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Differential
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aciduria
acquired immunodeficiency syndrome
acrocyanosis
acute ataxia of childhood
acute cerebellar ataxia
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
advances in neurology
affect, inappropriate
Africa
aggression
agitation
Aicardi-Goutieres syndrome
akinetic mute
alcohol
alcohol intolerance
alcohol, neurologic complications with
alcoholism
alopecia
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
alveolar hypoventilation
amimia
aminoacidurias
anemia
anemia, hemolytic
Angelman syndrome
angiitis
angiitis, granulomatous of CNS
ankle, swelling of
anomic aphasia
anorexia
antibiotics, neurologic complications with
anxiety
aphasia
aphasia, children
aphasia, classification of
aphasia, recovery from
aphonia
apraxia, speech
areflexia
arylsulfatase A
ascending paralysis
ascites
aspiration
asterixis
astrocytoma
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ATP1A3 gene
attention deficit disorder with hyperactivity
attention span
atypical
audiologic test to localize site of pathology
audiology
auditory dominance
auditory processing, impaired
autism
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
behavior, combative
behavioral disorder
Benedict's solution test
benign essential tremor
bifid uvula
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
blepharospasm
blindness
blood brain barrier
body image
bone marrow transplantation
botulinum toxin
brachycephaly
bradykinesia
brain atrophy
brain biopsy
brain biopsy, stereotaxic
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
Brown-Vialetto-Van Laere syndrome
bruxism
burning feet
burning feet, differential diagnosis of
CAG repeats
calcification, intracranial
calf hypertrophy
carcinoma
cardiomyopathy
carpo-pedal spasm
cassava
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, dense artery sign
catalepsy
cataplexy
catatonia
celiac disease, adult
Central America
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar lesion
cerebellar mutism
cerebellar vermis
cerebellitis
cerebellum, disease of
cerebellum, neoplasms of
cerebral cortex
cerebral cortical atrophy
cerebral dominance
cerebral embolism
cerebral embolism, mechanical extraction
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, young adult
Chagas'disease
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
chilbran skin lesions
children
choking
chorea
chorea, Sydenham's
choreoathetosis
chromosomal abnormality
chromosome 15
chromosome 7
cirrhosis
cirrhosis, causes of childhood
cleft palate
Clinical Pathologic Conference(C.P.C.)
clonus
clot retrieval
cochlear implant
cognition
cognitive delay
coma
comorbidities
complications
confusion
congenital bilateral perisylvian syndrome
congenital myasthenic syndromes
conjunctival biopsy
consanguinity
contractures, joint
conversion reaction
coronavirus
corpus callosum, infarction of
corpus callosum, lesion of
cortical blindness
cough
COVID-19
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
crying
crying, pathologic
cultured skin fibroblasts
cyanide poison
cytomegalic inclusion disease
cytomegalovirus infection
deafness
deafness, congenital
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, childhood
dementia, presenile
demyelinating disease
dense basilar artery sign
dense middle cerebral artery sign
dentate nuclei
dentate nuclei, lesion of
depression
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
dialysis
dialysis dementia
diarrhea
dichotic hearing
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
diplopia
disconnection syndrome
disease modifying agents
doll's head maneuver
dopa responsive dystonia
drooling
drought
dysarthria
dysdiadochokinesia
dysequilibrium syndrome
dyskinesia
dyskinesia, buccal lingual facial
dyslexia
dysmorphic
dysphagia
dysphonia
dysplasia of C.N.S.
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, children
dystonia, laryngeal
dystonia, painful
dystonia, treatment of
dystrophin
DYT1 mutation
echolalia
EDTA(ehtylenediamine tetraacetic acid)
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, sleep
electromyogram
electron microscopy
ELISA
embolism, paradoxical
embolism, vertebral-basilar artery
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, viral
encephalopathy
encephalopathy, acute
encephalopathy, metabolic
encephalopathy, parainfectious
encephalopathy, progressive
endovascular therapy
enuresis
enzyme, defect
epidemiology of neurology
epilepsia partialis continua
epileptic encephalopathy
epsilon sarcoglycan gene
equinovarus
exome sequencing
eye movement, disorders of
eyedness
face, inexpressive
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
FARS2 deficiency
fatigue
feeding disorder
ferric chloride test
fetal alcohol syndrome
fetus
fever
fine motor function, impaired
finger nose finger test
fingerprint bodies
fish
fluctuate
fluorescene in situ hybridization
folic acid
footedness
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frontal lobe, pathologic signs of
fucosidosis
fungal infection, CNS
gait disorder
gait, apraxic
galactorrhea
gastroenteritis
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycosuria
Gowers maneuver
grasp reflex
gray hair
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Hallervorden Spatz disease
hallucination
hallucination, visual
hand deformity
handedness
hands, fisted
handwriting
head circumference
head injury
head injury, pediatric
head lag
headache
headache, vascular
hearing loss
hearing problems in children
heavy metal intoxication
heel-knee-shin test
hemiballismus
hemichorea
hemiparesis
hemiparesis, transient
hemiplegia
hemisensory loss
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
herpes virus
hippocampus
hoarseness
human immunodeficiency virus type 1
hydrocephalus
hydroxyglutaric aciduria
hyperactivity
hyperintense vessel sign
hyperkalemia
hyperosmolality
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypokinetic left ventricle
hyponatremia
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
illusions
imbalance
immunodeficiency
immunosuppression
immunosuppressive agents
inattention
inborn errors of metabolism
inclusion bodies
incoordination
industrial neurologic disorders
infection
infection, recurrent
infertility
insomnia
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
interferon alpha
intestinal biopsy
intracerebral hemorrhage
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, young adult
intracranial pressure, increased
intrauterine
iron, brain
irritability
jaundice
joint hypermobility
karyotyping
Kayser-Fleischer ring
klippel feil syndrome
konzo
lactic acidemia
Landau-Kleffner syndrome
language
language delay
language development, neurologic basis of
language disorders in children
laughing, pathologic
L-dopa
learning disability
learning disability, in children
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
lethargy
leukemia
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
lipid storage disorder of CNS
liver disease
liver function enzymes
locked-in syndrome
Lyme disease
Lyme disease, children
lymphoma involving CNS
lysosomal storage disease
macrocephaly
macrognathia
magnetic source image
magnetoencephalography
malabsorption syndrome
manganese intoxication
maple syrup urine disease
marche a petits pas
masked facies
medulla oblongata, neoplasm of
medulloblastoma
megalencephaly
megalencephaly, idiopathic
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, CSF cell count-normal
meningitis, recurrent
meningoencephalitis
mental retardation
mental status, abnormal
MERCI trial
MERS
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methotrexate
microcephaly
micrographia
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
midline defect in children
miglustat
migraine
mimics
mirror writing
misdiagnosis
mitochondrial disease
molecular genetics
monoclonal antibodies
monoparesis
mood change
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abdomen
MRI, abnormal
MRI, cardiac
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR, hyperintense vessels
MRI, functional
MRI, negative
MRI, paramagnetic effect
MRI, pelvis
MRI, serial
MRI, T1 weighted high signal foci
MRS
muscle cramp
muscle stiffness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, familial incidence of
myelinolysis, extrapontine
myelodysplasia
myelopathy
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoglobinuria
nasal speech
negative
neoplasm, posterior fossa
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve biopsy
nerve conduction studies
neurofibromatosis 1
neurologic complications
neurologic complications of, burns
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic testing
neuromuscular junction
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neuropathy, painful
neuropathy, sensory
neurotoxic
neurotoxicity, acute
neurotoxin
Niemann-Pick disease
NMDA antagonists
non-dominant hemisphere
nonverbal
nystagmus
nystagmus, rotary
nystagmus, spontaneous
opened mouth
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
opisthotonus
optic atrophy
optic neuritis
osmotic demyelination syndrome
ovarian insufficiency
palatal myoclonus
palatopharyngeal incompetence
palilalia
pancytopenia
PANK2 mutation
papilledema
paralysis, acute
paralysis, acute areflexic
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
paresthesias
parietal lobe, syndromes of
Parkinson disease
Parkinson disease, freezing phenomena in
Parkinsonism syndrome
paroxysmal neurologic deficits
patent foramen ovale
penicillamine
penicillin
Penumbra System
peroxisomal disease
personality change
phenylketonuria
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
pneumonia
poison, mercury
poliosis
polyneuropathy
polyneuropathy, uremic
pons, infarction of
pons, lesion of
positional head-hanging test
postural abnormality
precipitating factors
pregnancy, neurologic complications in
prenatal
prevention of neurologic disorders
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
prosopagnosia
protozoan infection
pruritus
pseudobulbar palsy
pseudocoma
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
psychosomatic disease
ptosis
ptosis, bilateral
pulmonary infection
pure word deafness
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
reading disorder, acquired
recurrent
release phenomena
remote effect of cancer on the nervous system
renal transplantation
renal tubular acidosis
respirations in CNS disease
respirator
restless leg syndrome
reticulum cell sarcoma
retina, abnormal
retinal detachment
retinitis pigmentosa
Rett's syndrome
reversible neurologic disorder
reversible splenial lesion syndrome
review article
rhabdomyolysis
rheumatic brain disease
rheumatic fever
rheumatic heart disease
riboflavin transporter deficiency
rigidity
risk factors
rituximab
rocking
rooting reflex
rotavirus
rubella encephalitis, progressive
saccadic eye movements, abnormal
salivation, excessive
Saudi Arabia
schizophrenia
scoliosis
sea-blue histiocytes
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, focus
seizure, laughing as manifestation
seizure, psychosocial aspects of
seizure, recurrent
seizure, surgical treatment of
seizure, treatment of
seizure, workup of
sexual behavior, disorder of
sign language
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
slurred speech
smiling
snout reflex
South America
spastic diplegia
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech lateralization
speech therapy
speech, delayed development of
speech, loss of
speech, pressured
speech, slowed
spina bifida
spinocerebellar ataxia
spinocerebellar ataxia type 7
splenium of corpus callosum
splenomegaly
spongy degeneration of brain
stammering
startle reaction
stereotaxic surgery
stereotyped behavior
stimulation, deep brain
stimulation, deep brain, bilateral
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
stuttering
stuttering following CVA
subdural hematoma
substantia nigra
suck, poor
symmetric brain lesions
systemic illness
tandem gait, ataxic
tantrum
tauopathy
teeth, wide-spaced
telangiectases
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
term infant
testicular enlargement
tetany
thrombectomy
thrombus, mural
tick bite
tick paralysis
tinnitus
titubation
toe walking
tongue, impaired movements of
tongue, protrusion of
tonic foot response
tonic spasms
torticollis
toxoplasmosis, acquired
toxoplasmosis, CNS
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
tripping
Trousseau's sign
trypanosoma cruzi
tuberculosis
tuberculosis, miliary
tyrosine hydroxylase deficiency
upgaze, paralysis of
uremia
uremic encephalopathy
uremic twitching
uric acid, low
urine test for metabolic disorders
urine, dark
uveitis
vasculopathy
vertigo
very long chain fatty acids
vestibulopathy
vibratory sensation, abnormal
violent behavior
viral infection
viral infection, CNS
vision, blurred
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual impairment
visual loss
visual loss, progressive
visual loss, slow
vitamin supplementation
vitiligo
Vogt-Koyanagi-Harada syndrome
voice, abnormality of
Wada test
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weight loss
welder
Wernicke's aphasia
Wernicke's encephalopathy
wheelchair
white hair
white matter disease
wide based gait
word-finding difficulty
workup
wrist drop
writing
x-linked intellectual deficit
x-linked mental retardation
Showing articles 350 to 400 of 18064 << Previous Next >>

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

Surgery for Drug-Resistant Epilepsy in Children
NEJM 377:1639-1647, Dwivedi, R.,et al, 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
Front Neurol doi.10.3398/jneur.2017.00108, Piroth,T.,et al, 2017

Trial of Amitriptyline, Topiramate, and Placebo for Pediatric Migraine
NEJM 376:115-124, Powers, S.W.,et al, 2016

Clinicopathologic Conference, Aqueductal Stenosis with Hydrocephalus
NEJM 375:2583-2593, Case 40-2016, 2016

Carotid-Cavernous Fistula
Stroke 47:e207-e209, Gonzalez Castro, L.N.,et al, 2016

Complete Lingual Palsy from Bilateral Dejerine Syndrome (Bilateral Medial Medullary Stroke)
Neurol 87:550, Tsetsou, S.,et al, 2016

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

Congenital Zika Virus Syndrome in Brazil: A Case Series of the first 1501 livebirths with complete investigation
Lancet 388:891-897, Franca, G.V.A.,et al, 2016

Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
Ann Neurol 80:326-338, Messacar, K.,et al, 2016

Clinical Manifestations of Myasthenia Gravis
UptoDate Aug 2016, Bird, S.J., 2016

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

Hydrocephalus in Children
Lancet 387:788-799, Kahle, K.T.,et al, 2016

Rapid Multifocal Neurologic Decline in an Immunocompromised Patient
JAMA Neurol 73:226-231, Kromm, J.A.,et al, 2016

Cocaine Use and Risk of Ischemic Stroke in Young Adults
Stroke 47:918-922, Cheng, Y.C.,et al, 2016

Clinicopathologic Conference, Cerebral Infarction from Internal Carotid Occlusion Related to Sickle Cell Arteriopathy
NEJM 374:1265-1275, Case 10-2016, 2016

Metronidazole-Associated Encephalopathy
NEJM 374:1465, Baden, L.R., 2016

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016

Successful Corticosteroid Treatment of Refractory Spontaneous Vasoconstriction of Extracranial Internal Carotid and Corornary Arteries
Neurologist 21:55-57, Takeuchi, M.,et al, 2016

Acute Disseminated Encephalomyelitis in 228 Patients
Neurol 86:2085-2096, Koelman, D.L.H.,et al, 2016

Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
JIEMS 4:1-5, Politeri,J.M.,et al, 2016

Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
Ann Clin Trans Neurol 3:655-663, Venkatraman,A. & Opal,P., 2016

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

A 64-year-old Woman with Subacute Encephalopathy
Neurol 85:e64-e65, Bhai, S.,et al, 2015

Cavernous Sinus Thrombosis in Children
Stroke 46:2657-2660, Press, C.A.,et al, 2015

Recurrent Stroke in Childhood Cancer Survivors
Neurol 85:1056-1064, Fullerton, H.J.,et al, 2015

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Immediate Hemorrhagic Transformation After Intravenous Tissue-Type Plasminogen Activator Injection in 2 Cocaine Users
Stroke 46:e167-e169, Baud, M.O.,et al, 2015

Cryptic Loss of Consciousness in a 36-Year-Old Woman
Stroke 46:e164-e166, Martinez Majander, N.,et al, 2015

Clinicopathologic Conference, Primary Central Nervous System Diffuse Large B-cell Lymphoma
NEJM 373:367-377, Case 23-2015, 2015

Parry Romberg Syndrome: 7 Cases and Literature Review
AJNR 36:1355-1361, Wong, M.,et al, 2015

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

Radiation Necrosis in Pediatric Patients with Brain Tumors Treated with Proton Radiotherapy
AJNR 36:1572-1578, Kralik, S.F.,et al, 2015

Clinicopathologic Conference, CAT Scratch Disease (Encephalopathy Associated with Bartonella Henselae)
NEJM 372:2050-2058, Case 16-2015, 2015

Spinal Cord Ischemia: Practical Imaging Tips, Pearls, and Pitfalls
AJNR 36:825-830, Vargas, M.I.,et al, 2015

Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015

International Consensus Diagnostic Criteria for Neuromyelitis Optica Spectrum Disorders
Neurol 85:177-189, Wingerchuk, D.M.,et al, 2015

A 45 Year Old Patient with Headache, Fever, and Hyponatraemia
BMJ 350:h962, Fountas, A.,et al, 2015

Brain Swelling and Death in Children with Cerebral Malaria
NEJM 372:1126-1137, Seydel, K.B.,et al, 2015

MRI Characteristics of Globus Pallidus Infarcts in Isolated Methylmalonic Acidemia
AJNR 36:194-201, Baker, E.H.,et al, 2015

Community Based Case-Control Study of Childhood Stroke Risk Associated with Congenital Heart Disease
Stroke 46:336-340, Fox, C.K.,et al, 2015



Showing articles 350 to 400 of 18064 << Previous Next >>