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acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
algorithm
alpha glucosidase
alpha-fetoprotein
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
aphasia
aphasia, progressive, primary
apraxia of eye movements
areflexia
arm weakness
aspartate aminotransferase
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
Babinski sign
behavioral disorder
bulbar palsy
calf hypertrophy
camptocormia
cane
carcinoembryonic antigen
carcinoma
cardiomyopathy
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
cognition
congenital heart disease
congenital myopathy
congestive heart failure
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
degenerative diseases of CNS
delusion
dementia
dementia, age at onset
dementia, frontotemporal
dementia, presenile
developmental milestones
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
distal muscle atrophy
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dystonia
efficacy
emotional lability
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme treatment
enzyme, defect
epidemiology of neurology
exercise
eye movement, disorders of
facial weakness, bilateral
familial
fasciculation
floppy infant
fluency
foot drop
frontotemporal dementia, behavioral variant
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
growth retardation
hallucination
hand weakness
hemiparesis
hepatomegaly
heralding manifestation
history of neurology
hyperreflexia
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inflexibility, mental
intellectual deficit
intrinsic hand muscles, wasting of
jaw jerk, abnormal
Kugelberg-Welander syndrome
laughing, pathologic
leg atrophy
leg weakness, bilateral
leukemia
life expectancy
lobar atrophy
lymphoma
lysosomal storage disease
lysosomes, abnoral
mental retardation
Mills syndrome
mimics
misdiagnosis
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
motor system
movement disorder
movement disorder, extrapyramidal
MRI, abnormal
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
myelomalacia
myopathy
myotonia congenita
neck weakness
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic evaluation
neuronal degeneration
neuropathology
neuropathy
newborn, evaluation of
next-generation sequencing
nusinersen
ocular motility, disorders of
pain, increased response
palliative care
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinsonism syndrome
Parkinsonism-dementia complex
pathology
patient information and support
personality change
Pompe's disease of glycogen storage
preclinical
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
progeria
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract dysfunction
radiation hypersensitivity
release phenomena
respiratory failure
review article
risk factors
safety
scoliosis
scoliosis, neurologic association with
screening
single photon emission computed tomography
skin, lesions in neurologic disorders
SMN1 gene
spastic ataxia
spasticity
spinal cord
spinal cord degeneration
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
stereotyped behavior
superoxide dismutase
survival motor neuron gene
telangiectases
tongue, enlarged
tongue, fasciculations of
trauma
treatment of neurologic disorder
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
wheelchair
word-finding difficulty
workup
Showing articles 600 to 650 of 7669 << Previous Next >>

Multiple Sclerosis and Magnetic Resonance Imaging
Arch Neurol 58:35-36, Racke,M.K.,et al, 2001

Sensory Guillain-Barre Syndrome
Neurol 56:82-86, Oh,S.J.,et al, 2001

Disability and Quality of Life in Charcot-Marie-Tooth Disease Type 1
JNNP 70:548-550, Pfeiffer,G.,et al, 2001

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001

Longitudinal Assessment of Neurocognitive Function After Coronary-Artery Bypass Surgery
NEJM 344:395-402,451, Newman,M.F.,et al, 2001

APOE Genotype is a Major Predictor of Long-Term Progression of Disability in MS
Neurol 56:312-316, Chapman,J.,et al, 2001

La Crosse Encephalitis in Children
NEJM 344:801-807, McJunkin,J.E.,et al, 2001

Neuro-Ophthalmic Manifestations of Sarcoidosis. Clincal Spectrum, Evaluation and Management
J Neuroophthalmol 21:132-137, Frohman,L.P,et al, 2001

What Contributes to Quality of Life in Patients with Parkinson's Disease?
JNNP 69:308-312,289, Schrag,A. et al, 2000

A 44-Year-Old Woman with Difficulty Walking
JAMA 284:2632-2639, Iezzoni,L.I., 2000

Injections of Botulinum Toxin A Into the Salivary Glands Improve Sialorrhoea in Amyotrophic Lateral Sclerosis
JNNP 69:121-123, Giess,R. et al, 2000

Long-term Effect of Bone-marrow Transplantation for Childhood-onset Cerebral X-linked Adrenoleukodystrophy
Lancet 356:713-718, Shapiro,E. et al, 2000

Cerebral Infarctin in the Term Newborn: Clinical Presentation and Long-Term Outcome
J Pediatr 137:351-355, Sreenan,C. et al, 2000

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Recommendations for the Management of Patients with Unruptured Intracranial Aneurysms
Stroke 31:2742-2750, Bederson,J.B.,et al, 2000

Relapses and Progression of Disability in Multiple Sclerosis
NEJM 343:1430-1438,1486, Confavreux,C.,et al, 2000

Disability in Young People and Adults One Year after Head Injury: Prospective Cohort Study
BMJ 320:1631-1635, Thornhill,S. et al, 2000

Long-Term outcome in Patients With Guillain-Barre Syndrome Requiring Mechanical Ventilation
Neurol 54:2311-2315, Fletcher,D.D.,et al, 2000

Effect of Eliminating Compensation for Pain and Suffering on the Outcome of Insurance Claims for Whiplash Injury
NEJM 342:11790-1186,1211, Cassidy,J.D.,et al, 2000

Neurologic and Developmental Disability After Extremely Preterm Birth
NEJM 343:378-384,429, Wood,N.S. et al, 2000

Outcome of Surgery for Thoracic Outlet Syndrome in Washington State Workers' Compensation
Neurol 54:1252-1257, Franklin,G.M.,et al, 2000

The Split Hand in ALS has a Cortical Basis
J Neurol Sci 180:66-70, Weber,M.,et al, 2000

Amyotrophic lateral Sclerosis Mimic Syndromes, A Population-Based Study
Arch Neurol 57:109-113, Traynor,B.J.,et al, 2000

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Bicuspid Aortic Valve - A Silent Danger: Analysis of 50 Cases of Infective Endocarditis
Clin Inf Dis 30:336-341, Lamas, C.C. & Eykyn, S.J., 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Disorders of Upper & Lower Motor Neurons
Neurol in Clin Practice, 3rd Ed., Butterworth, Boston: Ch. 78 p. 2007, Mitasumoto,H., 2000

Botulinum Toxin is a Useful Treatment in Excessive Drooling of Saliva
JNNP 67:697, Bhatia,K.P.,et al, 1999

Safety and Factors Related to Survival After Percutaneous Endoscopic Gastrostomy in ALS
Neurol 53:1123-1125, Chio,A.,et al, 1999

Diagnosis and Treatment of Wilson's Disease
Semin Neurol 19:261-270, Brewer,G.J.,et al, 1999

Musculoskeletal and Neurologic Outcomes in Patients with Previously Treated Lyme Disease
Ann Int Med 131:919-926, Shadick,N.A.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Benign Multiple Sclerosis? Clinical Course, Long Term Follow Up, and Assessment of Prognostic Factors
JNNP 67:148-152,138, Hawkins,S.A.&McDonnell,G.V., 1999

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

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

Rehabilitation of Persons With Traumatic Brain Injury
JAMA 282:974-983,989, NIH Consensus Development Panel on Rehab with TBI, 1999

Multiple Sclerosis That is Progressive From the Time of Onset, Clinical Characteristics and Progression of Disability
Arch Neurol 56:1138-1142, Andersson,P.B.,et al, 1999

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

New Developments in the Neurobiology of the Tuberous Sclerosis Complex
Neurol 53:1384-1390, Crino,P.B.&Henske,E.P., 1999

An Algorithm for ALS Diagnosis and Management
Neurol 53:S58-S62, Swash,M., 1999

The Roussy-Levy Family:From the Original Description to the Gene
Ann Neurol 46:770-773, Plante-Bordeneuve,V.,et al, 1999

Fatal Guillain-Barre Syndrome
Neurol 52:635-638, Lawn,N.D.&Wijdicks,E.F.M., 1999

Quantitative MRI in Patients with Clinically Isolated Syndromes Suggestive of Demyelination
Neurol 52:599-606, Sailer,M.,et al, 1999

Clumsiness, Confusion, Coma, and Valproate
Lancet 353:1408, Ellaway,C.J.,et al, 1999

Fibromyalgia Syndrome a Decade Later
Arch Int Med 159:777-785, Goldenberg,D.L., 1999

Changes in Resource Use and Outcomes for Patients with Migraine Treated with Sumatriptan, A Managed Care Perspective
Arch Int Med 159:857-863, Lofland,J.H.,et al, 1999

Outcome in Severe Pediatric Guillain-Barre Syndrome after Immunotherapy or Supportive Care
Neurol 52:1494-1497, Graf,W.D.,et al, 1999

Atypical Form of Amyotrophic Lateral Sclerosis
JNNP 66:581-585, Sasaki,S.&Iwata,M., 1999

Brain Structure and Neurocognitive and Behavioural Function in Adolescents Who Were Born Very Preterm
Lancet 353:1653-1657, Stewart,A.L.,et al, 1999



Showing articles 600 to 650 of 7669 << Previous Next >>