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Differential
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Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
amyloid
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
diarrhea
distal muscle atrophy
distal muscle weakness
dysphagia
dyspnea
edema, leg
electromyogram
electron microscopy
familial
fatigue
Friedreich's ataxia
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Guillain Barre syndrome
hand weakness
heart block
heralding manifestation
hoarseness
hypercalcemia
immunoelectrophoresis, serum
immunohistochemistry
immunomodulation
immunosuppressive agents
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
jaw pain
klippel feil syndrome
leg weakness, bilateral
misdiagnosis
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mononeuropathy
motor neuron disease
MRI, abnormal
MRI, muscle
multiple myeloma
muscle biopsy
muscle diseases, characteristics of
muscle pain
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myopathy
myopathy, acquired
myopathy, amyloid
myopathy, autoimmune
myopathy, carcinomatous
myopathy, glycogen storage
myopathy, necrotizing
myopathy, painful
myopathy, quadriceps
myopathy, scleromyxedema
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nemaline rod myopathy
nemaline rod myopathy, adult onset
neuritis, causes of
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
neuropathy, amyloid
neuropathy, diabetic
neuropathy, hereditary peripheral
old age, neurology of
pain
pain, calf
pain, leg
plasma cell dyscrasia
plasma cell myeloma, CNS involvement associated with
poliomyelitis
polymyositis
polyneuropathy
polyneuropathy, familial
porphyria
practice guidelines
presenilin-1 gene
presenilin-2 gene
prognosis
proximal muscle atrophy
pseudohypertrophy
quadriceps atrophy
quadriceps weakness
review article
risk factors
sarcoidosis
sedimentation rate
sedimentation rate, elevated
stem cell transplantation
stiff man syndrome
systemic illness
tongue, enlarged
torticollis
treatment of neurologic disorder
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
Showing articles 700 to 750 of 1362 << Previous Next >>

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

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

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

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

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

Common Variable Immunodeficiency and Inclusion Body Myositis:A Distinct Myopathy Mediated by Natural Killer Cells
Ann Neurol 37:806-810, Dalakas,M.C.&Illa,I., 1995

Becker Muscular Dystrophy with Onset after 60 Years
Neurol 44:2388-2390, Heald,A.,et al, 1994

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

Hypokalemic Myopathy Induced by Giardia Lamblia
NEJM 330:66-67, Addiss,D.G.&Lengerich,e.J., 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

Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy
Ann Int Med 120:133-134, Skinner,M.,et al, 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

Clinical Genetics in Neurological Disease
JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994

Headache
JNNP 57:134-143, Pearce,J.M.S., 1994

Distal Vacuolar Myopathy in Nephropathic Cystinosis
Ann Neurol 35:181-188, Charnas,L.R.,et al, 1994

Relation of Alcoholic Myopathy to Cardiomyopathy
Ann Int Med 120:529-536, Fernandez-Sola,J.,et al, 1994

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

A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Alzheimer's-Disease-Like Changes in Tau Protein Processing:Assoc with Aluminium Accum in Brains of Dialysis Pts
Lancet 343:993-997, 9891994., Harrington,C.R.,et al, 1994

Antibiotic Induced Meningitis
JNNP 57:705-708, River,Y.,et al, 1994

Human Prion Diseases
Ann Neurol 35:385-395, Prusiner,S.B.&Hsiao,K.K., 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

Ekbom's Syndrome:Lypomas, Ataxia, and Neuropathy with MERRF
Muscle & Nerve 17:943-945994., Calabresi,P.,et al, 1994

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

Early-Onset Respiratory Failure Caused by Severe Congenital Neuromuscular Disease
J Pediatr 124:636-638, Sandler,D.L.,et al, 1994



Showing articles 700 to 750 of 1362 << Previous Next >>