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Differential
(Click to cross reference)
alcohol intolerance
alternating rapid movement
alternating rapid movement, impaired
anti Yo antibody
areflexia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxic gait
atypical
autoantibodies
Babinski sign
basal ganglia, lesion of
bedridden
brainstem, atrophy
CAG repeats
carcinoma
carcinoma of breast
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
cerebrospinal fluid, oligoclonal IgG in
choking
Clinical Pathologic Conference(C.P.C.)
clonus
cognition, slowed
cough
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
dementia
dementia, familial
diarrhea
difficulty climbing stairs
diplopia
dissociated sensory loss
dizziness
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
eye movement, disorders of
falling
familial
fatigue
fibrillations
finger nose finger test
gait disorder
gene mutation
genetic neurologic disorders
handwriting
head nodding
heel-knee-shin test
hot cross bun sign
hyperreflexia
hyporeflexia
imbalance
incoordination
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
memory, impairment of
midbrain, atrophy
mortality
MRI, abnormal
MRI, diffusion weighted
MRI, punctate pattern
myoclonus
nausea and vomiting
nerve conduction studies
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
optic atrophy
paraneoplastic cerebellar degeneration
pleocytosis of cerebrospinal fluid
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
positional head-hanging test
prognosis
progressive neurologic disorder
proprioception
pursuit eye movements, abnormal
reading disorder, acquired
real-time quaking-induced conversion
remote effect of cancer on the nervous system
Romberg's sign
saccadic eye movements, abnormal
spasticity
speech disorder
speech disorder, non aphasic
spinocerebellar ataxia
spinocerebellar ataxia type 7
startle myoclonus
tandem gait, ataxic
tauopathy
tremor
trinucleotide repeats
upgaze, paralysis of
vertigo
vestibulopathy
vibratory sensation
vibratory sensation, abnormal
visual acuity, decreased
voice, abnormality of
walking frame
walking, difficulty with
wheelchair
wide based gait
workup
Showing articles 50 to 60 of 60 << Previous

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Hand Contractures in Parkinson's Disease
JNNP 51:1221-1223, Kyriakides,T.&Hewer,R.L., 1988

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

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

Rigid Spine Syndrome:A Type I Fiber Myopathy
Arch Neurol 34:119, Seay,A.R.,et al, 1977

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968



Showing articles 50 to 60 of 60 << Previous