A5102755932- Congenital Diaphragmatic Hernia Studies
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
- Thyroid Cancer Diagnosis and Treatment
- Congenital Anomalies and Fetal Surgery
- Intestinal Malrotation and Obstruction Disorders
- Trauma Management and Diagnosis
- Esophageal and GI Pathology
- Injury Epidemiology and Prevention
- Gastrointestinal disorders and treatments
- Glioma Diagnosis and Treatment
- Homicide, Infanticide, and Child Abuse
- Vascular Malformations and Hemangiomas
- Infant Nutrition and Health
- Emergency and Acute Care Studies
- Foreign Body Medical Cases
- Child Abuse and Related Trauma
- Trauma and Emergency Care Studies
- Head and Neck Anomalies
- Ultrasound in Clinical Applications
- Autopsy Techniques and Outcomes
- Cardiovascular Conditions and Treatments
- Congenital Heart Disease Studies
- Appendicitis Diagnosis and Management
- Neonatal and Maternal Infections
University of Miami
2014-2023
Jackson Memorial Hospital
2014-2017
Memorial Medical Center
2014
Klinik und Poliklinik für Neurologie
2008
<b>Introduction</b> This study aims to update outcomes and predictors of survival on pediatric thyroid carcinoma, specifically examining patients with nonpapillary carcinoma who underwent surgical resection. <b>Methods</b> Surveillance, epidemiology, end results database were searched for cases (< 20 years old) surgically treated diagnosed from 1973 2011. Demographics, clinical characteristics, analyzed using standard statistical methods. All follicular, medullary, Hürthle-cell,...
To describe and discuss a case of superior mesenteric artery syndrome (SMAS) presenting with gastrointestinal signs symptoms mistakenly attributed to, treated as, diabetic gastroparesis.A report was compiled describing the clinical presentation, including history physical examination, evaluation, diagnosis, treatment patient type 1 diabetes complications.Clinical suspicion combined appropriate radiological evaluation led to diagnosis SMAS, classic findings reduced aortomesenteric angle...
Waardenburg syndrome (WS) type IV is characterized by pigmentary abnormalities, deafness and Hirschsprung's disease.This can be triggered dysregulation of the SOX10 gene, which belongs to SOX (SRY-related high-mobility group-box) family genes.We discuss first known case a frameshift mutation variant defined as c.895delC causing WS without female patient unrelated Kuwaiti parents, who tested negative for cystic fibrosis disease, was born with meconium ileus malrotation had multiple surgical...