Neudle.com: progressive muscular dystrophy

Differential
(Click to cross reference)

abdominal distention

abdominal muscle paralysis

abducens nerve paralysis, bilateral

abiotrophy

acanthocytosis

acid maltase deficiency

adrenoleukodystrophy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agammaglobulinemia

akinesia of eyelid function

algorithm

alopecia

alveolar hypoventilation

Alzheimer's disease

amniocentesis

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

ANA

analgesic

anesthesia, general

anterior interosseous neuropathy

anterior tibial muscle weakness

anxiety

apnea

apraxia of eyelid opening

areflexia

arrhythmia, cardiac

arthrogryposis multiplex

atrioventricular block

attention deficit disorder with hyperactivity

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

calf atrophy

calf hypertrophy

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

carnitine deficiency myopathy

case studies

CAT scan

CAT scan, abnormal

CAT scan, false negative

celiac disease, childhood

central core disease

central nervous system, infection of

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral palsy

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, multiple

cerebrovascular accident, young adult

cervical spine injury

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

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

conversion reaction

cornea, abnormal

corpus callosum, lesion of

cost

cost effectiveness

CPAP

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

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

diltiazem

diplopia

disability, neurological

distal muscle atrophy

distal muscle weakness

DNA probes

dropped head syndrome

drug induced neurologic disorders

dysthyroid ocularmyopathy

dystonia

dystroglycanopathies

dystrophin

dystrophin associated proteins

ejection fraction, abnormal

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram, abnormalities of

Emery-Dreifuss muscular dystrophy

Emery-Dreifuss muscular dystrophy, carrier

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, progressive

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

enzyme, serum

epidemiology of neurology

erythrocyte

ethics in neurology

euthanasia

evidence-based research

exercise

exercise intolerance

extraocular muscle atrophy

extraocular muscle enlargement

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye closure

eye movement, disorders of

eye, pain in

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

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

glycogen storage disease

glycosyltransferase

Gowers maneuver

Graves ophthalmopathy

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

hypoxic encephalopathy

idebenone

imbalance

immunohistochemistry

immunosuppressive agents

implantable cardioverter defibrillator

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

influenza

influenza immunization

intellectual deficit

intelligence quotient

intermittent positive pressure breathing

intestinal pseudoobstruction

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 closure, weakness of

life expectancy

life sustaining treatment

limb-girdle weakness

liver function enzymes

lymphocyte capping, diminished

machine learning

macrocephaly

malformation, CNS, congenital

malignancy screen

malignant hyperpyrexia

masked facies

medial rectus palsy

median neuropathy

medical-legal aspects of neurology

medulla oblongata, lesion of

MELAS syndrome

Melkersson's syndrome

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

MRI, muscle

MRI, serial

MRS

mucopolysaccharidoses

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle biopsy, extraocular

muscle cramp

muscle diseases, characteristics of

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, drug-induced

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, neurogenic hypothesis of

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myotonia dystrophica, classification

myotonia dystrophica, type 2

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

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

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

obicularis oculi, weakness of

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

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

paraspinal muscle weakness

Parkinson disease

Parkinsonism syndrome

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 therapy

physician assisted suicide

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

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

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

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

pulmonary function tests

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated and fixed, unilateral

respiratory depression

respiratory failure

respiratory tract infection

rippling muscle disease

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

skin, biopsy

skin, tight

sleep apnea

slit lamp examination

sloped shoulders

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 degeneration

standing difficulty

Stephens syndrome

steroid

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

thrombus, mural

toe walking

tongue, fasciculations of

torticollis

tracheostomy

transient ischemic attack

transverse smile

treatment of neurologic disorder

tricresylphosphate

trinucleotide repeats

tripping

tuberculoma of CNS

tuberculosis

tuberculosis, miliary

ventricular tachycardia

vertebral fracture

viral infection, CNS

vision, failure of in childhood

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

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked mental retardation

Showing articles 2350 to 2400 of 2426 << Previous Next >>

A Fatal Encephalopathy in Chronic Haemodialysis Patients
Lancet 764, Burks,J.S.,et al, 1976

Progressive Dialytic Encephalopathy
et al JNNP 39:411, Chokroverty,S., 1976

Bilateral Scalp Necrosis in Temporal Arteritis
Am J Med 61:541, Soderstrom,C.W.,et al, 1976

Progressive Rubella Panencephalitis
Arch Neurol 33:722, Wolinsky,J.S.,et al, 1976

Whipple's Disease of the Central Nervous System
Acta Neuropath 36:31, Silbert,S.W.,et al, 1976

Hypophosphatemia Mimicking Acute Guillain-Barre-Strohl Syndrome
JAMA 235:1040-1041, Weintraub,M.I., 1976

Dialysis Encephalopathy:A Possible Seizure Disorder
Neurol 26:1130-1134, Nadel,A.M.,et al, 1976

Limitations & Complications of Myelography, in Myelography
3rd Year Book Med Publ Inc, Chicago, 1975, p. 455-462., Shapiro,R., 1975

Neurologic Complications of Rheumatoid Arthritis
Orth Clin North Am 6:861-881, Nakano,K.K., 1975

Progressive Multifocal Leukoencephalophathy with 10-year Survival in a Patient with Montropical Sprue
Neurol 25:1006, Kepes,J.J.,et al, 1975

Acute Areflexic Paralysis
Arch Neurol 32:706, Furlan,A.J.,et al, 1975

Brachial Plexus Injuries
NEJM 291:1059, 1974 & 292, 4285., Leffert,R., 1975

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Sickle Cell Anemia
J Neurosurg 43:483, Ammoumi,A.A.,et al, 1975

Progressive Rubella Encephalitis
NEJM 292:990-993, 994-998, 1023-1024975., Townsend,J.J., 1975

Neuro-toxic Reaction to Haloperidol in a Thyrotoxic Pnt
NEJM 293:201, Yosselson,S.,et al, 1975

Acquired Toxoplasmosis
Arch Neurol 32:335, Townsend,J.,et al, 1975

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Progressive Rubella Panencephalitis
NEJM 292:990-993,1023, Townsend,J.,et al, 1975

Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
NEJM 292:994-998,1023, Weil, M.L.,et al, 1975

Case Records of MGH-NEJM 290:273
1974 Subacute Sclerosing Panencephalitis., , 1974

Isolated Facial Numbness
Ann Int Med 80:49, Horowitz,S., 1974

Subcortical Dementia of Progressive Supranuclear Palsy
JNNP 37:121, Albert,M.,et al, 1974

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Whipple'sDisease & the Nervous System-The Neurology of GI Disease
1974, Chapter 13, p. 207 Major Prob. In Neurology Vol. 3-Saunders., Pallis,C.A.&Lewis,P.D., 1974

Central Nervous System Infections in Patients with Cancer
Medicine 52:563, Chernik,N.L.,et al, 1973

Case Records of MGH-NEJM 289:628
1973 Necrotizing Giant Cell Arteritis., , 1973

Neurologic Manifestations of Progressive Systemic Sclerosis, 1972
Nebraska Med J 58:106, Aita,J.A., 1973

Etiology of Progressive Multifocal Leukoencephalopathy
NEJM 289:l278, Narayan,O.,et al, 1973

IUDR:Given Intraventricularly in the Treatment of PML
Cancer Chemoter Repts 57:73, Tarsy,D.,et al, 1973

Viral Infections & Demylinating Diseases
NEJM 288:1103, Weiner,J.,et al, 1973

Myasthenia, In System of Ophthalmology
Vol. VI Ocular Motility & Strabismus, CV Mosby Co, 1973, P. 755., Duke-Elder,W.S., 1973

Nitrofurantoin Polyneuropathy
Neurol 23:554-559, Toole,J.F.&Parrish,M.L., 1973

Papovaviruses & Human Disease
(Editorial) BMJ 3:540972., , 1972

Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972

Neurologic Manifestations of SLE 1972
Nebraska State Journ Med, Oct 1972, pp 395., Aita,J., 1972

Peripheral NR. Injuries & their Repairs
Surg Clin North Am Oct 1972., , 1972

Tapetoretinal Degeneration in Childhood Presenting as a Disturbance of Behavior
BMJ 202, 1972 Jan., Harcourt,B.,et al, 1972

Astrocytoma Mimicking the Features of Pheochromocytoms
NEJM 286:1397, Evans,C.,et al, 1972

Hypokalemic Periodic Paralysis withArrhythmia
NEJM 286:253, Levitt,L.,et al, 1972

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Case Records of MGH-NEJM 286:1047
1972 Progressive Multifocal Leukoencephalopathy., , 1972

Progressive Supranuclear Palsy:A Clinical, Pathological & Biochemical Study
Neurol 22:445, Antunes,J.L.,et al, 1972

Whipple's Disease-Dementia
ed. by Charles G. Wells, Chap. 10 by Gunther Haas-Contemporary Neuro. Series 192, 1971 Published by, . A. Davila., 1971

Trigeminal Neuropathy in Connective Tissue Disease
Neurol 21:609, Ashworth,B.,et al, 1971

Hemifacial Atrophy
Brit J Oral Surg 9:102, Vickery,I.M., 1971

Case Records of MGH-NEJM 285:394
1971 Glioblastoma Multiforme & Multiple Myeloma., , 1971

Case Records of MGH-NEJM 284:1023
1971 Herpes Simplex Encephalitis., , 1971

Diphosphonate Therapy in a Patient with Myosotis Ossificans Progressiva
Ann Int Med 74:933-936, Weiss,I.W.,et al, 1971

Neurologic Manifestation in Progressive Systemic Sclerosis
Arch Neurol 22:l26, Gordon,R.M.,et al, 1970

Supranuclear Abnorm. of the Vert. Ocular Motor Syst
Trans Ophth United King 90:433, Sanders,M.D.,et al, 1970

Showing articles 2350 to 2400 of 2426 << Previous Next >>