about
Acute neurological involvement in diarrhea-associated hemolytic uremic syndromeFamilial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variabilityContribution of single-photon emission computed tomography in the diagnosis and follow-up of CNS toxicity of a cytarabine-containing regimen in pediatric leukemiaQIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver diseaseSevere dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1.[Genetic and clinical aspects of lissencephaly]Diffusion magnetic resonance imaging of the fetal brain in intrauterine growth restriction.GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex.Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher diseaseEffect of transfusion therapy on cerebral vasculopathy in children with sickle-cell anemia.Mitochondrial acetoacetyl-CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosis.High-resolution heavily T2-weighted magnetic resonance imaging for evaluation of the pituitary stalk in children with ectopic neurohypophysis.Clinical and haematological risk factors for cerebral macrovasculopathy in a sickle cell disease newborn cohort: a prospective study.Headache with focal neurologic signs in children at the emergency department.Pediatric salivary gland carcinomas: Diagnostic and therapeutic management.Kingella kingae Sequence Type 25 Causing Endocarditis with Multiple and Severe Cerebral Complications.Subperiosteal orbital abscess: volumetric criteria for surgical drainage.Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory.Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification.New spastic paraplegia phenotype associated to mutation of NFU1.Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutations.Early-onset hyperargininaemia: a severe disorder?Activating Fgfr3 Y367C mutation causes hearing loss and inner ear defect in a mouse model of chondrodysplasia.Pediatric ischemic stroke: acute management and areas of research.SOX10 mutations mimic isolated hearing loss.Effects of systemic administration of methylprednisolone on residual hearing in an animal model of cochlear implantation.Fetal MRI: normal gestational landmarks for cerebral biometry, gyration and myelination.Central Diabetes Insipidus in Infancy With or Without Hypothalamic Adipsic Hypernatremia Syndrome: Early Identification and Outcome.Further delineation of the 17p13.3 microdeletion involving YWHAE but distal to PAFAH1B1: four additional patients.Design of the DREPAGREFFE trial: A prospective controlled multicenter study evaluating the benefit of genoidentical hematopoietic stem cell transplantation over chronic transfusion in sickle cell anemia children detected to be at risk of stroke by tIs fetal cerebral MRI worthwhile in antenatally diagnosed isolated cleft lip with or without palate?Pericallosal lipoma and middle cerebral artery aneurysm: a coincidence?Prenatal isolated mild ventriculomegaly: outcome in 167 cases.Increased cerebral blood flow velocity in children with sickle cell disease: adenotonsillectomy or transfusion regimens?A locus for sacral/anorectal malformations maps to 6q25.3 in a 0.3 Mb interval region.Protective effect of systemic administration of erythropoietin on auditory brain stem response and compound action potential thresholds in an animal model of cochlear implantation.The petrosquamosal sinus: CT and MR findings of a rare emissary vein.Fetal cerebral cortex: normal gestational landmarks identified using prenatal MR imaging.[Audiophonological evaluation of 16 children fitted with cochlear implants for sensorineural hearing loss induced by bacterial meningitis].[Computed tomography of the normal and pathologic temporal bone].
P50
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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type
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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El Maleh
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Elmaleh
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
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Monique Elmaleh-bergès
@sl
P106
P21
P31
P496
0000-0001-8190-8202