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Differential
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abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acyl CoA dehydrogenase deficiency
adverse drug reaction
algorithm
aneurysm
anterior tibial muscle weakness
arthralgia
arthritis
autoimmune disease
azathioprine
azidodeoxythymidine
brachial plexus neuropathy
brain biopsy
brain biopsy, stereotaxic
calf hypertrophy
carcinoma
cardiomegaly
CAT scan, abnormal
CD4 counts
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, recurrent
cerebrovascular disease
children
chloroquine
chromosomal abnormality
chromosome 9
cranial neuropathy
creatine phosphokinase(CPK)elevated
cryptococcal meningitis
cyclic vomiting
cystinosis
cytomegalovirus infection
delay in diagnosis
dementia
dermatitis
dermatomyositis
diaphragmatic paralysis
diarrhea
diarrhea, bloody
differential diagnosis
difficulty climbing stairs
disability rating scale, neurological
distal muscle atrophy
distal muscle weakness
dropped head syndrome
dysarthria
dysphagia
dyspnea
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalitis
encephalitis, focal
encephalitis, human immunodeficiency virus type 1
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
exercise
exercise intolerance
facial nerve palsy
facial nerve palsy, recurrent
facial weakness
falling
familial
fatigue
fibrillations
foot drop
foot drop, bilateral
fracture, long bone
gait disorder
gene
gene mutation
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen storage disease
Guillain Barre syndrome
hand weakness
headache
hearing loss
heart block
heart block, complete
hepatomegaly
heralding manifestation
histochemistry of muscle
human immunodeficiency virus type 1
human immunodeficiency virus type 1, pathogenesis
hyperreflexia
imbalance
immunosuppressive agents
inability to stand on tiptoes
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion body myositis
intrinsic hand muscles, wasting of
leg weakness, bilateral
limb-girdle weakness
lymphoma
lymphoma involving CNS
lysosomal storage disease
Melkersson's syndrome
memory, impairment of
methotrexate
misdiagnosis
mitochondrial disease
molecular genetics
mononeuritis multiplex
mononeuropathy multiplex
MRI
MRI, abnormal
MRI, brachial plexus
MRI, muscle
multiple sclerosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, classification
muscular dystrophy, distal, Miyoshi
myasthenia gravis
myelopathy
myelopathy, chronic progressive
myelopathy, vacuolar
myopathy
myopathy, distal
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, genetic
myopathy, hereditary
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, metabolic
myopathy, necrotizing
myopathy, proximal
myopathy, toxic
myopathy, vacuolar
myositis
myositis, ocular
myotonic discharges
nausea and vomiting
neck weakness
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuropathology
neuropathy
neurosyphilis
next-generation sequencing
optic neuritis
orthopnea
pain, abdominal
paraspinal muscle
paraspinal muscle weakness
phosphorylase b kinase deficiency
polymyositis
polyneuropathy, chronic inflammatory demyelinating
Pompe's disease of glycogen storage
prenatal diagnosis by amniocentesis
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proximal muscle atrophy
pseudomyotonia
quality of life
regional enteritis
research
respiratory failure
review article
riboflavin
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
short stature
standing difficulty
steppage gait
subarachnoid hemorrhage
syphilis, neurologic complications with
tongue, enlarged
tongue, weakness
toxoplasmosis, CNS
transient ischemic attack
treatment of neurologic disorder
ulcerative colitis
vital capacity
weakness
weakness, progressive
weakness, proximal
weight loss
winging of scapula
X-linked myopathy
x-linked myopathy with excessive autophagy
Showing articles 550 to 600 of 1025 << Previous Next >>

The Dropped Head Syndrome
Neurol 42:1625-1627, Suarez,G.A.&Kelly,J.J., 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Chronic Limb-Girdle Myasthenia Gravis
Neurol 42:1153-1156, Oh,S.J.&Kuruoglu,R., 1992

Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
Neurol 42:1422-1423, Bird,S.J., 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Pravastatin-Associated Inflammatory Myopathy
NEJM 327:649-650, Schalke,B.B.,et al, 1992

The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
Ann Neurol 32:207-214, Rowland,L.P., 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Fibromyalgia:The Copenhagen Declaration
Lancet 340:663-664, Csillag,C., 1992

Generalized Myositis in Behcet Disease:TReatment with Cyclosporine
Ann Int Med 116:651-653, Lingenfelser,T.,et al, 1992

Lyme Disease Associated with Fibromyalgia
Ann Int Med 117:281-285, Dinerman,H.&Steere,A.C., 1992

Controlled Trial of Plasma Exchange and Leukapheresis in Polymyositis and Dermatomyositis
NEJM 326:1380-1384, Miller,F.W.,et al, 1992

Dystrophinopathy in Isolated Cases of Myopathy in Females
Neurol 42:967-975, Hoffman,E.P.,et al, 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

A Chronic Illness of Fatigue, Neurologic and Immunologic Disorders, & Active Human Herpesvirus Type 6 Infection
Ann Int Med 116:103-113, Buchwald,D.,et al, 1992

Polymyalgia Rheumatica and Mitochondrial Myopathy:Clinicopathologic and Biochemical Studies in Five Cases
Am J Med 92:167-172, Harle,J.,et al, 1992

Headaches in Children Younger than 7 Years of Age
Arch Neurol 49:79-82, Chu,M.L.&Chinnar,S., 1992

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

Clinicopath Conf
Churg-Strauss Syndrome, Case 18-1992, NEJM 326:1204-1212992., , 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Acute Quadriplegic Myopathy:A Complic of Treat with Steroids, Nondepolarizing Blocking Agents, or Both
Neurol 42:2082-2087, Hirano,M.,et al, 1992

Ipecac Myopathy and Cardiomyopathy
JNNP 56:560-562, Dresser,L.P.,et al, 1992

Severe Phenytoin Hypersensitivity with Myopathy:A Case Report
Neurol 42:2303, Barclay,C.L.,et al, 1992

Travel and Ciguatera Fish Poisoning
Arch Int Med 152:2049-2053, Lange,W.R.,et al, 1992

Myopathy in Severe Asthma
Am Rev Respir Dis 146:517-519, Douglass,J.A.,et al, 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Clinical Signs in Severe Guillain-Barre Syndrome: Analysis of 63 Patients
J Neurol Sci 104:143-150, De Jager, A.E.J.,et al, 1991

Idiopathic Myelopathies with White Matter Vacuolation in Non-AIDS Patients
Human Pathol 22:816-824, Kamin,S.S.&Petito,C.K., 1991

Adult Reye's Syndrome:A Review with New Evidence for a Generalized Defect in Intramitochondrial Enzyme Processing
Neurol 41:1815-1821, VanCoster,R.N.,et al, 1991

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991

The Bruns-Garland Syndrome (Diabetic Amyotrophy) , Revisited 100 Years Later
Arch Neurol 48:1130-1135, Barohn,R.J.,et al, 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Cyclosporin in the Management of Polymyositis and Dermatomyositis
JNNP 54:1007-1008, Lueck,C.J.,et al, 1991

Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
Lancet 337:508-510, Arnaudo,E.,et al, 1991

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

N-Isopropyl-p- (123I) Iodoamphetamine SPECT in MELAS Syndrome:Comparison with CT & MR Imaging
J Comput Assist Tomogr 15:77-82, Satoh,M.,et al, 1991



Showing articles 550 to 600 of 1025 << Previous Next >>