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acrocyanosis
advances in neurology
affect, flat
aggression
agitation
Aicardi-Goutieres syndrome
alcohol
alternative medicine
alveolar hypoventilation
aminoacidurias
Angelman syndrome
ankle, swelling of
anxiety
aphasia
aphasia, children
apraxia, speech
arylsulfatase A
ascites
Asperger's syndrome
ataxia
ataxia, cerebellar
ataxia, truncal
ataxic gait
attention deficit disorder with hyperactivity
attention span
atypical
audiologic test to localize site of pathology
audiology
auditory processing, impaired
autism
autism, screening for
autoantibodies
autoimmune disease
automatism, postictal
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior
behavior, combative
behavioral disorder
Benedict's solution test
bifid uvula
brachial plexus neuropathy, children
brachycephaly
bradykinesia
brain atrophy
bruxism
calcification, intracranial
calf hypertrophy
carcinoma
CAT scan, abnormal
catatonia
cerebellar atrophy, primary
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar mutism
cerebellum, neoplasms of
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
chilbran skin lesions
children
chorea
chorea, Sydenham's
choreoathetosis
chromosomal abnormality
chromosome 15
chromosome 7
cleft palate
cochlear implant
cognition
comorbidities
complications
comprehension, impaired
compulsivity
confusion
congenital bilateral perisylvian syndrome
consanguinity
contractures, joint
creatine phosphokinase(CPK)elevated
deafness
deafness, congenital
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dentate nuclei, lesion of
depression
developmental disability
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
dichotic hearing
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
disorientation
dopa responsive dystonia
drooling
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyslexia
dysmorphic
dysphagia
dysplasia of C.N.S.
dyspraxia
dystonia
dystonia, children
dystrophin
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, depth electrode
electroencephalogram, sleep
electromyogram
ELISA
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, viral
encephalopathy
encephalopathy, progressive
enuresis
enzyme, defect
epidemiology of neurology
epsilon sarcoglycan gene
face, inexpressive
facial appearance, abnormal
facial expression abnormality
facial weakness, bilateral
falling
familial
fatigue
feeding disorder
ferric chloride test
fetal alcohol syndrome
fetus
fever
fine motor function, impaired
fish
fluorescene in situ hybridization
folic acid
gait disorder
gait, apraxic
galactorrhea
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
globus pallidus
globus pallidus, lesion of
Gowers maneuver
grimacing
growth retardation
Hallervorden Spatz disease
head circumference
head lag
hearing loss
hearing problems in children
hemichorea
hepatolenticular degeneration(Wilson's disease)
hippocampus
Huntington's chorea
hyperactivity
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
immunosuppression
immunosuppressive agents
inattention
insomnia
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
interferon alpha
intrauterine
iron, brain
irritability
jaundice
karyotyping
klippel feil syndrome
Landau-Kleffner syndrome
language
language delay
language development, neurologic basis of
language disorder in adults
language disorders in children
laughing, pathologic
L-dopa
learning disability
learning disability, in children
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
liver function enzymes
macrocephaly
macrognathia
magnetic source image
magnetoencephalography
maple syrup urine disease
medulloblastoma
megalencephaly
megalencephaly, idiopathic
memory, defect of recent
memory, impairment of
mental retardation
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
microcephaly
midline defect in children
misdiagnosis
monoclonal antibodies
mood change
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abdomen
MRI, abnormal
MRI, diffusion tensor
MRI, disappearing lesion on
MRI, functional
MRI, negative
MRI, paramagnetic effect
MRI, pelvis
muscle stiffness
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
mutism
myelodysplasia
myoclonic dystonia
myoclonus
myoclonus, action
myoglobinuria
nasal speech
neoplasm, posterior fossa
neoplasm, primary of CNS-children
nerve biopsy
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic evaluation
neurologic testing
neuropathology
neuropathology, brain
NMDA antagonists
nonverbal
nystagmus
opened mouth
operculum syndrome
operculum syndrome, bilateral
opisthotonus
optic atrophy
palatopharyngeal incompetence
PANK2 mutation
paraphasias
personality change
phenylketonuria
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
postictal neurologic deficits
postural abnormality
pregnancy, neurologic complications in
prenatal
prevention of neurologic disorders
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
pruritus
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
pure word deafness
pyramidal tract
pyramidal tract dysfunction
release phenomena
remote effect of cancer on the nervous system
respirations in CNS disease
respirator
retinitis pigmentosa
Rett's syndrome
review article
rhabdomyolysis
rheumatic brain disease
rheumatic fever
rheumatic heart disease
rigidity
risk factors
rituximab
rocking
scoliosis
screening
sea-blue histiocytes
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, focus
seizure, psychomotor-temporal lobe
seizure, psychosocial aspects of
seizure, recurrent
seizure, surgical treatment of
seizure, treatment of
seizure, workup of
sexual behavior, disorder of
sign language
skin, lesions in neurologic disorders
sleep pathology and physiology
smiling
socialisation
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech lateralization
speech therapy
speech, delayed development of
speech, slowed
spina bifida
stammering
startle reaction
stereotyped behavior, drug induced
stuttering
substantia nigra
symmetric brain lesions
systemic illness
teeth, wide-spaced
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
titubation
tongue, impaired movements of
tongue, protrusion of
treatment of neurologic disorder
tremor
tremor, intention
tripping
tyrosine hydroxylase deficiency
urine test for metabolic disorders
urine, dark
visual evoked response
visual impairment
vitamin supplementation
weakness, progressive
weight loss
wheelchair
white matter disease
workup
Showing articles 200 to 250 of 18014 << Previous Next >>

Pontine Tegmental Cap Dysplasia in a Neonate
Neuol 91:e2100-e2101, Bilgin, N.,et al, 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

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

Patent Foramen Ovale Closure, Antiplatelet Therapy or Anticoagulation Therapy Alone for Management of Cryptogenic Stroke?
BMJ 362:k2515, Kuijpers, T.,et al, 2018

Proptosis and Double Vision in a Child
JAMA Neurol 75:1142-1143, Lu, A.J.,et al, 2018

Trial of Fingolimod Versus Interferon Beta-1a in Pediatric Multiple Sclerosis
NEJM 379:1017-1027, Chitnis, T.,et al, 2018

Distinctive Imaging in a Paucisymptomatic Child with Leukodystrophy
Neruol 91:e1368-e1369, Sharawat, I.K.,et al, 2018

Abdominal Migraine
BMJ 360;k179, Angus-Leppan, H.,et al, 2018

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Cranial Cavernous Malformations
Stroke 49:1029-1035, Stapleton, C.J. & Barker, F.G., 2018

Recurrent Ischemic and Hemorrhagic Strokes in a Young Adult
JAMA Neurol 75:628-629, Rocha, E.A. & Singhal, A.B., 2018

Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018

Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
Neurol 90:974-976, Ishiyama, A.,et al, 2018

Neurologic Outcomes in Pediatric Cardiac Arrest Survivors Enrolled in the THAPCA trials
Neurol 91:e123-e131, Ichord, R.,et al, 2018

Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
Neurol 91:98-101, Marques-Matos, C.,et al, 2018

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

Pediatric HIV Infection: Classification, Clinical Manifestations, and Outcome
www.UptoDate.com, June, Gillespie, S.L., 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,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

Unique Gadolinium Enhancement Pattern in Spinal Dural Arteriovenous Fistulas
JAMA Neurol 75:1542-1545, Zalewski, N.L.,et al, 2018

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

Papillary Fibroelastoma, Unusual Cause of Stroke in a Young Man
J Cardiothorac Surg 12:33, Grolla, E.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

A 61-year-old woman with Lower Extremity Paralysis and Sensory Loss
Neurol 89:e257-e263, Manners, J.,et al, 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

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

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

Surgery for Drug-Resistant Epilepsy in Children
NEJM 377:1639-1647, Dwivedi, R.,et al, 2017

Maternal Use of antiepileptic Agents During Pregnancy and Major Congenital Malformations in Children
JAMA 318:1700-1701, Bromley, R.L.,et al, 2017

Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
Neurol 88:e26-e29, Qin, C.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Pregnancy, Hormonal Treatments for Infertility, Contraception, and Menopause in Women After Ischemic Stroke
Stroke 48:501-506, Caso, V.,et al, 2017

"Phacing" a New Cause of Carotid Artery Dissection
Neurologist 22:54-56, Kulyk, C.,et al, 2017

Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
NEJM 376:972-980, Case 7-2017, 2017

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

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

The Tadpole Pupil
JAMA Neurol 74:481, Aggarwal, K. & Hildebrand, G.D., 2017

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

Intracranial Dural Arteriovenous Fistulae
Stroke 48:1424-1431, Reynolds, M.R.,et al, 2017

Primary Angiitis of the Central Nervous System
Stroke 48:1248-1255, Boulouis, G.,et al, 2017



Showing articles 200 to 250 of 18014 << Previous Next >>