Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
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
aldolase
algorithm
allopurinol
alopecia
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
ANA
analgesic
anasarca
anesthesia, general
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
aspiration
aspirin
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
atelectasis
atrial fibrillation
atrial flutter
atrial paralysis
atrioventricular block
attention deficit disorder with hyperactivity
audiogram
auditory evoked brainstem potentials
autoimmune disease
automatic implantable cardioverter-defibrillator
axonopathy, distal
azathioprine
Babinski sign
baldness
basal ganglia, calcification of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
benign congenital hypotonia
bent spine syndrome
benzodiazepine
bladder dysfunction
blepharophimosis
blepharospasm
blindness
blood dyscrasias, neurologic findings with
bone age
botulism
brachial neuritis
bradycardia
brainstem, lesion of
brainstem, tuberculoma of
bulging of biceps
bulimia
bulimia nervosa
cachexia
CAG repeats
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 uterus
cardiac arrest
cardiac arrest and resuscitation
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
carotid angiogram
case studies
CAT scan
CAT scan, abnormal
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
Charcot-Marie-Tooth
Charcot's sign
chemosis
chewing, impaired
children
chloride channel dysfunction
cholestasis
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 17
chromosome 19
chromosome 3
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clofibrate
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
cornea, opacity of
corneal dystrophy
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cost
cost effectiveness
coumarin
CPAP
cranial neuropathy, multiple
creatine kinase
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
cry, weak
cyclosporine
cyst, parenchymal
cytochrome c oxidase
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
diaphragmatic paralysis
diarrhea
dieting
differential diagnosis
difficulty climbing stairs
digitalis intoxication
dilantin
dilantin, toxicity
diltiazem
diplopia
disability, neurological
distal muscle atrophy
distal muscle weakness
DNA probes
dropped head syndrome
drug induced neurologic disorders
dwarfism
dying
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspnea
dyspraxia
dysthyroid ocularmyopathy
dystonia
dystroglycanopathies
dystrophic calcification
dystrophin
dystrophin associated proteins
ear, abnormal
eating disorder
echinocyte
echocardiogram
edema, periorbital
efficacy
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electronystagmography, abnormal
electrophoretic pattern, serum
electroretinograph
ELISA
embolism
emerin
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
equinovarus
erythrocyte
ethics in neurology
euthanasia
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 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
foot drop
fracture, long bone
fragile-X syndrome
Friedreich's ataxia
frontal balding
F-wave response
gait disorder
gait, waddling
gargoylism
gastric dilatation, acute
gastrocnemius muscle weakness
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, horizontal
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glabellar sign
glaucoma
glioma
glucose tolerance test, abnormal
glycogen debranching enzyme deficiency
glycogen storage disease
glycosyltransferase
Gowers maneuver
Graves ophthalmopathy
gray matter
growth retardation
Guillain Barre syndrome
Guyon's canal
Hallgren's syndrome
hammertoes
hand weakness
head circumference
head injury
headache
hearing loss
hearing problems in children
heart block
heart block, complete
heart murmur
heavy metal intoxication
hemianopia, homonymous
hemophilia
hepatic failure
hepatomegaly
heralding manifestation
high arched feet
high arched palate
hip dysplasia
hip flexor weakness
hip pain
hippus
Hispanics
histochemistry
histochemistry of muscle
Holter monitoring
hospice
H-reflex testing
human immunodeficiency virus type 1
hunger
huntingtin
Huntington's chorea
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydrops fetalis
hypercapnia
hyperinsulinism
hyperkalemic periodic paralysis
hyperostosis
hyperparathyroidism
hypersomnia
hyperthyroidism
hypocalcemia
hypoglycemia
hypoglycemic coma
hypoglycorrhachia
hypogonadism
hypokalemia
hypokalemic periodic paralysis
hypoparathyroidism, idiopathic
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
idebenone
imbalance
immunohistochemistry
immunologic disease
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
jaw jerk, abnormal
Jewish
joint hypermobility
kaliuresis
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
lipid lowering agent
lipid storage disorder of CNS
lissencephaly
liver function enzymes
LMNA gene
locked-in syndrome
lordosis
low back pain
Lowe's syndrome
lymphocyte capping, diminished
machine learning
malformation, CNS, congenital
malignancy screen
malignant hyperpyrexia
manic-depressive
masked facies
medial rectus palsy
median neuropathy
medical-legal aspects of neurology
medulla oblongata, lesion of
megalencephaly
MELAS syndrome
Melkersson's syndrome
meningitis
meningitis, TB
mental retardation
merosin
MERRF syndrome
metabolic acidosis
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
MNGIE syndrome
modafinil
molecular genetics
mononeuropathy
morphine
mortality
motor neuron disease
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, functional
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 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, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, neurogenic hypothesis of
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
myasthenic crisis
myasthenic syndrome
myelomalacia
myeloneuropathy
myelopathy
myoblast transfer
myocardial biopsy
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, acute
myopathy, alcoholic
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
myopathy, vacuolar
myopia
myositis
myositis, ocular
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonia, causes of
myotonia, treatment of
myotonic discharges
nausea and vomiting
neck extension
neck weakness
negative
nemaline rod myopathy
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuritis
neuritis, causes of
neurocardiology
neuroendocrinology
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
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
Oppenheim muscular dystrophy
optic atrophy
optic disc edema
optic neuritis
optic neuropathy
orbicularis oculi muscle
orbit
orbit, lesions of
oxygen therapy
pacemaker, cardiac-transvenous
pain
pain, abdominal
pain, foot
pain, leg
palliative care
pancytopenia
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
POLG1 gene
poliomyelitis
polydactyly
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymicrogyria
polymyositis
polymyositis, infantile
polyneuropathy
pons, lesion of
porphyria
positive sharp waves
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
psychosis
ptosis
ptosis, bilateral
ptosis, familial
pulmonary embolism
pulmonary function tests
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated and fixed, unilateral
quadriceps atrophy
quadriceps weakness
quality of life
quinidine
radionuclide angiocardiography
ragged-red fibers
rash
Raynaud's phenomenon
recombinant DNA
recurrent
renal failure
respirator
respiratory depression
respiratory failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinal detachment
retinal dysplasia
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
RFLPs
rhabdomyolysis
right to die
rigid spine syndrome
rigidity
rippling muscle disease
risk factors
risk-benefit assessment
saccadic eye movements
saccadic eye movements, abnormal
safety
sarcoglycan
sarcoglycanopathy
sarcoidosis
scapulohumeral syndrome
scapuloperoneal syndrome
schizophrenia
Schwartz-Jampel syndrome
scintillations
scleroderma
scleroderma, neurologic involvement with
scoliosis
scoliosis, neurologic association with
screening
sedation
sedimentation rate
seizure
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
standing difficulty
statin therapy
Stephens syndrome
steppage gait
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
symptomatic
syncope
syringomyelia
systemic illness
taurine
Tay-Sachs disease
telangiectases
telangiectases, retinal
teleconsulting
telemedicine
teleneurology
telestroke
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
testicular atrophy
thalamus, lesion of-bilateral
thoracic outlet syndromes
thrombus, mural
thyrotoxicosis
tocainide
toe walking
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
twins
type 2 muscle fiber
ulnar neuropathy
ultrasonography
upgaze, paralysis of
urinary incontinence
urine, dark
Usher's syndrome
vaccine
valium
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
wide based gait
winging of scapula
workup
xanthopsia
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked mental retardation
x-ray, cervical spine
Showing articles 0 to 50 of 784 Next >>

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

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

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

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

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

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
AJNR 39:427-434, Gramegna, L.L.,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

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

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

Brain Imaging in Myotonic Dystrophy Type 1
Neurol 89:960-969, Okkersen, K.,et al, 2017

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

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

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,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

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

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

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

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

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

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

Mexiletine Is an Effective Antimyotonia Treatment in Myotonic Dystrophy Type 1
Neurol 74:1441-1448, Logigian,E.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

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

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

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

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

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

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

Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study
Lancet 369:37-42,5, Wilcken,B.,et al, 2007



Showing articles 0 to 50 of 784 Next >>