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Differential
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advances in neurology
allodynia
amyloidosis
anesthesia, general
anterior horn cell disease
areflexia
arm weakness
asymptomatic
autonomic dysfunction
bone scanning
bulging of biceps
burning paresthesia
calf amyotrophy
calf atrophy
calf hypertrophy
cardiomyopathy
children
Clinical Pathologic Conference(C.P.C.)
creatine phosphokinase(CPK)elevated
cyanosis
descending paralysis
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
DYSF gene
dysferlin
dysferlinopathy
dyspnea
edema, pedal
electromyogram
electron microscopy
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
foot drop
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic neurologic disorders
genetic testing
Gowers maneuver
guanethidine
hemidiaphragm, paralysis of
hereditary myopathy with early respiratory failure
hoarseness
hypercalcemia
hyperhidrosis
inability to sit up
India
Kugelberg-Welander syndrome
leg atrophy
leg weakness, unilateral
lid closure, weakness of
life expectancy
livedo reticularis
misdiagnosis
molecular genetics
monoclonal gammopathy
monomelic amyotrophy
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle hypertrophy
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, amyloid
myopathy, hereditary
myopathy, quadriceps
nerve conduction studies
neurologic disease, diagnoses of
neurologic examination
orthopnea
osteoporosis
pain
pain, leg
physical therapy
plasma cell dyscrasia
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
reflex sympathetic dystrophy
reflex sympathetic dystrophy, children
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
scoliosis
shoulder-girdle wasting
skin, temperature difference
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
steppage gait
steroid therapy, CNS treatment and complications with
survival motor neuron gene
sympathetic block
thermography
titinopathy
toe walking
tongue, enlarged
trauma
treatment of neurologic disorder
urine, dark
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
wheelchair
whistle, inability to
winging of scapula
Showing articles 800 to 850 of 2351 << Previous Next >>

MRI Findings in Mobius Syndrome: Correlation with Clinical Features
Neurol 55:1058-1060, Pedraza,S.,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

MR Imaging of the Cauda Equina in Hereditary Motor Sensory Neuropathies: Correlations with Sural Nerve Biopsy
AJNR 21:1793-1798,1779, Cellerini,M.,et al, 2000

Late Onset Postpartum Eclampsia Without Pre-Eclamptic Prodromi: Clinical and Neuroradiological Presentation in Two Patients
JNNP 69:824-827, Veltkamp,R.,et al, 2000

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

Glatiramer Acetate (Copaxone) Treatment in Relapsing-Remitting MS
Neurol 54:813-817, Ge,Y.,et al, 2000

Language Disturbances in Corticobasal Degeneration
Neurol 54:990-992, Frattali,C.M.,et al, 2000

Using Serial Registered Brain Magnetic Resonance Imaging to Measure Disease Progression in Alzheimer Disease
ArchNeurol 57:339-344, Fox,N.C.,et al, 2000

Palinopsia and Polyopia in the Absence of Drugs or Cerebral Disease
Neurol 54:855-859, Pomeranz,H.D. & Lessel,S., 2000

MR Characteristics of Muslin-Induced Optic Neuropathy: Report of Two Cases and Review of the Literature
AJNR 21:346-352, Bhatti,M.T.,et al, 2000

Progressive Cerebral Atrophy in MS
Neurol 54:807-812,782, Fox,N.C.,et al, 2000

Progressive Necrotic Myelopathy
ArchNeurol 57:355-361, Katz,J.D. & Ropper,A.H., 2000

Blindness in a Strict Vegan
NEJM 342:897-898, Milea,D.,et al, 2000

Cranial MR Imaging of Osteopetrosis
AJNR 21:1110-1115, Cure,J.K.,et al, 2000

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

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

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

Three-year Survival and Functional Outcome of Patients With Idiopathic Adult Hydrocephalus Syndrome
Neurol 55:576-578, Malm,J. et al, 2000

Intrathecal Baclofen for the Treatment of Dystonia in Patients with Reflex Sympathetic Dystrophy
NEJM 343:625-630,654, van Hilten,B.J. et al, 2000

Spinal Cord Stimulation in Patients with Chronic Reflex Sympathetic Dystrophy
NEJM 343:618-624, 654, Kemler,M.A. et al, 2000

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Hydrocephalus Is a Determinant of Early Mortality in Putaminal Hemorrhage
Stroke 31:2157-2162, Phan,T.G. et al, 2000

Neuroimaging in Deteriorating Patients with Cerebellar Infarcts and Mass Effect
Stroke 31:2062-2067, Koh,M.G. et al, 2000

The Central Nervous system and Infection by Candida Species
Diagn Microbial Infect Dis 37:169-179, Sanchez-Portocarrero, J.,et al, 2000

Fungal Meningitis
Semin Neurol 20:307-322, Gottfredsson, M. & Perfect J.R., 2000

Suprascapular Neuropathy
J Am Acad Orthop Surg 7:358-367, Romeo, A.A.,et al, 1999

Distal Myasthenic Gravis
Neurol 52:632-634, Nations,S.P.,et al, 1999

Magnetic Resonance Imaging-Based Volumetry Differentiates Idiopathic Parkinson's Syndrome from Multiple System Atrophy and Progressive Supranuclear Palsy
Ann Neurol 45:65-74, Schulz,J.B.,et al, 1999

Quantitative MRI in Patients with Clinically Isolated Syndromes Suggestive of Demyelination
Neurol 52:599-606, Sailer,M.,et al, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

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

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

Clinicopath Conf,Wegener's Granulomatosis with Pachymeningeal Granulomatous Inflammation, Case 9-1999
NEJM 340:945-953, , 1999

Quantitative MRI in CADASIL, Correlation with Disability and Cognitive Performance
Neurol 52:1361-1367, Dichgans,M.,et al, 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Clinicopath Conf:Multisystem Neurodegenerative Disease with Dementia Pugilistica
NEJM 340:1269-1277, Case 12-1999, 1999

MR Imaging of Acute Coccidioidal Meningitis
AJNR 20:509-514, Erly,W.K.,et al, 1999

Phenotypic Variability in Rippling Muscle Disease
Neurol 52:1453-1459, Vorgerd,M.,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

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Brain Structure and Neurocognitive and Behavioural Function in Adolescents Who Were Born Very Preterm
Lancet 353:1653-1657, Stewart,A.L.,et al, 1999

Medial Temporal Lobe Atrophy on MRI in Dementia with Lewy Bodies
Neurol 52:1153-1158, Barber,R.,et al, 1999



Showing articles 800 to 850 of 2351 << Previous Next >>