Search results for "lcsh:RJ1-570"

showing 10 items of 180 documents

Metabolic Consequences after Urinary Diversion

2014

Metabolic disturbances are well-known, but sometimes neglected immediate consequences or late sequelae following urinary diversion (UD) using bowel segments. Whereas subclinical disturbances appear to be quite common, clinically relevant metabolic complications, however, are rare. Exclusion of bowel segments for UD results in loss of absorptive surface for its physiological function. Previous studies demonstrated that at least some of the absorbtive and secreting properties of the bowel are preserved when exposed to urine.For each bowel segment typical consequences and complications have been reported. The use of ileal and/or colonic segments may result in hyperchloremic metabolic acidosis …

Diarrheamedicine.medical_specialtyMalabsorptionBowel habitmedicine.medical_treatmentUrineReview ArticleUrinary DiversionGastroenterologyPediatricsMetabolic complicationsInternal medicineMedicineVitamin B12Subclinical infectionAcidosisbusiness.industryUrinary diversionlcsh:RJ1-570lcsh:Pediatricsvitamin B12medicine.diseaseSurgeryDiarrheaVitamin B 12Pediatrics Perinatology and Child Healthmedicine.symptombusinessAcidosisFrontiers in Pediatrics
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The Role of Preschool Hours in Achieving Physical Activity Recommendations for Preschoolers

2021

Research on physical activity (PA) in different educational settings could elucidate which interventions promote a healthy school lifestyle in early childhood education (ECE). The aims of this study were: (a) to analyse the PA levels of preschoolers during school hours, as well as the rate of compliance with specific recommendations on total PA (TPA) and moderate-vigorous PA (MVPA)

Early childhood educationGerontologyeducationstructured movement sessionslcsh:RJ1-570Physical activityPsychological interventionHigh densityphysical activitylcsh:Pediatrics030229 sport sciencesArticlepreschoolAge and gender03 medical and health sciences0302 clinical medicineschool hoursPediatrics Perinatology and Child Healthearly childhood educationSchool environment030212 general & internal medicineeducational settingsPsychologyhuman activitiesChildren
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Gambling disorder in adolescents: what do we know about this social problem and its consequences?

2018

Abstract Gambling disorder (GD) is a psychiatric condition and it is characterized by a maladaptive pattern of gambling behavior that persists despite negative consequences in major areas of life functioning. In Italy, CNR (National Research Council) underlined how over 17 million, 42.8% of the population aged 15–64 have a gambling behavior. Among them, there are over one million students, aged 15–19, equal to 44.2% of Italian students; the number of minors in Italy with GD in 2017 was 580,000, equal to 33.6%. Various psychosocial treatment models have been adapted for GD; on the other hand no drug has received regulatory approval in any jurisdiction as a specific psychopharmacological trea…

Family therapymedicine.medical_specialtyAdolescentSocial ProblemsPopulationPsychological interventionGambling disorderAdolescentsSocial issuesYoung Adult03 medical and health sciencesRisk-Taking0302 clinical medicineIntervention (counseling)medicineHumans030212 general & internal medicineeducationPsychiatrygambling disordersConsequenceseducation.field_of_studyGovernmentbusiness.industryPublic healthlcsh:RJ1-570adolescenteslcsh:PediatricsSettore MED/38 - PEDIATRIA GENERALE E SPECIALISTICAItalyAdolescent BehaviorGamblingCommentaryConsequencebusinessPsychosocial030217 neurology & neurosurgeryItalian Journal of Pediatrics
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Effectiveness of cyclosporine and mycophenolate mofetil in a child with refractory evans syndrome

2011

Evans Syndrome is a rare autoimmune disease consisting of hemolytic anemia, thrombocytopenia and/or neutropenia. It may be associated with other autoimmune or lymphoproliferative diseases. Its course can be extremely serious and, rarely, even life-threatening

Hemolytic anemiaVincristinePediatricsmedicine.medical_specialtyEvans syndromeoutcome.CyclophosphamideEvans’ syndrome Cyclosporine Mycophenolate mofetil Treatment Outcomelcsh:MedicineCase ReportNeutropeniaPediatricshemic and lymphatic diseasesmedicineevans syndromeOutcomeAutoimmune diseasebusiness.industryMycophenolate mofetillcsh:Rlcsh:RJ1-570lcsh:PediatricsEvans’ syndromemedicine.diseaseDiscontinuationTreatmentImmunologyCyclosporineRituximabbusinessmedicine.drugPediatric Reports
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The predictive role of pelvic magnetic resonance in the follow up of spontaneous or induced puberty in turner syndrome

2018

Abstract Puberty is a critical age for patients with Turner syndrome (TS): infertility is reported to be linked to karyotype and spontaneous puberty and menarche occur in approximately 30% of patients, especially in mosaicism. However, it is not always predictable considering hormonal pattern and pelvic transabdominal ultrasound scan (US). The aim of the study is to compare the accuracy of Magnetic Resonance Imaging (MRI) and US to evaluate uterine and gonads volume, to visualize the presence of follicles and to predict spontaneous puberty and menarche in girls with TS. In a retrospective study, we evaluated 19 TS patients (age: 9–16 years), who underwent transabdominal pelvic US and pelvic…

Infertilitymedicine.medical_specialtyAdolescentPelviPrognosiTurner syndromeUterus030209 endocrinology & metabolismSensitivity and SpecificitySeverity of Illness Index03 medical and health sciencesYoung Adult0302 clinical medicineMagnetic resonance imagingRetrospective StudieTurner syndromemedicineStage (cooking)ChildLetter to the EditorUltrasonographyGynecologyMenarche030219 obstetrics & reproductive medicinemedicine.diagnostic_testbusiness.industryHypogonadismOvaryPubertylcsh:RJ1-570Magnetic resonance imagingRetrospective cohort studyKaryotypeUltrasonography Dopplerlcsh:PediatricsOrgan Sizemedicine.diseasemedicine.anatomical_structureUteruInfertilityPediatrics Perinatology and Child HealthMenarcheFemaleCohort StudiebusinessHumanItalian Journal of Pediatrics
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Internal Hernia Masquerading As Necrotizing Enterocolitis

2017

In extremely preterm infants, acute abdominal emergencies are fortunately less common with improving care. Spontaneous intestinal perforation and necrotizing enterocolitis are conditions where emergency surgery is most often needed. Conservative medical management and placement of temporary drain are often used in the initial management. Internal hernia (IH) is an uncommon cause of bowel obstruction in neonates, is difficult to diagnose and unfortunately are found only at autopsy. The presentation in preterm infants, distinction between these conditions, and the need for early diagnosis of IH are discussed.

Internal herniamedicine.medical_specialtyExploratory laparotomymedicine.medical_treatmentCase ReportAutopsyPediatrics030218 nuclear medicine & medical imagingacute abdomen03 medical and health sciences0302 clinical medicine030225 pediatricsSpontaneous Intestinal Perforationmedicineinternal herniasnecrotizing enterocolitisbusiness.industryGeneral surgeryexploratory laparotomylcsh:RJ1-570lcsh:Pediatricsmedicine.diseaseextreme preterm infantSurgeryBowel obstructionAcute abdomenPediatrics Perinatology and Child HealthNecrotizing enterocolitisPresentation (obstetrics)medicine.symptombusinessFrontiers in Pediatrics
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Early intestinal perforation secondary to congenital mesenteric defects

2016

Abstract Gastrointestinal perforation (GIP) in preterm neonates may be idiopathic, due to necrotizing enterocolitis (NEC), or mechanical obstruction. The predominant cause of GIP in the neonatal period is NEC. Differential diagnosis with congenital malformations, including mesenteric defects leading to internal hernias, is mandatory if the onset is early. We describe two newborns with trans-mesenteric herniation resulting in GIP, and we discuss the presence of possible additional risk factors such as prematurity and predisposing vascular disruption in connective tissue disorders (Ehlers-Danlos syndrome), twinning, and use of assisted reproductive technologies. These cases prompted us to rev…

Internal herniamedicine.medical_specialtyendocrine systemPerforation (oil well)lcsh:SurgeryConnective tissueReproductive technology03 medical and health sciencesInternal hernia0302 clinical medicineGastrointestinal perforation030225 pediatricsMedicinebusiness.industryDorsal mesentery; Ehlers-Danlos syndrome; Internal hernia; Twin; Pediatrics Perinatology and Child Health; Surgerylcsh:RJ1-570Twinlcsh:PediatricsDorsal mesenterylcsh:RD1-811medicine.diseasedigestive system diseasesSurgerymedicine.anatomical_structureEhlers–Danlos syndrome030220 oncology & carcinogenesisNecrotizing enterocolitisPediatrics Perinatology and Child HealthSurgeryDifferential diagnosisbusinessEhlers-Danlos syndromehormones hormone substitutes and hormone antagonists
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Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review

2019

Abstract Background Progressive lung involvement in Filamin A (FLNA)-related cerebral periventricular nodular heterotopia (PVNH) has been reported in a limited number of cases. Case presentation We report a new pathogenic FLNA gene variant (c.7391_7403del; p.Val2464Alafs*5) in a male infant who developed progressive lung disease with emphysematous lesions and interstitial involvement. Following lobar resection, chronic respiratory failure ensued necessitating continuous mechanical ventilation and tracheostomy. Cerebral periventricular nodular heterotopia was also present. Conclusions We report a novel variant of the FLNA gene, associated with a severe lung disorder and PNVH. The lung disord…

Lung DiseasesMalePathologymedicine.medical_specialtyFilaminsmedicine.medical_treatmentChildren; Congenital enphysema; Filamin a; Lung disease; Periventricular nodular heterotopiaCase ReportFilaminKeywords: Filamin a Congenital enphysema Lung disease Children Periventricular nodular heterotopiaFilamin aLung Disorder03 medical and health sciences0302 clinical medicineNeuroimagingLoss of Function Mutation030225 pediatricsmedicineHumansFLNA030212 general & internal medicineLungChildrenCongenital enphysemaGenetic testingMechanical ventilationLungmedicine.diagnostic_testbusiness.industrylcsh:RJ1-570BrainInfantlcsh:Pediatricsrespiratory systemRespiration ArtificialPeriventricular nodular heterotopiamedicine.anatomical_structurePulmonary EmphysemaRespiratory failureLung diseasePediatrics Perinatology and Child HealthRadiography ThoracicRespiratory InsufficiencyTomography X-Ray ComputedbusinessBMC Pediatrics
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Inhaled Surfactant in the treatment of accidental Talc Powder inhalation: a new case report

2011

Abstract The use of talcum powder is incorrectly part of the traditional care of infants. Its acute aspiration is a very dangerous condition in childhood. Although the use of baby powder has been discouraged from many authors and the reports of its accidental inhalation have been ever more rare, sometimes new cases with several fatalities have been reported. We report on a patient in which accidental inhalation of baby powder induced severe respiratory difficulties. We also point out the benefits of surfactant administration. Surfactant contributed to the rapid improvement of the medical and radiological condition, preventing severe early and late complications and avoiding invasive approac…

Lung Diseasesmedicine.medical_specialtymedicine.medical_treatmentTreatment outcomeCase Reportmacromolecular substancesTalcSettore MED/38 - Pediatria Generale E SpecialisticaPulmonary surfactantAdministration InhalationSurfactantmedicineHumansTalcum powderRespiratory physiotherapyIntensive care medicinePhospholipidsBiological ProductsInhalationRespiratory distressbusiness.industrylcsh:RJ1-570InfantRespiratory Physiotherapylcsh:PediatricsPulmonary SurfactantsBronchopulmonary LavageAccidental InhalationAnti-Bacterial AgentsBronchodilator AgentsRadiographyTreatment OutcomeCoughBaby powderTalcRespiratory DistressAccidentalDrug Therapy CombinationFemaleInhaled surfactant talc powder inhalationPowdersbusinessmedicine.drugItalian Journal of Pediatrics
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A Multicentre Pilot Study of a Two-Tier Newborn Sickle Cell Disease Screening Procedure with a First Tier Based on a Fully Automated MALDI-TOF MS Pla…

2019

The reference methods used for sickle cell disease (SCD) screening usually include two analytical steps: a first tier for differentiating haemoglobin S (HbS) heterozygotes, HbS homozygotes and β-thalassemia from other samples, and a confirmatory second tier. Here, we evaluated a first-tier approach based on a fully automated matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) platform with automated sample processing, a laboratory information management system and NeoSickle® software for automatic data interpretation. A total of 6701 samples (with high proportions of phenotypes homozygous (FS) or heterozygous (FAS) for the inherited genes for sickle h…

MALDI-TOFPediatricsmedicine.medical_specialtythalassemia[SDV]Life Sciences [q-bio]Sample (statistics)01 natural sciencesArticle03 medical and health sciencesImmunology and Microbiology (miscellaneous)preventionmedicineDisease Screening Procedure030304 developmental biologymass spectrometry0303 health sciencesNewborn screeningbusiness.industryMALDI-TOF; sickle cell disease; newborn screening; mass spectrometry; thalassemia; preventionnewborn screening010401 analytical chemistrylcsh:RJ1-570Obstetrics and GynecologyData interpretationlcsh:Pediatrics0104 chemical sciencesMatrix-assisted laser desorption/ionizationFully automatedSickle haemoglobinPediatrics Perinatology and Child Healthsickle cell diseaseSample collectionbusinessInternational Journal of Neonatal Screening
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