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Differential
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abdominal distention
areflexia
ataxia
atypical
autoimmune disease
cachexia
CAT scan
CAT scan, abnormal
CAT scan, orbits
cerebellar atrophy, secondary
cerebellar degeneration
chemosis
chronic progressive external ophthalmoplegia
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
conjunctival injection
consanguinity
cranial nerve enlargement
cranial neuropathy
creatine phosphokinase(CPK)elevated
cyst, benign intracranial
deafness
diarrhea
diplopia
diplopia, vertical
donut sign
dysthyroid ocularmyopathy
dysthyroidism
edema, periorbital
exophthalmus
extraocular muscle atrophy
extraocular muscle enlargement
extraocular muscle lesion
eye, pain in
familial
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gender
gene mutation
genetic neurologic disorders
granulomatosis with polyangiitis
Graves ophthalmopathy
heralding manifestation
hyperthyroidism
IgG4, serum
IgG4-related disease
immunotherapy
intestinal pseudoobstruction
Kearns-Sayre syndrome
lacrimal gland enlargement
leukodystrophy
lid
maxillary nerves
methotrexate
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, optic nerve
MRI, orbit
muscle biopsy
muscle biopsy, extraocular
muscle weakness, proximal
myasthenia gravis
myopathy, mitochondrial
myopathy, necrotizing
myopathy, steroid responsive
myositis
myositis, ocular
necrotizing vasculitis
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuroophthalmology
neuropathy
ocular myopathy
ophthalmoplegia
optic nerve
optic nerve sheath enhancement
optic nerve, compression of
optic nerve, enlarged
optic nerve, lesion of
optic neuropathy
optic neuropathy, bilateral
orbit
orbit, biopsy
orbit, inflammation in
orbit, lesions of
orbit, mass
orbital apex
pain
pain, abdominal
pathology
perineuritis
perineuritis, optic
photophobia
prognosis
progressive neurologic disorder
proptosis
proptosis, unilateral
ptosis
radiation therapy, CNS treatment and complications with
ragged-red fibers
restrictive ophthalmopathy
retina, abnormal
retinal lesion
review article
risk factors
rituximab
salivary gland enlargement
scotoma
sensorineural hearing loss
sialadenitis
sinuses, diseases of
sinusitis
steroid
steroid therapy, CNS treatment and complications with
systemic illness
thyrotoxicosis
tram-track sign
treatment of neurologic disorder
trigeminal nerve, lesion of
trinucleotide repeats
vasculitides
vision, blurred
visual acuity, decreased
visual field defect
visual loss
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
white matter disease
Showing articles 500 to 550 of 4226 << Previous Next >>

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991

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

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

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

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Neuromuscular Blockade
Lancet 335:382-384, , 1990

Clinical Study of 227 Patients with Lacunar Infarcts
Stroke 21:842-847, Arboix,A.,et al, 1990

Benign Plexus Neuropathy in Children
J Pediatr 116:276-278, Zeharia,A.,et al, 1990

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 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

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,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

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Syncope:Current Diagnostic Evaluation and Management
Ann Int Med 112:850-863, Manolis,A.S.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

MRI Demonstration of Cortical Laminar Necrosis and Delyaed White Matter Injury in Anoxic Encephalopathy
Neuroradiology 32:319-321, Sawada,H.,et al, 1990

Hypoxic-Ischemic Damage of the Basal Ganglia
Mov Disord 5:219-224, Hawker, K. & Lang, A.E., 1990

Computed Tomographic Features of Nonthyroid Extraocular Muscle Enlargement
Ophthalmol 96:1038-1047, Patrinely,J.R.,et al, 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Trochanteric Sciatic Neuropathy
Neurol 39:1539-1541, Crisci,C.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

Orbital Myositis and Giant Cell Myocarditis
Neurol 39:988-990, Klein,B.R.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989



Showing articles 500 to 550 of 4226 << Previous Next >>