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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
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muscular dystrophy, Duchenne, neonatal screening
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myelomalacia
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myocarditis
myoglobinuria
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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 1200 to 1250 of 1300 << Previous Next >>

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Weakness in Malignancy:Evidence for a Remote Effect of Tumor on Distal Axons
Ann Neurol 4:268-274, Barron,S.A.,et al, 1978

Human Pneumatic Tourniquet Paralysis
Neurol 28:787-793, Bolton,C.F.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Effect of Valproic Acid on Hepatic Function
Neurol 28:961-964, Willmore,L.J.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Neurological Involvement in the Epidermal Naevus Syndrome
JNNP 41:466, McAuley,D.L.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Clinical Pathological Conference
Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978

Possible Biochemical Basis of Memory Disorder in Alzheimer Disease
Ann Neurol 3:471, Smith,C.M.,et al, 1978

Creatine Kinase BB Isoenzyme Levels by Radioimmunoassay in Patients with Neurolological Disease
Ann Neurol 3:52, Bell,R.D.,et al, 1978

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Sarcoidosis & Its Ophthalmic Manifestations
Am J Ophthmol 86:648-655, Obenauf,C.D.,et al, 1978

Multiorgan Scans for Staging Lung Cancer
J Thorac Cardiovasc Surg 73:653-657, Ramsdell,J.W.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Bone Scanning & Diagnosis of Reflex Sympathetic Dystrophy Secondary to Herniated Lumbar Disks
Neurol 27:791, Carlson,D.H.,et al, 1977

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

Neuropathology of Sanfilippo Syndrome
Ann Neurol 2:161, Ghatak,N.R.,et al, 1977

Viruslike Particles in Amytrophic Lateral Sclerosis:Electron Microscopical Study of a Case
Ann Neurol 1:290, Pena,C.E., 1977

Chronic Neurogenic Quadriceps Amyotrophy
Ann Neurol 2:528, Furukawa,T.,et al, 1977

Plasma Anticonvulsant Concentrations During Pregnancy
Neurol 27:128, Lander,C.M.,et al, 1977

Abnormality of a Thiamine-Requiring Enzyme in Patients with Wernicke-Korsakoff Syndrome
NEJM 297:1367, Blass,J.P.,et al, 1977

Electrocardiographic Changes & Myocardial Damage in Patients with Acute Cerebrovascular Accidents
Stroke 8:448, Dimant,J.,et al, 1977

Lower Motor Neuron Disease with Spinocerebellar Degeneration
Ann Neurol 2:524, Page,R.W.,et al, 1977

Brain-Type Creatine Kinase Isoenzyme
Arch Neurol 34:142, Kaste,M.,et al, 1977

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

Cyclic AMP in CSF of Patients with Neurologic Disease
NEJM 296:691, Vapaatalo,H.,et al, 1977

Purine Phosphoribosyltransferase in Gilles de la Tourette Syndrome
NEJM 296:210, VanWoert,M.H.,et al, 1977

Drug Therapy of Parkinsonism
NEJM 295:814, Bianchine,J.R., 1976

Antibody Titers to Coxsackieviruses in Amyotrophic Lateral Sclerosis
NEJM 295:107, Cremer,N.E.,et al, 1976

Postradiation Motor Neuron Syndrome
Arch Neurol 33:786, Sadowsky,C.H.,et al, 1976

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Possible Pathophysiology of Neurologic Abnormalities assoc. with Nonketotic hyperglycinemia
NEJM 294:1295, Ramson,B.R., 1976

Phenytoin & Methadone Tolerance
NEJM 294:227, Finelli,P.F., 1976

Interaction of Quinidine with Anticonvulsant Drugs
NEJM 294:699, Data,J.L.,et al, 1976

Rifampin Induced Methadone Withdrawal
NEJM 294:1104, Kreek,M.J.,et al, 1976

Microsomal Enzume Induction by Methadone & its Implications on Toler. to Methad. Tox
Nature 253:200, Masten,L.W.,et al, 1975

Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in a Diabetic
Arch Neurol 32:564, Finelli,P.F., 1975

Brachial Plexus Injuries
NEJM 291:1059, 1974 & 292, 4285., Leffert,R., 1975

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975



Showing articles 1200 to 1250 of 1300 << Previous Next >>