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Differential
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abdominal distention

abducens nerve paralysis

acid maltase deficiency

acid maltase deficiency, adult

advances in neurology

adverse drug reaction

anesthesia, general

anterior horn cell disease

anticonvulsants

antineurofascin antibodies

arrhythmia, cardiac

autoimmune disease

autonomic dysfunction

bulging of biceps

calf hypertrophy

cardiovascular disease

CAT scan, emission, abnormal

cauda equina, enhancement

cauda equina, lesion of

cavernous sinus

cavernous sinus, lesion of

central nervous system, infection of

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

Charcot-Marie-Tooth

chewing, impaired

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

CLOVES syndrome

clubfoot as related to neurologic disease

congenital malformation

congenital myopathy

congestive heart failure

contactin associated protein like 1 antibodies

contractures, joint

conus medullaris, lesion of

corticotropin level

corticotropin-releasing factor

cortisol, elevated

cranial nerve enlargement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Cushing's syndrome

cysticercosis, cerebral

cysticercosis, disseminated

cysticercosis, intraventricular

cysticercosis, miliary

cysticercosis, spinal

cysticercosis, subarachnoid

Dejerine-Sottas syndrome

denervation of muscle

diabetes mellitus

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

distal muscle atrophy

distal muscle weakness

Dominican Republic

dysferlinopathy

dysplasia of C.N.S.

dystonia, post traumatic

echocardiogram, LVH

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

entrapment neuropathy

epidermal nevus syndrome

facial hair, excessive

facial pain, atypical

facial weakness

facial weakness, bilateral

failed back syndrome

failed medical management

fine motor function, impaired

fourth ventricle, cyst

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

Gowers maneuver

Guillain Barre syndrome, differential diagnosis of

helminthic infection of CNS

hemiatrophy, congenital

hemidiaphragm, paralysis of

hemihypertrophy, congenital

hemihypertrophy, facial

hemimegalencephaly

hereditary myopathy with early respiratory failure

herniated disc, lumbar

herniated disc, lumbar, recurrent

herniated disc, lumbar-laminectomy

high arched feet

H-reflex testing

hydrocephalus, non-communicating(obstructive)

hypoglycorrhachia

hypomelanosis of Ito

hypopigmentation of skin

IgG4-related disease

inability to sit up

incontinence, fecal

infantile spasm

intellectual deficit

intracranial pressure, increased

intrinsic hand muscles, wasting of

Isaacs syndrome

Kobberling-Dunnigan syndrome

kyphoscoliosis, neurologic causes of

left ventricular dilatation

leg weakness, bilateral

leg weakness, unilateral

life expectancy

limb hypertrophy

limb-girdle weakness

lumbosacral plexopathy

lymphoma, primary of CNS

malformation, CNS, congenital

malignant hyperpyrexia

meningitis, aseptic

meningitis, cysticercosis

meningitis, eosinophilic

mental retardation

mental status, abnormal

metabolic alkalosis

molecular genetics

monoclonal gammopathy

mononeuropathy chronic inflammatory demyelinating

motor neuron disease

movement disorder

MRI, contrast enhanced

MRI, contrast enhanced, postoperative

MRI, cranial nerves

MRI, lumbosacral plexus

MRI, peripheral nerve

MRI, spinal cord

MRI, spine, postoperative

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle hypertrophy

muscle hypertrophy, congenital

muscle stiffness

muscle swelling

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myeloradiculopathy

myopathy, amyloid

myopathy, focal

myopathy, hereditary

myopathy, metabolic

myopathy, monomelic

myopathy, quadriceps

myopathy, vacuolar

myotonia congenita

nausea and vomiting

neoplasm, hormone producing, ectopic

neoplasm, peripheral nerve

nephrotic syndrome

nerve conduction studies

nerve enlargement

nerve hypertrophy

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurologic disease, diagnoses of

neurologic examination

neurolymphomatosis

neuropathy, ataxic

neuropathy, autoimmune

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

night blindness

node of Ranvier

nodopathy, autoimmune

optic nerve, enlarged

parasitic infection, CNS

percussion induced muscle contraction

peripheral nerve, lesion of

peroxisomal disease

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

polyneuropathy, chronic inflammatory demyelinating

post polio syndrome

postoperative lumbar spine

postural abnormality

prenatal diagnosis by amniocentesis

progressive neurologic disorder

proximal muscle atrophy

pseudohypertrophy

pulmonary embolism

Refsum's disease

respiratory failure

retinitis pigmentosa

rippling muscle disease

root lesion, nerve

saddle anesthesia

sarcoglycanopathy

sciatic neuropathy

sedimentation rate, elevated

sensorineural hearing loss

serologic testing

shoulder, elevation

skin, lesions in neurologic disorders

spinal accessory nerve

spinal cord, compression of

spinal cord, extramedullary cyst of

spinal cord, neoplasm

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, intermediate form

standing difficulty

stem cell transplantation

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcutaneous nodules

survival motor neuron gene

tongue, enlarged

tongue, weakness

treatment of neurologic disorder

trigeminal nerve

trigeminal nerve, hypertrophy

urinary frequency

urinary incontinence

visual acuity, decreased

visual fields, constricted

weakness, generalized

weakness, progressive

weakness, proximal

winging of scapula

Showing articles 1100 to 1150 of 1523 << Previous Next >>

Origins of Cerebral Palsy
Am J Dis Child 143:1154-1160, Naeye,R.L.,et al, 1989

Lumbosacral Plexopathy Secondary to Perirectal Abscess in a Patient with HIV Infection
Neurol 39:1400-1401, Holtzman,D.M.,et al, 1989

Sciatic Nerve Damage Due to Toilet Seat Entrapment:Another Saturday Night Palsy
JNNP 52:1113-1114, Tyrrell,P.J.,et al, 1989

Idiopathic Granulomatous Meningitis
JNNP 52:1286-1289, Bakheit,A.M.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

Spinal Epidural Lipomatosis:A Serious Complication of Iatrogenic Cushing's Syndrome
Neurol 39:1031-1034, Kaplan,J.G.,et al, 1989

A Five-Year-Old Girl with Acute Renal Failure and Multiple Cerebral Infarctions
J Pediatr 115:816-823, Mauro,R.D.,et al, 1989

Clinicopath Conf
Diffuse Idiopathic Skeletal Hyperostosis, Case Record 43-1989, NEJM 321:1178-1187989., , 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

Endemic Fluorosis with Spinal Cord Compression, A Case Report and Review
Arch Int Med 149:697-700, Fisher,R.L.,et al, 1989

Pedal Pusher's Palsy
NEJM 320:63, Haig,A.J., 1989

Medical Problems of Musicians
NEJM 320:221-227, 246-2481989., Lockwood,A.H., 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Renal Replacement Treatment in Patients with Spina Bifida or Spinal Cord Injury
BMJ 299:1506, Muralikrishna,G.S.,et al, 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Bilateral Infarction of the Medullary Pyramids in Humans
Neurol 39:21-24, Jagiella,W.M.&Sung,J.H., 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

Maternal Alcohol Use During Breast-Feeding and Infant Mental and Motor Development at One Year
NEJM 321:425-430, Little,R.E.,et al, 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Zidovudine-Associated Myopathy
Am J Med 86:814-818, Gertner,E.,et al, 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Increased Replication of HTLV-I in HTLV-I-Associated Myelopathy
Ann Neurol 26:331-335, Yoshida,M.,et al, 1989

HTLV-I Myeloneuropathy in the Solomon Islands
NEJM 321:615-616, Ajdukiewicz,A.,et al, 1989

HTLV-I Polymyositis in a Patient Also Infected with the Human Immunodeficiency Virus
NEJM 320:992-995, Wiley,C.A.,et al, 1989

Man-In-The-Barrel Syndrome Caused by Cerebral Metastases
Neurol 39:1134-1135, Moore,A.P.&Humphrey,P.R.D., 1989

The Chronic Fatigue Syndrome-One Entity or Many?
NEJM 319:1726-1728, Swartz,M.N., 1989

Fatigue Syndrome:Neurasthenia Revived, Psychiatric Illnesses are Worth Considering
BMJ 298:1199-1200, White,P., 1989

The Alien Hand Syndrome, Clinical and Postmortem Findings
Arch Neurol 46:456-459, Banks,G.,et al, 1989

Guillain-Barre Syndrome Presenting as High-Altitude Cerebral Edema
NEJM 321:545, Shlim,D.R.&Cohen,M.T., 1989

Flaccid Quadriparesis Associated with Yersinia Enterocolitis-Induced Hypokalemia
Arch Int Med 149:1193-1194, Orman,R.A.&Lewis,J.B., 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Nocardial Spinal Epidural Abscess
Neurol 39:996, Siao,P.,et al, 1989

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Nicotinic Acid-Associated Myopathy:A Report of Three Cases
Am J Med 86:481-483, Litin,S.C.&Snderson,C.G., 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Laxative Abuse Causing Hypermagnesemia, Quadriparesis, & Neuromuscular Junction Defect
Neurol 39:746-747, Castelbaum,A.R.,et al, 1989

Hyponatremia and Inappropriate Secretion of Vasopressin (Antidiuretic Hormone) in Patients with Hypopituitarism
NEJM 321:492-496, 5381989., Oelkers,W., 1989

Diaphragmatic Paralysis
Am J Med 86:623-624, Javaheri,S.,et al, 1989

Infectious and Toxic Syndromes from Fish and Shellfish Consumption, A Review
Arch Int Med 149:1735-1740, Estaugh,J.&Shepherd,S., 1989

Nerve Conduction Study of Human Tetrodotoxication
Neurol 39:743-745, Oda,K.,et al, 1989

Showing articles 1100 to 1150 of 1523 << Previous Next >>