Publications
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Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.
Andolfo I,
Alper SL, De Franceschi L, Auriemma C, Russo R, De Falco L, Vallefuoco F, Esposito MR, Vandorpe DH, Shmukler BE, Narayan R, Montanaro D, D'Armiento M, Vetro A, Limongelli I, Zuffardi O, Glader BE, Schrier SL, Brugnara C, Stewart GW, Delaunay J, Iolascon A.
Blood.
2013;
121
(19):
3925-35
-
Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia.
Gazda HT,
Preti M, Sheen MR, O'Donohue MF, Vlachos A, Davies SM, Kattamis A, Doherty L, Landowski M, Buros C, Ghazvinian R, Sieff CA, Newburger PE, Niewiadomska E, Matysiak M, Glader B, Atsidaftos E, Lipton JM, Gleizes PE, Beggs AH.
Hum Mutat.
2012;
33
(7):
1037-44
-
Adenovirus-associated virus vector-mediated gene transfer in hemophilia B.
Nathwani AC,
Tuddenham EG, Rangarajan S, Rosales C, McIntosh J, Linch DC, Chowdary P, Riddell A, Pie AJ, Harrington C, O'Beirne J, Smith K, Pasi J, Glader B, Rustagi P, Ng CY, Kay MA, Zhou J, Spence Y, Morton CL, Allay J, Coleman J, Sleep S, Cunningham JM, Srivastava D, Basner-Tschakarjan E, Mingozzi F, High KA, Gray JT, Reiss UM, Nienhuis AW, Davidoff AM.
N Engl J Med.
2011;
365
(25):
2357-65
-
Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.
Stewart AK,
Kedar PS, Shmukler BE, Vandorpe DH, Hsu A, Glader B, Rivera A, Brugnara C, Alper SL.
Am J Physiol Cell Physiol.
2011;
300
(5):
C1034-46
-
Reduced ribosomal protein gene dosage and p53 activation in low-risk myelodysplastic syndrome.
McGowan KA,
Pang WW, Bhardwaj R, Perez MG, Pluvinage JV, Glader BE, Malek R, Mendrysa SM, Weissman IL, Park CY, Barsh GS.
Blood.
2011;
118
(13):
3622-33
-
Adrenal and renal corticomedullary junction iron deposition in red cell aplasia.
Rakow-Penner R,
Glader B, Yu H, Vasanawala S.
Pediatr Radiol.
2010;
40
(12):
1955-7
-
Development of antibodies to human thrombin and factor V in a pediatric patient exposed to topical bovine thrombin.
Lo CY,
Jones C, Glader B, Zehnder JL.
Pediatr Blood Cancer.
2010;
55
(6):
1195-7
-
Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia.
Doherty L,
Sheen MR, Vlachos A, Choesmel V, O'Donohue MF, Clinton C, Schneider HE, Sieff CA, Newburger PE, Ball SE, Niewiadomska E, Matysiak M, Glader B, Arceci RJ, Farrar JE, Atsidaftos E, Lipton JM, Gleizes PE, Gazda HT.
Am J Hum Genet.
2010;
86
(2):
222-8
-
Monthly recombinant tissue plasminogen activator administration to implantable central venous access devices decreases infections in children with haemophilia.
Jeng MR,
O'Brien M, Wong W, Zoland J, Lea J, Tang N, Glader B.
Haemophilia.
2009;
15
(6):
1272-80
-
One year follow-up of children and adolescents with chronic immune thrombocytopenic purpura (ITP) treated with rituximab.
Mueller BU,
Bennett CM, Feldman HA, Bussel JB, Abshire TC, Moore TB, Sawaf H, Loh ML, Rogers ZR, Glader BE, McCarthy MC, Mahoney DH, Olson TA, Feig SA, Lorenzana AN, Mentzer WC, Buchanan GR, Neufeld EJ.
Pediatr Blood Cancer.
2009;
52
(2):
259-62
-
Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.
Vlachos A,
Ball S, Dahl N, Alter BP, Sheth S, Ramenghi U, Meerpohl J, Karlsson S, Liu JM, Leblanc T, Paley C, Kang EM, Leder EJ, Atsidaftos E, Shimamura A, Bessler M, Glader B, Lipton JM.
Br J Haematol.
2008;
142
(6):
859-76
-
Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients.
Gazda HT,
Sheen MR, Vlachos A, Choesmel V, O'Donohue MF, Schneider H, Darras N, Hasman C, Sieff CA, Newburger PE, Ball SE, Niewiadomska E, Matysiak M, Zaucha JM, Glader B, Niemeyer C, Meerpohl JJ, Atsidaftos E, Lipton JM, Gleizes PE, Beggs AH.
Am J Hum Genet.
2008;
83
(6):
769-80
-
Cold agglutinin syndrome in pediatric liver transplant recipients.
Wong W,
Merker JD, Nguyen C, Berquist W, Jeng M, Viele M, Glader B, Fontaine MJ.
Pediatr Transplant.
2007;
11
(8):
931-6
-
Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura.
Bennett CM,
Rogers ZR, Kinnamon DD, Bussel JB, Mahoney DH, Abshire TC, Sawaf H, Moore TB, Loh ML, Glader BE, McCarthy MC, Mueller BU, Olson TA, Lorenzana AN, Mentzer WC, Buchanan GR, Feldman HA, Neufeld EJ.
Blood.
2006;
107
(7):
2639-42
-
Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia.
Gazda HT,
Grabowska A, Merida-Long LB, Latawiec E, Schneider HE, Lipton JM, Vlachos A, Atsidaftos E, Ball SE, Orfali KA, Niewiadomska E, Da Costa L, Tchernia G, Niemeyer C, Meerpohl JJ, Stahl J, Schratt G, Glader B, Backer K, Wong C, Nathan DG, Beggs AH, Sieff CA.
Am J Hum Genet.
2006;
79
(6):
1110-8
-
Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response.
Manno CS,
Pierce GF, Arruda VR, Glader B, Ragni M, Rasko JJ, Rasko J, Ozelo MC, Hoots K, Blatt P, Konkle B, Dake M, Kaye R, Razavi M, Zajko A, Zehnder J, Rustagi PK, Nakai H, Chew A, Leonard D, Wright JF, Lessard RR, Sommer JM, Tigges M, Sabatino D, Luk A, Jiang H, Mingozzi F, Couto L, Ertl HC, High KA, Kay MA.
Nat Med.
2006;
12
(3):
342-7
-
AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B.
Manno CS,
Chew AJ, Hutchison S, Larson PJ, Herzog RW, Arruda VR, Tai SJ, Ragni MV, Thompson A, Ozelo M, Couto LB, Leonard DG, Johnson FA, McClelland A, Scallan C, Skarsgard E, Flake AW, Kay MA, High KA, Glader B.
Blood.
2003;
101
(8):
2963-72
-
Approach to the bleeding child.
Allen GA,
Glader B.
Pediatr Clin North Am.
2002;
49
(6):
1239-56
-
Resolution of severe Donath-Landsteiner autoimmune hemolytic anemia temporally associated with institution of plasmapheresis.
Roy-Burman A,
Glader BE.
Crit Care Med.
2002;
30
(4):
931-4
-
Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemia.
Gripp KW,
McDonald-McGinn DM, La Rossa D, McGain D, Federman N, Vlachos A, Glader BE, McKenzie SE, Lipton JM, Zackai EH.
Am J Med Genet.
2001;
101
(3):
268-74
-
Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease.
Gazda H,
Lipton JM, Willig TN, Ball S, Niemeyer CM, Tchernia G, Mohandas N, Daly MJ, Ploszynska A, Orfali KA, Vlachos A, Glader BE, Rokicka-Milewska R, Ohara A, Baker D, Pospisilova D, Webber A, Viskochil DH, Nathan DG, Beggs AH, Sieff CA.
Blood.
2001;
97
(7):
2145-50
-
Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector.
Kay MA,
Manno CS, Ragni MV, Larson PJ, Couto LB, McClelland A, Glader B, Chew AJ, Tai SJ, Herzog RW, Arruda V, Johnson F, Scallan C, Skarsgard E, Flake AW, High KA.
Nat Genet.
2000;
24
(3):
257-61
-
Hemolytic anemia in children.
Glader BE,
Clin Lab Med.
1999;
19
(1):
87-111, vi
-
Bone marrow transplant in thalassemia. A role for radiation?
Lee YS,
Kristovich KM, Ducore JM, Vichinsky E, Crouse VL, Glader BE, Amylon MD.
Ann N Y Acad Sci.
1998:
850
503-5
-
Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitors.
Key NS,
Aledort LM, Beardsley D, Cooper HA, Davignon G, Ewenstein BM, Gilchrist GS, Gill JC, Glader B, Hoots WK, Kisker CT, Lusher JM, Rosenfield CG, Shapiro AD, Smith H, Taft E.
Thromb Haemost.
1998;
80
(6):
912-8
-
Acute idiopathic thrombocytopenic purpura--management in childhood.
Buchanan GR,
de Alarcon PA, Feig SA, Gilchrist GS, Lukens JN, Moertel CL, Cohen AR, Dickerman JD, Forman EN, Glader BE, Lusher JM.
Blood.
1997;
89
(4):
1464-5; author reply 1466
-
Hematologic disorders in children from southeast Asia.
Glader BE,
Look KA.
Pediatr Clin North Am.
1996;
43
(3):
665-81
-
Loss of elbow and wrist motion in hemophilia.
Gamble JG,
Vallier H, Rossi M, Glader B.
Clin Orthop Relat Res.
1996;
(328):
94-101
-
Frequency of inhibitor development in haemophiliacs treated with low-purity factor VIII.
Addiego J,
Kasper C, Abildgaard C, Hilgartner M, Lusher J, Glader B, Aledort L.
Lancet.
1993;
342
(8869):
462-4
-
Langerhans' cell histiocytosis presenting with the superior vena cava syndrome: a case report.
Mogul M,
Hartman G, Donaldson S, Gelb A, Link M, Amylon M, Glader B.
Med Pediatr Oncol.
1993;
21
(6):
456-9
-
Arthropathy of the ankle in hemophilia.
Gamble JG,
Bellah J, Rinsky LA, Glader B.
J Bone Joint Surg Am.
1991;
73
(7):
1008-15
-
Cryptococcus infection in a nine-year-old child with hemophilia and the acquired immunodeficiency syndrome.
Ting SF,
Glader BE, Prober CG.
Pediatr Infect Dis J.
1991;
10
(1):
76-7
-
Congenital hypoplastic (Diamond-Blackfan) anemia in seven members of one kindred.
Viskochil DH,
Carey JC, Glader BE, Rothstein G, Christensen RD.
Am J Med Genet.
1990;
35
(2):
251-6
-
Red blood cell aplasias in children.
Glader BE,
Pediatr Ann.
1990;
19
(3):
168-9, 173-6
-
Treatment of neutropenia associated with dyskeratosis congenita with granulocyte-macrophage colony-stimulating factor.
Russo CL,
Glader BE, Israel RJ, Galasso F.
Lancet.
1990;
336
(8717):
751-2
-
Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7.
Shannon KM,
Turhan AG, Chang SS, Bowcock AM, Rogers PC, Carroll WL, Cowan MJ, Glader BE, Eaves CJ, Eaves AC.
J Clin Invest.
1989;
84
(3):
984-9
-
Hb F-M-Osaka or alpha 2G gamma 2(63)(E7)His----Tyr in a Caucasian male infant.
Glader BE,
Zwerdling D, Kutlar F, Kutlar A, Wilson JB, Huisman TH.
Hemoglobin.
1989;
13
(7-8):
769-73
-
Hemoglobin FM-Fort Ripley: another lesson from the neonate.
Glader BE,
Pediatrics.
1989;
83
(5):
792-3
-
Reduced neutrophil counts in children with transient erythroblastopenia of childhood.
Rogers ZR,
Bergstrom SK, Amylon MD, Buchanan GR, Glader BE.
J Pediatr.
1989;
115
(5 Pt 1):
746-8
-
SUP-HD1: a new Hodgkin's disease-derived cell line with lymphoid features produces interferon-gamma.
Naumovski L,
Utz PJ, Bergstrom SK, Morgan R, Molina A, Toole JJ, Glader BE, McFall P, Weiss LM, Warnke R.
Blood.
1989;
74
(8):
2733-42
-
Clinical and biologic characterization of T-cell neoplasias with rearrangements of chromosome 7 band q34.
Smith SD,
Morgan R, Gemmell R, Amylon MD, Link MP, Linker C, Hecht BK, Warnke R, Glader BE, Hecht F.
Blood.
1988;
71
(2):
395-402
-
Elevated red cell adenosine deaminase activity: a marker of disordered erythropoiesis in Diamond-Blackfan anaemia and other haematologic diseases.
Glader BE,
Backer K.
Br J Haematol.
1988;
68
(2):
165-8
-
Philadelphia chromosome-positive acute lymphoblastic leukemia cell lines without classical breakpoint cluster region rearrangement.
Naumovski L,
Morgan R, Hecht F, Link MP, Glader BE, Smith SD.
Cancer Res.
1988;
48
(10):
2876-9
-
Transient erythroblastopenia of childhood.
Glader BE,
West J Med.
1988;
149
(4):
453-4
-
Diagnosis and management of red cell aplasia in children.
Glader BE,
Hematol Oncol Clin North Am.
1987;
1
(3):
431-47
-
Establishment and characterization of a common acute lymphoblastic leukemia cell line with a deletion of chromosome 3 band q26.
Smith SD,
Morgan R, Galili N, Amylon MD, Link MP, Hecht F, Sklar J, Glader BE.
Cancer Res.
1987;
47
(6):
1652-6
-
Chronic infectious mononucleosis syndrome, pancytopenia, and polyclonal B-lymphoproliferation terminating in acute lymphoblastic leukemia.
Finlay J,
Luft B, Yousem S, Wood GS, Link M, Arvin A, Glader B, Lennette E, Shatsky M, Olds L.
Am J Pediatr Hematol Oncol.
1986;
8
(1):
18-27
-
Comparative activity of erythrocyte adenosine deaminase and orotidine decarboxylase in Diamond-Blackfan anemia.
Glader BE,
Backer K.
Am J Hematol.
1986;
23
(2):
135-9
-
Pancytopenia with myelofibrosis. An unusual presentation of childhood Hodgkin's disease.
Carroll WL,
Berberich FR, Glader BE.
Clin Pediatr (Phila).
1986;
25
(2):
106-8
-
Prednisone stimulation of erythropoiesis in leukemic children during remission.
Amylon MD,
Perrine SP, Glader BE.
Am J Hematol.
1986;
23
(2):
179-81
-
Pyruvate kinase deficiency in dog and human erythrocytes: effects of energy depletion on cation composition and cellular hydration.
Muller-Soyano A,
Platt O, Glader BE.
Am J Hematol.
1986;
23
(3):
217-21
-
Screening for anemia and erythrocyte disorders in children.
Glader BE,
Pediatrics.
1986;
78
(2):
368-9
-
Transient erythroblastopenia of adolescence.
Zwerdling T,
Finlay J, Glader BE.
Clin Pediatr (Phila).
1986;
25
(11):
563-5
-
Childhood bone marrow monosomy 7 syndrome: a familial disorder?
Carroll WL,
Morgan R, Glader BE.
J Pediatr.
1985;
107
(4):
578-80
-
Monovalent cation changes in sickle erythrocytes: a direct reflection of alpha-globin gene number.
Embury SH,
Backer K, Glader BE.
J Lab Clin Med.
1985;
106
(1):
75-9
-
Acute nonlymphocytic leukemia developing during the course of Ewing's sarcoma.
Link MP,
Donaldson SS, Kempson RL, Wilbur JR, Glader BE.
Med Pediatr Oncol.
1984;
12
(3):
194-200
-
Comparative monovalent cation transport in neonatal and adult red blood cells.
Muller-Soyano A,
Ramsey BW, Glader BE.
Pediatr Res.
1984;
18
(8):
778-80
-
Fatal myocardial infarction following therapy with prothrombin complex concentrates in a young man with hemophilia A.
Sullivan DW,
Purdy LJ, Billingham M, Glader BE.
Pediatrics.
1984;
74
(2):
279-81
-
Immune thrombocytopenia associated with acute nonlymphocytic leukemia.
Amylon MD,
Link MP, Glader BE.
J Pediatr.
1984;
105
(5):
776-8
-
Monoclonal antibody and enzymatic profiles of human malignant T-lymphoid cells and derived cell lines.
Smith SD,
Shatsky M, Cohen PS, Warnke R, Link MP, Glader BE.
Cancer Res.
1984;
44
(12 Pt 1):
5657-60
-
Elevated erythrocyte adenosine deaminase activity in congenital hypoplastic anemia.
Glader BE,
Backer K, Diamond LK.
N Engl J Med.
1983;
309
(24):
1486-90
-
Platelet-associated immunoglobulin G in childhood idiopathic thrombocytopenic purpura.
Cheung NK,
Hilgartner MW, Schulman I, McFall P, Glader BE.
J Pediatr.
1983;
102
(3):
366-70
-
The red blood cell as a biopsy tool.
Glader BE,
Sullivan DW.
Clin Haematol.
1981;
10
(1):
209-22
-
Erythrocyte enzyme disorders in children.
Sullivan DW,
Glader BE.
Pediatr Clin North Am.
1980;
27
(2):
449-62
-
Hereditary spherocytosis.
Sullivan DW,
Glader BE.
Pediatr Ann.
1980;
9
(8):
308-11
-
Eosinophilia in children.
Foung S,
Glader BE.
Pediatr Ann.
1979;
8
(6):
39-51
-
Erythrocyte disorders leading to potassium loss and cellular dehydration.
Glader BE,
Sullivan DW.
Prog Clin Biol Res.
1979:
30
503-13
-
Microcytosis associated with sickle cell anemia.
Glader BE,
Propper RD, Buchanan GR.
Am J Clin Pathol.
1979;
72
(1):
63-4
-
Cation permeability alterations during sickling: relationship to cation composition and cellular hydration of irreversibly sickled cells.
Glader BE,
Nathan DG.
Blood.
1978;
51
(5):
983-9
-
Energy reserve and cation composition of irreversibly sickled cells in vivo.
Glader BE,
Lux SE, Muller-Soyano A, Platt OS, Propper RD, Nathan DG.
Br J Haematol.
1978;
40
(4):
527-32
-
Haemolytic disorders of infancy.
Glader BE,
Platt O.
Clin Haematol.
1978;
7
(1):
35-61
-
Leukocyte counts in children with sickle cell disease. Comparative values in the steady state, vaso-occlusive crisis, and bacterial infection.
Buchanan GR,
Glader BE.
Am J Dis Child.
1978;
132
(4):
396-8
-
Physiologic features of hemolysis axxociated with altered cation and 2,3-diphosphoglycerate content.
Albala MM,
Fortier NL, Glader BE.
Blood.
1978;
52
(1):
135-41
-
Red blood cell size and glycolytic enzyme activity: relationship to number of intramedullary cell divisions.
Glader BE,
McCrimmons D, Müller-Soyano A, Platt O.
Pediatr Res.
1978;
12
(4 Pt 1):
308-9
-
Benign course of extreme hyperbilirubinemia in sickle cell anemia: analysis of six cases.
Buchanan GR,
Glader BE.
J Pediatr.
1977;
91
(1):
21-4
-
Cation specificity of propranolol-induced changes in RBC membrane permeability: comparative effects in human, dog and cat erythrocytes.
Müller-Soyano A,
Glader BE.
J Cell Physiol.
1977;
91
(2):
317-21
-
Care of the critically ill child: the bleeding neonate.
Glader BE,
Buchanan GR.
Pediatrics.
1976;
58
(4):
548-55
-
Evaluation of the hemolytic role of aspirin in glucose-6-phosphate dehydrogenase deficiency.
Glader BE,
J Pediatr.
1976;
89
(6):
1027-8
-
Salicylate-induced injury of pyruvate-kinase-deficient erythrocytes.
Glader BE,
N Engl J Med.
1976;
294
(17):
916-8
-
Energy metabolism in human erythrocytes: the role of phosphoglycerate kinase in cation transport.
Segel GB,
Feig SA, Glader BE, Muller A, Dutcher P, Nathan DG.
Blood.
1975;
46
(2):
271-8
-
Haemolysis due to pyruvate kinase deficiency and other glycolytic enzymopathies.
Glader BE,
Nathan DG.
Clin Haematol.
1975;
4
(1):
123-38
-
In vivo hepatic and intestinal toxicity of sodium cyanate in rats: cyanate-induced alterations in hepatic glycogen metabolism.
Haut MJ,
Toskes PP, Hildenbrandt PK, Glader BE, Conrad ME.
J Lab Clin Med.
1975;
85
(1):
140-54
-
Role of elevated glucose concentrations in the hemolysis of glucose-6-phosphate dehydrogenase deficient erythroycytes (38474).
Glader BE,
Proc Soc Exp Biol Med.
1975;
148
(1):
50-3
-
Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss.
Glader BE,
Fortier N, Albala MM, Nathan DG.
N Engl J Med.
1974;
291
(10):
491-6
-
Effect of cyanate on erythrocyte deformability.
Durocher JR,
Glader BE, Gaines LT, Conrad ME.
Blood.
1974;
43
(2):
277-80
-
Oncorna virus disease. The syndrome of hemolytic anemia and lymph node cystic disease.
Siegler R,
Moran S, Glader B, Lane I, Frosch Y.
Lab Invest.
1974;
30
(5):
626-38
-
Effect of cyanate on erythrocyte membrane surface charge.
Durocher JR,
Glader BE, Conrad ME.
Proc Soc Exp Biol Med.
1973;
144
(1):
249-51
-
Hemolysis by diphenylsulfones: comparative effects of DDS and hydroxylamine-DDS.
Glader BE,
Conrad ME.
J Lab Clin Med.
1973;
81
(2):
267-72
-
Intravascular hemolysis associated with intravenous urea infusions in normal individuals.
Bensinger TA,
Glader BE, Conrad ME.
Blood.
1973;
41
(3):
461-4
-
Cyanate inhibition of erythrocyte glucose-6-phosphate dehydrogenase.
Glader BE,
Conrad ME.
Nature.
1972;
237
(5354):
336-8
-
Decreased glutathione peroxidase in neonatal erythrocytes: lack of relation to hydrogen peroxide metabolism.
Glader BE,
Conrad ME.
Pediatr Res.
1972;
6
(12):
900-4
-
Mechanism of methemoglobin formation by diphenylsulfones. Effect of 4-amino-4'-hydroxyaminodiphenylsulfone and other p-substituted derivatives.
Kramer PA,
Glader BE, Li TK.
Biochem Pharmacol.
1972;
21
(9):
1265-74
-
Effect of cobalt upon iron absorption.
Schade SG,
Felsher BF, Glader BE, Conrad ME.
Proc Soc Exp Biol Med.
1970;
134
(3):
741-3
-
2,4-dinitrophenol inhibition of P32 release from human red cells.
Omachi A,
Scott CB, Glader BE.
Experientia.
1968;
24
(3):
244-5
-
Observations on the effect of testosterone and hydrocortisone on erythropoiesis.
Glader BE,
Rambach WA, Alt HL.
Ann N Y Acad Sci.
1968;
149
(1):
383-8
-
Phosphate release from human erythrocytes.
Glader BE,
Omachi A.
Biochim Biophys Acta.
1968;
163
(1):
30-6
-
Role of cellular Pi in Pi transport and metabolism in human red cells.
Glader BE,
Omachi A.
Biochim Biophys Acta.
1968;
150
(3):
524-7
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