Neudle.com: muscular dystrophy classification

Differential
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abdominal distention

abdominal muscle paralysis

abducens nerve paralysis, bilateral

abiotrophy

acanthocytosis

acetazolamide

acid maltase deficiency

acquired immunodeficiency syndrome

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agammaglobulinemia

airway obstruction

akinesia of eyelid function

alcohol, neurologic complications with

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, familial

aminoacidurias

amniocentesis

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anterior interosseous neuropathy

anterior tibial muscle weakness

antiarrhythmic drugs

antibodies to voltage-gated calcium channels

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, untoward effects of

antihistamines

anxiety

apnea

apraxia of eyelid opening

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

arrhythmia, cardiac

arthrogryposis multiplex

atrioventricular block

attention deficit disorder with hyperactivity

audiogram

auditory evoked brainstem potentials

autoimmune disease

automatic implantable cardioverter-defibrillator

basal ganglia, calcification of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

benign congenital hypotonia

blood dyscrasias, neurologic findings with

brainstem, tuberculoma of

calcification, intracranial

calcium antagonist

calcium channel dysfunction

calf atrophy

calf hypertrophy

calpain III deficiency

camptocormia

cancer of colon

carbamazepine

carbamazepine, toxicity

carcinoma

carcinoma of ovary

carcinoma of pancreas

carcinoma of uterus

cardiac arrest

cardiac arrest and resuscitation

cardiac surgery, neurologic complications with

cardiac transplantation

cardiomegaly

cardiomyopathy

cardiovascular disease

carnitine deficiency myopathy

CAT scan, false negative

CAT scan, muscle

cataracts

cataracts, congenital

cathartic

cause of death

celiac disease, childhood

central core disease

central nervous system, infection of

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebral blood flow

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral ischemia

cerebral palsy

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, multiple

cerebrovascular accident, prevention of

cerebrovascular accident, young adult

cervical spine

cervical spine abnormality

cervical spine injury

chloride channel dysfunction

cholestasis

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clofibrate

Coats syndrome

Cockayne's syndrome

coenzyme Q10 deficiency

cogwheel rigidty

collagen vascular disease

coma

complications

compression fracture

compression neuropathy

concussion

conduction block

confidentiality

congenital birth defects

congenital heart disease

congenital myopathy

congestive heart failure

conjunctival injection

consanguinity

contractures, joint

controversies in neurology

corpus callosum, lesion of

corpus callosum, thinning

cranial neuropathy, multiple

creatine kinase

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cytochrome c oxidase, deficiency

deafmute

deafness

deep gray nuclei

defibrillator, implanted

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, thalamic

dentatorubral-pallidoluysian atrophy

dermatomyositis

descending paralysis

developmental disability

developmental milestones

developmental retardation

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

diarrhea

dieting

differential diagnosis

difficulty climbing stairs

digitalis intoxication

disability, neurological

distal muscle atrophy

distal muscle weakness

DNA probes

dropped head syndrome

drug induced neurologic disorders

dysthyroid ocularmyopathy

dystonia

dystroglycanopathies

dystrophic calcification

dystrophin

dystrophin associated proteins

ejection fraction, abnormal

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

electronystagmography, abnormal

electrophoretic pattern, serum

Emery-Dreifuss muscular dystrophy

Emery-Dreifuss muscular dystrophy, carrier

encephalitis

encephalocele

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, progressive

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

enzyme, serum

epidemiology of neurology

evidence-based research

evoked potentials

exercise

exercise electrocardiography

exercise intolerance

extraocular muscle atrophy

extraocular muscle enlargement

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye closure

eye movement, disorders of

eye, pain in

Fabry's disease

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

falling

false negative

familial

familial hemiplegic migraine

family planning

fasciculation

fatigue

Fazio-Londe's disease

feeding disorder

femoral neuropathy

fetal movements, reduced

fetus

fever

fibrillations

fine motor function, impaired

Fisher C.M.

fistula, arterio-venous, carotid-cavernous

floppy infant

fluorescein angiography

gastric dilatation, acute

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, horizontal

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glucose tolerance test, abnormal

glycogen debranching enzyme deficiency

glycogen storage disease

glycosyltransferase

Gowers maneuver

Graves ophthalmopathy

gray matter

growth retardation

Guillain Barre syndrome

hearing problems in children

heart block

heart block, complete

heart murmur

heavy metal intoxication

hemianopia, homonymous

hemophilia

hepatic failure

hepatomegaly

heralding manifestation

histochemistry of muscle

Holter monitoring

hospice

H-reflex testing

human immunodeficiency virus type 1

hydrocephalus, congenital

hydrops fetalis

hypercapnia

hyperinsulinism

hyperkalemic periodic paralysis

hypokalemic periodic paralysis

hypoparathyroidism, idiopathic

hypoxic encephalopathy

immunosuppressive agents

implantable cardioverter defibrillator

inability to stand on tiptoes

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

influenza

influenza immunization

INR values

insulin

intellectual deficit

intelligence quotient

intermittent positive pressure breathing

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

iris, abnormal

ischemic exercise test

Kearns-Sayre syndrome

keratoconus

klippel feil syndrome

Kugelberg-Welander syndrome

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

laminopathies

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

left ventricular dilatation

leg weakness, bilateral

Leigh's disease

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

lid abnormalities

lid closure, weakness of

lid retraction, lower

life expectancy

life sustaining treatment

limb-girdle weakness

lipid lowering agent

lipid storage disorder of CNS

lissencephaly

liver function enzymes

lymphocyte capping, diminished

machine learning

macrocephaly

malformation, CNS, congenital

malignancy screen

malignant hyperpyrexia

medical-legal aspects of neurology

medulla oblongata, lesion of

megalencephaly

MELAS syndrome

Melkersson's syndrome

metachromatic leukodystrophy

methotrexate

mexiletine

microangiopathy, brain

microcephaly

micrognathia

micropthalmia

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve prolapse

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

mucopolysaccharidoses

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle biopsy, extraocular

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle relaxant

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, intermediate onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

muscular dystrophy, lymphocyte capping, diminished

muscular dystrophy, neurogenic hypothesis of

muscular dystrophy, pattern of muscle involvement

muscular dystrophy, systemic membrane defect

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, drug-induced

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, neurogenic hypothesis of

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonia, causes of

myotonia, treatment of

nemaline rod myopathy

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal migration disorder

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, ataxia, retinitis pigmentosa

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, peripheral

neuropathy, sensory

newborn, evaluation of

next-generation sequencing

nifedipine

normal

nucleotidase-5 activity

nystagmus

nystagmus, vertical

obesity

obicularis oculi, weakness of

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

oculovestibular reflex

old age, neurology of

one and a half syndrome

opened mouth

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

Oppenheim muscular dystrophy

orbicularis oculi muscle

pacemaker, cardiac-transvenous

paramyotonia congenita

paraparesis

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

pathology

pediatric neurology

pediatric neurology, transition to adult care

percussion induced muscle contraction

periodic paralysis

phosphorylase b kinase deficiency

photophobia

photophobia, central

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

pigmentary retinopathy

pinched face

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pleural effusion

pneumonia

poison, mercury

poison, neurologic problems with

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymicrogyria

polymyositis

polymyositis, infantile

posterior interosseous neuropathy

postoperative neurologic complications

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

procainamide

progeria

prognosis

progressive infantile poliodystrophy

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proptosis

proptosis, bilateral

proptosis, unilateral

prostigmine

proteinuria

proximal muscle atrophy

proximal myotonic myopathy

pseudobulbar palsy

pseudohypertrophy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pulmonary function tests

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated and fixed, unilateral

radionuclide angiocardiography

respiratory depression

respiratory failure

respiratory tract infection

rippling muscle disease

risk factors

risk-benefit assessment

saccadic eye movements

saccadic eye movements, abnormal

scapulohumeral syndrome

scapuloperoneal syndrome

schizophrenia

Schwartz-Jampel syndrome

scintillations

scleroderma

scleroderma, neurologic involvement with

scoliosis

scoliosis, neurologic association with

sensorineural hearing loss

sensory loss

seronegative

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

short stature

shoulder, pain in

shoulder-girdle wasting

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

skin, tight

sleep apnea

slit lamp examination

sloped shoulders

sodium channel dysfunction

somnolence

Southern immunoblot test

spasticity

speech disorder, childhood

speech, delayed development of

Spielmeyer Vogt syndrome

spinal cord, injury of

spinal cord, neoplasm

spinal fusion

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 6

spinocerebellar degeneration

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

strokelike episodes

succinate dehydrogenase deficiency

suck, poor

sudden death

symmetric brain lesions

telangiectases, retinal

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

term infant

testicular atrophy

thalamus, lesion of-bilateral

thoracic outlet syndromes

tongue, fasciculations of

torticollis

toxoplasma gondii

toxoplasmosis, muscle

tracheostomy

transient ischemic attack

transverse smile

treatment of neurologic disorder

tricresylphosphate

trinucleotide repeats

tripping

tuberculoma of CNS

tuberculosis

tuberculosis, miliary

tubular aggregates, muscle

ventricular tachycardia

vertebral fracture

viral infection, CNS

visceral neuropathy

vision, failure of in childhood

visual evoked response

visual field defect

visual fields, constricted

visual loss

vital capacity

Walker-Warburg syndrome

walking frame

walking, difficulty with

weakness

weakness, congenital

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

weight loss

Werdnig-Hoffman disease

Western immunoblot test

wheelchair

whistle, inability to

white matter disease

white matter disease, pattern

white matter disease, periventricular

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked mental retardation

x-ray, cervical spine

Showing articles 850 to 873 of 873 << Previous

Neurocutaneous Disease
in Dermatology in General Medicine, Fitzpatrick, et al, eds, McGraw Hill, 1971, pp. 1379-1434., Adams,R., 1971

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969

Parietal Lobe Syndromes
In Handbk of Clinical Neurology, Vinken & Bruyn, Ed, North-Holland Publ Co, Amsterdam, V2, Ch21, p., 84wesbury,E.C.O., 1969

Nine Neuropathies
Med Ann of the Dist of Columbia 37:89, Stevens,H., 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

Amyotrphic Lateral Sclerosis
Arch Neurol 16:357, Hirano,A.,et al, 1967

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

"Myopathic"Changes in Chronically Denervated Muscle
Arch Neurol 16:14-24, Drachman,D.B.,et al, 1967

Motor Neurone Disease as a Manifestation of Neoplasm
Brain 88:479, Brain,L.,et al, 1965

Seronegative Ocular Syphilis & Neurosyphilis, Neuro-Ophthalmology Symposium, U. of Miami
(Ed) , St. Louis:C. V. Mosby Co. , 1965, p. 1, Smith,J.L., 1965

Cervical Myelopathy with Fasciculations in the Lower Extremities
J Neurosurg 20:948, King,R.B.,et al, 1963

Course & Prognosis in Amyotrophic Lateral Sclerosis
Arch Neurol 8:17, Mackay,R., 1963

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Causalgia of the Face, Two Cases Successfully Treated by Sympathectomy
BMJ 1:804-805, Bingham,J.A.W., 1947

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Showing articles 850 to 873 of 873 << Previous