المؤلفون: Ballmaier, M., Balduini, C., Welte, K., Germeshausen, M.

المصدر: Monatsschrift Kinderheilkunde: Organ der Deutschen Gesellschaft für Kinderheilkunde und JugendmedizinOrgan der Österreichischen Gesellschaft für Kinder- und Jugendmedizin. June 2006 154(6):510-521

المؤلفون: Germeshausen, M^{Aff1, ID2403663_cor1}, Schulze, H, Kratz, C, Wilkens, L, Repp, R, Shannon, K, Welte, K, Ballmaier, M

المصدر: Leukemia. 19(4):611-617

المؤلفون: Cremer, M., Schulze, H., Linthorst, G., Folman, C. C., Wehnert, S., Strauß, G., von dem Borne, A. E. G. Kr., Welte, K., Ballmaier, M.

المصدر: Annals of Hematology. September 1999 78(9):401-407

المؤلفون: Hussein, K, Bock, O, Ballmaier, M, Göhring, G, Steinemann, D, Lehmann, U, Kemper, J, Buhr, T, Kreipe, H^{Aff1, ID2404846_cor9}

المصدر: Leukemia. 21(12):2566-2568

المؤلفون: Ockenga, J., Rohde, F., Süttmann, U., Herbarth, L., Ballmaier, M., Schedel, I.

المصدر: European Journal of Clinical Pharmacology. May 1996 50(3):167-170

المؤلفون: Pecci, A, Klersy, C, Gresele, P, Lee, K, De Rocco, D, Bozzi, V, Russo, G, Heller, Pg, Loffredo, G, Ballmaier, M, Fabris, F, Beggiato, E, Kahr, Wha, Pujol-Moix, N, Platokouki, H, Matthijs, G, Noris, P, Yerram, P, Hermans, C, Batzios, S, De Groot, M, Zieger, B, De Candia, E, Fraticelli, V, Kersseboom, R, Piccoli, Gb, Zimmermann, S, Zaninetti, C, Nicchia, E, Baronci, C, Seri, M, Knight, Pj, Balduini, Cl, Savoia, A, Van Geet, C, Geber, B, Economou, M, Fierro, T, Glembotsky, Ac, Vianello, F, Guthner, C.

المساهمون: Pecci, A, Klersy, C, Gresele, P, Lee, Kj, De Rocco, D, Bozzi, V, Russo, G, Heller, Pg, Loffredo, G, Ballmaier, M, Fabris, F, Beggiato, E, Kahr, Wh, Pujol-Moix, N, Platokouki, H, Van Geet, C, Noris, P, Yerram, P, Hermans, C, Gerber, B, Economou, M, De Groot, M, Zieger, B, De Candia, E, Fraticelli, V, Kersseboom, R, Piccoli, Gb, Zimmermann, S, Fierro, T, Glembotsky, Ac, Vianello, F, Zaninetti, C, Nicchia, E, Güthner, C, Baronci, C, Seri, M, Knight, Pj, Balduini, Cl, Savoia, A., DE ROCCO, Daniela, Pujol Moix, N, Nicchia, Elena, Savoia, Anna, University of Zurich

المصدر: Human Mutation, 35(2), 236-247. Wiley
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

مصطلحات موضوعية: Male, Oncology, thrombocytopenia, Medicina Clínica, Disease, Malattia MYH9 associata, Myh9 related disease, MYH9 RELATED DISEASE, Myh9, MYH9, Risk Factors, purl.org/becyt/ford/3.2 [https], Genotype, Genetics(clinical), CRYSTAL-STRUCTURE, Age of Onset, IIA, Genetics (clinical), deafne, MYOSIN HEAVY-CHAIN, EPSTEIN-SYNDROME, Molecular Motor Proteins, FECHTNER SYNDROMES, Trombocitopenia, Penetrance, POWER STROKE STATE, Phenotype, Italy, nephropathy, Female, purl.org/becyt/ford/3 [https], Miosina No Muscular Iia, Adult, 2716 Genetics (clinical), medicine.medical_specialty, CIENCIAS MÉDICAS Y DE LA SALUD, MOTOR DOMAIN, Hearing Loss, Sensorineural, Genetic counseling, 610 Medicine & health, Biology, nonmuscle myosin, Article, Cataract, Nephropathy, 1311 Genetics, Internal medicine, deafness, Genetics, medicine, Humans, Hematología, Gene, Genetic Association Studies, Hereditaria, Myosin Heavy Chains, MUTATIONS, Settore MED/09 - MEDICINA INTERNA, medicine.disease, Amino Acid Substitution, Epstein Syndrome, Mutation, 10032 Clinic for Oncology and Hematology, Linear Models, SMOOTH-MUSCLE MYOSIN

وصف الملف: STAMPA; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0b3202308793ba3d6d45b4fe01ee6e8
https://research.rug.nl/en/publications/8f687127-8140-4108-abe8-7c14ccda866a

المؤلفون: Moschny, N., Jahn, K., Maier, H., Khan, A., Liepach, K., Bajbouj, M., Ballmaier, M., Sack, M., Kreitlow, A., Bleich, S., Frieling, H., Neyazi, A.

المصدر: In European Neuropsychopharmacology December 2019 29 Supplement 6:S438-S439

المؤلفون: SAVOIA, ANNA, DE ROCCO, DANIELA, Germeshausen M., Henschel B., Kratz C., Kuhlen M., Rath B., Steuhl K. P., Wermes C., Ballmaier M.

المساهمون: Savoia, Anna, Germeshausen, M., DE ROCCO, Daniela, Henschel, B., Kratz, C., Kuhlen, M., Rath, B., Steuhl, K. P., Wermes, C., Ballmaier, M.

مصطلحات موضوعية: Malattia MYH9 associata (MYH9RD), piastrinopenia, gene MYH9

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3d7db4650da2a395c5bfd58d0999ff83
http://hdl.handle.net/11368/2304117

المؤلفون: Ballmaier, M., Maurizio MEMO

المصدر: Scopus-Elsevier

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::67165c68c2766de0a627992b90aa4c2e
http://hdl.handle.net/11379/25505

المؤلفون: Ballmaier, M., Zoli, M., Mazzoncini, R., Gennarelli, Massimo, Spano, Pier Franco

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3662::f3a8e92551744fb4310d5f24ac31b683
http://hdl.handle.net/11379/22068