Neudle.com: proximal myopathy

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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

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

Addison's disease

adverse drug reaction

alcohol, heart involvement with

alcohol, neurologic complications with

alpha glucosidase

amaurosis fugax

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

angiotensin-converting enzyme

anterior horn cell disease

anterior tibial muscle weakness

anti HMGCR antibody

anti Jo1 antibody

anti Ku antibody

anti Mi2 antibody

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

arrhythmia, cardiac

arthrogryposis multiplex

aspartate aminotransferase

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

ataxia, truncal

atrial fibrillation

atrioventricular block

autoimmune disease

autonomic dysfunction

axonal degeneration

azidodeoxythymidine

Balint's syndrome

beta adrenergic blocker

biologic markers

blepharophimosis

bone marrow transplantation

brachial plexus neuropathy

brain natriuretic peptide

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

calf hypertrophy

cancer associated myopathy

carcinoma of esophagus

carcinoma of lung

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, false negative

cauda equina, enhancement

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

chewing, impaired

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cigarette smoking

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

collagen vascular disease

conduction block

confidentiality

congenital heart disease

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

contractures, joint

corticotropin level

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

Cushing's syndrome

deep tendon reflexes

delay in diagnosis

dementia, frontotemporal

dementia, rapidly progressive

dermatomyositis

descending paralysis

developmental retardation

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diamond on quadriceps

diaphragmatic paralysis

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

dilantin, hypersensitivity to

diplegia, brachial

disability, neurological

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug induced neurologic disorders

dysferlinopathy

dystrophic calcification

echocardiogram, LVH

electrocardiogram, abnormal

electromyogram, decremental response

electromyogram, fasciculation potentials

electromyogram, incremental response

electron microscopy

Emery-Dreifuss muscular dystrophy

encephalopathy, progressive

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

eosinophilia-myalgia syndrome

epidemiology of neurology

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

evoked potentials

exercise intolerance

exercise-induced neurologic dysfunction

exercise-related muscle strength increase

exome sequencing

extraocular muscle lesion

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

fatigable chewing

finger flexor weakness

finger weakness

Fisher's syndrome

flu-like illness

foot ulcer, neuropathic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

gag reflex, depressed

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

glycogen debranching enzyme deficiency

glycogen storage disease

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

hallucination, auditory

heart block, complete

heat intolerance

hepatosplenomegaly

heralding manifestation

high arched feet

high arched palate

hip flexor weakness

histochemistry of muscle

HMGcoA reductase inhibitors

H-reflex testing

human immunodeficiency virus type 1

hyperadrenalism

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperparathyroidism

hyperparathyroidism, secondary

hyperphosphatasia

hypersensitivity reaction

hyperthyroidism

hypokalemic periodic paralysis

hypoosmolality of serum

hypoparathyroidism

hypopituitarism

hypotonia, infants

iatrogenic neurologic disorders

idiopathic inflammatory myopathy

ileus, paralytic

immune checkpoint inhibitors

immune-related adverse events

immunohistochemistry

immunomodulation

immunosuppressive agents

inability to stand on tiptoes

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

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

intellectual deficit

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

ischemic exercise test

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

leg weakness, bilateral

leg weakness, unilateral

lid closure, weakness of

life expectancy

limb-girdle weakness

lipid storage myopathy

lipomatosis, multiple symmetrical

livedo reticularis

liver function enzymes

lumbosacral radiculopathy

lung transplantation

lymphadenopathy

lymphocytic meningoradiculitis

lysosomal storage disease

lysosomes, abnoral

malabsorption syndrome

malignancy screen

malignant hyperpyrexia

McArdle's disease

McArdle's disease, adult onset

McLeod syndrome

Melkersson's syndrome

memory, impairment of

meningitis, aseptic

mental retardation

mental status, abnormal

metabolic acidosis

metabolic alkalosis

middle cerebellar peduncle

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

mononeuropathy multiplex

motor neuron disease

movement disorder

MRI, brachial plexus

MRI, disappearing lesion on

multicore myopathy

multiple myeloma

multiple sclerosis

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphorylase deficiency

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, chronic progressive

myopathy, acquired

myopathy, acute

myopathy, alcoholic

myopathy, amyloid

myopathy, autoimmune

myopathy, carcinomatous

myopathy, critically ill

myopathy, drug-induced

myopathy, glycogen storage

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, scleromyxedema

myopathy, steroid induced

myopathy, steroid responsive

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myositis, focal

myositis, granulomatous

myositis, ocular

myotonia dystrophica

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonic discharges

myxedema, neurologic manifestations of

nausea and vomiting

Nelson's syndrome

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing, ectopic

neoplasm, metastatic to muscle

nerve conduction studies

nerve root enhancement

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, 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

next-generation sequencing

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

oral contraceptives

overlap syndrome

pacemaker, cardiac-transvenous

Paget's disease

pain, abdominal

paralysis, acute areflexic

paraproteinemia

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinsonism syndrome

parotid gland swelling

perhexiline maleate

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

personality change

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

poison, organophosphate

polymerase chain reaction

polymyositis, eosinophilic

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

Pompe's disease of glycogen storage

positive sharp waves

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive neurologic disorder

proximal muscle atrophy

proximal myotonic myopathy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

purkinje cell cytoplastic autoantibody

quadriceps atrophy

quadriceps weakness

quadriparesis, acute

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

Raynaud's phenomenon

regional enteritis

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retina, abnormal

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rigid spine syndrome

sarcoglycanopathy

Schwartz-Jampel syndrome

sclerosis, bone

scoliosis, neurologic association with

sedimentation rate, elevated

sensorineural hearing loss

serum alanine aminotransferase

sex reassignment surgery

shoulder, pain in

single-fiber electromyography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sloped shoulders

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar degeneration

spirochete infection

splinter hemorrhages

standing difficulty

starvation, therapeutic

statin therapy, discontinuation

status asthmaticus

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

strokelike episodes

subarachnoid hemorrhage

subcutaneous edema

survival motor neuron gene

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

telangiectases, periungual

temporal lobe, lesion

temporalis muscle wasting

tensilon test, false positive

thyroid function tests

tongue, enlarged

tongue, fasciculations of

tongue, weakness

toxins, nervous system

transient ischemic attack

transverse smile

treatment of neurologic disorder

tremor, intention

trinucleotide repeats

type 1 muscle fiber

type 2 muscle fiber

ulcerative colitis

upgaze, paralysis of

urinary frequency

urine osmolality, elevated

vestibular migraine

vincristine neurotoxicity

viral infection

vision, blurred

vitamin deficiency

vitamin E deficiency

walking, difficulty with

Watson-Schwartz reaction

weakness, acute

weakness, episodic

weakness, fatiguable

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

white matter disease

winging of scapula

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 800 to 850 of 1051 << Previous Next >>

Suxamethonium Myalgia
Editorial, Lancet 2:945-9461988., , 1988

The Neuromuscular Manifestations of Human Immunodeficiency Virus Infections
Arch Neurol 45:1084-1088, Lange,D.J.,et al, 1988

Genetic Markers for Neurofibromatosis
Editorial, Lancet 2:719-7201988., , 1988

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

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

Diagnosis & Follow-up of Mitochondrial Encephalomyopathy:CT and MR Studies
J Comput Assist Tomogr 12:696-697, Taverni,N.,et al, 1988

Distal Vacuolar Myopathy with Complete Heart Block
Arch Neurol 45:698-699, Krendel,D.A.,et al, 1988

Pyomyositis in a Patient with the Acquired Immunodeficiency Syndrome
Arch Int Med 148:1608-1610, Gaut,P.,et al, 1988

Successful Treatment of Ciguatera Fish Poisoning with Intravenous Mannitol
JAMA 259:2740-2742, Palafox,N.A.,et al, 1988

Overuse Syndrome:A Muscle Biopsy Study
Lancet 1:905-908, Dennett,X.&Fry,H.J.H., 1988

Neuromuscular Diseases Associated with Human Immunodeficiency Virus Infection
Ann Neurol 23:S38-S48, Dalakas,M.C.&Pezeshkpour,G.H., 1988

Fatal Adult Respiratory Distress Syndrome in a Patient with Lyme Disease
JAMA 259:2737-2739, Kirsch,M.,et al, 1988

Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 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

Lyme Myositis:Muscle Invasion by Borrelia Burgdorferi
Ann Int Med 109:245-246, Atlas,E.,et al, 1988

Subacute Structural Myopathy Associated with Human Immunodeficiency Virus Infection
Arch Neurol 45:585-587, Gonzales,M.F.,et al, 1988

Trauma-Triggered Migraine:An Explanation for Common Neurological Attacks after Mild Head Injury
J Neurosurg 68:181-188, Haas,D.C.&Lourie,H., 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Dysphagia in Inclusion Body Myositis
JNNP 51:1542-1545, Wintzen,A.R.,et al, 1988

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

Pyogenic Myositis:CT Evaluation
J Comput Assist Tomogr 12:1002-1005, Tumeh,S.S.,et al, 1988

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

Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis
NEJM 392:1461-1464, Gahl,W.A.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

Whiplash and Its Relationship to Migraine
Headache 27:452-457, Winston,K.R., 1987

Cluster Headache after Head Injury
Headache 27:509-510, Reik,L., 1987

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

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Acute Lead Poisoning in Two Users of Illicit Methamphetamine
JAMA 258:510-511, Allcott,J.V.,et al, 1987

Acetazolamide-Responsive Myotonia Congenita
Neurol 37:488-491, Trudell,R.G.,et al, 1987

Neurologic Disease as the Presenting Manifestation of Acquired Immunodefieicney Syndrome
South Med J 80:683-686, Berger,J.R.,et al, 1987

The Spectrum of Neurol Dis Assoc with Antiphospholipid Antibd, Lupus Anticoag & Anticardiolipin Antibd
Arch Neurol 44:876-883, Levin,S.R.&Welch,K.M.A., 1987

Repetition Strain Injury
Editorial, Lancet 2:3161987., , 1987

Fibromyalgia Syndrome, An Emerging but Controversial Condition
JAMA 257:2782-2787, 2802-28031987., Goldenberg,D.L., 1987

Unusual Manifestations of Nervous System Borrelia Burgdorferi Infection
Arch Neurol 44:781-783, Midgard,R.&Hofstad,H., 1987

Treatment of Myotonia
Editorial, Lancet 1:1242-12441987., , 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

Peripheral Neuropathy Associated with Mitochondrial Myopathy
Ann Neurol 20:249-257, Yiannikas,C.,et al, 1986

Preventive Screening for Fragile X Syndrome
Editorial, Lancet 2:1191-11921986., , 1986

Phenytoin Hypersensitivity:A Case of Severe Acute Rhabdomyolysis
Am J Med 81:928-930, Engel,J.N.,et al, 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Clinicopath Conf
Malignant Lymphoma, Intravascular, Large-Cell, Immunoblastic type (Malignant Angioendotheliomatosis), , Case86,NEJM 315:874-885,1986., 1986

Myopathy After Short Term Administration of Procainamide
BMJ 292:593-594, Lewis,C.A.,et al, 1986

Polyarteritis Manifesting as Calf Myositis & Fever
Am J Med 80:312-315, Ferreiro,J.E.,et al, 1986

Successful Treatment with Tocainide of Recessive Generalized Congenital Myotonia
Ann Neurol 19:501-504, Streib,E.W., 1986

Granulomatous Inflammatory Myopathy Associated with Myasthenia Gravis, A Case Report & Review of the Literature
Arch Neurol 43:621-623, Pascuzzi,R.M.,et al, 1986

Neurologic Complications of Carcinoid
Neurol 36:745-749, Parchell,R.A.&Posner,J.B., 1986

Showing articles 800 to 850 of 1051 << Previous Next >>