Erytrocyte-related phenotypes and genetic susceptibility to thrombosis von Remacha, Angel F., Vilalta, Noèlia, Sardà, M. Pilar, Millón, Joan, Pujol-Moix, Nuria, Ziyatdinov, Andrey, Fontcuberta, Jordi, Nomdedeu, Josep, Soria, José Manuel, Souto, Juan Carlos

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Hydrops fetalis–associated congenital dyserythropoietic anemia treated with intrauterine transfusions and bone marrow transplantation von Remacha, Angel F., Badell, Isabel, Pujol-Moix, Núria, Parra, Juan, Muñiz-Diaz, Eduardo, Ginovart, Gemma, Sardà, M. Pilar, Hernández, Angel, Moliner, Elisenda, Torrent, Montserrat

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Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene von Altès, Albert, Bach, Vanessa, Ruiz, Angels, Esteve, Anna, Felez, Jordi, Remacha, Angel F, Sardà, M. Pilar, Baiget, Montserrat

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Vitamin B-12 metabolism in HIV-infected patients in the age of highly active antiretroviral therapy: role of homocysteine in assessing vitamin B-12 status von REMACHA, Angel F, CADAFALCH, Josep, SARDA, Pilar, BARCELO, Montserrat, FUSTER, Montserrat

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Influence of cobalamin deficiency compared with that of cobalamin absorption on serum holo-transcobalamin II von Chen, X, Remacha, A.F, Sarda, M.P, Carmel, R

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Does the SLC40A1 gene modify HFE-related haemochromatosis phenotypes? von Altès, Albert, Bach, Vanessa, Ruiz, Angels, Esteve, Anna, Remacha, Angel F, Sardà, M. Pilar, Felez, Jordi, Baiget, Montserrat

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Vitamin B12 deficiency, hyperhomocysteinemia and thrombosis: a case and control study von Remacha, Angel F., Souto, Joan Carles, Piñana, José Luis, Sardà, María Pilar, Queraltó, Josep Maria, Martí-Fabregas, Joan, García-Moll, Xavier, Férnandez, Cristina, Rodriguez, Alvaro, Cuesta, Jorge

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The “Thomas Plot”: Its Usefulness in the Assessment of Iron Status in Anemia von Canals, Carmen, Sardà, Pilar, Piazuelo, Jose María, Remacha, Ángel F.

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Hematologic response to four weeks of intermittent hypobaric hypoxia in highly trained athletes von Abellan, R, Remacha, AF, Ventura, R, Sarda, MP, Segura, J, Rodriguez, FA

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Iron Deficiency and Vitamin B12/Folate Levels. A Case-Control Study von Remacha, Angel F., Sardà, Pilar, Royo, Teresa, Fernández, Nieves, Rojas, Ester, Canals, Carmen, Altés, Albert

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Tumor cells induce COX-2 and mPGES-1 expression in microvascular endothelial cells mainly by means of IL-1 receptor activation von Casós, Kelly, Siguero, Laura, Fernández-Figueras, María-Teresa, León, Xavier, Sardá, María-Pilar, Vila, Luis, Camacho, Mercedes

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Genotype-phenotype correlation in a Spanish population homozygous for the H63D mutation of the HFE gene von Remacha, Angel F, Sardà, M Pilar, Barceló, M Jesús, Bach, Vanessa, Altès, Albert, Baiget, Montserrat, Guarner, Carlos, Blesa, Irene

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The V617F mutation of JAK2 is very uncommon in patients with thrombosis von Remacha, Angel F, Estivill, Camino, Sarda, M. Pilar, Mateo, Jose, Souto, Joan Carles, Canals, Carme, Nomdedeu, Josep, Fontcuberta, Jordi

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Early clinical impact of iron overload in stem cell transplantation. A prospective study von Altes, Albert, Remacha, Angel Francisco, Sarda, Pilar, Baiget, Montserrat, Sureda, Anna, Martino, Rodrigo, Briones, Javier, Brunet, Salut, Canals, Carme, Sierra, Jorge

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Occurrence of the JAK2 V617F mutation in the WHO provisional entity: myelodysplastic/myeloproliferative disease, unclassifiable-refractory anemia with ringed sideroblasts associate... von Remacha, AF, Nomdedeu, JF, Puget, G, Estivill, C, Sarda, MP, Canals, C, Aventin, A

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Evaluation of V617F mutation of JAK2 in negative chromosome Philadelphia chronic myeloproliferative disorders von Remacha, Angel F, Puget, Guiomar, Nomdedéu, Josep F, Estivill, Camino, Sardà, M Pilar, Canals, Carme

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Valoración de la mutación V617F del gen JAK2 en síndromes mieloproliferativos crónicos con cromosoma Filadelfia negativo von Remacha, Ángel F., Puget, Guiomar, Nomdedéu, Josep F., Estivill, Camino, Pilar Sardà, M., Canals, Carme

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Use of random amplified microsatellites to type isolates from an outbreak of nosocomial aspergillosis in a general medical ward von Guarro, Josep, Solé, María, Castany, Roser, Cano, Josep, Teixidó, Anna, Pujol, Isabel, Gené, Josepa, Castro, Antoni, Sardà, Pilar

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Genomewide linkage analysis of soluble transferrin receptor plasma levels von Remacha, Angel F, Souto, Joan C, Soria, José Manuel, Buil, Alfonso, Sardà, M Pilar, Lathrop, Mark, Blangero, John, Almasy, Laura, Fontcuberta, Jordi

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Treatment of type 1 hereditary haemochromatosis with oral magnesium von Altés, Albert, Ruiz, M Angels, Remacha, Angel F, Sardá, Pilar, Baiget, Montserrat, Sierra, Jordi

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