Neudle.com: hip disease

Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

abducens nerve paralysis

abducens nerve paralysis, bilateral

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acne fulminans

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome-related complex

acromegaly

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

Addison's disease

advance directives

adverse drug reaction

agitation

alcohol

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic withdrawal states, DT's, convulsions, etc.

alcoholism

aldolase

Alzheimer's disease

Alzheimer's disease, risk factors in

Alzheimer's disease, treating associated medical problems in

amaurosis fugax

amphotericin B

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

angiotensin-converting enzyme

anorexia

anterior horn cell disease

anterior tibial muscle weakness

anti Jo1 antibody

anti Ku antibody

anti Mi2 antibody

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

anticoagulant, complications of

anticoagulant, discontinuation

anticoagulant, restarting

anticoagulant, reversal of

anticoagulant, treatment

anticonvulsants

anticonvulsants, compliance

anticonvulsants, effectiveness

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

apraxia of eyelid opening

arthrogryposis multiplex

atrioventricular block

autonomic dysfunction

beta adrenergic blocker

blepharophimosis

blepharospasm

blood gases, arterial

brachial plexus neuropathy

calcification, intracranial

cancer associated myopathy

canned food

carbenoxolone

carcinoma

carcinoma of esophagus

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carotid sinus pressure

carotid sinus syndrome

carpal tunnel syndrome

CAT scan, emission, abnormal

CAT scan, false negative

cavernous sinus, expansion

cavernous sinus, lesion of

CD4 counts

central core disease

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral palsy

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, complications with

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, postoperative

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, time of onset

cerebrovascular accident, young adult

cerebrovascular disease

ceruloplasmin, serum

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chest pain

chest x-ray, abnormal

chromosomal abnormality

chromosome 3

chromosome 5

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

colonoscopy

coma

compartment syndrome

complex regional pain syndrome

compliance

complications

compression fracture

compression neuropathy

conduction block

confusion

confusional state, acute

congenital heart disease

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

corticotropin-releasing factor

cortisol, elevated

coumarin

coumarin, stopping treatment

Coxa saltans

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, unilateral

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein

C-reactive protein, elevated

creatine kinase

creatine phosphokinase(CPK)elevated

crossed straight leg raising test

dementia, frontotemporal

dementia, rapidly progressive

dementia, subcortical

dental procedure, neurologic complications with

developmental retardation

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diagnostic criteria

diaphragmatic paralysis

diarrhea

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

dilantin

dilantin, hypersensitivity to

diphosphonates

diplegia, brachial

diplopia

disability, neurological

dislocated hip

dislocated hip, congenital

disorientation

distal muscle atrophy

distal muscle weakness

drug abuse, inhalation

drug induced neurologic disorders

dystrophic calcification

echocardiogram, transesophageal

edema, pedal

efficacy

Ehlers-Danlos syndrome

ejection fraction, abnormal

electrical injury of nervous system

electrocardiogram, abnormal

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

embolism

embolism, fat

embolism, paradoxical

emergency room

Emery-Dreifuss muscular dystrophy

encephalitis, human immunodeficiency virus type 1

encephalopathy

encephalopathy, progressive

endoscopic surgery

endoscopy

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

epicanthal folds

epidemiology of neurology

epidural steroid

epsilon-aminocaproic acid(E.A.C.A.)

evoked potentials

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

extraocular muscle lesion

eye closure

eye movement, disorders of

face, elongated

facial anomalies

facial appearance, abnormal

facial hair, excessive

facial nerve palsy

facial nerve palsy, recurrent

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fetal alcohol syndrome

foot ulcer, neuropathic

fracture, long bone

fracture, long bones, nerve injury with

fracture, pathologic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frontal lobe, pathologic signs of

gadolinium

gag reflex, depressed

gait disorder

gait training

gait, waddling

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

give-way weakness

glucose tolerance test, abnormal

glycogen debranching enzyme deficiency

glycogen storage disease

gout

Gowers maneuver

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

grimacing

groin pain

guanethidine

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, variant forms of

gunshot wounds

gynecomastia

hallucination

hallucination, auditory

hallucination, visual

heart block, complete

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, differential diagnosis of

herniated disc, lumbar

herniated disc, lumbar-conservative vs.surgical treat.of

herniated disc, lumbar-laminectomy

herpes zoster

high arched feet

high arched palate

highly active antiretroviral therapy

histochemistry of muscle

HLA

HMGcoA reductase inhibitors

human immunodeficiency virus type 1

hung reflex

hyperadrenalism

hypercalcemia

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperparathyroidism

hyperparathyroidism, secondary

hyperphosphatasia

hyperreflexia

hypersensitivity reaction

hypertension

hyperthyroidism

hypertrophic intracranial pachymeningitis

hypertrophic spinal pachymeningitis

hypoglycemia

hypokalemia

hypokalemic periodic paralysis

hypomagnesemia

hyponatremia

hypoosmolality of serum

hypotension, systemic

iatrogenic neurologic disorders

idiopathic inflammatory myopathy

ileus, paralytic

imbalance

immune checkpoint inhibitors

immune-related adverse events

immunohistochemistry

immunologic disease

immunomodulation

immunosuppressive agents

impotence

impulsivity

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inclusion bodies

inclusion body myositis

infant, evaluation of

intellectual deterioration

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intracerebral hemorrhage

intrinsic hand muscles, wasting of

ipecac

ipilimumab

ischemic exercise test

jaw contractures

jaw jerk, abnormal

jaw pain

Kayser-Fleischer ring

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

leg weakness, bilateral

leg weakness, unilateral

lesions too numerous to count

lethargy

leukocytosis

leukodystrophy

level of consciousness, decreased

lid closure, weakness of

limb-girdle weakness

lip, abnormal

lipid storage myopathy

lipoma of skin

lipomatosis

lipomatosis, multiple symmetrical

liver transplantation

long bone lesion

lordosis

low back pain

lumbosacral radiculopathy

lymphadenopathy

lymphocytic meningoradiculitis

lymphoma

lymphoma involving CNS

lymphoma, meningeal

lymphopenia

lysosomal storage disease

magnetic susceptibility

malabsorption

malabsorption syndrome

malignant hyperpyrexia

McArdle's disease

McArdle's disease, adult onset

median neuropathy

MELAS syndrome

Melkersson's syndrome

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis

meningitis, aseptic

meningitis, lymphomatous

mental retardation

mental status, abnormal

microhemorrhage, intracerebral

middle cerebellar peduncle

migraine

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

mononeuropathy, children

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, punctate pattern

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, starfield pattern

multiple sclerosis, relapsing

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphorylase deficiency

muscle spasm

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myocardial infarction

myopathy, carcinomatous

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, hypocalcemic

myopathy, hypokalemic

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, proximal

myopathy, steroid induced

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myositis

myositis, granulomatous

myxedema, neurologic manifestations of

needle induced neuropathy

negative

Nelson's syndrome

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing, ectopic

neoplasm, metastatic to muscle

nerve biopsy

nerve conduction studies

nerve injury

nerve root compression

nerve root, lumbar, lesion of

neuritis, causes of

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, diabetic

neuropathy, iatrogenic

neuropathy, ischemic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, postoperative

neuropathy, recurrent

neuropathy, sensory

neuropathy, short-fiber

neuropathy, toxic

neuropathy, vasculitic, systemic

neurotoxic

neurotoxin

neutropenia

next-generation sequencing

old age, neurology of

opened mouth

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

optic atrophy

optic nerve, lesion of

orthostatic hypotension

osteolytic lesion, causes of

osteomalacia

osteoporosis

overlap syndrome

pacemaker, cardiac-transvenous

palpebral fissure, short

palpitations

paralysis, acute areflexic

paraspinal muscle weakness

Parkinsonism syndrome

parotid gland swelling

parvovirus

patent foramen ovale

patient information and support

periodic paralysis, thyrotoxic

peripheral nerve, lesion of

personality change

petechiae

philtrum, hypoplastic

phlebotomy

physical therapy

pinched face

piriformis muscle syndrome

plasma cell dyscrasia

plasmapheresis

platelet inhibiting drugs

platelet inhibiting drugs, discontinuation

pleocytosis of cerebrospinal fluid

pleurisy

pneumonia

poison, neurologic problems with

poison, organophosphate

poliomyelitis

polymerase chain reaction

polymyalgia rheumatica

polymyositis

polymyositis, eosinophilic

polyneuritis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyradiculoneuropathy

polyuria

Pompe's disease of glycogen storage

porphyria

position sensation, abnormal

positive sharp waves

post traumatic pain syndrome

posterior column disease

postoperative neurologic complications

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognosis

progressive neurologic disorder

progressive supranuclear palsy

propranolol

proteinuria

proximal muscle atrophy

proximal myotonic myopathy

pseudohypertrophy

pseudomyotonia

psychiatric problems in neurologic disorders

psychological testing

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

radial nerve, palsy of

radiculitis

radiculopathy

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

recurrent

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

regional enteritis

rehabilitation for neurologic disorders

release phenomena

remote effect of cancer on the nervous system

renal failure

renal stones

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retina, abnormal

retinal lesion

retroperitoneal hemorrhage

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

Schwartz-Jampel syndrome

scoliosis, neurologic association with

screening

sedation

sedimentation rate

sedimentation rate, elevated

seizure

seizure, complications following

seizure, focal

seizure, injury following

sensorineural hearing loss

sensory loss

seroconversion

short stature

shoulder, dislocation

shoulder, fracture

shoulder, pain in

single-fiber electromyography

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

spinal cord, compression of

spinal cord, injury of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal pachymeningitis

spinal stenosis

spinal stenosis, cervical canal

spinocerebellar degeneration

spirochete infection

splenomegaly

splinter hemorrhages

sports medicine, neurology of

standing difficulty

starvation, therapeutic

statin therapy

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

stiff joints

stiff man syndrome

straight leg raising test

strokelike episodes

subarachnoid hemorrhage

survival motor neuron gene

sweating, abnormality of

systemic lupus erythematosus

telangiectases, periungual

temporal artery, biopsy

temporal lobe, lesion

temporalis muscle wasting

tenderness

tensilon test, false positive

thermography

third nerve palsy

third nerve palsy, pupil sparing in

thirst

thyroid function tests

tissue plasminogen activator, intravenous

toe walking

tongue, enlarged

tongue, fasciculations of

tongue, weakness

torticollis

toxic shock syndrome

toxins, nervous system

transient ischemic attack

transluminal angioplasty, coronary artery

transurethral prostatectomy

transverse smile

trauma

treatment of neurologic disorder

tremor

tremor, intention

trichopoliodystrophy

trinucleotide repeats

type 1 muscle fiber

type 2 muscle fiber

ulcerative colitis

ulnar nerve, compression of

urine osmolality, elevated

urine test for metabolic disorders

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral myopathy

vision, blurred

visual acuity, decreased

vitamin supplementation

vitamin therapy

walking frame

walking, difficulty with

Watson-Schwartz reaction

weakness, fluctuating

weakness, functional

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

X-linked bulbospinal neuronopathy

Showing articles 100 to 150 of 219 << Previous Next >>

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

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

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,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

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,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

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

Osteomalacic Myopathy
Muscle & Nerve 17:578-580994., Russell,J.A., 1994

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Pediatric Median Mononeuropathies:A Clinical and Electromyographic Study
Muscle & Nerve 17:755-762994., Deymeer,F.&Jones,H.R., 1994

Sciatic Neuropathy:Clinical and Prognostic Features in 73 Patients
Neurol 44:1669-1674, Yuen,E.C.,et al, 1994

Seizure-Induced Thoracic Burst Fractures
Spine 19:77-79, McCullen,G.M.&Brown,C.C., 1994

Brief Report:Fulminating Fat Embolism Syndrome Caused by Paradoxical Embolism Through a Patent Foramen Ovale
NEJM 329:926-929, 9611993., Pell,A.C.H.,et al, 1993

The Treatment of Inclusion Body Myositis:A Retrospective Review & Random, Prospective Trial of Immunosupp Therapy
Medicine 72:225-235, Leff,R.L.,et al, 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Clinical Characteristics of Vasodepressor, Cardioinhibitory, and Mixed Carotid Sinus Syndrome in the Elderly
Am J Med 95:203-208, McIntosh,S.J.,et al, 1993

Trauma and Multiple Sclerosis:A Population-Based Cohort Study from Olmsted County, Minnesota
Neurol 43:1878-1882, 18711993., Siva,A.,et al, 1993

Cranial Neuropathy Heralding Otherwise Occult AIDS-Related Large Cell Lymphoma
J Clin Neuro-Ophthalmol 13:113-118, Berger,J.R.,et al, 1993

Neuromuscular Manifestations of Wegener's Granulomatosis:A Case Report
Neurol 43:617-618, Finkelman,R.,et al, 1993

Rate and Types of Fractures in Corticosteroid-Treated Multiple Sclerosis Patinets
Neurol 42:1389-1391, Troiano,R.A.,et al, 1992

Pravastatin-Associated Inflammatory Myopathy
NEJM 327:649-650, Schalke,B.B.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Chronic Limb-Girdle Myasthenia Gravis
Neurol 42:1153-1156, Oh,S.J.&Kuruoglu,R., 1992

Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
Neurol 42:1422-1423, Bird,S.J., 1992

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Dystrophinopathy in Isolated Cases of Myopathy in Females
Neurol 42:967-975, Hoffman,E.P.,et al, 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Acute Compartment Syndromes Resulting from Anticoagulant Treatment
BMJ 305:1474-1475, Hay,S.M.,et al, 1992

The Bruns-Garland Syndrome (Diabetic Amyotrophy) , Revisited 100 Years Later
Arch Neurol 48:1130-1135, Barohn,R.J.,et al, 1991

Prognosis in AZT Myopathy
Neurol 41:1181-1184, Chalmers,A.C.,et al, 1991

Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
Ann Neurol 29:606-614, Mhiri,C.,et al, 1991

Clinical Follow-Up and Immunogenetic Studies of 32 Patients with Eosinophilia-Myalgia Syndrome
Lancet 337:1071-1074, Kaufman,L.D.,et al, 1991

Colchicine-Induced Myopathy and Neuropathy
Neurol 41:943, Younger,D.S.,et al, 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Delirium in the Elderly Patient
NEJM 320:578-582, Lipowski,Z.J., 1989

Prevention of Falls Among the Elderly
NEJM 320:1055-1059, Tinetti,M.E.&Speechley,M., 1989

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

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

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

Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Clin Characteristics, Course, & Diag Criteria
Arch Neurol 46:878-884, Barohn,R.J.,et al, 1989

Compartment Syndrome of the Thigh
Editorial, Lancet 2:485-4861989., , 1989

Seizure as a Cause of Fracture
& Cardi, J. K. , Neurol 39:858-860, Finelli,P.F., 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

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

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Showing articles 100 to 150 of 219 << Previous Next >>