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advances in neurology
adverse drug reaction
alcohol
alcohol, neurologic complications with
algorithm
aminoacidurias
amyloidosis
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anemia
anemia, hemolytic
anterocollis
anticholinergic drugs
aphonia
artane
arthrogryposis multiplex
athetosis
athetosis, causes of
attention deficit disorder with hyperactivity
Babinski sign
basal ganglia
basal ganglia, lesion, bilateral
benign essential tremor
bent spine syndrome
biopterin deficiency
blepharospasm
botulinum toxin
bradykinesia
Brueghel's syndrome
camptocormia
carbamazepine
CAT scan
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catecholamine
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cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
chorea, causes of
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 14
cirrhosis
cirrhosis, causes of childhood
Clinical Pathologic Conference(C.P.C.)
clonazepam
cogwheel rigidty
complications
conversion reaction
creatine phosphokinase(CPK)elevated
dementia
depression
dermatomyositis
developmental retardation
diurnal variation
dopa responsive dystonia
dopamine
drug induced neurologic disorders
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphonia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
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dystonia, painful
dystonia, post traumatic
dystonia, prevalence of
dystonia, symptomatic
dystonia, treatment of
DYT1 mutation
efficacy
electromyogram
encephalitis, brainstem
epidemiology of neurology
equinovarus
familial
gait disorder
gamma amino butyric acid
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genetic counselling
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, lesion of, bilateral
Guillain Barre syndrome
Hallervorden Spatz disease
handwriting
head nodding
head tilt
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatitis
hepatolenticular degeneration(Wilson's disease)
homovanillic acid
Huntington's chorea
hyperekplexia
hyperreflexia
iron, brain
Kayser-Fleischer ring
klippel feil syndrome
kyphosis
laminectomy
laminectomy, lumbar
laterocollis
L-dopa
leg spasms
leg spasms, painful
low back pain
migraine
migraine, children
misdiagnosis
molecular genetics
monoamines
mononeuropathy
motor neuron disease
movement disorder
movement disorder, drug induced
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movement disorder, treatment of
MRI, abnormal
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multiple sclerosis
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muscle diseases, characteristics of
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
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myasthenia gravis
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myotonia dystrophica
nerve conduction studies
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neurodegeneration with brain iron accumulation
neurologic complications of, surgery
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neurotransmitter
norepinephrine
obsessive-compulsive disorder
old age, neurology of
pain
pancytopenia
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paraspinal muscle
paraspinal muscle weakness
Parkinson disease
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Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
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patient information and support
penicillamine
phenylketonuria
poliomyelitis
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porphyria
postoperative neurologic complications
postural abnormality
prognosis
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psychiatric problems in neurologic disorders
psychosis
radiculopathy
reflex sympathetic dystrophy
retrocollis
reversible neurologic disorder
review article
rigidity
Riley-Day syndrome
salivation, excessive
sarcoidosis
schizophrenia
scoliosis
seizure
seizure, stimulus sensitive
sensory tricks
sinemet
slit lamp examination
spastic dysphonia
speech disorder
speech disorder, non aphasic
splenomegaly
startle reaction
stiff man syndrome
stimulation, deep brain
stooped posture
tardive dyskinesia
tardive dystonia
tetrabenazine
tic
toe walking
tonic foot response
torticollis
torticollis, benign paroxysmal
torticollis, familial
torticollis, infants and children
torticollis, post traumatic
trauma
treatment of neurologic disorder
tremor
tremor, jaw
tremor, leg
tremor, post traumatic
tremor, postural
tremor, treatment of
tremor, voice
uric acid, low
vasospasm, cerebral
walking, difficulty with
weakness, progressive
Werdnig-Hoffman disease
wheelchair
workup
writers cramp
Showing articles 1400 to 1450 of 1744 << Previous Next >>

Machado-Joseph-Azorean Disease
Arch Neurol 41:921-925, Fowler,H.L., 1984

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome
Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

Adrenoleukodystrophy:Clinical & Biochemical Manifestations in Carriers
Neurol 34:798-801, O'Neill,B.P.,et al, 1984

Parental Transmission in Huntington's Disease
Lancet 1:1100-1102, Went,L.N.,et al, 1984

Wilson's Disease
BMJ 288:1180-1181, Parkes,D., 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Metoprolol Compared with Propranolol in the Treatment of Essential Tremor
Arch Neurol 41:171-172, Koller,W.C.,et al, 1984

Autosomal Dominant Transmission of the"Photic Sneeze Reflex"
NEJM 310:599-600, Peroutka,S.J.,et al, 1984

Molecular Genetics, Recombinant DNA Techniques, & Genetic Neurological Disease
Ann Neurol 15:511-520, Rosenberg,R.N., 1984

Familial Occurrence of Idiopathic Normal-Pressure Hydrocephalus
Arch Neurol 41:335-337, Portenoy,R.K.,et al, 1984

Nemaline Myopathy Appearing in Adults as Cardio-myopathy
Arch Neurol 41:443-445, Meier,C.,et al, 1984

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

Leber's Congenital Amaurosis
Arch Neurol 41:204-206, Weinstein,J.M.,et al, 1984

The Cerebrohepatorenal (Zellweger) Syndrome
NEJM 310:1141-1146, Moser,A.E.,et al, 1984

Alcoholic Myelopathy without Substantial Liver Disease
Arch Neurol 41:999-1001, Sage,J.I.,et al, 1984

Familial Occurrences of Adult-Type Neuronal Ceroid Lipofuscinosis
Arch Neurol 41:1091-1094, Tobo,M.,et al, 1984

Adrenoleukodystrophy:Survey of 303 Cases:Biochemistry, Diagnosis, & Therapy
Ann Neurol 16:628-641, Moser,H.W.,et al, 1984

Abnormal Metabolism of y-Trace Alkaline Microprotein
NEJM 311:1547-1549, Grubb,A.,et al, 1984

Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
NEJM 311:1649-1652, Berginer,V.M.,et al, 1984

Familial Spastic Paraplegia, Mental Retardation, & Precocious Puberty
Arch Neurol 40:809-810, Raphaelson,M.I.,et al, 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Conjugal Amyotrophic Lateral Sclerosis
Ann Neurol 14:699, Paolino,E.,et al, 1983

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

Acute Infectious Torticollis
Neurol 33:1344-1346, Neng,T.,et al, 1983

High Dosage Anticholinergic Therapy in Dystonia
Neurol, 33:1255-12611983., Fahn,S., 1983

Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
Ann Neurol 14:670-678, Hudson,A.J.,et al, 1983

Idiopathic Hemochromatosis (IHC) :Dementia & Ataxia as Presenting Signs
Neurol 33:1479-1483, Royden,H.,et al, 1983

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
Neurol 33:237-240, Djupesland,G.,et al, 1983

Chronic Progressive External Ophthalmoplegia (CPEO) :Clinical, Morphologic, & Biochemical Studies
Neurol 33:452-461, Mitsumoto,H.,et al, 1983

Primary Position Vertical Nystagmus & Cerebellar Ataxia
Arch Neurol 40:310-314, Kattah,J.C.,et al, 1983

Parkinson's Disease in 65 Pairs of Twins & in a Set of Quadruplets
Neurol 33:815-824, Ward,C.D.,et al, 1983

Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
Arch Neurol 40:416-418, Bianco,G.,et al, 1983

Neurogenic Arthropathy & Recurring Fractures with Subclinical Inherited Neuropathy
Neurol 33:357-367, Dyck,P.J.,et al, 1983

Infantile Osteopetrosis & Neuronal Storage Disease
Neurol 33:437-441, Ambler,M.W.,et al, 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Dominant Chondrodysplasia Punctata with Neurologic Symptoms
Neurol 33:1095-1097, Curless,R.G., 1983

Familial Porencephaly
Arch Neurol 40:567-569, Berg,R.A.,et al, 1983

Evoked Response Studies in Patients with Adreno-leukodystrophy & Heterozygous Relatives
Arch Neurol 40:356-359, Garg,B.P.,et al, 1983

Torticollis in Three Children with Syringomyelia & Spinal Cord Tumor
Neurol 33:956-958, Kiwak,K.J.,et al, 1983

Acetazolamide-Responsive Episodic Ataxia Syndrome
Neurol 33:1212-1214, Zasorin,N.L.,et al, 1983

Treatment of Dystonia with Tetrahydrobiopterin
NEJM 308:157-158, LeWitt,P.A.,et al, 1983

A Family with Histologially Confirmed Alzheimer's Disease
Arch Neurol 40:203-208, Nee,L.E.,et al, 1983

Lipomembranous Polycystic Osteodysplasia (Brain, Bone, & Fat Disease)
Neurol 33:81-86, Bird,T.D.,et al, 1983

Hyperekplexia
Arch Neurol 40:246-248, Kurczysnki,T.W., 1983

Taste & Smell in Disease (First of Two Parts)
NEJM 308:1275-1279, Schiffman,S.S., 1983

The Malignant Hyperthermia Syndrome
NEJM 309:416-418, Nelson,T.E.,et al, 1983



Showing articles 1400 to 1450 of 1744 << Previous Next >>