Neudle.com: progressive muscular dystrophy

Differential
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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 1800 to 1850 of 2426 << Previous Next >>

Progressive Multifocal Leukoencephalopathy Complicating Wiskott-Aldrich Syndrome
Arch Neurol 51:422-426, Katz,D.A.,et al, 1994

Osteomalacic Myopathy
Muscle & Nerve 17:578-580994., Russell,J.A., 1994

Clinicopath Conf
PML in Bone Marrow Transplant Patient, BMJ 309:262-2651994., , 1994

Progressive Spastic Paraparesis Revealing Primary Hyperparathyroidism
Neurol 44:178-179, Thomas,P.&Lebrun,C., 1994

Intravascular Malignant Lymphomatosis Manifes Clin as Bilat Sudden Hearing Loss & Cytomegalovirus Encephal
Neurol 44:1518-1520, Nagayama,M.,et al, 1994

Intravascular Lymphomatosis:A Clinicopathological Study of Three Cases
J Cancer Res Clin Oncol 120:164-168, Liszka,U.,et al, 1994

Demetia with Leucoaraiosis and Dural Arteriovenous Malformation:Clinical and PET Case Study
JNNP 56:929-931, Nencini,P.,et al, 1994

Progressive Supranuclear Palsy:Neuropathologic and Clinical Heterogeneity
Neurol 44:1015-1024, Gearing,M.,et al, 1994

The Syndrome of'Pure Akinesia'and Its Relationship to Progressive Supranuclear Palsy
Neurol 44:1025-1029, Riley,D.E.,et al, 1994

Are Magnetic Resonance Findings Pred of Clinical Outcome in Therapeutic Trials in MS? The Dilemma of Interferon-B
Ann Neurol 36:14-18, McDonald,W.I.,et al, 1994

Cladribine in Treatment of Chronic Progressive Multiple Sclerosis
Lancet 344:3-13, Sipe,J.C.,et al, 1994

Myasthenia Gravis
NEJM 330:1797-1810, Drachman,D.B., 1994

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Progressive Multifocal Leukoencephalopathy in HIV Infection Presenting as Balint's Syndrome
Neurol 44:1339-1340, Ayuso-Peralta,L.,et al, 1994

Eye Movements in Parkinsonian Syndromes:Vidailhet
M. , et al, Neurol 35:420-42694., , 1994

Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
JNNP 57:278-284, Burn,D.J.,et al, 1994

MRI in Chronic Progressive Radiation Myelopathy
J Comput Asisst Tomogr 18:1-6, Melki,P.S.,et al, 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
Ann Neurol 36:362-367, Haltia,M.,et al, 1994

Familial Progressive Subcortical Gliosis
Neurol 44:1633-1643, Lanska,D.J.,et al, 1994

Treatment of Stiff-Man Syndrome with Intravenous Immunoglobulin
Neurol 44:1652-1654, Amato,A.A.,et al, 1994

Peripheral Nerve Injury and Causalgia Secondary to Routine Venipuncture
Neurol 44:962-964, Horowitz,S.H., 1994

Pathologic Findings in a Case of Primary Progressive Aphasia
Neurol 44:279-282, Scheltens,P.,et al, 1994

Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
Ann Neurol 35:273-279, 2571994., Al-Lozi,M.T.,et al, 1994

Botulinum Toxin-A Improves the Rigidity of Progressive Supranuclear Palsy
Ann Neurol 35:237-239, Polo,K.B.&Jabbari,B., 1994

Concentric Sclerosis (Balo) :Morphometric and In Situ Hybridization Study of Lesions in Six Patients
Ann Neurol 35:18-30, Yao,D-L.,et al, 1994

Experience with Brain Biopsy in AIDS Related Focal Lesions of the Central Nervous System
Br J Surg 81:1508-1511, Iocoangeli,M.,et al, 1994

Prolonged Paralysis Due to Nondepolarizing Neuromuscular Blocking Agents and Corticosteroids
Muscle & Nerve 17:647-654994., Barohn,R.J.,et al, 1994

Gliomas of the Anterior Visual Pathway
Surv Ophthalmol 38:427-452, Dutton, J., 1994

Hemorrhagic Necrosis and Vascular Injury in Carbon Monoxide Poisoning:MR Demonstration
AJNR 14:168-170, Silverman,C.S.,et al, 1993

Stiff-Man Syndrome Treated with Intrathecal Baclofen
Neurol 43:2412, Penn,R.D.&Mangieri,E.A., 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Sudden Hearing Loss as the Initial Monosymptom of Multiple Sclerosis
Neurol 43:2703-2705, Drulovic,B.,et al, 1993

Myositis-Specific Autoantibodies, Touchstones for Understanding the Inflammatory Myopathies
JAMA 270:1846-1849, Miller,F.W., 1993

Progressive Multifocal Leukoencephalopathy:Contrast Enhancement on CT Scans and MR Images
AJR 161:1049-1051, Wheeler,A.L.,et al, 1993

The Clinical Spectrum of Cerebral Amyloid Angiopathy:Presentations Without Lobar Hemorrhage
Neurol 43:2073-2079, Greengerg,S.M.,et al, 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Olfactory Testing Differentiates Between Progressive Supranuclear Palsy & Idiopathic Parkinson's Dis
Neurol 43:962-965, Doty,R.L.,et al, 1993

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

Accelerated Neuropathy of Renal Failure
Arch Neurol 50:536-539, Ropper,A.H., 1993

Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Visual Impairment in Patients with Neurofibromatosis 2
Neurol 43:622-623, Bouzas,E.A.,et al, 1993

Successful Outcome of Progressive Multifocal Leukoencephalopathy with Cytarabine and Interferon
Ann Neurol 33:407-411, Steiger,M.J.,et al, 1993

Progressive Multifocal Leukoencephalopathy in 47 HIV-Sero (+) Pts:Neuroimaging, Clin, Path Correl
Radiolgoy 187:233-240, Whiteman,M.L.H.,et al, 1993

Catastrophic Visual Loss Due to Cryptococcus Neoformans Meningitis
Medicine 72:207-224, Rex,J.H.,et al, 1993

Spastic Ataxia Associated with Human T-Cell Lymphotropic Virus Type II Infection
Ann Neurol 33:411-414, Harrington,W.J.,et al, 1993

Isolation of HTLV-II from Pt with Chronic, Prog Neurol Dis Clin Indistinguish from HAM/Tropical Spastic Paraparesis
Ann Neurol 33:392-396, Jacobson,S.,et al, 1993

Hyperintense Globus Pallidus on T1-Weighted MRI in Cirrhotic Pts is Associated with Severity of Liver Failure
Neurol 43:65-69, Pujol,A.,et al, 1993

Showing articles 1800 to 1850 of 2426 << Previous Next >>