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Differential
(Click to cross reference)
anterior horn cell disease
aqueduct of Sylvius, obstruction
arachnoiditis
areflexia
arm weakness
arrhythmia, cardiac
asthma
asthma, poliomyelitis-like syndrome with
cachexia
calcification, intracranial
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, disappearing lesion on
CAT scan, false negative
CAT scan, serial
cerebral cortex
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
children
cisterna magna
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
coma
congenital myopathy
congestive heart failure
Creutzfeldt-Jakob disease, genetic
cyst, cortical parenchyma
cyst, ventricular
cysticercosis
cysticercosis, cerebral
cysticercosis, intraventricular
cysticercosis, subarachnoid
dementia
dermatomyositis
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetic amyotrophy
dropped head syndrome
dysphagia
electromyogram
encephalitis
endemic area
entrapment neuropathy
epidemiology of neurology
episodic neurologic deficits
falling
familial
fibrillations
flaccid paralysis
foot drop
fourth ventricle, cyst
gait disorder
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
headache
headache, severe
helminthic infection of CNS
hemianopia, homonymous
hemiparesis
hip flexor weakness
Hispanics
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hydrocephalus, transient
imbalance
inclusion body myositis
interstitial pulmonary fibrosis
intracranial hypertension, benign
intracranial pressure, increased
Jakob-Creutzfeldt disease
kyphoscoliosis, neurologic causes of
leg atrophy
leg numbness
leg weakness, bilateral
leg weakness, unilateral
linear lesion
meningitis
meningitis, aseptic
meningitis, chronic
meningitis, cysticercosis
meningitis, eosinophilic
Mexican
Mexico
misdiagnosis
mixed connective tissue disease
monomelic myositis
monoparesis
mortality
motor cortex
motor neuron disease
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, muscle
MRI, susceptibility weighted
multiple myeloma
muscle biopsy
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle weakness
muscle weakness, proximal
myasthenia gravis
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, stimulus sensitive
myopathy
myopathy, axial
myopathy, focal
myopathy, monomelic
myopathy, thyroid disease causing
myositis
myositis, bacterial
myositis, eosinophilic
myositis, focal
myositis, fungal
myositis, granulomatous
myositis, ocular
myositis, parasitic
neck extension
neck weakness
nerve conduction studies
neurologic disease, diagnoses of
neuropathy
neuropathy, diabetic
pain
pain, abdominal
pain, leg
pain, thigh
paraplegia
paraproteinemia
parasitic infection, CNS
paraspinal muscle
paraspinal muscle weakness
pleocytosis of cerebrospinal fluid
poliomyelitis-like illness
polymyositis
polyradiculoneuropathy
posterior interosseous neuropathy
prion disease
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
quadriceps atrophy
quadriplegia
rapidly progressing neurologic illness
real-time quaking-induced conversion
review article
rhabdomyolysis
rheumatoid arthritis
Romberg's sign
scleroderma
seizure
seizure, focal
serologic testing
shunt procedure, ventricular
Sjogren's syndrome
systemic lupus erythematosus, neurologic complications with
tandem gait, ataxic
thyrotoxicosis
treatment of neurologic disorder
vertigo
viral myopathy
walking, difficulty with
weakness, acute
weakness, focal
weight loss
wheelchair
wide based gait
Showing articles 450 to 500 of 1121 << Previous Next >>

Clinicopath Conf
Skeletal-Muscle Infarction Associated with Diabetes Mellitus, Case 29-1997, NEJM 337:839-845997., , 1997

Clinical Characteristics of Patients with Motor Disability Due to Conversion Disorder:A Prospective Study
JNNP 63:83-88, Binzer,M.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Acute Corticosteroid Myopathy in Intensive Care Patients
Muscle & Nerve 20:1371-1380997., Hanson,P.,et al, 1997

Hemiparetic Acute Myopathy of Intensive Care Progressing to Triplegia
Arch Neurol 54:1420-1422, Sun,D.Y.,et al, 1997

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

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

Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996

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

Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
Neurol 47:1269-1277, Baser,M.E., 1996

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

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

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

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

Clozapine-Induced Myotoxicity in Patients with Chronic Psychotic Disorders
Neurol 47:1518-1523, Scelsa,S.N.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Linomide Reduces the Rate of Active Lesions in Relapsing-Remitting Multiple Sclerosis
Neurol 47:895-900, Anderson,O.,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

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

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

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

Motor Neuropathy Due to Docetaxel and Paclitaxel
Neurol 47:115-118, Freilich,R.J.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,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

Apolipoprotein E Genotyping in Alzheimer's Disease
Lancet 347:1091-1095, Tanzi,R.,et al, 1996

Intravenous Immunoglobulin Treatment of Neurological Disease
JNNP 60:359-361, Otten,A.,et al, 1996

The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
JNNP 60:449-451, Jamal,G.A.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Chronic Post-Traumatic Headache Often a Myth
Neurol 46:915-916, Warner,J.S.&Fenichel,G.M., 1996

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,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

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,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

Mushroom Myopathy
Muscle & Nerve 19:790-792996., Gonzalez,J.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

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

Peripheral Neuropathy Secondary to Docetaxel (Taxotere)
Neurol 46:108-111, 21996., New,P.Z.,et al, 1996



Showing articles 450 to 500 of 1121 << Previous Next >>