-Nielsen,K., 1990

Perineural Spread of Cutaneous Head and Neck Cancer
Arch Neurol 47:73-77, Clouston,P.D.,et al, 1990

Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy
NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

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

Peripheral Neuropathy Associated with Mitochondrial Myopathy
Ann Neurol 20:249-257, Yiannikas,C.,et al, 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Clin. Path. Conference
External Ophthalmoplegia with Mitochondrial Myopathy, Case Record 3-1985, NEJM 312:171-177985., , 1985

Mitochondrial Myopathies
Ann Neurol 17:521-538, DiMauro,S.,et al, 1985

Relapsing Ophthalmoparesis-Sensory Neuropathy Syndrome
Neurol 35:595-596, Kaplan,J.G.,et al, 1985

Abnormalities of Eyelid Closure
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, 2:967, Miller,M.R., 1985

Graves'Disease Presenting with Bilateral Acute Painful Proptosis, Ptosis, Ophthalmoplegia, & Visual Loss
Lancet 2:431-433, Leonard,T.J.K.,et al, 1984

Nystagmus in Motor Neuron Disease:Clinicopathological Study of Two Cases
Ann Neurol 16:71-77, Kushner,M.J.,et al, 1984

Small Bowel Resection with Vitamin E Deficiency & Progressive Spinocerebellar Syndrome
Neurol 34:1046-1052, Bertoni,J.M.,et al, 1984

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

Isolated Ocular Myopathy & Celiac Disease in Childhood
Neurol 33:792, Sandyk,R.,et al, 1983

Chronic Progressive External Ophthalmoplegia (CPEO) :Clinical, Morphologic, & Biochemical Studies
Neurol 33:452-461, Mitsumoto,H.,et al, 1983

Brainstem Encephalitis & The Syndrome Of Miller Fisher
Brain 105:481-495, Al-Din,A.N.,et al, 1982

External Carotid-Cavernous Sinus Fistula Simulating Unilateral Graves Ophthalmopathy
J Comput Assist Tomogr 6:1006-1009, Merlis,A.L.,et al, 1982

Abrupt Neurological Deterioration in Children With Kearns-Sayre Syndrome
Arch Neurol 38:247-250, Coulter,D.L.,et al, 1981

Ophthalmoplegia-Plus
Arch Neurol 38:423-426, Okamoto,T.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Neuropathy & Mitochondrial Myopathy
Ann Neurol 7:262-268, Peyronnard,M.J.,et al, 1980

Mitral Valve Prolapse & Ophthalmoplegia:A Progressive, Cardioneurologic Syndrome
Ann Int Med 92:735-741, Darsee,J.R.,et al, 1980

Demyelinating Radiculopathy in the Kearns-Sayre Syndrome:A Clinicopathological Study
Ann Neurol 8:373-380, Groothuis,D.R.,et al, 1980

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Reversibility of Human Myopathy Caused by Vitamin E Deficiency
Neurol 29:1182-1186, Tomasi,L.G., 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979



Showing articles 50 to 100 of 5792 << Previous Next >>