Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
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 750 to 800 of 845 << Previous Next >>

Prolonged Partial Complex Status Epilepticus:EEG & Behavioral Observations
Neurol 28:863-869, Engel,J.Jr.,et al, 1978

Complex Partial Status Epilepticus:Case Report & Proposal for Diagnostic Criteria
Neurol 28:957-961, Mayeux,R., 1978

Effect of Valproic Acid on Spike & Wave Discharges in Patients with Absence Seizures
Neurol 28:886-891, Villarreal,H.J.,et al, 1978

Imipramine in Absence & Myoclonic-astatic Seizures
Neurol 28:953-957, Fromm,G.H.,et al, 1978

Aphasias & Related Disturbances
Textbook of Medicine. Ed. R. W. Wilkins Little Brown & Co. , Boston, p. 867, Benson,D.F., 1978

Neuromuscular Diseases that Affect the Eye
International Ophthal Clx 18:103, Black,J., 1978

Methyl Bromide Intoxication:Neurologic Features, Including Simulation of Reye Syndrome
Neurol 27:959, Shield,L.K.,et al, 1977

Neonatal Ophthalmoplegia with Microfibers:A Reversible Myopathy
Neurol 27:974, Hanson,P.A.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Sodium Valproate & Clonazepam in the Treatment of Intractable Epilepsy
Arch Neurol 34:14, Lance,W.,et al, 1977

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

Clonazepam & Branchial Myoclonus
Ann Neurol 1:306, Gledhill,R.F., 1977

Insensitivity to Pain in Psychotic Patients
NEJM 296:1480, Geschwind,N., 1977

Fisher's Syndrome:A Pharmacological Study of the Pupils
Ann Neurol 2:63, Okajima,T.,et al, 1977

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

Case Record of the M. G. H.
Glioblastoma Multiforme of Pons, NEJM 296:8651977., , 1977

Cervical Myelographic Changes in Hypertrophic Interstitial Polyneuropathy
Ann Neurol 2:83, Hammerschlag,S.B.,et al, 1977

Thalamic Hemorrhage:A Computed Yomographic-clinical Correlation
Neurol 27:217, Walshe,T.M.,et al, 1977

Reversible Subacute Peripheral Neuropathy Induced by Phenytoin
Arch Neurol 34:189, Dobkin,B.H., 1977

Paroxysmal Choreoathetosis as a Presenting Symptom in Idiopathic Hypoparathyroidism
JNNP 40:692, Soffer,D.,et al, 1977

Lymphomatoid Granulomatosis Clinically Confined to the CNS
Arch Neurol 34:782, Kokmen,E., 1977

Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977

Tonic Pupils with Acute Ophthalmoplegic Polyneuritis
Ann Neurol 2:393, Keane,J.R., 1977

Blepharospasm-oromandibular Dystonia Dyndrome (Brueghel's syndrome) :A Variant of Adult-onset Torsion Dystonia
JNNP 39:1204, Marsden,C.D., 1976

Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976

Case Record MGH
Necrotizing Myelopathy with Carcinoma, NEJM 294:14471976., , 1976

Case Records of the MGH
Giant cell Angiitis, intracranial NEJM 295:9441976., , 1976

Progressive Rubella Panencephalitis
Arch Neurol 33:722, Wolinsky,J.S.,et al, 1976

A Fatal Encephalopathy in Chronic Haemodialysis Patients
Lancet 764, Burks,J.S.,et al, 1976

Progressive Dialytic Encephalopathy
et al JNNP 39:411, Chokroverty,S., 1976

Phenytoin-induced Ophthalmoplegia
Neurol 26:1031, Spector,R.H.,et al, 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
Neurol Sciences 28:17-40, Salisachs,P.J., 1976

Dialysis Encephalopathy:A Possible Seizure Disorder
Neurol 26:1130-1134, Nadel,A.M.,et al, 1976

Neuro-toxic Reaction to Haloperidol in a Thyrotoxic Pnt
NEJM 293:201, Yosselson,S.,et al, 1975

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Recurrent Aseptic Meningitis in an Elderly Male, Unusual Prodromal Manifestation of SLE
JAMA 235:1142, Finelli,P.F.,et al, 1975

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Acute Areflexic Paralysis
Arch Neurol 32:706, Furlan,A.J.,et al, 1975

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Acute Bulbar Dysfunction & Hyperthyroidism
Am J Med 56:464, Kammer,G.M.,et al, 1974

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974

Bulbar Paralysis in Chronic Alcoholic with Recovery,
Dis Nerv Syst 1974, Mar p. 135., Khurana,K.,et al, 1974

Case Records of MGH-Polycythemia
Carotid Occlusion & Cerebral Infarcts, NEJM 291:96674., , 1974

Emergency Management of the Patient with Seizures
Postgrad Med 55:59, Conomy,J.,et al, 1974

Pseudointernuclear Ophthalmoplegia in Acute Idiopathic Polyneuritis (Fisher's Syndrome)
Am J Ophthalmol 77:725, Swick,H.M., 1974

Speech Defects in Children Aged 7 yrs, A National Study
BMJ 253, 1973 Feb., Butler,N.,et al, 1973

Case Records of MGH-NEJM 287:1291
1972, 289:1039, 1973 Arterio-Venous Malformation of Cerebellum., , 1973



Showing articles 750 to 800 of 845 << Previous Next >>