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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
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
atrial fibrillation
atrial flutter
atrial paralysis
atrioventricular block
attention deficit disorder with hyperactivity
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
blepharospasm
blindness
blood dyscrasias, neurologic findings with
botulism
brachial neuritis
bradycardia
brainstem, lesion of
brainstem, tuberculoma of
bulging of biceps
bulimia
bulimia nervosa
cachexia
CAG repeats
calcification, intracranial
calcium antagonist
calf atrophy
calf hypertrophy
calpain III deficiency
camptocormia
cancer of colon
carcinoma
carcinoma of ovary
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
CAT scan, muscle
cataracts
cathartic
cause of death
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
Charcot-Marie-Tooth
Charcot's sign
chemosis
children
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.)
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
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
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
dwarfism
dying
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspnea
dyspraxia
dysthyroid ocularmyopathy
dystonia
dystroglycanopathies
dystrophin
dystrophin associated proteins
eating disorder
echinocyte
echocardiogram
edema, periorbital
efficacy
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram, abnormalities of
electromyogram
electron microscopy
ELISA
embolism
emerin
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
falling
false negative
familial
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
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
glycogen storage disease
glycosyltransferase
Gowers maneuver
Graves ophthalmopathy
Guillain Barre syndrome
Guyon's canal
Hallgren's syndrome
hammertoes
hand weakness
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 pain
hippus
Hispanics
histochemistry
histochemistry of muscle
Holter monitoring
hospice
hunger
huntingtin
Huntington's chorea
Hurler's syndrome
hydrocephalus
hypercapnia
hypersomnia
hyperthyroidism
hypoglycemia
hypoglycemic coma
hypoglycorrhachia
hypogonadism
hypokalemia
hyporeflexia
hypotonia
hypotonia, infants
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
iris, abnormal
jaw jerk, abnormal
Jewish
joint hypermobility
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
LMNA gene
locked-in syndrome
lordosis
low back pain
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
meningitis
meningitis, TB
mental retardation
merosin
MERRF syndrome
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitral valve prolapse
MNGIE syndrome
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, 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 relaxant
muscle stiffness
muscle swelling
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
myasthenic crisis
myasthenic syndrome
myelomalacia
myeloneuropathy
myelopathy
myoblast transfer
myocardial biopsy
myocarditis
myoclonus
myoglobinuria
myopathy
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
myopathy, vacuolar
myopia
myositis
myositis, ocular
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonic discharges
nausea and vomiting
neck weakness
negative
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
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
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
normal
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
old age, neurology of
one and a half syndrome
opened mouth
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
ovarian tumor
oxygen therapy
pacemaker, cardiac-transvenous
pain
pain, abdominal
pain, foot
pain, leg
palliative care
pancytopenia
paraparesis
paraparesis, spastic
paraspinal muscle
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
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
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
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
ragged-red fibers
Raynaud's phenomenon
recombinant DNA
recurrent
respirator
respiratory depression
respiratory failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinal detachment
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
RFLPs
rhabdomyolysis
right to die
rigid spine syndrome
rigidity
rippling muscle disease
risk factors
safety
sarcoglycan
sarcoglycanopathy
sarcoidosis
schizophrenia
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
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
symptomatic
syncope
syringomyelia
systemic illness
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
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
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
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
wide based gait
winging of scapula
workup
xanthopsia
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked mental retardation
Showing articles 50 to 100 of 2310 << Previous Next >>

Case 35-2006: A Newborn Boy with Hypotonia
NEJM 355:2132-2142, Brown,R.H.,et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

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

Practice Parameter: Corticosteroid Treatment of Duchenne Dystrophy
Neurol 64:13-20, Moxley,R.T. III.,et al, 2005

Intermittent Prednisone Therapy in Duchenne Muscular Dystrophy
Arch Neurol 62:128-132, Beenakker,E.A.C.,et al, 2005

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

Neurological and Neuromuscular Disease as a Risk Factor for Respiratory Failure in Children Hospitalized With Influenza Infection
JAMA 294:2188-2194, Keren,R.,et al, 2005

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

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

Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy
Stroke 34:901-908, Boriani,G.,et al, 2003

New Strategy for Prenatal Diagnosis of X-Linked Disorders
NEJM 346:1502, Costa,J.,et al, 2002

A Novel, Blood-Based Diagnostic Assay for Limb Girdle Muscular Dystrophy 2B and Miyoshi Myopathy
Ann Neurol 51:129-133, Ho,M.,et al, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
JAMA 286:2437-2440, Becher,M.W.,et al, 2001

Clinical and Genetic Aspects of Distal Myopathies
Muscle Nerve 24:1440-1450, Saperstein,D.S.,et al, 2001

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

GCG Genetic Expansions in Italian Patients with Oculopharyngeal Muscular Dystrophy
Neurol 54:608-614, Mirabella,M.,et al, 2000

New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
Neurol 54:1218-1221, The International Myotonic Dystrophy Consortium (I, 2000

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

Pressure-Controlled Ventilation Via a Mini-Tracheostomy Tube for Patients with Neuromuscular Disease
Neurol 55:698-702,613,615, 611, Nomori,H. & Ishihara,T., 2000

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 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

Age and Cause of Death in Mitochondrial Diseases
Neurol 53:855-857, Klopstock,T.,et al, 1999

Getting a Grip on the Myotonic Dystrophies
Neurol 52:12-13, Thornton,C.A.&Ashizawa,T., 1999

The Clinical Spectrum of Sarcoglycanopathies
Neurol 52:176-179, Angelini,C.,et al, 1999

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

Cardiac Involvement in Genetically Confirmed Facioscapulohumeral Muscular Dystrophy
Neurol 51:1454-1456, Laforet,P.,et al, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997

The Muscular Dystrophies-Clarity or Chaos
NEJM 336 650-651, Dubowitz,V., 1997

Obstetric Aspects in Women with FSH Muscular Dystrophy, Limb-Girdle Musc Dyst, & Cogen Myopathies
Arch Neurol 54:888-894, Rudnik-Schoneborn,S.,et al, 1997

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample
Ann Neurol 42:249-253, Mora,M.,et al, 1997

Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Prenatal Diagnosis of Duchenne Muscular Dystrophy Using a Single Fetal Nucleated Erythrocyte in Maternal Blood
Neurol 46:1350-1353, Sekizawa,A.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Development of Cardiomyopathy in Female Carriers of Duchenne and Becker Muscular Dystrophies
JAMA 275:1335-1338, Politano,L.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

Palliative Care in Neurology
Neurol 46:870-872, 5981996., Bernat,J.L.,et al, 1996



Showing articles 50 to 100 of 2310 << Previous Next >>