Managing Construction Projects: Developing Complexity into Complicatedness von Eber, W

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The international personality item pool and the future of public-domain personality measures von Goldberg, Lewis R., Johnson, John A., Eber, Herbert W., Hogan, Robert, Ashton, Michael C., Cloninger, C. Robert, Gough, Harrison G.

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Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study von Grace, Rachael F., Bianchi, Paola, van Beers, Eduard J., Eber, Stefan W., Glader, Bertil, Yaish, Hassan M., Despotovic, Jenny M., Rothman, Jennifer A., Sharma, Mukta, McNaull, Melissa M., Fermo, Elisa, Lezon-Geyda, Kimberly, Morton, D. Holmes, Neufeld, Ellis J., Chonat, Satheesh, Kollmar, Nina, Knoll, Christine M., Kuo, Kevin, Kwiatkowski, Janet L., Pospíšilová, Dagmar, Pastore, Yves D., Thompson, Alexis A., Newburger, Peter E., Ravindranath, Yaddanapudi, Wang, Winfred C., Wlodarski, Marcin W., Wang, Heng, Holzhauer, Susanne, Breakey, Vicky R., Kunz, Joachim, Sheth, Sujit, Rose, Melissa J., Bradeen, Heather A., Neu, Nolan, Guo, Dongjing, Al-Sayegh, Hasan, London, Wendy B., Gallagher, Patrick G., Zanella, Alberto, Barcellini, Wilma

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Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study von van Beers, Eduard J, van Straaten, Stephanie, Morton, D Holmes, Barcellini, Wilma, Eber, Stefan W, Glader, Bertil, Yaish, Hassan M, Chonat, Satheesh, Kwiatkowski, Janet L, Rothman, Jennifer A, Sharma, Mukta, Neufeld, Ellis J, Sheth, Sujit, Despotovic, Jenny M, Kollmar, Nina, Pospíšilová, Dagmar, Knoll, Christine M, Kuo, Kevin, Pastore, Yves D, Thompson, Alexis A, Newburger, Peter E, Ravindranath, Yaddanapudi, Wang, Winfred C, Wlodarski, Marcin W, Wang, Heng, Holzhauer, Susanne, Breakey, Vicky R, Verhovsek, Madeleine, Kunz, Joachim, McNaull, Melissa A, Rose, Melissa J, Bradeen, Heather A, Addonizio, Kathryn, Li, Anran, Al-Sayegh, Hasan, London, Wendy B, Grace, Rachael F

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Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis von Eber, Stefan W, Gonzalez, Jennifer M, Lux, Marcia L, Scarpa, Alphonse L, Tse, William T, Dornwell, Marion, Herbers, Jutta, Kugler, Wilfried, Ozcan, Refik, Pekrun, Arnulf, Gallagher, Patrick G, Schroter, Werner, Forget, Bernard G, Lux, Samuel E

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Comorbidities and complications in adults with pyruvate kinase deficiency von Boscoe, Audra N., Yan, Yan, Hedgeman, Elizabeth, van Beers, Eduard J., Al‐Samkari, Hanny, Barcellini, Wilma, Eber, Stefan W., Glader, Bertil, Yaish, Hassan M., Chonat, Satheesh, Sharma, Mukta, Kuo, Kevin H. M., Neufeld, Ellis J., Wang, Heng, Verhovsek, Madeleine, Sheth, Sujit, Grace, Rachael F.

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Pyruvate kinase deficiency in children von Chonat, Satheesh, Eber, Stefan W., Holzhauer, Susanne, Kollmar, Nina, Morton, D. Holmes, Glader, Bertil, Neufeld, Ellis J., Yaish, Hassan M., Rothman, Jennifer A., Sharma, Mukta, Ravindranath, Yaddanapudi, Wang, Heng, Breakey, Vicky R., Sheth, Sujit, Bradeen, Heather A., Al‐Sayegh, Hasan, London, Wendy B., Grace, Rachael F.

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Mode of splenectomy and immunogenicity of meningococcal vaccination in patients with hereditary spherocytosis von Stoehr, G. A., Luecken, J., Zielen, S., Eber, S. W., Borrow, R., Rose, M. A.

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Characterization of the severe phenotype of pyruvate kinase deficiency von Al‐Samkari, Hanny, Beers, Eduard J., Morton, D. Holmes, Barcellini, Wilma, Eber, Stefan W., Glader, Bertil, Yaish, Hassan M., Chonat, Satheesh, Kuo, Kevin H. M., Kollmar, Nina, Despotovic, Jenny M., Pospíšilová, Dagmar, Knoll, Christine M., Kwiatkowski, Janet L., Pastore, Yves D., Thompson, Alexis A., Wlodarski, Marcin W., Ravindranath, Yaddanapudi, Rothman, Jennifer A., Wang, Heng, Holzhauer, Susanne, Breakey, Vicky R., Verhovsek, Madeleine M., Kunz, Joachim, Sheth, Sujit, Sharma, Mukta, Rose, Melissa J., Bradeen, Heather A., McNaull, Melissa N., Addonizio, Kathryn, Al‐Sayegh, Hasan, London, Wendy B., Grace, Rachael F.

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Near-total splenectomy: A new technique for the management of hereditary spherocytosis von STOEHR, Gerhard A, STAUFFER, Urs G, EBER, Stefan W

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Health-related quality of life and fatigue in children and adults with pyruvate kinase deficiency von Al-Samkari, Hanny, van Beers, Eduard J., Morton, D. Holmes, Eber, Stefan W., Chonat, Satheesh, Kuo, Kevin H.M., Kollmar, Nina, Wang, Heng, Breakey, Vicky R., Sheth, Sujit, Sharma, Mukta, Forbes, Peter W., Klaassen, Robert J., Grace, Rachael F.

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Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants von Bianchi, Paola, Fermo, Elisa, Lezon-Geyda, Kimberly, Gallagher, Patrick G., Morton, D Holmes, Barcellini, Wilma, Glader, Bertil, Eber, Stefan W., Despotovic, Jenny M., Knoll, Christine M., Yaish, Hassan M., Newburger, Peter E., Rothman, Jennifer, Thompson, Alexis A., Ravindranath, Yaddanapudi, Nottage, Kerri A, Wang, Heng, van Beers, Eduard J., Kunz, Joachim, Wlodarski, Marcin W, Sharma, Mukta, Rose, Melissa J., Pastore, Yves D., Giardina, Patricia J., Rhodes, Melissa, Kuo, Kevin, Guo, Dongjing, London, Wendy B., Grace, Rachael F.

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Diagnosis and management of pyruvate kinase deficiency: international expert guidelines von Al-Samkari, Hanny, Shehata, Nadine, Lang-Robertson, Kelly, Bianchi, Paola, Glenthøj, Andreas, Sheth, Sujit, Neufeld, Ellis J, Rees, David C, Chonat, Satheesh, Kuo, Kevin H M, Rothman, Jennifer A, Barcellini, Wilma, van Beers, Eduard J, Pospíšilová, Dagmar, Shah, Ami J, van Wijk, Richard, Glader, Bertil, Mañú Pereira, Maria Del Mar, Andres, Oliver, Kalfa, Theodosia A, Eber, Stefan W, Gallagher, Patrick G, Kwiatkowski, Janet L, Galacteros, Frédéric, Lander, Carl, Watson, Alejandra, Elbard, Riyad, Peereboom, Dore, Grace, Rachael F

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Interactions between intelligence and personality: results from two large samples von Austin, Elizabeth J, Hofer, Scott M, Deary, Ian J, Eber, Herbert W

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Favorable response of pediatric stem cell recipients to human protein C concentrate substitution for veno-occlusive disease von Eber, S. W., Gungor, T., Veldman, A., Sykora, K., Scherer, F., Fischer, D., Grigull, L.

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Immunogenicity of sequential pneumococcal vaccination in subjects splenectomised for hereditary spherocytosis von Stoehr, Gerhard A., Rose, Markus A., Eber, Stefan W., Heidemann, Katrin, Schubert, Ralf, Zielen, Stefan

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Near‐total splenectomy for hereditary spherocytosis: clinical prospects in relation to disease severity von Stoehr, Gerhard A., Sobh, Julian N., Luecken, Jan, Heidemann, Kathrin, Mittler, Uwe, Hilgers, Reinhard, Eber, Stefan W.

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Frequency of very late fatal sepsis after splenectomy for hereditary spherocytosis : impact of insufficient antibody response to pneumococcal infection von EBER, S. W, LANGENDÖRFER, C. M, DITZIG, M, REINHARDT, D, STÖHR, G, SOLDAN, W, SCHRÖTER, W, TCHERNIA, G

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Application of RHD and RHCE genotyping for correct blood group determination in chronically transfused patients von Legler, T.J., Eber, S.W., Lakomek, M., Lynen, R., Maas, J.H., Pekrun, A., Repas-Humpe, M., Schröter, W., Köhler, M.

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Radiographic and MRI features of deferiprone-related arthropathy of the knees in patients with β-thalassemia von KELLENBERGER, Christian J, SCHMUGGE, Markus, SAURENMANN, Traudel, DI GENNARO, Lin, EBER, Stefan W, WILLI, Ulrich V, BABYN, Paul S

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