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Differential
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abdominal distention
abscess, intracerebral
abulia
acrocyanosis
acute disseminated encephalomyelitis
addiction, heroin
addiction, heroin-neurologic complications with
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, inappropriate
Aicardi-Goutieres syndrome
akinetic mute
Alexanders disease
Alexanders disease, adult onset
algorithm
amenorrhea
aminoacidopathies
aminoacidurias
amnestic syndrome
amniocentesis
anatomy of
anterior tibial muscle weakness
antiviral agents
aphasia
apraxia
areflexia
arylsulfatase A
arylsulfatase A pseudodeficiency
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
attention deficit disorder with hyperactivity
atypical
auditory evoked brainstem potentials
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bladder dysfunction
blindness
bone biopsy
bone marrow transplantation
bone survey
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brainstem, lesion of
bulbar palsy
burning feet
cachexia
CAG repeats
calcification, intracranial
calcifications, intracranial, punctate
Canavan's disease
carcinoma of pancreas
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
celiac disease, adult
centrum semiovale
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral edema, cytotoxic
cerebral edema, vasogenic
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, pressure increased
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
chemotherapy, CNS treatment and complications with
chilbran skin lesions
children
cholelithiasis
chorea
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
cocaine
Cockayne's syndrome
cognition
color vision
color vision, impaired
coma
complications
confusion
conjunctival biopsy
consanguinity
controversies in neurology
cornea, abnormal
cornea, opacity of
corpus callosum
corpus callosum, hypoplastic
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cranial nerve enhancement
cranial nerve enlargement
creatine phosphokinase(CPK)elevated
cry, abnormal
crying
crying, pathologic
cultured skin fibroblasts
Cushing's syndrome
cyst, bone
cyst, parenchymal
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
delayed dentition
dementia
dementia, childhood
dementia, frontal lobe type
dementia, presenile
dementia, subcortical
dementia, thalamic
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
diarrhea
diet
differential diagnosis
difficulty going down stairs
distal muscle weakness
DNA probes
drug abuse
drug abuse, neurologic complications of
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dyscalculia
dysdiadochokinesia
dysmorphic
dysphagia
dyspraxia
dystonia
dystonia, children
dystonia, focal
efficacy
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
emergencies, ocular
empyema, subdural
encephalitis
encephalitis, diagnosis of
encephalitis, viral
encephalopathy
encephalopathy, progressive
enzyme treatment
enzyme, defect
epicanthal folds
epidemiology of neurology
episodic neurologic deficits
erucic acid therapy
evoked potentials
exercise intolerance
exome sequencing
extraocular muscle lesion
Fabry's disease
facial appearance, abnormal
failure to thrive
falling
familial
fatigue
fatty acid, elevated plasma content
feeding disorder
fever
flow study, carotid artery
fluorescein angiography
fracture, pathologic
frontal lobe, anatomy and physiology
frontal lobe, behavior with disease of
frontal lobe, lesion of
frontal lobe, pathologic signs of
gadolinium
gait disorder
gait, spastic
galactocerebrosidase
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis, generalized
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
GFAP gene
glioma
globoid cells
growth hormone deficiency
Hallervorden Spatz disease
hallucination
hallucination, auditory
hands, fisted
handwriting
head circumference
head lag
head nodding
headache
hearing loss
hearing problems in children
hemiparesis
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
heralding manifestation
high arched feet
hormone replacement
Hurler's syndrome
hydrocephalus
hydrocephalus, exvacuo
hyperadrenalism
hyperparathyroidism
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypersomnia
hyperthyroidism
hypertonia
hypodontia
hypoglycemia
hypogonadism
hypomyelination
hypoparathyroidism
hypothyroidism
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunofluorescent exam of CSF cells
immunosuppressive agents
inattention
inborn errors of metabolism
inclusion bodies, intracytopasmic
incoordination
intellectual deficit
intellectual deterioration
intelligence testing in children
interferon alpha
internal capsule
intestinal pseudoobstruction
intrathecal chemotherapy
intrauterine
irritability
Kearns-Sayre syndrome
Krabbe's disease
lactic acidemia
lacunar infarction
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukodystrophy, 4H
leukodystrophy, pigmented orthochromatic
leukoencephalitis, acute necrotizing hemorrhagic
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
leukoencephalopathy, toxic
level of consciousness, decreased
lipid storage disorder of CNS
lipomembranous polycystic osteodysplasia
liver transplantation
Lorenzo's oil
lysosomal storage disease
lysosomes, abnoral
macrocephaly
meconium staining
medulla oblongata, lesion of
MELAS syndrome
memory, impairment of
meningitis
meningitis, aseptic
meningitis, leptospira
meningitis, noninfectious
meningoencephalitis
meningoencephalitis, diagnosis of
mental retardation
mental status, abnormal
merosin
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
methotrexate
microcephaly
microdontia
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, spinal cord
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, cognitive presenttion
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
mumps virus
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, congenital
muscular dystrophy, Duchenne
myelin basic protein
myelinolysis, extrapontine
myelomalacia
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
myopia
N-acetyl-L-aspartic acid
nausea and vomiting
neoplasm, intracranial
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroaxonal leukodystrophy
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neurologic testing
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, peripheral
neuropsychiatry
neurotoxic
neurotoxin
next-generation sequencing
Niemann-Pick disease
nystagmus
nystagmus, pendular
nystagmus, primary position of gaze
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
occupational neurologic disorders
oculodentodigital dysplasia
oleic acid therapy
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
optic nerve, lesion of
organ transplantation
ovarian dysgenesis
pain, abdominal
palatal myoclonus
palmoplantar keratoderma
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paroxysmal neurologic deficits
PAS positive material in the brain
Pelizaeus Merzbacher
penicillamine
pernicious anemia
peroxisomal disease
personality change
pes cavus
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLR3B
pons, lesion of
porphyria
posterior fossa, lesion of
prenatal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
progressive myoclonic epilepsy
progressive neurologic disorder
pseudobulbar palsy
psychiatric manifestations of brain tumors
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
psychosis, cause of
pterygoid muscle weakness
ptosis
pyramidal
pyramidal tract
pyramidal tract dysfunction
pyrimethamine
quadriparesis
radiation therapy, CNS treatment and complications with
radioimmunoassay
ragged-red fibers
renal failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinal ischemia
retinal lesion
retinal vasculitis
retinal vasculopathy
retinal vasculopathy with cerebral leukodystrophy
retinopathy
review article
RFLPs
rigidity
Rosenthal fibers
rubeola virus
safety
Salla disease
Sandhoff's disease
Schilder's disease
schizophrenia
seizure
sensorineural hearing loss
sensory loss
short stature
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
solvent
somatosensory evoked potentials
somnolence
spasticity
speech disorder
speech disorder, childhood
sphingolipodoses
spinal cord
spinal cord, lesion of
spinal cord, pathologic exam of
spongy degeneration of brain
startle reaction
stem cell transplantation
steroid therapy, CNS treatment and complications with
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subcortical U fibers
succinate dehydrogenase deficiency
sudanophilic leukodystrophy
sural nerve
symmetric brain lesions
syndactyly
syphilis, neurologic complications with
systemic illness
systemic lupus erythematosus
tacrolimus
tandem gait, ataxic
Tay-Sachs disease
teeth, abnormal
teeth, number of in infants
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular atrophy
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
titubation
toe walking
tonic spasms
top of the basilar syndrome
toxins, nervous system
transient neurologic deficit
transitional sclerosis
treatment of neurologic disorder
tremor
tremor, intention
tripping
umbilical-cord blood transplantation
uncal herniation
urea-cycle enzymopathies
urinary incontinence
urinary sulfatidase excretion
urine test for metabolic disorders
uveitis
vanishing white matter
very long chain fatty acids
vibratory sensation, abnormal
viral infection, CNS
visual evoked response
visual field defect
visual loss
visual loss, slow
walking, delayed
walking, difficulty with
Wallerian degeneration
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
Wernicke's encephalopathy
white matter disease
white matter disease, pattern
white matter disease, periventricular
white matter disease, unilateral
wide based gait
writing
Showing articles 0 to 50 of 146 Next >>

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Lentiviral Haematopoietic stem-cell gene therapy for early-onset metachromatic leukodystrophy: long-term results from a non-randomised, open-label, phase 1/2 trial and expanded access
Lancet 399:372-383, Fumagalli, F.,et al, 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Bilateral Temporal Pole Involvement in Adult-Onset X-Linked Adrenoleukodystrophy
JAMA Neurol 78:367-368, Liu, M.,et al, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

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

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Spinal Cord Involvement in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
JAMA Neurol 77:1169-1170, Li, S.,et al, 2020

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

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

A Rare Case of Metachromatic Leukodystrophy with Multiple Bilateral Cranial Nerve Enhancement
Neurol 93:e1742-e1743, Sonowal, P.,et al, 2019

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

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

A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
Ann Neurol 79:507-519, Vodopivec, I.,et al, 2016

Long-Term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Juvenile Metachromatic Leukodystrophy Compared with Nontransplanted Control Patients
JAMA Neurol 73:1133-1140, Groeschel, S.,et al, 2016

Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease
Neurol 82:49-56, Graff-Radford, J.,et al, 2014

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
Adams & Victors Principles of Neurology, Chp 37, pg 959, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Metachromatic Leukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 971, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Intracranial Optic Nerve Enlargement in Infantile Krabbe Disease
Neurol 78: e126, Shah, S.,et al, 2012

Unilateral White Matter Involvement in Krabbe Disease
Arch Neurol 68:130-131, Lemmens,R.,et al, 2011

Patient with Unilateral White Matter Involvement Does Not Have Krabbe Disease
Arch Neurol 68:1345, Van der Knaap, M.S. and Wenger, D.A., 2011

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

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

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

Leukodystrophies: Classification, Diagnosis, and Treatment
Neurologist 15:319-328, Costello,D.,et al, 2009

Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
Neurol 71:925-929, Van Gerpen,J.A.,et al, 2008

Sporadic Adult-Onset Leukoencephalopathy with Neuroaxonal Spheroids Mimicking Cerebral MS
Neurol 70:1128-1133, Keegan,B.M.,et al, 2008

Adult-Onset Vanishing White Matter Leukoencephalopathy Presenting as Psychosis
Neurol 68:1538-1539, Denier,C.,et al, 2007

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia
AJNR 27:1037-1039, Mascalchi,M.,et al, 2006

Peripheral Neuropathy in Krabbe Disease. Effect of Hematopoietic Stem Cell Transplantation
Neurol 67:268-272, Siddiqi, Z.A.,et al, 2006

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

Diffusion-Weighted MR Imaging in Leukodystrophies
Eur Radiol 15:2284-2303, Patay,Z., 2005

Unusual Variants of Alexander's Disease
Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Diffusion-Weighted Imaging Findings in Juvenile Metachromatic Leukodystrophy
Neuropediatrics 35:279-282, Oguz,K.K.,et al, 2004

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Metachromatic Leukodystrophy:Diffusion MR Imaging Findings
AJNR 23:1424-1426, Sener,R.N., 2002

Toxic Leukoencephalopathy
NEJM 345:425-432, Filley,C.M. &Kleinschmidt-DeMasters,B.K., 2001

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Long-term Effect of Bone-marrow Transplantation for Childhood-onset Cerebral X-linked Adrenoleukodystrophy
Lancet 356:713-718, Shapiro,E. et al, 2000

MR Imaging and Proton MR Spectorscopy in Adult Krabbe Disease
AJNR 21:1478-1482, Farina,L. et al, 2000



Showing articles 0 to 50 of 146 Next >>