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acid maltase deficiency
acid maltase deficiency, adult
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
alpha glucosidase
alpha-synuclein
Alzheimer's disease
Alzheimer's disease, treatment of
anesthesia, general
anterior horn cell disease
arthritis
aspartate aminotransferase
asymptomatic
atidarsagene autotemcel
biologic markers
bone marrow transplantation
bradykinesia
calf hypertrophy
cardiomyopathy
carotid artery disease
cataracts
central nervous system, infection of
cerebrovascular accident
cerebrovascular disease
ceruloplasmin, serum
chelation therapy
children
choreoathetosis
chromosomal abnormality
cirrhosis
clinical trials
coenzyme Q10 deficiency
complications
congestive heart failure
copper
copper metabolism, abnormal
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
degenerative diseases of CNS
dementia, childhood
demyelinating disease
developmental retardation
diet
differential diagnosis
dysarthria
dyskinesia
dysphagia
dystonia
dystroglycanopathies
dystrophin
efficacy
Emery-Dreifuss muscular dystrophy
enzyme treatment
enzyme, defect
epidemiology of neurology
ethambutol
ethics in neurology
fatty acid, elevated plasma content
Gaucher's disease
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glioblastoma multiforme(astrocytoma Gr.III)
glutamic acid decarboxylase
glycogen storage disease
Gowers maneuver
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
history of neurology
Hurler's syndrome
hypogonadism
hypotonia
in situ hybridization
inborn errors of metabolism, screening
Kayser-Fleischer ring
Kearns-Sayre syndrome
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
Lesch-Nyhan syndrome
leukemia
leukocyte enzyme abnormality
leukodystrophy
Lewy body
life expectancy
lipid storage disorder of CNS
liver disease
liver transplantation
Lorenzo's oil
lysosomal storage disease
lysosomes, abnoral
MELAS syndrome
MERRF syndrome
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
motor system
MRI
MRI, abnormal
mucopolysaccharidoses
muscle biopsy
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
myelodysplasia
myoblast transfer
myopathy, mitochondrial
myopathy, quadriceps
neonatal screening, genetic neurologic disorders
neoplasm, primary intracerebral
neoplasm, primary of CNS
neoplasm, primary of CNS-recurrent
neoplasm, primary of CNS-treatment of
neuroleptic, atypical
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuropathy, ataxia, retinitis pigmentosa
ophthalmoplegia, progressive external
pancreatitis
paraparesis, spastic
Parkinson disease
Parkinson disease, etiology of
Parkinson disease, nonmotor problems of
Parkinson disease, on-off phenomena in
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
peroxisomal disease
polymerase chain reaction
Pompe's disease of glycogen storage
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
ProSavin
psychiatric problems in neurologic disorders
quality of life
respirator
respiratory failure
review article
rigidity
rippling muscle disease
safety
scoliosis
screening
seizure
sham surgery
sinemet
skin, darkening of
SMN1 gene
spinal muscular atrophy
spinal muscular atrophy, classification
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
subarachnoid hemorrhage
subthalamic nucleus
survival motor neuron gene
synucleinopathy
systemic illness
testicular atrophy
toe walking
tongue, enlarged
treatment of neurologic disorder
tremor
viral infection
viral infection, CNS
weakness
weakness, progressive
weakness, proximal
web sites
Werdnig-Hoffman disease
white matter disease
Showing articles 1600 to 1650 of 1660 << Previous Next >>

Juvenile Diabetes Mellitus & Optic Atrophy
Arch Neurol 34:759, Lessell,S.,et al, 1977

Intracranial Aneurysms:Characteristics of Aneurysms in Siblings
NEJM 297:115, 1977. (Letter), Andrews,R.J., 1977

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

Familial Spasmodic Torticollis
Neurol 27:11, Gilbert,G.J., 1977

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Familial Nonprogressive Involuntary Movements of Childhood
Ann Neurol 1:602 1977., Damasio,H.,et al, 1977

Gilles de la Tourette's syndrome:Clinical, Genetic, Psychologic, & Biochemical Aspects in 21 Selected Families
Neurol 27:115, Eldridge,R.,et al, 1977

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

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Myasthenia Gravis, Study of Humoral Immune Mechanisms by Passive Transfer to Mice
NEJM 296:125, Toyka,K.V.,et al, 1977

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

Duane Syndrome & Congential Upper-Limb Anomalies:A Familial Occurrence
Arch Neurol 34:174, Okihiro,M.M.,et al, 1977

Juvenile Parkinsonism Treated with Levodopa
Arch Neurol 34:244, Sachdev,K.K.,et al, 1977

Familial Essential Myoclonus
Brain 93:131-138, Korten,J.J.,et al, 1977

Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976

Low Activities of the Pyruvate & Oxoglutarate Dehydrogenase Complexes in Five Patients with Friedreich's Ataxia
NEJM 295:62, Blass,J.P.,et al, 1976

Cause of Weakness in Myasthenia Gravis
NEJM 294:722, Grob,D., 1976

Myasthenic Abduction Nystagmus in a Patient with Hyperthyroidism
Neurol 26:589, Finelli,P.F.&Hoyt,W., 1976

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Specific Laboratory Test for Diagnosis of MS
BMJ 1:412, Field,E.J.,et al, 1974

Diagnosis of Fabry's Disease by Tear-Galactosidase A-Correspondence NEJM 290:57
1974., , 1974

Unrecognized Adult Phenylketonuria
NEJM 289:395, 1973, 289:1040, 1973, 290:1084., Perry,T.,et al, 1974

Ataxia-Telangiectasia-Clonal Growth of Translocation Lymphocytes
NEJM 289:286, Hecht,F.,et al, 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Niemann-Pick Disease
Correspondence NEJM 289:590, Dacremont,G.,et al, 1973

Infantile Metachromatic Leukodystrophy
NEJM 288:1365, 14051973., Leroy,J.,et al, 1973

Tay-Sachs Disease-The Use of Tears for the Detection of Heterozygotes
NEJM 289:1072, Carmody,P.,et al, 1973

Teratogenic Effect of Anticonvulsnats
Lancet 198, 1973 Jan., , 1973

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973

Treating Problem Children with Stimulant Drugs
NEJM 289:407, Sroufe,L.A.,et al, 1973

Hereditary Quadriceps Myopathy
JNNP 36:1041, Espir,M.L.E.,et al, 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Familiar Basilar Impression
Neurol 22:554, Paradis,R.,et al, 1972

Maternal Epilepsy & Abnormalities of the Fetus & Newborn
Lancet 839, Oct1972., Speidel,B.,et al, 1972

Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
Neurol 22:49, Nakano,K.K.,et al, 1972

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971

Myasthenia Gravis & Hyperthyroidism Occurring in Two Sisters
Neurol 21:377, Namba,T.,et al, 1971

Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971

Polyneroupathies of Undetermined Cause
Acta Neurol Scand (Supp) :5970., Prineas,J., 1970

Prenatal Genetic Diagnosis
NEJM 283:1370, Milunsky,A.,et al, 1970

Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970



Showing articles 1600 to 1650 of 1660 << Previous Next >>