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abducens nerve paralysis
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
areflexia
arterial dissection
arterial dissection, vertebral
arteriopathy
arteritis, temporal
astrocytoma
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
attention deficit disorder with hyperactivity
atypical
autism
autoimmune disease
autonomic dysfunction
autosomal dominant leukodystrophy
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Bickerstaff's brainstem encephalitis
brain atrophy
brain biopsy
brain biopsy, stereotaxic
brainstem, glioma
brainstem, hypoplasia
brainstem, infarction of
brainstem, lesion of
brainstem, malformation
brainstem, neoplasms of
CAG repeats
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
comorbidities
confusion
congenital malformation
conus medullaris, lesion of
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cyst, parenchymal
deafness, bilateral
deep gray nuclei
degenerative diseases of CNS
dementia
demyelinating disease
developmental retardation
diagnostic criteria
diaschisis
differential diagnosis
diplopia
dysarthria
dysdiadochokinesia
dysmetria
electroencephalogram, periodic complexes
encephalitis
encephalitis, brainstem
encephalitis, viral
encephalopathy
encephalopathy, progressive
epicanthal folds
erectile dysfunction
exome sequencing
eye movement, disorders of
face, numbness of
facial appearance, abnormal
facial pain
falling
familial
Fisher's syndrome
fluorescein angiography
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
hammertoes
headache
headache, recurrent
headache, severe
hearing loss
hearing loss, bilateral
hearing loss, sudden, bilateral
hemiparesis
heralding manifestation
HGPPS
hiccoughs
Horner's syndrome
H-sign, spinal cord
human immunodeficiency virus type 1
hyperactivity
hyperreflexia
hypomyelination
hypothalamus, lesion of
hypotonia
imbalance
immune-mediated pathogenesis
immunologic disease
immunosuppression
impulsivity
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
infection
infertility
intellectual deficit
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia
JC virus
joint hypermobility
Kearns-Sayre syndrome
lactic acidemia
lateral medullary syndrome
lateropulsion
lethargy
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
low back pain
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malformation, CNS, congenital
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
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
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
mycoplasma
mycoplasma pneumoniae
myelitis, longitudinal
myelitis, transverse
myelomalacia
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
nutritional deficiency
nystagmus
nystagmus, gaze-evoked
ocular dysmetria
ocular motility, disorders of
oculodentodigital dysplasia
old age, neurology of
ophthalmoplegia
optic neuritis
optic neuritis, bilateral
optic neuritis, recurrent
orthostatic hypotension
ovarian insufficiency
pain, back
paraparesis
paraparesis, spastic
Parkinsonism syndrome
periaqueductal lesion
personality change
PLEDs
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
pons, hypoplasia
pons, infarction of
pons, lesion of
pontine glioma
precipitating factors
pregnancy, neurologic complications in
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pyramidal tract, uncrossed
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
reading disorder, acquired
recurrent
Red flags
regional enteritis
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
speech, delayed development of
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
Susac's syndrome
symmetric brain lesions
syncope
syndactyly
tandem gait, ataxic
tantrum
teeth, abnormal
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular enlargement
thalamus, lesion of
thalamus, lesion of-bilateral
third ventricle, wall
tinnitus
treatment of neurologic disorder
tremor
tremor, intention
tremor, writing
trinucleotide repeats
tumefactive lesion
urinary incontinence
vaccination, neurologic complications with
vertebral artery
vertigo
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
x-linked intellectual deficit
x-linked mental retardation
Showing articles 100 to 150 of 13666 << Previous Next >>

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
Neurol 94:710-712, Kim, D.D. & Prasad, A.N., 2020

Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
Neurologist 25:82-84, Uzawa, A.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

Acute Lateral Medullary Infarct Due to Giant Cell Arteritis
Stroke 50:e290-e293, Dardick, J.M.,et al, 2019

Isolated and Persistent Hiccup by Tiny Ischemia at Dorsolateral Medulla
Neurol 93:e934, Seo,J.H., 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Non-Bacterial Thrombotic Endocarditis
Infective Endocarditis doi:10.5772/intechopen.84398, Busca-Arenzana, C.,et al, Chp 6, pg 315, 2019

Posterior Circulation Thrombectomy - Pc-ASPECT Score Applied to Preintervention Magnetic Resonance Imaging Can Accurately Predict Functional Outcome
World Neurosurg 129:e566-e571, Khatibi, K.,et al, 2019

Cerebellar Hippocampal and Basal Nuclei Transient Edema with Restricted Diffusion (CHANTER) Syndrome
Neurocrit Care 31:228-296, Jasne, A.S.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

Gasperini Syndrome
Neurol 90:e261, Lorio, R., 2018

Headache and Altered Mental Status
Neurol 90:e1267-e1270, Spera, K.M.,et al, 2018

Neurologic Abnormalities After Atrial Fibrillation Ablative Procedure
JAMA Neurol 75:1144-1145, Stanton, R.J.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

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

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

Acute Viral Encephalitis
NEJM 379:357-366, Tyler,K.L., 2018

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

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

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

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

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

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,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

Holmes Tremor
Neurol 86:931-938, Raina, G.B.,et al, 2016

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

MRI Characteristics of Globus Pallidus Infarcts in Isolated Methylmalonic Acidemia
AJNR 36:194-201, Baker, E.H.,et al, 2015

Clinical Pathologic Conference, A 20-Year-Old Man with Back Pain and Lower Extremity Weakness
JAMA Neurol 72:363-366, Etherton, M.R.,et al, 2015

Significant Period Between Presentation and Diagnosis in Basilar Artery Occlusion
Stroke 46:e79-e81, Organek, N.,et al, 2015

Cavernous Sinus Thrombosis in Children
Stroke 46:2657-2660, Press, C.A.,et al, 2015

Basilar Occlusion Syndromes: An Update
Neurohosp 5:142-150, Demel, S.L. & Broderick, J.P., 2015

Clinicopathologic Conference, Cerebral Granulomatosis with Polyangiitis
NEJM 371:162-173, Case 21-2014, 2014

Hyperintense Basilar Artery on FLAIR MR Imaging: Diagnostic Accuracy and Clinical Impact in Patients with Acute Brain Stem Stroke
AJNR 35:1520-1526, Gawlitza, M.,et al, 2014

Clinicopathologic Conference, Parainfectious Encephalomyelitis Associated with Systemic Mycoplasma Infection
NEJM 370:2427-2438, Case 19-2012, 2014

Diagnosis and Management of Acute Cerebellar Infarction
Stroke 45:e56-e58, Wright, J.,et al, 2014

Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
UptoDate Oct. 2014, McClain, K.L., 2014

Neuroimaging Features and Predictors of Outcome in Eclamptic Encephalopathy: A Prospective Observational Study
AJNR 35:1728-1734, Junewar, V.,et al, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
Adams & Victors Principles of Neurology Chp 41, pg 1172, Ropper, A.H.,et al, 2014



Showing articles 100 to 150 of 13666 << Previous Next >>