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Differential
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abducens nerve paralysis
abducens nerve paralysis, bilateral
abiotrophy
acanthocytosis
acquired immunodeficiency syndrome
adrenoleukodystrophy
advances in neurology
adverse drug reaction
agammaglobulinemia
akinesia of eyelid function
aminoacidopathies
amyotrophic lateral sclerosis
ANA
anterior tibial muscle weakness
anti GQ1b IgG antibody
aphasia
apraxia of eyelid opening
areflexia
arrhythmia, cardiac
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxic gait
atrial fibrillation
atypical
azidodeoxythymidine
basal ganglia, calcification of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
blepharospasm
blindness
blindness, sudden
botulism
brainstem, lesion of
brainstem, tuberculoma of
bulbar palsy
calcification, intracranial
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
celiac disease, childhood
central core disease
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral glucose metabolism
cerebral infarction
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
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
chromosomal abnormality
chromosome 14
chronic progressive external ophthalmoplegia
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
coenzyme Q10 deficiency
cogwheel rigidty
collagen vascular disease
coma
congenital myopathy
congestive heart failure
conjunctival biopsy
conjunctival injection
consanguinity
cornea, abnormal
corpus callosum, lesion of
cortical blindness
cranial neuropathy, multiple
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
cyst, parenchymal
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, rapidly progressive
diabetes mellitus
diarrhea
differential diagnosis
digitalis intoxication
diplopia
distal muscle atrophy
distal muscle weakness
DNA probes
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, brainstem
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 weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
familial
fasciculation
fatigue
fibrillations
Fisher C.M.
Fisher's syndrome
fistula, arterio-venous, carotid-cavernous
foot drop
Friedreich's ataxia
fundus, abnormality of
gait disorder
gangliosides
gangliosidosis GM1
gangliosidosis, generalized
gargoylism
gastrointestinal motility
gaze palsy
gaze palsy, horizontal
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
Graves ophthalmopathy
Guillain Barre syndrome, ophthalmoplegia in
Hallervorden Spatz disease
Hallgren's syndrome
headache
headache, sudden onset of
hearing loss
heart block
heart murmur
hemianopia
hemianopia, homonymous
hemianopia, transient
hemiparesis
hepatic failure
hippus
Hispanics
histochemistry of muscle
human immunodeficiency virus type 1
Hurler's syndrome
hyperthyroidism
hypocalcemia
hypoglycorrhachia
hypogonadism
hypomagnesemia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypophonia
hyporeflexia
hypothyroidism
hypotonia
imbalance
immunohistochemistry
impulsivity
inclusion body myositis
intellectual deficit
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal pseudoobstruction
iridoplegia
ischemic exercise test
jaw jerk, abnormal
Kearns-Sayre syndrome
keratoconus
lactic acidemia
Lafora's disease
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lid closure, weakness of
life expectancy
lordosis
macular degeneration
malabsorption
malformation, CNS, congenital
masked facies
medial rectus palsy
medulla oblongata, lesion of
MELAS syndrome
Melkersson's syndrome
memory, impairment of
meningitis
meningitis, TB
mental retardation
MERRF syndrome
metabolic acidosis
metachromatic leukodystrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitral valve lesion
mitral valve prolapse
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, muscle
mucopolysaccharidoses
multicore myopathy
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
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, seronegative
myasthenic syndrome
myelopathy
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
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
neuritis
neuroaxonal dystrophy
neuroendocrinology
neurogenic vs.myopathic atrophy
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal ceroid-lipofuscinosis
neuronopathy, sensory
neuroophthalmology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, peripheral
Niemann-Pick disease
night blindness
normal
nystagmus
nystagmus, dissociated
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular myopathy
ocular myopathy, differential diagnosis
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, total
optic atrophy
optic disc edema
optic nerve
optic neuritis
optic neuropathy
orbicularis oculi muscle
orbit
orbit, lesions of
overlap syndrome
pain
pancytopenia
papillitis
paraparesis
paraparesis, spastic
Parkinsonism syndrome
periodic paralysis
peroxisomal disease
personality change
photophobia
photophobia, central
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLG1 gene
polydactyly
polymerase chain reaction
polymyalgia rheumatica
polymyositis
pons, lesion of
prognosis
progressive infantile poliodystrophy
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
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
radiculopathy
ragged-red fibers
rapidly progressing neurologic illness
Raynaud's phenomenon
refractive errors
Refsum's disease
renal failure
renal tubular acidosis
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
rhabdomyolysis
rigidity
schizophrenia
scintillations
scleroderma
scleroderma, neurologic involvement with
scoliosis
screening
sedimentation rate
seizure
sensorineural hearing loss
serologic testing
seronegative
short stature
skin, biopsy
skin, tight
Southern immunoblot test
spasticity
Spielmeyer Vogt syndrome
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
Stephens syndrome
steroid therapy, CNS treatment and complications with
strabismus
strokelike episodes
succinate dehydrogenase deficiency
sudden death
symmetric brain lesions
tandem gait, ataxic
tapetoretinal degeneration
temporal lobe, lesion
tetany
thalamus, lesion of-bilateral
tongue, fasciculations of
transverse smile
treatment of neurologic disorder
trigeminal nerve
trigeminal nerve, lesion of
trinucleotide repeats
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
Usher's syndrome
vestibulopathy
visual field defect
visual fields, constricted
visual loss
vitamin deficiency
vitamin E
vitamin E deficiency
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
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 97 of 97 << Previous

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

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

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

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

Familial Kearns-Sayre syndrome
Neurol 29:1172-1174, Schnitzler,E.R.,et al, 1979

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 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

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers
Arch Neurol 35:643-647, Bertorini,T.,et al, 1978

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Chronic Progressive External Ophthalmoplegia
Arch Ophthalmol 82:845, Daroff,R., 1969

Progressive Ophthalmoplegia
Arch Neurol 19:362, Rosenberg,R.,et al, 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Some Neuro-ophthalmological Observations
JNNP 30:383, Fisher,C.M., 1967



Showing articles 50 to 97 of 97 << Previous