J. Goede

发表

Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1

H. Lutz, A. Iolascon, R. Ficarella, 2005, Nature Genetics.

Washing stored red blood cells in an albumin solution improves their morphologic and hemorheologic properties

S. Shevkoplyas, A. Makhro, A. Bogdanova, 2015, Transfusion.

Oral iron supplements increase hepcidin and decrease iron absorption from daily or twice-daily doses in iron-depleted young women.

D. Swinkels, G. Brittenham, H. Tjalsma, 2015, Blood.

Diagnosis of hypersplenism with the epinephrine stimulation test - 23 years of experience at a tertiary care hospital.

J. Fehr, B. Misselwitz, J. Goede, 2012, Swiss medical weekly.

South‐east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects

L. Bruce, G. Stewart, Penny J Harrison, 2011, British journal of haematology.

Asymptomatic elevation of the hyperchromic red blood cell subpopulation is associated with decreased red cell deformability

H. Lutz, B. Misselwitz, J. Deuel, 2012, Annals of Hematology.

sIL2R ratio as early marker for response in hairy cell leukemia and the prognostic relevance of IL28B genotype to interferon-α therapy

K. Spanaus, O. Senn, M. Manz, 2017, Annals of Hematology.

R-hyper-CVAD versus R-CHOP/cytarabine with high-dose therapy and autologous haematopoietic stem cell support in fit patients with mantle cell lymphoma: 20 years of single-center experience

S. Balabanov, M. Manz, B. Gerber, 2018, Annals of Hematology.

A pilot clinical phase II trial MemSID: Acute and durable changes of red blood cells of sickle cell disease patients on memantine treatment

M. Gassmann, M. Manz, L. Kaestner, 2020, EJHaem.

Human L-ferritin deficiency is characterized by idiopathic generalized seizures and atypical restless leg syndrome

M. Muckenthaler, V. Broccoli, B. Garavaglia, 2013, The Journal of experimental medicine.

Hyperlipidemic myeloma: review of 53 cases

B. Misselwitz, J. Goede, B. Pestalozzi, 2010, Annals of Hematology.

Lysophosphatidic Acid-Activated Calcium Signaling Is Elevated in Red Cells from Sickle Cell Disease Patients

L. Birnbaumer, L. Kaestner, Sandra L Ruppenthal, 2021, Cells.

Cryohydrocytosis: increased activity of cation carriers in red cells from a patient with a band 3 mutation

H. Lutz, I. Bernhardt, A. Bogdanova, 2010, Haematologica.

Haemosiderin-Laden Sputum Macrophages for Diagnosis in Pulmonary Veno-Occlusive Disease

R. Speich, S. Ulrich, S. Stämpfli, 2014, PloS one.

MEMSID: Results From a Phase 2 Pilot Study on Memantine Treatment for Sickle Cell Disease

M. Gassmann, M. Manz, A. Makhro, 2020, HemaSphere.

Red blood cells of sickle cell disease patients exhibit abnormally high abundance of N‐methyl D‐aspartate receptors mediating excessive calcium uptake

M. Gassmann, A. Makhro, A. Bogdanova, 2014, British journal of haematology.

inv(16) and NPM1mut AMLs engraft human cytokine knock-in mice.

R. Flavell, M. Manz, U. Wagner, 2016, Blood.

A phase 3 randomized placebo-controlled trial of darbepoetin alfa in patients with anemia and lower-risk myelodysplastic syndromes

M. Delforge, J. Franklin, U. Platzbecker, 2017, Leukemia.

Real-world Data From the Swiss Lenalidomide in MDS del(5q) (SLIM)—Registry Identify New Chances and Challenges in Lenalidomide Treatment of Patients With MDS del(5q)

N. Bonadies, A. Calderoni, A. Rüfer, 2022, HemaSphere.

Efficacy of Azacitidine in De Novo and Relapsed Acute Myeloid Leukemia: A Retrospective Comparative Study.

O. Senn, M. Manz, B. Gerber, 2015, Clinical lymphoma, myeloma & leukemia.

Hemoglobin is an oxygen-dependent glutathione buffer adapting the intracellular reduced glutathione levels to oxygen availability

A. Makarov, V. Mitkevich, I. Petrushanko, 2022, Redox biology.

Necrobiotic xanthogranuloma successfully treated with autologous stem cell transplantation

A. Dispenzieri, R. Trüeb, J. Fehr, 2007, Annals of Hematology.

Does venous blood gas analysis provide accurate estimates of hemoglobin oxygen affinity?

K. Bloch, T. Latshang, Fabienne L. Huber, 2011, Annals of Hematology.

Functional plasticity of the N-methyl-d-aspartate receptor in differentiating human erythroid precursor cells

M. Gassmann, A. Bogdanova, P. Kemp, 2015, American journal of physiology. Cell physiology.

A New α1-Globin Mutation, Hb Brugg [α20(B1)His→Gln]

M. Schmugge, J. Goede, M. Nardi, 2011, Hemoglobin.

Effect of osmolality on erythrocyte rheology and perfusion of an artificial microvascular network.

S. Shevkoplyas, N. Z. Piety, W. Reinhart, 2015, Microvascular research.

Primary immune thrombocytopenia

Y. Beguin, D. Selleslag, J. Goede, 2013 .

Clonal Hematopoiesis in Hospitalized Elderly Patients With COVID-19

H. Moch, A. Kahraman, S. Balabanov, 2020, HemaSphere.

Erythrocyte storage in hypertonic (SAGM) or isotonic (PAGGSM) conservation medium: influence on cell properties

W. Reinhart, T. Schulzki, J. Goede, 2008, Vox sanguinis.

MPL expression on AML blasts predicts peripheral blood neutropenia and thrombocytopenia.

M. Manz, B. Löwenberg, Hitoshi Takizawa, 2016, Blood.

Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation.

K. Schwarz, H. Heimpel, H. Tamary, 2006, Blood.

Donor Age and Red Cell Age Contribute to the Variance in Lorrca Indices in Healthy Donors for Next Generation Ektacytometry: A Pilot Study

K. Dey, I. Petrushanko, A. Bogdanova, 2021, Frontiers in Physiology.

Patients with an extraordinarily elevated serum ferritin: think of haemophagocytic lymphohistiocytosis.

V. Briner, J. Goede, M. Schweizer, 2015, Swiss medical weekly.

clinical appearance, and prognosis based on long-term observation Congenital dyserythropoietic anemia type I (CDA I): molecular genetics,

K. Schwarz, H. Heimpel, H. Tamary, 2013 .

Sequestration of extracellular hemoglobin within a haptoglobin complex decreases its hypertensive and oxidative effects in dogs and guinea pigs.

P. Buehler, A. Alayash, D. Schaer, 2009, The Journal of clinical investigation.

Abdominal pain in a patient with acute lymphoblastic leukaemia

E. Minder, C. Renner, A. Breitenstein, 2010, Annals of Hematology.

Diagnosis and treatment of follicular lymphoma: an update.

S. Cogliatti, F. Stenner, M. Bargetzi, 2018, Swiss medical weekly.

Feasibility of electronic patient-reported outcome monitoring and self-management program in aplastic anemia and paroxysmal nocturnal hemoglobinuria—a pilot study (ePRO-AA-PNH)

J. Passweg, S. Gerull, B. Drexler, 2022, Annals of Hematology.

Feasibility of electronic patient-reported outcome monitoring with self-management advice and warning system in aplastic anemia and paroxysmal nocturnal hemoglobinuria – a pilot study (ePRO-AA-PNH)

J. Passweg, M. Bargetzi, S. Gerull, 2021 .

Frequency of congenital dyserythropoietic anemias in Europe

K. Schwarz, H. Heimpel, S. Perrotta, 2010, European journal of haematology.

Human F(ab')2-containing immune complexes together with anti-hinge natural antibodies stimulate complement amplification in vitro and in vivo.

H. Lutz, J. Goede, M. Fischler, 2008, Molecular immunology.

Marginal Zone Lymphoma Complicated by Protein Losing Enteropathy

M. Manz, C. Reiner, H. Heinrich, 2016, Case reports in hematology.

Asymptomatic hyperchromasia of red blood cells is associated with decreased red cell deformability

J. Goede, 2018 .

Influence of Standard Laboratory Procedures on Measures of Erythrocyte Damage

B. Seifert, D. de Zélicourt, V. Kurtcuoglu, 2017, Front. Physiol..

bout of resistance exercise in humans Leg glucose and protein metabolism during an acute

D. Chinkes, R. Wolfe, A. Brüggemann, 2015 .

[Sickle cell anemia].

E. Battegay, A. von Keudell, M. Schmugge, 2010, Praxis.

Modelling of a genetically diverse evolution of Systemic Mastocytosis with Chronic Myelomonocytic Leukemia (SM-CMML) by Next Generation Sequencing

H. Moch, P. Wild, M. Tinguely, 2014, Experimental Hematology & Oncology.

Alternate-day dosing of pomalidomide in relapsed/ refractory multiple myeloma: a multicenter, single-arm phase 2 trial

S. Aebi, T. Pabst, S. Schär, 2023, Leukemia.

N-methyl-D-aspartate receptors in human erythroid precursor cells and in circulating red blood cells contribute to the intracellular calcium regulation.

M. Gassmann, A. Brüggemann, L. Kaestner, 2013, American journal of physiology. Cell physiology.

Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapy

K. Schwarz, H. Heimpel, J. Goede, 2006, Annals of Hematology.

Frequency of congenital dyserythropoietic anemias in

K. Schwarz, H. Heimpel, S. Perrotta, 2010 .

A New Highly Unstable α Chain Variant Causing α+‐Thalassemia: Hb Zurich Albisrieden [α59(E8)Gly→Arg (α2)]

H. Troxler, J. Fehr, J. Goede, 2004, Hemoglobin.

Response to Tyrosine Kinase Inhibitors in Myeloproliferative Neoplasia with 8p11 Translocation and CEP110-FGFR1 Rearrangement.

M. Manz, A. Müller, J. Goede, 2017, The Oncologist.

High karyotypic complexity is an independent prognostic factor in patients with CLL treated with venetoclax combinations.

M. Hallek, G. Juliusson, S. Stilgenbauer, 2023, Blood.

[Approach to the Patient with Elevated Serum Ferritin].

J. Goede, A. Nowak, P. Krayenbühl, 2016, Praxis.