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Differential
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acid maltase deficiency
advances in neurology
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, misdiagnosis
anterior horn cell disease
anterior tibial muscle weakness
areflexia
arthrogryposis multiplex
bulbar palsy
CAG repeats
calf atrophy
calf hypertrophy
cardiomyopathy
central core disease
Charcot-Marie-Tooth
children
chromosome 5
congenital heart disease
congenital myopathy
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
developmental retardation
diabetes mellitus
differential diagnosis
distal muscle atrophy
distal muscle weakness
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dystrophin
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, muscle disease
epidemiology of neurology
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
floppy infant
foot drop
fragile-X syndrome
gait disorder
gait, waddling
gastrocnemius muscle weakness
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
gynecomastia
hand weakness
heavy metal intoxication
Huntington's chorea
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
intrinsic hand muscles, wasting of
Kugelberg-Welander syndrome
leg weakness, bilateral
lid closure, weakness of
lordosis
misdiagnosis
molecular genetics
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, distal, vacuolar
myopathy, distal, Welander's
myopathy, mitochondrial
myopathy, quadriceps
myopathy, vacuolar
myotonia congenita
myotonia dystrophica
neck weakness
nemaline rod myopathy
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurofibrillary degeneration
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuronal migration disorder
neuronopathy
neuropathy
newborn, evaluation of
nusinersen
old age, neurology of
poison, mercury
poison, neurologic problems with
polymerase chain reaction
polymyositis
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
proximal muscle atrophy
quadriceps atrophy
quadriceps weakness
respiratory failure
review article
RFLPs
scoliosis
scoliosis, neurologic association with
screening
SMN1 gene
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar degeneration
steppage gait
survival motor neuron gene
tongue, fasciculations of
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trinucleotide repeats
walking frame
walking, difficulty with
weakness
weakness, progressive
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 600 to 650 of 2055 << Previous Next >>

The Role of Muscle Biopsy in Investigating Isolated Muscle Pain
Neurol 68:181-186,170, Filosto,M.,et al, 2007

Ischemic and Hemorrhagic Complications After Intra-Arterial Fibrinolysis in Vertebrobasilar Occlusion
AJNR 28:378-381, Schulte-Altedorneburg,G.,et al, 2007

Detection of Intracranial Atherosclerotic Steno-Occlusive Disease With 3D Time-Of-Flight Magnetic Resonance Angiography With Sensitivity Encoding at 3T
AJNR 28:439-446, Choi,C.G.,et al, 2007

Admission Facility Is Associated With Outcome of Basilar Artery Occlusion
Stroke 38:1380-1383, Muller,R.,et al, 2007

Mechanical Thrombectomy of Intracranial Internal Carotid Occlusion: Pooled Results of the MERCI and Multi MERCI Part I Trials
Stroke 38:1274-1280, Flint,A.C.,et al, 2007

Neurologic Complications of Gastric Bypass Surgery for Morbid Obesity
Neurol 68:1843-1850, Juhasz-Pocsine,K.,et al, 2007

A 46-Year-Old Woman With Severe Weakness Following Acute Respiratory Distress Syndrome
Neurol 68:1529-1535, Waclawik,A.J.,et al, 2007

Inclusion Body Mositis With Human Immunodeficiency Virus Infection: Four Cases with Clonal Expansion of Viral-Specific T Cells
Ann Neurol 61:466-475, Dalakas,M.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Palliative Care for Patients With Amyotrophic Lateral Sclerosis
JAMA 298:207-216,248, Mitsumoto,H. &Rabkin,J.G., 2007

Clinicopath Conf., Severe Microangiopathy of Diabetic Vasculopathy with Multiple Cerebral Infarcts
NEJM 357:164-173, Case Study 21-2007, 2007

"Salt and Pepper" in the Eye and Face: A Prelude to Brainstem Ischemia
Am J Ophthalmol 144:322-325, Conforto, A.B.,et al, 2007

Polyarteritis Nodosa Presenting as Rhabdomyolysis
J Korean Rheum Assoc Mar13(1):76-81, Bae,Y.D.,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

Mechanical Thrombolysis in Ischemic Stroke Attributable to Basilar Artery Occlusion as First-Line Treatment
Stroke 37:145-150, Bergui,M.,et al, 2006

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

The Natural History of Primary Lateral Sclerosis
Neurol 66:647-653, Gordon,P.H.,et al, 2006

Natural History of Homonymous Hemianopia
Neurol 66:901-905, Zhang,X.,et al, 2006

Homonymous Hemianopias
Neurol 66:906-910, Zhang,X.,et al, 2006

Predictors for Malignant Middle Cerebral Artery infarctions
Neurol 66:815-820, Jaramillo,A.,et al, 2006

Frontotemporal Lobar Degeneration with Motor Neuron Disease
Arch Neurol 63:489-490, Clark,C.M. &Forman,M.S., 2006

Orgasmic Headache and Middle Cerebral Artery Dissection
JNNP 77:693-694, Szatmary,Z.,et al, 2006

Mycophenolate Mofetil in Dermatomyositis: Is It Safe?
Neurol 66:1245-1247, Rowin,J.,et al, 2006

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

Clinicopath Conf, Acute Ischemic Stroke
NEJM 354:2263-2271, Case 16:2006, 2006

Intra-Arterial Thrombolysis Is the Treatment of Choice for Basilar Thrombosis: Pro
Stroke 37:2436-2437,2440, Schellinger,P.D. &Hacke,W., 2006

Intra-Arterial Thrombolysis Is the Treatment of Choice for Basilar Thrombosis: Con
Stroke 37:2438-2439,2440, Ford,G.A., 2006

Tandem Internal Carotid Artery/Middle Cerebral Artery Occlusion: An Independent Predictor of Poor Outcome After Systemic Thrombolysis
Stroke 37:2301-2305, Rubiera,M.,et al, 2006

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

West Nile Virus Neuroinvasive Disease
Ann Neurol 60:286-300, Davis,L.E.,et al, 2006

The Tuberous Sclerosis Complex
NEJM 355:1345-1356, Crino,P.B.,et al, 2006

Outcome of Acute Vertebrobasilar Occlusions Treated with Intra-Arterial Fibrinolysis in 180 Patients
AJNR 27:2042-2047, Schulte-Altedorneburg,G.,et al, 2006

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

The Association of Chronic Hepatitis B and Myopathy
Neurol 67:1467-1469, Capasso,M.,et al, 2006

Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Frequently Missed Diagnosis?
Neurol 67:1519, Koppel,S.,et al, 2006

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

The Hyperdense Posterior Cerebral Artery Sign
Stroke 37:399-403, Krings,T.,et al, 2006

Therapy of Basilar Artery Occlusion, A Systematic Analysis Comparing Intra-Arterial and Intravenous Thrombolysis
Stroke 37:922-928, Lindsberg,P.J.&Mattle,H.P., 2006

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Underappreciated Statin-Induced Myopathic Weakness Causes Disability
Neurorehabil Neural Repair 19:259-263, Dobkin,B.H., 2005

Clinicopath Conf., MELAS Syndrome
NEJM 353:2271-2280, Case 36-2005, 2005

Patent Foramen Ovale in Young Adults with Unexplained Stroke
NEJM 353:2361-2372, Kizer,J.R. &Devereux,R.B., 2005

Meningovascular syphilis as a cause of basilar artery stenosis
Neurol 64:391-392, Flint, A.C., et al, 2005

High-Resolution MRI Identifies Basilar Artery Plaques in Paramedian Pontine Infarct
Neurol 64:551-552, Klein, I.F., et al, 2005

West Nile Virus: A Case Report with Flaccid Paralysis and Cervical Spinal Cord MR Imaging Findings
AJNR 26:26-29, Kraushaar, G., et al, 2005

Sensorineural Hearing Loss in Children
Lancet 365:879-890, Smith, R.J.H.,et al, 2005

Sonothrombolysis in Acute Ischemic Stroke for Patients Ineligible for rt-PA
Neurol 64:1052-1054, Eggers,J., et al, 2005

Clinicopath Conf, Human Granulocytic Ehrlichiosis
NEJM 352:1358-1364, Case 10-2005, 2005

Comparison of Warfarin and Aspirin for Symptomatic Intracranial Arterial Stenosis
NEJM 352:1305-1316, 1368, Chimowitz,M.I.,et al, 2005



Showing articles 600 to 650 of 2055 << Previous Next >>