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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 300 to 350 of 845 << Previous Next >>

"Salt and Pepper" in the Eye and Face: A Prelude to Brainstem Ischemia
Am J Ophthalmol 144:322-325, Conforto, A.B.,et al, 2007

Concomitant Chronic Inflammatory Demyelinating Polyneuropathy and Myasthenia Gravis Following Cytomegalovirus Infection
J Neurol Sci 240:103-106, Mori, M.,et al, 2006

Botulism in 4 Adults Following Cosmetic Injections With an Unlicensed, Highly Concentrated Botulinum Preparation
JAMA 296:2476-2479,2512, Chertow,D.S.,et al, 2006

Pallidal Deep-Brain Stimulation in Primary Generalized or Segmental Dystonia
NEJM 355:1978-1990, Kupsch,A.,et al, 2006

Tiagabine-Induced Nonconvulsive Status Epilepticus in an Adolescent Without Epilepsy
Neurol 67:1514-1515, Jette,N.,et al, 2006

Cerebellar Infarction int he Territory of the Medial Branch of the Superior Cerebellar Artery
Neurol 66:115-117, Sohn,S.-I.,et al, 2006

Clinical Study of 39 Patients with Atypical Lacunar Syndrome
JNNP 77:381-384, Arboix,A.,et al, 2006

Nonconvulsive Status Epilepticus in Metastatic CNS Disease
Neurol 66:1261-1263, Blitshteyn,S. &Jaeckle,K.A., 2006

Diagnosis of Psychogenic Nonepileptic Status Epilepticus in the Emergency Setting
Neurol 66:1727-1729, Holtkamp,M.,et al, 2006

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Late-Onset Friedreich Ataxia
Arch Neurol 62:1865-1869, Bhidayasiri,R.,et al, 2005

Rehabilitation After Stroke
NEJM 352:1677-1684, Dobkin,B.H., 2005

Does This Patient Have Myasthenia Gravis?
JAMA 293:1906-1914, Scherer,K.,et al, 2005

Is This Patient Having a Stroke?
JAMA 293:2391-2402, Goldstein,L.B. &Simel,D.L., 2005

A Floppy Child with Failure to Thrive
Lancet 366:176, Loma-Sanner,I.,et al, 2005

Dysphagia as the Sole Manisfestation of Myasthenia Gravis
JNNP 76:1297-1300, Llabrs,M.,et al, 2005

The "Electrocuted" Hippocampus
Lancet 366:956-957, Uncini,A.,et al, 2005

Diffusion-weighted and Perfusion MRI Demonstrates Parenchymal Changes in Complex Partial Status Epilepticus
Brain 128:1369-1376, Szabo, K.,et al, 2005

Agreement Between Ambulance Paramedic- and Physician-Recorded Neurological Signs with Face Arm Speech Test (FAST) in Acute Stroke Patients
Stroke 35:1355-1359, Nor,A.M.,et al, 2004

Strokes in the Subinsular Territory
Neurol 63:2429-2432, Kumral,E.,et al, 2004

Riversible Diffusion MRI Abnormalities and Transient Mutism after Liver Trnasplantation
Neurol 62:981-983, Bianco,F.,et al, 2004

Magnetoencephalography (MEG) and Magnetic Source Imaging (MSI)
The Neurologist 10:138-153, Wheless,J.W.,et al, 2004

Reversible Corpus Callosum Lesion in Legionnaires Disease
JNNP 75:651-654, Morgan, J.C.,et al, 2004

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Neuropathological Findings in West Nile Virus Encephalitis: A Case Report
Ann Neurol 54:547-551, Agamanolis,D.P.,et al, 2003

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Diagnostic Accuracy of Stroke Referrals from Primary Care, Emergency Room Physicians, and Ambulance Staff Using the Face Arm Speech Test
Stroke 34:71-76, Harbison,J.,et al, 2003

Antivonvulsants for Creutzfeldt-Jakob Disease?
Lancet 361:224, Fioel,A.,et al, 2003

Non-convulsive Status Epilepticus: Usefulness of Clinical Features in Selecting Patients for Urgent EEG
JNNP 74:189-191, Husain,A.M.,et al, 2003

Clinicopath Conf., Chronic Inflammatory Demyelinating Polyneuropathy
NEJM 348:735-743, Case 6-2003, 2003

Clinical Features and Natural Histry of Progressive Supranuclear Palsy, A Clinical Cohort Study
Neurol 60:910-916, Nath,W.,et al, 2003

Status Epilepticus: A Review of Different Syndromes, Their Current Evaluation, and Treatment
The Neurologist 9:61-76, Gaitanis,J.N. &Drislane,F.W., 2003

Pure Dysarthria Due to Small Cortical Stroke
Neurol 60:1178-1180, Kim,J.S.,et al, 2003

Emergency Calls in Acute Stroke
Stroke 34:1005-1009, Handschu,R.,et al, 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Neurotoxicity Following Addition of Intravenous Valproate to Lamotrigine Therapy
Neurol 60:1991-1992, Burneo,J.G.,et al, 2003

Clinicopath Conf., Giant-Cell Arteritis
NEJM 349:170-180, Case 21-2003, 2003

Polymyositis Masquerading as Motor Neuron Disease
Arch Neurol 60:1001-1003, Ryan,A.,et al, 2003

Language Function and Dysfunction in Corticobasal Degeneration
Neurol 61:493-499, Graham,N.L.,et al, 2003

Left Internal Carotid Artery Dissection Presenting with Headache, Collet-Sicard Syndrome and Sustained Hypertension
Eur J Neurol 10:731-732, Walker, S.,et al, 2003

Clinicopath Conf., Acute Disseminated Encephalomyelitis
NEJM 347:1433-1440, Case 34-2002, 2002

A Reversible Paralysis
Lancet 360:1160, Maury,E.,et al, 2002

Reversible Metronidazole-Induced Lesions of the Cerebellar Dentate Nuclei
NEJM 346:68-69, Woodruff,B.K.,et al, 2002

Refractory Status Epilepticus
Arch Neurol 59:205-210,188, Mayer,S.A.,et al, 2002

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

A Poliomyelitis-like Syndrome from West Nile Virus Infection
NEJM 347:1279-1280, Leis,A.A., et al, 2002

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001

Sensory Guillain-Barre Syndrome
Neurol 56:82-86, Oh,S.J.,et al, 2001



Showing articles 300 to 350 of 845 << Previous Next >>