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acetylcholine
advances in neurology
Alzheimer's disease
anticholinesterase
areflexia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
auditory evoked brainstem potentials
autonomic dysfunction
Babinski sign
baclofen
blindness
bradykinesia
brainstem, atrophy
CAG repeats
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
chorea
chromosome 14
chromosome 6
Clinical Pathologic Conference(C.P.C.)
controversies in neurology
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
depression
down-beat nystagmus, primary position of gaze
dysarthria
enzyme, defect
evoked potentials
excitotoxin
familial
fragile-X syndrome
Friedreich's ataxia
gaze palsy, supranuclear
genetic neurologic disorders
genetic screening
genetic testing
glutamate dehydrogenase deficiency
glutamic acid
HLA
hot cross bun sign
huntingtin
Huntington's chorea
hydroxytryptophan L-5(L-5 HTP)
hypoxia
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
L-dopa
life expectancy
macular degeneration
molecular genetics
movement disorder, extrapyramidal
MRI
MRI, abnormal
multiple system atrophy
myelomalacia
myoclonic jerks
myotonia dystrophica
neurologic disease
neurologic disease, diagnoses of
neuropathology
neurotoxin
neurotransmitter
nystagmus
ocular motility, disorders of
ophthalmoplegia
optic atrophy
orthostatic hypotension
palatal myoclonus
Parkinson disease
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
physostigmine
pons, atrophy
pontocerebellar atrophy
prognosis
pseudobulbar palsy
psychological testing
psychological testing, neurologic problems
Purkinje cell
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
retinal degeneration
retinitis pigmentosa
review article
seizure
Shy-Drager syndrome
sleep apnea
sleep pathology and physiology
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinopontine atrophy, dominant
striatonigral degeneration
trazodone
treatment of neurologic disorder
trinucleotide repeats
X-linked bulbospinal neuronopathy
Showing articles 2100 to 2150 of 2376 << Previous Next >>

Computed Tomography in Aneurysmal Subarachnoid Hemorrhage
Neurol 29:802-808, Weisberg,L.A., 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Cortical Atrophy, Ventricular Enlargement & Intellectual Impairment in the Aged
Neurol 29:1138-1143, Earnest,M.P.,et al, 1979

Cerebral Atrophy, EEG Slowing, Age, Education, & Cognitive Functioning in Suspected Dementia
Neurol 29:1273-1279, Kaszniak,A.W.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Visual Evoked Potentials in Infants with Hydrocephalus
Neurol 29:1541-1544, Ehle,A.,et al, 1979

Dementia Paralytica:Deterioration From Communicating Hydrocephalus
JNNP 42:501-508, Gimenez-Roldan,S.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Deficiency of Arylsulfatase B in 2 Brothers Aged 40 & 38 Years (Maroteaux-Lamy Syndrome, Type B)
Ann Neurol 6:315-325, Pilz,H.,et al, 1979

Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
Ann Neurol 6:302-314, Dyck,P.J.,et al, 1979

Facial Recognition in Patients With Focal Brain Lesions
Arch Neurol 36:837-839, Hamsher,K.deS.,et al, 1979

Familial Fatal Parkinsonism with Alveolar Hypoventilation & Mental Depression
Ann Neurol 6:523-531, Purdy,A.,et al, 1979

Left-to-right Transfer of Language Dominance:A Case Study
Neurol 29:1547-1550, Cummings,J.L.,et al, 1979

Clinical Pathological Conference, Peripheral Neuropathy in Leprosy
NEJM 300:546-553, Dawson,D., 1979

Clinical Pathological Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 18-1979, NEJM 300:1037-104579., , 1979

Acute Hydrocephalus in Cerebellar Infarct & Hemorrhage
Neurol 29:409-413, Greenberg,J.,et al, 1979

Regional Cerebral Blood Flow Comparison of Right & Left Hand Movement
Jr. , et al, Neurol 29:21-2879., Halsey,H.H., 1979

Cranial Computed Tomography in the Diagnosis of Systemic Lupus Erythematosus
Ann Neurol 5:158-165, Gonzalez-Scarano,F.,et al, 1979

Seasonal Variation in the Birth of Left-Handed Schoolgirls
Arch Neurol 36:115-116, Leviton,A.,et al, 1979

Computed Tomography in a Verified Case of Tuberculous Meningitis
Neurol 29:384-386, Arimitsu,T.,et al, 1979

Optic Neuropathy & Ophthalmoplegia in Herpes Zoster Oticus
Neurol 29:726-729, Carroll,W.M.,et al, 1979

Acute Anterior Myelitis Complicating West Nile Fever
Arch Neurol 36:172-173, Gadoth,N.,et al, 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Arachnoid Cyst of the Fourth Ventricle & "Arrested"Hydrocephalus
Surg Neurol 12:467-471, DiRocco,C.,et al, 1979

Interhemispheric Subdural Hematoma
Surg Neurol 10:119-122, Glista,G.G.,et al, 1978

CT Scan Appearances in Leigh's Disease (Subacute Necrotizing Encephalomyelopathy)
Neuroradiology 16:48-50, Hall,K.,et al, 1978

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

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,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

Central Nervous System Lesions in Childhood Leukemia
Neurol 28:678, Crosley,C.J.,et al, 1978

Visual Dysfunction in Optic Tract Lesions
et al. , Ann Neurol 3:187978., Bender,M.B., 1978

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

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

Hydrocephalus Caused by Increased Intracranial Venous Pressure:A Clinicopathological Study
Ann Neurol 3:445, Rosman,N.P.,et al, 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

The Syndrome of Facial Nevi, Anomalous Cerebral Venous Return, & Hydrocephalus
Ann Neurol 3:316, Orr,L.S.,et al, 1978

Posterior Fossa Subdural Hematomas in Neonates
Arch Neurol 35:108, Blank,N.K.,et al, 1978

The EEG Manifestations of Chronic Ethanol Abuse:Relation to Cerebral Cortical Atrophy
Ann Neurol 3:299, Newman,S.E., 1978

Alexia & Left Homonymous Hemianopia in a Non-right-hander
Ann Neurol 3:549, Erkulvrawatr,S., 1978

Identification of Speech Lateralization by Intracarotid Injection of Methohexital
Ann Neurol 4:86, Willmore,L.J.,et al, 1978

Speech Arrest in a Dextral with a Right MesialFfrontal Astrocytoma
Arch Neurol 35:252, Caplan,L.R.,et al, 1978

Intracranial Arteriovenous Malformations in Childhood
Ann Neurol 3:338, Kelly,J.J.,et al, 1978

Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
Ann Neurol 3:253, Bird,T.D.,et al, 1978

Developmental Dyslexia
Arch Neurol 35:90, Hier,D.B.,et al, 1978

Medical Implications of Computed Tomography ("Cat scanning")
NEJM 298:255, Abrams,H.L.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978



Showing articles 2100 to 2150 of 2376 << Previous Next >>