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Differential
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acid maltase deficiency
acid maltase deficiency, adult
acyl CoA dehydrogenase deficiency
adverse drug reaction
alpha glucosidase
aminoacidopathies
anterior horn cell disease
aspartate aminotransferase
aspiration
asymptomatic
ataxia
attention span
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
cardiomyopathy
carnitine deficiency
carnitine deficiency myopathy
CAT scan, abnormal
cataplexy
cerebral cortical atrophy
cerebrovascular accident
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
coma
complications
congestive heart failure
cornea, abnormal
corneal dystrophy
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cystinosis
delay in diagnosis
dementia
developmental milestones, loss of
developmental retardation
differential diagnosis
drooling
dropped head syndrome
dysarthria
dysphagia
dystonia
echocardiogram
electromyogram
enzyme treatment
enzyme, defect
enzyme, muscle disease
enzyme, serum
exercise
exercise intolerance
exercise-induced neurologic dysfunction
Fabry's disease
familial
fatigue
fluctuate
foam cells
gangliosidosis GM2
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glucocerebrosidase
glycogen storage disease
growth retardation
hepatic failure
hepatomegaly
hepatosplenomegaly
heralding manifestation
hexosaminidase-A
hypoglycemia
hypoglycemic coma
hypomyelination
hyporeflexia
hypotonia
inattention
inborn errors of metabolism, screening
incoordination
intellectual deficit
jaundice
Jewish
lactic dehydrogenase(LDH)
leg weakness, bilateral
limb-girdle weakness
lipid storage disorder of CNS
lipid storage myopathy
lysosomal storage disease
lysosomes, abnoral
metabolic acidosis
mitral valve prolapse
molecular genetics
mortality
MRI, abnormal
MRI, hypointense signal foci on
mucopolysaccharidoses
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
myoglobinuria
myopathy
myopathy, metabolic
myopathy, proximal
myopathy, vacuolar
neck weakness
neurofibrillary degeneration
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neuropathology
neurosis
next-generation sequencing
Niemann-Pick disease
pain
pain, leg
patient in waiting
pediatric neurology
photophobia
polymerase chain reaction
Pompe's disease of glycogen storage
Pompe's disease, infantile
postpartum
precipitating factors
preclinical
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
progressive neurologic disorder
propranolol
proteinuria
psychiatric problems in neurologic disorders
psychological testing
psychosis
quadriplegia
recurrent
renal failure
respiratory failure
respiratory tract infection
review article
rhabdomyolysis
rigidity
screening
seizure
skin, lesions in neurologic disorders
slit lamp examination
sodium valproate
sodium valproate, toxicity
spasticity
sphingolipodoses
spinocerebellar degeneration
splenomegaly
startle reaction
storage disease of CNS
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
tone, muscle, increased
tongue, enlarged
treatment of neurologic disorder
type 1 muscle fiber
urine, dark
weakness
weakness, chronic
weakness, fluctuating
weakness, generalized
weakness, progressive
weakness, proximal
white matter disease
Showing articles 850 to 900 of 1299 << Previous Next >>

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Polymyositis after Ciguatera Toxin Exposure
Arch Neurol 48:874-877, Stommel,E.W.,et al, 1991

Colchicine-Induced Myopathy and Neuropathy
Neurol 41:943, Younger,D.S.,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

Eosinophilia-Myalgia Syndrome, A Clinical Case Series of 21 Patients
Arch Int Med 151:533-537, Philen,R.M.,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

Serum Cholesterol Concentration and Risk of Primary Brain Tumours
BMJ 302:90, Knekt,P.,et al, 1991

Polymyositis Mediated by T Lymphocytes that Express the y/8 Receptor
NEJM 324:877-881, Hohlfeld,R.,et al, 1991

Lisch Nodules in Neurofibromatosis Type I
NEJM 324:1264-1266, 1283-12851991., Lubs,M-L.E.,et al, 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Cervical Dystonia:Clinical Findings and Associated Movement Disorders
Neurol 41:1088-1091, Jankovic,J.,et al, 1991

Myopathy Associated with Ketoconazole Treatment
Am J Dis Child 145:970-971, Garty,B-Z.,et al, 1991

Cramp-Fasciculation Syndrome:A Treatable Hyperexcitable Peripheral Nerve Disorder
Neurol 41:1021-1024, Tahmoush,A.J.,et al, 1991

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 1991

Prognosis in AZT Myopathy
Neurol 41:1181-1184, Chalmers,A.C.,et al, 1991

Myopathy in Human Immunodeficiency Virus-Infected Children Receiving Long-Term Zidovudine Therapy
J Pediatr 119:152-155, Walter,E.B.,et al, 1991

Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
Ann Neurol 29:606-614, Mhiri,C.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Legionella Myositis
Neurol 41:750-752, Warner,C.L.,et al, 1991

Rickettsial Meningitis and Encephalitis
Arch Int Med 151:1753-1757, Silpapojakul,K.,et al, 1991

Treatment of Dermatomyositis with Intravenous Gammaglobulin
Am J Med 91:169-172, Lang,B.A.,et al, 1991

Efficacy of Intravenous Gammaglobulin Therapy in Chronic Refactory Polymyositis & Dermatomyositis:20 Adult Patients
Am J Med 91:162-168, Cherin,P.,et al, 1991

The Idiopathic Inflammatory Myopathies and Their Treatment
JNNP 54:285-287, Walton,J., 1991

Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
Lancet 337:1311-1313, Hammans,S.R.,et al, 1991

The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
Neurol 41:1491-1496, Arikawa,E.,et al, 1991

Steroid-Induced Weakness in Patients with Primary Brain Tumors
Neurol 41:1235-1239, Dropcho,E.J.&Soong,S., 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991

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

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

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

Tangier Disease in a Black Patient:An Unusual Clinical Presentation
Am J Med 89:105-108, Lo,W.D.,et al, 1990

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

Scleroderma, fasciitis, and Eosinophilia Associated with the Ingestion of Tryptophan
NEJM 322:874-881, 9261990., Silver,R.M.,et al, 1990

Association of the Eosinophilia-Myalgia Syndrome with the Ingestion of Tryptophan
NEJM 322:869-873, 9261990., Hertzman,P.A.,et al, 1990

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990



Showing articles 850 to 900 of 1299 << Previous Next >>