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acid maltase deficiency
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
advances in neurology
adverse drug reaction
alpha-fetoprotein
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis-like syndrome
anterior horn cell disease
anterior tibial muscle weakness
antiviral agents
apraxia of eye movements
areflexia
arm atrophy
arm weakness
arthrogryposis multiplex
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
brachial amyotrophic diplegia
Brugada syndrome
bulbar palsy
bulbar palsy, progressive
CAG repeats
calf hypertrophy
carcinoembryonic antigen
carcinoma
CD4 counts
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
Clinical Pathologic Conference(C.P.C.)
clinodactyly
coma
complications
congenital heart disease
congenital myopathy
constipation
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
Dejerine-Sottas syndrome
dementia
denervation of muscle
denervation potentials
dentatorubral-pallidoluysian atrophy
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
diplegia, brachial
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dysarthria
dysphagia
dystonia
dystrophin
efficacy
electrocardiogram, abnormal
electromyogram
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
fragile-X syndrome
Friedreich's ataxia
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
growth retardation
gynecomastia
heavy metal intoxication
heralding manifestation
highly active antiretroviral therapy
history of neurology
human immunodeficiency virus type 1
huntingtin
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
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Isaacs syndrome
jaw closure weakness
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
leukemia
lid closure, weakness of
life expectancy
liver disease
lordosis
lymphoma
Man-In-The-Barrel syndrome
masseter muscle weakness
mental retardation
misdiagnosis
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
motor system
movement disorder
movement disorder, extrapyramidal
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle hypertrophy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myeloradiculopathy
myocardial injury
myocytolysis
myokymia
myopathy
myopathy, centronuclear
myopathy, mitochondrial
myopathy, quadriceps
myotonia congenita
myotonia dystrophica
nemaline rod myopathy
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurogenic vs.myopathic atrophy
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromyotonia
neuronal degeneration
neuronal migration disorder
neuronopathy
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, motor, multifocal
newborn, evaluation of
nusinersen
ocular motility, disorders of
Parkinson disease
pathology
patient information and support
peroneal muscle atrophy, causes of
placebo
poison, mercury
poison, neurologic problems with
polymerase chain reaction
polymyositis
polyneuropathy
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
progeria
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudohypertrophy
quadriceps atrophy
quadriceps weakness
radiation hypersensitivity
radiculopathy
Refsum's disease
respiratory failure
retrovirus
review article
RFLPs
risdiplam
risk-benefit assessment
Roussy Levy syndrome
safety
scoliosis
scoliosis, neurologic association with
screening
skin, lesions in neurologic disorders
SMN1 gene
spinal cord
spinal cord degeneration
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
sudden death
survival motor neuron gene
telangiectases
term infant
testicular atrophy
tongue, fasciculations of
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trinucleotide repeats
viral infection
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 700 to 750 of 7326 << Previous Next >>

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Optic Nerve Enhancement and Restricted Diffusion in Postoperative Visual Loss
Neuro-Ophthalmol 43:337-339, Finelli, P.F., 2019

A 65-year-old man with Asymmetric Weakness and Parethesias
Neurol 93:856-861, Harada, Y.,et al, 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

Toxoplasmosis in HIV-Infected Patients
www.UptoDate.com, May, Gandhi, R.T., 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Subacute Progressive Sensorimotor Symptoms
BMJ 365:doi:10.1136/bmj.l1923, Francis, A.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

Central Nervous System Infections Due to Coccidioidomycosis
J Fungi 5:2-12, Jackson, N.R.,et al, 2019

Pediatric HIV Infection: Classification, Clinical Manifestations, and Outcome
www.UptoDate.com, June, Gillespie, S.L., 2018

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

Deep Brain Nuclei T1 Shortening after Gadobenate Dimeglumine in Children: Influence of Radiation and Chemotherapy
AJNR 39:24-30, Kinner, S.,et al, 2018

Long-term Effects of Glucocorticoids on Function, Quality of Life, and Survival in Patients with Duchenne Muscular Dystrophy: A Prospective Cohort Study
Lancet 391:451-461, McDonald, C.M.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

Gummatous Neurosyphilis
Neurol 90:e913-e914, Silva, H.S.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

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

A 48-year-old woman with confusion, personality change, and multiple enhancing brain lesions
Neurol 90:e1724-e1729, Hills, J.M.,et al, 2018

Trypanosoma cruzi Reactivation in the Brain
NEJM 378:1824, Sacks, C.A.,et al, 2018

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

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

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

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,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

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

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

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

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

Cerebral Amyloid Angiopathy-Related Inflammation Presenting with Isolated Leptomeningitis
Neurol 89:e66-e67, Kang, P.,et al, 2017

A Comparative Study of CIDP in a Cohort of HIV-Infected and HIV-Uninfected Patients
Neurol Neuroimmunol Neuroinflamm 4:e315, Moodley, K.,et al, 2017

CNS Cryptococcosis in HIV
eMedicine.com Nov 2017, Gliksman, F.J. & Singh, N.N., 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

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

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

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

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

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

Human Immunodeficiency Virus Presenting as Progressive Multifocal Leukoencephalopathy Restricted to the Posterior Fossa
JAMA Neurol 74:597-598, Schubert, R.D. & Richie, M.B., 2017

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

Anal Carcinoma
NCCN.org April 2017 V2.2017, , 2017

Candida Meningitis in an Immunocompetent Patient Detected Through (1?3)-beta-?-glucan
Int J Infect Dis 51:25-26, Farrugia, M.K.,et al, 2016

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Rapid Multifocal Neurologic Decline in an Immunocompromised Patient
JAMA Neurol 73:226-231, Kromm, J.A.,et al, 2016



Showing articles 700 to 750 of 7326 << Previous Next >>