2015
A Pediatrician’s Practical Guide to Diagnosing and Treating Hereditary Spherocytosis in Neonates
Christensen RD, Yaish HM, Gallagher PG. A Pediatrician’s Practical Guide to Diagnosing and Treating Hereditary Spherocytosis in Neonates. Pediatrics 2015, 135: 1107-1114. PMID: 26009624, PMCID: PMC4444801, DOI: 10.1542/peds.2014-3516.Peer-Reviewed Original ResearchConceptsHereditary spherocytosisDiagnosis of HSABO hemolytic diseaseGlucose-6-phosphate dehydrogenase deficiencyHazardous hyperbilirubinemiaErythrocyte transfusionSymptomatic anemiaNeurologic dysfunctionPrompt diagnosisAdverse outcomesEmergency departmentNewborn periodNeonatal presentationNewborn infantsHemolytic diseaseAppropriate treatmentEarly suspicionHemolytic anemiaHemolytic conditionsAnticipatory guidanceNeonatesFirst monthAnemiaDehydrogenase deficiencyHyperbilirubinemia
1995
Hematologic disorders and nonimmune hydrops fetalis
Arcasoy M, Gallagher P. Hematologic disorders and nonimmune hydrops fetalis. Seminars In Perinatology 1995, 19: 502-515. PMID: 8822334, DOI: 10.1016/s0146-0005(05)80057-6.Peer-Reviewed Original ResearchConceptsNonimmune hydrops fetalisHematologic disordersHydrops fetalisTwin-twin transfusionFetal blood lossGlucose-6-phosphate dehydrogenase deficiencyFinal common denominatorBlood lossHeart failureFetomaternal hemorrhageNonimmune hydropsErythrocyte lossDehydrogenase deficiencyErythrocyte abnormalitiesErythrocyte productionDisordersHemorrhageAnemiaFetalisAnasarcaTransfusionAscitesEdemaHydropsFailure