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Differential
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aminoacidopathies
aminoacidurias
aneurysm
aneurysm, intracranial
anosognosia
aphasia
aphasia, global
aphasia, transcortical
areflexia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
ataxic-dystonia syndromes
athetosis
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
bilirubin encephalopathy
blindness, sudden
brain atrophy
brain damage
brainstem, lesion of
breast feeding
bulbar palsy
CAG repeats
CAT scan
CAT scan, abnormal
cerebellar ataxia, hereditary
cerebellar lesion
cerebrospinal fluid, glycine
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cherry red spot
cherry red spot-myoclonus syndrome
children
choreoathetosis
chromosomal abnormality
chromosome 6
Clinical Pathologic Conference(C.P.C.)
congenital myasthenic syndromes
conjugate gaze, forced
cortical blindness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
cry, abnormal
cry, high-pitched
degenerative diseases of CNS
dementia
dementia, rapidly progressive
developmental milestones, loss of
developmental retardation
dinitrophenylhydrazine(D.N.P.H.)reaction
downward gaze, paralysis of
dysarthria
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
epidemiology of neurology
exercise intolerance
exome sequencing
eye movement, disorders of
facial weakness
facial weakness, bilateral
falling
false negative
familial
fever
floppy infant
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
Guillain Barre syndrome, infantile and childhood form
head injury
headache
hearing loss
hemiparesis
hemorrhage, thalamic
hoarseness
hydrocephalus
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hypophonia
hyporeflexia
imbalance
impulsivity
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia, bilateral
intracerebral hemorrhage
intracerebral hemorrhage, location of
intracerebral hemorrhage, volume
intraventricular hemorrhage
jaundice
kernicterus
lactic acidemia
leucine
lid closure, weakness of
lysosomal storage disease
maple syrup urine disease
MELAS syndrome
meningitis
meningitis, aseptic
mental retardation
metabolic disorder, primary
migraine
miosis
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
moro reflex
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, familial incidence of
myopathy
myopathy, mitochondrial
nasal speech
nausea and vomiting
neglect
neoplasm, primary of CNS
nerve conduction studies
neurologic examination, focal
neuromuscular junction
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neurotoxic
neurotoxin
nystagmus
ocular motility, disorders of
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, head injury causing
ophthalmoplegia, neonatal
ophthalmoplegia, progressive external
ophthalmoplegia, total
ophthalmoplegic migraine
opisthotonus
personality change
premature infant
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
psychosis
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pyramidal tract dysfunction
ragged-red fibers
rapidly progressing neurologic illness
renal failure
retinal degeneration
retropulsion
review article
seizure
seizure, children
sensorimotor stroke
sensorineural hearing loss
setting sun phenomena
short stature
skew deviation
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 28
spinocerebellar degeneration
strokelike episodes
subthalamic nucleus
suck, poor
temporal lobe, lesion
term infant
thalamic aphasia
third nerve palsy
third nerve palsy, childhood
third nerve palsy, congenital
third nerve palsy, cyclic
transverse smile
treatment of neurologic disorder
tremor
trinucleotide repeats
upgaze, paralysis of
ventricular enlargement
vertical gaze
viral infection
viral infection, CNS
visual acuity, decreased
visual fields, constricted
visual loss
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
wheelchair
wide based gait
Showing articles 100 to 150 of 1755 << Previous Next >>

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
Neurol 95:e3153-e3159, Russ, J.B.,et al, 2020

Clinicopathologic conference, Vitamin D deficiency
NEJM 383:2462-2470, Case 39-2020, 2020

Efficacy and Safety of Adjunctive Lacosamide in the Treatment of Primary Generalised Tonic-Clonic Seizures: A Double-Blind, Randomised, Placebo-Controlled Trial
JNNP 91:1067-1075, Vossler, D.G.,et al, 2020

Acute Ischemic Stroke in Adolescents
Neurol 94:e158-e169, Rambaud, R.,et al, 2020

Feasibility, Safety, and Outcome of Endovascular Recanalization in Childhood Stroke
JAMA Neurol 77:25-34, Sporns, P.B.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Clinicopathologic Conference, Intraparenchymal & Intracranial Hemorrhage due to Birth Trauma
NEJM 382:656-664, Case 5-2020, 2020

Young Woman with Orbital Pain and Diplopia
Neurol 94:e752-e757, Infante, R.,et al, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
Neurologist 25:82-84, Uzawa, A.,et al, 2020

Carotid-Cavernous Fistula Presenting with Bilateral Abducens Palsy
Stroke 51:e107-e110, Peng, T.J.,et al, 2020

A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
Neurol 94:994-999, Wildman, J.,et al, 2020

Contrast-Induced Encephalopathy Following Coronary Angiography
Neurol 94:e2491-e2494, Harada, Y.,et al, 2020

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Distal Symmetric Polyneuropathy in 2020
JAMA 324:90-92, Callaghan, B.C.,et al, 2020

Long Survival Sporadic Creutzfeldt-Jakob Disease
Neurol 95:87-88, Liu, X.Y.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

COVID-19 Presenting with Ophthalmoparesis from Cranial Nerve Palsy
Neurol 95:221-223, Dinkin, M.,et al, 2020

Recurrent Cerebral Ischemia During Pregnancies
Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020

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

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Acute Maternal Confusion and Neonatal Seizure Postpartum
BMJ 364:k5399, Jakes, A.D.,et al, 2019

Management of Stroke in Neonates and Children
Stroke 50:e51-e96, Ferriero, D.M.,et al, 2019

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

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

Dog Licks Baby. Baby gets Pasteurella Multocida Meningitis
Lancet 393:e41, Ryan, J.M. & Feder Jr., H.M., 2019

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

Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019

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

Bilateral Claude Syndrome
Neurol 93:599-600, Witsch, J.,et al, 2019

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

Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019

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

Rare Presentation of Spontaneous, Direct, Carotid Cavernous Fistula in Late Pregnancy:A Case Report
Ophthalmol Clin Res 2:73-77, Agrawal,N.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Posttraumatic Isolated Intraventricular Hemorrhage A Rare Entity: Case Series
Asian J Neurorsurg 14:162-165, Ravi,K.,et al, 2019

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

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 2018

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

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,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

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Childhood Seizures After Phototherapy
Pediatrics 142:e20180648, Newman, T.B.,et al, 2018



Showing articles 100 to 150 of 1755 << Previous Next >>