Chapter 77 – Erythrocyte Disorders in Infancy

[1]  G. Kupfer,et al.  Inherited Bone Marrow Failure Syndromes , 2007 .

[2]  L. Wranne.  Transient erythroblastopenia in infancy and childhood. , 2009, Scandinavian journal of haematology.

[3]  R. Ehrenkranz,et al.  Anemia in the preterm infant: erythropoietin versus erythrocyte transfusion--it's not that simple. , 2009, Clinics in perinatology.

[4]  E. Lopriore,et al.  Fetal and neonatal haematological complications in monochorionic twins. , 2008, Seminars in fetal & neonatal medicine.

[5]  L. Zon,et al.  Hematopoiesis: An Evolving Paradigm for Stem Cell Biology , 2008, Cell.

[6]  K. Barrington,et al.  The Premature Infants in Need of Transfusion (PINT) study: a randomized, controlled trial of a restrictive (low) versus liberal (high) transfusion threshold for extremely low birth weight infants. , 2006, The Journal of pediatrics.

[7]  B. Vohr,et al.  Delayed Cord Clamping in Very Preterm Infants Reduces the Incidence of Intraventricular Hemorrhage and Late-Onset Sepsis: A Randomized, Controlled Trial , 2006, Pediatrics.

[8]  K. Barrington,et al.  Crystalloid or colloid for partial exchange transfusion in neonatal polycythemia: A systematic review and meta‐analysis , 2005, Acta paediatrica.

[9]  E. Bell,et al.  Randomized Trial of Liberal Versus Restrictive Guidelines for Red Blood Cell Transfusion in Preterm Infants , 2005, Pediatrics.

[10]  K. Moise,et al.  Management of Rhesus Alloimmunization in Pregnancy , 2002, Obstetrics and gynecology.

[11]  W. Judd.  Practice guidelines for prenatal and perinatal immunohematology, revisited , 2001, Transfusion.

[12]  C. Hammerman,et al.  Onset of jaundice in glucose-6-phosphate dehydrogenase-deficient neonates. , 2001, Pediatrics.

[13]  M. Goldman,et al.  Reduction of Donor Exposures in Premature Infants by the Use of Designated Adenine–Saline Preserved Split Red Blood Cell Packs , 2001, Journal of Perinatology.

[14]  A. Vlachos,et al.  The Diamond Blackfan Anemia Registry: tool for investigating the epidemiology and biology of Diamond-Blackfan anemia. , 2001, Journal of pediatric hematology/oncology.

[15]  A. Kappas,et al.  A single dose of Sn-mesoporphyrin prevents development of severe hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient newborns. , 2001, Pediatrics.

[16]  M. Daly,et al.  Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease. , 2001, Blood.

[17]  M. V. van Gemert,et al.  Twin-twin transfusion syndrome: etiology, severity and rational management , 2001, Current opinion in obstetrics & gynecology.

[18]  R. Strauss,et al.  Meta‐analysis of controlled clinical trials studying the efficacy of rHuEPO in reducing blood transfusions in the anemia of prematurity , 2001, Transfusion.

[19]  E. Beutler,et al.  Hyperbilirubinaemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome , 2001, European Journal of Pediatrics.

[20]  H. Reesink,et al.  Red cell transfusions in neonatal care , 2001, Vox sanguinis.

[21]  J. Abramson,et al.  Hematopoietic stem cell transplantation for Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry , 2001, Bone Marrow Transplantation.

[22]  N. Mohandas,et al.  Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. , 2001, Blood.

[23]  J. Lipton,et al.  Osteogenic Sarcoma Associated With Diamond–Blackfan Anemia: A Report From the Diamond–Blackfan Anemia Registry , 2001, Journal of pediatric hematology/oncology.

[24]  W. Erber,et al.  Detection of massive transplacental haemorrhage by flow cytometry. , 2000, Clinical and laboratory haematology.

[25]  V. Rajadurai,et al.  Twin-twin transfusion syndrome: a five year review , 2000, Archives of disease in childhood. Fetal and neonatal edition.

[26]  S. Fucharoen,et al.  Clinical Manifestation of &bgr;-Thalassemia/Hemoglobin E Disease , 2000, Journal of pediatric hematology/oncology.

[27]  E. Vichinsky,et al.  Changing outcome of homozygous alpha-thalassemia: cautious optimism. , 2000, Journal of pediatric hematology/oncology.

[28]  V. Chan,et al.  Genetic and clinical features of hemoglobin H disease in Chinese patients. , 2000, The New England journal of medicine.

[29]  A. Zipursky.  Erythropoietin Therapy for Premature Infants: Cost without Benefit? , 2000, Pediatric Research.

[30]  R. Couper.  Methaemoglobinaemia secondary to topical lignocaine/ prilocaine in a circumcised neonate , 2000, Journal of paediatrics and child health.

[31]  C. Comstock,et al.  Fetal schistocytic hemolytic anemia and umbilical vein varix. , 2000, Journal of pediatric hematology/oncology.

[32]  C R Bird,et al.  Fumaric aciduria: Clinical and imaging features , 2000, Annals of neurology.

[33]  C. Hammerman,et al.  Predischarge Bilirubin Screening in Glucose-6-Phosphate Dehydrogenase-Deficient Neonates , 2000, Pediatrics.

[34]  A. Zanella,et al.  Red cell pyruvate kinase deficiency: from genetics to clinical manifestations. , 2000, Bailliere's best practice & research. Clinical haematology.

[35]  E. Vichinsky,et al.  Sickle-cell disease not identified by newborn screening because of prior transfusion. , 2000, The Journal of pediatrics.

[36]  L. Burmeister,et al.  Feasibility and safety of AS-3 red blood cells for neonatal transfusions. , 2000, The Journal of pediatrics.

[37]  P. Rohrlich,et al.  Natural history of hereditary spherocytosis during the first year of life. , 2000, Blood.

[38]  I. Georgiou,et al.  Effect of recombinant human erythropoietin in preterm infants , 1999, European journal of haematology.

[39]  N. Olivieri.  The β-Thalassemias , 1999 .

[40]  D. Stevenson,et al.  Neonatal Hyperbilirubinemia in Glucose-6-Phosphate Dehydrogenase-deficient Heterozygotes , 1999, Pediatrics.

[41]  Hyde,et al.  The estimation of fetomaternal haemorrhage , 1999 .

[42]  D. Stevenson,et al.  Favism by proxy in nursing glucose-6-phosphate dehydrogenase-deficient neonates. , 1998, Journal of perinatology : official journal of the California Perinatal Association.

[43]  Chi-kong Li,et al.  Treatment of hemoglobin Bart's hydrops with bone marrow transplantation. , 1998, The Journal of pediatrics.

[44]  D. Chui,et al.  Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem , 1998 .

[45]  M. Malloy,et al.  Impact of transfusion guidelines on neonatal transfusions. , 1998, Journal of perinatology : official journal of the California Perinatal Association.

[46]  J. Kattwinkel,et al.  Inhaled Nitric Oxide for the Early Treatment of Persistent Pulmonary Hypertension of the Term Newborn: A Randomized, Double-Masked, Placebo-Controlled, Dose-Response, Multicenter Study , 1998, Pediatrics.

[47]  P. Nilsson,et al.  Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb , 1997, Nature Genetics.

[48]  K. Craig,et al.  Efficacy and safety of lidocaine-prilocaine cream for pain during circumcision. , 1997, The New England journal of medicine.

[49]  S. Weed,et al.  Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia. , 1997, The Journal of clinical investigation.

[50]  B. Glader,et al.  Hematologic disorders in children from southeast Asia. , 1996, Pediatric clinics of North America.

[51]  F. Ovalı,et al.  Management of Late Anemia in Rhesus Hemolytic Disease: Use of Recombinant Human Erythropoietin (A Pilot Study) , 1996, Pediatric Research.

[52]  R. Porat,et al.  Methylene blue-induced phototoxicity: an unrecognized complication. , 1996, Pediatrics.

[53]  L Luzzatto,et al.  Hematologically important mutations: glucose-6-phosphate dehydrogenase. , 1996, Blood cells, molecules & diseases.

[54]  H. Fujii,et al.  Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: Tabulation of mutant enzymes , 1996 .

[55]  T. Tang,et al.  Neonatal jaundice and molecular mutations in glucose‐6‐phosphate dehydrogenase deficient newborn infants , 1996, American journal of hematology.

[56]  L. Zon,et al.  Developmental biology of hematopoiesis. , 1995, Blood.

[57]  K. Barrington,et al.  Methemoglobinemia Associated with Prilocaine Use in Neonatal Circumcision , 1995, American journal of perinatology.

[58]  T. Zwerdling,et al.  Hemoglobin F‐Cincinnati, α2Gγ2 41(C7) Phe → Ser in a newborn with cyanosis , 1995 .

[59]  B. Kaplan,et al.  Use of Erythropoietin in Premature Neonates: Controversies and the Future , 1995, The Annals of pharmacotherapy.

[60]  R. Ehrenkranz,et al.  Recombinant human erythropoietin stimulates erythropoiesis and reduces erythrocyte transfusions in very low birth weight preterm infants. , 1995, Pediatrics.

[61]  S. Gross,et al.  Premature infants require additional folate and vitamin B-12 to reduce the severity of the anemia of prematurity. , 1994, The American journal of clinical nutrition.

[62]  B. Berman,et al.  Transient Erythroblastopenia of Childhood in Infants <6 Months of Age , 1994, The American journal of pediatric hematology/oncology.

[63]  J. Widness,et al.  Myocardial, erythropoietic, and metabolic adaptations to anemia of prematurity. , 1994, The Journal of pediatrics.

[64]  N. Fisk,et al.  Clinical utility of fetal RhD typing in alloimmunized pregnancies by means of polymerase chain reaction on amniocytes or chorionic villi. , 1994, American journal of obstetrics and gynecology.

[65]  T. Lane,et al.  Prospective, randomized trial of the safety and efficacy of a limited donor exposure transfusion program for premature neonates. , 1994, The Journal of pediatrics.

[66]  O. Linderkamp,et al.  Effects of red cell transfusion on cardiac output and blood flow velocities in cerebral and gastrointestinal arteries in premature infants. , 1994, Archives of disease in childhood. Fetal and neonatal edition.

[67]  M. Meyer,et al.  Recombinant human erythropoietin in the treatment of the anemia of prematurity: results of a double-blind, placebo-controlled study. , 1994, Pediatrics.

[68]  J. Widness,et al.  Recombinant human erythropoietin vs transfusions in the treatment of anemia of prematurity. A cost-benefit analysis. , 1994, Archives of pediatrics & adolescent medicine.

[69]  R. Strauss.  Erythropoietin and neonatal anemia. , 1994, The New England journal of medicine.

[70]  G. Duc,et al.  The effect of epoetin beta (recombinant human erythropoietin) on the need for transfusion in very-low-birth-weight infants , 1994 .

[71]  C. Henschke,et al.  Control of jaundice in preterm newborns by an inhibitor of bilirubin production: studies with tin-mesoporphyrin. , 1994, Pediatrics.

[72]  J. Palek,et al.  Clinical expression and laboratory detection of red blood cell membrane protein mutations. , 1993, Seminars in hematology.

[73]  J. Cartron,et al.  Molecular genetic basis of the human Rhesus blood group system , 1993, Nature Genetics.

[74]  N. Fisk,et al.  Prenatal determination of fetal RhD type by DNA amplification. , 1993 .

[75]  M. Norman,et al.  Skin microcirculation in neonatal polycythaemia and effects of haemodilution. Interaction between haematocrit, vasomotor activity and perfusion , 1993, Acta paediatrica.

[76]  J. Bussel,et al.  Suppression of erythropoiesis by intrauterine transfusions in hemolytic disease of the newborn: use of erythropoietin to treat the late anemia. , 1993, The Journal of pediatrics.

[77]  S. Cook,et al.  Effective use of a strategy using assigned red cell units to limit donor exposure for neonatal patients , 1993, Transfusion.

[78]  N. Mohandas,et al.  Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis , 1993 .

[79]  S. Izraeli,et al.  Lactic acid as a predictor for erythrocyte transfusion in healthy preterm infants with anemia of prematurity. , 1993, The Journal of pediatrics.

[80]  T. Pearson,et al.  Double blind trial of recombinant human erythropoietin in preterm infants. , 1993, Archives of disease in childhood.

[81]  R. Ehrenkranz,et al.  Erythropoietin therapy for anemia of prematurity. , 1993, Clinics in perinatology.

[82]  Audrey K. Brown.  Hyperbilirubinemia in Black Infants , 1992, Clinical pediatrics.

[83]  J. Spinnato.  Hemolytic disease of the fetus: a plea for restraint. , 1992, Obstetrics and gynecology.

[84]  A. Sola,et al.  Neonatal polycythemia in appropriately grown infants of hypertensive mothers , 1992, Acta paediatrica.

[85]  B. Fagrell,et al.  Effects of neonatal polycythemia and hemodilution on capillary perfusion. , 1992 .

[86]  D. Batton,et al.  Reducing neonatal transfusions. , 1992, Journal of perinatology : official journal of the California Perinatal Association.

[87]  D. P. Davies,et al.  Case study. Erythropoietin for anaemia in a preterm Jehovah's Witness baby. , 1992, Early human development.

[88]  F. Smith,et al.  Relationship between determinants of oxygen delivery and respiratory abnormalities in preterm infants with anemia. , 1992, The Journal of pediatrics.

[89]  J. Widness,et al.  Management of fetal hemolytic disease by cordocentesis. II. Outcome of treatment. , 1991, American journal of obstetrics and gynecology.

[90]  K. Schibler,et al.  Administration of erythropoietin to newborn rats results in diminished neutrophil production. , 1991, Blood.

[91]  R. Strauss,et al.  Transfusion therapy in neonates. , 1991, American journal of diseases of children.

[92]  R. Ware,et al.  Transient erythroblastopenia in the first year of life , 1991, American journal of hematology.

[93]  F. Chehab,et al.  Detection of the Hemoglobin E Mutation Using the Color Complementation Assay: Application to Complex Genotyping , 1990 .

[94]  E. Berman,et al.  Prediction of the need for transfusion during anemia of prematurity. , 1990, Jornal de Pediatria.

[95]  H. D. Heese,et al.  Prevention of iron deficiency in preterm neonates during infancy. , 1990, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

[96]  E. McCabe,et al.  Transient organic aciduria and methemoglobinemia with acute gastroenteritis. , 1990, Pediatrics.

[97]  P. Merlob,et al.  Neonatal polycythaemia: Effect of partial dilutional exchange transfusion with human albumin on whole blood viscosity , 1990, European Journal of Pediatrics.

[98]  M. Amylon,et al.  Reduced neutrophil counts in children with transient erythroblastopenia of childhood. , 1989, The Journal of pediatrics.

[99]  R. Kimura,et al.  A randomized trial to develop criteria for administering erythrocyte transfusions to anemic preterm infants 1 to 3 months of age. , 1989, Journal of perinatology : official journal of the California Perinatal Association.

[100]  F. Oski,et al.  Assessing the need for transfusion of premature infants and role of hematocrit, clinical signs, and erythropoietin level. , 1989, Pediatrics.

[101]  A. Pramanik,et al.  Diagnostic errors in neonatal polycythemia based on method of hematocrit determination. , 1989, The Journal of pediatrics.

[102]  J. Neilson,et al.  Twin-to-Twin Transfusion Syndrome: What Are Appropriate Diagnostic Criteria? , 1989, American journal of obstetrics and gynecology.

[103]  I. Hudson,et al.  PREVENTION OF TRANSFUSION-ACQUIRED CYTOMEGALOVIRUS INFECTION IN INFANTS BY BLOOD FILTRATION TO REMOVE LEUCOCYTES , 1989, The Lancet.

[104]  J. Priest,et al.  Mutant fetal hemoglobin causing cyanosis in a newborn. , 1989, Pediatrics.

[105]  V. Diaz-Barrios.  New York's Experience , 1989, Pediatrics.

[106]  B. Swanson,et al.  Neonatal hyperviscosity association with lower achievement and IQ scores at school age. , 1989, Pediatrics.

[107]  M. Gaston,et al.  Newborn screening for sickle cell disease and other hemoglobinopathies. , 1989, Pediatrics.

[108]  H. Kazazian,et al.  Molecular basis and prenatal diagnosis of beta-thalassemia. , 1988, Blood.

[109]  C. van der Heiden,et al.  WHAT IS THE BEST PREDICTOR OF THE SEVERITY OF ABO-HAEMOLYTIC DISEASE OF THE NEWBORN? , 1988, The Lancet.

[110]  J. Parer.  Severe Rh isoimmunization--current methods of in utero diagnosis and treatment. , 1988, American journal of obstetrics and gynecology.

[111]  J. Hobbins,et al.  The reversal of hydrops fetalis by intravascular intrauterine transfusion in severe isoimmune fetal anemia. , 1988, American journal of obstetrics and gynecology.

[112]  A. Kappas,et al.  Sn-protoporphyrin use in the management of hyperbilirubinemia in term newborns with direct Coombs-positive ABO incompatibility. , 1988, Pediatrics.

[113]  K. Shannon,et al.  Circulating erythroid progenitors in the anemia of prematurity. , 1987, The New England journal of medicine.

[114]  B. Glader.  Diagnosis and management of red cell aplasia in children. , 1987, Hematology/oncology clinics of North America.

[115]  E. Bancalari,et al.  Blood transfusion effect on the respiratory pattern of preterm infants. , 1987, Pediatrics.

[116]  H. Ha,et al.  Partial exchange transfusion in term, polycythemic neonates: absence of association with severe gastrointestinal injury. , 1987 .

[117]  R. Ramamurthy,et al.  Postnatal alteration in hematocrit and viscosity in normal and polycythemic infants. , 1987, The Journal of pediatrics.

[118]  N. Mohandas,et al.  Modulation of erythrocyte membrane mechanical stability by 2,3-diphosphoglycerate in the neonatal poikilocytosis/elliptocytosis syndrome. , 1987, The Journal of clinical investigation.

[119]  E. Bell,et al.  Oral vitamin E supplementation for the prevention of anemia in premature infants: a controlled trial. , 1987, Pediatrics.

[120]  E Vichinsky,et al.  Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial. , 1986, The New England journal of medicine.

[121]  J. Hobbins,et al.  In utero exchange transfusion by direct intravascular injection in severe erythroblastosis fetalis. , 1986, The New England journal of medicine.

[122]  Y. Kan,et al.  Survival of a hydropic infant with homozygous α-thalassemia-1 , 1986 .

[123]  D. Anderson,et al.  Posttransfusion cytomegalovirus infection in neonates: role of saline-washed red blood cells. , 1986, The Journal of pediatrics.

[124]  A. Stark,et al.  Normal long-term survival with α-thalassemia , 1986 .

[125]  L. Lubchenco,et al.  Gastrointestinal injury in polycythemic term infants. , 1985, Pediatrics.

[126]  J. Richardson,et al.  Nuchal Cord as a Cause of Neonatal Anemia , 1985, American journal of diseases of children.

[127]  K. Nicolaides,et al.  The management of severe rhesus isoimmunization by fetoscopic intravascular transfusions. , 1984, American journal of obstetrics and gynecology.

[128]  J. Stockman,et al.  Anemia of prematurity: determinants of the erythropoietin response. , 1984, The Journal of pediatrics.

[129]  J. Stockman,et al.  Weight gain: a response to transfusion in selected preterm infants. , 1984, American journal of diseases of children.

[130]  B. Puppala,et al.  The role of RBC transfusion in the premature infant. , 1984, American journal of diseases of children.

[131]  D. Anderson,et al.  Use of deglycerolized red blood cells to prevent posttransfusion infection with cytomegalovirus in neonates. , 1984, The Journal of infectious diseases.

[132]  L. Osborn,et al.  Phototherapy in full-term infants with hemolytic disease secondary to ABO incompatibility. , 1984, Pediatrics.

[133]  M. Shohat,et al.  Neonatal polycythemia: I. Early diagnosis and incidence relating to time of sampling. , 1984, Pediatrics.

[134]  W. Schröter,et al.  Diagnosis of hereditary spherocytosis in newborn infants. , 1983, The Journal of pediatrics.

[135]  E. Danish,et al.  Transient methemoglobinemia with acidosis in infants. , 1982, The Journal of pediatrics.

[136]  C. Prober,et al.  Prevention of transfusion-acquired cytomegalovirus infections in newborn infants , 1981 .

[137]  K. Matthay,et al.  Erythrocyte enzymopathies in the newborn. , 1981, Clinics in haematology.

[138]  O. P. Gray,et al.  Nonphysiological anaemia of prematurity. , 1978, Archives of disease in childhood.

[139]  Mentzer Wc.  Polycythaemia and the hyperviscosity syndrome in newborn infants. , 1978 .

[140]  J. Graeber,et al.  The use of intramuscular vitamin E in the premature infant. Optimum dose and iron interaction. , 1977, The Journal of pediatrics.

[141]  Richards Bw.  Letter: Consultant involvement in planning super specialties. , 1976 .

[142]  D. Phelps,et al.  Placenta to lamb fetus transfusion in utero during acute hypoxia. , 1975, American journal of obstetrics and gynecology.

[143]  V. Freda,et al.  Prevention of Rh hemolytic disease--ten years' clinical experience with Rh immune globulin. , 1975, The New England journal of medicine.

[144]  W. Mentzer,et al.  Hydrops fetalis associated with erythrocyte G-6-PD deficiency and maternal ingestion of fava beans and ascorbic acid. , 1975, The Journal of pediatrics.

[145]  H. Bard.  The postnatal decline of hemoglobin F synthesis in normal full-term infants. , 1975, The Journal of clinical investigation.

[146]  F. Rosen,et al.  Graft-versus-host disease after intrauterine and exchange transfusions for hemolytic disease of the newborn. , 1974, The New England journal of medicine.

[147]  J. Keating,et al.  Infantile methemoglobinemia caused by carrot juice. , 1973, The New England journal of medicine.

[148]  S. Halvorsen,et al.  Regulation of erythropoiesis in the fetus and newborn. , 1972, Archives of disease in childhood.

[149]  Y. Kan,et al.  Gamma-beta thalassemia: a cause of hemolytic disease of the newborn. , 1972, The New England journal of medicine.

[150]  M. Delivoria-Papadopoulos,et al.  Postnatal Changes in Oxygen Transport of Term, Premature, and Sick Infants: The Role of Red Cell 2,3-Diphosphoglycerate and Adult Hemoglobin , 1971, Pediatric Research.

[151]  M. A. Williams,et al.  An Explanation of the Failure of the Direct Antiglobulin Test to Detect Erythrocyte Sensitization in ABO Haemolytic Disease of the Newborn and Observations on Pinocytosis of IgG Anti‐A Antibodies by Infant (Cord) Red Cells , 1971, British journal of haematology.

[152]  J. Harley,et al.  NEONATAL METHÆMOGLOBINÆMIA AND THE " RED-BROWN " SCREENING-TEST , 1970 .

[153]  M. Delivoria-Papadopoulos,et al.  The red cell, 2,3-diphosphoglycerate, and tissue oxygen release. , 1970, The Journal of pediatrics.

[154]  Lacelle Pl.  Alteration of membrane deformability in hemolytic anemias. , 1970 .

[155]  M. Stahlman,et al.  Symptomatic posthemorrhagic anemia in the newborn. , 1970, Pediatric clinics of North America.

[156]  J. Arey,et al.  Possible graft-versus-host reaction after intrauterine transfusion for Rh erythroblastosis fetalis. , 1969, The New England journal of medicine.

[157]  J. Desforges,et al.  Hereditary elliptocytosis: an unusual presentation of hemolysis in the newborn associated with transient morphologic abnormalities. , 1969, Pediatrics.

[158]  L. Diamond,et al.  Splenectomy in childhood and the hazard of overwhelming infection. , 1969, Pediatrics.

[159]  C. Bauer,et al.  Different effects of 2.3 diphosphoglycerate and adenosine triphosphate on the oxygen affinity of adult and foetal human haemoglobin , 1968 .

[160]  M. Grossman,et al.  Edema and hemolytic anemia in premature infants. A vitamin E deficiency syndrome. , 1968, The New England journal of medicine.

[161]  J. Desforges,et al.  Fetomaternal hemorrhage from diagnostic transabdominal amniocentesis. , 1967, American journal of obstetrics and gynecology.

[162]  F. Oski,et al.  The relationship of erythrocyte glucose-6-phosphate dehydrogenase deficiency to byperbilirubinemia in Negro premature infants. , 1967, The Journal of pediatrics.

[163]  H. Pearson.  Life-span of the fetal red blood cell. , 1967, The Journal of pediatrics.

[164]  F. Oski,et al.  Vitamin E deficiency: a previously unrecognized cause of hemolytic anemia in the premature infant. , 1967, The Journal of pediatrics.

[165]  R. B. Cole,et al.  Neonatal polycythemia with transient cyanosis and cardiorespiratory abnormalities. , 1966, The Journal of pediatrics.

[166]  P. Finne.  Erythropoietin Levels in Cord Blood as an Indicator of Intrauterine Hypoxia , 1966, Acta paediatrica Scandinavica.

[167]  J. Desforges,et al.  Erythrocyte DPNH dependent diaphorase levels in infants. , 1966, Pediatrics.

[168]  W. Oh,et al.  Venous and Capillary Hematocrit in Newborn Infants and Placental Transfusion , 1966, Acta paediatrica Scandinavica.

[169]  J. Lind,et al.  Blood Volume of the Newborn Premature Infant , 1965, Acta paediatrica Scandinavica.

[170]  A. Rausen,et al.  Twin transfusion syndrome , 1965 .

[171]  T. Valaes,et al.  The Clinical Picture of Glucose 6-Phosphate Dehydrogenase Deficiency in Early Infancy , 1964, Archives of disease in childhood.

[172]  W. Zuelzer,et al.  MECHANISMS OF ISOIMMUNIZATION. I. THE TRANSPLACENTAL PASSAGE OF FETAL ERYTHROCYTES IN HOMOSPECIFIC PREGNANCIES. , 1964, Blood.

[173]  T. Huisman,et al.  Formation of Ferrihæmoglobin of Isolated Human Hæmoglobin Types by Sodium Nitrite , 1963, Nature.

[174]  A. W. Liley.  Intrauterine Transfusion of Foetus in Haemolytic Disease , 1963, British medical journal.

[175]  Secundino Veiga,et al.  Massive Intravascular Sickling after Exchange Transfusion with Sickle Cell Trait Blood * , 1963, Transfusion.

[176]  J. Lind,et al.  The Blood Volume of the Newborn Infant and Placental Transfusion , 1963, Acta paediatrica.

[177]  D. Hsia,et al.  Serum Bilirubin Levels and Glucose-6-Phosphate Dehydrogenase Deficiency in Newborn American Negroes. , 1963 .

[178]  A. W. Liley.  Liquor amnii analysis in the management of the pregnancy complicated by rhesus sensitization , 1961 .

[179]  M. Lyon.  Gene Action in the X-chromosome of the Mouse (Mus musculus L.) , 1961, Nature.

[180]  P. Lanzkowsky.  The Influence of Maternal Iron-deficiency Anaemia on the Haemoglobin of the Infant , 1961, Archives of disease in childhood.

[181]  B. Anthony,et al.  Giant cephalhematoma of newborn with hemorrhagic disease and hyperbilirubinemia. , 1961, American journal of diseases of children.

[182]  L. Jacobson,et al.  Studies on erythropoiesis. XII. The effect of transfusion-induced polycythemia in the mother on the fetus. , 1959, Blood.

[183]  A. Rawson,et al.  Studies of Blood Group Antibodies , 1959, The Journal of Immunology.

[184]  J. Marks,et al.  The Fluid Shift from the Vascular Compartment Immediately after Birth , 1958, Archives of disease in childhood.

[185]  L. Diamond,et al.  Congenital hemolytic anemia in the newborn; relationship to kernicterus. , 1957, A.M.A. journal of diseases of children.

[186]  J. Wyman,et al.  The oxygen equilibrium of fetal and adult human hemoglobin. , 1953, The Journal of biological chemistry.

[187]  H. H. Comly.  Cyanosis in Infants caused by Nitrates in Well Water. , 1945 .

[188]  P. Levine,et al.  The role of iso-immunization in the pathogenesis of erythroblastosis fetalis , 1941 .

[189]  R. Cabot,et al.  Case 19331: A Mediastinal Mass with Pulmonary Collapse , 1933 .

[190]  R. Strauss.  Controversies in the management of the anemia of prematurity using single-donor red blood cell transfusions and/or recombinant human erythropoietin. , 2006, Transfusion medicine reviews.

[191]  H. Witkowska,et al.  Universal newborn screening for Hb H disease in California. , 2001, Genetic testing.

[192]  B. Frey,et al.  The value of capillary whole blood lactate for blood transfusion requirements in anaemia of prematurity , 2001, Intensive Care Medicine.

[193]  S. De Virgiliis,et al.  Clinical experience of management of thalassemia: the Sardinian experience. , 1996, Seminars in hematology.

[194]  F. Lorey,et al.  Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state , 1996, Genetic epidemiology.

[195]  T. Vulliamy,et al.  HEMOTOLOGICALLY IMPORTANT MUTATIONS : GLUSOSE-6-PHOSPHATE DEHYDROGENASE , 1996 .

[196]  D. Christie,et al.  Dietary protein intolerance in infants with transient methemoglobinemia and diarrhea. , 1993, The Journal of pediatrics.

[197]  D. Pr.  Anemia of prematurity: the prospects for avoiding blood transfusions by treatment with recombinant human erythropoietin. , 1993, Advances in pediatrics.

[198]  P. Merlob,et al.  Polycythemia of the preterm and full-term newborn infant: relationship between hematocrit and gestational age, total blood solutes, reticulocyte count, and blood pH. , 1992, Biology of the neonate.

[199]  G. Forteleoni,et al.  Marked decline of favism after neonatal glucose-6-phosphate dehydrogenase screening and health education: the northern Sardinian experience. , 1992, Acta haematologica.

[200]  K. Shannon.  Anemia of prematurity: progress and prospects. , 1990, The American journal of pediatric hematology/oncology.

[201]  K. Titani,et al.  A New Abnormal Fetal Hemoglobin, Hb FM-Osaka (α2γ263His→Tyr) , 1980 .

[202]  J. Stockman,et al.  Rapid correction of anemia with partial exchange transfusion. , 1977, American journal of diseases of children.

[203]  F. Herz,et al.  ABO hemolytic disease of the newborn, without hyperbilirubinemia , 1976, American journal of hematology.

[204]  A. Montague,et al.  Transplacental hemorrhage in cesarean section. , 1966, American journal of obstetrics and gynecology.

[205]  J. Mestyán,et al.  THE BASAL METABOLIC RATE OF PREMATURE INFANTS. , 1964, Biologia neonatorum. Neo-natal studies.