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acid maltase deficiency
advances in neurology
alveolar hypoventilation
Alzheimer's disease
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
analgesic
anesthesia, general
anterior interosseous neuropathy
anterior tibial muscle weakness
anxiety
apnea
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
asymptomatic
atrioventricular block
axonopathy, distal
baldness
benign congenital hypotonia
benzodiazepine
brachial neuritis
bulbar palsy
bulging of biceps
cachexia
CAG repeats
calf atrophy
carcinoma
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, abnormal
cataracts
central core disease
cerebrovascular accident
cervical spine injury
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 19
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
coma
complications
compression neuropathy
concussion
congenital myopathy
congestive heart failure
contractures, joint
controversies in neurology
cost
cost effectiveness
CPAP
creatine phosphokinase(CPK)elevated
deafness
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
dermatomyositis
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
dying
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspnea
dystrophic calcification
dystrophin
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
entrapment neuropathy
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
ethics in neurology
euthanasia
evidence-based research
exercise
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
foot drop
fragile-X syndrome
gastrocnemius muscle weakness
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Guillain Barre syndrome
Guyon's canal
hand weakness
head injury
headache
heart block
heavy metal intoxication
hepatomegaly
high arched palate
hospice
hunger
huntingtin
Huntington's chorea
hypercapnia
hypoglycemia
hypoglycemic coma
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
immunologic disease
immunosuppressive agents
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion body myositis
intermittent positive pressure breathing
intrinsic hand muscles, wasting of
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, bilateral
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
lid closure, weakness of
life sustaining treatment
locked-in syndrome
lordosis
median neuropathy
medical-legal aspects of neurology
mental retardation
methotrexate
misdiagnosis
molecular genetics
mononeuropathy
morphine
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, muscle
multiple sclerosis
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle relaxant
muscle stiffness
muscle strength, testing
muscle swelling
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenic crisis
myocarditis
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, distal, vacuolar
myopathy, distal, Welander's
myopathy, mitochondrial
myopathy, necrotizing
myopathy, neurogenic hypothesis of
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myotonia
myotonia congenita
myotonia dystrophica
neck weakness
nemaline rod myopathy
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
neuritis, causes of
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurogenic vs.myopathic atrophy
neurologic complications of, systemic cancer
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neuromuscular blockade
neuromuscular junction, abnormality of
neuronal migration disorder
neuropathy
neuropathy, diabetic
neuropathy, motor, multifocal
neuropathy, peripheral
newborn, evaluation of
next-generation sequencing
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
Oppenheim muscular dystrophy
oxygen therapy
palliative care
Parkinson disease
percussion induced muscle contraction
phosphorylase b kinase deficiency
phrenic nerve pacemaker
physician assisted suicide
poison, mercury
poison, neurologic problems with
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
porphyria
posterior interosseous neuropathy
practice guidelines
pregnancy, neurologic complications in
prognosis
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudohypertrophy
ptosis
quadriceps atrophy
quadriceps weakness
quality of life
rash
recombinant DNA
respirator
respiratory depression
respiratory failure
retinitis pigmentosa
review article
RFLPs
right to die
sarcoidosis
sedation
seizure
sensorineural hearing loss
short stature
sleep apnea
slit lamp examination
spinal cord, injury of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
steppage gait
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
teleconsulting
telemedicine
teleneurology
telestroke
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
thoracic outlet syndromes
torticollis
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
ulnar neuropathy
valium
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 200 to 250 of 1542 << Previous Next >>

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

An ALS-Like Syndrome with New HIV Infection and Complete Response to Antiretroviral Therapy
Neurol 57:1094-1097,945, MacGowan,D.J.L.,et al, 2001

Reversible ALS-Like Disorder in HIV Infection
Neurol 57:995-1001,945, Moulignier,A.,et al, 2001

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

Inclusiong Body Myositis Mimicking Motor Neuron Disease
Arch Neurol 58:1253-1256, Dabby,R.,et al, 2001

Nonpoliovirus Poliomyelitis Simulating Guillain-Barre Syndrome
Arch Neurol 58:1460-1464, Gorson,K.C.&Ropper,A.H., 2001

Hospitalization in Amyotrophic Lateral Sclerosis, Causes, Costs, and Outcomes
Neurol 56:753-757, Lechtzin,N.,et al, 2001

Amyotrophic Lateral Sclerosis
NEJM 344:1688-1700, Rowland,L.P. & Shneider,N.A., 2001

The Split Hand in ALS has a Cortical Basis
J Neurol Sci 180:66-70, Weber,M.,et al, 2000

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

Amyotrophic lateral Sclerosis Mimic Syndromes, A Population-Based Study
Arch Neurol 57:109-113, Traynor,B.J.,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

Injections of Botulinum Toxin A Into the Salivary Glands Improve Sialorrhoea in Amyotrophic Lateral Sclerosis
JNNP 69:121-123, Giess,R. et al, 2000

Poliomyelitic-Like Illness in Central European Encephalitis
Neurol 55:299-302, Schellinger,P.D. et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 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

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

A 44-Year-Old Woman with Difficulty Walking
JAMA 284:2632-2639, Iezzoni,L.I., 2000

Disorders of Upper & Lower Motor Neurons
Neurol in Clin Practice, 3rd Ed., Butterworth, Boston: Ch. 78 p. 2007, Mitasumoto,H., 2000

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

Botulinum Toxin is a Useful Treatment in Excessive Drooling of Saliva
JNNP 67:697, Bhatia,K.P.,et al, 1999

An Algorithm for ALS Diagnosis and Management
Neurol 53:S58-S62, Swash,M., 1999

Antithrombotic Therapy to Prevent Stroke in Patients with Atrial Fibrillation:A Meta-Analysis
Ann Int Med 131:492-501,537, Hart,R.G.,et al, 1999

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

A 10-Year Study of Mortality in a Cohort of Patients with Myotonic Dystrophy
Neurol 52:1658-1662, Mathieu,J.,et al, 1999

Atypical Form of Amyotrophic Lateral Sclerosis
JNNP 66:581-585, Sasaki,S.&Iwata,M., 1999

Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
Neurol 52:1311-1323, Miller,R.G.,et al, 1999

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

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 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

A Prospecitve Study of Preferences and Actual Treatment Choices in ALS
Neurol 53:278-283,248, Albert,S.M.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

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

Safety and Factors Related to Survival After Percutaneous Endoscopic Gastrostomy in ALS
Neurol 53:1123-1125, Chio,A.,et al, 1999

Brachial Amyotrophic Diplegia, A Slowly Progressive Motor Neuron Disorder
Neurol 53:1071-1076, Katz,J.S.,et al, 1999

Attitudes of Patients with Amyotrophic Lateral Sclerosis and Their Care Givers Toward Assisted Suicide
NEJM 339:967-973,987, Ganzini,L.,et al, 1998

Olfactory Dysfunction in Guamanian ALS,Parkinsonism,and Dementia
Neurol 51:1672-1677, Ahlskog,J.E.,et al, 1998

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

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,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 Findings of Werdnig-Hoffmann Disease in Two Infants
AJNR 19:550-552, Hsu,C.,et al, 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Estimation of Brainstem Neuronal Loss in ALS with in Vivo Proton Magnetic Resonance Spectroscopy
Neurol 50:72-77, Cwik,V.A.,et al, 1998

Risk of Amyotrophic Lateral Sclerosis & History of Physical Activity, A Population Study
Arch Neurol 55:201-206, Longstreth,W.T.,et al, 1998

Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
Neurol 50:768-772, Ross,M.A.,et al, 1998

Hirayama Disease:MR Diagnosis
AJNR 19:365-368, Chen,C.,et al, 1998

Proton Spectroscopy in Myotonic Dystrophy, Correlations with CTG Repeats
Arch Neurol 55:305-311, 2911998., Chang,L.,et al, 1998



Showing articles 200 to 250 of 1542 << Previous Next >>