المؤلفون: Kozyra, EJ, Gohring, G, Hickstein, DD, Calvo, KR, DiNardo, CD, Dworzak, M, de Haas, V, Stary, J, Hasle, H, Shimamura, A, Fleming, MD, Inaba, H, Lewis, S, Hsu, AP, Holland, SM, Arnold, DE, Mecucci, C, Keel, SB, Bertuch, AA, Tawana, K, Barzilai, S, Hirabayashi, S, Onozawa, M, Lei, SH, Alaiz, H, Andrikovics, H, Betts, D, Beverloo, BH, Buechner, J, Cermak, M, Cervera, J, Haus, O, Jahnukainen, K, Manola, KN, Nebral, K, Pasquali, F, Tchinda, J, Turkiewicz, D, Van Roy, N, Zemanova, Z, Pastor, VB, Strahm, B, Noellke, P, Niemeyer, CM, Schlegelberger, B, Yoshimi, A, Wlodarski, MW

المصدر: Blood. 138(23):2441-2445

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:148647321

المؤلفون: Pasińska M, Łazarczyk E, Repczyńska A, Sobczyńska-Tomaszewska A, Zimowski J, Runge A, Haus O

المصدر: The Application of Clinical Genetics, Vol Volume 15, Pp 27-38 (2022)

مصطلحات موضوعية: x chromosome, structural aberrations, genetic diagnostics, genetic counseling, intellectual disability., Medicine (General), R5-920, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.dovepress.com/clinical-importance-of-acgh-in-genetic-counselling-of-children-with-ps-peer-reviewed-fulltext-article-TACG; https://doaj.org/toc/1178-704X

URL الوصول: https://doaj.org/article/6c0bb40dc2214c83b38cc2f65717c06f

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المؤلفون: Haus, O.^{Aff4, Aff6}, Mucha, B.^Aff4, Kurylak, A.^Aff5, Soszynska, K.^Aff4, Debski, R.^Aff5, Wysocki, M.^Aff5

المساهمون: Hiddemann, Wolfgang, editor^Aff1, Haferlach, Torsten, editor^Aff1, Unterhalt, Michael, editor^Aff1, Büchner, Thomas, editor^Aff2, Ritter, Jörg, editor^Aff3

المصدر: Acute Leukemias IX : Basic Research, Experimental Approaches and Novel Therapies. 41:332-337

المؤلفون: Haus, O.^{Aff5, Aff6}, Czarnecka, M.^Aff5, Kotlarek-Haus, S.^Aff5, Kuliczkowski, K.^Aff5, Duszenko, E.^Aff5, Makowska, I.^Aff5

المساهمون: Büchner, T., editor^Aff1, Hiddemann, W., editor^Aff2, Wörmann, B., editor^Aff3, Schellong, G., editor^Aff4, Ritter, J., editor^Aff4, Creutzig, U., editor^Aff4

المصدر: Acute Leukemias VIII : Prognostic Factors and Treatment Strategies. 40:49-53

المؤلفون: Sahoo S. S., Pastor V. B., Goodings C., Voss R. K., Kozyra E. J., Szvetnik A., Noellke P., Dworzak M., Stary J., Locatelli F., Masetti R., Schmugge M., De Moerloose B., Catala A., Kallay K., Turkiewicz D., Hasle H., Buechner J., Jahnukainen K., Ussowicz M., Polychronopoulou S., Smith O. P., Fabri O., Barzilai S., de Haas V., Baumann I., Schwarz-Furlan S., Moerloose B. D., Smith O., Haas V. D., Gohring G., Niemeyer C., Nebral K., Simonitsch-Kluppp I., Paepe P. D., Van Roy N., Campr V., Zemanova Z., Clasen-Linde E., Plesner T., Schlegelberger B., Rudelius M., Manola K., Stefanaki K., Csomor J., Andrikovics H., Betts D., O'Sullivan M., Zohar Y., Jeison M., Vito R. D., Pasquali F., Maldyk J., Haus O., Alaiz H., Kjollerstrom P., Lemos L. M., Bodova I., Cermak M., Plank L., Gazic B., Kavcic M., Podgornik H., Ros M. L., Cervera J., Gengler C., Tchinda J., Beverloo B., Leguit R., Niewisch M. R., Sauer M. G., Burkhardt B., Lang P., Bader P., Beier R., Muller I., Albert M. H., Meisel R., Schulz A., Cario G., Panda P. K., Wehrle J., Hirabayashi S., Derecka M., Durruthy-Durruthy R., Yoshimi-Noellke A., Ku M., Lebrecht D., Erlacher M., Flotho C., Strahm B., Niemeyer C. M., Wlodarski M. W.

المساهمون: Sahoo S.S., Pastor V.B., Goodings C., Voss R.K., Kozyra E.J., Szvetnik A., Noellke P., Dworzak M., Stary J., Locatelli F., Masetti R., Schmugge M., De Moerloose B., Catala A., Kallay K., Turkiewicz D., Hasle H., Buechner J., Jahnukainen K., Ussowicz M., Polychronopoulou S., Smith O.P., Fabri O., Barzilai S., de Haas V., Baumann I., Schwarz-Furlan S., Moerloose B.D., Smith O., Haas V.D., Gohring G., Niemeyer C., Nebral K., Simonitsch-Kluppp I., Paepe P.D., Van Roy N., Campr V., Zemanova Z., Clasen-Linde E., Plesner T., Schlegelberger B., Rudelius M., Manola K., Stefanaki K., Csomor J., Andrikovics H., Betts D., O'Sullivan M., Zohar Y., Jeison M., Vito R.D., Pasquali F., Maldyk J., Haus O., Alaiz H., Kjollerstrom P., Lemos L.M., Bodova I., Cermak M., Plank L., Gazic B., Kavcic M., Podgornik H., Ros M.L., Cervera J., Gengler C., Tchinda J., Beverloo B., Leguit R., Niewisch M.R., Sauer M.G., Burkhardt B., Lang P., Bader P., Beier R., Muller I., Albert M.H., Meisel R., Schulz A., Cario G., Panda P.K., Wehrle J., Hirabayashi S., Derecka M., Durruthy-Durruthy R., Yoshimi-Noellke A., Ku M., Lebrecht D., Erlacher M., Flotho C., Strahm B., Niemeyer C.M., Wlodarski M.W., Clinical Genetics

المصدر: Nat Med
Nature Medicine, 27(10), 1806-1817. Nature Publishing Group
Sahoo, S S, Pastor, V B, Goodings, C, Voss, R K, Kozyra, E J, Szvetnik, A, Noellke, P, Dworzak, M, Starý, J, Locatelli, F, Masetti, R, Schmugge, M, De Moerloose, B, Catala, A, Kállay, K, Turkiewicz, D, Hasle, H, Buechner, J, Jahnukainen, K, Ussowicz, M, Polychronopoulou, S, Smith, O P, Fabri, O, Barzilai, S, de Haas, V, Baumann, I, Schwarz-Furlan, S, Niewisch, M R, Sauer, M G, Burkhardt, B, Lang, P, Bader, P, Beier, R, Müller, I, Albert, M H, Meisel, R, Schulz, A, Cario, G, Panda, P K, Wehrle, J, Hirabayashi, S, Derecka, M, Durruthy-Durruthy, R, Göhring, G, Yoshimi-Noellke, A, Ku, M, Lebrecht, D, Erlacher, M, Flotho, C, Strahm, B, Niemeyer, C M, European Working Group of MDS in Children (EWOG-MDS) & Wlodarski, M W 2021, ' Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes ', Nature Medicine, vol. 27, no. 10, pp. 1806-1817 . https://doi.org/10.1038/s41591-021-01511-6

مصطلحات موضوعية: Oncology, Male, medicine.medical_specialty, Monosomy, Adolescent, Somatic cell, Medizin, Bone Marrow Cells, Kaplan-Meier Estimate, General Biochemistry, Genetics and Molecular Biology, Germline, Article, Clonal Evolution, Germline mutation, SDG 3 - Good Health and Well-being, Internal medicine, medicine, Humans, Child, Germ-Line Mutation, Chromosome 7 (human), Cytopenia, clonal hemopoiesis, business.industry, Myelodysplastic syndromes, Tumor Suppressor Proteins, Intracellular Signaling Peptides and Proteins, High-Throughput Nucleotide Sequencing, Infant, General Medicine, medicine.disease, GATA2 Transcription Factor, SAMD9 and SAMD9L mutations, Pediatric Myelodysplastic syndromes, medicine.anatomical_structure, HEK293 Cells, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, Child, Preschool, Myelodysplastic Syndromes, Female, Bone marrow, Clonal Hematopoiesis, Single-Cell Analysis, business

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6e81b72e27d4c9c76679649a64ad2cf
http://hdl.handle.net/11585/836418

المؤلفون: Haus, O.^Aff5, Czarnecka, M.^Aff6, Kuliczkowski, K.^Aff6, Makowska, I.^Aff6, Kotlarek-Haus, S.^Aff6

المساهمون: Hiddemann, W., editor^Aff1, Büchner, T., editor^Aff2, Wörmann, B., editor^Aff1, Ritter, J., editor^Aff3, Creutzig, U., editor^Aff3, Keating, M., editor^Aff4, Plunkett, W., editor^Aff4

المصدر: Acute Leukemias VII : Experimental Approaches and Novel Therapies. 39:253-258

Degree: MD PhD

المؤلفون: Sahoo, S. S., Pastor, V. B., Goodings, C., Voss, R. K., Kozyra, E. J., Szvetnik, A., Noellke, P., Dworzak, M., Stary, J., Locatelli, Franco, Masetti, R., Schmugge, M., De Moerloose, B., Catala, A., Kallay, K., Turkiewicz, D., Hasle, H., Buechner, J., Jahnukainen, K., Ussowicz, M., Polychronopoulou, S., Smith, O. P., Fabri, O., Barzilai, S., de Haas, V., Baumann, I., Schwarz-Furlan, S., Smith, O., Haas, V. D., Gohring, G., Niemeyer, C., Nebral, K., Simonitsch-Kluppp, I., Paepe, P. D., Van Roy, N., Campr, V., Zemanova, Z., Clasen-Linde, E., Plesner, T., Schlegelberger, B., Rudelius, M., Manola, K., Stefanaki, K., Csomor, J., Andrikovics, H., Betts, D., O'Sullivan, M., Zohar, Y., Jeison, M., Vito, R. D., Pasquali, F., Maldyk, J., Haus, O., Alaiz, H., Kjollerstrom, P., Lemos, L. M., Bodova, I., Cermak, M., Plank, L., Gazic, B., Kavcic, M., Podgornik, H., Ros, M. L., Cervera, J., Gengler, C., Tchinda, J., Beverloo, B., Leguit, R., Niewisch, M. R., Sauer, M. G., Burkhardt, B., Lang, P., Bader, P., Beier, R., Muller, I., Albert, M. H., Meisel, R., Schulz, A., Cario, G., Panda, P. K., Wehrle, J., Hirabayashi, S., Derecka, M., Durruthy-Durruthy, R., Yoshimi-Noellke, A., Ku, M., Lebrecht, D., Erlacher, M., Flotho, C., Strahm, B., Niemeyer, C. M., Wlodarski, M. W.

مصطلحات موضوعية: Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, SAMD9/SAMD9L syndromes

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2601::111388b43ff6bd962c380c112da05bd2
https://hdl.handle.net/10807/229515

المؤلفون: Lubiński, J., Górski, B., Huzarski, T., Byrski, T., Gronwald, J., Serrano-Fernández, P., Domagała, W., Chosia, M., Uciński, M., Grzybowska, E., Lange, D., Mąka, B., Mackiewicz, A., Karczewska, A., Bręborowicz, J., Lamperska, K., Stawicka, M., Gozdecka-Grodecka, S., Bębenek, M., Sorokin, D., Wojnar, A., Haus, O., Sir, J., Mierzwa, T., Niepsuj, S., Gugała, K., Góźdź, S., Sygut, J., Kozak-Klonowska, B., Musiatowicz, B., Posmyk, M., Kordek, R., Morawiec, M., Zambrano, O., Waśko, B., Fudali, L., Skręt, J., Surdyka, D., Urbański, K., Mituś, J., Ryś, J., Szwiec, M., Rozmiarek, A., Dziuba, I., Wandzel, P., Wiśniowski, R., Szczylik, C., Kozak, A., Kozłowski, W., Narod, S.A.

المصدر: Breast Cancer Research and Treatment. September 2006 99(1):71-76

المؤلفون: Dębniak, T., Scott, R.J., Huzarski, T., Byrski, T., Masojć, B., van de Wetering, T., Serrano-Fernandez, P., Górski, B., Cybulski, C., Gronwald, J., Dębniak, B., Maleszka, R., Kładny, J., Bieniek, A., Nagay, L., Haus, O., Grzybowska, E., Wandzel, P., Niepsuj, S., Narod, S.A., Lubinski, and J.

المصدر: Breast Cancer Research and Treatment. July 2006 98(2):209-215