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abiotrophy
adult polyglucosan body disease
advances in neurology
algorithm
Alzheimer's disease
aminoacidopathies
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amyotrophic lateral sclerosis, bulbar
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amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, conjugal
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
aphasia
aphasia, progressive, primary
areflexia
arm weakness
arthrogryposis multiplex
ataxia
ataxia, progressive
autonomic dysfunction
axonal degeneration
Babinski sign
behavioral disorder
bladder dysfunction
brain atrophy
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
C0ORF72
CAG repeats
calf hypertrophy
camptocormia
cane
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
central core disease
cerebellar atrophy, primary
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
Charcot-Marie-Tooth
children
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Dejerine-Sottas syndrome
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dermatomyositis
developmental retardation
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differential diagnosis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dying
dysarthria
dysphagia
dyspnea
dystonia
electromyogram
emotional lability
epidemiology of neurology
episodic neurologic deficits
exercise
exercise intolerance
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
fluency
foot drop
free radical
Friedreich's ataxia
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gait disorder
gait, spastic
gene
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gene therapy
genetic counselling
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genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
Guillain Barre syndrome
gynecomastia
hallucination
hand weakness
hearing loss
heavy metal intoxication
hemiparesis
heralding manifestation
history of neurology
hoarseness
Huntington's chorea
hyperpigmentation of skin
hyperreflexia
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinentia pigmenti
infant, evaluation of
inflexibility, mental
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
Isaacs syndrome
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Jewish
klippel feil syndrome
Kugelberg-Welander syndrome
lactic acidemia
lathyrism
laughing
laughing, pathologic
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
leukodystrophy
leukoencephalopathy
Lewy body
life expectancy
lobar atrophy
lysosomal storage disease
malformation, CNS, congenital
memory, defect of recent
memory, impairment of
mental retardation
metabolic disorder, primary
Mills syndrome
mimics
misdiagnosis
molecular genetics
monomelic amyotrophy
mononeuropathy
mortality
motor neuron disease
MRI, abnormal
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelomalacia
myeloneuropathy
myokymia
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nasal speech
neck weakness
nerve conduction studies
neuritis, causes of
neuroendocrinology
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neurofibromatosis 2
neurogenic bladder
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neuropathy, hereditary peripheral
next-generation sequencing
nusinersen
optic atrophy
pain, increased response
palliative care
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, familial
Parkinson disease, rapid progression
Parkinson disease, young onset
Parkinsonism syndrome
Parkinsonism-dementia complex
paroxysmal neurologic deficits
patient information and support
peroneal muscle atrophy, causes of
peroxisomal disease
personality change
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
poliomyelitis
polyglucosan body
polyglucosan body disease
polymyositis
polyneuropathy
porphyria
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
pseudobulbar palsy
pseudohypertrophy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
recombinant DNA
Refsum's disease
release phenomena
respirator
respiratory failure
review article
RFLPs
riluzole
risk factors
Roussy Levy syndrome
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
single photon emission computed tomography
skin, lesions in neurologic disorders
SMN1 gene
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord degeneration
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
stereotyped behavior
stiff man syndrome
superoxide dismutase
survival motor neuron gene
temporal lobe, atrophy
term infant
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
torticollis
trauma
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trinucleotide repeats
urea-cycle enzymopathies
urinary incontinence
vestibular function, tests of
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
word-finding difficulty
X-linked bulbospinal neuronopathy
Showing articles 700 to 750 of 4485 << Previous Next >>

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

"Better Explanations" in Multiple Sclerosis Diagnostic Workup
Neurol 92:e2527-e2537, Calabrese, M.,et al, 2019

Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
NEJM 381:164-172, Case 21-2019, 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Acute Lateral Medullary Infarct Due to Giant Cell Arteritis
Stroke 50:e290-e293, Dardick, J.M.,et al, 2019

Vaccine-Preventable Infections and Immunization in Multiple Sclerosis
Neurol 93:584-594, Farez, M.F.,et al, 2019

Ehlers-Danlos Syndromes
BMJ 366:I4966, Ghali, N.,et al, 2019

Empty Sella Is a Sign of Symptomatic Lateral Sinus Stenosis and Not Intracranial Hypertension
AJNR 40:1695-1700, Zetchi, A.,et al, 2019

Inebilizumab for the Treatment of Neuromyelitis Optica Spectrum Disorder (N-MOmentum): A Double-Blind, Randomised Placebo-Controlled Phase 2/3 Trial
Lancet 394:1352-1363,1304, Cree, B.A.C.,et al, 2019

Recurrent Epistaxis in an Adolescent
BMJ 367:I5393, McLaren, O. & Ronan, N., 2019

Effects of Tranexamic Acid on Death, Disability, Vascular Occlusive Events and Other Morbidities in Patients with Acute Traumatic Brain Injury (CRASH-3): A Randomised, Placebo-Controlled Trial
Lancet 394:1713-1723,1687, The CRASH-3 trial collaborators, 2019

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

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

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Long-Term Treatment Effect in Cerebrotendinous Xanthomatosis Depends on Age at Treatment Start
Neurol 92:e83-e95, Stelten, B.M.L.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,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

Compressive Lateral Femoral Cutaneous Neuropathy Secondary to Sartorius Muscle Fibrosis
JAMA Neurol 76:109-110, Triplett, J.D.,et al, 2019

Association of Initial Disease-Modifying Therapy with Later Conversion to Secondary Progressive Multiple Sclerosis
JAMA 32:175-187, Brown, J.W.L.,et al, 2019

Effect of Nonmyeloablative Hematopoietic Stem Cell Transplantation vs Continued Disease-Modifying Therapy on Disease Progression in Patients with Relapsing-Remitting Multiple Sclerosis
JAMA 32:165-174,153, Burt, R.K.,et al, 2019

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

Simultaneous CMV and Listeria Infection Following Alemtuzumab Treatment for Multiple Sclerosis
Neurol 92:296-298, Pappolla, A.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

Acute Toxic Limbic Encephalopathy Following Glyphosate Intoxication
Neurol 92:534-536, Planche, V.,et al, 2019

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

Diagnostic Tools for Immune Causes of Encephalitis
Clin Microbiol Infect 25:431-436, Lascano, A.M.,et al, 2019

Clinical Epidemiology of Familial Sarcoidosis
Respir Med 149:36-41, Terwiel, M. & Van Moorsel, C.H.M., 2019

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

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

Neuromyelitis Optica Spectrum Disorder (NMOSD) in a Male with Hiccups and Quadriparesis
IJCMR 5:K28-K30, Tuteja,H.S.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

Area Postrema Syndrome
Neurol 91:e1642-e1651, Shosha, E.,et al, 2018

Congenital Myasthenic Syndromes in Adult Neurology Clinic
Neurol 91:e1770-e1777, Kao, J.C.,et al, 2018

Use of Newer Disease-Modifying Therapies in Pediatric Multiple Sclerosis in the US
Neurol 91:e1778-e1787, Krysko, K.M.,et al, 2018

Application of the 2017 Revised McDonald Criteria for Multiple Sclerosis to Patients with a Typical Clinically Isolated Syndrome
JAMA Neurol 75:1392-1398, Van Der Vuurst De Vries, R.M.,et al, 2018

Foot Drop
WebMD, Bernstein, L., 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Use of Vitamins and Dietary Supplements by Patients with Multiple Sclerosis, A Review
JAMA Neurol 75:1013-1021, Evans,E.,et al, 2018

Prodromal Symptoms of Multiple Sclerosis in Primary Care
Ann Neurol 83:1162-1173, Disanto,G.,et al, 2018

Valsalva-Triggered Pseudotumor Cerebri Syndrome
Neurol 91:e746-e750, Chan, T.L.H.,et al, 2018

Trial of Fingolimod Versus Interferon Beta-1a in Pediatric Multiple Sclerosis
NEJM 379:1017-1027, Chitnis, T.,et al, 2018

Inclusion of Optic Nerve Involvement in Dissemination in Space Criteria for Multiple Sclerosis
Neurol 91:e1130-e1134,545, Brownlee, W.J.,et al, 2018



Showing articles 700 to 750 of 4485 << Previous Next >>