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Differential
(Click to cross reference)
acquired immunodeficiency syndrome
Alexanders disease
algorithm
altered states of consciousness, driving with
Alzheimer's disease
Alzheimer's disease, driving with
Alzheimer's disease, familial
amniocentesis
anemia
anemia, hemolytic
anticonvulsants
anticonvulsants, discontinuation in seizure-free epileptics
anticonvulsants, selection of
arrhythmia, cardiac
automobile accidents
basal ganglia, degeneration
basal ganglia, lesion of
blindness
brainstem, lesion of
carcinoma
CAT scan, false negative
cerebellar lesion
cerebellum, neoplasms of
cerebrovascular accident
cerebrovascular accident, complications with
cerebrovascular accident, driving with
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 11
chromosome 9
cognition
conflict of interest
controversies in neurology
creatine phosphokinase(CPK)elevated
cryptococcal meningitis
cyst, neoplastic cerebellum
dementia
dementia, driving with
dentate nuclei
dentate nuclei, lesion of
developmental retardation
disability, neurological
DNA probes
Driver's license
driving
driving restrictions
driving restrictions, compliance
driving test
dysmorphic
dystonia
dystonia musculorum deformens
dystrophin
employment
familial
gadolinium
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
hemangioblastoma
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatosplenomegaly
Hunter's syndrome
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, presymptomatic detection of
hypotonia
hypotonia, infants
immunohistochemistry
inclusion bodies, intracytopasmic
lawsuit
Leber's hereditary optic neuropathy
leukocytes
leukodystrophy
leukoencephalopathy
macrocephaly
manic-depressive
McArdle's disease
medical-legal aspects of neurology
meningitis
meningitis, recurrent
meningitis, relapse
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
mucopolysaccharidoses
mucopolysacchariduria
muscle biopsy
muscle phosphorylase deficiency
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, limb-girdle
myotonia dystrophica
neoplasm, metastatic to CNS
neoplasm, posterior fossa
neurofibromatosis 1
neurofibromatosis 2
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neuropathy, amyloid
old age, driving and
old age, neurology of
optic atrophy, hereditary
optic neuropathy
optic neuropathy, hereditary
Parkinson disease
Parkinson disease, driving with
patient information and support
pheochromocytoma
polymerase chain reaction
posterior fossa, lesion of
practice guidelines
precipitating factors
prenatal diagnosis by amniocentesis
prognosis
quality of life
recombinant DNA
recurrent
renal cell carcinoma
retinal degeneration
retinal hemangioma
review article
RFLPs
risk factors
Rosenthal fibers
safety
screening
seizure
seizure, children
seizure, driving with
seizure, employment with
seizure, new onset
seizure, precipitating factors
seizure, prognosis in adults
seizure, prognosis in childhood
seizure, recurrent
seizure, restrictions following
seizure, treatment of
seizure, treatment of, first
seizure, workup of
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spine, metastasis to
treatment of neurologic disorder
visual acuity, decreased
visual impairment
visual loss
Von Hippel Lindau
Von Hippel Lindau, carrier
Von Hippel Lindau, screening protocol for
Western immunoblot test
white matter disease
work loss
Showing articles 0 to 37 of 37

Seizures, Driver Licensure, and Medical Reporting
Neurol 104:e213459, Tolchin,B.,et al, 2025

When it is Safe to Return to Driving Following First-Ever Seizure?
JNNP 86:60-64, Brown, J.W.L.,et al, 2015

Doctors and Dangers of Driving
NEJM 370:8-11, Jones, D.S., 2014

Screening for Fitness to Drive After Stroke: A Systematic Review and Meta-Analysis
Neurol 76:747-756, e35, Devos,H.,et al, 2011

The Older Adult Driver with Cognitive Impairment: "Its a Very Frustrating Life"
JAMA 303:1632-1641, 1642, 1660, Carr,D.B. &Ott,B.R., 2010

Risk of Recurrence After a First Seizure and Implications for Driving: Further Analysis of the Multicentre Study of Early Epilepsy and Single Seizures
BMJ 341:c6477, 1227, Bonnet,L.J.,et al, 2010

The Safety of Driving a Commercial Motor Vehicle After a Stroke
Stroke 41:2991-2996, Rabadi,M.H.,et al, 2010

A longitudinal Study of Drivers With Alzheimer Disease
Neurol 70:1171-1178, Ott, B.R.,et al, 2008

Parkinsons Disease and Driving Ability
JNNP 78:363-366, Singh,R.,et al, 2007

American Academy of Neurology Position Statement on Physician Reporting of Medical Conditions That May Affect Driving Competence
Neurol 68: 1174-1177,1170, Bacon,D.,et al, 2007

Predictors of Fitness to Drive in People With Parkinson Disease
Neurol 69:1434-1441, Devos,H.,et al, 2007

The First Seizure and Its Management in Adults and Children
BMJ 332:339-342, Pohlmann-Eden,B.,et al, 2006

Factors Associated With Poor Compliance of Patients with Epilepsy Driving Restrictions
Neurol 67:869-871, Polychronopoulos,P.,et al, 2006

Impaired Visual Search in Drivers with Parkinsons Disease
Ann Neurol 60:407-413,387, Uc,E.Y.,et al, 2006

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

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Rapid Direct Diagnosis of Deletions Carriers of Duchenne and Becker Muscular Dystrophies
Lancet 344:302-303, Fassati,A.,et al, 1994

Persistence of Initial Infection in Recurrent Cryptococcus Neuformans Meningitis
Lancet 341:595-596, Spitzer,E.D.,et al, 1993

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
NEJM 327:57, Cossu,P.,et al, 1992

Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
J Pediatr 120:394-398, Hofman,K.J.&Boehm,C.D., 1992

Screening for von Hippel-Lindau Disease by DNA Polymorphism Analysis
JAMA 267:1226-1231, Glenn,G.M.,et al, 1992

Central Nervous System Lesions in von Hippel-Lindau Syndrome
JNNP 55:898-901, Neumann,H.P.H.,et al, 1992

Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
Clin genet 37:355-362, Clarke,J.T.,et al, 1990

Dystonia Gene in Ashkenazi Jewish Population is Located on Chromosome 9q32-34
Ann Neurol 27:114-120, Kramer,P.L.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

Dystrophin Analysis in Duchenne & Becker Muscular Dystrophy Carriers:Correl with Intracellular Calcium & Albumin
Ann Neurol 28:674-679, Morandi,L.,et al, 1990

Homing in on Wilson's Disease
Editorial, Lancet 1:822-8231989., , 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
NEJM 318:535-542, Meissen,G.J.,et al, 1988

Prenatal Testing for Duchenne & Becker Muscular Dystrophy
Lancet 1:262-266, Cole,C.G.,et al, 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987



Showing articles 0 to 37 of 37