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Differential
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abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
acrocyanosis
Adies pupil
adult polyglucosan body disease
advances in neurology
adverse drug reaction
agenesis of corpus callosum
Aicardi-Goutieres syndrome
Alexanders disease
alpha glucosidase
alveolar hypoventilation
Alzheimer's disease
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
anesthesia, general
angiography, cerebral, false negative
angiography, cerebral, negative
ankylosing spondylitis
anterior horn cell disease
anterior tibial muscle weakness
antibodies to measles
antiviral agents
apnea
areflexia
arm atrophy
arm weakness
arrhythmia, cardiac
arthralgia
arylsulfatase A
ascending paralysis
aspartate aminotransferase
aspartocyclase
aspiration
aspirin
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxic gait
attention deficit disorder with hyperactivity
atypical
audiogram
auditory evoked brainstem potentials
autoimmune disease
autonomic dysfunction
autonomic neuropathy
B 12 deficiency
Babinski sign
bacterial infection
baldness
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basement membrane
basement membrane thickening
biologic markers
BiPAP
bladder dysfunction
bone marrow biopsy
bradycardia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
bulbar palsy, progressive
burning skin
cachexia
CAG repeats
calcification, intracranial
Canavan's disease
cardiac arrest
cardiac arrest and resuscitation
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, spine
cataracts
cataracts, congenital
cauda equina, enhancement
CD4 counts
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral venous thrombosis
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, women
cervical spine
Charcot-Marie-Tooth
chilbran skin lesions
children
chorea
choreoathetosis
chromosome 12
chromosome 19
chromosome 3
chromosome 5
Clinical Pathologic Conference(C.P.C.)
cognition
coma
complications
confusion
congestive heart failure
consanguinity
copper deficiency
corona radiata
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
cortical blindness
cortical blindness, transient
cortical infarction
cranial nerve enhancement
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
critical care unit
crying, pathologic
cultured skin fibroblasts
cyanosis
cyst
cyst, parenchymal
deafness
deafness, bilateral
deafness, sudden
deep gray nuclei
degenerative diseases of CNS
Dejerine-Sottas syndrome
delayed dentition
dementia
dementia, childhood
dementia, frontotemporal
denervation of muscle
denervation potentials
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diagnostic criteria
diarrhea
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
diffuse idiopathic skeletal hyperostosis
diplopia
diplopia, transient
disability, neurological
distal muscle weakness
disulfiram
drooling
dural sinus thrombosis
dying
dysarthria
dysdiadochokinesia
DYSF gene
dysferlinopathy
dysmetria
dysphagia
dyspnea
dystonia
dystonia, children
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electromyogram
electron microscopy
emotional lability
encephalitis
encephalitis, focal
encephalopathy
encephalopathy, acute
encephalopathy, anoxic
encephalopathy, metabolic
encephalopathy, post anoxic
enzyme treatment
enzyme, defect
enzyme, muscle disease
episodic neurologic deficits
evoked potentials
exercise intolerance
exome sequencing
extraocular muscle lesion
eye movement, disorders of
facial appearance, abnormal
facial nerve palsy
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fever
fibrillations
flail arm syndrome
foot deformity
foot drop
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
frontal lobe, atrophy
frontal lobe, pathologic signs of
fundus, abnormality of
funduscopic exam
gait disorder
gastric partitioning
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
genu of corpus callosum
globus pallidus, hemorrhage
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycogen storage disease
GM1 ganglioside antibodies
gray matter
Guillain Barre syndrome, differential diagnosis of
hand weakness
head bobbing
head circumference
head lag
headache
headache, positional
hearing loss
hearing loss, bilateral
hearing loss, sudden, bilateral
heart block
hemiparesis
hemiparesis, transient
hepatomegaly
heralding manifestation
high arched feet
high arched palate
highly active antiretroviral therapy
hoarseness
hospice
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hypercapnia
hyperhomocysteinemia
hyperpyrexia, CNS disorder causing
hyperreflexia
hypodontia
hypoglycorrhachia
hypomyelination
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunosuppressive agents
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
incoordination
infection
intellectual deficit
intellectual deterioration
interferon alpha
intestinal pseudoobstruction
intrauterine
intrinsic hand muscles, wasting of
irritability
Jakob-Creutzfeldt disease
Japan
Jewish
Kernig's sign
Krabbe's disease
laminar necrosis, cortical
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
Lewy body disease, diffuse
life expectancy
life support, withdrawal of
lobar atrophy
lymphoma
lymphoma involving CNS
lysosomal storage disease
lysosomes, abnoral
macrocephaly
Marinesco-Sjogren syndrome
masseter muscle wasting
MELAS syndrome
memory, impairment of
meningeal biopsy
meningeal enhancement
meningismus
meningitis, melanomatous
mental retardation
merosin
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methylene tetrahydrofolate reductase
methylenetetrahydrofolate reductase deficiency
microangiopathy, brain
microangiopathy, retina
microcephaly
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
Middle east
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoclonal gammopathy
monoparesis
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, functional
MRI, high signal foci on
MRI, negative
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRI, susceptibility weighted
multiple organ failure
multiple sclerosis
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, congenital
muscular dystrophy, limb-girdle
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myopathy
myopathy, acute
myopathy, critically ill
myopathy, drug-induced
myopathy, steroid induced
myopia
myotonia
myotonia dystrophica
nasal speech
nausea and vomiting
neck weakness
nerve biopsy
nerve conduction studies
nerve root enhancement
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic evaluation
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuronal degeneration
neuronopathy
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, sensory
neuroprotective agents
neurotoxic
neurotoxicity, acute
next-generation sequencing
nutritional deficiency
nystagmus
obesity
occipital lobe, lesion of
old age, neurology of
ophthalmoplegia
optic atrophy
optic nerve, hypoplasia of
optic neuropathy
pain
pain, abdominal
pain, foot
paralysis
paralysis, recurrent
paraparesis
paraparesis, spastic
paresthesias
Parkinson disease
pathology
patient information and support
pediatric neurology
percussion induced muscle contraction
persistent vegetative state
personality change
pes cavus
pleocytosis of cerebrospinal fluid
POLR3B
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, critically ill
polyneuropathy, critically ill, children
polyradiculoneuropathy
Pompe's disease of glycogen storage
pons, atrophy
pons, lesion of
posterior column disease
posterior longitudinal ligament, ossification of
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
proximal muscle atrophy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pupil, abnormality in neurologic disorders
pupil, tonic
pyramidal tract dysfunction
quadriparesis
quadriplegia
quadriplegia, transient
ragged-red fibers
rapidly progressing neurologic illness
reading disorder, acquired
recurrent
respirator
respiratory failure
retina, abnormal
retinal artery occlusion
retinal branch artery occlusion
retinal infarction
retinal lesion
retinopathy
retrovirus
reversible neurologic disorder
review article
rigidity
riluzole
risk factors
Rosenthal fibers
rubeola virus
saccadic eye movements, abnormal
Schilder's disease
sedimentation rate, elevated
seizure
seizure, children
sensorineural hearing loss
sensory loss
septicemia
serologic testing
sicca syndrome
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
slit lamp examination
slow virus infection of CNS
small vessel disease
SMN1 gene
spasticity
speech disorder, childhood
spinal cord
spinal cord degeneration
spinal cord, cervical
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinal stenosis
spinal stenosis, cervical canal
splenium of corpus callosum
spondylosis
spongy degeneration of brain
spontaneous remission
staggering
standing difficulty
startle reaction
steroid
steroid therapy, CNS treatment and complications with
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subdural hematoma
superior sagittal sinus thrombosis
sural nerve
survival motor neuron gene
Susac's syndrome
symmetric brain lesions
systemic illness
tandem gait, ataxic
teeth, abnormal
teeth, number of in infants
temporal lobe, atrophy
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
titubation
toe walking
tongue, atrophy
tongue, enlarged
tongue, fasciculations of
tongue, weakness
toxic encephalopathy
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trigeminal neuralgia
trinucleotide repeats
tripping
urinary incontinence
urine test for metabolic disorders
vasculopathy
vein of Galen
vertigo
viral infection
viral infection, CNS
virus, slow
visual acuity, decreased
visual loss
visual tracking
visuospatial disturbance
vitamin deficiency
vitamin E deficiency
Waldenstrom's macroglobulinemia
walking, delayed
walking, difficulty with
weakness
weakness, acute
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
weight loss
wheelchair
white matter disease
white matter disease, periventricular
white matter disease, subcortical
wide based gait
winging of scapula
word-finding difficulty
workup
xerophthalmia
xerostomia
X-linked neuropathy
Showing articles 0 to 50 of 4710 Next >>

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
Neurol 90:518-519, Peddawad, D.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Cerebral White Matter Abnormalities in Patients with Charcot-Marie-Tooth Disease
Ann Neurol 81:147-151, Lee, M.,et al, 2017

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

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
NEJM 371:847-858, Case 27-2014, 2014

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010

Ascending Paralysis from Malignant Leptomeningeal Melanomatosis
JNNP 81:449-450, Burrows,A.M., et al, 2010

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

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: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Neurologic Complications of Gastric Bypass Surgery for Morbid Obesity
Neurol 68:1843-1850, Juhasz-Pocsine,K.,et al, 2007

Clinicopath Conf., Severe Microangiopathy of Diabetic Vasculopathy with Multiple Cerebral Infarcts
NEJM 357:164-173, Case Study 21-2007, 2007

Cerebral Cortical and White Matter Lesions in Amyotrophic Lateral Sclerosis With Dementia; Correlation With MR and Pathologic Examinations
AJNR 28:1505-1510, Matsusue,E.,et al, 2007

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease
Neurol 61:1475-1478, Taylor,R.A.,et al, 2003

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Subacute Sclerosing Panencephalitis Clinical and Magnetic Resonance Imaging Evaluation of 36 Patients
J Child Neurol 17:25-29, Ozturk, A.,et al, 2002

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Reversible ALS-Like Disorder in HIV Infection
Neurol 57:995-1001,945, Moulignier,A.,et al, 2001

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Diagnosis and Treatment of Ossification of the Posterior Longitudinal Ligament of the Spine:8 Cases and Lit Review
Am J Med 92:296-306, Trojan,D.A.,et al, 1992

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

MRI Demonstration of Cortical Laminar Necrosis and Delyaed White Matter Injury in Anoxic Encephalopathy
Neuroradiology 32:319-321, Sawada,H.,et al, 1990

Critical Illness Polyneuropathy:A Complication of Sepsis and Multiple Organ Failure
Brain 110:819-842, Zochodne,D.W.,et al, 1987

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024



Showing articles 0 to 50 of 4710 Next >>