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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 1300 to 1350 of 1523 << Previous Next >>

Diagnosis & Treatment of Lumbosacral Plexopathies in Patients with Cancer
Arch Neurol 41:1282-1285, Pettigrew,L.C.,et al, 1984

Enterogenous Intraspinal Cysts
J Neurosurg 61:834-840, Agnoli,A.L.,et al, 1984

Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983

Hypertrophic Neuropathy & Multiple Sclerosis
Neurol 33:1361-1364, Rosenberg,N.L.,et al, 1983

Idiopathic Recurrent Myoglobinuria & Persistent Weakness
Neurol 33:1613-1615, Bermils,C.,et al, 1983

Endocrine Myopathies
BMJ 287:705-708, Kendall-Taylor,P.,et al, 1983

Paraparesis Following Intrathecal Chemotherapy
Neurol 33:1032-1038, Hahn,A.F.,et al, 1983

"Claudication"of the Sciatic Nerve
BMJ 286:1785-1786, Lamerton,A.J.,et al, 1983

Dominant Chondrodysplasia Punctata with Neurologic Symptoms
Neurol 33:1095-1097, Curless,R.G., 1983

Acute Flaccid Neonatal Paraplegia:A Case Report
Neurol 33:93-95, Haldeman,S.,et al, 1983

Myopathy & Hypersensitivity to Phenytoin
Neurol 33:790-791, Harney,J.,et al, 1983

Paraplegia Associated with Intraaortic Balloon Pump Counter-pulsation
Stroke 14:983-986, Singh,B.M.,et al, 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Myelomalacia & Hypoglycorrhachia in Malignant Atrophic Papulosis
Neurol 33:936-939, Label,L.S.,et al, 1983

Isaacs'Syndrome with Muscle Hypertrophy Reversed by Phenytoin Therapy
Arch Neurol 40:241-242, Zisfein,J.,et al, 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Proximal Myopathy Due to Discrete Carcinomatous Metastases in Muscle
JNNP 46:358-360, Doshi,R.,et al, 1983

An Unusual Cause of Hypokalemic Muscle Weakness
Neurol 33:1242-1243, Valeriano,J.,et al, 1983

Myositis of Chronic Graft Versus Host Disease
Neurol 33:1222-1224, Reyes,M.G.,et al, 1983

Quadriplegia Secondary to Hematoma after Lateral C-1, C-2 Puncture in a Leukemic Child
Neurosurgery 12:230-231, Mapstone,T.B.,et al, 1983

Aortic Saddle Embolus, A Twenty-Year Experience
Ann Surg 197:698-706, Busuttil,R.W.,et al, 1983

Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
Pathology 14:435-438, Ojeda,V.J., 1982

The Jamaica Ginger Paralysis
JAMA 248:1864-1867, Morgan,J.P.,et al, 1982

Clinical Features of Ciguatera Fish Poisoning, A Study of the Disease in the US Virgin Islands
Jr. , et al, Arch Int Med 142:1090-109282., Morris,J.G., 1982

Transient Areflexia & Quadriplegia Following Metrizamide Myelography
Ann Neurol 12:406-407, Peroutka,S.J.,et al, 1982

Recurrent Paraplegia with Total Recovery from Spontaneous Spinal Epidural Hematoma
Ann Neurol 11:623-624, Hernandez,D.,et al, 1982

Clin. Path. Conference
Spinal Epidural Hematoma, With Compression of Cauda Equina, Case Record 14-1982, NEJM 306:855-86082., , 1982

Radiculomyelopathy Due To Genital Herpes
Lancet 2:987-988, Handler,O.E.,et al, 1982

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Inclusion Body Myositis
Arch Neurol 39:760-764, Danon,M.J.,et al, 1982

A Prospective Study of Lacunar Infarction Using Computerized Tomography
Neurol 32:49-56, Donnan,G.A.,et al, 1982

Neurological Aspect of Hyponatraemia
Postgrad Med J 58:737-740, Daggett,P.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Tethered Cord Syndrome in Adults
J Neurosurg 57:32-47, Pang,D.&Wilberger,J.E.Jr., 1982

Atlanto-Axial Instability in Children with Down Syndrome
Pediat Radiol 10:129-132, Pueschel,S.M.,et al, 1981

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Neurologic Manifestations of Systemic Vasculitis
Am J Med 71:517-524, Moore,P.M.,et al, 1981

Sjogren Syndrome:Central Nervous System Manifestations
Neurol 31:1391-1396, Alexander,G.E.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Bilateral Vocal Cord Paralysis in a Patient With Familial Hypertrophic Neuropathy
Arch Neurol 38:532, Johnson,J.A.,et al, 1981

Lumbosacral Plexus Neuropathy
Neurol 31:1327-1330, Evans,B.A.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

Acute Quadriplegia Due to Bilateral Cerebral Metastases
Neurol 31:343-346, Levine,D.N.,et al, 1981

Lumbosacral Plexus Neuritis
Neurol 31:470-473, Sander,J.E.,et al, 1981

Unicyclist's Sciatica-A Case Report
NEJM 305:231-232, Gold,S., 1981

Spinal Subarachnoid Hematoma
NEJM 303:1020-1021, Brem,S.S., 1981

Familial Spastic Paraplg, Peroneal Neuropathy, & Crural Hypopig, A New Neurocut Synd
Neurol 31:754-757, Stewart,R.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Showing articles 1300 to 1350 of 1523 << Previous Next >>