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acanthocytosis
acetazolamide
acid maltase deficiency
adrenoleukodystrophy
advances in neurology
adverse drug reaction
airway obstruction
alveolar hypoventilation
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anesthesia, general
anterior tibial muscle weakness
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticonvulsants
antihistamines
aqueduct of Sylvius, stenosis
aqueductal stenosis
arrhythmia, cardiac
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, paroxysmal
autoimmune disease
automatic implantable cardioverter-defibrillator
baldness
Bassen-Kornzweig syndrome
benign congenital hypotonia
blindness
botulism
brainstem, lesion of
calcium antagonist
calcium channel dysfunction
carbamazepine
carcinoma
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
cataracts, congenital
central core disease
central nervous system, infection of
cerebellar hypoplasia
cerebral cortical atrophy
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
chromosomal abnormality
chromosome 1
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Coats syndrome
Cockayne's syndrome
complications
conduction block
congenital birth defects
congenital heart disease
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
controversies in neurology
cornea, abnormal
cornea, opacity of
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
cry, weak
deafmute
deafness
degenerative diseases of CNS
developmental disability
developmental milestones
developmental retardation
differential diagnosis
dilantin
disability, neurological
distal muscle weakness
dropped head syndrome
drug induced neurologic disorders
dwarfism
dystroglycanopathies
dystrophin
dystrophin associated proteins
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
epidemiology of neurology
eye closure
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
familial hemiplegic migraine
Fazio-Londe's disease
feeding disorder
fetal movements, reduced
fetus
floppy infant
foot drop
Friedreich's ataxia
frontal balding
gait disorder
gargoylism
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glaucoma
glycosyltransferase
Gowers maneuver
Hallgren's syndrome
heart block
heavy metal intoxication
high arched feet
high arched palate
histochemistry
histochemistry of muscle
Huntington's chorea
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hyperkalemic periodic paralysis
hypokalemia
hypokalemic periodic paralysis
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
joint hypermobility
kaliuresis
Kearns-Sayre syndrome
keratoconus
Kugelberg-Welander syndrome
laminopathies
Laurence-Moon-Bardet-Biedl syndrome
leukodystrophy
lid closure, weakness of
life expectancy
lissencephaly
LMNA gene
lordosis
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
Melkersson's syndrome
mental retardation
merosin
metabolic acidosis
mexiletine
micrognathia
micropthalmia
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
motor neuron disease
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, muscle
MRI, serial
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, LAMA2
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopia
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia, treatment of
neck weakness
nemaline rod myopathy
neoplasm, metastatic to CNS
neoplasm, primary of CNS
neuritis
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuropathology, brain
neuropathy
newborn, evaluation of
nifedipine
obesity
ocular myopathy
oculopharyngeal muscular dystrophy
opened mouth
ophthalmoplegia
Oppenheim muscular dystrophy
orbicularis oculi muscle
pacemaker, cardiac-transvenous
paramyotonia congenita
paresthesias
paroxysmal neurologic deficits
percussion induced muscle contraction
periodic paralysis
poison, mercury
poison, neurologic problems with
polydactyly
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymicrogyria
polymyositis
polymyositis, infantile
postoperative neurologic complications
potassium channel antibodies
potassium channel dysfunction
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
procainamide
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
psychomotor retardation
ptosis
quality of life
respirator
respiratory failure
retinal detachment
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
rhabdomyolysis
rigid spine syndrome
schizophrenia
scoliosis
seizure
skin, biopsy
sloped shoulders
sodium channel dysfunction
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
steroid
suck, poor
sudden death
syncope
systemic illness
temporalis muscle wasting
term infant
tocainide
transverse smile
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
ultrasonography
Usher's syndrome
viral infection, CNS
visual field defect
visual fields, constricted
vital capacity
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weaning from respirator, failure to
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
wide based gait
winging of scapula
workup
x-linked hydrocephalus
x-linked mental retardation
Showing articles 1000 to 1050 of 1896 << Previous Next >>

The Spectrum of Brain MR Abnormalities in Sickle-Cell Disease:A Report from the Cooperative Study of Sickle Cell Disease
AJNR 17:965-972, Moser,F.G.,et al, 1996

Brain and Spinal Cord MRI in Motor Neuron Disease
JNNP 61:314-317, Thorpe,J.W.,et al, 1996

Amyotrophic Lateral Sclerosis and Occupational History
Arch Neurol 53:730-733, Strickland,D.,et al, 1996

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Pituitary Enlargement on Magnetic Resonance Imaging in Congenital Hypothyroidism
Arch Pediatr Adolesc Med 150:623-628, Desai,M.P.,et al, 1996

The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
NEJM 334:821-827, 8571996., Reuss,M.L.,et al, 1996

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Motor Neuron Disease:A Paraneoplastic Process Associated with Anti-Hu Antibody and Small-Cell Lung Carcinoma
Ann Neurol 40:112-116, Verma,A.,et al, 1996

Development of General Weakness in a Patient with Amyotrophic Lateral Sclerosis after Focal Botulinum Toxin Injection
Neurol 46:845-846, Mezaki,T.,et al, 1996

Three-Dimensional CT Angiography in the Detection and Characterization of Intracranial Berry Aneurysms
AJNR 17:439-445, Hope,J.K.A.,et al, 1996

Cerebral Aneurysms:Evaluation with Three-Dimensional CT Angiography
AJNR 17:447-454, Ogawa,T.,et al, 1996

X-Linked Malformation of Neuronal Migration
Neurol 47:331-339, Dobyns,W.B.,et al, 1996

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

MR Evaluation of Patients with Congenital Hyposmia or Anosmia
AJR 166:439-443, Yousem,D.M.,et al, 1996

Is Marfan Syndrome Associated with Symptomatic Intracranial Aneurysms?
Stroke 27:10-12, van den Berg,J.S.P.,et al, 1996

Stroke in Williams Syndrome
Stroke 27:143-146, Wollack,J.B.,et al, 1996

Congenital Unilateral Facial Paralysis
Pediatrics 97:261-265, Shapiro,N.L.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

MRI of White Matter Changes in the Sjogren-Larsson Syndrome
Neuroradiology 37:576-577, Hussain,M.Z.&Aihara,M., 1996

Aneurysmal Third-Nerve Palsies Presenting with Pleocytosis
Neurol 46:1176, Keane,J.R., 1996

Misdiagnosis of Symptomatic Cerebral Aneurysm Prevalence & Correlation with Outcome at Four Institutions
Stroke 27:1558-1563, Mayer,P.L.,et al, 1996

White Matter MR Hyperintensities in Adult Patients with Congenital Rubella
AJNR 17:99-103, Barton Lane,E.,et al, 1996

Visual Loss after Neurosurgical Repair of Paraclinoid Aneurysms
Ophthalmol 102:905-910, Rizzo,J.F.,III, 1995

Detection and Assessment of Intracranial Aneurysms:Value of CT Angiography with Shaded Surface Display
AJR 165:1497-1502, Liang,E.Y.,et al, 1995

Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
Ann Neurol 38:960-964, North,K.N.,et al, 1995

Effects of HIV on Cognitive & Motor Devel in Children Born to HIV-Seropositive Women with no Reported Drug Use:Birth-24 mo
Pediatrics 96:1078-1082, Gay,C.L.,et al, 1995

Interventional Neuroradiology
BMJ 311:789-792, Taylor,W.&Rodesch,G., 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Relative Pupillary Sparing Third Nerve Palsies:To Arteriogram or Not?
J Neuro-Ophthalmol 15:136-141, Cullom,M.E.,et al, 1995

Folate Levels and Neural Tube Defects:Implications for Prevention
JAMA 274:1698-1702, 17171995., Daly,L.E.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
Ann Neurol 38:929-934, Bromberg,J.E.C.,et al, 1995

CT & MRI of Intracavernous Carotid Art Aneurysm with Occlusion of Cervical Internal Carotid Art
J Comput Assist Tomogr 19:1006-1007, Holemans,J.A.&Cox,T.C., 1995

Is Blood Pressure Really a Trigger for the Circadian Rhythm of Subarachnoid Hemorrhage?
Stroke 26:1805-1810, Kleinpeter,G.,et al, 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

Folic Acid and the Prevention of NEural Tube Defects
BMJ 310:1019-1020, Wald,N.J.&Bower,C., 1995

Ischemic Stroke and Intracranial Multifocal Cerebral Arteriopathy in Williams Syndrome
J Pediatr 126:945-958, Soper,R.,et al, 1995

Cerebral Artery Stenosis in Williams Syndrome Causes Strokes in Childhood
J Pediatr 126:943-945, Kaplan,P.,et al, 1995

MRI in Acute Hemiplegia of Childhood
J Comput Assist Tomogr 19:492-494, Connolly,B.,et al, 1995

Eval of the Circle of Willis with Three-Dimentional CT Angiography in Pts with Suspected Intracran Aneurysms
AJNR 16:1571-1578, 15791995., Alberico,R.A.,et al, 1995

Intracranial Arteries:Prospective Blinded Comparative Study of MR Angiography and DSA in 50 patients
Radiology 195:451-456, Klaus,W.S.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Familial Autoimmune Myasthenia Gravis:Report of Four Families
JNNP 58:729-731, Evoli,A.,et al, 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Encephalopathy in Children with Perinatally Acquired Immunodeficiency Virus Infection
J Pediatr 126:710-715, Lobato,M.N.,et al, 1995



Showing articles 1000 to 1050 of 1896 << Previous Next >>