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acquired immunodeficiency syndrome
acyl CoA dehydrogenase deficiency
adult polyglucosan body disease
advances in neurology
adverse drug reaction
alcohol, neurologic complications with
aldolase
aminoacidurias
amniocentesis
arrhythmia, cardiac
atrioventricular block
Babinski sign
bladder dysfunction
blood dyscrasias, neurologic findings with
bone age
bulimia
bulimia nervosa
calf hypertrophy
carcinoma
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
cathartic
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
clofibrate
coenzyme Q10 deficiency
complications
congestive heart failure
contractures, joint
creatine kinase
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
delay in diagnosis
dermatomyositis
developmental retardation
diagnostic criteria
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
DNA probes
drug induced neurologic disorders
dysphagia
dystrophic calcification
dystrophin
eating disorder
electrocardiogram, abnormal
electromyogram
ELISA
encephalitis
encephalopathy
enzyme, defect
enzyme, muscle disease
enzyme, serum
exercise
exercise intolerance
Fabry's disease
falling
familial
fatigue
femoral neuropathy
fever
fine motor function, impaired
gait disorder
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
growth retardation
heart block
hemophilia
hepatomegaly
hip flexor weakness
human immunodeficiency virus type 1
hypocalcemia
hypoglycemia
hypokalemia
hypoparathyroidism, idiopathic
hyporeflexia
imbalance
immunologic disease
immunosuppressive agents
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion body myositis
insulin
ischemic exercise test
Jewish
Kearns-Sayre syndrome
Kugelberg-Welander syndrome
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lipid lowering agent
lipid storage disorder of CNS
liver function enzymes
Lowe's syndrome
MELAS syndrome
MERRF syndrome
metachromatic leukodystrophy
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
mononeuropathy
mortality
motor neuron disease
MRI
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle strength, testing
muscle tenderness
muscle weakness
muscle weakness, causes of
muscle weakness, insidious onset of
muscle weakness, intermediate onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
myelomalacia
myeloneuropathy
myelopathy
myocarditis
myoglobinuria
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, hypokalemic
myopathy, inflammatory
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, vacuolar
myositis
neck weakness
neonatal screening, genetic neurologic disorders
nerve biopsy
nerve conduction studies
neurogenic bladder
neurologic complications of, surgery
neurologic disease, diagnoses of
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, sensory
oculopharyngeal muscular dystrophy
ophthalmoplegia, progressive external
pain
pain, foot
pain, leg
paraparesis
paraparesis, spastic
phosphorylase b kinase deficiency
polyglucosan body
polyglucosan body disease
polymyositis
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proteinuria
quinidine
rash
recurrent
renal failure
review article
rhabdomyolysis
sensory loss
serum glutamic oxaloacetic transaminase
serum glutamic pyruvic transaminase
short stature
skin, lesions in neurologic disorders
spasticity
speech disorder, childhood
speech, delayed development of
spinal muscular atrophy
spinal muscular atrophy, adult onset
standing difficulty
statin therapy
steroid
systemic illness
Tay-Sachs disease
toxoplasma gondii
toxoplasmosis, muscle
treatment of neurologic disorder
tripping
type 2 muscle fiber
urinary incontinence
urine, dark
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
wheelchair
white matter disease
Showing articles 950 to 1000 of 1214 << Previous Next >>

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Lyme Disease:Of Ticks and Titers
J Pediatr 114:328-333, Eichenfield,A.H.&Athreya,B.H., 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.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

Pergolide and Selegiline for Parkinson's Disease
The Medical Letter, 31:81-841989., , 1989

Long-Term Efficacy and Safety of Deprenyl (Selegiline) in Advanced Parkinson's Disease
Neurol 39:1109-1111, Golbe,L.I.,et al, 1989

Neuroaxonal Dystrophy Due to Lysosomal a-N-Acetylgalactosaminidase Deficiency
NEJM 320:1735-1740, Schindler,D.,et al, 1989

Clinicopath Conf
Lyme Disease, Case Record 51-1988, NEJM 319:1654-1662988., , 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Reflex Sympathetic Dystrophy in Children:Treatment with Transcutaneous Electric Nerve Stimulation
Pediatrics 82:728-732, Kesler,R.W.,et al, 1988

Reflex Sympathetic Dystrophy Syndrome in Children and Adolescents, Reports of 18 Cases and Review
Am J Dis Child 142:1325-1330, Silber,T.J.&Majd,M., 1988

Magnetic Resonance Imaging in Amyotrophic Lateral Sclerosis
Ann Neurol 23:418-420, Goodin,D.S.,et al, 1988

A Double-Blind Study of the Effectiveness of Cyclosporine in Amyotrophic Lateral Sclerosis
Arch Neurol 45:381-386, Appel,S.H.,et al, 1988

Motoneuron Disease and Past Poliomyelitis in England and Wales
Lancet 1:1319-1322, Martyn,C.N.,et al, 1988

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

Amyotrophic Lateral Sclerosis, Recent Advances in Pathogenesis & Therapeutic Trials
Arch Neurol 45:189-202, Mitsumoto,H.,et al, 1988

The Natural History of Motoneuron Loss in Amyotrophic Lateral Sclerosis
Neurol 38:409-413, Munsat,T.L.,et al, 1988

Use of Composite Scores (Megascores) to Measure Deficit in Amyotrophic Lateral Sclerosis
Neurol 38:405-408, Andres,P.L.,et al, 1988

Amaurotic Family Idiocy
Am J Dis Child 142:53-56, Abt,I.A., 1988

Reduced Felodipine Bioavailability in Pts Taking Anticonvulsants
Lancet 2:480-482, Capewell,S.,et al, 1988

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

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

Inborn Errors of Metabolism in Children Referred with Reye's Syndrome, A Changing Pattern
JAMA 260:3167-3170, 3178-31801988., Rowe,P.C.,et al, 1988

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

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

Hypoparathyroidism
Cecil Textbook of Medicine 18th Ed, W B Saunders Co, Phila, p149688., Arnaud,C.D., 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

Motor Neuron Disease & Paraproteinemia
Neurol 37:335-337, Rudnicki,S.,et al, 1987

Reflex Sympathetic Dystrophy, A Review
Arch Neurol 44:555-561, Schwartzman,R.J.&McLellan,T.L., 1987

Thermography in Childhood Reflex Sympathetic Dystrophy
J Pediatr 111:551-555, Lightman,H.I.,et al, 1987

Neurological Clues from Environmental Neurotoxins
BMJ 295:346-347, Martyn,C.N., 1987

Ocular Complications of Tangier Disease
Am J Med 83:991-994, Pressley,T.A.,et al, 1987

Current Status of Thyrotropin-Releasing Hormone Therapy in Amyotrophic Lateral Sclerosis
Comm. on Health Care Issues, Amer Neuro Assoc, Ann Neurol 22:541-54387., , 1987

A Rating Scale for Amyotrophic Lateral Sclerosis:Description & Preliminary Experience
Ann Neurol 22:328-333, Appel,V.,et al, 1987

Motor Neuron Disease in the US, 1971 & 1973-1978:Patterns of Mortality & Associated Conditions at Time of Death
Neurol 37:1339-1343, Leone,M.,et al, 1987

Clinincopath Conf
Progressive Muscular Atrophy & Diabetic Neuromuscular Disease, Case 21-1987, NEJM 316:1326-13357., , 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Lyme Disease, A Neuro-Ophthalmologic View
J Clin Neuro-ophthalmol 7:185-190, MacDonald,A.B., 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Temporal Arteritis After Normalization of Erythrocyte Sedimentation Rate in Polymyalgia Rheumatica
Arch Int Med 146:2283-2284, Papadakis,M.A.&Schwartz,N.D., 1986

Optic-Nerve Degeneration in Alzheimer's Disease
NEJM 315:485-487, Hinton,D.R.,et al, 1986



Showing articles 950 to 1000 of 1214 << Previous Next >>