2,792 results match your criteria: "Schneider Children`s Medical Center of Israel[Affiliation]"

Diabetes Technologies and the Human Factor.

Diabetes Technol Ther

March 2024

Faculty of Health and Social Sciences, Bournemouth University, Bournemouth, United Kingdom.

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Diabetes Technology and Therapy in the Pediatric Age Group.

Diabetes Technol Ther

March 2024

Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.

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Using Digital Health Technology to Prevent and Treat Diabetes.

Diabetes Technol Ther

March 2024

Jesse Z. and Sara Lea Shaffer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.

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Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.

Am J Hum Genet

March 2024

Center for Medical Genetics Ghent, Department of Biomolecular Medicine, Ghent University Hospital, 9000 Ghent, Belgium; Department of Biomolecular Medicine, Ghent University, 9000 Ghent, Belgium. Electronic address:

Article Synopsis
  • Neurodevelopmental disorders (NDDs) stem from brain development issues, and research identifies loss-of-function (LoF) variations in the ZFHX3 gene as a cause of syndromic intellectual disability (ID).
  • A study of 42 individuals shows that variants in ZFHX3 lead to diverse symptoms like intellectual disability, autism spectrum disorder, distinct facial features, and developmental delays.
  • ZFHX3 plays a vital role in brain development, influences gene expression related to the nervous system, and has specific DNA methylation patterns linked to its function.
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Article Synopsis
  • Rapid trio genome sequencing (rtGS) is being implemented in Israeli neonatal intensive care units (NICUs) to provide advanced care for critically ill newborns suspected of having genetic issues.
  • A study conducted from October 2021 to December 2022 involved 130 neonates, leading to a diagnostic rate of 50% for disease-causing genetic variants and 11% for variants of unknown significance (VUS).
  • Results showed a mean turnaround time for rapid reports of 7 days, with high engagement from medical staff regarding the clinical utility of the results (82% response rate to questionnaires).
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Celiac disease (CeD) is likely to be associated with growth impairment and poor weight gain. However, long-term growth patterns following diagnosis are poorly characterized. We evaluated long-term anthropometric changes in a large cohort of pediatric patients with CeD.

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Carbamoyl phosphate synthetase 1 (CPS1) and ornithine transcarbamylase (OTC) deficiencies are rare urea cycle disorders, which can lead to life-threatening hyperammonemia. Liver transplantation (LT) provides a cure and offers an alternative to medical treatment and life-long dietary restrictions with permanent impending risk of hyperammonemia. Nevertheless, in most patients, metabolic aberrations persist after LT, especially low plasma citrulline levels, with questionable clinical impact.

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Pathogenic variants in solute carrier family 34, member 3 (SLC34A3), the gene encoding the sodium-dependent phosphate cotransporter 2c (NPT2c), cause hereditary hypophosphatemic rickets with hypercalciuria (HHRH). Here, we report a pooled analysis of clinical and laboratory records of 304 individuals from 145 kindreds, including 20 previously unreported HHRH kindreds, in which two novel SLC34A3 pathogenic variants were identified. Compound heterozygous/homozygous carriers show above 90% penetrance for kidney and bone phenotypes.

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Long-term outcomes and electrophysiological measures of children with inner ear malformations and cochlear implants.

Int J Pediatr Otorhinolaryngol

March 2024

Institute for Audiology and Clinical Neurophysiology, Schneider Children's Medical Center, Israel; Department of Communication Sciences & Disorders, University of Haifa, Haifa, Israel.

Article Synopsis
  • The study aimed to compare the auditory and speech outcomes of children with cochlear implants (CIs) who have inner ear malformations (IEMs) versus those with normal ear anatomy.
  • Researchers conducted a retrospective analysis involving 41 children with IEMs and 41 age-matched controls with normal anatomy.
  • Results showed that children with normal anatomy had better auditory performance; specifically, those with isolated enlarged vestibular aqueduct (EVA) performed better than other IEM subgroups, while SIR scores were lower in IEMs without EVA compared to all other groups.
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The coronavirus disease 2019 (COVID-19) pandemic substantially impacted different age groups, with children and young people not exempted. Many have experienced enduring health consequences. Presently, there is no consensus on the health outcomes to assess in children and young people with post-COVID-19 condition.

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Background: Pediatric immune thrombocytopenia (ITP) may precede systemic autoimmune disorders. In adolescent patients with ITP, routine screening for systemic lupus erythematosus (SLE) may be performed by testing for antinuclear antibody (ANA) titer. Hydroxychloroquine (HCQ) is a safe and effective immunomodulatory drug in patients with SLE but rarely used in ITP.

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Patients with active ulcerative colitis (UC) display a misalignment of the circadian clock, which plays a vital role in various immune functions. Our aim was to characterize the expression of clock and inflammation genes, and their mutual regulatory genes in treatment-naïve pediatric patients with UC. Using the Inflammatory Bowel Disease Transcriptome and Metatranscriptome Meta-Analysis (IBD TaMMA) platform and R algorithms, we analyzed rectal biopsy transcriptomic data from two cohorts (206 patients with UC vs.

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Background: Data on breastfeeding rates and targeted interventions in women with pre-gestational diabetes mellitus are inconclusive. The aim of the study was to evaluate breastfeeding rates up to one year postpartum and whether targeted counseling towards the end of pregnancy can impact breastfeeding rates and duration. An additional goal was to evaluate whether counseling affected women's perceptions regarding breastfeeding.

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Background: Global education in psychiatry is heavily influenced by knowledge from Western, high-income countries, which obscures local voices and expertise.

Aim: To adapt a human simulation model to psychiatric education in a context that is specific to local languages and cultures.

Methods: We conducted an observational study consisting of six human simulation sessions with standardized patients from two host countries, speaking their native languages, and following an adaptation of the co-constructive patient simulation (CCPS) model.

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Article Synopsis
  • Common cutaneous non-genital viral warts are a frequent skin condition in kids, leading to discomfort and requiring multiple visits for treatment.
  • This study examined the effectiveness of oral Verrulyse Methionine (VM) as a standalone treatment for children and adolescents with persistent warts that did not respond to previous therapies.
  • Of the 25 patients treated with VM, 56% showed significant improvement within 4 months, and this method was painless with no reported side effects, making it a viable alternative to painful local treatments.
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Parent-child couples display shared neural fingerprints while listening to stories.

Sci Rep

February 2024

Educational Neuroimaging Group, Faculty of Biomedical Engineering, Faculty of Education in Science and Technology, Technion - Israel Institute of Technology, Haifa, Israel.

Neural fingerprinting is a method to identify individuals from a group of people. Here, we established a new connectome-based identification model and used diffusion maps to show that biological parent-child couples share functional connectivity patterns while listening to stories. These shared fingerprints enabled the identification of children and their biological parents from a group of parents and children.

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Tissue markers may predict treatment response to antitumor necrosis factor-α agents in children with Crohn's disease.

J Pediatr Gastroenterol Nutr

March 2024

Schneider Children's Medical Center of Israel, Institute of Gastroenterology, Nutrition and Liver Diseases, Petah Tikva, Israel.

Objectives: Patients with moderate-severe Crohn's disease (CD) who are treated with antitumor necrosis factor alpha (TNF-α) agents may be subjected to primary nonresponse or partial response. We aimed to identify tissue markers that may predict response to these agents.

Methods: Pediatric patients (6-18 years) with either ileal or ileo-colonic CD who were treated with anti-TNF-α were stratified into three different groups based on their overall response to therapy at the end of induction including clinical and laboratory parameters (group 1-full responders [FR], group 2-partial responders [PR], group 3-nonresponders [NR]).

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Joint ESPGHAN/NASPGHAN Guidelines on Childhood Eosinophilic Gastrointestinal Disorders Beyond Eosinophilic Esophagitis.

J Pediatr Gastroenterol Nutr

January 2024

Digestive Health Institute, Section of Pediatric Gastroenterology, Hepatology and Nutrition, Children's Hospital Colorado, Gastrointestinal Eosinophilic Disease Program, Mucosal Inflammation Program, University of Colorado School of Medicine, Aurora, CO.

Introduction: Eosinophilic gastrointestinal disorders beyond eosinophilic esophagitis (non-EoE EGIDs) are rare chronic inflammatory disorders of the gastrointestinal (GI) tract. Diagnosis is based on clinical symptoms and histologic findings of eosinophilic inflammation after exclusion of a secondary cause or systemic disease. Currently, no guidelines exist for the evaluation of non-EoE EGIDs.

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Hydrocephalus is rarely described in Joubert-Boltshauser syndrome (JBTS). The aim of this study was to investigate whether this association is a chance occurrence or potentially signifies a new phenotypic subtype. The databases of Wolfson Medical Center, Sourasky Medical Center, and EB's personal collection were reviewed.

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Background: Although extremely premature birth disrupts lung development, adolescent survivors of extreme prematurity show good clinical and physiologic outcomes. Cardiopulmonary limitations may not be clinically evident at rest. Data regarding exercise limitation in adolescents following preterm birth in the postsurfactant era are limited.

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Background: Early life respiratory syncytial virus (RSV) bronchiolitis is a significant risk factor for childhood asthma. In vitro and in vivo studies suggested that decreasing levels of airway matrix metalloproteinase (MMP)-9 during RSV bronchiolitis may be associated with clinical benefits.

Objective: To investigate whether azithromycin therapy during severe RSV bronchiolitis reduces upper airway MMP-9 levels, whether upper airway MMP-9 levels correlate with upper airway interleukin IL-8 levels, and whether MMP-9 level reduction is associated with reduced post-RSV recurrent wheeze (RW).

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Objective: Pigtail thoracostomy (PT) has become the mainstay technique for the drainage of pediatric pleuropneumonic effusions (PLPe). However, its efficacy and complication profile has been questioned when compared with video-assisted thoracoscopic surgery and larger bore traditional tube thoracostomy. The aim of this study was to assess the efficacy, safety, and complications associated with PT.

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