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	1.	Hb Johnstown [beta109(G11)Val-->Leu]: A high oxygen affinity variant associated with beta0-thalassemia. [electronic resource] by Feliu-Torres, Aurora Eberle, Silvia Eandi Roldán, Ariel González, Silvia Sciuccati, Gabriela Producer: 20050511 In: Hemoglobin vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Von Willebrand disease in children: diagnosis and management of a pediatric cohort in one single center in Argentina. [electronic resource] by Bonduel, Mariana Frontroth, Juan Pablo Hepner, Mirta Sciuccati, Gabriela Feliu-Torres, Aurora Pieroni, Graciela Producer: 20120328 In: Seminars in thrombosis and hemostasis vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Prospective study of low-dose ristocetin-induced platelet aggregation to identify type 2B von Willebrand disease (VWD) and platelet-type VWD in children. [electronic resource] by Frontroth, Juan Pablo Hepner, Mirta Sciuccati, Gabriela Feliú Torres, Aurora Pieroni, Graciela Bonduel, Mariana Producer: 20110324 In: Thrombosis and haemostasis vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Factor V Leiden and prothrombin gene G20210A mutation in children with venous thromboembolism. [electronic resource] by Bonduel, Mariana Hepner, Mirta Sciuccati, Gabriela Pieroni, Graciela Feliú-Torres, Aurora Mardaraz, Claudia Frontroth, Juan Pablo Producer: 20030825 In: Thrombosis and haemostasis vol. 87 Availability: No items available. Save to lists Add to cart (remove)
	5.	α-globin gene quadruplication and heterozygous β-thalassemia: a not so rare cause of thalassemia intermedia. [electronic resource] by Origa, Raffaella Sollaino, Maria Carla Borgna-Pignatti, Caterina Piga, Antonio Feliu Torres, Aurora Masile, Valentina Galanello, Renzo Producer: 20140602 In: Acta haematologica vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Hb Southampton [beta106(G8)Leu-->Pro, CTG-->CCG] in an Argentinean boy. [electronic resource] by Eandi Eberle, Silvia Noguera, Nélida I Sciuccati, Gabriela Bonduel, Mariana Díaz, Lilian Staciuk, Raquel Feliu-Torres, Aurora Producer: 20060810 In: Hemoglobin vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	[Hereditary xerocytosis. Presentation of two pediatric cases]. [electronic resource] by Eandi Eberle, Silvia Pepe, Carolina Aguirre, Fernando Milanesio, Berenice Fernández, Diego Ávalos Gómez, Vanesa Kinen, Analía Feliu Torres, Aurora Producer: 20200826 In: Archivos argentinos de pediatria vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Hb Alesha [beta67(E11)Val-->Met, GTG-->ATG] in an Argentinean girl. [electronic resource] by Eberle, Silvia Eandi Noguera, Nélida I Sciuccati, Gabriela Bonduel, Mariana Díaz, Lilian Staciuk, Raquel Targovnik, Héctor M Feliu-Torres, Aurora Producer: 20071005 In: Hemoglobin vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Two novel DNA variants associated with glucose-6-phosphate dehydrogenase deficiency found in Argentine pediatric patients. [electronic resource] by Chaves, Alejandro Eberle, Silvia Eandi Defelipe, Lucas Pepe, Carolina Milanesio, Berenice Aguirre, Fernando Fernandez, Diego Turjanski, Adrian Feliú-Torres, Aurora Producer: 20170214 In: Clinical biochemistry vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Corrigendum to 'Two novel DNA variants associated with glucose-6-phosphate dehydrogenase deficiency found in Argentine pediatric patients' [Clin. Biochem. 49 (2016) 808-810]. [electronic resource] by Chaves, Alejandro Eandi Eberle, Silvia Defelipe, Lucas Pepe, Carolina Milanesio, Berenice Aguirre, Fernando Fernandez, Diego Turjanski, Adrian Feliú-Torres, Aurora Publication details: Clinical biochemistry 08 2018 In: Clinical biochemistry vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	[Hemoglobin Woodville associated with double point mutation in the gene of glucose-6-phosphate dehydrogenase]. [electronic resource] by Mansini, Adrián P Fernández, Diego A Aguirre, Fernando M Pepe, Carolina Milanesio, Berenice Chaves, Alejandro Eandi Eberle, Silvia Feliú Torres, Aurora Producer: 20160602 In: Medicina vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	12.	[Glucose 6 phosphate dehydrogenase deficiency: a case series]. [electronic resource] by Eandi Eberle, Silvia García Rosolen, Nerina Urtasun, Carolina Sciuccati, Gabriela Díaz, Lilian Savietto, Valeria Candás, Andrea Avalos Gómez, Vanesa Cervio, Carolina Bonduel, Mariana Feliú Torres, Aurora Producer: 20120110 In: Archivos argentinos de pediatria vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	[Severe hemolytic anemia due to hemoglobin Southampton: case report]. [electronic resource] by Avalos Gómez, Vanesa Eandi Eberle, Silvia Pepe, Carolina Sciuccati, Gabriela García Rosolen, Nerina Cervio, Carolina Díaz, Lilian Candás, Andrea Bonduel, Mariana Piazza, Guillermo Chaves, Darío Feliú Torres, Aurora Producer: 20131119 In: Archivos argentinos de pediatria vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	[Beta thalassemia intermedia: clinical characteristics and molecular analysis. Case series]. [electronic resource] by Eandi Eberle, Silvia Pepe, Carolina Aguirre, Fernando Milanesio, Berenice Fernández, Diego Mansini, Adrián Chávez, Alejandro Sciuccati, Gabriela Díaz, Lilian Candás, Andrea Avalos Gómez, Vanesa Bonduel, Mariana Feliú Torres, Aurora Producer: 20170707 In: Archivos argentinos de pediatria vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Phenotypic and genotypic characterization of glucose-6-phosphate dehydrogenase deficiency in Argentina. Retrospective and descriptive study. [electronic resource] by Eandi Eberle, Silvia Pepe, Carolina Chaves, Alejandro Aguirre, Fernando Milanesio, Berenice Fernández, Diego Ávalos Gómez, Vanesa Sciuccati, Gabriela Díaz, Lilian A Candas, Andrea Cervio, Carolina Bonduel, Mariana Feliu Torres, Aurora Producer: 20200716 In: Archivos argentinos de pediatria vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Hb S-San Martin: a new sickling hemoglobin with two amino acid substitutions [β6(A3)Glu→Val;β105(G7)Leu→Pro] in an Argentinean family. [electronic resource] by Feliu-Torres, Aurora Eberle, Silvia Eandi Bragós, Irma M Sciuccati, Gabriela Ojeda, Mara J Calvo, Karina L Voss, María E Pratti, Arianna F Milani, Angela C Bonduel, Mariana Díaz, Lilian Noguera, Nélida I Producer: 20110303 In: Hemoglobin vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	A new β(0) frameshift mutation, HBB: c.44delT (p.Leu14ArgfsX5), identified in an Argentinean family associated with secondary genetic modifiers of β-thalassemia. [electronic resource] by Pepe, Carolina Eberle, Silvia Eandi Chaves, Alejandro Milanesio, Berenice Aguirre, Fernando M Gómez, Vanesa Avalos Diaz, Lilian Mansini, Adrian P Fernandez, Diego A Sciuccati, Gabriela Candas, Andrea Cervio, Carolina Bonduel, Mariana Feliú-Torres, Aurora Producer: 20150708 In: Hemoglobin vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)