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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 650 to 700 of 1299 << Previous Next >>

Low Total Serum Cholesterol and Intracerebral Hemorrhagic Stroke:Is the Assoc Confined to Elderly Men
Stroke 27:1993-1998, Iribarren,C.,et al, 1996

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

Predictors of Stroke in Middle-Aged Patients with Non-Insulin-Dependent Diabetes
Stroke 27:63-68, Lehto,S.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Reduction in Carotid Arterial Wall Thickness Using Lovastatin & Dietary Therapy
Ann Int Med 124:548-556, Hodis,H.N.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

Lipids and Stroke
Arch Neurol 53:303-308, Hachinski,V.,et al, 1996

Apolipoprotein E Genotyping in Alzheimer's Disease
Lancet 347:1091-1095, Tanzi,R.,et al, 1996

Intravenous Immunoglobulin Treatment of Neurological Disease
JNNP 60:359-361, Otten,A.,et al, 1996

The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
JNNP 60:449-451, Jamal,G.A.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Chronic Post-Traumatic Headache Often a Myth
Neurol 46:915-916, Warner,J.S.&Fenichel,G.M., 1996

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Mushroom Myopathy
Muscle & Nerve 19:790-792996., Gonzalez,J.,et al, 1996

Isolated Neck Extensor Myopathy:A Common Cause of Dropped Head Syndrome
Neurol 46:917-921, Katz,J.S.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Motor Neuropathy Due to Docetaxel and Paclitaxel
Neurol 47:115-118, Freilich,R.J.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
Stroke 26:1950-1952, Kosinski,C.,et al, 1995

Primary Prevention of Stroke
NEJM 333:1392-1400, Bronner,L.L.,et al, 1995

Parkinsonism Unmasked by Lovastatin
Ann Neurol 37:685-686, Muller,T.,et al, 1995

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Apolipoprotein E Allele E4, Dementia, and Cognitive Decline in a Population Sample
Lancet 346:1387-1390, Henderson,A.S.,et al, 1995

Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
JAMA 274:1627-1629, Farrer,L.A.,et al, 1995

Apoliprprotein E E4 Allele & the Lifetime Risk of Alzheimer's Disease:What Physicians Know, & What They Should Know
Arch Neurol 52:1074-1079, Seshadri,S.,et al, 1995

Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
Ann Neurol 38:797-808, Farrer,L.A.,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

Apolipoprotein E E4 in Inclusion Body Myositis
Ann Neurol 38:957-959, Garlepp,M.J.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Lipoprotein (a) & Asympt Carotid Art Disease:Evidence of a Prominent Role in the Evol of Advanced Carotid Plaques
Stroke 26:1582-1587, Willeit,J.,et al, 1995

Plasma Concentration of Lipoprotein (a) and the Risk of Future Stroke
JAMA 273:1269-1273, Ridker,P.M.,et al, 1995

Medical Complications During Stroke Rehabilitation
Stroke 26:990-994, Kalra,L.,et al, 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



Showing articles 650 to 700 of 1299 << Previous Next >>