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Differential
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acromicria
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
advances in neurology
affect, inappropriate
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
Angelman syndrome
antidepressant
antitoxin
apnea
applause sign
arm weakness
aspiration
ataxia
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
behavior, combative
behavioral disorder
BiPAP
blindness
bone marrow transplantation
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brainstem, infarction of
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
cachexia
calcification, intracranial
caries
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cerebral dominance
cerebrovascular accident
cerebrovascular accident, bilateral
children
chromosomal abnormality
chromosome 15
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
constipation
contractures, joint
conversion reaction
cortical blindness
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
crying, pathologic
cryptorchidism
cultured skin fibroblasts
deafness
decerebrate posture
degenerative diseases of CNS
dementia
dementia, frontotemporal
depression
developmental disability
developmental retardation
differential diagnosis
disability rating scale, neurological
disability, neurological
distal muscle weakness
drooling
dying
dysarthria
dysmorphic
dysphagia
dysphonia
dystonia
dystonia, cervical
eating disorder
efficacy
electroencephalogram, abnormalities of
electromyogram
emotional lability
epidemiology of neurology
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fibrillations
flail arm syndrome
floppy infant
fluoxetine
food poisoning
food-borne infection
foot drop
gait disorder
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
growth hormone deficiency
growth retardation
hand flapping
head bobbing
hearing loss
hemiparesis
heralding manifestation
honey
hospice
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypertension
hypogonadism
hypometric saccades
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
imbalance
inappropriate antidiuretic(A.D.H.)hormone
infant, evaluation of
intellectual deficit
intellectual deterioration
internal capsule
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
intubation
irritability
irritable baby
jaw jerk, abnormal
laughing, pathologic
leg weakness, unilateral
lethargy
leukodystrophy
life expectancy
locked-in syndrome
masked facies
mental retardation
merosin
mimics
misdiagnosis
molecular genetics
monoparesis
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, mouse ears
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle cramp
muscle wasting, diffuse
muscular dystrophy
muscular dystrophy, congenital
mutism
neck weakness
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuroprotective agents
neurotoxin
obesity
ocular bobbing
opened mouth
ophthalmoplegia
optic neuropathy
palliative care
paraparesis, spastic
Parkinsonism syndrome
peroxisomal disease
personality change
photosensitivity, skin
pigmentary retinopathy
polymerase chain reaction
polymicrogyria
pons, infarction of
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychomotor retardation
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
rash
respirator
respiratory arrest
respiratory failure
retinopathy
review article
riluzole
risk factors
saccadic eye movements, abnormal
seizure
sensorineural hearing loss
sertraline
short stature
skew deviation
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
spasticity
speech disorder
speech, loss of
stooped posture
strabismus
suck, poor
symmetric brain lesions
tachycardia
temper tantrums
term infant
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, protrusion of
toxins, nervous system
tracheostomy
trauma
treatment of neurologic disorder
tremulousness
tripping
very long chain fatty acids
walking, difficulty with
weakness
weakness, generalized
weakness, infant
wheelchair
white matter disease
wide based gait
Showing articles 0 to 50 of 2522 Next >>

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Pharmaceutical Interventions for Emotionalism After Stroke
Stroke 54:e213-e214, Hackett,M.L.,et al, 2023

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

My Weeping Patient
Neurol 89:e202, Peters, J.,et al, 2017

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

Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1096, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

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

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Human Botulism Immune Globulin for the Treatment of Infant Botulism
NEJM 354:462-471, Arnon,S.S.,et al, 2006

Case 35-2006: A Newborn Boy with Hypotonia
NEJM 355:2132-2142, Brown,R.H.,et al, 2006

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Infant Botulism:A Review of 12 Years'Experience at the Children; s Hosp of Phila
Pediatrics 87:159-165, Schreiner,M.S.,et al, 1991

Emotionalism after Stroke
BMJ 298:991-994, House,A.,et al, 1989

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Pathological Laughter & Crying
In Frederiks, J. A. M. (Ed) Handbook of Clinical Neurology, Elsevier Science Publ, 45:219, Poeck,K., 1985

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Clinical and Imaging Features of Cobb Syndrome
Neurol 102:e208118, Yang,X.,et al, 2024

Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024

Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

Progressive Hemiparesis and White Matter Abnormalities in an HIV-Negative Patient
Neurol 100:1156-1163, Jabbari,E.,et al, 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

A 40-Year-Old Woman Presenting with Encepatholopathy and Paraparesis
Neurol 101:e94-e98, AlSabah,A.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Clinical Features and Diagnosis of Intramedullary Spinal Cord Abscess in Adults, A Systematic Review
Neurol 101:e836-e844, Harrold,G.K.,et al, 2023

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

A Woman With Multifocal Ischemic Strokes and Progressive Cognitive Impairment Due to Intravascular Lymphoma
Stroke 54:e488-e451, Stamm,B., et al, 2023

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

MR Imaging Patterns and Prognosis in Powassan Virus Encephalitis
Neurologist doi.10.1097/NRI.0000000000000533, Finelli,P.F., 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

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

Cerebral Alveolar Echinococcosis
NEJM 388:453, Ju,H. & Liu,C., 2023

Cashew Nut Sign:A Concave Parenchymal Hemorrhage Caused by Cerebral Venous Thrombosis
Stroke 54:e38-e39, Schlechter,M.,et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Occult Breast Cancer with Anti-Ri Antibody Positivity and Pontine Hot Cross Bun Sign
JAMA Neurol 80:207-208, Liu,Y.,et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Clinicopathological Conference, Systemic Lupus Erythematosus with Antiphospholipid Syndrome
NEJM 386:1560-1570, Case 12-2022, 2022



Showing articles 0 to 50 of 2522 Next >>