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Differential
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abscess, intracerebral
acetazolamide
acetylcholinesterase
acid maltase deficiency
acid maltase deficiency, adult
acoustic neurinoma
acoustic neurinoma, bilateral
acrocyanosis
acromicria
ACTH
Addison's disease
adducted thumb
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
agenesis of corpus callosum
Aicardi-Goutieres syndrome
algorithm
alpha glucosidase
alpha-fetoprotein
alveolar hypoventilation
aminoacidurias
ammonia
amniocentesis
anemia
anencephaly
anesthesia, general
aneurysm
Angelman syndrome
angiofibroma, facial
angiography, spinal
angiokeratoma
ankle edema
anterior horn cell disease
anticonvulsants
anticonvulsants, absorption
anticonvulsants, bioavailability
anticonvulsants, blood level determination of
anticonvulsants, compliance
anticonvulsants, subtherapeutic
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
anxiety
arbovirus
areflexia
arm weakness
arrhythmia, cardiac
arteriovenous malformation
arteriovenous malformation, pulmonary
arthralgia
arylsulfatase B
ascites
aspartate aminotransferase
aspartocyclase
aspiration
asymptomatic
ataxia
ataxia, hereditary
ataxia, paroxysmal
attention deficit disorder with hyperactivity
atypical
audiogram
auditory evoked brainstem potentials
autism
Babinski sign
baldness
basal ganglia, calcification of
behavior, combative
behavioral disorder
birth injury
bleeding disorder
body odor
bone marrow transplantation
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
brain atrophy
Brazil
breast feeding
bruit
cachexia
cafe au lait spots
CAG repeats
calcification, intracranial
calf hypertrophy
Canavan's disease
carbamazepine
carcinoma
cardiac surgery, hypothermia and circulatory arrest for
cardiac surgery, neurologic complications with
cardiomegaly
cardiomyopathy
caribbean
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, indications for
cataracts
cataracts, congenital
Central America
central nervous system, infection of
cerebellar ataxia, children
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral embolism
cerebral infarction
cerebral palsy
cerebral palsy, risk factors
cerebral palsy, work up
cerebro hepato renal syndrome
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, intrauterine
cerebrovascular accident, multiple
cerebrovascular accident, neonatal
cerebrovascular accident, recurrent
cerebrovascular disease
ceruloplasmin, serum
cesarean section
Charcot-Marie-Tooth
chilbran skin lesions
children
chorea
choroid plexus
choroid plexus, abnormality of
choroid plexus, cyst
chromosomal abnormality
chromosome 15
chromosome 19
chromosome 3
chromosome 5
chronic graft versus host disease
cleft lip
Clinical Pathologic Conference(C.P.C.)
clonazepam
clubbing of fingers
cocaine
Cockayne's syndrome
cognition
cold temperature
coma
complications
confidentiality
congenital birth defects
congenital heart disease
congenital infection, CNS
congenital infection, viral
congenital malformation
congenital malformation, dilantin therapy causing
congenital malformation, non CNS
congestive heart failure
consanguinity
constipation
contractures, joint
controversies in neurology
copper metabolism, abnormal
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corpus callosum, atrophy of
counselling
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
cultured skin fibroblasts
cyanosis
cyst, porencephalic
deafness
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dentate nuclei, lesion of
depression
developmental abnormality of brain
developmental disability
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
diaphragmatic paralysis
diet
differential diagnosis
digits, abnormal
dilantin
dilantin, toxicity
disability, neurological
dissociated sensory loss
distal muscle weakness
diurnal variation
DNA probes
dopamine agonist
drooling
drug abuse
drug interactions
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmorphic
dysostosis multiplex
dysphagia
dysphasia
dyspnea
dyspraxia
dystonia
dystonia, children
dystrophin
ear, abnormal
eating disorder
echocardiogram
eczema
edema, pedal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, monitoring, continuous
electromyogram
electron microscopy
embolism, paradoxical
employment
encephalitis, viral
encephalocele
encephalopathy
encephalopathy, neonatal
endovascular therapy
enzyme treatment
enzyme, defect
enzyme, induction
epidemic
epidemiology of neurology
epileptic encephalopathy
epistaxis
epistaxis, recurrent
epoxide hydrolase
esophageal varices
ethics in neurology
extracorporeal membrane oxygenation
Fabry's disease
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
failure to thrive
familial
fasciculation
fatty acid, elevated plasma content
feeding disorder
fetus
fever
fibroma, ungual
fistula, arterio-venous
fistula, arterio-venous, dural
fistula, arterio-venous, dural, spinal
flavivirus
flow study, carotid artery
folic acid
fragile-X syndrome
fragile-X syndrome, carrier
fucosidosis
gabapentin
gait disorder
galactocerebrosidase
gangliosidosis GM1
gangliosidosis GM2
gastrointestinal bleeding
Gaucher's disease
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glucocerebrosidase
glycogen storage disease
glycoprotein
granular osmiphilic material
gray matter
grimacing
growth hormone deficiency
growth retardation
Guillain Barre syndrome
hamartin
hamartoma
hand flapping
head bobbing
head lag
headache
health insurance
hearing loss
heart block
hemiparesis
hemiplegia
hemiplegia, congenital
hemorrhage, intracranial, newborn
hemorrhage, periventricular
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatomegaly
hepatosplenomegaly
hereditary hemorrhagic telangiectasia(HHT)
hexosaminidase-A
high arched palate
hormone replacement
human genome
human T-lymphotropic virus type I(HTLV-I)
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, presymptomatic detection of
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hyperactivity
hypercapnia
hyperphagia
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypoalbuminemia
hypogonadism
hypokinesia
hypopigmentation of skin
hyporeflexia
hypotelorism
hypothermia
hypothyroidism
hypothyroidism, congenital
hypothyroxinemia
hypotonia
hypotonia, infants
hypoxia
hypoxic-ischemic leukoencephalopathy
hypsarrhythmia
imbalance
immunohistochemistry
in situ hybridization
inborn errors of metabolism
inborn errors of metabolism, screening
infant, evaluation of
infantile spasm
infection
infection, recurrent
intellectual deficit
intellectual deterioration
intelligence quotient
intelligence testing in children
interferon alpha
internet
intracranial hemorrhage
intrauterine
intrauterine growth retardation
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intraventricular hemorrhage
iris, abnormal
iron, brain
iron, serum
irritability
karyotyping
Kayser-Fleischer ring
klippel feil syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lamotrigine
learning disability
learning disability, in children
leg weakness, bilateral
lens, dislocation of
leukodystrophy
leukoencephalopathy
leukopenia
levonorgestrel
lipid storage disorder of CNS
Lisch nodules
lissencephaly
liver disease
liver function enzymes
long bone lesion
Lorenzo's oil
low birth weight
lymphangiomyomatosis
lymphoma
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malformation, CNS, congenital
malformation, vascular, cerebral
medical-legal aspects of neurology
meningocele
mental retardation
mental retardation, familial
metabolic disorder, primary
metachromatic leukodystrophy
microcephaly
micrognathia
migraine
Miller-Dieker syndrome
misdiagnosis
mitral valve prolapse
molecular genetics
molybdenum cofactor deficiency
mongolism
mortality
mosquito
motor dysfunction
motor neuron disease
mousy odor
movement disorder
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, fetal
MRI, indications for
MRI, intrauterine
mucopolysaccharidoses
multiple sclerosis, misdiagnosis
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myelomeningocele
myelopathy
myelopathy, chronic progressive
myopathy
myopathy, distal
myopathy, metabolic
myopathy, vacuolar
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
nasal bridge, wide
nausea and vomiting
neonatal epilepsy syndromes
neonatal epileptic encephalopathy
neoplasm, primary of CNS
nerve conduction studies
nerve growth factor
neural tube defect
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic practice
neurologic signs
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neurosis
newborn, evaluation of
Niemann-Pick disease
nose, abnormal
Notch3 gene
nusinersen
nystagmus, hereditary
nystagmus, periodic
obesity
obstetric neurologic injuries
oculopharyngeal muscular dystrophy
omphalocele
opiate
optic atrophy
oral contraceptives
ornithine transcarbamylase deficiency
orthopnea
pain
pain, severe
papilledema
paraparesis
paraparesis, spastic
parasitic infection, CNS
paresthesias
Parkinsonism syndrome
paroxysmal neurologic deficits
partruition
pathology
patient information and support
penicillamine
percussion induced muscle contraction
periventricular leukomalacia
peroxisomal disease
peroxisomes
personality change
phakomatoses
phenylketonuria
pheochromocytoma
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy, chronic inflammatory demyelinating
Pompe's disease of glycogen storage
post hemorrhagic hydrocephalus
postoperative neurologic complications
postpartum
postpartum coma
postural abnormality
practice guidelines
Prader-Labhart-Willi syndrome
pramipexole
precipitating factors
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
premature infant
premature infant, problems in
prenatal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
proximal muscle atrophy
proximal myotonic myopathy
pruritus
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
ptosis
puerperium
pyramidal tract dysfunction
quadriparesis
Rankin score
rash
recombinant DNA
recurrent
Refsum's disease
renal cyst
renal stones
respiratory failure
restless leg syndrome
retinal degeneration
retinal hamartoma
reversible neurologic disorder
review article
RFLPs
rhabdomyoma, cardiac
rigidity
risk factors
rubella syndrome
scoliosis
scoliosis, neurologic association with
screaming
screening
seizure
seizure, complications following
seizure, crying as manifestation of
seizure, diagnosis of
seizure, etiology of
seizure, familial
seizure, intractable
seizure, neonatal
seizure, pregnancy
seizure, treatment of
seizure, treatment of, monotherapy
seizure, women
seizure, workup of
self-mutilation
shagreen patch
short stature
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
slit lamp examination
SMN1 gene
South America
Southern immunoblot test
speech disorder
speech disorder, childhood
sphingolipodoses
spina bifida
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal cord, vascular malformation of
spinal muscular atrophy
spinal muscular atrophy, classification
splenomegaly
spongy degeneration of brain
startle reaction
stem cell transplantation
strabismus
subarachnoid fluid collection, benign
subarachnoid hemorrhage
subdural hematoma
subdural hematoma, neonates and infants
subependymal nodules
suck, poor
sudden infant death syndrome
suicide
Tay-Sachs disease
telangiectases
temper tantrums
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
teratogenesis
teratogenic drugs
term infant
testicular atrophy
testicular enlargement
thrombocytopenia
thyroxine
tissue plasminogen activator, intravenous
titinopathy
tongue, enlarged
tongue, fasciculations of
tongue, protrusion of
tongue, weakness
toxoplasmosis, CNS
toxoplasmosis, congenital
transplacental virus infections
trauma
treatment of neurologic disorder
tremor
tremulousness
trichopoliodystrophy
trientine dihydrochloride
trinucleotide repeats
trisomes
trisomy 18
tuber, cortical
tuberin
tuberous sclerosis
tuberous sclerosis, screening for
twins
ultrasonography
ultrasonography, head
ultrasonography, head, fetus-neonate
umbilical-cord blood transplantation
undiagnosed
urea-cycle enzymopathies
uric acid, low
urine test for metabolic disorders
vertigo, episodic
very long chain fatty acids
viral infection
viral infection, CNS
visual loss
vital capacity
vitamin K
vitamin supplementation
walking, difficulty with
weakness
weakness, congenital
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
white freckles
white matter disease
wide based gait
Wood's light
workup
x-linked hydrocephalus
x-linked mental retardation
Zika virus infection
zinc
Showing articles 150 to 200 of 2244 << Previous Next >>

Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
Neurol 104: e213682, Hayakawa,I.,et al, 2025

AAV9-Mediated Gene Therapy for Infantile-Onset Pompes Disease
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The Spectrum of Fragile X Disorders
NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025

Brain Death in Pregnancy - Abortion, Advance-Directive, or End-of-Life Law?
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A 2-Year-Old Girl with Acute Encephalopathy After Febrile Systemic Illness
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
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Pneumocephalus Leading to Basilar Artery Compression After Epidural Anesthesia
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A 32-Year-Old Woman Presenting with Thunderclap Headache in the Third Trimester
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RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

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

Diagnosis and Management of Cerebral Venous Thrombosis:A Scientific Statement From the American Heart Association
Stroke 55:e77-e90, Saposnik,G.,et al, 2024

Cavernous Maliformations of the Central Nervous System
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Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Vascular Malformations of the Central Nervous System
www.UptoDate.Com, March, Singer,R.J.,et al, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
NEJM 391:1015-1027, Al-Samkari,H.,et al, 2024

A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
Neurol 103:e209796, Bouchart,J.,et al, 2024

Newborn Screening and Presymptomatic Treatment of Metachromatic Leukodystrophy
NEJM 391:1256-1258, Laugwitz,L.,et al, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

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

Multiple Contrast Enhancing Subdural Lesions
BMJ 387:e079362, Liu,J. & Sun,Z., 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

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

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

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

Cavernous Sinus Thrombosis
StatPearls PMID:28846357, Plewa,M.C.,et al, 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Primary Brain Tumours in Adults
Lancet 402:1564-1579, van den Bent,M.,et al, 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
Stroke 54:e512-e515, Silveira,L.,et al, 2023

A 24-Year-Old Pregnant Woman with Headache and Behavioral Change Progressing to Coma
Neurol 101:e2331-e2337, Barnardes,C.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

Subarachnoid Hemmorhage During Pregnancy and Puerperium:A Population-Based Study
Stroke 54:198-207, Korhonen,A., et al, 2023

Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
Lancet 401:e2, Kovalchuk,B. & Khoramnia,R., 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

Cashew Nut Sign:A Concave Parenchymal Hemorrhage Caused by Cerebral Venous Thrombosis
Stroke 54:e38-e39, Schlechter,M.,et al, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

Cauda Equina Syndrome in the Third Trimester
BMJ 395:e078711, Ugas,M.A. & Ashkan,K., 2023



Showing articles 150 to 200 of 2244 << Previous Next >>