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Differential
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acanthocytosis
accomodation, abnormal
acral sensory symptoms
alternating rapid movement
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
anal wink response
anorexia
antecedent illness
anti GQ1b IgG antibody
antiganglioside antibodies
antioxidant
areflexia
arrhythmia, cardiac
ascending paralysis
astrocytoma
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
athetosis
atypical
autoantibodies
axonal degeneration
Babinski sign
botulism
brain atrophy
Brown-Vialetto-Van Laere syndrome
bulbar palsy
bulbar palsy, acute
burning paresthesia
campylobacter infection
cardiomyopathy
CAT scan
CAT scan, abnormal
caudate nucleus, atrophy
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellum, disease of
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrospinal fluid, xanthochromia of
Charcot-Marie-Tooth
children
chorea
chorein
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Collier's sign
congestive heart failure
consanguinity
constipation
contractures, joint
corneal reflex, abnormal
corpus callosum, hypoplastic
corpus callosum, lesion of
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dementia
denervation of muscle
denervation potentials
developmental disability
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diarrhea
diplopia
dopa responsive dystonia
dysarthria
dysdiadochokinesia
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dystonia
dystonia, children
electromyogram
electromyogram, decremental response
encephalopathy
encephalopathy, progressive
enteritis
enzyme, defect
episodic neurologic deficits
exome sequencing
eye movement, disorders of
facial appearance, abnormal
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fever
Fisher's syndrome
flaccid paralysis
flu-like illness
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
F-wave response
gait disorder
galactorrhea
gaze palsy
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
glioma
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
gynecomastia
hammertoes
hand deformity
hearing loss
heel-knee-shin test
hoarseness
hydrocephalus
hyperreflexia
hypertonia
hypophosphatemia
hyporeflexia
hypotonia
imbalance
immunoelectrophoresis, serum
incoordination
intellectual deficit
L-dopa
leg weakness, bilateral
leg weakness, unilateral
lethargy
lid
lid abnormalities
lip, biting
liver disease
lymphadenopathy
malabsorption
meningismus
mental retardation
microcephaly
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
movement disorder
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, spinal cord
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
myelomalacia
nasal speech
nausea and vomiting
neoplasm, primary intracerebral
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic signs
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, sensory
neurotoxin
next-generation sequencing
numbness, ascending
numbness, extremity
nystagmus
nystagmus, gaze-evoked
nystagmus, vertical
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
overlap syndrome
pain, abdominal
palatal myoclonus
papilledema
paralysis
paralysis, acute
paralysis, acute areflexic
parenteral alimentation
paresthesias
Parkinson disease
Parkinsonism syndrome
perioral numbness
pes cavus
philtrum, tented
POLG1 gene
positional head-hanging test
postoperative neurologic complications
prevention of neurologic disorders
prion disease
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
prolactin, elevated
proprioception, abnormal
ptosis
ptosis, bilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
Purkinje cell
quadriparesis
quadriplegia
reading disorder, acquired
recurrent
renal tubular acidosis
ReNU syndrome
repetitive nerve stimulation
respiratory failure
respiratory tract infection
reversible neurologic disorder
review article
riboflavin transporter deficiency
Romberg's sign
saccadic eye movements, abnormal
scannig speech
scoliosis
seizure
sensory loss
sensory nerve action potentials
short stature
single photon emission computed tomography
slurred speech
spastic ataxia
spasticity
speech arrest
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, absence of
speech, loss of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spinopontine atrophy, dominant
spontaneous remission
stool culture
subdural hematoma
tandem gait, ataxic
tauopathy
telangiectases
temporal lobe, status
thalamus, lesion of
thalamus, lesion of-bilateral
tick bite
tick paralysis
tongue, biting
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, postural
trinucleotide repeats
tyrosine hydroxylase deficiency
upgaze, paralysis of
vestibulopathy
vibratory sensation, abnormal
vision, blurred
vital capacity
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin supplementation
vocalizations
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
white matter disease
whole genome sequencing
wide based gait
workup
wrist drop
X-linked bulbospinal neuronopathy
Showing articles 650 to 700 of 845 << Previous Next >>

Aphasia with a Left Frontal Interhemispheric Hematoma
Neurol 34:1261-1264, Tijssen,C.C.,et al, 1984

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Transient Neurologic Dysfunction Following Moderate-Dose Methotrexate for Undifferentiated Lymphoma
Cancer 54:2003-2005, Martino,R.L.,et al, 1984

Voice Changes after Thyroidectomy:Role of the External Laryngeal Nerve
BMJ 289:1412-1415, Kark,A.E.,et al, 1984

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

Nonconvulsive Status Epilepticus Following Metrizamide Myelography
Ann Neurol 16:252-254, Pritchard,P.B.,et al, 1984

Bilateral Adie's Tonic Pupil with Anhidrosis & Hyperthermia
Arch Neurol 41:342-343, Spector,R.H.,et al, 1984

Mutism Following Left Hemisphere Infarction
JNNP 47:1342-1344, David,A.S.,et al, 1984

Effectiveness of Speech Therapy for Aphasic Stroke Patients
Lancet l:1197-1200, Lincoln,N.B.,et al, 1984

Speech Arrest & Supplementary Motor Area Seizures
Neurol 34:110-111, Peled,R.,et al, 1984

Long-Lasting Neurological Sequelae After Lithium Intoxication
Acta Psychiatr Scand 70:594-602, Schou,M., 1984

Aphemia Clinical-Anatomic Correlations
Arch Neurol 40:720-727, Schiff,H.B.,et al, 1983

Mutism after Closed Head Injury
Arch Neurol 40:601-606, Levin,H.S.,et al, 1983

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

Unrecognized Chronic Lithium Neurotoxic Reactions
JAMA 250:2029-2030, Lewis,D.A., 1983

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

Motor Aphasia Unaccompanied by Faciobrachial Weakness
Neurol 33:519-521, Masdeu,J.C.,et al, 1983

Blepharospasm & Orofacial-Cervical Dystonia:Clinical & Pharmacological Findings in 100 Patients
Ann Neurol 13:402-411, Jankovic,J.,et al, 1983

Juvenile Progressive Bulbar Palsy
Arch Neurol 40:351-353, Albers,J.W.,et al, 1983

Dialysis Encephalopathy, Clinical, Electroencephalographic & Interventional Aspects
Medicine 62:129-141, O'Hare,J.A., 1983

Delayed Neurologic Sequelae in Carbon Monoxide Intoxication
Arch Neurol 40:433-435, Choi,I.I.S., 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Epilepsies of Infancy & Childhood
Ann Neurol 13:113-124, Gomez,M.R.,et al, 1983

Long-Term Prognosis in Two Forms of Childhood Epilepsy:Absence Seizures & Epilepsy with Rolandic EEG Foci
Ann Neurol 13:642-648, Loiseau,P.,et al, 1983

Absence Status Manifested by Compulsive Masturbation
Arch Neurol 40:523-524, Jacome,D.E.,et al, 1983

Complex Partial Status Epilepticus
Arch Neurol 40:90-92, Shalev,R.S.,et al, 1983

Long-Term Follow-up of Absence Seizures
Neurol 33:1590-1595, Sato,S.,et al, 1983

De Novo Minor Status Epilepticus of Late Onset Presenting as Stupor
BMJ 287:1673-1674, Spriggs,E.A., 1983

Partial Complex Status Epilepticus
Neurol 33:1545-1552, Ballenger,C.E.,et al, 1983

Valproate-Ethosuximide Combination Therapy for Refractory Absence Seizures
Arch Neurol 40:797-802, Rowan,A.J.,et al, 1983

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

Brainstem Encephalitis & The Syndrome Of Miller Fisher
Brain 105:481-495, Al-Din,A.N.,et al, 1982

"Tip-of-the-tongue"Phenomenon in Parkinson Disease
Neurol 32:567-570, Matison,R.,et al, 1982

The Child Who is Slow to Talk
BMJ 285:671-672, Robinson,R.J., 1982

Transient Areflexia & Quadriplegia Following Metrizamide Myelography
Ann Neurol 12:406-407, Peroutka,S.J.,et al, 1982

Aphasia With Nonhemorrhagic Lesions in the Basal Ganglia & Internal Capsule
Arch Neurol 39:15-20, Damasio,A.R.,et al, 1982

Valproic Acid Versus Ethosuximide in the Treatment of Absence Seizures
Neurol 32:157-163, Sato,S.,et al, 1982

Ross Syndrome & Skin Changes
Neurol 32:1041-1042, Heath,P.D.,et al, 1982

Global Aphasia Without Hemiparesis:A Sign of Embolic Encephalopathy
Neurol 32:403-406, VanHorn,G.,et al, 1982

Localization in Transcortical Sensory Aphasia
Arch Neurol 39:475-478, Kertesz,A.,et al, 1982

Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
Ann Int Med 96:616-617, Faillace,R.T.,et al, 1982

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Neurological Manifestation of Accidental Hypothermia
Ann Neurol 10:384-387, Fischbeck,K.H.,et al, 1981

Pronounced Cerebellar Features in Legionnaires'Disease
BMJ 283:276, Maskill,M.R., 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Speech Disorders of Parkinsonism:A Review
JNNP 44:751-758, Critchley,E.M.R., 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Metastasis to the Base of the Skull:Clinical Findings in 43 Patients
Neurol 31:530-537, Greenberg,H.S.,et al, 1981

Complex Partial Status Epilepticus in Young Children
Ann Neurol 9:526-530, McBride,M.C.,et al, 1981



Showing articles 650 to 700 of 845 << Previous Next >>