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
Nutritional Anemias in Infancy
Gallagher P, Ehrenkranz R. Nutritional Anemias in Infancy. Clinics In Perinatology 1995, 22: 671-692. PMID: 8521688, DOI: 10.1016/s0095-5108(18)30275-6.Peer-Reviewed Original ResearchConceptsNutritional anemiaUnderlying nutritional deficiencyLong-term sequelaeRole of vitaminsImportant warning signYears of lifeImpact of nutritionAspects of healthPrompt diagnosisNew therapiesNutritional deficienciesAnemiaTreatment of diseasesWarning signsTreatmentDeficiencySequelaeTherapyCliniciansDiseaseDiagnosis