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Differential
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abdominal distention

abdominal muscle paralysis

abducens nerve paralysis, bilateral

acid maltase deficiency

adrenoleukodystrophy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agammaglobulinemia

akinesia of eyelid function

alveolar hypoventilation

Alzheimer's disease

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anesthesia, general

anterior interosseous neuropathy

anterior tibial muscle weakness

apraxia of eyelid opening

arrhythmia, cardiac

arthrogryposis multiplex

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

atrial fibrillation

atrial paralysis

atrioventricular block

attention deficit disorder with hyperactivity

autoimmune disease

automatic implantable cardioverter-defibrillator

axonopathy, distal

basal ganglia, calcification of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

benign congenital hypotonia

bent spine syndrome

bladder dysfunction

blood dyscrasias, neurologic findings with

brachial neuritis

brainstem, lesion of

brainstem, tuberculoma of

bulging of biceps

bulimia nervosa

calcification, intracranial

calcium antagonist

calf hypertrophy

calpain III deficiency

cancer of colon

carcinoma of ovary

carcinoma of pancreas

carcinoma of uterus

cardiac arrest and resuscitation

cardiac surgery, neurologic complications with

cardiac transplantation

cardiovascular disease

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, false negative

CAT scan, muscle

celiac disease, childhood

central core disease

central nervous system, infection of

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, multiple

cerebrovascular accident, young adult

cervical spine injury

Charcot-Marie-Tooth

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10 deficiency

cogwheel rigidty

collagen vascular disease

compression fracture

compression neuropathy

conduction block

confidentiality

congenital birth defects

congenital heart disease

congenital myopathy

congestive heart failure

conjunctival injection

contractures, joint

controversies in neurology

conversion reaction

cornea, abnormal

corpus callosum, lesion of

cost effectiveness

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

defibrillator, implanted

degenerative diseases of CNS

delay in diagnosis

dentatorubral-pallidoluysian atrophy

dermatomyositis

descending paralysis

developmental disability

developmental milestones

developmental retardation

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

digitalis intoxication

disability, neurological

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug induced neurologic disorders

dysferlinopathy

dysthyroid ocularmyopathy

dystroglycanopathies

dystrophin associated proteins

eating disorder

edema, periorbital

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram, abnormalities of

electron microscopy

Emery-Dreifuss muscular dystrophy

Emery-Dreifuss muscular dystrophy, carrier

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, progressive

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

ethics in neurology

evidence-based research

exercise intolerance

extraocular muscle atrophy

extraocular muscle enlargement

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

family planning

Fazio-Londe's disease

feeding disorder

femoral neuropathy

fetal movements, reduced

fine motor function, impaired

fistula, arterio-venous, carotid-cavernous

fluorescein angiography

fracture, long bone

fragile-X syndrome

Friedreich's ataxia

frontal balding

gastric dilatation, acute

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, horizontal

gaze palsy, vertical

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glycogen storage disease

glycosyltransferase

Gowers maneuver

Graves ophthalmopathy

Guillain Barre syndrome

Hallgren's syndrome

hearing problems in children

heart block, complete

heavy metal intoxication

hemianopia, homonymous

hepatic failure

heralding manifestation

high arched feet

high arched palate

histochemistry of muscle

Holter monitoring

Huntington's chorea

Hurler's syndrome

hyperthyroidism

hypoglycemic coma

hypoglycorrhachia

hypotonia, infants

hypoxic encephalopathy

immunohistochemistry

immunosuppressive agents

implantable cardioverter defibrillator

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

influenza immunization

intellectual deficit

intelligence quotient

intermittent positive pressure breathing

intestinal pseudoobstruction

jaw jerk, abnormal

joint hypermobility

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

lactic acidemia

lactic dehydrogenase(LDH)

Laurence-Moon-Bardet-Biedl syndrome

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

left ventricular dilatation

leg weakness, bilateral

Leigh's disease

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

lid closure, weakness of

life expectancy

life sustaining treatment

limb-girdle weakness

liver function enzymes

locked-in syndrome

lymphocyte capping, diminished

machine learning

malformation, CNS, congenital

malignancy screen

malignant hyperpyrexia

medial rectus palsy

median neuropathy

medical-legal aspects of neurology

medulla oblongata, lesion of

Melkersson's syndrome

mental retardation

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

motor neuron disease

movement disorder

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

mucopolysaccharidoses

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy, extraocular

muscle diseases, characteristics of

muscle hypertrophy

muscle relaxant

muscle stiffness

muscle swelling

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, intermediate onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

muscular dystrophy, lymphocyte capping, diminished

muscular dystrophy, neurogenic hypothesis of

muscular dystrophy, pattern of muscle involvement

muscular dystrophy, systemic membrane defect

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myasthenic crisis

myasthenic syndrome

myeloneuropathy

myoblast transfer

myocardial biopsy

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, neurogenic hypothesis of

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myopathy, vacuolar

myositis, ocular

myotonia congenita

myotonia dystrophica

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonic discharges

nausea and vomiting

nemaline rod myopathy

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

neuritis, causes of

neurocardiology

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal migration disorder

neuroophthalmology

neuropathy, amyloid

neuropathy, ataxia, retinitis pigmentosa

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, peripheral

neuropathy, sensory

newborn, evaluation of

next-generation sequencing

nystagmus, vertical

obicularis oculi, weakness of

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

old age, neurology of

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

Oppenheim muscular dystrophy

optic disc edema

optic neuropathy

orbicularis oculi muscle

orbit, lesions of

pacemaker, cardiac-transvenous

pain, abdominal

palliative care

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinsonism syndrome

pediatric neurology

pediatric neurology, transition to adult care

percussion induced muscle contraction

periodic paralysis

phosphorylase b kinase deficiency

photophobia, central

phrenic nerve pacemaker

physical therapy

physician assisted suicide

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyositis, infantile

pons, lesion of

positive sharp waves

posterior interosseous neuropathy

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive infantile poliodystrophy

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proptosis, bilateral

proptosis, unilateral

proximal muscle atrophy

proximal myotonic myopathy

pseudobulbar palsy

pseudohypertrophy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

ptosis, bilateral

ptosis, familial

pulmonary embolism

pulmonary function tests

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated and fixed, unilateral

quadriceps atrophy

quadriceps weakness

quality of life

ragged-red fibers

Raynaud's phenomenon

recombinant DNA

respiratory depression

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinal detachment

retinitis pigmentosa

rigid spine syndrome

rippling muscle disease

sarcoglycanopathy

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sedimentation rate

sensorineural hearing loss

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

shoulder, pain in

shoulder-girdle wasting

slit lamp examination

sloped shoulders

Southern immunoblot test

speech disorder, childhood

speech, delayed development of

Spielmeyer Vogt syndrome

spinal cord, injury of

spinal cord, neoplasm

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar degeneration

standing difficulty

Stephens syndrome

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

strokelike episodes

succinate dehydrogenase deficiency

symmetric brain lesions

systemic illness

Tay-Sachs disease

telangiectases, retinal

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular atrophy

thalamus, lesion of-bilateral

thoracic outlet syndromes

thrombus, mural

tongue, fasciculations of

transient ischemic attack

transverse smile

treatment of neurologic disorder

tricresylphosphate

trinucleotide repeats

tuberculoma of CNS

tuberculosis, miliary

type 2 muscle fiber

ulnar neuropathy

ultrasonography

upgaze, paralysis of

urinary incontinence

Usher's syndrome

ventricular tachycardia

vertebral fracture

viral infection, CNS

vision, failure of in childhood

visual field defect

visual fields, constricted

Walker-Warburg syndrome

walking, difficulty with

weakness, congenital

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Werdnig-Hoffman disease

Western immunoblot test

whistle, inability to

white matter disease

white matter disease, pattern

wide based gait

winging of scapula

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked mental retardation

Showing articles 2050 to 2100 of 2426 << Previous Next >>

Seizures in Progressive Supranuclear Palsy
Neurol 39:138-140, Nygaard,T.G.,et al, 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

The Significance of MRI Abnormalities in Children with Neurofibromatosis
Neurol 39:373-378, Duffner,P.K.,et al, 1989

Phenobarbital Rheumatism in Patients with Brain Tumor
Ann Neurol 25:92-94, Taylor,L.P.&Posner,J.B., 1989

Chronic Myelopathies Associated with HTLV-I, A Clinical, Serologic, and Immunovirologic Study of 10 Patients in France
Arch Neurol 46:255-260, Gout,O.,et al, 1989

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

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

Reflex Sympathetic Dystrophy Syndrome in Children and Adolescents, Reports of 18 Cases and Review
Am J Dis Child 142:1325-1330, Silber,T.J.&Majd,M., 1988

MR Imaging of the Brain in Myelopathy Associated with Human T-Cell Lymphotropic Virus Type I
J Comput Assist Tomogr 12:750-754, Hara,Y.,et al, 1988

Plasmapheresis in Treatment of Human T-Lymphotropic Virus Type-I Associated Myelopathy
Lancet 2:1109-1113, Matsuo,H.,et al, 1988

Elevated Serum Antibody Titers to Epstein-Barr Virus in HTLV-I Associated Myelopathy (HAM)
Neurol 38:1650-1653, Itoyama,Y.,et al, 1988

Correlation of Neuropsychological and MRI Findings in Chronic/Progressive Multiple Sclerosis
Neurol 38:1826-1829, Franklin,G.M.,et al, 1988

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

Risk Factors for Progressive Supranuclear Palsy
Neurol 38:1546-1552, Davis,P.H.,et al, 1988

Involvement of JC Virus-Infected Mononuclear Cells From the Bone Marrow & Spleen in the Pathogen of PML
NEJM 318:301-305, 315-3171988., Houff,S.A.,et al, 1988

Nervous System Complications in Uremia
Ann Int Med 109:143-153, Frasser,C.L.&Arieff,A.I., 1988

Acute Paralysis from Inhaled Barium Carbonate
Arch Neurol 45:579-580, Shankle,R.&Keane,J.R., 1988

Chronic Unilateral Optic Neuropathy:A Magnetic Resonance Study
Ann Neurol 24:3-11, Eidelberg,D.,et al, 1988

Progressive Language Impairment without Dementia:A Case with Isolated Category Specific Semantic Defect
JNNP 51:1201-1207, Basso,A.,et al, 1988

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy, Chronic Lymphocytic Leukemia, Case Record 45-1988, NEJM, 19:8-1280,1988., 1988

MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988

CT & MRI in Maple Syrup Urine Disease
Neurol 38:486-488, Uziel,G.,et al, 1988

Role of Contrast Enhancement in Cerebral CT of Carbon Monoxide Poisoning
J Comput Assist Tomogr 12:341-343, Zeiss,J.&Brinker,R., 1988

Malignant Monophasic Multiple Sclerosis or"Marburg's Disease"
Neurol 38:1153-1155, Mendez,M.F.&Pogacar,S., 1988

Prevalence and Natural History of Progressive Supranuclear Palsy
Neurol 38:1031-1034, Golbe,L.I.,et al, 1988

Cerebral Hypometabolism in Progressive Supranuclear Palsy Studied with Positron Emission Tomography
Ann Neurol 24:399-406, Foster,N.L.,et al, 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

Stiff-Man Syndrome, An Autoimmune Disease
NEJM 318:1060-1062, Layzer,R.B., 1988

Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
Ann Neurol 24:79-84, Simpson,D.M.&Bender,A.N., 1988

Acquired Immunodeficiency Syndrome, Magnetic Resonance Patterns of Brain Involvement with Pathologic Correlation
Arch Neurol 45:731-736, Jarvik,J.G.,et al, 1988

Detection of HTLV-I DNA & Antigen in Spinal Fluid & Blood of Pts with Chronic Progressive Myelopathy
NEJM 318:1141-1147, 11951988., Bhagavati,S.,et al, 1988

Prolonged Survival & Partial Recovery in AIDS-Associated Progressive Multifocal Leukoencephalopathy
Neurol 38:1060-1065, Berger,J.R.&Mucke,L., 1988

Progressive Multifocal Leukoencephalopathy after Cardiac Transplantation
Neurol 38:995-996, Hall,W.A.,et al, 1988

Paraplegia and Quadriplegia after Intrathecal Chemotherapy
Arch Phys Med Rehabil 69:1054-1056, Werner,R.A., 1988

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

Positron Emission Tomography in a Patient with Progressive Multifocal Leukoencephalopathy
Neurol 38:1864-1867, Kiyosawa,M.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

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

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

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

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Radiculomeningeal Vascular Malformations of the Spine:MR Imaging
Radiology 164:845-849, Nasaryk,T.J.,et al, 1987

Iodinated Contrast Agents in Myasthenia Gravis
Neurol 37:1400-1402, Frank,J.H.,et al, 1987

Computed Tomography Abnormalities in Hanging
Neuroradiology 29:297-298, Bianco,F.&Floris,R., 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Miliary Metastasis to the Brain:Clinical & Radiologic Features
Neurol 37:1817-1818, Floeter,M.K.,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

Showing articles 2050 to 2100 of 2426 << Previous Next >>