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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 700 to 750 of 1026 << Previous Next >>

Dissociation of AIDS-Related Vacuolar Myelopathy and Productive HIV-1 Infection of the Spinal Cord
Neurol 39:892-896, Rosenblum,M.,et al, 1989

HTLV-I Polymyositis in a Patient Also Infected with the Human Immunodeficiency Virus
NEJM 320:992-995, Wiley,C.A.,et al, 1989

Computeritis, Who's Responsible When PCs Make Employees Sick?
Infoworld 11:51-54, Flynn,L., 1989

The Chronic Fatigue Syndrome-One Entity or Many?
NEJM 319:1726-1728, Swartz,M.N., 1989

Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,et al, 1989

Flaccid Quadriparesis Associated with Yersinia Enterocolitis-Induced Hypokalemia
Arch Int Med 149:1193-1194, Orman,R.A.&Lewis,J.B., 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Pyomyositis in a Child with Acquired Immunodeficiency Syndrome
Am J Dis Child 143:779-781, Raphael,S.A.,et al, 1989

Nicotinic Acid-Associated Myopathy:A Report of Three Cases
Am J Med 86:481-483, Litin,S.C.&Snderson,C.G., 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

Orbital Myositis and Giant Cell Myocarditis
Neurol 39:988-990, Klein,B.R.,et al, 1989

Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Clin Characteristics, Course, & Diag Criteria
Arch Neurol 46:878-884, Barohn,R.J.,et al, 1989

HTLV-1 and Polymyositis in Jamaica
Lancet 2:1184-1187, Morgan,O.S.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

Genetic Markers for Neurofibromatosis
Editorial, Lancet 2:719-7201988., , 1988

Pyomyositis in a Patient with the Acquired Immunodeficiency Syndrome
Arch Int Med 148:1608-1610, Gaut,P.,et al, 1988

Successful Treatment of Ciguatera Fish Poisoning with Intravenous Mannitol
JAMA 259:2740-2742, Palafox,N.A.,et al, 1988

Overuse Syndrome:A Muscle Biopsy Study
Lancet 1:905-908, Dennett,X.&Fry,H.J.H., 1988

Neuromuscular Diseases Associated with Human Immunodeficiency Virus Infection
Ann Neurol 23:S38-S48, Dalakas,M.C.&Pezeshkpour,G.H., 1988

Severe Polymyositis-Like Syndrome Associated with Zidovudine Therapy of AIDS & ARC
NEJM 318:708, Bessen,L.J.,et al, 1988

Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Lyme Myositis:Muscle Invasion by Borrelia Burgdorferi
Ann Int Med 109:245-246, Atlas,E.,et al, 1988

Subacute Structural Myopathy Associated with Human Immunodeficiency Virus Infection
Arch Neurol 45:585-587, Gonzales,M.F.,et al, 1988

Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
Ann Neurol 24:79-84, Simpson,D.M.&Bender,A.N., 1988

Fatal Adult Respiratory Distress Syndrome in a Patient with Lyme Disease
JAMA 259:2737-2739, Kirsch,M.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988

Diagnosis & Follow-up of Mitochondrial Encephalomyopathy:CT and MR Studies
J Comput Assist Tomogr 12:696-697, Taverni,N.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

The Neuromuscular Manifestations of Human Immunodeficiency Virus Infections
Arch Neurol 45:1084-1088, Lange,D.J.,et al, 1988

Human Immunodeficiency Virus in Vacuolar Myelopathy of the Acquired Immunodeficiency Syndrome
NEJM 319:1667-1668, Budka,H.,et al, 1988

Suxamethonium Myalgia
Editorial, Lancet 2:945-9461988., , 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Dysphagia in Inclusion Body Myositis
JNNP 51:1542-1545, Wintzen,A.R.,et al, 1988

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

Pyogenic Myositis:CT Evaluation
J Comput Assist Tomogr 12:1002-1005, Tumeh,S.S.,et al, 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis
NEJM 392:1461-1464, Gahl,W.A.,et al, 1988

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988



Showing articles 700 to 750 of 1026 << Previous Next >>