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acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
adverse drug reaction
alpha glucosidase
alpha-synuclein
anesthesia, general
anterior horn cell disease
aspartate aminotransferase
biologic markers
bionic reconstruction
brachial plexus injury
bradykinesia
calf hypertrophy
cardiomyopathy
children
chromosomal abnormality
complications
congestive heart failure
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
developmental retardation
disability, neurological
dystroglycanopathies
efficacy
Emery-Dreifuss muscular dystrophy
enzyme treatment
enzyme, defect
epidemiology of neurology
gene
gene mutation
gene therapy
genetic neurologic disorders
glycogen storage disease
Gowers maneuver
Guillain Barre syndrome
Guillain Barre syndrome, passive transfer of
hepatomegaly
history of neurology
hypotonia
immunology and the nervous system
L-dopa
Lewy body
life expectancy
lysosomal storage disease
lysosomes, abnoral
molecular genetics
mortality
motor neuron disease
motor system
MRI, abnormal
muscle biopsy
muscle transfer
muscle wasting, diffuse
muscle weakness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myopathy
myopathy, metabolic
myopathy, quadriceps
nerve transfer
neuroleptic, atypical
neurologic disease, diagnoses of
Parkinson disease
Parkinson disease, etiology of
Parkinson disease, nonmotor problems of
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Pompe's disease of glycogen storage
Pompe's disease, infantile
preclinical
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
quality of life
respirator
respiratory failure
respiratory tract infection
review article
rigidity
rippling muscle disease
safety
scoliosis
sinemet
SMN1 gene
spinal muscular atrophy
spinal muscular atrophy, classification
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
storage disease of CNS
survival motor neuron gene
synucleinopathy
systemic illness
toe walking
tongue, enlarged
treatment of neurologic disorder
tremor
weakness
weakness, progressive
weakness, proximal
web sites
Werdnig-Hoffman disease
Showing articles 2700 to 2750 of 3223 << Previous Next >>

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Ataxic Hemiparesis with Trigeminal Weakness
Neurol 31:635-636, Sakai,T.,et al, 1981

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

Myoclonic Seizures Following Chlorambucil Overdose
Jr. , Ann Neurol 9:191-194981., Byrne,T.N., 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Cimetidine Toxic Reactions Masquerading as Delirium Tremens
JAMA 245:1058-1059, Weddington,W.W.,et al, 1981

Tick Paralysis With Persistent Weakness & Electromyographic Abnormalities
Arch Neurol 38:59-61, Donat,J.R., 1981

Arthrogryposis Multiplex Congenita
Editorial, BMJ 283:2-31981., , 1981

Raised Plasma Renin Activity in the Hypertension of the Guillain-Barre Syndrome
BMJ 282:1272-1273, Laufer,J.,et al, 1981

Successful Treat. of Echovirus Meningoenceph & Myo Fasciitis With Immune Glob Therapy In X-Linked Agammaglob
NEJM 304:1278-1281, Mease,P.J.,et al, 1981

Neurologic Disease Associated with Mycoplasma Pneumoniae Pneumonitis
Ann Int Med 94:15-20, Bayer,A.S.,et al, 1981

Atlanto-Axial Instability in Children with Down Syndrome
Pediat Radiol 10:129-132, Pueschel,S.M.,et al, 1981

Neurological Aspects of Thyroid Dysfunction
Mayo Clin Proc 56:504-512, Swanson,J.W.,et al, 1981

Congenital Hemihypertrophy:Oncogenic Potential of the Hypertrophic Side
Ann Neurol 10:199-201, Furukawa,T.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Cephaloridine Encephalopathy
BMJ 283:409-410, Taylor,R.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Biotin Deficiency:An Unusual Complication Of Parenteral Alimentation
NEJM 304:820-823, Mock,D.M.,et al, 1981

Post-encephalitic Parkinsonism:Current Experience
JNNP 44:670-676, Rail,D.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Plasmapheresis in the Treatment of Four Cases of Guillain-Barre Syndrome (acute form)
Ital. J Neurol Sci 4:331-3361981., Zerbi,D.,et al, 1981

Pattern Reversal Visual Evoked Potentials
Arch Neurol 38:739-741, Bird,T.D.,et al, 1981

Acute Rhabdomyolysis Associated With An Echovirus 9 Infection
Arch Int Med 140:1671-1672, Josselson,J.,et al, 1980

Myelopathy in Mucopolysacchariodsis Type II (Hunter Syndrome)
Ann Neurol 7:382-385, Ballenger,C.E.,et al, 1980

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Brachial Plexus Neuropathy, An Electrophysiologic Evaluation
Arch Neurol 37:160-164, Flaggman,P.D.,et al, 1980

Arm-diaphragm Synkinesis:Electrodiagnostic Studies of Aberrant Regeneration of Phrenic Motor Neurons
Neurol 30:339-344, Swift,T.R.,et al, 1980

Penicillamine-associated Myasthenia Gravis
Neurol 30:1246-1250, Albers,J.W.,et al, 1980

Proximal Muscle Weakness in Uremia
Arch Neurol 37:555-558, Lazaro,R.P.,et al, 1980

Hypokalemic Periodic Paralysis in Chronic Toluene Exposure
Arch Neurol 37:673, Bennett,R.H.,et al, 1980

Clin. Path. Conference
Type B Botulism, Unclassified Form, Case Record 48-1980, NEJM 303:1347-135580., , 1980

Dysthyroid & Myasthenic Myopathy of the Medial Rectus:A Clinical Pathologic Report
Neurol 30:939-944, Spoor,T.C.,et al, 1980

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Clonazepam Treatment of Insomnia Due to Sleep Myoclonus
Arch Neurol 37:119-120, Oshtory,M.A.,et al, 1980

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Neurologic Prognosis after Cardiopulmonary Arrest:III. Seizure Activity
Neurol 30:1292-1297, Snyder,B.D.,et al, 1980

Mitral Valve Prolapse & Ophthalmoplegia:A Progressive, Cardioneurologic Syndrome
Ann Int Med 92:735-741, Darsee,J.R.,et al, 1980

Lobar Cerebral Hemorrhages:Acute Clinical Syndromes in 26 Cases
Ann Neurol 8:141-147, Ropper,A.H.,et al, 1980

Phencyclidine Abuse Mimicking Head Injury
JAMA 243:2323-2324, Corales,R.L.,et al, 1980

A pedigree of Amyotrophic Chorea With Acantho-cytosis
Arch Neurol 37:514-517, Kito,S.,et al, 1980

Diagnosis & Treatment, Physiologic & Pathologic Tremors
Ann Int Med 93:460-465, Jankovic,J.,et al, 1980

Lafora Disease:Diagnosis by Liver Biopsy
Ann Neurol 8:409-415, Nishimura,R.N.,et al, 1980

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

Masticatory Spasm in Facial Hemiatrophy
Ann Neurol 7:585-587, Kaufman,M.D., 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Pathogenesis of Papilloedema & Raised Intra-cranial Pressure in Guillain-Barre Syndrome
BMJ 281:1393-1394, Reid,A.C.,et al, 1980

Guillain-Barre Syndrome in Recipients of A/New Jersey Influenza Vaccine
JAMA 243:2490-2494, Marks,J.S.,et al, 1980



Showing articles 2700 to 2750 of 3223 << Previous Next >>