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Differential
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abdominal reflex, absent
abducens nerve paralysis
abscess, intracerebral
acute disseminated encephalomyelitis
acute disseminated encephalomyelitis, multiphasic
adrenoleukodystrophy
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
amenorrhea
ammonia
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ANA
anemia
ankle clonous
anomic aphasia
anterior spinal artery
antiviral agents
aphasia
areflexia
Arnold Chiari malformation
arteritis, temporal
arthralgia
asterixis
asterixis, causes of
asterixis, unilateral
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
atlanto-axial subluxation
atypical
autonomic dysfunction
B 12 deficiency
B12
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, infarction
behavioral disorder
bladder dysfunction
brain atrophy
brain biopsy
brain biopsy, false negative
brainstem, dysfunction
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
burning feet
burning paresthesia
camptocormia
cardiomyopathy
carotid angiogram
CAT scan
CAT scan, abnormal
central nervous system, infection of
cerebral edema
cerebritis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, amonia
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, glutamine
cerebrospinal fluid, pressure increased
cerebrovascular accident
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
coma
complications
confusion
consanguinity
cornea, opacity of
coronavirus
corpus callosum, lesion of
cough
COVID-19
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
C-reactive protein, elevated
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
decerebrate posture
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
depression
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
diaphragmatic paralysis, causes of
differential diagnosis
digiti quinti sign
diplopia
disability, neurological
distal muscle weakness
drowsiness
dysarthria
dysmorphic
dysphagia
dyspnea
electrical sensation
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
emotional lability
encephalopathy
encephalopathy, acute
encephalopathy, metabolic
ependymal
epidemiology of neurology
eye movement, disorders of
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial weakness
falling
fasciculation
fatigue
fever
foot drop
frataxin
Friedreich's ataxia
frontal lobe, pathologic signs of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
genu valgum
girdle sensation
glutamine
gram negative rod
granulomatosis with polyangiitis
granulomatous disease
hand weakness
headache
headache, recurrent
headache, severe
hearing loss
hearing problems in children
hemianopia
hemiparesis
hepatic encephalopathy
hepatolenticular degeneration, non-Wilsonian
Hispanics
Horner's syndrome
horse bite
hypercapnia
hyperreflexia
hypersegmented polys
hypertension
hypothalamus
hypothalamus, disturbance of
hypothermia
hypothermia, causes of
imbalance
incontinence, fecal
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intrinsic hand muscles, wasting of
irritability
Jakob-Creutzfeldt disease
jaw jerk, abnormal
kyphoscoliosis, neurologic causes of
leg weakness, bilateral
lethargy
leukodystrophy
leukopenia
Lhermitte's sign
lymphadenopathy
lymphadenopathy, hilar
lymphoma involving CNS
lymphomatoid granulomatosis
lysosomal storage disease
mediastinum, lymph-node biopsy
mediastinum, mass of
medulla oblongata, lesion of
memory, impairment of
meningeal enhancement
meningitis
meningitis, bacterial
meningitis, brucellosis
meningitis, pneumococcal
mental retardation
mental status, abnormal
midbrain, lesion of
middle cerebellar peduncle, lesion
Mills syndrome
molecular genetics
mononeuropathy multiplex
Morquio syndrome
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, linear enhancement
MRI, nodular enhancement
MRI, ring sign
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
mucopolysaccharidoses
multiple sclerosis
muscle biopsy
muscle cramp
muscle weakness
myelitis, longitudinal
myelomalacia
myelopathy
myelopathy hand
nausea and vomiting
neck stiffness
neck weakness
nerve root enhancement
neuroendocrinology
neurogenic bladder
neurologic complications
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathy
neuropathy, peripheral
neuropathy, vasculitic, systemic
neuropsychiatry
nystagmus
nystagmus, dissociated
nystagmus, vertical
ophthalmoplegia
optic nerve
optic nerve, lesion of
optic neuropathy
orthostatic hypotension
osteoporosis
papilledema
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
paresthesias
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, asymmetric onset
Parkinson disease, hemiparesis in
Parkinson disease, L-dopa nonresponsive
Parkinson disease, tremor, absence of
Parkinson disease, unilateral
Parkinson disease, young onset
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathologic reflex
pernicious anemia
pes cavus
pituitary stalk
pituitary stalk, lesion of
pleocytosis of cerebrospinal fluid
posterior column disease
posterior leukoencephalopathy syndrome
postural abnormality
prognosis
progressive neurologic disorder
proprioception, abnormal
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pyramidal tract
pyramidal tract dysfunction
pyramidal tract dysfunction, unilateral
quadriparesis
rash
recurrent
remdesivir
renal failure
respiratory failure
retinal degeneration
retinal exudates
retinopathy
retropulsion
reversible neurologic disorder
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
risk factors
sarcoidosis
sarcoidosis, CNS
Saudi Arabia
scoliosis
scotoma
seizure
seizure, children
sensorineural hearing loss
sensory loss
sensory loss, cutaneous
short neck
short stature
skin, lesions in neurologic disorders
slow virus infection of CNS
spasticity
spinal cord
spinal cord, compression of
spinal cord, ischemic lesion of
spinal cord, lesion of
spinal cord, pathologic exam of
splenomegaly
spongy degeneration of brain
startle myoclonus
startle reaction
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
syringomyelia
temporal lobe, lesion
temporal lobe, lesion, bilateral
thrombocytopenia
tinnitus
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
unconsciousness
urinary frequency
urinary incontinence
urinary urgency
vaccination, neurologic complications with
ventricular enlargement
vertigo
vertigo, episodic
vibratory sensation, abnormal
viral infection, CNS
visual acuity, decreased
visual fields, constricted
visual loss
vitamin deficiency
weakness
weakness, progressive
weaning from respirator, failure to
weight loss
wheelchair
white matter disease
wide based gait
zoonoses
Showing articles 50 to 100 of 5803 << Previous Next >>

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

Finger Clonus
Neurol 86:e118-e119, Moccia,M.,et al, 2016

Idiopathic Thoracic Spontaneous Spinal Epidural Hematoma
Case Reports Surg doi:10.1155/2016/5430708, Aycan, A.,et al, 2016

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

Corticosteroid-Induced Paraplegia - A Diagnostic Clue for Spinal Dural Arterial Venous Fistula
JAMA Neurol 72:833-834, Hocker, S., 2015

Cyclical Konzo Epidemics and Climate Variability
Ann Neurol 77:371-380, Oluwole, O.S.A., 2015

DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
Neurol 84:226-230,218, Wolf, N.I.,et al, 2015

Multiple-System Atrophy
NEJM 372:249-263, Fanciulli, A. & Wenning, G.K., 2015

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

A 73-year-old Man with Diplopia and Ataxia
Neurol 85:e96-e100, Gupta, H.V.,et al, 2015

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Tropical Spastic Paraparesis, HTLV-1 Infection
Adams & Victors Principles of Neurology, Chp 33, pg 762, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1107, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Familial Dementia with Spastic Paraparesis
Adams & Victors Principles of Neurology, Chp 39, pg 1081, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Rubella Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Clinical Case Conference: A 41-Year-Old Woman with Progressive Weakness and Sensory Loss
Ann Neurol 75:9-19, Stephen, C.D.,et al, 2014

A Case of Slowly Progressive Painful Paraparesis
Neurol 82:1476-1479, Corbetto, M.,et al, 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

A Young Woman with Rapid Mental Deterioration and Leukoencephalopathy
Neurol 83:e182-e186, Biotti, D.,et al, 2014

Longitudinally Extensive Transverse Myelitis in Neuro-Beh�et Disease
Neurol 80:e189-e190, Graham, D.,et al, 2013

Clinical Reasoning: A Case of Treatable Spastic Paraparesis
Neurol 79: e50-e53, McKinnon, J.H. & Bosch E.P., 2012

Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
AJNR 33:1945-1950, Lee,H.,et al, 2012

Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct
Stroke 42:e1-e3, Ng, A.S.L.,et al, 2011

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Clinicopath Conf., Gliomatosis Cerebri
Neurol 69:600-606, Fleming,J.O.,et al, 2007

Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
Neuropathology 27:434-441, Iwasaki,Y.,et al, 2007

Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
Neurol 67:859-863, Rauschka,H.,et al, 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

Hereditary Spastic Paraplegia
Arch Neurol 61:849-855,830, Orlacchio,A.,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

The Hereditary Spastic Paraplegias
Arch Neurol 60:1045-1049, Fink,J.K., 2003

Prevalence and Clinical Features of HTLV Neurologic Disease in the HTLV Outcomes Study
Neurol 61:1588-1594, Orland,J.R.,et al, 2003

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
JNNP 71:795-797, Kasim,S.,et al, 2001

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

Recurrent Reversible Paraplegia
Lancet 357:1092, Haran,M. & Ni,S., 2001

Dysarthria in Acute Ischemic Stroke
Neurol 56:1021-1027, Urban,P.P.,et al, 2001

Ipsilateral Hemiparesis After Putaminal Hemorrhage Due to Uncrossed Pyramidal Tract
Neurol 54:1801-1805, Terakawa,H.,et al, 2000

Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Hereditary Spastic Paraparesis: A Review of New Developments
JNNP 69:150-160, McDermott,C.J. et al, 2000



Showing articles 50 to 100 of 5803 << Previous Next >>