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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 2350 to 2376 of 2376 << Previous

Optic Atrophy in Childhood
Pediatrics 34:670, 1964 (Nov) ., Schwartz,J.F.,et al, 1964

Neuro CPC of MGH
Congenital Toxoplasmosis Involving CNS, NEJM 269:369-3741963., , 1963

Cervical Myelopathy with Fasciculations in the Lower Extremities
J Neurosurg 20:948, King,R.B.,et al, 1963

Course & Prognosis in Amyotrophic Lateral Sclerosis
Arch Neurol 8:17, Mackay,R., 1963

Sarcoid of the Fundus
Arch Ophthalmol 65:161, Gould,H.,et al, 1961

Clinical Syndromes in Cerebral Arterial Occlusion
(Ed) , Fields, Wm. Pathogenesis & Treatment of CVD, Charles C. Thomas, Publisher, Fisher,C.M., 1961

The Brain in Uremia
Acta Psychiatr Scand 36 (Suppl 156) :1-128961., Olsen,S., 1961

Neuro CPC of MGH
Glioblastoma Multiforme, NEJM 262:413-4161960., , 1960

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

Motivational & Structural Factors in the Denial of Hemiplegia
Arch Neurol 3:306-318, Ullman,M.,et al, 1960

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Cysticercosis Cerebri
NEJM 256:479-486, White,J.C.,et al, 1957

Left Hemiplegia & Motor Impersistence
J Nerv Ment Dis 123:201, Fisher,C.M., 1956

Neurologic Signs & Symptoms as Early Manifestations of SLE
Neurol 5:84, Siekert,R.,et al, 1955

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Rheumatic Brain Disease
JAMA 134:450, Bruetsch,W.L., 1947

Causalgia of the Face, Two Cases Successfully Treated by Sympathectomy
BMJ 1:804-805, Bingham,J.A.W., 1947

Mirror Writing (Book)
Psyche Miniatures Med. Series1928., Critchley,M., 1928

Alcoholism
Clin Neurol Chap 22 p. 1084, A. B. Baker Text Book of Neurology., Victor,M., 1850

Neurology & Psychiatry Section-Year book of Pediatrics
Pediatr Abstract p. 406-449., , 1850

Failure of Vision in Childhood
Proc Royal Soc Medicine, pp 494-500., , 1850

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

An 81-Year-Old Man with Imbalance and Memory Impairment
, Golbe,L.I.,et al,

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,



Showing articles 2350 to 2376 of 2376 << Previous