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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 1750 to 1800 of 2440 << Previous Next >>

The Canadian Coop Trial of Cyclophosphamide and Plasma Exchange in Progr MS
The Canadian Coop MS Study Group, Lancet 337:441-4461991., , 1991

Syphilitic Meningomyelitis
Neurol 41:325-326, Strom,T.&Schneck,S.A., 1991

Myelopathic Neurosarcoidosis:Diagnostic Value of Enhanced MRI
Neurol 41:150-151, Sauter,M.K.,et al, 1991

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

The Role of HTLV in HIV-1 Neurologic Disease
Neurol 41:197-202, Berger,J.R.,et al, 1991

HTLV-I-Associated Myelopathy Associated with Blood Transfusion in the US:Epidemiologic & Molecular Evidence
Neurol 41:192-197, Kaplan,J.E.,et al, 1991

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Radiation Injury of the Brain
AJNR 12:45-62, Valk,P.E. & Dillon,W.P., 1991

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Perineal Reflex Sympathetic Dystrophy Treated with Bilateral Lumbar Sympathectomy
Ann Int Med 113:633-634, Olson,W.L., 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Guillain Barre Syndrome, Case Record 39-1990, NEJM 323:895-908990., , 1990

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

Incomplete Unilateral Ophthalmoplegia as the Presenting Manifestation of Waldenstrom's Macroglobulinemia
Neurol 40:1801-1802, Lossos,A.,et al, 1990

Causalgia and Other Reflex Sympathetic Dystrophies
In the Management of Pain, Lea & Febiger, Phila, p. 220, Bonica,J.J., 1990

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

A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
Neurol 40:1359-1363, Coppeto,J.R.&Lessel,S., 1990

Trigeminal Sensory Neuropathy Associated with Connective Tissue Diseases
Neurol 40:891-896, Hagen,N.A.,et al, 1990

Chronic Injuries of the Spinal Cord:Assessment with MR Imaging
Radiology 175:849-854, Yamashita,Y.,et al, 1990

Primary progressive Aphasia
Arch Neurol 47:1329-1336, Weintraub,S.,et al, 1990

Slowly Progressive Aphasia:Three Cases with Language, Memory, CT and PET Data
JNNP 53:987-993, Kempler,D.,et al, 1990

Clinicopath Conf
Acute Multiple Sclerosis, Case Record 42-1990, NEJM 323:1123-1135990., , 1990

Fulminant Monophasic Multiple Sclerosis, Marburg's Type
JNNP 53:918-921, Johnson,M.D.,et al, 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

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

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

Acute Intermittent Porphyria
JAMA 264:1290-1293, 1315-13161990., Sack,G.H., 1990

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.R.,et al, 1990

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

Follow-up MR STudies in Hallervorden-Spatz Disease
J Comput Assist Tomogr 14:118-120, Gallucci,M.,et al, 1990

Patterns of Disease Activity in Multiple Sclerosis:Clinical and Magnetic Resonance Imaging Study
BMJ 300:631-634, Thompson,A.J.,et al, 1990

Scleroderma, fasciitis, and Eosinophilia Associated with the Ingestion of Tryptophan
NEJM 322:874-881, 9261990., Silver,R.M.,et al, 1990

PET Study in Progressive Supranuclear Palsy, Hypometabolic Pattern
Arch Neurol 47:747-752, Blin,J.,et al, 1990

Excessive Muscular Fatigue in Patients with Spastic Paraparesis
Neurol 40:1271-1274, Miller,R.G.,et al, 1990

Efficacy & Toxicity of Cyclosporine in Chronic Progressive Multiple Sclerosis:A Randomized Clinical Trial
M. S. Study Group, Ann Neurol 27:591-605, 5890., , 1990

Autoantibodies to Gaba-Ergic Neurons & Pancreatic Beta Cells in Stiff-Man Syndrome
NEJM 322:1555-1560, Solimena,M.,et al, 1990

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

A Patient with Progressive Myelopathy and Antibodies to HTLV-I & HIV Type I in Serum and Cerebrospinal Fluid
Arch Neurol 47:477-479, Aboulafia,D.M.,et al, 1990

Transvrse Myelitis and Spastic Paraparesis in a Patient with HIV Infection
NEJM 322:1322, Dodson,D., 1990

Nationwide Survey of HTLV-I-Associated Myelopathy in Japan:Ass with Blood Transufsion
Ann Neurol 28:50-56, Osame,M.,et al, 1990



Showing articles 1750 to 1800 of 2440 << Previous Next >>