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Differential
(Click to cross reference)
abdominal distention
amaurosis fugax
amyloid
amyloidosis
areflexia
arteritis, temporal
arthralgia
ataxia
atypical
cachexia
cardiomyopathy
carpal tunnel syndrome
CAT scan, abnormal
CAT scan, orbits
cerebellar atrophy, secondary
cerebellar degeneration
chemosis
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
congestive heart failure
consanguinity
cough
creatine phosphokinase(CPK)elevated
deafness
diarrhea
diplopia
dysthyroid ocularmyopathy
edema, periorbital
eosinophilic granulomatosis with polyangiitis
episcleritis
extraocular muscle enlargement
extraocular muscle lesion
extraocular muscle, metastasis to
eye, pain in
familial
fatigue
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gene mutation
genetic neurologic disorders
giant cell arteritis
granulomatosis with polyangiitis
headache
headache, bitemporal
heralding manifestation
histochemistry of muscle
IgG4-related disease
immunotherapy
infraorbital nerve
intestinal pseudoobstruction
Kearns-Sayre syndrome
lacrimal gland enlargement
lateral rectus palsy
leukodystrophy
lymph node biopsy
medial rectus palsy
melanoma, malignant
methotrexate
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
MRI, abnormal
MRI, contrast enhanced
MRI, extraocular muscle enhancement
MRI, orbit
muscle biopsy
muscle biopsy, extraocular
muscle weakness, proximal
myasthenia gravis, ocular
myopathy, necrotizing
myopathy, steroid responsive
myositis
myositis, ocular
necrotizing vasculitis
neoplasm, metastatic to CNS
neoplasm, metastatic to muscle
neoplasm, metastatic to orbit
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
oculopharyngeal muscular dystrophy
ophthalmoplegia
optic neuropathy
orbit
orbit, biopsy
orbit, inflammation in
orbit, lesions of
orbit, mass
orbital apex
pain, abdominal
perineuritis
perineuritis, optic
prognosis
progressive neurologic disorder
proptosis
proptosis, unilateral
ptosis
ptosis, unilateral
purpura
ragged-red fibers
rash
retina, abnormal
retinal lesion
rituximab
salivary gland enlargement
scotoma
sedimentation rate, elevated
sensorineural hearing loss
sialadenitis
skin, biopsy
skin, lesions in neurologic disorders
Stephens syndrome
steroid therapy, CNS treatment and complications with
systemic illness
temporal artery, biopsy
tongue, enlarged
transient neurologic deficit
treatment of neurologic disorder
vasculitides
visual field defect
visual loss
visual loss, alternating
visual loss, sudden-unilateral
visual loss, transient
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
white matter disease
Showing articles 200 to 250 of 3683 << Previous Next >>

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Ten Steps in Characterizing and Diagnosing Patients with Peripheral Neuropathy
Neurol 47:10-17, Dyck,P.J.,et al, 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Angiotropic Large-Cell Lymphoma with Peripheral Nerve & Skeletal Muscle Involvement:Early Diagnosis & Treatment
Neurol 47:1009-1011, Levin,K.H.&Lutz,G., 1996

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
J Pediatr 128:230-233, Pollard,F.,et al, 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Isolated Neck Extensor Myopathy:A Common Cause of Dropped Head Syndrome
Neurol 46:917-921, Katz,J.S.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
Neurol 45:1828-1832, Oh,S.J.,et al, 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

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

Investigation of Peripheral Neuropathy
JNNP 58:274-283, McLeod,J.G., 1995

Inclusion Body Myositis Presenting with Isolated Erector Spinae Paresis
Neurol 45:993-994, Hund,E.,et al, 1995

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

Extreme Eyelid Swelling as an Unusual Presentation of Dysthyroid Orbitopathy
J Neuro-Ophthalmol 15:84-89, Rosen,C.E.&Kennerdell,J.S., 1995

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

Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995

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

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

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

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

POEMS Syndrome:A Study of 25 Cases and a Review of the Literature
Am J Med 97:543-553, Soubrier,M.J.,et al, 1994

Clinicopath Conf
Polyarteritis Nodosa, with Neuropathy, Case 40-1994, NEJM 331:1293-130094., , 1994

Neurologic Manifestations of HIV Infection
Ann Int Med 121:769-785, Simpson,D.M.&Tagliati,M., 1994

Clinicopath Conf
Chronic Idiopathic Anhidrosis, Case 29-1994, NEJM 331:259-265994., , 1994

Benign Familial Disease with Muscle Mounding and Rippling
JNNP 57:344-347, Burns,R.J.,et al, 1994

Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
Lancet 343:1397-1398, Nakai,A.,et al, 1994

Congenital Myopathies
Muscle & Nerve 17:131-144994., Bodensteiner,J.B., 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
Ann Neurol 35:273-279, 2571994., Al-Lozi,M.T.,et al, 1994

Extraocular Muscles in Graves Ophthalmopathy:Usefulness of T2 Relaxation Time Measurements
Radiology 190:857-862, Ohnishi,T.,et al, 1994

Ocular Myasthenia:A Protean Disorder
Survey of Ophthalmology 39:169-210, Weinberg,D.A.,et al, 1994

Prolonged Paralysis Due to Nondepolarizing Neuromuscular Blocking Agents and Corticosteroids
Muscle & Nerve 17:647-654994., Barohn,R.J.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Pathogenesis of Graves'Ophthalmopathy
NEJM 329:1468-1475, Bahn,R.S.&Heufelder,A.E., 1993

Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993



Showing articles 200 to 250 of 3683 << Previous Next >>