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Differential
(Click to cross reference)
abducens nerve paralysis, bilateral
abiotrophy
acanthocytosis
advances in neurology
agammaglobulinemia
akinesia of eyelid function
ANA
apraxia of eyelid opening
arrhythmia, cardiac
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
atrial fibrillation
basal ganglia, calcification of
Bassen-Kornzweig syndrome
blepharospasm
blindness
botulism
brainstem, lesion of
brainstem, tuberculoma of
calcification, intracranial
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cause of death
celiac disease, childhood
cerebellar ataxia, primary
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
conjunctival injection
consanguinity
cornea, abnormal
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
deafmute
deafness
dementia
diabetes mellitus
digitalis intoxication
diplopia
dwarfism
dysarthria
dysphagia
dyspraxia
dysthyroid ocularmyopathy
dystonia
dystrophin
edema, periorbital
electroencephalogram, abnormalities of
electromyogram
encephalopathy
encephalopathy, progressive
enzyme, muscle disease
epidemiology of neurology
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
familial
fasciculation
fatigue
fibrillations
Fisher C.M.
fistula, arterio-venous, carotid-cavernous
Friedreich's ataxia
gait disorder
gargoylism
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
hippus
Hispanics
histochemistry of muscle
Hurler's syndrome
hyperthyroidism
hypoglycorrhachia
hypogonadism
hypotonia
imbalance
immunohistochemistry
intestinal pseudoobstruction
jaw jerk, abnormal
Kearns-Sayre syndrome
keratoconus
lactic acidemia
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
lid closure, weakness of
malformation, CNS, congenital
masked facies
medial rectus palsy
medulla oblongata, lesion of
MELAS syndrome
Melkersson's syndrome
meningitis
meningitis, TB
mental retardation
MERRF syndrome
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, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, seronegative
myasthenic syndrome
myelopathy
myoclonus
myopathy
myopathy, distal
myopathy, mitochondrial
myopia
myositis
myositis, ocular
myotonia dystrophica
neck weakness
negative
neuritis
neuroendocrinology
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular junction, abnormality of
neuroophthalmology
neuropathy
normal
nystagmus
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular myopathy
ocular myopathy, differential diagnosis
oculopharyngeal muscular dystrophy
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
pancytopenia
paraparesis
paraparesis, spastic
Parkinsonism syndrome
photophobia
photophobia, central
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLG1 gene
polydactyly
polymerase chain reaction
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
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
Raynaud's phenomenon
retinitis pigmentosa
retinopathy
retropulsion
review article
rigidity
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
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
upgaze, paralysis of
Usher's syndrome
visual field defect
visual fields, constricted
visual loss
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weight loss
wheelchair
white matter disease
wide based gait
xanthopsia
Showing articles 1450 to 1500 of 2440 << Previous Next >>

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Differentiation of Central Nervous System Lesions in AIDS Patients Using Positron Emission Tomography (PET)
Int J STD AIDS 7:337-346, Heald,A.E.,et al, 1996

Neurologic manifestations of intravascular lymphomatosis
Acta Neurol Scand 91:494-499, Chapin, J.E.,et al, 1995

Polyarteritis Nodosa-Induced Quadriplegia
Ann Int MEd 122:731-732, Smith,D.L.,et al, 1995

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Diagnostic Value of Detecting JC Virus DNA in Cerebropsinal Fluid of Patients with Progressive Multifocal Leukoencephalopathy
J Clin Microbiol 33:484-486, Fong,I.W.,et al, 1995

Extrapyramidal Symptoms in a BMT Recipient with Hyperintense Basal Ganglia and Elevated Manganese
Bone Marrow Transplantation 15:989-992, Fredstrom,S.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
Ann Neurol 38:825-828, Rosenow,F.,et al, 1995

Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
Stroke 26:1950-1952, Kosinski,C.,et al, 1995

Benign Episodic Unilateral Mydriasis
Ophthalmol 102:1623-1627, Jacobson,D.M., 1995

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Comparison of Triple Dose vs Std Dose Gadolinium-DTPA for Detect of MRI Enhanc Lesions in Pts with Primary Progr MS
JNNP 59:540-544, Filippi,M.,et al, 1995

The Natural History of Progressive Mutlifocal Leukoencephalopathy in Patients with AIDS
Clin Inf Dis 20:1305-1310, Fong,I.W.,et al, 1995

Chronic Myelopathy Associated with Human Herpesvirus-6
Neurol 45:2015-2017, Mackenzie,I.R.A.,et al, 1995

Systemic Sclerosis Sine Scleroderma:An Unusual Presentation in Scleroderma Renal Crisis
J Rheumatol 22:557-560, Molina,J.F.,et al, 1995

Systemic Sclerosis (Scleroderma) :Clinical Management of Its Major Complications
Rheum Dis Clin North America 21:203-216, Legerton,C.W.,et al, 1995

Intrathecal Baclofen Therapy in Stiff-Man Syndrome:A Double-blind, Placebo-controlled Trial
Neurol 45:1893-1897, Silbert,P.L.,et al, 1995

Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
Ann Neurol 38:714-722, 7011995., Shillito,P.,et al, 1995

Acute Bilateral Ophthalmoplegia Secondary to Metastatic Prostatic Carcinoma:Demonstr of Magnetic Resonance Imaging
J Neuro-Ophthalmol 15:45-47, Agarwal,P.,et al, 1995

Stereotactic Ventral Pallidotomy for Parkinson's Disease
Neurol 45:753-761, Dogali,M.,et al, 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Spinal Dural Arteriovenous Fistula:The Pathology of Venous Hypertensive Myelopathy
Neurol 45:1309-1313, Hurst,R.W.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

JC Virus DNA in CSF of HIV-Infected Pts:Predictive Value for Progressive Multifocal Leukoencephalopathy
Ann Neurol 37:395-399, McGuire,D.,et al, 1995

Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Progressive Multifocal Leukoencephalopathy:Unusual MR Findings
J Comput Assist Tomogr 19:302-305, Ng,S.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy & Systemic Lupus Erythematosus, Case 20-1995, NEJM 332:17, 3-17995., 1995

Neurofibromatosis Type 1:Pathologic Substrate of High-Signal-Intensity Foci in the Brain
Radiology 195:721-724, DiPaolo,D.P.,et al, 1995

MRI of the Brain in Wilson Disease:T2 Signal Loss Under Therapy
J Comput Assist Tomogr 19:635-638, Engelbrecht,V.,et al, 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Persistence of MRI Hyperintensity of the Globus Pallidus in Cirrhotic Patients:A 2-year Follow-up Study
Neurol 45:995-997, Kulisevsky,J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

AIDS-Associated Progressive Multifocal Leukoencephalopathy Revealed by New-Onset Seizures
Am J Med 99:64-68, Moulignier,A.,et al, 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995



Showing articles 1450 to 1500 of 2440 << Previous Next >>