Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acid maltase deficiency
advances in neurology
adverse drug reaction
alpha-fetoprotein
Alzheimer's disease
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
anterior tibial muscle weakness
apraxia of eye movements
areflexia
arthrogryposis multiplex
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
atlanto axial dislocation, congenital
benign congenital hypotonia
Brugada syndrome
bulbar palsy, progressive
calf hypertrophy
carcinoembryonic antigen
carcinoma
cavernous sinus, syndrome
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
coma
complications
congenital heart disease
congenital myopathy
congestive heart failure
constipation
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
denervation of muscle
denervation potentials
dermatomyositis
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dysarthria
dystonia
dystrophin
efficacy
electrocardiogram, abnormal
electromyogram
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, muscle disease
epidemiology of neurology
eye movement, disorders of
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
foot drop
Friedreich's ataxia
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
growth retardation
Guillain Barre syndrome
gynecomastia
heavy metal intoxication
hemangioma
history of neurology
Huntington's chorea
hypercapnia
hypertension
hypoglycemia
hypoglycemic coma
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infant, evaluation of
infantile tremor syndrome
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Isaacs syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
leukemia
lid closure, weakness of
life expectancy
liver disease
lordosis
lymphoma
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
mental retardation
misdiagnosis
molecular genetics
mononeuropathy
mortality
motor neuron disease
motor neuron disease, juvenile form
motor system
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, spinal cord
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, treatment of
myasthenic crisis
myocardial injury
myocytolysis
myokymia
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, mitochondrial
myopathy, thyroid disease causing
myositis
myotonia congenita
myotonia dystrophica
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic evaluation
neuromyotonia
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, peripheral, treatment
newborn, evaluation of
nusinersen
ocular motility, disorders of
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, painful
Oppenheim muscular dystrophy
paraparesis, familial spastic
Parkinson disease
pathology
patient information and support
periodic paralysis
periodic paralysis, thyrotoxic
phrenic nerve
placebo
poison, mercury
poison, neurologic problems with
poliomyelitis
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
porphyria
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
radiation hypersensitivity
radiculopathy
respiratory failure
review article
RFLPs
risk-benefit assessment
safety
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, treatment of
skin, lesions in neurologic disorders
SMN1 gene
spina bifida
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
stiff man syndrome
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
sudden death
survival motor neuron gene
telangiectases
term infant
Tolosa Hunt syndrome
tongue, fasciculations of
torticollis
treatment of neurologic disorder
tremor
tricresylphosphate
trinucleotide repeats
tuberous sclerosis
vitamin E
vitamin E deficiency
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
West disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 1150 to 1200 of 8383 << Previous Next >>

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Cholesterol Embolism:Experience with 22 Histologically Proven Cases
Surgery 105:737-746, Dahlberg,P.J.,et al, 1989

Acute Ascending Myelopathy of the Spine
Spine 14:1084-1089, Yablon,I.G.,et al, 1989

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Transverse Sinus Thrombosis in Newborns:Clinical and Magnetic Resonance Imaging Findings
Ann Neurol 24:792-794, Baram,T.Z.,et al, 1988

Compressive Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in Cyclists
JNNP 51:1588-1590, Hankey,G.J.&Gubbay,S.S., 1988

Nontraumatic Frontal Lobe Hemorrhages:Clinical-computed Tomographic Correlations
Neuroradiology 30:500-505, Weisberg,L.A.&Stazio,A., 1988

Neurologic and Cognitive Deficits in Children with Cystinosis
J Pediatr 112:912-914, Trauner,D.A.,et al, 1988

Corpus Callostomy for Intractable Generalized Epilepsy
J Pediatr 113:255-261, Wyllie,E., 1988

Reflex Sympathetic Dystrophy in Children:Treatment with Transcutaneous Electric Nerve Stimulation
Pediatrics 82:728-732, Kesler,R.W.,et al, 1988

Pain Syndromes in Multiple Sclerosis
Neurol 38:1830-1834, Moulin,D.E.,et al, 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
Arch Int Med 148:1739-1740, Eichacker,P.Q.,et al, 1988

Distal Vacuolar Myopathy with Complete Heart Block
Arch Neurol 45:698-699, Krendel,D.A.,et al, 1988

Hypertrophy of the Calf with S-1 Radiculopathy
Arch Neurol 45:660-664, Ricker,K.,et al, 1988

Opsoclunus, Myoclonus, Ataxia & Encephalopathy in Adults with Cancer:A Distinct Paraneoplastic Syndrome
Medicine 67:100-109, Anderson,N.E.,et al, 1988

Hypoplasia of Cerebellar Vermal Lobules VI and VII in Autism
NEJM 318:1349-1354, 13901988., Courchesne,E.,et al, 1988

Magnetic Resonance Imaging in the Assessment of Medullary Compression in Achondroplasia
Am J Dis Child 142:989-992, Thomas,I.T.,et al, 1988

Neurocysticercosis, Two Hundred Thirty-Eight Cases from a California Hospital
Arch Neurol 45:777-780, Scharf,D., 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Deep Branch Ulnar Neuropathy Due to Giant Cell Tumor:Report of a Case
Neurol 38:327-329, Rafecas,J.C.,et al, 1988

Chronic Ureaplasma Urealyticum & Mycoplasma Hominis Infections of Central Nervous System in Preterm Infants
Lancet 1:17-21, Waites,K.B.,et al, 1988

Magnetic Resonance Imaging of the Central Nervous System Council on Scientific Affairs
Report of the Panel on MRI, JAMA 259:1211-12221988., , 1988

Dialysis Myelopathy:Quardiparesis Due to Extradural Amyloid of B2 Microglobulin Origin
BMJ 296:752-753, Allain,T.J.,et al, 1988

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Severe Polymyositis-Like Syndrome Associated with Zidovudine Therapy of AIDS & ARC
NEJM 318:708, Bessen,L.J.,et al, 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

Headaches in Pregnancy
Semin Neurol 8:187-192, Reik,L., 1988

CT, MR, and Pathlogy in HIV Encephalitis and Meningitis
AJR 151:373-380, Post,M.J.D.,et al, 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Progressive Nemaline (Rod) Myopathy Associated with HIV Infection
NEJM 317:1602-1603, Dalakas,M.C.,et al, 1987

Symptomatic Atlantoaxial Dislocation in Down's Syndrome
Ann Neurol 21:606-609, Chaudhry,V.,et al, 1987

Diagnosis of Thoracic Outlet Syndrome, Value of Sensory & Motor Conduction Studies & Quantitative EMG
Arch Neurol 44:1161-1163, Smith,T.&Trojabor,W., 1987

Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987

Late Denervation in Patients with Antecedent Paralytic Poliomyelitis
NEJM 317:7-12, Cashman,N.R.,et al, 1987

Chronic Muscle Weakness Caused by Borrelia Burgdorferi Meningoradiculitis
Ann Neurol 22:389-392, Wokke,J.H.J.,et al, 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Spectrum of Inclusion Body Myositis
Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987

Proximal Weakness of the Extremities as Main Feature of Amyloid Myopathy
JNNP 50:1353-1358, Jennekens,F.G.I.&Wokke,J.H.J., 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

The Spectrum of Neurol Dis Assoc with Antiphospholipid Antibd, Lupus Anticoag & Anticardiolipin Antibd
Arch Neurol 44:876-883, Levin,S.R.&Welch,K.M.A., 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Transient Traumatic Quadriplegia
Editorial, Lancet 1:8441987., , 1987

Reflex Sympathetic Dystrophy, A Review
Arch Neurol 44:555-561, Schwartzman,R.J.&McLellan,T.L., 1987

Tick-Bite Meningoradiculoneuritis:Clinical, Electrophysiologic, & Histolic Findings in 10 Cases
Neurol 37:749-753, Vallat,J.M.,et al, 1987

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987



Showing articles 1150 to 1200 of 8383 << Previous Next >>