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Differential
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abdominal distention
abducens nerve paralysis, bilateral
abiotrophy
acanthocytosis
advances in neurology
agammaglobulinemia
akinesia of eyelid function
ANA
apraxia of eyelid opening
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arrhythmia, cardiac
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
atrial fibrillation
audiogram
auditory evoked brainstem potentials
basal ganglia, calcification of
Bassen-Kornzweig syndrome
blepharospasm
blindness
botulism
brainstem, lesion of
brainstem, tuberculoma of
cachexia
calcification, intracranial
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cataracts, congenital
cause of death
celiac disease, childhood
central core disease
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot's sign
chemosis
children
chromosomal abnormality
chromosome 14
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
cogwheel rigidty
collagen vascular disease
coma
congenital myopathy
conjunctival injection
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
corneal dystrophy
cranial neuropathy, multiple
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
dementia
dermatomyositis
diabetes mellitus
diarrhea
digitalis intoxication
diplopia
distal muscle weakness
dwarfism
dysarthria
dysphagia
dyspraxia
dysthyroid ocularmyopathy
dystonia
dystrophin
edema, periorbital
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electronystagmography, abnormal
electroretinograph
encephalocele
encephalopathy
encephalopathy, progressive
enzyme, muscle disease
epidemiology of neurology
evoked potentials
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, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
fatigue
fever
fibrillations
Fisher C.M.
fistula, arterio-venous, carotid-cavernous
Friedreich's ataxia
gait disorder
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, horizontal
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
glabellar sign
glaucoma
Graves ophthalmopathy
Hallgren's syndrome
headache
hearing loss
heart block
heart murmur
hemianopia, homonymous
hepatic failure
hepatomegaly
heralding manifestation
hippus
Hispanics
histochemistry of muscle
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hyperthyroidism
hypoglycorrhachia
hypogonadism
hypotonia
imbalance
immunohistochemistry
immunologic disease
immunosuppressive agents
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
intestinal pseudoobstruction
jaw jerk, abnormal
joint hypermobility
Kearns-Sayre syndrome
keratoconus
lactic acidemia
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
leukodystrophy
leukoencephalopathy
lid closure, weakness of
lissencephaly
malformation, CNS, congenital
masked facies
medial rectus palsy
medulla oblongata, lesion of
MELAS syndrome
Melkersson's syndrome
meningitis
meningitis, TB
mental retardation
MERRF syndrome
methotrexate
micropthalmia
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
movement disorder
MRI
MRI, abnormal
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
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, 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
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, mitochondrial
myopathy, steroid induced
myopia
myositis
myositis, ocular
myotonia dystrophica
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
neuritis
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
normal
nystagmus
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
oculopharyngeal muscular dystrophy
oculovestibular reflex
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
optic disc edema
optic neuritis
optic neuropathy
orbicularis oculi muscle
orbit
orbit, lesions of
pain, abdominal
pancytopenia
paraparesis
paraparesis, spastic
Parkinsonism syndrome
photophobia
photophobia, central
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLG1 gene
polydactyly
polymerase chain reaction
polymyositis
polyneuropathy
pons, lesion of
prognosis
progressive infantile poliodystrophy
progressive neurologic disorder
progressive supranuclear palsy
proptosis
proptosis, bilateral
proptosis, unilateral
prostigmine
pseudobulbar palsy
pseudomyasthenia
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
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
ragged-red fibers
rash
Raynaud's phenomenon
retina, abnormal
retinal degeneration
retinal detachment
retinal dysplasia
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
rigidity
saccadic eye movements
saccadic eye movements, abnormal
schizophrenia
scintillations
scleroderma
scleroderma, neurologic involvement with
screening
sedimentation rate
seizure
sensorineural hearing loss
seronegative
short stature
skin, tight
Southern immunoblot test
spasticity
Spielmeyer Vogt syndrome
standing difficulty
Stephens syndrome
steroid therapy, CNS treatment and complications with
strokelike episodes
symmetric brain lesions
systemic illness
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
upgaze, paralysis of
Usher's syndrome
visceral neuropathy
visual field defect
visual fields, constricted
visual loss
Walker-Warburg syndrome
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
weight loss
wheelchair
white matter disease
wide based gait
xanthopsia
Showing articles 850 to 900 of 1786 << Previous Next >>

Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis
JNNP 65:950-951, Hu, M.T.M.,et al, 1998

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Ophthalmoplegic Migraine:Reversible Enhancement and Thickening of the Cisternal Segment of the Oculomotor Nerve on Contrast-Enhanced MR Images
AJNR 19:1887-1891, Mark,A.S.,et al, 1998

MR Findings of Werdnig-Hoffmann Disease in Two Infants
AJNR 19:550-552, Hsu,C.,et al, 1998

Estimation of Brainstem Neuronal Loss in ALS with in Vivo Proton Magnetic Resonance Spectroscopy
Neurol 50:72-77, Cwik,V.A.,et al, 1998

Risk of Amyotrophic Lateral Sclerosis & History of Physical Activity, A Population Study
Arch Neurol 55:201-206, Longstreth,W.T.,et al, 1998

Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
Neurol 50:768-772, Ross,M.A.,et al, 1998

Hirayama Disease:MR Diagnosis
AJNR 19:365-368, Chen,C.,et al, 1998

Occult Giant Cell Arteritis:Ocular Manifestations
Am J Ophthalmol 125:521-526, Hayreh,S.S.,et al, 1998

Migrainous Visual Accompaniments are not Rare in Late Life:The Framingham Study
Stroke 29:1539-1543, Wijman,C.A.C.,et al, 1998

An Analysis of Extended Survival in Patients with Amyotrophic Lateral Sclerosis Treated with Riluzole
Arch Neurol 55:526-528, Riviere,M.,et al, 1998

Magnetic Resonance Imaging of Muscle in Amyotrophic Lateral Sclerosis
Neurol 51:110-113, Bryan,W.W.,et al, 1998

Pupil Involvement in Patients with Diabetes-Associated Oculomotor Nerve Palsy
Arch Ophthalmol 116:723-727, 7981998., Jacobson,D.M., 1998

Managing Oculomotor Nerve Palsy
Arch Ophthalmol 116:798, Trobe,J.D., 1998

Ischemic Optic Neuropathy Associated with Internal Carotid Artery Dissection
Arch Neurol 55:715-719, Biousse,V.,et al, 1998

Pregnant,Vomiting,and Going Blind
Lancet 352:1594, Tesfaye,S.,et al, 1998

Paroxysmal Tonic Upgaze:a Reappraisal of Outcome
Ann Neurol 43:514-520, Hayman,M.,et al, 1998

Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Mydriatic Pupil as the Presenting Sign of Common Carotid Artery Dissection
Stroke 29:2653-2655, Koennecke,H.C. & Seyfert,S., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

MR Findings in Isolated Oculomotor Nerve Palsy Associated with Infectious Mononucleosis Caused by Epstein-Barr Virus Infection
J Comput Assist Tomogr 22:995-997, Ishibashi,A.,et al, 1998

Attitudes of Patients with Amyotrophic Lateral Sclerosis and Their Care Givers Toward Assisted Suicide
NEJM 339:967-973,987, Ganzini,L.,et al, 1998

Olfactory Dysfunction in Guamanian ALS,Parkinsonism,and Dementia
Neurol 51:1672-1677, Ahlskog,J.E.,et al, 1998

Most Diabetic Third Nerve Palsies are Peripheral
Neurol 51:1510, Keane,J.R.&Ahmadi,J., 1998

Silent Sinus Syndrome:An Unusual Cause of Vertical Diplopia
Klinische Monatsblatter fur Augenheilkunde 212:397-399, Durig,J.,et al, 1998

Binocular Vertical Diplopia
Mayo Clin Proc 73:55-66, Brazis,P.W.&Lee,A.G., 1998

Spontaneous Dural Carotid Cavernous Sinus Fistula Pres Isolat Ophthalmoplegia:Eval with MR Angiogr
Neurol 50:814-816, Uehara,T.,et al, 1998

Clinicopath Conf
Cat Scratch Encephalitis Due to B. Quintana, Case 1-1998, NEJM 338:112-11998., , 1998

Axonal Transection in the Lesions of Multiple Sclerosis
NEJM 338:278-285, 3231998., Trapp,B.D.,et al, 1998

More on Reflex Sympathetic Dystrophy Syndrome Following Air-Bag Inflation
NEJM 338:334-335, Quarino,H.A., 1998

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Complete Ophthalmoplegia After Zoster Ophthalmicus
J Neuro-Ophthalmol 17:262-265, Chang-Godinich,A.,et al, 1997

Cocaine and Pupillary-Sparing Oculomotor Nerve Paresis
Neurol 49:1466-1467, Migita,D.S.,et al, 1997

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Peripheral Neuropathy Associated with Sicca Complex
Neurol 48:855-862, Grant,I.A.,et al, 1997

Neuro-Ophthalmic Manifestations of Lyme Disease
J Neuro-Ophthalmol 17:108-121, Balcer,L.J.,et al, 1997

ALS Standard of Care Consensus
Neurol 48 (Suppl 4) :S33-S37997., Miller,R.G.,et al, 1997

Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
Ann Int Med 127:450-453, Aboussouan,L.S.,et al, 1997

Practice Advisory on the Trtm of ALS with Riluzole
Quality Standards Subcommittee of the AAN, Neurol 49:657-6591997., , 1997

Motor Neuron Syndromes in Cancer Patients
Ann Neurol 41:722-730, 7031997., Forsyth,P.A.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Lymphoproliferative Disorders and Motor Neuron Disease:An Update
Neurol 48:1671-1678, Gordon,P.H.,et al, 1997

Bilateral Trochlear Nerve Palsy and Downbeat Nystagmus in a Patient with Cephalic Tetanus
Neurol 49:894-895, Orwitz,J.I.,et al, 1997

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

Multifocal Motor Neuropathy Presenting as Ophthalmoplegia
Muscle & Nerve 20:347-351997., Pringle,C.E.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997



Showing articles 850 to 900 of 1786 << Previous Next >>