747 results match your criteria: "and The Perelman School of Medicine at the University of Pennsylvania[Affiliation]"
Pract Radiat Oncol
November 2024
Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Purpose: Increasing concern that brainstem toxicity incidence after proton radiation therapy might be higher than with photons led to a 2014 University of Florida (UF) landmark paper identifying its risk factors and proposing more conservative dose constraints. We evaluated how practice patterns changed among the Pediatric Proton/Photon Consortium Registry (PPCR).
Material And Methods: This prospective multicenter cohort study gathered data from patients under the age of 22 years enrolled on the PPCR, treated between 2002 and 2019 for primary posterior fossa brain tumors.
J Clin Oncol
October 2024
Department of Pediatrics and the Ben Towne Center for Childhood Cancer Research, Seattle Children's Hospital, University of Washington, Seattle, WA.
Am J Hum Genet
August 2024
Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Pathology and Laboratory Medicine, The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, PA 19104, USA.
Pathogenic variants in the JAG1 gene are a primary cause of the multi-system disorder Alagille syndrome. Although variant detection rates are high for this disease, there is uncertainty associated with the classification of missense variants that leads to reduced diagnostic yield. Consequently, up to 85% of reported JAG1 missense variants have uncertain or conflicting classifications.
View Article and Find Full Text PDFJ Perinatol
December 2024
Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Objectives: The primary objective of this study was to profile the childhood health, development, and health-related quality of life (HR QoL) for children with the most severe bronchopulmonary dysplasia (BPD), those discharged from a quaternary referral program.
Study Design: We collected cross-sectional data through telephone interviews with 282 families of children ages 18 months to 11 years who had been discharged from a BPD referral program.
Results: Respiratory morbidities were near universal, with 42% of children ever having required a tracheostomy and severity of these morbidities correlated with parent-reported health and QoL.
Pediatr Crit Care Med
June 2024
Division of General Pediatrics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA.
Kidney Med
June 2024
Kidney Health Research Collaborative, San Francisco VA Medical Center & University of California, San Francisco, San Francisco, CA.
Rationale & Objective: Tubulointerstitial damage is a feature of early chronic kidney disease (CKD), but current clinical tests capture it poorly. Urine biomarkers of tubulointerstitial health may identify risk of CKD.
Study Design: Prospective cohort (Atherosclerosis Risk in Communities [ARIC]) and case-cohort (Multi-Ethnic Study of Atherosclerosis [MESA] and Reasons for Geographic and Racial Differences in Stroke [REGARDS]).
N Engl J Med
May 2024
From the Perelman School of Medicine at the University of Pennsylvania, Philadelphia (M.C.); Massachusetts General Hospital, Boston (M.F.); and Yale School of Medicine, New Haven, CT (S.N., G.S.).
N Engl J Med
May 2024
From the Perelman School of Medicine at the University of Pennsylvania, Philadelphia (E.A., J.T.); Boston Medical Center (C.M.C.) and Massachusetts General Hospital (M.F., S.S.-V.) - both in Boston; and Yale School of Medicine, New Haven, CT (G.S.).
bioRxiv
April 2024
Center for Biomedical Image Computing and Analytics (CBICA), the Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104 USA.
Personalized functional networks (FNs) derived from functional magnetic resonance imaging (fMRI) data are useful for characterizing individual variations in the brain functional topography associated with the brain development, aging, and disorders. To facilitate applications of the personalized FNs with enhanced reliability and reproducibility, we develop an open-source toolbox that is user-friendly, extendable, and includes rigorous quality control (QC), featuring multiple user interfaces (graphics, command line, and a step-by-step guideline) and job-scheduling for high performance computing (HPC) clusters. Particularly, the toolbox, named personalized functional network modeling (pNet), takes fMRI inputs in either volumetric or surface type, ensuring compatibility with multiple fMRI data formats, and computes personalized FNs using two distinct modeling methods: one method optimizes the functional coherence of FNs, while the other enhances their independence.
View Article and Find Full Text PDFJ Am Acad Orthop Surg Glob Res Rev
May 2024
From the Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA (Mr. Huffman, Mr. Ayotte, and Ms. Jia); the Department of Orthopaedic Surgery, Yale-New Haven Hospital, New Haven, CT (Dr. Pirruccio); the Department of Orthopaedic Surgery, Boston University Medical Center, Boston, MA (Dr. Li); the Department of Orthopaedic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA (Dr. Kelly IV); and the Department of Orthopaedic Surgery, Mount Sinai, New York, NY (Dr. Parisien).
N Engl J Med
May 2024
From the Perelman School of Medicine at the University of Pennsylvania, Philadelphia (E.A., J.T.); Boston Medical Center (C.M.C.) and Massachusetts General Hospital (M.F., S.S.-V.) - both in Boston; and Yale School of Medicine, New Haven, CT (S.N., G.S.).
J Clin Endocrinol Metab
August 2024
The Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
After birth, healthy neonates undergo a period of altered glucose metabolism, known as "transitional hypoglycemia." During the first 0 to 4 hours of life, the mean plasma glucose concentration decreases to 57 mg/dL, then by 72 to 96 hours of life increases to 82 mg/dL, well within the normal adult range. Recent data suggest that transitional hypoglycemia is due to persistence of the fetal beta cell's lower threshold for insulin release, resulting in a transient hyperinsulinemic state.
View Article and Find Full Text PDFWe performed a qualitative review of 50 consent forms posted on Clinicaltrials.gov, examining the content of key information sections. We found that key information disclosures are typically focused on procedures, risks, potential benefits, and alternatives.
View Article and Find Full Text PDFCurr Probl Pediatr Adolesc Health Care
August 2024
The Children's Hospital of Philadelphia, Section Chief, Neuropsychology & Assessment, United States. Electronic address:
Epilepsy is one of the most common neurological problems affecting 470,000 children in the United States. While most youth will achieve seizure freedom using medication, up to a third will continue to have seizures and are therefore considered to have drug-resistant epilepsy (DRE). Children and adolescents with epilepsy are at higher risk of behavioral, cognitive, and emotional disorders.
View Article and Find Full Text PDFJ Neuroophthalmol
June 2024
Neuro-ophthalmology Service, Division of Ophthalmology, Children's Hospital of Philadelphia and Division of Neuro-Ophthalmology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania; and Departments of Neurology and Ophthalmology at the Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
Brain
September 2024
Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Biallelic SORD mutations cause one of the most frequent forms of recessive hereditary neuropathy, estimated to affect ∼10 000 patients in North America and Europe alone. Pathogenic SORD loss-of-function changes in the encoded enzyme sorbitol dehydrogenase result in abnormally high sorbitol levels in cells and serum. How sorbitol accumulation leads to peripheral neuropathy remains to be elucidated.
View Article and Find Full Text PDFSci Rep
March 2024
Departments of Neurology, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Neurovascular coupling is a vital mechanism employed by the cerebrovascular system, including the eye, to regulate blood flow in periods of neuronal activation. This study aims to investigate if laser speckle flowgraphy (LSFG) can detect coupling response elicited by flickering light stimuli and how variations in stimulus type and duration can affect the magnitude and evolution of blood flow in the optic nerve head (ONH) and peripapillary vessels. Healthy adults were exposed to two types of 10-Hz flicker stimuli: a photopic negative response-like stimulus (PhNR-S) or a visual evoked potential-like stimulus (VEP-S)-each presented in separate 10- and 60-s epochs.
View Article and Find Full Text PDFMany racial-ethnic minoritized individuals are repeatedly exposed to subtle actions reflecting racial slights, termed racial microaggressions (RMAs), which are associated with adjustment problems in early adult and adult populations. Early adolescence represents a unique developmental period when minoritized youth begin their racial-ethnic identity exploration and are subjected to stereotypes and prejudice, thereby making them vulnerable to RMAs. Based upon the Preferred Reporting Items for Systematic Reviews and Meta-Analyses checklist, a systematic literature search, screening and review of RMA literature focusing on high schoolers and younger youth was conducted and yielded 54 publications.
View Article and Find Full Text PDFNeoreviews
March 2024
Department of Pediatrics, Norton Children's Research Institute Affiliated with the University of Louisville School of Medicine, Louisville, KY.
Clinicians practicing in a modern NICU are noticing an increase in the proportion of patients who undergo genetic testing as well as changes in the types of genetic testing patients receive. These trends are not surprising given the increasing recognition of the genetic causes of neonatal illness and recent advances in genetic technology. Yet, the expansion of genetic testing in the NICU also raises a number of ethical questions.
View Article and Find Full Text PDFJAMA Netw Open
February 2024
Joslin Diabetes Center, Harvard Medical School, Boston, Massachusetts.
JAMA Netw Open
February 2024
Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Leukemia
April 2024
Department of Biostatistics, Colleges of Medicine, Public Health and Health Professions, University of Florida, Gainesville, FL, USA.
Pediatr Blood Cancer
April 2024
Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada.
Background: The primary objective was to measure the proportion of episodes where care delivery was inconsistent with selected recommendations of a clinical practice guideline (CPG) on fever and neutropenia (FN) management. The influence of site size on CPG-inconsistent care delivery, and association between patient outcomes and CPG-inconsistent care were described.
Methods: This retrospective, multicenter study included patients less than 21 years old with cancer who were at high risk of poor FN outcomes and were previously enrolled to a Children's Oncology Group (COG) study at participating National Cancer Institute Community Oncology Research Program (NCORP) institutions from January 2014 through December 2015.