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abdominal distention

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

Alexanders disease

alpha glucosidase

alveolar hypoventilation

Alzheimer's disease

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anesthesia, general

angiography, cerebral, false negative

angiography, cerebral, negative

ankylosing spondylitis

anterior horn cell disease

anterior tibial muscle weakness

antibodies to measles

antiviral agents

arrhythmia, cardiac

arylsulfatase A

ascending paralysis

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autonomic neuropathy

axonal degeneration

B 12 deficiency

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

biologic markers

bladder dysfunction

bone marrow biopsy

brainstem, atrophy

brainstem, lesion of

brucellosis, nervous system involvement with

bulbar palsy, progressive

calcification, intracranial

Canavan's disease

cardiac arrest and resuscitation

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, spine

cataracts, congenital

cauda equina, enhancement

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, women

Charcot-Marie-Tooth

chilbran skin lesions

choreoathetosis

Clinical Pathologic Conference(C.P.C.)

congestive heart failure

copper deficiency

corpus callosum

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical infarction

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

critical care unit

crying, pathologic

cultured skin fibroblasts

cyst, parenchymal

deafness, bilateral

deafness, sudden

deep gray nuclei

degenerative diseases of CNS

Dejerine-Sottas syndrome

delayed dentition

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diffuse idiopathic skeletal hyperostosis

diplopia, transient

disability, neurological

distal muscle weakness

dural sinus thrombosis

dysdiadochokinesia

dysferlinopathy

dystonia, children

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electron microscopy

emotional lability

encephalitis, focal

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, post anoxic

enzyme treatment

enzyme, muscle disease

episodic neurologic deficits

evoked potentials

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial weakness

facial weakness, bilateral

failure to thrive

feeding disorder

flail arm syndrome

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontal lobe, pathologic signs of

fundus, abnormality of

funduscopic exam

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen storage disease

GM1 ganglioside antibodies

Guillain Barre syndrome, differential diagnosis of

head circumference

headache, positional

hearing loss, bilateral

hearing loss, sudden, bilateral

hemiparesis, transient

heralding manifestation

high arched feet

high arched palate

highly active antiretroviral therapy

human immunodeficiency virus type 1

Huntington's chorea

hyperhomocysteinemia

hyperpyrexia, CNS disorder causing

hypoglycorrhachia

hypomyelination

hypotension, systemic

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

immunosuppressive agents

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

intellectual deficit

intellectual deterioration

interferon alpha

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Krabbe's disease

laminar necrosis, cortical

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

Marinesco-Sjogren syndrome

masseter muscle wasting

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis, melanomatous

mental retardation

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

microangiopathy, brain

microangiopathy, retina

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal gammopathy

motor neuron disease

movement disorder

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, high signal foci on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multiple organ failure

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, congenital

muscular dystrophy, limb-girdle

myeloneuropathy

myelopathy, chronic progressive

myoclonic jerks

myopathy, acute

myopathy, critically ill

myopathy, drug-induced

myopathy, steroid induced

myotonia dystrophica

nausea and vomiting

nerve conduction studies

nerve root enhancement

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal degeneration

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

neuroprotective agents

neurotoxicity, acute

next-generation sequencing

nutritional deficiency

occipital lobe, lesion of

old age, neurology of

ophthalmoplegia

optic nerve, hypoplasia of

optic neuropathy

optic neuropathy, nutritional

pain, abdominal

paralysis, recurrent

paraparesis, spastic

Parkinson disease

patient information and support

pediatric neurology

percussion induced muscle contraction

persistent vegetative state

personality change

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyradiculoneuropathy

Pompe's disease of glycogen storage

pons, lesion of

posterior column disease

posterior longitudinal ligament, ossification of

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

primary lateral sclerosis

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

quadriplegia, transient

ragged-red fibers

rapidly progressing neurologic illness

reading disorder, acquired

respiratory failure

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

reversible neurologic disorder

Rosenthal fibers

saccadic eye movements, abnormal

Schilder's disease

sedimentation rate, elevated

seizure, children

sensorineural hearing loss

serologic testing

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

speech disorder, childhood

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

splenium of corpus callosum

spongy degeneration of brain

spontaneous remission

standing difficulty

startle reaction

steroid therapy, CNS treatment and complications with

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subdural hematoma

superior sagittal sinus thrombosis

survival motor neuron gene

Susac's syndrome

symmetric brain lesions

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

temporal lobe, atrophy

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

toxic encephalopathy

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trigeminal neuralgia

trinucleotide repeats

urinary incontinence

urine test for metabolic disorders

viral infection

viral infection, CNS

visual acuity, decreased

visual tracking

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

weakness, acute

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

X-linked neuropathy

Showing articles 500 to 550 of 4861 << Previous Next >>

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

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 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

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

Autonomic Ganglionitis with Severe Hypertension, Migraine, and Episodic but Fatal Hypotension
Neurol 47:817-821, Lee,H.C.,et al, 1996

Palliative Care in Neurology
Neurol 46:870-872, 5981996., Bernat,J.L.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

MR Findings in Methanol Intoxication
AJNR 16:1783-1786, Gaul,H.P.,et al, 1995

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

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

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

Leukoencephalopathy with Swelling & A Discrepantly Mild Clinical Course in Eight Children
Ann Neurol 37:324-334, van der Knaap,M.S.,et al, 1995

MR Findings in Adult-Onset Adrenoleukodystrophy
AJNR 16:1227-1237, Kumar,A.J.,et al, 1995

Binswanger's Disease-Revisited
Neurol 45:626-633, Caplan,L.R., 1995

Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Hypoglycaemia in Spinal Muscular Atrophy
Lancet 346:609-610, Bruce,A.K.,et al, 1995

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

Bilateral Ulnar Handcuff Neuropathies with Segmental Conduction Block
Muscle & Nerve 18:1021-1023995., Satkunam,L.&Zochodne,D., 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,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

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 1995

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Becker Muscular Dystrophy with Onset after 60 Years
Neurol 44:2388-2390, Heald,A.,et al, 1994

Detection of Cortical Neuron Loss in Motor Neuron Disease by Proton Magnetic Resonance Spectroscopic Imaging in Vivo
Neurol 44:1933-1938, Pioro,E.P.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

Bilateral Distal Upper Limb Amyotrophy and Watershed Infarcts from Vertebral Dissection
Stroke 25:1870-1872, Pullicino,P., 1994

Distal Vacuolar Myopathy in Nephropathic Cystinosis
Ann Neurol 35:181-188, Charnas,L.R.,et al, 1994

Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
Lancet 343:1397-1398, Nakai,A.,et al, 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Intestinal Pseudo-Obstruction in Adult Spinal Muscular Atrophy
Muscle & Nerve 17:946-948994., Ionasescu,V.,et al, 1994

Location of the Corticospinal Tract in the Internal Capsule at MR Imaging
Radiology 191:455-460, Yagishita,A.,et al, 1994

Showing articles 500 to 550 of 4861 << Previous Next >>