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Differential
(Click to cross reference)
abducens nerve paralysis
abscess, intracerebral
achilles tendon, enlarged
acoustic nerve
acquired immunodeficiency syndrome
acute disseminated encephalomyelitis
acute disseminated encephalomyelitis, multiphasic
addiction, heroin
addiction, heroin-neurologic complications with
akinetic mute
alopecia
angiotensin-converting enzyme
anterior commissure
anterior inferior cerebellar artery
anti MAG antibodies
antibodies to measles
aphasia
aphonia
arbovirus
areflexia
arterial dissection
arterial dissection, vertebral
arteriopathy
arteriovenous malformation
arteritis, temporal
astrocytoma
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoimmune disease
autonomic dysfunction
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bickerstaff's brainstem encephalitis
brain atrophy
brain biopsy
brain biopsy, stereotaxic
brainstem, dysfunction
brainstem, glioma
brainstem, hypoplasia
brainstem, infarction of
brainstem, lesion of
brainstem, malformation
brainstem, neoplasms of
cachexia
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
central nervous system, infection of
centrum semiovale
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellar infarction, bilateral
cerebellar lesion
cerebellar peduncle
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral cortical encephaliis
cerebral edema, cytotoxic
cerebral edema, vasogenic
cerebral infarction, subcortical
cerebral peduncle
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, bilateral
children
chorea
chromosomal abnormality
chromosome 11
cognition
coma
complications
confusion
congenital malformation
conus medullaris, lesion of
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cranial nerve palsies
crying, pathologic
cyst, parenchymal
cystatin C mutation
deafness, bilateral
deep gray nuclei
degenerative diseases of CNS
dementia
demyelinating disease
Dengue fever
developmental retardation
diagnostic criteria
diaschisis
diplopia
dysarthria
dysdiadochokinesia
dysmetria
electroencephalogram, periodic complexes
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, viral
encephalopathy
encephalopathy, progressive
epicanthal folds
epidemiology of neurology
Erdheim-Chester disease
erectile dysfunction
exome sequencing
eye movement, disorders of
face, numbness of
facial appearance, abnormal
facial nerve palsy
facial pain
facial weakness
falling
familial
finger nose finger test
Fisher's syndrome
fluorescein angiography
foam cells
fourth ventricle, enlargement of
fourth ventricle, floor
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
gadolinium
gait disorder
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
giant cell arteritis
glioma
glutamic acid decarboxylase, antibody
hammertoes
headache
headache, recurrent
headache, severe
hearing loss
hearing loss, bilateral
hearing loss, sudden, bilateral
heel swelling
hemiparesis
heralding manifestation
herpes simplex encephalitis
herpes simplex encephalitis, atypical
herpes simplex encephalitis, extra temporal
HGPPS
hiccoughs
highly active antiretroviral therapy
histiocytosis
Horner's syndrome
H-sign, spinal cord
human immunodeficiency virus type 1
hypomyelination
hypothalamus
hypothalamus, lesion of
hypotonia
imbalance
immune reconstitution inflammatory syndrome
immune-mediated pathogenesis
immunocompetent
immunologic disease
immunosuppression
impulsivity
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
infection
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia
intracerebral hemorrhage
JC virus
Kearns-Sayre syndrome
lactic acidemia
lateral medullary syndrome
lateropulsion
laughing, pathologic
lethargy
leukemia
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
listeria monocytogenes
listeriosis, CNS
locked-in syndrome
low back pain
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malformation, CNS, congenital
malformation, vascular, cerebral
Marchiafava-Bignami disease
medulla oblongata
medulla oblongata, infarction of
medulla oblongata, lesion of
medulla oblongata, malformation
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
mental status, abnormal
metabolic acidosis
microdontia
microhemorrhage, intracerebral
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
MNGIE syndrome
molecular genetics
monoclonal antibodies
mortality
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, contrast enhanced, cloud-like
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, mass effect on
MRI, optic nerve
MRI, snowball lesions
MRI, spinal cord
MRS
multiple sclerosis
multiple system atrophy
muscle weakness, proximal
mycoplasma
mycoplasma pneumoniae
myelitis, longitudinal
myelitis, transverse
myoclonus
nausea and vomiting
neoplasm, primary of CNS
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuronal intranuclear inclusion disease
neuronopathy, sensory
neuroophthalmology
neuropathology
next-generation sequencing
nonverbal
nutritional deficiency
nystagmus
nystagmus, gaze-evoked
ocular motility, disorders of
oculodentodigital dysplasia
old age, neurology of
ophthalmoplegia
opportunistic infection, CNS
optic chiasm
optic chiasm, lesion of
optic neuritis
optic neuritis, bilateral
optic neuritis, recurrent
pain, back
paraparesis
paraparesis, spastic
Parkinsonism syndrome
pathologic reflex
periaqueductal lesion
personality change
pituitary
pituitary, lesion of
PLEDs
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
polymerase chain reaction, false negative
pons, hypoplasia
pons, infarction of
pons, lesion of
pontine glioma
posterior fossa, arteriovenous malformation
precipitating factors
pregnancy, neurologic complications in
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pseudobulbar palsy
pyramidal tract, uncrossed
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
reading disorder, acquired
recurrent
Red flags
regional enteritis
release phenomena
renal failure
renal failure, acute
respiratory tract infection
restiform body
retinal branch artery occlusion
reversible neurologic disorder
review article
rigidity
rubeola virus
sarcoidosis
sarcoidosis, CNS
scoliosis
scoliosis, neurologic association with
screening
seizure
sensorineural hearing loss
sensory loss
sensory loss, crossed pattern
serologic testing
seronegative
skin, biopsy
snout reflex
spinocerebellar ataxia
splenium of corpus callosum
spondylolysis
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subacute sclerosing panencephalitis, adult onset
subcortical U fibers
succinate dehydrogenase deficiency
superior cerebellar peduncle
Susac's syndrome
symmetric brain lesions
syndactyly
systemic illness
tandem gait, ataxic
teeth, abnormal
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
third ventricle, wall
tinnitus
treatment of neurologic disorder
tremor
tremor, intention
tremor, writing
trigeminal artery, persistent
trinucleotide repeats
tropical disease
tumefactive lesion
urinary incontinence
vaccination, neurologic complications with
vertebral artery
vertigo
viral infection
viral infection, CNS
visual loss
visuospatial disturbance
walking, difficulty with
Wallerian degeneration
weakness
weight loss
wheelchair
white matter disease
white matter disease, pattern
white matter disease, subcortical
wide based gait
writing
Showing articles 250 to 300 of 1987 << Previous Next >>

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Coma
Neurol 90:e1638-e1645, Schievink, W.I.,et al, 2018

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

A 77-year-old man presenting with episodic expressive aphasia
Neurol 90:e1822-e1826, Shanklin, A.,et al, 2018

Diagnosis and Management of Active Intracranial Atherosclerotic Disease
Stroke 49:e221-e223, Narwal, P.,et al, 2018

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Human Immunodeficiency Virus Presenting as Progressive Multifocal Leukoencephalopathy Restricted to the Posterior Fossa
JAMA Neurol 74:597-598, Schubert, R.D. & Richie, M.B., 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Clinical Imaging Factors Associated with Infarct Progression in Patients with Ischemic Stroke During Transfer for Mechanical Thrombectomy
JAMA Neurol 74:1361-1367,1298, Boulouis, G.,et al, 2017

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

Imaging Characteristics of Venous Parenchymal Abnormalities
Stroke 48:3258-3265, Arnoux, A.,et al, 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

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

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

A Case of Fulminant Encephalopathy in a 69-year-old Woman
Neurol 89:e109-e114, Lamotte, G. and Williams, C, 2017

Intracranial Carotid Artery Calcification Relates to Recanalization and Clinical Outcome after Mechanical Thrombectomy
Stroke 48:342-347, Hernandez-Perez, M.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Patient with Severe Moyamoya Disease Who Presents with Acute Cortical Blindness
Stroke 48:e126-e129, Sajja, A.,et al, 2017

Intracranial and Extracranial Neurovascular Manifestations of Takayasu Arteritis
AJNR 38:766-772, Bond, K.M.,et al, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

The Contrast Enhancement of Intracranial Arterial Wall on High-Resolution MRI and Its Clinical Relevance in Patients with Moyamoya Vasculopathy
Sci Rep 7:44264 doi:10.1038/srep44264, Wang, M.,et al, 2017

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

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

Emerging Cases of Powassan Virus Encephalitis in New England:Clinical Presentation, Imaging, and Review of the Literature
CID 62:707-713, Piantadosi,A.,et al, 2016

Intracerebral Hemorrhage Due To Developmental Venous Anomalies
J Clin Neurosci 26:95-100, Li, X.et al, 2016

Extensive Vasogenic Edema in Bickerstaff Brainstem Encephalitis
Neurol 86:e38-e39, Nerrant, E.,et al, 2016

Atypical Presentations of Intracranial Hypotension: Comparison with Classic Spontaneous Intracranial Hypotension
AJNR 37:1256-1261, Capizzano, A.A.,et al, 2016

Imaging Signs in Spontaneous Intracranial Hypotension: Prevalence and Relationship to CSF Pressure
AJNR 37:1374-1378, Kranz, P.G.,et al, 2016

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

Fat Embolism Syndrome Secondary to Bone Marrow Necrosis in Patients with Hemoglobinopathies
SMJ 109:549-553, Gangaraju, R.,et al, 2016

Antibiotic-Associated Encephalopathy
Neurol 86:963-971, Bhattacharyya, S.,et al, 2016

Computed Tomographic Findings in Microcephaly Associated with Zika Virus
NEJM 374:2193-2195, Hazin, A.,et al, 2016

Metronidazole-Associated Encephalopathy
NEJM 374:1465, Baden, L.R., 2016

Minimally Invasive Surgery for Intracerebral and Intraventricular Hemorrhage
Stroke 47:1399-1406, Fiorella, D.,et al, 2016

Neuroradiologic Patterns and Novel Imaging Findings in Aicardi-Goutieres Syndrome
Neurol 86:28-35, La Piana, R.,et al, 2016

Spontaneous Intracranial Hypotension and Posterior Reversible Encephalopathy Syndrome
Neurol 86:e55-e57, Santillan, A.,et al, 2016

Infective Endocarditis
Lancet 387:882-893, Cahill, T.J. & Prendergast, B.D., 2016

A 57-year-old Man with Subacute Gait Difficulty and Hand Tremor
Neurol 87:e110-e113, Paliwal, V.K.,et al, 2016

Incidence and Clinical Significance of Acute Reocclusion after Emergent Angioplasty or Stenting for Underlying Intracranial Stenosis in Patients with Acute Stroke
AJNR 37:1690-1695, Kim, G.E.,et al, 2016

Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

A 52-year-old Man with Diplopia and Ataxia
Neurol 87:e140-e143, Bradshaw, M.J.,et al, 2016

A Benign But Potentially Life-Threatening Headache
Neurol 87:e168-e173, Zhang, D.,et al, 2016

Emerging Risk Factors for Recurrent Vascular Events in Patients with Embolic Stroke of Unertermined Source
Stroke 47:2714-2721, Ueno, Y.,et al, 2016



Showing articles 250 to 300 of 1987 << Previous Next >>