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Differential
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acanthocytosis
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, infants and children
acyl CoA dehydrogenase deficiency
adriamycin
advances in neurology
adverse drug reaction
alcohol
alcohol intoxication
alcohol, heart involvement with
alcohol, neurologic complications with
alcoholic blackout
alcoholic coma
alcoholic dementia
alcoholic polyneuropathy
alcoholic withdrawal states, DT's, convulsions, etc.
alcoholism
alopecia
alpha glucosidase
amenorrhea
amyloid
amyloidosis
amyotrophic chorea-acanthocytosis
ANA
anasarca
anemia
anesthesia, general
aneurysm
aneurysm, intracranial
aneurysm, intracranial, familial
angiography, cerebral
angiotensin-converting enzyme
ankle edema
anosmia
anterior horn cell disease
anti signal recognition particle antibody
anticholinergic drugs
anticoagulant, restarting
anticoagulant, treatment
anticoagulant, treatment in CVD
antineutrophil cytoplasmic autoantibodies
antiphospholipid antibody syndrome
anxiety
aortic valve, stenosis
areflexia
arrhythmia, cardiac
arsenic
arterial dissection
arterial dissection, carotid
arterial dissection, vertebral
arthralgia
arthritis
ascending paralysis
aspartate aminotransferase
aspiration
aspirin
asthma
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, truncal
ataxic gait
atrial fibrillation
atrial flutter
atrial myxoma
atrial septal defect
atrioventricular block
autoantibodies
autoimmune disease
automatic implantable cardioverter-defibrillator
autonomic cardiovascular reflexes
autonomic dysfunction
Babinski sign
bacterial infection
BAL
baldness
basal cistern
basal ganglia, calcification of
basophilic stippling of red blood cells
blacks
blood pressure
bone marrow suppression
bradycardia
brain natriuretic peptide
brainstem, lesion of
burning paresthesia
calcification, intracranial
calf hypertrophy
carcinoma
cardiac enzymes
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency
carnitine deficiency myopathy
carotid artery disease
carotid artery occlusion, intracranial
carotid sinus syndrome
carpal tunnel syndrome
CAT scan
CAT scan, abdomen
CAT scan, abnormal
CAT scan, dense artery sign
CAT scan, perfusion
cataracts
catecholamine
cavernous hemangioma
CD4 counts
Central America
central core disease
central pontine myelinolysis
cerebellar degeneration
cerebellar infarction
cerebral atherosclerosis
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral embolism, carotid origin
cerebral infarction
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, clinical diagnosis
cerebrovascular accident, familial occurrence
cerebrovascular accident, incidence of
cerebrovascular accident, infancy and childhood
cerebrovascular accident, location of
cerebrovascular accident, nonvascular territory
cerebrovascular accident, postpartum
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, secondary prevention
cerebrovascular accident, silent
cerebrovascular accident, women
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
cerebrovascular disease, risk factors in
ceruloplasmin, serum
Chagas'disease
chelation therapy
chemosis
chest pain
chest x-ray, abnormal
children
chloroquine
chorea
choreoathetosis
chromosomal abnormality
chromosome 9
chronic progressive external ophthalmoplegia
Churg-Strauss syndrome
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clofibrate
clubfoot as related to neurologic disease
coagulopathy
cobalt toxicity
cocaine
collateral circulation
coma
complications
conduction block
congenital heart disease
congenital heart disease, CNS complications with
congestive heart failure
conjunctivitis
consanguinity
contractures, joint
controversies in neurology
conversion reaction
copper
copper metabolism, abnormal
corpus callosum, atrophy of
cortical infarction
coumarin
coumarin, restarting treatment
cranial neuropathy
cranial neuropathy, multiple
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
cryptorchidism
cultured skin fibroblasts
cyclophosphamide
cyst, bone
cytochrome c oxidase
cytochrome c oxidase, deficiency
Danon disease
deep tendon reflexes
degenerative diseases of CNS
dementia
depression
dermatitis
dermatomyositis
desmin
developmental retardation
dexterity, impaired
diabetes mellitus
diarrhea
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
disulfiram
dropped head syndrome
drug induced neurologic disorders
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysgraphia
dysmorphic
dysphagia
dyspnea
dystonia
dystroglycanopathies
dystrophic calcification
dystrophin
dystrophin associated proteins
echocardiogram
echocardiogram, contrast
echocardiogram, LVH
echocardiogram, transesophageal
echocardiogram, transesophageal, false negative
edema, leg
edema, pedal
edema, periorbital
Ehlers-Danlos syndrome
ejection fraction
ejection fraction, abnormal
ejection fraction, abnormal, transient
electrocardiogram, abnormal
electrocardiogram, LVH
electromyogram
electron microscopy
embolic stroke of unknown source
embolism
embolism, air
embolism, amniotic fluid
embolism, fat
embolism, paradoxical
embolism, systemic
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy, carrier
encephalopathy
endarterectomy, carotid
endocardial fibrosis
endocarditis
endocarditis, marantic
endocarditis, subacute bacterial
enzyme treatment
enzyme, defect
enzyme, muscle disease
eosinophilia
eosinophilic granulomatosis with polyangiitis
epidemiology of neurology
episcleritis
erythrocyte
evidence-based research
exercise intolerance
exercise-induced neurologic dysfunction
extraocular muscle enlargement
Fabry's disease
facial anomalies
facial appearance, abnormal
facial nerve palsy
facial weakness
falling
false negative
familial
fasciculation
fatigue
feeding disorder
fetal alcohol syndrome
fever
fibrillations
fibromuscular dysplasia
fingernails, abnormal
fingers, abnormal
fingolimod
fluctuate
flu-like illness
fluorescein angiography
frataxin
Friedreich's ataxia
frontal balding
fundus, abnormality of
gait disorder
gait, waddling
gastrocnemius muscle weakness
gastroenteritis
gastrointestinal bleeding
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
granuloma, eosinophilic
granulomatous disease
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
hammertoes
hand weakness
handwriting
head circumference
headache
headache, episodic
headache, progressive
hearing loss
heart block
heart rate
heart rhythm
heart valve, prosthetic
heart wall motion dysfunction
heavy metal intoxication
hemianopia
hemisensory loss
hemoglobin abnormality, neurologic complications of
hemoglobinuria
hemorrhagic diathesis
heparin
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
hepatosplenomegaly
hereditary hemorrhagic telangiectasia(HHT)
high arched feet
high arched palate
hip arthroplasty
hip pain
hirsutism
histochemistry
histochemistry of muscle
Holter monitoring
homocystinuria
human immunodeficiency virus type 1
hydrocephalus
hyperamylasemia
hypercalcemia
hyperhidrosis
hyperkeratosis
hyperreflexia
hypertelorism
hypertension
hypertensive emergency
hypertrophic cardiomyopathy
hypertrophy, ventricular
hypocalcemia
hypoglycemia
hypoglycemic coma
hypogonadism
hypokinetic left ventricle
hypomagnesemia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypoplastic left heart syndrome
hyporeflexia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
idiopathic hypertrophic subaortic stenosis
imbalance
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
incoordination
INR values
insular cortex
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracardiac electrophysiologic testing
intracerebral hemorrhage
intracerebral hemorrhage, young adult
intracranial pressure, increased
ipecac
isolated left ventricular noncompaction
jaundice
joint hypermobility
Kayser-Fleischer ring
Kearns-Sayre syndrome
ketamine
kyphoscoliosis, neurologic causes of
kyphosis
lactic acidemia
laminopathies
Leber's hereditary optic neuropathy
left ventricular dilatation
left ventricular dysfunction
leg swelling
leg weakness, bilateral
Leigh's disease
leukemia
leukopenia
life expectancy
lipid lowering agent
lipid storage myopathy
liver disease
liver function enzymes
liver transplantation
LMNA gene
lordosis
lung biopsy
lysosomal storage disease
lysosomes, abnoral
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malignant hyperpyrexia
Marchiafava-Bignami disease
Mees lines
MELAS syndrome
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, basilar
mental retardation
mental retardation, familial
MERRF syndrome
metabolic acidosis
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitoxantrone
mitral valve prolapse
mitral valve vegetation
molecular genetics
mononeuritis multiplex
mortality
movement disorder
moyamoya
moyamoya, adult
MRI
MRI, abnormal
MRI, cardiac
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, muscle
MRI, optic nerve
MRI, orbit
multiple sclerosis
multiple sclerosis, treatment of
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle hypertrophy
muscle pain
muscle stiffness
muscle strength, testing
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset 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, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenic syndrome
myelopathy
myocardial biopsy
myocardial infarction
myocardial infarction, acute
myocardial injury
myocarditis
myoclonus
myocytolysis
myoglobinuria
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, amyloid
myopathy, desmin
myopathy, drug-induced
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, necrotizing
myopathy, painful
myopathy, proximal
myopathy, quadriceps
myopathy, steroid induced
myopathy, toxic
myositis
myositis, bacterial
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonic discharges
nausea and vomiting
neck weakness
neck, webbed
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, metastatic to CNS
nephritis
nephrotic syndrome
nerve biopsy
nerve conduction studies
neuritis, heavy metals causing
neurocardiology
neurocutaneous disease
neurofibromatosis 1
neurogenic stunned myocardium
neurologic complications
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, toxic
neurotoxic
neurotoxin
neutropenia
non-dominant hemisphere
Noonan Syndrome
nutritional deficiency
nystagmus
occipital lobe, infarction, bilateral
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic nerve, lesion of
optic neuropathy
orthopnea
orthostatic hypotension
overlap syndrome
pacemaker, cardiac-transvenous
pain
pain, abdominal
pain, calf
pain, leg
pancreatitis
pancytopenia
paresthesias
paresthesias, feet
paresthesias, hands
Parkinsonism syndrome
patent foramen ovale
patent foramen ovale, surgical treatment of
pathology
pectus excavatum
pellagra
pericardial effusion
perineuritis
perineuritis, optic
peripheral blood smear
peripheral blood smear, abnormal
pes cavus
pheochromocytoma
physical therapy
pigmentary retinopathy
platelet inhibiting drugs
pleural effusion
poison, neurologic problems with
POLG1 gene
polycythemia, primary
polyhydramnios
polymyositis
polyneuropathy
Pompe's disease of glycogen storage
position sensation, abnormal
postoperative neurologic complications
postpartum
postpartum cardiomyopathy
postpartum cortical blindness
practice guidelines
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
progeria
prognosis
progressive neurologic disorder
proprioception, abnormal
protein C deficiency
proteinuria
protozoan infection
proximal muscle atrophy
pseudohypertrophy
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychosis
ptosis
ptosis, unilateral
pulmonary edema
pulmonary embolism
pulmonary infiltrates
pulmonary stenosis
quadriceps atrophy
quadriparesis
quadriplegia
quality of life
race
radionuclide imaging, heart
ragged-red fibers
RAPID CT perfusion maps
rash
renal biopsy
renal failure
renal failure, acute
renal stones
repetitive nerve stimulation
respirator
respiratory failure
retinal vasculitis
retinopathy
review article
rheumatic heart disease
rhinitis
rigid spine syndrome
rippling muscle disease
risk factors
Romberg's sign
sarcoglycan
sarcoidosis
sarcoidosis, CNS
scoliosis
scoliosis, neurologic association with
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, injury following
seizure, withdrawal
sensorineural hearing loss
sensory loss
short stature
shoulder, pain in
sick sinus syndrome
sickle cell disease
sinuses, diseases of
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
South America
spinocerebellar ataxia
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
Stokes-Adams syndrome
stress, emotional
strokelike episodes
subarachnoid hemorrhage
subarachnoid hemorrhage, prognosis
sudden death
sweating, abnormality of
symptomatic
syncope
syncope, differential diagnosis of
systemic illness
tachycardia
Takotsubo cardiomyopathy
tetany
the metabolic syndrome
thrombin inhibitor
thrombocytopenia
thrombophlebitis
thrombotic microangiopathy
thrombotic thrombocytopenia purpura
thrombus, atrial
thrombus, intracardiac
thrombus, mural
thymoma
toe walking
tongue, enlarged
tongue, numbness of
top of the basilar syndrome
toxins, nervous system
transdermal medication
transderm-V
transient ischemic attack
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
troponin T
trypanosoma cruzi
tuberous sclerosis
type 1 muscle fiber
ultrasonography
upright-tilt test
uremia
urinary catecholamines
urinary tract infection
urine test in toxic screen
uveitis
valvulopathy
vanilmandelic acid, urine
vasculitides
vasculopathy
vertebral-basilar insufficiency
viral myopathy
visual acuity, decreased
visual evoked response
visual field defect
visual impairment
visual loss
vitreous opacities
vomiting, recurrent
Von Hippel Lindau
walking frame
walking, difficulty with
weakness
weakness, acute
weakness, chronic
weakness, fluctuating
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
weight loss
Wernicke's encephalopathy
wheelchair
winging of scapula
word-finding difficulty
workup
ximelagatran
Showing articles 0 to 50 of 121 Next >>

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

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

A 63-Year-Old Woman Presenting with Bilateral Leg Pain
Neurol 96:343-348, Budhu, J.,et al, 2021

Clinicopathologic Conference, Pheochromocytoma
NEJM 384:1145-1155, Case 9-2021, 2021

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Undetermined Stroke Genesis and Hidden Cardiomyopathies Determined by Cardiac Magnetic Resonance
Neurol 94:e107-e113,14, Fonseca, A.C.,et al, 2020

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

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

A 61-Year-Old Woman with Acute Onset Dysgraphia
Neurol 92:e386-e391, Smith, L.R.,et al, 2019

Hearing and Vision Loss in an Older Man
JAMA Neurol 75:1439-1440, Ho, V.M.,et al, 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

Diagnostic Challenges in a Young Patient with Hypereosinophilia
Neurol 89:e159-e165, Ortiz, J.G.,et al, 2017

Stroke and Embolic Events in Hypertrophic Cardiomyopathy
Stroke 47:936-942, Haruki, S.,et al, 2016

Clinical Outcomes after Neurogenic Stress Induced Cardiomyopathy in Aneurysmal Sub-Arachnoid Hemorrhage: A Prospective Cohort Study
Clin Neurol Neurosurg 128:4-9, Kilbourn, K.J.,et al, 2015

Cardiovascular Dysfunction in Multiple Sclerosis
Neurologist 20:108-114, Kaplan, T.B.,et al, 2015

Progressive Development of Cardiomyopathy Following Altered Autonomic Activity in Status Epilepticus
Am J Physiol Heart Circ 309:1554-1564, Read, M.I.,et al, 2015

A 32-year-old Woman with Right-Sided Numbness and Word-Finding Difficulties
Neurol 83:e98-e102, Busza, A.,et al, 2014

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

Alcohol and Alcoholism
Adams & Victors Principles of Neurology Chp 42, pg 1186, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Friedreich Ataxia
Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014

A Case of Necrotizing Myopathy with Proximal Weakness and Cardiomayopathy
Neurol 78:1527-1532, Matthews,E.,et al, 2012

MELAS
MedLink.com, August, Klopstock, T., 2012

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

Guidelines for the Prevention of Stroke in Patients With Stroke or Transient Ischemic Attack: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:227-276, Furie,K.L.,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

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

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

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

Autoimmune Targets of Heart and Skeletal Muscles in Myasthenia Gravis
Arch Neurol 66:1334-1338, 1322, Suzuki,S.,et al, 2009

Clinicopath Conference, Postpartum Renal Failure Due to Thrombotic Microangiopathy Associated With Antiphospholipid Antibodies
NEJM 358:275-289, Case 2-2008, 2008

Extension of the Clinical Spectrum of Danon Disease
Neurol 70:1358-1359, van der Kooi,A.J.,et al, 2008

Takotsubo Cardiomyopathy in Acute Ischemic Stroke
Ann Neurol 64:547-554, Yoshimura,S.,et al, 2008

An Unusual Cause of Cardioembolic Stroke
Neurologist 14:125-127, Sahin, S.,et al, 2008

When the Worst Headache Becomes the Worst Heartache!
Stroke 38:3292-3295, Hakeem,A.,et al, 2007

Antithrombotic and Interventional Treatment Options in Cardioembolic Transient Ischaemic Attack and Ischaemic Stroke
JNNP 78:14-24, McCabe,D.J.H. &Rakhit,R.D., 2007

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Mitoxantrone Treatment of Multiple Sclerosis
Neurol 63(Suppl 6):S28-S32, Cohen,B.A. &Mikol,D.D., 2004

Sudden Cardiac Death in Myotonic Dystrophy Type 2
Neurol 63:2402-2404, Schoser,B.G.H.,et al, 2004

The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
Neurol 60:1246-1251,1230, Poppe,M.,et al, 2003

Mitochondrial Respiratory-Chain Diseases
NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003

Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
J Am Coll Cardiol 39:301-307, Maron,B.J.,et al, 2002

Hypertrophic Cardiomyopathy A Systematic Review
JAMA 287:1308-1320, Maron, B.J., 2002

Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
NEJM 342:770-780, Dalakas,M.C.,et al, 2000

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Churg-Strauss Syndrome, Clinical Study and Long-Term Follow-Up of 96 Patients
Medicine 78:26-37, Guillevin,L.,et al, 1999

Signs and Symptoms of Duchenne Muscular Dystrophny and Becker Muscular Dystrophy Among Carriers in the Netherlands: A Cohort Study
Lancet 353:2116-2119, Hoogerwaard,E.M.,et al, 1999



Showing articles 0 to 50 of 121 Next >>