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abdominal distention
acetazolamide
acid maltase deficiency
advances in neurology
adverse drug reaction
airway obstruction
algorithm
amniocentesis
anesthesia, general
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticonvulsants
antihistamines
arrhythmia, cardiac
ataxia
ataxia, paroxysmal
calcium antagonist
calcium channel dysfunction
calf hypertrophy
carbamazepine
cardiac transplantation
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, muscle
central core disease
chewing, impaired
children
chloride channel dysfunction
clubfoot as related to neurologic disease
complications
congenital myopathy
congestive heart failure
contractures, joint
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
differential diagnosis
dilantin
disability, neurological
distal muscle atrophy
distal muscle weakness
DNA probes
drug induced neurologic disorders
dystrophin
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electrocardiogram, LVH
electromyogram
electron microscopy
ELISA
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
erythrocyte
facial weakness, bilateral
falling
familial
familial hemiplegic migraine
floppy infant
Friedreich's ataxia
gait disorder
gait, waddling
gastric dilatation, acute
gastrointestinal motility
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genetic counselling
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genetic linkage
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Gowers maneuver
Guillain Barre syndrome
hand weakness
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high arched feet
histochemistry
hydrocephalus
hyperkalemic periodic paralysis
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hypokalemic periodic paralysis
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
inclusion body myositis
intellectual deficit
intestinal pseudoobstruction
kaliuresis
left ventricular dilatation
life expectancy
lordosis
lymphocyte capping, diminished
malignant hyperpyrexia
mental retardation
metabolic acidosis
mexiletine
micrognathia
migraine
molecular genetics
mortality
MRI
MRI, abnormal
MRI, muscle
muscle biopsy
muscle cramp
muscle hypertrophy
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muscle weakness
muscular dystrophy
muscular dystrophy, Becker
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muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
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muscular dystrophy, female occurrence of
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myoglobinuria
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myotonia congenita
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neurologic disease, diagnoses of
neurologic evaluation
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neuropathy, amyloid
newborn, evaluation of
nifedipine
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paresthesias
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potassium channel antibodies
potassium channel dysfunction
prenatal diagnosis by amniocentesis
procainamide
prognosis
pseudohypertrophy
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quadriceps atrophy
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review article
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spinocerebellar ataxia type 6
steroid therapy, CNS treatment and complications with
symptomatic
temporalis muscle wasting
term infant
tocainide
toe walking
treatment of neurologic disorder
trinucleotide repeats
tubular aggregates, muscle
weakness
weakness, progressive
web sites
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workup
Showing articles 600 to 650 of 788 << Previous Next >>

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Perineal Reflex Sympathetic Dystrophy Treated with Bilateral Lumbar Sympathectomy
Ann Int Med 113:633-634, Olson,W.L., 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
Neurol 40:1359-1363, Coppeto,J.R.&Lessel,S., 1990

Causalgia and Other Reflex Sympathetic Dystrophies
In the Management of Pain, Lea & Febiger, Phila, p. 220, Bonica,J.J., 1990

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

The Movement Disorder of Reflex Sympathetic Dystrophy
Neurol 40:57-61, Schwartzman,R.J.&Kerrigan,J., 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 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

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

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

Phenobarbital Rheumatism in Patients with Brain Tumor
Ann Neurol 25:92-94, Taylor,L.P.&Posner,J.B., 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

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

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

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

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

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

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

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

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

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



Showing articles 600 to 650 of 788 << Previous Next >>