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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 650 to 700 of 1026 << Previous Next >>

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Fluctuating MR Images with Mitochondrial Encephalopathy, Lactic Acidosis, Stroke-Like Syndrome (MELAS)
Neuroradiology 32:77, Abe,K.,et al, 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Mitochondrial Encephalomyopathy (MELAS) with Mental Disorder, CT, MRI and SPECT Findings
Neuroradiology 32:74-76, Suzuki,T.,et al, 1990

Myopathy and Rhabdomyolysis Associated with Lovastatin-Gemfibrozil Combination Therapy
JAMA 264:71-75, Pierce,L.R.,et al, 1990

Peripheral Neuropathy in the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Neurol 40 1035-1040, Smith,B.E.&Dyck,P.J., 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Eosinophilia-Myalgia Syndrome (L-Tryptophan-Associated Neuromyopathy)
Neurol 40:1793-1796, Turi,G.K.,et al, 1990

L-Tryptophan-Induced Eosinophila-Myalgia Syndrome and Myopathy
Neurol 40:1629-1630, Sagman,D.L.&Melamed,J.C., 1990

New Muscle Power Test in Neuromuscular Disease
Am J Dis Child 144:1083-1087, Tirosh,E.,et al, 1990

Myopathy with Human Immunodeficiency Virus Type I (HIV-1) Infection:HIV-1 or Zidovudine?
Ann Int Med 113:492-493, Till,M.&MacDonell,K., 1990

Human Immunodeficiency Virus Assoc Myopathy:Immunocytochemical Ident of an HIV Antigen (gp41) in Muscle Macrophages
Ann Neurol 28:579-582, Chad,D.A.,et al, 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Multifocal Vacuolar Leucoencephalopathy:A Distinct HIV-Associated Lesion of the Brain
Neuropath Appl Neurobiol 16:437-443, Schmidbauer,M.,et al, 1990

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

Spinal Cord Pathology in Pediatric Acquired Immunodeficiency Syndrome
Neurol 39:227-235, Dickson,D.W.,et al, 1989

Polymyositis and HTLV-I Antibodies
Ann Neurol 25:311, Francis,D.A.&Hughes,R.A.C., 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Predictive Testing for Huntington's Disease, Progress and Problems
BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Zidovudine-Associated Myopathy
Am J Med 86:814-818, Gertner,E.,et al, 1989

Spinal Cord and Peripheral Nerve Pathology in AIDS:The Roles of CMV & HIV
Ann Neurol 25:561-566, Grafe,M.R.&Wiley,C.A., 1989



Showing articles 650 to 700 of 1026 << Previous Next >>