Neudle.com: myopathy proximal

Differential
(Click to cross reference)

abdominal distention

abdominal muscle paralysis

abdominal protrusion

abducens nerve paralysis

abducens nerve paralysis, bilateral

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

acromegaly

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

Addison's disease

adverse drug reaction

alcohol

alcohol, heart involvement with

alcohol, neurologic complications with

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

ANA

anemia

aneurysm

angiotensin-converting enzyme

ankle edema

anterior horn cell disease

anterior tibial muscle weakness

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

arthrogryposis multiplex

Asians

aspartate aminotransferase

atrioventricular block

atypical

autoantibodies

autoimmune disease

autonomic dysfunction

axonal degeneration

azidodeoxythymidine

Balint's syndrome

beta adrenergic blocker

bone marrow transplantation

bone pain

bone scanning

botulism

brachial plexus neuropathy

bradycardia

brain natriuretic peptide

bulbar palsy

bulbar palsy, progressive

calcification, intracranial

calf atrophy

calf hypertrophy

camptocormia

cancer associated myopathy

canned food

carbenoxolone

carcinoma

carcinoma of esophagus

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, emission, abnormal

CAT scan, false negative

cataracts

central core disease

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chromosomal abnormality

chromosome 19

chromosome 3

chromosome 5

chronic graft versus host disease

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clofibrate

Coats syndrome

colchicine

collagen vascular disease

congenital heart disease

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

corticotropin-releasing factor

cortisol, elevated

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine kinase

creatine phosphokinase(CPK)elevated

critical care unit

cultured skin fibroblasts

dementia, frontotemporal

dementia, rapidly progressive

developmental retardation

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diamond on quadriceps

diaphragmatic paralysis

diarrhea

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

dilantin

dilantin, hypersensitivity to

diplegia, brachial

diplopia

disability, neurological

dislocated hip, congenital

disorientation

distal muscle atrophy

distal muscle weakness

diuretic

docetaxel

dropped head syndrome

drug induced neurologic disorders

dystrophic calcification

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

Emery-Dreifuss muscular dystrophy

encephalopathy

encephalopathy, progressive

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

epidemiology of neurology

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 appearance, abnormal

facial hair, excessive

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

finger flexor weakness

foot ulcer, neuropathic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

gag reflex, depressed

gait disorder

gait, waddling

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

glycogen debranching enzyme deficiency

glycogen storage disease

gout

Gowers maneuver

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, variant forms of

gynecomastia

hallucination

hallucination, auditory

heart block, complete

heralding manifestation

histochemistry of muscle

HLA

HMGcoA reductase inhibitors

hoarseness

hot bath test

H-reflex testing

human immunodeficiency virus type 1

hung reflex

hyperadrenalism

hypercalcemia

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperparathyroidism

hyperparathyroidism, secondary

hyperphosphatasia

hyperreflexia

hypersensitivity reaction

hypokalemic periodic paralysis

hypomagnesemia

hyponatremia

hypoosmolality of serum

iatrogenic neurologic disorders

idiopathic inflammatory myopathy

ileus, paralytic

imbalance

immune checkpoint inhibitors

immune-related adverse events

immunohistochemistry

immunomodulation

immunosuppressive agents

impotence

impulsivity

inability to stand on tiptoes

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

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

insecticides

insulin

intellectual deficit

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

ipecac

ipilimumab

ischemic exercise test

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

leg atrophy

leg numbness

leg swelling

leg weakness, bilateral

leg weakness, unilateral

lethargy

leukocytosis

leukodystrophy

lid closure, weakness of

life expectancy

limb-girdle weakness

lipid storage myopathy

lipoma of skin

lipomatosis

lipomatosis, multiple symmetrical

liquorice

livedo reticularis

liver disease

liver function enzymes

lordosis

lumbosacral radiculopathy

lung transplantation

lymphadenopathy

lymphocytic meningoradiculitis

lymphopenia

lysosomal storage disease

lysosomes, abnoral

malabsorption

malabsorption syndrome

malignant hyperpyrexia

McArdle's disease

McArdle's disease, adult onset

MELAS syndrome

Melkersson's syndrome

memory, impairment of

meningitis

meningitis, aseptic

mental retardation

mental status, abnormal

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

MRI, disappearing lesion on

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, Becker

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

muscular dystrophy, pattern of muscle involvement

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

myelopathy

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, critically ill

myopathy, drug-induced

myopathy, hereditary

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, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, painful

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, steroid responsive

myopathy, thyroid disease causing

myositis, granulomatous

myositis, ocular

myotonia

myotonia dystrophica

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonic discharges

myxedema, neurologic manifestations of

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing, ectopic

neoplasm, metastatic to muscle

nerve biopsy

nerve conduction studies

neuritis, causes of

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology, brain

neuropathy

neuropathy, diabetic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, short-fiber

neuropathy, toxic

neuropathy, vasculitic, systemic

neurotoxin

neutropenia

next-generation sequencing

oculopharyngeal muscular dystrophy

old age, neurology of

opened mouth

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

pacemaker, cardiac-transvenous

paralysis, acute areflexic

paraspinal muscle weakness

Parkinsonism syndrome

parotid gland swelling

periodic paralysis, thyrotoxic

personality change

pinched face

plasma cell dyscrasia

plasmapheresis

pleurisy

pneumonia

poison, neurologic problems with

poison, organophosphate

poliomyelitis

polymerase chain reaction

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

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

propranolol

proteinuria

proximal muscle atrophy

proximal myotonic myopathy

pseudohypertrophy

pseudomyotonia

psychiatric problems in neurologic disorders

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

renal failure

renal stones

repetitive nerve stimulation

respirator

respiratory failure

respiratory tract infection

retina, abnormal

retinal lesion

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

Schwartz-Jampel syndrome

scleroderma

sclerosis, bone

scoliosis

scoliosis, neurologic association with

screening

sedimentation rate, elevated

seizure

seizure, focal

sensorineural hearing loss

sensory loss

serum alanine aminotransferase

sex reassignment surgery

short stature

shoulder, pain in

single-fiber electromyography

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

sleep apnea

sloped shoulders

SMN1 gene

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar degeneration

starvation, therapeutic

statin therapy

statin therapy, discontinuation

status asthmaticus

status epilepticus

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcutaneous edema

sudden death

suicide

survival motor neuron gene

systemic illness

systemic lupus erythematosus

telangiectases, periungual

temporal lobe, lesion

temporalis muscle wasting

tensilon test, false positive

thirst

thyroid function tests

tongue, fasciculations of

tongue, weakness

torticollis

toxins, nervous system

transgender

transient ischemic attack

transverse smile

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

urine osmolality, elevated

urine, dark

vasculitides

vecuronium

vincristine neurotoxicity

walking, difficulty with

Watson-Schwartz reaction

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 100 to 150 of 1030 << Previous Next >>

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

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

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

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

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

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

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Severe Polymyositis-Like Syndrome Associated with Zidovudine Therapy of AIDS & ARC
NEJM 318:708, Bessen,L.J.,et al, 1988

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

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

Syndrome De Gougerot Sjogren Primitif Avec Polymyosite Necrosante:Effet Favorable de L'Hydroxychloroquine
Rev Neurol 143:147-148, Ponge,T.,et al, 1987

Progressive Nemaline (Rod) Myopathy Associated with HIV Infection
NEJM 317:1602-1603, Dalakas,M.C.,et al, 1987

Spectrum of Inclusion Body Myositis
Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987

Proximal Weakness of the Extremities as Main Feature of Amyloid Myopathy
JNNP 50:1353-1358, Jennekens,F.G.I.&Wokke,J.H.J., 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Colchicine Myopathy & Neuropathy
NEJM 316:1562-1568, Kuncl,R.W.,et al, 1987

Neurotoxic Effects of Organophosphorus Insecticides:An Intermediate Syndrome
NEJM 316:761-763, 807-8081987., Senanayake,N.&Karalliedde,L., 1987

Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
Am J Med 82:447-455, Estes,M.L.,et al, 1987

Tick-Bite Meningoradiculoneuritis:Clinical, Electrophysiologic, & Histolic Findings in 10 Cases
Neurol 37:749-753, Vallat,J.M.,et al, 1987

Clinicopath Conf
Myopathy Due to Adult Acid Maltase Deficiency, 36-1986, NEJM 315:694-701986., , 1986

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

Clin. Path. Conference
External Ophthalmoplegia with Mitochondrial Myopathy, Case Record 3-1985, NEJM 312:171-177985., , 1985

Improved Neurologic Function After Long-Term Correction of Vitamin E Deficiency in Children with Chronic Cholestasis
NEJM 313:1580-1586, Sokol,R.J.,et al, 1985

Reversible Ipecac Myopathy
Arch Neurol 42:188-190, Mateer,J.E.,et al, 1985

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

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

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

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

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

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

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

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

Myopathy Induced by Rifampicin
BMJ 283:105-106, Jenkins,P.,et al, 1981

Chronic Focal Polymyositis in the Adult
JNNP 44:419-425, Bharucha,N.E.,et al, 1981

Proximal Muscle Weakness in Uremia
Arch Neurol 37:555-558, Lazaro,R.P.,et al, 1980

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Proximal Myopathy after Prolonged Total Therapeutic Starvation
BMJ 280:1212-1213, Scobie,I.N.,et al, 1980

Eosinophilic Polymyositis
Arch Neurol 36:721-722, 1979, Stark,R.J., 1979

Reversibility of Human Myopathy Caused by Vitamin E Deficiency
Neurol 29:1182-1186, Tomasi,L.G., 1979

Insulin-Induced Weakness in Hypokalemic Myopathy
Ann Neurol 6:139-140, Ruff,R.L., 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Proximal Myopathy During Beta-blockade
BMJ 2:1331-1332, Forfar,J.C.,et al, 1979

Drug-Induced Myopathies In Man
Lancet 2:562-566, Lane,R.J.M.,et al, 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Showing articles 100 to 150 of 1030 << Previous Next >>