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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 200 to 250 of 2351 << Previous Next >>

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

A 30-year-old man with headache and sleep disturbance
Neurol 90:e1535-e1540, English, S.W.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
Neurol 90:974-976, Ishiyama, A.,et al, 2018

An 18-year-old man with progressive headache and visual loss
Neurol 90:1076-1081, Jiang, N.,et al, 2018

Postoperative Visual Loss After Anesthesia for Nonocular Surgery
UptoDate May, Lee, L.A. & Newman, N.J., 2018

A Fatal Case of Undiagnosed Candida Meningitis-Role of Computer-assisted Diagnosis
Neurologist 23:138-140, Finelli, P.F., 2018

Alexander Disease with Features of Both Frontal and Bulbospinal Involvement
Neurol 91:e396-e397, Nam,T-S.,et al, 2018

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Atrophy Patterns in Cerebral Amyloid Angiopathy With and Without Cortical Superficial Siderosis
Neurol 90:e1751-e1758, Kim,J.,et al, 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Posterior Ischemic Optic Neuropathy
UptoDate Aug, Tamhankar, M. & Volpe, N., 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Neuropsychiatric Involvement of Behcets Disease
www.SMGEbooks.com Dec, Soyak, M., 2017

Hydrocephalus as the Sole Presentation of Primary Diffuse Large B-cell Lymphoma of the Brain
Surg Neurol Internatl 8:165, Boshrabadi, A.P.,et al, 2017

Powassan Virus-A New Reemerging Tick-Borne Disease
Front Public Health 5:342, Fatmi,S.S., et al, 2017

IGG4-Related Hypertrophic Pachymeningitis Coexpressing Antineutrophil Cytoplasmic Antibodies
Neurol 4:e341-e343, Massey, J., 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Cerebral White Matter Abnormalities in Patients with Charcot-Marie-Tooth Disease
Ann Neurol 81:147-151, Lee, M.,et al, 2017

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

Acute Hydrocephalus Caused by Radiographically Occult Fourth Ventricular Outlet Obstruction
Neurol 88:e36-e37, Duran, D.,et al, 2017

Rheumatoid Pannus of the Cervical Spine
Neurol 88:e51, Weerasinghe, D.,et al, 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

MRI Findings in Collet-Sicard Syndrome
Neurol 88:811, , 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

A Woman in Her 60s with Chronic Meningitis from Aspergillus
JAMA Neurol 74:348-352, Pichler, M.R.,et al, 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 10-year-old boy with Bilateral Vision Loss
Neurol 88:e221-e224, Bulwa, Z.,et al, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Subarachnoid Hemorrhage
NEJM 377:257-266, Lawton, M.T. & Vates, G.E., 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

Alemtuzumab CARE-MS I 5-year follow-up
Neurol 89:1107-1116, Havrdova, E.,et al, 2017

Alemtuzumab CARE-MS II 5-year follow-up
Neurol 89:1117-1126, Coles, A.J.,et al, 2017

Brain Imaging in Myotonic Dystrophy Type 1
Neurol 89:960-969, Okkersen, K.,et al, 2017

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017



Showing articles 200 to 250 of 2351 << Previous Next >>