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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 1850 to 1900 of 7326 << Previous Next >>

Myelitis-Predominant Agressive Phenotype:Unveiling Unique Paterns of Late-Onset Neuromyelitis Optica Spectrum Disorders
Ann Neurol 99:1139-1151, Pu,Y-L.,et al, 2026

Bilateral Posterior Limb Internal Capsule T2 Hyperintensity and Severe Cerebellar Atrophy in 2 Lifelong Friends
Neurol 106:e218014, Inoue,H.,et al, 2026

Deep Venous Dural Arteriovenous Fistula Mimicking Progressive Dementia
Stroke 57:e180-181, Langlois-Therien,T.,et al, 2026

A 28-Year-Old Man with Seizures and Thalamic Lesions
Neurol 106:e218065, Santos-Rojo,A.B.,et al, 2026

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

A 32-Year-Old Woman with Progressive Vision Loss and Confusion
Neurol 106:e214988, Kumar,A.B.,et al, 2026

Cerebral Syphilitic Vasculitis Presenting with Recurrent Stroke
Stroke 57:e197-e198, Yilmaz,E.,et al, 2026

High-Grade Gliomas with Autoimmune Encephalitis-Like Presentation: Case Report and Systematic Review of the Literature
Neurological Sci 46:3559-3572, Creda,G.S.et al, 2025

Trident Sign in GFAP-Associated Meningoencephalomyelitis
Neurol 106:e214566, Mallett,N.S.,et al, 2025

An 83-Year-Old Female Patient with a Pupil Involving Oculomotor Nerve Palsy
Neurol 105:e214383, Riegel,D.C.,et al, 2025

A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2198-2209, 2264, Luciano,M.G.,et al, 2025

Ribbon-Like Cortical Calcifications in Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type
Neurol 106:e214464, Chen,Y.,et al, 2025

Recurrent Ischemic Strokes Due to Os Odontoideum
Ann Neurol 98:1315-1317, Wang,J.,et al, 2025

Acromegaly
NEJM 393:1926-1939, Giustina,A. & Colao,A.,, 2025

Clinical Core Symptoms of Posterior Spinal Artery Ischemia
Eur Neurol 65:183-186, Struhal,S.,et al, 2025

Pneumocephalus Leading to Basilar Artery Compression After Epidural Anesthesia
Neurol 105:e214089, Schick,J.,et al, 2025

Frequency, Risk Factors, and Outcomes of Strokes in Patients with Primary Glioma After Cranial Radiation
Neurol 105:e213902, Ryan,D.,et al, 2025

A 64-Year-Old Man with Confusion, Nausea, Seizure, and Fever
Neurol 104:e213659, Xu,A.,et al, 2025

Bobble-Head Doll Syndrome in a Child
Neurol 104: e213694, Chityala,A.,et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
Neurol 105:e214297, Chen,Z., et al, 2025

A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
Neurol 105:e214381, Gomez,A.C.et al, 2025

Sjogren Syndrome Presenting with Craniospinal Hypertrophic Pachymeningitis
Neurol 105:e214382, Nayak,A.,et al, 2025

Isolated Cervical Radiculopathy as an Unusual Presentation of Vertebral Artery Dissection
Neurol 105:e214389, Guo,K.,et al, 2025

Neurosyphilis
Ann Neurol 98:1070-1076, Minter,D.J. & Chow,F.C., 2025

Clinicopathologic Conference, Lyme Carditis
NEJM 393:799-807, Case 24-2025, 2025

Cervical Radiculopathy Due to Vertebral Artery Dissection
Neurol 105:e214090, Guadalupi,P.,et al, 2025

A 9-Year-Old Girl with CNS Immune Dysregulation
Neurol 105:e213999, Marefi,A.,et al, 2025

A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
Neurol 105:e214173, Wold,K.J.,et al, 2025

A Woman with Subacute Progression of Distal Upper Extremity Weakness
Neurol 105:e214212, Zhao,A.J.,et al, 2025

The Multifactorial Nature of Ischemic Stroke in Malignancy
Stroke 56:e303-e306, Doyle,C.L.,et al, 2025

A 66-Year-Old Female Patient with Rapidly Progressive Memory Changes
Neurol 105:e214211, Fokas,J.A.,et al, 2025

Atypical Diabetic Neuropathies
BMJ 390:e081109, McCray,B.A.,et al, 2025

Acute Subarachnoid MRI-FLAIR Signal in severe Tick-Borne Encephalitis: A Potential Prognostic Marker
Life 15:1655, Bohm,V.,et al, 2025

Idiopathic Intracranial Hypertension
NEJM 393:1409-1414, Horton,J.C., 2025

A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
Neurol 105:e214233, Bu,S.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

Use of Advance Vessel Wall Imaging to Detect Vertebral Artery Dissection
Neurol 104:e213542, Hu,X.,et al, 2025

Primary Central Nervous System Vasculitis with Thalamic Involvement
Neurol 104:e213665, Sarikaya,C.,et al, 2025

A 72-Year-Old Man With Meningoencephalitis
Neurol 104:e213658, Isaza-Pierotti,D.F.,et al, 2025

Clinicopathologic Conference, Cryptococcus Neoformans and Cushings Syndrome
NEJM 392:1847-1856, Case 13-2025, 2025

A 62-Year-Old Man with Symmetric Saddle Hypoesthesia and Sphincter Dysfunction
Neurol 104:e213712, Crausaz,L.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Clinicopathological Conference, Powasan Virus Encephalitis
NEJM 393:176-184, Case 19-2025, 2025

Neuroimaging Spectrum of Erdheim-Chester Disease:An Image-Based Review
AJNR 46:1300-1308, Rai,P.,et al, 2025

AAV9-Mediated Gene Therapy for Infantile-Onset Pompes Disease
NEJM 392:2438-2446, 2477, Ma,X.,et al, 2025

Acute and Progressive Cognitive Decline in a 38-Year-Old Man
Neurol 105: e213871, Wu,L.,et al, 2025

A 27-Year-Old Man with Progressive Bilateral Vision Loss Resistant to Steroid Therapy
Neurol 105: e213897, Zhang,W.,et al, 2025

Clinicopathologic conference, Malignant Mixed Germ-Cell Tumor and Anti-NMDA Receptor Encephalitis
NEJM 303:488-496, Case 22-2025, 2025

Automated Detection of Normal Pressure Hydrocephalus Using CT Imaging for Calculating the Ventricle-to-Subarachnoid Volume Ratio
AJNR 46:141-146, Knittel,J.J.,et al, 2025

Automated Idiopathic Normal Pressure Hydrocephalus Diagnosis via Artificial Intelligence-Based 3D T1 MRI Volumetric Analysis
AJNR 46:33-40, Lee,J.,et al, 2025



Showing articles 1850 to 1900 of 7326 << Previous Next >>