B. Glader

B. Glader, M. Conrad, J. Durocher, 1973, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Approach to the Newborn Who Has Thrombocytopenia

B. Glader, W. Wong, 2004 .

Comorbidities and complications in adults with pyruvate kinase deficiency

E. Neufeld, S. Sheth, B. Glader, 2019, European journal of haematology.

TNF-mediated inflammation represses GATA1 and activates p38 MAP kinase in RPS19-deficient hematopoietic progenitors.

Shuo Lin, N. Danilova, K. Sakamoto, 2014, Blood.

Red Blood Cell Enzyme Disorders.

B. Glader, R. Grace, 2018, Pediatric clinics of North America.

The active component of ginseng, ginsenoside Rb1, improves erythropoiesis in models of Diamond–Blackfan anemia by targeting Nemo-like kinase

K. Sakamoto, B. Glader, A. Narla, 2021, The Journal of biological chemistry.

SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature

M. Fleming, J. Boudreaux, T. Olson, 2021, Human mutation.

L‐leucine improves anemia and growth in patients with transfusion‐dependent Diamond‐Blackfan anemia: Results from a multicenter pilot phase I/II study from the Diamond‐Blackfan Anemia Registry

Jason E. Farrar, Ellen V. Muir, G. Nalepa, 2020, Pediatric blood & cancer.

Metformin-induced suppression of NLK improves erythropoiesis in pre-clinical models of Diamond Blackfan Anemia through induction of miR-26a.

K. Sakamoto, Jun Chen, M. Serrano, 2020, Experimental Hematology.

Increased Prevalence of Congenital Heart Disease in Children With Diamond Blackfan Anemia Suggests Unrecognized Diamond Blackfan Anemia as a Cause of Congenital Heart Disease in the General Population: A Report of the Diamond Blackfan Anemia Registry

Jason E. Farrar, I. Dianzani, K. Onel, 2018, Circulation. Genomic and precision medicine.

A novel pathogenic mutation in RPL11 identified in a patient diagnosed with diamond Blackfan anemia as a young adult.

D. Yuan, B. Glader, J. Ulirsch, 2016, Blood cells, molecules & diseases.

Erythrocyte adenosine deaminase levels are elevated in Diamond Blackfan anemia but not in the 5q− syndrome

B. Glader, A. Narla, N. Davis, 2016, American journal of hematology.

Erythrocyte adenosine deaminase: diagnostic value for Diamond‐Blackfan anaemia

S. Savage, N. Giri, B. Alter, 2013, British journal of haematology.

Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia Cell Lines without Classical Breakpoint Cluster Region Rearrangement 1

F. Hecht, M. Link, L. Naumovski, 2006 .

Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7.

A. Bowcock, C. Eaves, K. Shannon, 1989, The Journal of clinical investigation.

Acute nonlymphocytic leukemia developing during the course of Ewing's sarcoma.

S. Donaldson, R. Kempson, M. Link, 1984, Medical and Pediatric Oncology.

Establishment and characterization of a common acute lymphoblastic leukemia cell line with a deletion of chromosome 3 band q26.

F. Hecht, J. Sklar, S. Smith, 1987, Cancer research.

Clinical and biologic characterization of T-cell neoplasias with rearrangements of chromosome 7 band q34.

R. Warnke, F. Hecht, S. Smith, 1988, Blood.

One year follow‐up of children and adolescents with chronic immune thrombocytopenic purpura (ITP) treated with rituximab

M. Loh, S. Feig, E. Neufeld, 2009, Pediatric blood & cancer.

Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency

J. Segovia, J. Hoyer, B. Glader, 2018, American journal of hematology.

Immunosuppressive therapy for pediatric aplastic anemia: a North American Pediatric Aplastic Anemia Consortium study

David A. Williams, T. Olson, A. Bertuch, 2019, Haematologica.

Long‐term hematologic and clinical outcomes of splenectomy in children with hereditary spherocytosis and sickle cell disease

J. Scott, Rebeccah L. Brown, B. Warner, 2020 .

Resolution of severe Donath-Landsteiner autoimmune hemolytic anemia temporally associated with institution of plasmapheresis

B. Glader, A. Roy-Burman, A. Roy‐Burman, 2002, Critical care medicine.

Monthly recombinant tissue plasminogen activator administration to implantable central venous access devices decreases infections in children with haemophilia

B. Glader, J. Lea, M. Jeng, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Effect of Cyariate on Erythrocyte Deformability

B. Glader, M. Conrad, Durocher, 2005 .

Cyanate Inhibition of Erythrocyte Glucose-6-phosphate Dehydrogenase

B. Glader, M. Conrad, 1972, Nature.

Haemolytic disorders of infancy.

O. Platt, B. Glader, 1978, Clinics in Haematology.

Animal models of Diamond-Blackfan anemia: updates and challenges

M. Barna, K. Sakamoto, Y. L. Liu, 2022, Haematologica.

Transient Erythroblastopenia of Adolescence

J. Finlay, B. Glader, T. Zwerdling, 1986, Clinical pediatrics.

Hematologic disorders in children from southeast Asia.

B. Glader, K. Look, 1996, Pediatric clinics of North America.

Leukocyte counts in children with sickle cell disease. Comparative values in the steady state, vaso-occlusive crisis, and bacterial infection.

B. Glader, G. Buchanan, 1978, American journal of diseases of children.

Elevated erythrocyte adenosine deaminase activity in congenital hypoplastic anemia.

B. Glader, L. Diamond, K. Backer, 1983, The New England journal of medicine.

Thrombocytopenia in Neonates Who Have Physical Abnormalities or Dysmorphic Features

B. Glader, W. Wong, 2004 .

Erratum: Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia (DOI:10.1016/j.ajhg.2009.12.015)

P. Newburger, R. Arceci, M. O'Donohue, 2010 .

Loss of Elbow and Wrist Motion in Hemophilia

H. Vallier, B. Glader, J. Gamble, 1996, Clinical orthopaedics and related research.

Arthropathy of the ankle in hemophilia.

B. Glader, J. Gamble, L. Rinsky, 1991, The Journal of bone and joint surgery. American volume.

Updated analysis: central venous access device infection rates in an expanded cohort of paediatric patients with severe haemophilia receiving prophylactic recombinant tissue plasminogen activator

B. Glader, J. Andrews, M. Jeng, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

Adenovirus-associated virus vector-mediated gene transfer in hemophilia B.

Pratima Chowdary, Savita Rangarajan, Cecilia Rosales, 2011, The New England journal of medicine.

AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B.

Alan McClelland, Arthur Thompson, Roland W Herzog, 2003, Blood.

Fatal myocardial infarction following therapy with prothrombin complex concentrates in a young man with hemophilia A.

B. Glader, M. Billingham, L. J. Purdy, 1984, Pediatrics.

Early Clinical Trial Results Following Administration of a Low Dose of a Novel Self Complementary Adeno-Associated Viral Vector Encoding Human Factor IX In Two Subjects with Severe Hemophilia B

M. Kay, A. Nienhuis, J. Gray, 2010 .

Approach to the bleeding child.

B. Glader, G. Allen, 2002, Pediatric clinics of North America.

1002. Immune Responses to AAV and to Factor IX in a Phase I Study of AAV-Mediated, Liver-Directed Gene Transfer for Hemophilia B

J. Rasko, M. Kay, M. Ozelo, 2004 .

Care of the critically ill child: the bleeding neonate.

B. Glader, G. Buchanan, 1976, Pediatrics.

Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.

D. Vandorpe, S. Alper, C. Brugnara, 2011, American journal of physiology. Cell physiology.

Cation specificity of propranolol‐induced changes in RBC membrane permeability: Comparative effects in human, dog and cat erythrocytes

B. Glader, Aixa Müller‐Soyano, 1977, Journal of cellular physiology.

Energy metabolism in human erythrocytes: the role of phosphoglycerate kinase in cation transport.

B. Glader, D. Nathan, G. Segel, 1975, Blood.

Cryptococcus infection in a nine-year-old child with hemophilia and the acquired immunodeficiency syndrome.

B. Glader, C. Prober, S. Ting, 1991, The Pediatric infectious disease journal.

Salicylate-induced injury of pyruvate-kinase-deficient erythrocytes.

B. Glader, 1976, The New England journal of medicine.

Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemia.

E. Zackai, K. Gripp, D. McDonald-McGinn, 2001, American journal of medical genetics.

Congenital hypoplastic (Diamond-Blackfan) anemia in seven members of one kindred.

J. Carey, D. Viskochil, B. Glader, 1990, American journal of medical genetics.

Congenital Hypoplastic Anemia (Diamond — Blackfan Anemia)

B. Glader, 1990 .

Chapter 77 – Erythrocyte Disorders in Infancy

B. Glader, D. Matthews, 2012 .

Mechanism of methemoglobin formation by diphenylsulfones. Effect of 4-amino-4'-hydroxyaminodiphenylsulfone and other p-substituted derivatives.

B. Glader, T. Li, P. Kramer, 1972, Biochemical pharmacology.

Loss of Forkhead box M1 promotes erythropoiesis through increased proliferation of erythroid progenitors

K. Sakamoto, B. Glader, A. Narla, 2017, Haematologica.

Comparative activity of erythrocyte adenosine deaminase and orotidine decarboxylase in Diamond‐Blackfan anemia

B. Glader, K. Backer, 1986, American journal of hematology.

Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia.

A. Beggs, L. D. Da Costa, C. Niemeyer, 2006, American journal of human genetics.

Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss.

B. Glader, D. Nathan, N. Fortier, 1974, The New England journal of medicine.

Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference

S. Karlsson, S. Sheth, T. Leblanc, 2008, British journal of haematology.

Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency.

D. Morton, C. Kung, S. Sheth, 2019, The New England journal of medicine.

Prednisone stimulation of erythropoiesis in leukemic children during remission

M. Amylon, B. Glader, Susan P. Perrlne, 1986, American journal of hematology.

Reduced neutrophil counts in children with transient erythroblastopenia of childhood.

M. Amylon, B. Glader, G. Buchanan, 1989, The Journal of pediatrics.

Diamond Blackfan anemia is mediated by hyperactive Nemo-like kinase

H. Nakauchi, M. Serrano, M. Porteus, 2020, Nature Communications.

The role of the DNA damage response in zebrafish and cellular models of Diamond Blackfan anemia

Shuo Lin, N. Danilova, K. Sakamoto, 2014, Disease Models & Mechanisms.

Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond–Blackfan anemia

P. Newburger, A. Beggs, M. O'Donohue, 2013, Human Genetics.

Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients.

Alan H Beggs, Pierre-Emmanuel Gleizes, Joerg J Meerpohl, 2008, American journal of human genetics.

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.

Ivan Limongelli, Gordon W Stewart, Achille Iolascon, 2013, Blood.

RED CELLS , IRON , AND ERYTHROPOIESIS Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO 1

S. Schrier, D. Vandorpe, A. Iolascon, 2013 .

Pklr Intron Splicing-Associated Mutations and Alternate Diagnoses Are Common in Pyruvate Kinase Deficient Patients with Single or No Pklr Coding Mutations

B. Glader, P. Bianchi, H. Yaish, 2018, Blood.

Philadelphia chromosome-positive acute lymphoblastic leukemia cell lines without classical breakpoint cluster region rearrangement.

F Hecht, F. Hecht, S. Smith, 1988, Cancer research.

Reduced ribosomal protein gene dosage and p53 activation in low-risk myelodysplastic syndrome.

I. Weissman, G. Barsh, S. Mendrysa, 2011, Blood.

Langerhans' cell histiocytosis presenting with the superior vena cava syndrome: a case report.

M. Amylon, S. Donaldson, M. Link, 1993, Medical and pediatric oncology.

Monoclonal antibody and enzymatic profiles of human malignant T-lymphoid cells and derived cell lines.

R. Warnke, S. Smith, M. Link, 1984, Cancer research.

Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease.

M. Daly, A. Beggs, C. Niemeyer, 2001, Blood.

Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura.

M. Loh, E. Neufeld, J. Bussel, 2006, Blood.

Anti‐Mur as the most likely cause of mild hemolytic disease of the newborn

B. Glader, J. Andrews, Sara Bakhtary, 2016, Transfusion.

The Bleeding Neonate

B. Glader, G. Buchanan, 1976, Pediatrics.

Hemolysis by diphenylsulfones: comparative effects of DDS and hydroxylamine-DDS.

B. Glader, M. Conrad, 1973, The Journal of laboratory and clinical medicine.

Role of cellular Pi in Pi transport and metabolism in human red cells.

B. Glader, A. Omachi, 1968, Biochimica et biophysica acta.

Phosphate release from human erythrocytes.

B. Glader, A. Omachi, 1968, Biochimica et biophysica acta.

Development of antibodies to human thrombin and factor V in a pediatric patient exposed to topical bovine thrombin

J. Zehnder, B. Glader, C. Lo, 2010, Pediatric blood & cancer.

Red blood cell aplasias in children.

B. Glader, 1990, Pediatric annals.

Array Comparative Genomic Hybridization of Ribosomal Protein Genes In Diamond-Blackfan Anemia Patients; Evidence for Three New DBA Genes, RPS8, RPS14 and RPL15, with Large Deletion or Duplication

P. Newburger, A. Beggs, J. Lipton, 2010 .

Transient erythroblastopenia of childhood.

B. Glader, 1988, The Western journal of medicine.

Diagnosis and management of red cell aplasia in children.

B. Glader, 1987, Hematology/oncology clinics of North America.

Genotype‐phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency

P. Newburger, D. Morton, M. Wlodarski, 2020, American journal of hematology.

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study.

P. Newburger, D. Morton, E. Neufeld, 2018, Blood.

Hemolytic anemia in children.

B. Glader, 1999, Clinics in laboratory medicine.

Pancytopenia with Myelofibrosis

W. Carroll, B. Glader, F. Berberich, 1986, La Clinica pediatrica.

Acute idiopathic thrombocytopenic purpura--management in childhood.

S. Feig, C. Moertel, B. Glader, 1997, Blood.

Childhood bone marrow monosomy 7 syndrome: a familial disorder?

W. Carroll, B. Glader, R. Morgan, 1985, The Journal of pediatrics.

Neonatal Hematology: Neonatal hemolysis

B. Glader, G. Allen, 2005 .

Hemoglobin FM-Fort Ripley: another lesson from the neonate.

B. Glader, 1989, Pediatrics.

Diamond Blackfan anemia is mediated by hyperactive Nemo-like kinase

H. Nakauchi, K. Sakamoto, T. Lundbäck, 2020, Nature Communications.

The pyruvate kinase (PK) to hexokinase enzyme activity ratio and erythrocyte PK protein level in the diagnosis and phenotype of PK deficiency

D. Morton, C. Kung, Y. Ravindranath, 2020, British journal of haematology.

The variable manifestations of disease in pyruvate kinase deficiency and their management.

B. Glader, P. Bianchi, H. Al‐Samkari, 2020, Haematologica.

Pyruvate kinase deficiency in dog and human erythrocytes: Effects of energy depletion on cation composition and cellular hydration

B. Glader, Aixa Muller‐Soyano, Orah Platt, 1986, American journal of hematology.

Erythrocyte enzyme disorders in children.

B. Glader, D. Sullivan, 1980, Pediatric clinics of North America.

Pyruvate kinase deficiency in children

D. Morton, E. Neufeld, S. Sheth, 2021, Pediatric blood & cancer.

Characterization of the severe phenotype of pyruvate kinase deficiency

D. Morton, S. Sheth, M. Wlodarski, 2019, American journal of hematology.

Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study

P. Newburger, D. Morton, E. Neufeld, 2018, Haematologica.

Decreased Glutathione Peroxidase in Neonatal Erthyrocytes: Lack of Relation to Hydrogen Peroxide Metabolism

B. Glader, M. Conrad, 1972, Pediatric Research.

Immune thrombocytopenia associated with acute nonlymphocytic leukemia.

M. Amylon, M. Link, B. Glader, 1984, The Journal of pediatrics.

Physiologic features of hemolysis axxociated with altered cation and 2,3-diphosphoglycerate content.

B. Glader, N. Fortier, M. Albala, 1978, Blood.

MMP9 inhibition increases erythropoiesis in RPS14-deficient del(5q) MDS models through suppression of TGF-β pathways.

P. Greenberg, Shuo Lin, Haigen Huang, 2019, Blood advances.

Benign course of extreme hyperbilirubinemia in sickle cell anemia: analysis of six cases.

B. Glader, G. Buchanan, 1977, The Journal of pediatrics.

Hematologic outcomes after total splenectomy and partial splenectomy for congenital hemolytic anemia.

J. Scott, Rebeccah L. Brown, C. Thornburg, 2016, Journal of pediatric surgery.

Diagnosis of Pyruvate Kinase Deficiency

B. Glader, P. Gallagher, 2016, Pediatric blood & cancer.

Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants

P. Newburger, D. Morton, M. Wlodarski, 2015 .

Effects of AG-348, a Pyruvate Kinase Activator, on Anemia and Hemolysis in Patients with Pyruvate Kinase Deficiency: Data from the DRIVE PK Study

D. Morton, C. Kung, J. Hixon, 2016 .

Erratum: CORRIGENDUM: Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response

M. Kay, M. Ozelo, J. F. Wright, 2006 .

Novel protocol including liver biopsy to identify and treat CD8+ T‐cell predominant acute hepatitis and liver failure

L. Hofmann, K. Nadeau, B. Glader, 2014, Pediatric transplantation.

The Genetic Landscape of Diamond-Blackfan Anemia.

Beryl B. Cummings, Jacob C. Ulirsch, Michael H. Guo, 2019, American journal of human genetics.

Clinical outcomes of splenectomy in children: Report of the splenectomy in congenital hemolytic anemia registry

J. Scott, Rebeccah L. Brown, C. Thornburg, 2015, American journal of hematology.

ERRATUM: People to watch

J. Rasko, M. Kay, J. Zehnder, 2006, Nature Medicine.

Leucine for the Treatment of Transfusion Dependence in Patients with Diamond Blackfan Anemia

Ellen V. Muir, G. Nalepa, J. Lipton, 2018, Blood.

Platelet-associated immunoglobulin G in childhood idiopathic thrombocytopenic purpura.

N. Cheung, M. Hilgartner, B. Glader, 1983, The Journal of pediatrics.

Cold agglutinin syndrome in pediatric liver transplant recipients

J. Merker, B. Glader, M. Fontaine, 2007, Pediatric transplantation.

Anemia in Children

B. Glader, W. Wong, 2017 .

Comparative Monovalent Cation Transport in Neonatal and Adult Red Blood Cells

B. Ramsey, B. Glader, A. Muller-Soyano, 1984, Pediatric Research.

Erythrocyte disorders leading to potassium loss and cellular dehydration.

B. Glader, D. Sullivan, 1979, Progress in clinical and biological research.

Hb F-M-Osaka or alpha 2G gamma 2(63)(E7)His----Tyr in a Caucasian male infant.

A. Kutlar, B. Glader, T. Huisman, 1989, Hemoglobin.

Point-of-Care Quantitative Measure of Glucose-6-Phosphate Dehydrogenase Enzyme Deficiency

Michael Kaplan, Bertil Glader, Vamsee Pamula, 2015, Pediatrics.

The Pyruvate Kinase Deficiency Global Longitudinal (Peak) Registry: rationale and study design

D. Pospíšilová, V. Viprakasit, Junlong Li, 2023, BMJ Open.

Adrenal and renal corticomedullary junction iron deposition in red cell aplasia

S. Vasanawala, Huanzhou Yu, B. Glader, 2010, Pediatric Radiology.

The variable manifestations of disease in pyruvate kinase deficiency and their management

B. Glader, P. Bianchi, H. Al‐Samkari, 2020, Haematologica.

Monovalent cation changes in sickle erythrocytes: a direct reflection of alpha-globin gene number.

B. Glader, S. Embury, K. Backer, 1985, The Journal of laboratory and clinical medicine.

Immune Thrombocytopenia in Children Less Than 1 Year of Age: A Single-institution 10-year Experience

B. Glader, W. Wong, M. Jeng, 2013, Journal of pediatric hematology/oncology.

A Congenital Anemia Reveals Distinct Targeting Mechanisms for Master Transcription Factor GATA1.

Christopher M. Vockley, A. Regev, A. Kundaje, 2022, Blood.

The birth, life, and death of red blood cells: Erythropoiesis, the mature red blood cell, and cell destruction

J. Quigley, B. Glader, R. Means, 2013 .

Chronic Infectious Mononucleosis Syndrome, Pancytopenia, and Polyclonal B‐Lymphoproliferation Terminating in Acute Lymphoblastic Leukemia

J. Finlay, M. Link, G. Wood, 1986, The American journal of pediatric hematology/oncology.

Glucose Phosphate Isomerase Deficiency In 2 Patients With Novel Mutations Presenting As Severe Neurologic Abnormalities and Transfusion Dependent Hemolytic Anemia

T. Coates, B. Glader, P. Gallagher, 2013 .

The red blood cell as a biopsy tool.

B. Glader, D. Sullivan, 1981, Clinics in Haematology.

DRIVE PK: A Phase 2 Trial of AG-348 in Patients with Pyruvate Kinase Deficiency

C. Kung, Hua Yang, B. Silver, 2015 .

Evaluation of the hemolytic role of aspirin in glucose-6-phosphate dehydrogenase deficiency.

B. Glader, 1976, The Journal of pediatrics.

Comorbidities and complications in adults with pyruvate kinase deficiency

E. Neufeld, S. Sheth, B. Glader, 2020, European journal of haematology.

Red Blood Cell Size and Glycolytic Enzyme Activity: Relationship to Number of Intramedullary Cell Divisions

O. Platt, B. Glader, A. Müller-Soyano, 1978, Pediatric Research.

Haploinsufficiency of Ribosomal Protein S6 In Mice Mimics Bone Marrow Failure Syndromes In Humans

I. Weissman, G. Barsh, K. McGowan, 2010 .

Neutral-Coating Capillary Electrophoresis Coupled with High-Resolution Mass Spectrometry for Top-Down Identification of Hemoglobin Variants.

J. Zehnder, B. Glader, R. Shi, 2022, Clinical chemistry.

Physician review of the peripheral blood smear: When and Why An opinion

David J. Blomberg, Bertil Glader, J. Nosanchuk, 2001 .

Wintrobe's clinical hematology: Fourteenth edition

F. Appelbaum, D. Arber, A. Dispenzieri, 2018 .

Clinical outcomes of splenectomy in children: Report of the splenectomy in congenital hemolytic anemia registry

J. Scott, Rebeccah L. Brown, C. Thornburg, 2015, American journal of hematology.

Energy Reserve and Cation Composition of Irreversibly Sickled Cell in Vivo

O. Platt, B. Glader, D. Nathan, 1978, British journal of haematology.

Bleeding symptoms and laboratory correlation in patients with severe von Willebrand disease

R. Watts, E. Kraut, B. Kerlin, 2009, Haemophilia.

Neonatal Hematology: Neonatal hemolysis

B. Glader, G. Allen, 2005 .

Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.

D. Vandorpe, S. Alper, C. Brugnara, 2011, American journal of physiology. Cell physiology.

Urea Infusions in Normal Individuals

B. Glader, M. Conrad, T. A. Bensinger, 2017 .