11 results match your criteria: "Health Sciences Center Children's Hospital of New Orleans[Affiliation]"

Male-specific late effects after hematopoietic cell transplantation (HCT) include genital chronic graft-versus-host disease (GvHD), hypogonadism, sexual dysfunction, infertility, and subsequent malignancies. They may be closely intertwined and cause prolonged morbidity and decreased quality of life after HCT. We provide a systematic review of male-specific late effects in a collaboration between transplant physicians, endocrinologists, urologists, dermatologists, and sexual health professionals through the Late Effects and Quality of Life Working Committee of the Center for International Blood and Marrow Transplant Research, and the Transplant Complications Working Party of the European Society of Blood and Marrow Transplantation.

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Male-specific late effects after hematopoietic cell transplantation (HCT) include genital chronic graft-versus-host disease (GVHD), hypogonadism, sexual dysfunction, infertility, and subsequent malignancies, such as prostate, penile, and testicular cancer. These effects may be closely intertwined and cause prolonged morbidity and decreased quality of life after HCT. Here we provide a systematic review of male-specific late effects in a collaboration among transplantation physicians, endocrinologists, urologists, dermatologists, and sexual health professionals through the Late Effects and Quality of Life Working Committee of the Center for International Blood and Marrow Transplant Research and the Transplant Complications Working Party of the European Society of Blood and Marrow Transplantation.

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Pharmacotherapy training for pediatric residents is an important part of their overall education. Limited data exist describing formal engagement of clinical pharmacists in residency training. The objective of this study was to evaluate a novel pharmacotherapy rotation for learner gains and program feasibility.

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Systematic reviews apply rigorous methodologies to address a prespecified, clearly formulated clinical research question. The conclusion that results is often cited to more robustly inform decision making by clinicians, third-party payers, and managed care organizations about the clinical question of interest. Although systematic reviews provide a rigorous standard, they may be infeasible when the task is to create general disease-focused guidelines comprising multiple clinical practice questions versus a single major clinical practice question.

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Systematic reviews apply rigorous methodologies to address a pre-specified, clearly formulated clinical research question. The conclusion that results is often cited to more robustly inform decision-making by clinicians, third-party payers and managed care organizations about the clinical question of interest. While systematic reviews provide a rigorous standard, they may be unfeasible when the task is to create general disease-focused guidelines comprised of multiple clinical practice questions versus a single major clinical practice question.

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Article Synopsis
  • The study aimed to assess the prevalence of functional gastrointestinal disorders (FGIDs) among patients in a pediatric gastroenterology clinic using Rome 3 diagnostic criteria.
  • Over a 19-month period, data were collected from 976 new patients, with parents completing a demographic survey and a symptom questionnaire before appointments.
  • The results showed that 52% of children under 4 years and 75% of children over 4 years met the criteria for at least one FGID, indicating a significant presence of these disorders among pediatric patients.
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Monosomy 18p and immunologic dysfunction: review of the literature and a new case report with thyroiditis, IgA deficiency, and systemic lupus erythematosus.

Clin Dysmorphol

April 2011

Departments of Pathology Pediatrics, Division of Clinical Genetics Department of Pediatrics, Division of Rheumatology, Louisiana State University, Health Sciences Center Children's Hospital of New Orleans, New Orleans, Louisiana, USA.

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45,X/47,XX,+18 and ring (18) mosaicism with mild phenotypic features including normal stature: clinical report and review of the literature.

Clin Dysmorphol

January 2009

Departments of Pathology Pediatrics, Division of Clinical Genetics, Louisiana State University Health Sciences Center Children's Hospital of New Orleans, New Orleans, Louisiana Department of Pediatrics, Weisskopf Child Evaluation Center, University of Louisville, Louisville, Kentucky, USA.

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Blast crisis of chronic myeloid leukemia: diagnosis prompted by T(8;9).

J Pediatr Hematol Oncol

November 2002

Department of Pediatric Hematology/Oncology, LSU Health Sciences Center/Children's Hospital of New Orleans, 200 Henry Clay Avenue, New Orleans, LA 70118, USA.

T(8;9) is a relatively new translocation that has been reported in a few patients with chronic myeloid leukemia (CML) but never in acute myeloid leukemia (AML). We report here a patient who presented with AML with t(8; 9). He lacked the Philadelphia chromosome but tested positive for the gene by the polymerase chain reaction method.

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