Neudle.com: "progressive muscular dystrophy"

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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.)

clubfoot as related to neurologic disease

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 0 to 50 of 2310 Next >>

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

Cancer Risk in Patients with Muscular Dystrophy and Myotonic Dystrophy
Neurol 103:e209883, Maya-Gonzalez,C.,et al, 2024

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Accuracy of a Machine Learning Muscle MRI - Based Tool for the Diagnosis of Muscular Dystrophies
Neurol 94:e1094-e1102, Verdu-Diaz, J.,et al, 2020

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018

Long-term Effects of Glucocorticoids on Function, Quality of Life, and Survival in Patients with Duchenne Muscular Dystrophy: A Prospective Cohort Study
Lancet 391:451-461, McDonald, C.M.,et al, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Efficacy of Idebenone on Respiratory Function in Patients with Duchenne Muscular Dystrophy not using Glucocorticoids (DELOS): A Double-Blind Randomised Placebo-Controlled Phase 3 Trial
Lancet 385:1748-1757,1704, Buyse, G.M.,et al, 2015

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Electrophysiological Study with Prophylactic Pacing and Survival in Adults with Myotonic Dystrophy and Conduction System Disease
JAMA 307:1292-1301, Wahbi,K.,et al, 2012

Evidence-Based Path to Newborn Screening for Duchenne Muscular Dystrophy
Ann Neurol 71:304-313, Mendell,J.R.,et al, 2012

The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
Ann Neurol 72:9-17, Mercuri, E. & Muntoni, F., 2012

LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011

Cancer Risk Among Patients with Myotonic Muscular Dystrophy
JAMA 306:2480-2486, Gadalla, S.M.,et al, 2011

Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
Neurol 76:194-195, Mathews,K.D.,et al, 2011

Muscle Histology vs MRI in Duchenne Muscular Dystrophy
Neurol 76:346-353, Kinali,M.,et al, 2011

Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy
Neurol 77:62-66, Schade van Westrum, S.M.,et al, 2011

Transition to Adult Care for Children with Chronic Neurological Disorders
Ann Neurol 69:437-444, Camfiled, P. & Camfield, C., 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Clinical Features of Facioscapulohumeral Muscular Dystrophy 2
Neurol 75:1548-1554, Greef,J.C.,et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1
NEJM 358:2688-2697, Groh,W.J.,et al, 2008

Cardiac Involvement in Patients With Limb-Girdle Muscular Dystrophy Type 2 and Becker Muscular Dystrophy
Arch Neurol 65:1196-1201, Sveen,M.-L.,et al., 2008

Diagnosis and Etiology of Congenital Muscular Dystrophy
Neurol 71:312-321,308, Peat,R.A.,et al., 2008

Congenital Muscular Dystrophy
eMedicine (Jan), Lopate,G., 2007

Orthopedic Outcomes of Long-Term Daily Corticosteroid Treatment in Duchenne Muscular Dystrophy
Neurol 68:1607-1613, King,W.M.,et al, 2007

Gene Therapy for Duchenne Muscular Dystrophy: Expectations and Challenges
Arch Neurol 64:1236-1241, Rodino-Klapac,L.R.,et al, 2007

Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
Neurol 66:1585-1587, Fernandez,C.,et al, 2006

Showing articles 0 to 50 of 2310 Next >>