Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
achilles tendon, enlarged
acromicria
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adult polyglucosan body disease
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
asymmetric crying facies
ataxia
autonomic dysfunction
axonal degeneration
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
behavior, combative
behavioral disorder
BiPAP
bladder dysfunction
blindness
bone marrow transplantation
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brainstem, infarction of
brainstem, lesion 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
congenital birth defects
congenital heart disease
congenital malformation
constipation
contractures, joint
conversion reaction
cortical blindness
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
crying, pathologic
cryptorchidism
cultured skin fibroblasts
cystatin C mutation
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
dysdiadochokinesia
dysmorphic
dysphagia
dysphonia
dystonia
dystonia, cervical
eating disorder
echocardiogram
efficacy
electroencephalogram, abnormalities of
electromyogram
emotional lability
epidemiology of neurology
Erdheim-Chester disease
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
facial asymmetry
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fibrillations
flail arm syndrome
floppy infant
fluoxetine
foam cells
food poisoning
food-borne infection
foot drop
gait disorder
gait, spastic
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen storage disease
growth hormone deficiency
growth retardation
hand flapping
head bobbing
hearing loss
heel swelling
hemiparesis
heralding manifestation
histiocytosis
honey
hospice
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypertension
hypogonadism
hypometric saccades
hypopigmentation of skin
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
inappropriate antidiuretic(A.D.H.)hormone
inclusion bodies
infant, evaluation of
intellectual deficit
intellectual deterioration
internal capsule
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
intubation
irritability
irritable baby
jaw jerk, abnormal
Jewish
laughing
laughing, pathologic
leg weakness, unilateral
lethargy
leukodystrophy
leukoencephalopathy
life expectancy
locked-in syndrome
masked facies
memory, defect of recent
memory, impairment of
mental retardation
merosin
middle cerebellar peduncle, lesion
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
myelomalacia
myeloneuropathy
neck weakness
neurogenic bladder
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuropathy
neuroprotective agents
neurotoxin
next-generation sequencing
obesity
ocular bobbing
opened mouth
ophthalmoplegia
optic neuropathy
palliative care
paraparesis, spastic
Parkinsonism syndrome
pathologic reflex
peroxisomal disease
personality change
photosensitivity, skin
pigmentary retinopathy
polyglucosan body
polyglucosan body disease
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
radiculopathy
rash
release phenomena
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
systemic illness
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
ultrasonography
urinary incontinence
very long chain fatty acids
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
wheelchair
white matter disease
wide based gait
Showing articles 950 to 1000 of 2560 << Previous Next >>

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Drug Points, Transient Hemiparesis with Topiramate
BMJ 318:845, Stephen,L.J.,et al, 1999

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

Pain and the Guillain-Barre Syndrome in Children Under 6 Years
J Pediatr 134:773-776, Nguyen,D.K.,et al, 1999

Spinal Cord Schistosomiasis, A Report of 2 Cases and Review Emphasizing Clinical Aspects
Medicine 78:176-190, Ferrari,T.C.A., 1999

Signs and Symptoms of Duchenne Muscular Dystrophny and Becker Muscular Dystrophy Among Carriers in the Netherlands: A Cohort Study
Lancet 353:2116-2119, Hoogerwaard,E.M.,et al, 1999

Focal, Steroid Responsive Myositis Causing Dropped Head Syndrome
Muscle & Nerve 22:769-771, Biran,I.,et al, 1999

Generalised Muscular Weakness after Botulinum Toxin Injections for Dystonia:A Report of Three Cases
JNNP 67:90-93, Bhatia,K.P.,et al, 1999

Posttraumatic Syringomyelia:Pathogenesis, Imaging, and Treatment
AJR 173:487-492, Schwartz,E.D.,et al, 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Demyelinative Brainstem Encephalitis Responsive to Intravenous Immunoglobulin Therapy
Pediatrics 104:301-304, Assa,A.,et al, 1999

Intravenous Immunoglobulin Treatment in Neurologic Disorders
Arch Neurol 56:1025-1027,1032, Sorensen,P.S., 1999

Is the Routine Use of Intravenous Immunoglobulin Treatment in Neurologic Disorders Justified?
Arch Neurol 56:1028-1032, Karussis,D.&Abramsky,O., 1999

Tracheostomy, In Guillain- Barre Syndrome
Muscle & Nerve 22:1058-1062, Lawn,N.D.&Wijdicks,E.F.M., 1999

Prognostic Factors of Guillain-Barre Syndrome After Intravenous Immunoglobulin or Plasma Exchange?
Neurol 53:598-604, Visser,L.H.,et al, 1999

Amyloid Myopathy:An Underdiagnosed Entity
Ann Neurol 43:719-728, Spuler,S.,et al, 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

Neurologic Complications Associated with Hepatitis C Virus Infection
Neurol 53:861-864, Tembl,J.I.,et al, 1999

Adult-Onset "Infant" Botulism:An Unusual Cause of Weakness in the Intensive Care Unit
Neurol 53:891, Li,L.Y.J.,et al, 1999

The Clinical Course of Neuromyelitis Optica (Devic's Syndrome)
Neurol 53:1107-1114, Wingerchuk,D.M.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Brachial Amyotrophic Diplegia, A Slowly Progressive Motor Neuron Disorder
Neurol 53:1071-1076, Katz,J.S.,et al, 1999

Neurologic Manifestations of Compressive Radiculopathy of the First Thoracic Root
Neurol 53:1149-1151, Levin,K.H., 1999

A Man with Progressive Weakness in His Legs
Lancet 354:830, van der Meulen,M.F.G.,et al, 1999

MR Appearance of an Intracranial Dural Arteriovenous Fistula Leading to Cervical Myelopathy
Neurol 51:1131-1135, Hahnel,S.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

A 29-Year-Old Man with Multiple Sclerosis
JAMA 280:1432-1439, Rudick,R.A., 1998

Pertussis Encephalopathy with High Cerebrospinal Fluid Antibody Titers to Pertussis Toxin and Filamentous Hemagglutinin
Pediatrics 102:986-990, Grant,C.C.,et al, 1998

Anterior Spinal Artery Syndrome Associated with Severe Stenosis of the Vertebral Artery
AJNR 19:1353-1355, Suzuki,K.,et al, 1998

Transdural Spinal Cord Herniation:Imaging and Clinical Spectra
AJNR 19:1337-1344, 11851998., Watters,M.R.,et al, 1998

Clinicopath Conf
Wegener's Granulomatosis Involving Sinuses, Skull, and Cranial Nerves, Case 28-1998, NEJM 339:755-76, , 199, 1998

Varicella Zoster Virus-Associated Focal Vasculitis Without Herpes Zoster:Recovery After Treatment with Acyclovir
Neurol 51:914-915, Nau,R.,et al, 1998

Basilar Artery Occlusion Associated with Pathological Crying:'Folles Larmes Prodromiques'
Neurol 51:916-917, Larner,A.J., 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Minimal Number of Plasma Exchanges Needed to Reduce Immunoglobulin in Guillain-Barre Syndrome
Neurol 51:875-877, Yuki,N.,et al, 1998

Myasthenic Hand
Neurol 51:913-914, Janssen,J.C.,et al, 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

Paraneoplastic Necrotizing Myopathy, Clinical and Pathologic Features
Neurol 50:764-767, Levin,M.I.,et al, 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Acute Myopathy After Liver Transplantation
Neurol 50:46-53, Campellone,J.V.,et al, 1998

Secondary Hyperkalaemic Paralysis
JNNP 64:249-252, Evers,S.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Clinicopath Conf
Demyelinating Process Consistent with Multiple Sclerosis, Case 26-1998, NEJM 339:542-549998., , 1998

Mortality in People Taking Selegiline:Observational Study
BMJ 317:252-254, Thorogood,M.,et al, 1998

Incoordination in Patients with Overuse Syndrome
Neurol 51:512-519, Fry,H.J.H.,et al, 1998

Clinicopath Conf
Chronic Inflammatory Demyelinating Polyneuropathy, Case 13-1998, NEJM 338:1212-1219998., , 1998

Facial Nerve is Liable to Pressure Palsy
Neurol 51:320-322, Foloni,T.E.,et al, 1998

Isolated Weakness of the Fingers in Cortical Infarction
Neurol 50:823-824, Lee,P.,et al, 1998

Respiratory Management in Acute Neurologic Illness
Neurol 50:11-20, Wijdicks,E.F.M.&Borel,C.O., 1998



Showing articles 950 to 1000 of 2560 << Previous Next >>