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Differential
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aciduria
acoustic neurinoma
acoustic neurinoma, bilateral
acquired immunodeficiency syndrome
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
Alexanders disease
algorithm
alopecia
alpha-fetoprotein
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
amniocentesis
amyloid
amyloid angiopathy, cerebral
amyloid angiopathy, hereditary cystatin C
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, familial
anemia
anemia, hemolytic
anesthesia, general
anosmia
apolipoprotein E
APP gene
apraxia of eye movements
arteriopathy
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
attention deficit disorder with hyperactivity
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
benign familial neonatal convulsions
brachial neuritis
brachial plexus neuropathy
brachial plexus neuropathy, familial
brain biopsy
brainstem, lesion of
brainstem, neoplasms of
bulbar palsy, progressive
cafe au lait spots
calcification, intracranial
calcitonin gene-related peptide receptor blocker
cane
carcinoembryonic antigen
carcinoma
carcinoma of pancreas
CAT scan
CAT scan, abnormal
cataracts
caudate nucleus, atrophy
cavernous hemangioma
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellum, neoplasms of
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral infarction
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chorea
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 17
chromosome 2
chromosome 22
chromosome 3
chromosome 7
chromosome 9
clindamycin
clonazepam
clubfoot as related to neurologic disease
Cockayne's syndrome
cognition
coma
compression neuropathy
compression neuropathy, recurrent
corpus callosum, lesion of
cost effectiveness
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
cryptococcal meningitis
cyst, neoplastic cerebellum
cytomegalovirus infection
degenerative diseases of CNS
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
disability rating scale, neurological
DNA probes
dopa responsive dystonia
drooling
drug induced neurologic disorders
dysarthria
dysmorphic
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, children
dystonia, paroxysmal
dystrophin
ear, abnormal
electroencephalogram
electronystagmography
electroretinograph
encephalitis
encephalitis, autoimmune
encephalitis, focal
encephalitis, Rasmussen's
encephalitis, viral
enzyme, muscle disease
epidemiology of neurology
ethics in neurology
eye movement, disorders of
Fabry's disease
face, elongated
facial appearance, abnormal
familial
fasciculation
fatal familial insomnia
fragile-X syndrome
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
GFAP gene
globus pallidus
globus pallidus, lesion of, bilateral
GLUT1 deficiency syndrome
gonadotropin-releasing hormone
growth retardation
gynecomastia
hair analysis
Hallervorden Spatz disease
hallucination
hamartoma
head circumference
headache
headache, positional
headache, recurrent
hearing loss
hemangioblastoma
hemiparesis
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatosplenomegaly
Hispanics
HTRA1 gene
Hunter's syndrome
huntingtin
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, presymptomatic detection of
Huntington's disease, children
hyperactivity
hyperekplexia
hyperhidrosis
hyperkalemic periodic paralysis
hyperreflexia
hyperthermia
hypogonadism
hypotelorism
hypotonia
hypotonia, infants
imbalance
immunodeficiency
immunohistochemistry
immunoperoxidase staining
immunosuppression
in situ hybridization
inborn errors of metabolism
inclusion bodies, intracytopasmic
insomnia
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, young adult
iron, brain
Jakob-Creutzfeldt disease
joint hypermobility
Kallmann's syndrome
Kearns-Sayre syndrome
KRIT1 gene
Kugelberg-Welander syndrome
lacunar infarction
Laurence-Moon-Bardet-Biedl syndrome
leukemia
leukodystrophy
leukoencephalopathy
lymphoma
macrocephaly
macular degeneration
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malignant hyperpyrexia
manic-depressive
medulla oblongata
medulla oblongata, atrophy
medulla oblongata, lesion of
memory, impairment of
meningitis
meningitis, recurrent
meningitis, relapse
mental retardation
mental retardation, familial
metachromatic leukodystrophy
Mexican
Mexico
microcephaly
microhemorrhage, intracerebral
migraine
migraine, children
migraine, pathogenesis
migraine, prophylaxis
migraine, treatment of
mimics
misdiagnosis
molecular genetics
mongolism
monoclonal antibodies
mononeuropathy
mononeuropathy, recurrent
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, eye of tiger sign
MRI, gradient-echo
MRI, paramagnetic effect
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, susceptibility weighted
mucopolysaccharidoses
mucopolysacchariduria
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle spasm
muscle stiffness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
myelin basic protein gene
myoclonus
myopathy
myopathy, mitochondrial
myopathy, proximal
myopia
myotonia
myotonia dystrophica
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, posterior fossa
neoplasm, primary intracranial
neoplasm, primary of CNS
neurocutaneous disease
neurodegeneration with brain iron accumulation
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurologic disease
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
neurotomy
next-generation sequencing
night blindness
nonsteroidal anti-inflammatory drug
Notch3 gene
ocular motility, disorders of
oculopharyngeal muscular dystrophy
olfactory bulb
optic atrophy
optic glioma
optic nerve
optic neuropathy
pain
pain, flank
PANK2 mutation
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal neurologic deficits
pathology
patient information and support
periodic paralysis
peroxisomal disease
pheochromocytoma
pigmentary retinopathy
polycystic kidneys
polymerase chain reaction
polyneuropathy, familial
posterior fossa, lesion of
practice guidelines
prenatal diagnosis by amniocentesis
presenilin-1 gene
presenilin-2 gene
prevention of neurologic disorders
prion disease
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal myotonic myopathy
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
radiation hypersensitivity
recombinant DNA
recurrent
refractive errors
Refsum's disease
renal cell carcinoma
renal cyst
retinal degeneration
retinal hemangioma
retinal lesion
retinal tumor
retinitis pigmentosa
retinopathy
review article
RFLPs
rigidity
risk factors
Rosenthal fibers
screening
seizure
seizure, children
seizure, familial
seizure, focal
seizure, intractable, treatment of
seizure, neonatal
sensorineural hearing loss
serotonin agonist
simian crease
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep pathology and physiology
small vessel disease
small vessel disease, cerebral
Southern immunoblot test
spastic ataxia
spasticity
spinal cord
spinal cord, lesion of
spinal cord, neoplasm
spinal muscular atrophy
spine, metastasis to
spinocerebellar ataxia
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spondylosis
spongy degeneration of brain
startle reaction
striatal encephalitis
stuporous
subarachnoid hemorrhage
synkinesis
tapetoretinal degeneration
telangiectases
testicular enlargement
thalamus, lesion of
tinnitus
tomaculous neuropathy
trauma
treatment of neurologic disorder
trigeminovascular system
trinucleotide repeats
triptans
Usher's syndrome
ventricular garlands
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual field defect
visual loss
Von Hippel Lindau
Von Hippel Lindau, carrier
Von Hippel Lindau, screening protocol for
walking, difficulty with
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
white matter disease
white matter disease, subcortical
workup
X-linked bulbospinal neuronopathy
x-linked mental retardation
X-linked neuropathy
Showing articles 1450 to 1500 of 1870 << Previous Next >>

Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease
Ann Neurol 25:440-443, Panayiotopoulos,C.P.&Obeid,T., 1989

Radiologic Screening for von Hippel-Lindau Disease:Role of Gd-DTPA Enhanced MR Imaging of the CNS
J Comput Assist Tomogr 13:743-755, Filling-Katz,M.R.,et al, 1989

Magnetic Resonance Imaging in a Family with Hereditary Cerebral Arteriovenous Malformations
Arch Neurol 46:184-187, Allard,J.C.,et al, 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,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

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

REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
Eur Neurol 29:61-66, Martinelli,P.,et al, 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

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

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

Risk of Brain Infarction in Familial Hypercholesterolemia
Stroke 19:1097-1100, Kaste,M.&Koivisto,P., 1988

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988

Characterization of Dystrophin in Muscle-Biopsy Spec from Pts with Duchenne's or Becker's Muscular Dystrophy
NEJM 318:1363-1368, 13921988., Hoffman,E.P.,et al, 1988

Dystrophin
Editorial, Lancet 2:429-4301988., , 1988

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

Clinicopath Conf
Mastoiditis with Right Transverse-Sinus and Sigmoid-Sinus Thrombosis, Case Record 20-1988, NEJM 318:, 321328,1988., 1988

Familial Parkinsonism, Apathy, Weight Loss & Central Hypoventilation:Successful Long-Term Management
Neurol 38:637-639, Roy,E.P.,et al, 1988

Parkinson's Disease in a Nationwide Twin Cohort
Neurol 38:1217-1219, Marttila,R.J.,et al, 1988

Neurofibromatosis 2:Clinical & DNA Linkage Studies of a Large Kindred
Wertelecki. W. , et al, NEJM 319:276-2838., , 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Genetic Factors in Myasthenia Gravis:A Family Study
Neurol 38:38-42, Kerzin-Storrar,L.,et al, 1988

Leigh Disease (Subacute Necrotizing Encephalomyelopathy) :CT & MR in Five Cases
J Comput Assist Tomogr 12:40-44, Geyer,C.A.,et al, 1988

Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 1988

Amaurotic Family Idiocy
Am J Dis Child 142:53-56, Abt,I.A., 1988

Cerebral Cavernous Malformations:Incidence and Familial Occurrence
NEJM 319:343-347, Rigamonti,D.,et al, 1988

Neurofibromatosis
Conference Statement, National Institutes of Health Consensus Development Conference, Arch Neurol 45, 57578,1988., 1988

Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
Lancet 1:1263-1265, Burton,J.L., 1988

The Familial Nature of Multiple Sclerosis:Age-Correlated Empiric Recurrence Risks for Children & Siblings of Pts
Neurol 38:990-991, Sadovnick,A.D.,et al, 1988

Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
Arch Neurol 45:1004-1008, Schwankhaus,J.D.,et al, 1988

Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988

Risk of Dementia in Relatives of Patient with Alzheimer's Disease
Neurol 38:786-790, Huff,F.J.,et al, 1988

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

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

Transient Tic Disorder and the Spectrum of Tourette's Syndrome
Arch Neurol 45:1200-1201, Kurlan,R.,et al, 1988

Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
Arch Neurol 45:1097-1100, Duffy,P.,et al, 1988

Brain Abscess:Association with Pulmonary Arteriovenous Fistula and Hereditary Hemorrhagic Telangiectasia:3 Cases
Am J Med 85:718-720, Gelfand,M.S.,et al, 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Essential Tremor:A Review
Neurol 37:1194-1197, Findley,L.J.&Koller,W.C., 1987

A Rating Scale for Gilles de la Tourette's Syndrome:Description, Reliability, & Validity Data
Neurol 37:1542-1544, Goetz,C.G.,et al, 1987

False Negative Results in Patients with fra (X) (q) Mental Retardation Taking Oral Vitamin Supplements
NEJM 316:1093, Froster-Iskenius,U.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Ocular Complications of Tangier Disease
Am J Med 83:991-994, Pressley,T.A.,et al, 1987

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

Cervicomedullary Compression in Young Patients with Achondroplasia:Value of Neurologic & Respiratory Eval
J Pediatr 110:522-530, Reid,C.S.,et al, 1987

The Autosomal Dominant Form of"Pure"Familial Spastic Paraplegia:Clinical Findings & Linkage Analysis of a Pedigree
Neurol 37:910-915, Boustany,R.M.N.,et al, 1987

MR Imaging of Pelizaeus-Merzbacher Disease
J Comput Assist Tomogr 11:591-593, Penner,M.W.,et al, 1987

Magnetic Resonance Imaging in Pelizaeus-Merzbacher Disease
Neuroradiology 29:403-405, Journel,H.,et al, 1987



Showing articles 1450 to 1500 of 1870 << Previous Next >>