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Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
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amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, misdiagnosis
ankle edema
apolipoprotein E
APP gene
arrhythmia, cardiac
arthrogryposis multiplex
Bence Jones protein
cardiomyopathy
carpal tunnel syndrome
Charcot-Marie-Tooth
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
congestive heart failure
Congo red stain
creatine phosphokinase(CPK)elevated
dermatomyositis
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distal muscle weakness
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electromyogram
electron microscopy
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genetic screening
genetic testing
Guillain Barre syndrome
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heralding manifestation
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immunoelectrophoresis, serum
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
jaw pain
klippel feil syndrome
leg weakness, bilateral
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuropathy
motor neuron disease
MRI, abnormal
MRI, muscle
multiple myeloma
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muscle diseases, characteristics of
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muscle weakness, causes of
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muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myopathy
myopathy, amyloid
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myopathy, carcinomatous
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myopathy, painful
myopathy, quadriceps
myopathy, thyroid disease causing
myositis
myotonia dystrophica
neuritis, causes of
neurologic disease, diagnoses of
neuropathy
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old age, neurology of
pain
pain, calf
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plasma cell dyscrasia
plasma cell myeloma, CNS involvement associated with
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polyneuropathy
polyneuropathy, familial
porphyria
practice guidelines
presenilin-1 gene
presenilin-2 gene
proximal muscle atrophy
pseudohypertrophy
quadriceps atrophy
quadriceps weakness
review article
risk factors
sarcoidosis
sedimentation rate
sedimentation rate, elevated
stiff man syndrome
tongue, enlarged
torticollis
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
Showing articles 650 to 700 of 1335 << Previous Next >>

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

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

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Amyloid Angiopathy-Related Cerebellar Hemorrhage
Surg Neurol 46:235-239, Cuny,E.,et al, 1996

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

Image Analysis of B-Amyloid Load in Alzheimer's Disease and Relation to Dementia Severity
Lancet 346:1524-1528, Cummings,B.J.&Cotman,C.W., 1995

Apolipoprotein E Allele E4, Dementia, and Cognitive Decline in a Population Sample
Lancet 346:1387-1390, Henderson,A.S.,et al, 1995

Apolipoprotein E, Dementia, and Cortical Deposition of B-Amyloid Protein
NEJM 333:1242-1247, 12831995., Polvikoski,T.,et al, 1995

Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
JAMA 274:1627-1629, Farrer,L.A.,et al, 1995

Apoliprprotein E E4 Allele & the Lifetime Risk of Alzheimer's Disease:What Physicians Know, & What They Should Know
Arch Neurol 52:1074-1079, Seshadri,S.,et al, 1995

Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
Ann Neurol 38:797-808, Farrer,L.A.,et al, 1995

Regional Distrib of Neurofibrillary Tangles & Senile Plaques in Cerebral Cortex of Very Old Pts
Arch Neurol 52:1150-1159, Gioannakopoulos,P.,et al, 1995

Cystatin C Mutation in an Elderly Man with Sporadic Amyloid Angiopathy and Intracerebral Hemorrhage
Stroke 26:2190-2193, Graffagnino,C.,et al, 1995

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

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.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

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,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

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 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

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

Anticonvulsant Hypersensitivity Syndrome
Arch Int Med 155:2285-2290, Vittorio,C.C.&Muglia,J.J., 1995

Subacute Enlarging Cerebral Hematoma From Amyloid Angiopathy: Case Report
Neurosurg 36:403-406, Leblanc,R.,et al, 1995

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

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Acute Bacterial Myositis Due to Staphylococcus Aureus Septicemia
Neurol 45:390-391, Sato,K.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

The Neuropathology of Williams Syndrome
Arch Neurol 52:209-212, Golden,J.A.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

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

Recurrence of Bleeding in Patients with Primary Intracerebral Hemorrhage
Stroke 26:1189-1192, Passero,S.,et al, 1995

Apolipoprotein E e4 and Cerebral Hemorrhage Associated with Amyloid Angiopathy
Ann Neurol 38:254-259, Greenberg,S.M.,et al, 1995

Clin Features & Pathog of Intracerebral Hemorrhage after rt-PA & Heparin Therapy for Acute Myocardial Infarct
Neurol 45:649-658, Sloan,M.A.,et al, 1995

Medical Complications During Stroke Rehabilitation
Stroke 26:990-994, Kalra,L.,et al, 1995

Is Alzheimer's Disease an Apolipoprotein E Amyloidosis?
Lancet 345:956-958, Wisniewski,T.,et al, 1995

Down's Syndrome and the Links with Alzheimer's Disease
JNNP 59:111-114, Holland,A.J.&Oliver,C., 1995

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

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Mild Traumatic Brain Injury:Pathophysiology, Natural History, and Clinical Management
Neurol 45:1253-1260, 12511995., Alexander,M.P., 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

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

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

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

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



Showing articles 650 to 700 of 1335 << Previous Next >>