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Differential
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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 1300 << Previous Next >>

Late Onset Globoid Cell Leukodystrophy
JNNP 54:1011-1012, Grewal,R.P.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

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

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

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

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

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

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,et al, 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

Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
NEJM 322:1652-1669, Arn,P.H.,et al, 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

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Extraneural Manifestations of Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Am J Med 89:531-534, Romanick-Schmiedl,S.,et al, 1990

New Uses and Old for Carbamazepine
Patient Care 24:48-81, Browne,T.R.,et al, 1990

Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
JNNP 53:76-78, Fiorelli,M.,et al, 1990

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

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

Clinicopath Conf
Sarcoidosis of CNS and Mediastinal Lymph Nodes, Case Record 6-1990, NEJM 322:388-397990., , 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

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

The Widening Spectrum of Infectious Neurological Disease
JNNP 53:629-632, Kennedy,P.G., 1990

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

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,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

Cerebrospinal Fluid Lactate Dehydrogenase Levels in Early Stroke and Transient Ischemic Attacks
Stroke 21:854-857, Lampl,Y.,et al, 1990

Clinicopath Conf
Malignant Angioendotheliomatosis, Am J Med 88:522-5281990., , 1990

Dantrolene Sodium and Hepatic Injury
Neurol 40:1427-1432, Chan,C.H., 1990

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

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

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

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

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

Selegiline Use to Prevent Progression of Parkinson's Disease
Arch Neurol 46:1275-1279, Elizan,T.S.,et al, 1989

Abnormal Blood Clotting after Head Injury
Editorial, Lancet 2:957-9581989., , 1989

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

Human Ehrlichiosis Associated with Cerebrospinal Fluid Pleocytosis:A Case Presentation
Am J Med 87:677-678, Dimmitt,D.C.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989



Showing articles 950 to 1000 of 1300 << Previous Next >>