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acid maltase deficiency
advances in neurology
adverse drug reaction
alpha-fetoprotein
Alzheimer's disease
amyloidosis
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, Parkinson-dementia-complex
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
anterior tibial muscle weakness
apraxia of eye movements
areflexia
arthrogryposis multiplex
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
atlanto axial dislocation, congenital
benign congenital hypotonia
Brugada syndrome
bulbar palsy, progressive
calf hypertrophy
carcinoembryonic antigen
carcinoma
cavernous sinus, syndrome
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
coma
complications
congenital heart disease
congenital myopathy
congestive heart failure
constipation
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
denervation of muscle
denervation potentials
dermatomyositis
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dysarthria
dystonia
dystrophin
efficacy
electrocardiogram, abnormal
electromyogram
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, muscle disease
epidemiology of neurology
eye movement, disorders of
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
foot drop
Friedreich's ataxia
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
growth retardation
Guillain Barre syndrome
gynecomastia
heavy metal intoxication
hemangioma
history of neurology
Huntington's chorea
hypercapnia
hypertension
hypoglycemia
hypoglycemic coma
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infant, evaluation of
infantile tremor syndrome
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Isaacs syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
leukemia
lid closure, weakness of
life expectancy
liver disease
lordosis
lymphoma
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
mental retardation
misdiagnosis
molecular genetics
mononeuropathy
mortality
motor neuron disease
motor neuron disease, juvenile form
motor system
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, spinal cord
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
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, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, treatment of
myasthenic crisis
myocardial injury
myocytolysis
myokymia
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, mitochondrial
myopathy, thyroid disease causing
myositis
myotonia congenita
myotonia dystrophica
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic evaluation
neuromyotonia
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, peripheral, treatment
newborn, evaluation of
nusinersen
ocular motility, disorders of
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, painful
Oppenheim muscular dystrophy
paraparesis, familial spastic
Parkinson disease
pathology
patient information and support
periodic paralysis
periodic paralysis, thyrotoxic
phrenic nerve
placebo
poison, mercury
poison, neurologic problems with
poliomyelitis
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
porphyria
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
radiation hypersensitivity
radiculopathy
respiratory failure
review article
RFLPs
risk-benefit assessment
safety
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, treatment of
skin, lesions in neurologic disorders
SMN1 gene
spina bifida
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
stiff man syndrome
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
sudden death
survival motor neuron gene
telangiectases
term infant
Tolosa Hunt syndrome
tongue, fasciculations of
torticollis
treatment of neurologic disorder
tremor
tricresylphosphate
trinucleotide repeats
tuberous sclerosis
vitamin E
vitamin E deficiency
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
West disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 1700 to 1750 of 8383 << Previous Next >>

Lumbar Spinal Stenosis
BMJ 373:m1581, Kruger Jensen, R.,et al, 2021

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Clinical Presentation and Management of SMART Syndrome
Neurol 97:118-120, Winter, S.F.,et al, 2021

A 68-Year-Old Man with Proximal Weakness and Seizures
Neurol 97:e423-e428, Chen, T., 2021

Silent Myocardial Infarction and Subsequent Ischemic Stroke in the Cardiovascular Health Study
Neurol 95:e436-e443, Merkler, A.E.,et al, 2021

Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021

Radiation-Induced Bilateral Oculomotor Nerve Palsy 20 Years After Radiation Treatment
Neurol 96:955-957, Grassmeyer, J.J.,et al, 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

A 42-Year-Old Woman with Mysterious Monocytic Meningitis
Neurol 97:449-454, Nothem, M.E., et al, 2021

Nitromethane-Induced Acute Reversible Encephalopathy
Neurol 97:e1361-e1362, Palumbo, G.,et al, 2021

Dural Arteriovenous Fistula Presenting with Reversible Dementia
Ann Neurol 90:512-513, Yoon, J.Y.,et al, 2021

COVID-19 Associated Myelitis Involving the Dorsal and Lateral White Matter Tracts
AJNR 42:1912-1917, Huang, H.Y.,et al, 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Nocardial Brain Abscesses
NEJM 385:e53, Sherman, S.V., 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

An Intramedullary Mass
BMJ 374:m1948, Yang, J.S.,et al, 2021

A 40-Year-Old Woman With Scapular Winging and Dysphonia
Neurol 97:503-507, Aladawi, M.,et al, 2021

When Should a Brain MRI Be Performed in Children with New-Onset Seizures? Results of a Large Prospectice Trial
AJNR 42:1645-1701, Hourani, R.,et al, 2021

A 7-Year-Old Boy with Acute-Onset Altered Mental Status
Neurol 96:e2774-e2778, Wong, G.J.,et al, 2021

Vagus Nerve Stimulation and Seizure Outcomes in Pediatric Refractory Epilepsy
Neurol 96:1041-1051, Jain, P. & Arya, R., 2021

Pain in Right Buttock after Carbon Monoxide Poisoning
BMJ 373:n1233, Hu, H. & Sun, Q., 2021

Fluorosis
Neurol 97:e1973-e1974, Saluja, A.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

An Unusual Case of Acute Psychosis and Tetraparesis in a Young Zambian Man
Neurol 97:1002-1005, Zimba, S.,et al, 2021

The First Examination of Diagnostic Performance of Automated Measurement of the Callosal Angle in 1856 Elderly Patients and Volunteers Indicates that 12.4% of Exams Met the Criteria for Possible Normal Pressure Hydrocephalus
AJNR 42:1942-1948, Morzage, M.,et al, 2021

Digital Health
Stroke 52:351-355, Silva, G.S. & Schwamm, L.H., 2021

Leg Weakness and Paraesthesia Provide a Clue to Sudden Death due to Aortic Dissection
Lancet 397:128, Agarwal, M.,et al, 2021

A 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021

Chorioretinopathy After Corticosteroid Treatment for Optic Neuritis
Neurol 96:e305-e306, Ling, J. and Micieli, J.A., 2021

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

Cranial Nerve Disorders Associated with Immune Checkpoint Inhibitors
Neurol 96:e866-e875, Vogrig, A.,et al, 2021

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

Immunoglobulin G4-related Hypertrophic Pachymeningitis Mimicking Temporal Arteritis
Neurol 94:(15 suppl), Han, J.Y.,et al, 2020

Neurotoxic Manifestations of High-Dose Intrathecal Gadolinium Administration for CT Myelogram
Radiol Case Reports 15:1992-1995, Malalur, P. & Rajacic, P.C., 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

A Patient with a History of Weight Loss Presenting with Seizures
Neurol 95:e2038-e2042, Tang, G. & Benavides, D.R., 2020

Clinicopathologic conference, Cryptococcal meningoencephalitis and advanced HIV infection
NEJM 383:2572-2580, Case 40-2020, 2020

Neurological Impairments in a Patient Returning from Cuba
JAMA Neurol 77:1570-1571, Serlin, Y.,et al, 2020

Covd-19-Associated Myopathy Caused by Type 1 Interferonopathy
NEJM 383:2389-2390, Manzano, A.C.,et al, 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

Headache, Confusion, and Somnolence in a 27-Year-Old Woman
JAMA doi:10-1001/JAMA.2020.10167, Sastry, R.,et al, 2020

A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
Ann Neurol 88:637-638, Wu, H.,et al, 2020

Spinal Cord Involvement in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
JAMA Neurol 77:1169-1170, Li, S.,et al, 2020

Tattoo Reaction - A Diagnostic Clue in Neurosarcoidosis
JAMA Neurol 77:1167-1168, Halliday, A.J.,et al, 2020

Encephalomyelitis and Lymphadenopathy in a Man in His Early 40s
JAMA Neurol 77:1171-1172, Bakirtzis, C.,et al, 2020



Showing articles 1700 to 1750 of 8383 << Previous Next >>