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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 700 to 750 of 1860 << Previous Next >>

Use of Specialized Coagulation Testing in the Evaluation of Patients with Acute Ischemic Stroke
Neurol 56:624-627, Bushnell,C.,et al, 2001

The Incidence of Mitochondrial Encephalomyopathies in Childhood: Clinical Features and Morphological, Biochemical, and DNA Abnormalities
Ann Neurol 49:377-383, Darin,N.,et al, 2001

Transtentorial Herniation After Unilateral Infarction of the Anterior Cerebral Artery
Stroke 32:649-651, Leistner,S.,et al, 2001

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

A Blind Panic
Lancet 357:1262, Ayuk,J.,et al, 2001

Arterial Hyperintensity on Fast Fluid-attenuated Inversion Recovery Images: A Subtle Finding for Hyperacute Stroke Undetected by Diffusion-weighted MR Imaging
AJNR 22:632-636, 599, Maeda,M.,et al, 2001

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

Radial Entrapment Neuropathy Due to Chronic Injection-induced Triceps Fibrosis
Muscle Nerve 24:134-137, Midroni,G. & Moulton,R., 2001

Rescue Treatment with Abciximab in Acute Ischemic Stroke
Neurol 56:1585-1587, Lee,K.Y.,et al, 2001

Diagnosis of X-Linked Myotubular Myopathy by Detection of Myotubularin
Ann Neurol 50:42-46, Laporte,J.,et al, 2001

Acute Compartment Syndrome After Forearm Ischemic Work Test in a Patient with McArdle's Disease
Neurol 56:1779-1780, Lindner,A.,et al, 2001

Predominant Involvement of a Particular Group of Fingers Due to Small, Cortical Infarction
Neurol 56:1677-1682, Kim,J.S., 2001

Focal Myopathy Mimicking Posterior Interosseous Nerve Syndrome
Muscle Nerve 24:969-972, Erdem,S.,et al, 2001

CT Angiography in the Rapid Triage of Patients with Hyperacute Stroke to Intraarterial Thrombolysis: Accuracy in the Detection of Large Vessel Thrombus
J Comput Assist Tomogr 25:520-528, Lev,M.H.,et al, 2001

Two Controlled Trials of Antibiotic Treatment in Patients with Persistent Symptoms and a History of Lyme Disease
NEJM 345:85-92, Klempner,M.S.,et al, 2001

Fluid-attenuated Inversion Recovery Intraarterial Signal: An Early Sign of Hyperacute Cerebral Ischemia
AJNR 22:1021-1029,1015, Toyoda,K.,et al, 2001

Alcohol Related Neuropathy
Diagnosis and Management of Peripheral Nerve Disorders :332, Mendell,J.R.,et al, 2001

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

Moyamoya-like Vasculopathy from Cocaine Dependency
AJNR 21:1008-1010, Storen,E.C.,et al, 2000

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

Dermatomyositis
Lancet 355:53-57, Callen,J.P., 2000

Intracranial Percutaneous Transluminal Angioplasty for Arteriosclerotic Stenosis
Arch Neurol 57:1625-1630, Alazzaz,A.,et al, 2000

Clinicopath Conf, Granulomatous and Lymphocytic Hypophysitis
NEJM 343:1399-1406, Case 34-2000, 2000

Visual Manifestations of Giant Cell Arteritis
Medicine 79:283-292, Gonzalez-Gay,M.A.,et al, 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

Dilated Stomach and Weak Muscles
Lancet 356:1898, Rigby,S.P.,et al, 2000

Critical Illness Myopathy
Muscle Nerve 23:1785-1788, Lacomis,D.,et al, 2000

Posttraumatic Headache-A Myth?
Arch Neurol 57:1778-1780, Warner,J.S., 2000

Posttraumatic Headache
Arch Neurol 57:1776-1778,1780, Saper,J.R., 2000

Weak and Numb Feet in a Man with Knobby Hands, Report of a Case
Arch Neurol 57:271, Kaplan,P.W.,et al, 2000

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

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

Neurological Manifestations of Dengue Infection
Lancet 355:1053-1059, Solomon,T.,et al, 2000

Pseudoulnar Palsy From a Small Infarct of the Precentral Knob
Neurol 54:2185, Phan,T.G.,et al, 2000

The DYT1 Phenotype and Guidelines for Diagnostic Testing
Neurol 54:1746-1753,1718, Bressman,S.B.,et al, 2000

Transcranial Doppler Ultrasound Criteria for Recanalization After Thrombolysis for Middle Cerebral Artery Stroke
Stroke 31:1128-1132, Burgin,W.S.,et al, 2000

Motor Strokes Sparing the Leg
Arch Neurol 57:513-518, de Freitas,G.R.,et al, 2000

Disease Progression in Sporadic Inclusion Body Myositis: Observations in 78 Patients
Neurol 55:296-198, Peng,A. et al, 2000

Detection of Early CT Signs of >1/3 Middle Cerebral Artery Infarctions
Stroke 31:1667-1671, Kalafut,M.A. et al, 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

Symptomatic Intracranial Atherosclerosis
Neurol 55:490-497, 465, Thijs,V.N. & Albers,G.W., 2000

Amusement Park Stroke
, Burneo,J.G. et al, 2000

Neuromuscular Findings in Thyroid Dysfunction: A Prospective Clinical and Electrodiagnostic Study
JNNP 68:750-755, Duyff,R.F. et al, 2000

Incidence and Prevalence of Neurological Disorders Associated with HIV Since the Introduction of Highly Active Antiretroviral Therapy (HAART)
JNNP 69:376-380, Maschke,M. et al, 2000

Prediction of Malignant Middle Cerebral Artery Infarction by Diffusion-Weighted Imaging
Stroke 31:2175-2181, Oppenheim,C. et al, 2000

Treatable Dropped Head Syndrome in Hypothyroidism
Neurol 55:896-897, Askmark,H. et al, 2000



Showing articles 700 to 750 of 1860 << Previous Next >>