Neudle.com: muscle cramp

Differential
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abdominal cramps

abdominal distention

abdominal muscle paralysis

abdominal muscle spasms

abdominal protrusion

abdominal reflex, absent

abducens nerve paralysis

abscess, vertebral

acquired immunodeficiency syndrome

acute intermittant porphyria

Addison's disease

adverse drug reaction

agitation

alcohol, neurologic complications with

alcoholism

alopecia

alternating hemiplegia

amaurosis fugax

amenorrhea

amphetamines

amphiphysin antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

ANA

anasarca

anemia

anemia, megaloblastic

anterior horn cell disease

anti citrullinated antibody

antibiotics

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticholinergic drugs

antineutrophil cytoplasmic autoantibodies

antispasticity drugs

aqueduct of Sylvius, obstruction

autoimmune cerebellar ataxia

autoimmune disease

autonomic dysfunction

autonomic dysfunction, acute

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

bedridden

benign essential tremor

bone demineralization

bone pain

botulinum toxin

botulism

brachial plexus neuropathy

brain biopsy

brainstem, infarction of

burning feet, differential diagnosis of

calcification, intracranial

calf hypertrophy

camptocormia

campylobacter infection

cancer, unknown origin

carcinoma of unknown origin

cardiomegaly

cardiomyopathy

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, disappearing lesion on

CAT scan, false negative

CAT scan, serial

cataracts

catecholamine

cauda equina, enhancement

CD4 counts

cecum perforation

celiac disease, adult

celiac disease, epilepsy and cerebral calcification

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, secondary

cerebellar degeneration

cerebellum, disease of

cerebral edema

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, familial occurrence

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

Charcot-Marie-Tooth

chest pain

chest x-ray, abnormal

chewing, impaired

children

chills

Chinese paralytic syndrome

chorea

chromosomal abnormality

Churg-Strauss syndrome

Chvostek sign

cisterna magna

Clinical Pathologic Conference(C.P.C.)

clonus

clostridium tetani

coenzyme Q10

coenzyme Q10 deficiency

collagen vascular disease

congestive heart failure

conjunctivitis

consanguinity

constipation

contactin associated protein like 2 antibodies

contractures, joint

corneal reflex, abnormal

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Cuba

cultured skin fibroblasts

cyclophosphamide

cylindrical spiral

cyst, bone

cyst, cortical parenchyma

cyst, ventricular

cysticercosis

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cystoisospora belli

cytomegalic inclusion disease

cytomegalovirus infection

degenerative diseases of CNS

delirium

dementia

demyelinating disease

denervation of muscle

denervation potentials

Dengue fever

depression

dermatitis

dermatitis herpetiformis

dermatomyositis

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diabetic radiculopathy

dialysis

dialysis disequilibrium syndrome

differential diagnosis

dilantin

diplopia

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dizziness

drooling

dropped head syndrome

drowsiness

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

dura, thickened

dying

dysarthria

dysequilibrium syndrome

dystonia, drug induced

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electromyogram, incremental response

electrophoretic pattern, serum

emergencies, neurologic

emotional lability

empyema, epidural-spinal

encephalitis

encephalomyopathy

encephalopathy

encephalopathy, Hashimoto's

encephalopathy, metabolic

endemic area

enteritis

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemic

epidemiology of neurology

epilepsia partialis continua

episcleritis

episodic neurologic deficits

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

face, numbness of

facial movement disorder

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

fasciculation, benign

fine motor function, impaired

fourth ventricle, cyst

frontal lobe, pathologic signs of

fundus, abnormality of

fungal infection, CNS

gamma amino butyric acid

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric dilatation, acute

gastroenteritis

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

glutamic acid decarboxylase, antibody

glycogen storage disease

GM1 ganglioside antibodies

gram positive rod

granuloma, eosinophilic

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

gynecomastia

hallucination

hallucination, auditory

hallucination, visual

headache, chronic daily

headache, severe

headache, vascular

hearing loss

hearing loss, sudden, bilateral

heart block

heavy metal intoxication

heliotrope rash

helminthic infection of CNS

hematuria, microscopic

hemianopia, homonymous

hemiballismus

hemiparesis

hemiparesis, transient

hemorrhagic diathesis

hepatitis

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, thoracic

herpes simplex virus

herpes virus

herpes virus infection

histochemistry of muscle

HMGcoA reductase inhibitors

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hypereosinophilic syndrome(HES)

hyperexcitable peripheral nerve disorder

hypergammaglobulinemia

hyperhidrosis

hyperkalemia

hyperkalemic periodic paralysis

hyperparathyroidism

hyperpathia

hyperphosphatasia

hyperpigmentation of skin

hypokalemic paralysis

hypokalemic periodic paralysis

hypomyelination

hyponatremia

hyponatremia with cerebral disorders

hyponatremic encephalopathy

hypoosmolality of serum

hypoparathyroidism

hypoparathyroidism, idiopathic

hypoprothrombinemia

hyporeflexia

hyposmia

hypothalamus, disturbance of

hypothyroidism

hypoxia

iatrogenic neurologic disorders

immunosuppressive agents

impotence

inappropriate antidiuretic(A.D.H.)hormone

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

inborn errors of metabolism

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrinsic hand muscles, wasting of

iritis

irritability

Isaacs syndrome

ischemic exercise test

juvenile distal and segmental muscular atrophy

Kearns-Sayre syndrome

keratitis, interstitial

lactic acidemia

lactic dehydrogenase(LDH)

laughing, pathologic

lead and the nervous system

leg weakness, bilateral

leg weakness, unilateral

leptospirosis

leukocytosis

leukodystrophy

level of consciousness, decreased

lid lag

limbic encephalitis

lipid lowering agent

lipid storage disorder of CNS

livedo reticularis

liver biopsy

liver disease

liver function enzymes

lymphadenopathy, axillary

lymphocytic meningoradiculitis

lymphoma involving CNS

lysosomal storage disease

malabsorption

malabsorption syndrome

malaise

malignant hyperpyrexia

malignant papulosis

mastoiditis

McArdle's disease

McArdle's disease, adult onset

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, leptospira

meningitis, noninfectious

meningoencephalitis

mental status, abnormal

metabolic disorder, primary

methylmalonic acid, serum

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

monoparesis

mortality

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, psychogenic

MRI, contrast enhanced

MRI, gradient-echo

MRI, hypointense signal foci on

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle cramp, nocturnal

muscle pain

muscle pain-fasciculation syndrome

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle relaxant

muscle spasm

muscle spasm, paraspinal

muscle stiffness

muscle strength, testing

muscle tenderness

muscle twitching

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker, carrier

myasthenia gravis

myasthenic syndrome

myelopathy

myelopathy, chronic progressive

myeloradiculitis

myocardial infarction

myocardial infarction, acute

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, hypocalcemic

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, proximal

myopathy, thyroid disease causing

nasal septum, perforation of

nausea and vomiting

neck pain

neck weakness

neoplasm, primary of CNS-intraventricular

nephritis

nephrotic syndrome

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

neuroendocrinology

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuropathology, brain

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, thoracoabdominal

neuropathy, toxic

neuropathy, vasculitic, systemic

nutritional deficiency

nystagmus

occupational neurologic disorders

oculomasticatory myorhythmia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

ophthalmoplegic migraine

opisthotonus

optic neuritis

optic neuritis, bilateral

oral contraceptives

oral ulcerations

orthostatic hypotension

osteomyelitis

osteomyelitis, spinal

osteoporosis

otitis, neurologic complications with

paralysis, acute areflexic

paraparesis

paraparesis, spastic

paraplegia

parasitic infection, CNS

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal neurologic disorder

PAS positive

PAS positive material in the brain

periodic paralysis, thyrotoxic

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

phosphorylase b kinase deficiency

photophobia

pituitary stalk

pituitary stalk, lesion of

plasmapheresis

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleurisy

poison, organophosphate

polymerase chain reaction

polymyalgia rheumatica

polymyositis

polymyositis, eosinophilic

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polyneuropathy, uremic

polyps, gastrointestinal tract

polyradiculoneuropathy

porphyria

posterior column disease

posterior leukoencephalopathy syndrome

postoperative neurologic complications

postural abnormality

potassium

potassium channel antibodies

practice guidelines

precipitating factors

pressure sores

primary aldosteronism

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive neurologic disorder

progressive spinal muscular atrophy

proteinuria

protozoan infection

proximal muscle atrophy

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pupil, oval

pyramidal tract dysfunction

quadriparesis

quadriplegia

quadriplegia, transient

quinidine

quinine

rabies, nervous system involvement with

race

radial nerve, palsy of

reflex sympathetic dystrophy

reflex, brainstem

reflex, brainstem, absent

refractory sprue

regional enteritis

remote effect of cancer on the nervous system

renal failure

renal stones

renal transplantation

repetitive nerve stimulation

respiratory failure

respiratory tract infection

restless leg syndrome

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rhinorrhea

rickets

rigidity

rippling muscle disease

risus sardonicus

Romberg's sign

rooting reflex

Sabin-Feldman dye test

saccadic eye movements, abnormal

safety

salivation, excessive

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure

seizure, children

seizure, differential diagnosis of

seizure, focal

sensorineural hearing loss

sensory loss, band distribution

sensory polyneuropathy

serologic testing

serum glutamic oxaloacetic transaminase

serum lipase, elevated

shoulder, pain in

shunt procedure, ventricular

sick sinus syndrome

single-fiber electromyography

sinusitis

skin, biopsy

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

skin, thickened

sleep pathology and physiology

spasticity, treatment of

spinal cord

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, infarction of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 2

spinocerebellar degeneration

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage, prognosis

suspended sensory loss

sweating

sweating, abnormality of

temporal artery, biopsy

temporalis muscle wasting

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, fasciculations of

tongue, impaired movements of

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

transcutaneous electrical nerve stimulation

transient ischemic attack

travel, foreign

treatment of neurologic disorder

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

trismus

tropical disease

Trousseau's sign

truncal polyneuropathy

tubular aggregates, muscle

uremic encephalopathy

uremic twitching

urinary 17 hydroxycorticosteroids

urinary 17 ketosteroids

urinary catecholamines

urinary retention

urine osmolality, elevated

vanilmandelic acid, urine

visual acuity, decreased

visual evoked response

visual field defect

visual impairment

visual loss

visual loss, transient

walking, difficulty with

Watson-Schwartz reaction

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight loss

Wernicke's encephalopathy

X-linked bulbospinal neuronopathy

X-linked myopathy

yersinia enterocolitica

Showing articles 2900 to 2950 of 3286 << Previous Next >>

Cranial Neuropathy, Myeloradiculopathy, & Myositis, Complications of Mycoplasma Pneumoniae Infection
Arch Neurol 36:476-477, Rothstein,T.L.,et al, 1979

Benign Acute Childhood Myositis
Neurol 29:1068-1071, Henly,J.,et al, 1979

5'-Nucleotidase Activity in Duchenne Muscular Dystrophy
NEJM 301:726, Scholte,H.R.,et al, 1979

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

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

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Neonatal Myasthenia Gravis in the Infant of a Myasthenic Mother in Remission
Ann Neurol 6:72-75, Elias,S.B.,et al, 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Disorders of Neuromuscular Transmission Caused by Drugs
NEJM 301:409-413, Argov,Z.,et al, 1979

Primary Hyperparathyroidism Presenting as Fever of Unknown Origin with Unremitting Headache
Ann Int Med 91:575-576, Blair,D.C.,et al, 1979

Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
Ann Neurol 6:302-314, Dyck,P.J.,et al, 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Acute Generalized Polyneuropathy Accompanying Lithium Poisoning
Ann Neurol 6:360-362, Brust,J.C.M.,et al, 1979

Sciatic Nerve Entrapment by Pentazocine-Induced Muscle Fibrosis, A Case Report
Arch Neurol 36:723-724, Rousseau,J.J.,et al, 1979

Gyrate Atrophy of the Choroid & Retina with Hyperornithinemia:Tubular Aggreg. & Type 2 Fiber Atrophy
Neurol 29:966, Sipila,I.,et al, 1979

Electromyographic Abnormalties Following Myelography
Arch Neurol 36:588-589, Weber,R.J.,et al, 1979

Clinical Pathological Conference
Foramen Magnum Meningioma, Case Record 29-1979, NEJM 301:147-154979., , 1979

Phenytoin Hypersensitivity:38 Cases
Neurol 29:1480-1485, Harunda,F., 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Periodic Lateralized Epileptiform Discharges in Infants & Children
Ann Neurol 6:47-50, PeBenito,R.,et al, 1979

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

HLA-B8 in Polymyositis
NEJM 298:1260, Behan,W.M.H.,et al, 1978

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

Inclusion Body Myositis:A Distinct Variety of Idiopathic Inflammatory Myopathy
Neurol 28:8, Carpenter,S.,et al, 1978

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978

Jamaica Ginger Paralysis
Arch Neurol 35:530, Morgan,J.P.,et al, 1978

Urban Lead Mining:Lead Intoxication Among Deleaders
NEJM 298:1143, Feldman,R.G., 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

Amanita Mushroom Poisoning with Recovery from Coma:A Case Report
Ann Neurol 3:177, Teutsch,C.,et al, 1978

Polyneuropathy From Inhalation of N2O Cartridges Through a Whipped-cream Dispenser
Neurol 28:485, Sahenk,Z.,et al, 1978

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

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

The Cervical Myelopathy Associated with Rheumatoid Arthritis:Analysis of 32 Patients, with Two Post-mortem Cases
Ann Neurol 3:144, Nakano,K.K.,et al, 1978

Post-anoxic Action Myoclonus:Improvement with Valproic Acid
NEJM 299:313, Fah,S., 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Recurrent Guillain-Barre Syndrome Following Influenza Vaccine
Neurol 28:725, Seyal,M.,et al, 1978

Criteria for Diagnosis of Guillain-Barre Syndrome
Ann Neurol 3:565, , 1978

Treatment of Bell Palsy with Prednisone:A Prospective Randomized Study
Neurol 28:158, Wolf,S.M.,et al, 1978

HLA Antigens in the Landry-Guillain-Barre Syndrome & Chronic Relapsing Polyneuritis
Ann Neurol 4:285-289, Stewart,G.J.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Showing articles 2900 to 2950 of 3286 << Previous Next >>