Neudle.com: Duchenne muscular dystrophy

Differential
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abdominal distention

abdominal muscle paralysis

abiotrophy

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy

advances in neurology

adverse drug reaction

algorithm

allopurinol

alopecia

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, familial

amniocentesis

amyloidosis

amyotrophic lateral sclerosis

analgesic

anesthesia, general

anterior tibial muscle weakness

anxiety

apnea

arrhythmia, cardiac

arthrogryposis multiplex

atrioventricular block

attention deficit disorder with hyperactivity

autoimmune disease

automatic implantable cardioverter-defibrillator

axonopathy, distal

azathioprine

baldness

benign congenital hypotonia

calpain III deficiency

carcinoma of pancreas

carcinoma of uterus

cardiac arrest

cardiac arrest and resuscitation

cardiac surgery, neurologic complications with

cardiac transplantation

cardiomegaly

cardiomyopathy

cardiovascular disease

central nervous system, infection of

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral palsy

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, young adult

cervical spine injury

Charcot-Marie-Tooth

children

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

congenital birth defects

congenital heart disease

congenital myopathy

congestive heart failure

contractures, joint

controversies in neurology

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cry, weak

cyclosporine

defibrillator, implanted

degenerative diseases of CNS

developmental disability

developmental milestones

developmental retardation

diagnostic criteria

diaphragmatic paralysis

dieting

differential diagnosis

difficulty climbing stairs

diltiazem

disability, neurological

distal muscle atrophy

distal muscle weakness

DNA probes

dropped head syndrome

drug induced neurologic disorders

dystrophin associated proteins

ejection fraction, abnormal

electrocardiogram, abnormal

electrocardiogram, LVH

Emery-Dreifuss muscular dystrophy

Emery-Dreifuss muscular dystrophy, carrier

enzyme, defect

enzyme, muscle disease

enzyme, serum

epidemiology of neurology

erythrocyte

ethics in neurology

euthanasia

evidence-based research

eye closure

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fetal movements, reduced

fetus

fibrillations

fine motor function, impaired

floppy infant

fluorescein angiography

gastric dilatation, acute

gastrocnemius muscle weakness

gastrointestinal motility

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glioma

glycogen storage disease

glycosyltransferase

Gowers maneuver

Guillain Barre syndrome

hearing problems in children

heart block

heart block, complete

histochemistry of muscle

immunosuppressive agents

implantable cardioverter defibrillator

inability to stand on tiptoes

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion body myositis

influenza

influenza immunization

intellectual deficit

intelligence quotient

intermittent positive pressure breathing

intestinal pseudoobstruction

iris, abnormal

joint hypermobility

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

kyphosis

lactic dehydrogenase(LDH)

laminopathies

learning disability

learning disability, in children

left ventricular dilatation

leg weakness, bilateral

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

lid closure, weakness of

life expectancy

life sustaining treatment

lipid storage disorder of CNS

liver function enzymes

lymphocyte capping, diminished

machine learning

macrocephaly

malignancy screen

malignant hyperpyrexia

manic-depressive

medical-legal aspects of neurology

megalencephaly

Melkersson's syndrome

mental retardation

merosin

metachromatic leukodystrophy

migraine

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MRI, disappearing lesion on

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

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, systemic membrane defect

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, neurogenic hypothesis of

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonic discharges

neck weakness

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

neurogenic vs.myopathic atrophy

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal migration disorder

neuropathy

neuropathy, amyloid

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, peripheral

next-generation sequencing

nucleotidase-5 activity

obesity

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

opened mouth

ophthalmoplegia

Oppenheim muscular dystrophy

orbicularis oculi muscle

ovarian tumor

oxygen therapy

pacemaker, cardiac-transvenous

pain, abdominal

palliative care

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

pathology

pediatric neurology

pediatric neurology, transition to adult care

percussion induced muscle contraction

periodic paralysis

phrenic nerve pacemaker

physical therapy

physician assisted suicide

poliomyelitis

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymicrogyria

polymyositis

polymyositis, infantile

polyneuropathy

porphyria

positive sharp waves

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progeria

prognosis

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

proximal myotonic myopathy

pseudohypertrophy

psychiatric disorder

psychological testing

psychological testing, children

ptosis

ptosis, bilateral

pulmonary embolism

pulmonary function tests

respiratory depression

respiratory failure

respiratory tract infection

rippling muscle disease

scoliosis, neurologic association with

screening

sedation

seizure

sensorineural hearing loss

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

shoulder, pain in

shoulder-girdle wasting

skin, biopsy

sleep apnea

slit lamp examination

sloped shoulders

somnolence

speech disorder, childhood

speech, delayed development of

spinal cord, injury of

spinal cord, neoplasm

spinal fusion

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar degeneration

standing difficulty

steroid

steroid therapy, CNS treatment and complications with

telangiectases, retinal

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

transient ischemic attack

transverse smile

treatment of neurologic disorder

trinucleotide repeats

ventricular tachycardia

vertebral fracture

viral infection, CNS

vision, failure of in childhood

visual loss

vital capacity

Walker-Warburg syndrome

walking frame

walking, difficulty with

weakness

weakness, congenital

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

wide based gait

winging of scapula

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked mental retardation

Showing articles 700 to 750 of 788 << Previous Next >>

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Heredopathia Atactica Polyneuritiformis
Arch Neurol 38:605-606, Refsum,S., 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

The Reflex Sympathetic Dystrophy Syndrome (RSDS)
Am J Med 70:23-30, Kozin,F.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Horner Syndrome with Causalgia
Neurol 30:534-535, Bernad,P.G.,et al, 1980

Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
Arch Neurol 37:214-216, Alberica,R.,et al, 1980

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

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

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

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

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

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Neurological Involvement in the Epidermal Naevus Syndrome
JNNP 41:466, McAuley,D.L.,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

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,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

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Weakness in Malignancy:Evidence for a Remote Effect of Tumor on Distal Axons
Ann Neurol 4:268-274, Barron,S.A.,et al, 1978

Human Pneumatic Tourniquet Paralysis
Neurol 28:787-793, Bolton,C.F.,et al, 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Clinical Pathological Conference
Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978

Sarcoidosis & Its Ophthalmic Manifestations
Am J Ophthmol 86:648-655, Obenauf,C.D.,et al, 1978

Chronic Neurogenic Quadriceps Amyotrophy
Ann Neurol 2:528, Furukawa,T.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Showing articles 700 to 750 of 788 << Previous Next >>