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Differential
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adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
alternating hemiplegia
alternating hemiplegia of childhood
Alzheimer's disease
Alzheimer's disease, familial
amimia
anterior tibial muscle weakness
antiviral agents
areflexia
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic-dystonia syndromes
ATP1A3 gene
attention deficit disorder with hyperactivity
autonomic dysfunction
Babinski sign
basal ganglia, lesion, bilateral
beta-D-glucon
bladder dysfunction
brainstem, atrophy
bronchoscopy
bulbar palsy
candida albicans
CAT scan, abnormal
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar atrophy, primary
cerebral palsy
cerebral palsy, etiology
cerebral palsy, work up
cerebrospinal fluid, beta-D-glucan
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, familial occurrence
ceruloplasmin, serum
Charcot-Marie-Tooth
chelation therapy
chest x-ray, abnormal
children
choreoathetosis
chromosomal abnormality
chromosome 12
chromosome 5
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
cobalamin C deficiency
cogwheel rigidty
complications
congenital myasthenic syndromes
consanguinity
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cranial nerve enhancement
degenerative diseases of CNS
dementia
dementia, presenile
developmental disability
developmental retardation
diet
difficulty going down stairs
distal muscle atrophy
distal muscle weakness
DNA sequencing
double-cortex syndrome
dysarthria
dysmetria
dysphagia
dystonia
electromyogram
Embryonal tumors
encephalopathy
eosinophilia
ependymoma
exome sequencing
facial weakness
falling
false negative
familial
fatigue
fish
floppy infant
fourth ventricle, compression
fungal infection
fungal infection, CNS
gait disorder
gait, spastic
GAMT gene
gene
gene mutation
genetic counselling
genetic diagnosis
genetic neurologic disorders
genetic screening
genetic testing
glioblastoma multiforme(astrocytoma Gr.III)
glioma
glioma, low-grade
globus pallidus, lesion of, bilateral
gram positive cocci
Guillain Barre syndrome
hammertoes
headache
headache, awakening with
headache, positional
headache, progressive
hearing loss
helminthic infection of CNS
hemiparesis, transient
hepatolenticular degeneration(Wilson's disease)
heterotopia
high arched feet
high arched palate
human genome
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperbilirubinemia
hyperhomocysteinemia
hyperreflexia
hypoglycorrhachia
hypogonadism
hypogonadism, hypogonadotropic
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
imbalance
inborn errors of metabolism
inclusion bodies, intranuclear
incoordination
India
intellectual deficit
intracerebral hemorrhage
intrauterine infection, viral
intrauterine infection, viral of CNS
intravenous drug abuse
intrinsic hand muscles, wasting of
Jewish
Krabbe's disease
lactic acidemia
Leber's hereditary optic neuropathy
leg weakness, bilateral
lethargy
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
life expectancy
linear lesion
liver biopsy
liver function enzymes
lung nodule
lung-brain syndromes
lysosomal storage disease
malformation, CNS, congenital
masked facies
medulloblastoma
megalencephaly
memory, impairment of
meningeal enhancement
meningeal sarcomatosis
meningitis
meningitis, basilar
meningitis, candida
meningitis, chronic
meningitis, fungal
meningitis, neutrophilic
mental retardation
mestinon
metabolic acidosis
methylmalonic acidemia
microcephaly
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mineralization
misdiagnosis
mitochondrial disease
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI, abnormal
MRI, blooming effect
MRI, contrast enhanced
MRI, diffusion weighted
MRI, mass effect on
MRI, nodular enhancement
MRI, spinal cord
muscle stiffness
muscle weakness, proximal
mutism
myelomalacia
myeloneuropathy
myelopathy
nasal speech
nausea and vomiting
needle tracks
neonatal intensive care unit
neonatal screening, genetic neurologic disorders
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-classification
neoplasm, primary of CNS-treatment of
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic practice
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathy
neuropathy, demyelinating
newborn, evaluation of
next-generation sequencing
night blindness
normal
NOTCH2NLC
nystagmus
ocular motility, disorders of
opened mouth
ophthalmoplegia
ovarian dysgenesis
pachygyria
papilledema
paragonimiasis
paraparesis, familial spastic
paraparesis, spastic
parasitic infection, CNS
Parkinson disease
Parkinson disease, early symptoms
Parkinson disease, familial
Parkinsonism syndrome
paroxysmal neurologic deficits
patient information and support
Perrault syndrome
pes cavus
phonophobia
photophobia
PICU
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
polyglucosan body disease
polymicrogyria
pons, lesion of
precipitating factors
PRKN gene
prognosis
progressive neurologic disorder
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia
quality of life
recurrent
respiratory tract infection
review article
risk factors
risus sardonicus
Romberg's sign
salivation, excessive
scissors gait
scotoma
screening
seizure
seizure, drug-induced
sensorineural hearing loss
shunt procedure, ventricular
shunt procedure, ventricular-complications of
spastic ataxia
spastic paraplegia, type 7
spasticity
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
symmetric brain lesions
tandem gait, ataxic
tinnitus
toe walking
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
tripping
urinary urgency
vasculitides
vasculopathy
vegetarianism
viral infection
viral infection, CNS
vision loss, sequential
vision, blurred
visual loss
visual loss, transient
visual obscurations, transient
walking, delayed
walking, difficulty with
weakness
weakness, fatiguable
weakness, proximal
weight loss
wheelchair
white matter disease
wide based gait
workup
x-linked intellectual deficit
x-linked mental retardation
Zika virus infection
Showing articles 0 to 32 of 32

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

A 26-Year-OldWoman with Headache and Eosinophilia
Neurol 104:e213434, Goh,W.G.W.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era
JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022

Brain Tumors in Children
NEJM 386:1922-1931, Cohen, A.R., 2022

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021

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

Muscle Stiffness, Gait Instability, and Liver Cirrhosis in Wilsons Disease
Lancet 396:990, Kronlage, C.,et al, 2020

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Zika Virus as a Cause of Neurologic Disorders
NEJM 374:1506-1509, Broutet, N.,et al, 2016

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

Somatic Mutations in Cerebral Cortical Malformations
NEJM 371:733-743, Jamuar, S.S.,et al, 2014

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Genomewide Association Studies of Stroke
NEJM 360:1718-1728, Ikram,M.A.,et al, 2009

Alzheimer's Disease and Parkinson's Disease
NEJM 348:1356-1364, Nussbaum,R.L. &Ellis,C.E., 2003

Impact of the Human Genome Projects and Identification of a Stroke Gene
Stroke 32:1239-1241, Alberts,M.J., 2001

Complete Genomic Screen in Parkinson Disease
JAMA 286:2239-2244, Scott,W.K.,et al, 2001

The Brain Code in Health and Disease
Arch Neurol 57:50-51, Rosenberg,R.N., 2000

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998



Showing articles 0 to 32 of 32