Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Peretz Resnitzky"'
Autor:
Sharon Noy-Lotan, Orly Dgany, Roxane Lahmi, Nathaly Marcoux, Tanya Krasnov, Nissan Yissachar, Doron Ginsberg, Benny Motro, Peretz Resnitzky, Isaac Yaniv, Gary M. Kupfer, Hannah Tamary
Publikováno v:
Haematologica, Vol 94, Iss 5 (2009)
Background Congenital dyserythropoietic anemia type I is an inherited autosomal recessive macrocytic anemia associated with ineffective erythropoiesis and the development of secondary hemochromatosis. Distinct erythroid precursors with internuclear c
Externí odkaz:
https://doaj.org/article/53d77ab182cb4ac887fb5899e36c705e
Autor:
Tanya Krasnov, Orly Dgany, Hannah Tamary, Peretz Resnitzky, Dina Shaft, Joseph Kapelushnik, Hanna Shalev
Publikováno v:
European Journal of Haematology. 99:366-371
Introduction Congenital dyserythropoietic anemias are rare blood disorders characterized by congenital anemia and a wide range of morphological and functional abnormalities of erythroid precursors. Objectives To analyze the relative frequency of both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa2f24edbfb7c61c621749e18cb53455
https://doi.org/10.1111/ejh.12931
https://doi.org/10.1111/ejh.12931
Autor:
Dvora Filon, Evgeny Chubar, Carina Levin, Peretz Resnitzky, Ariel Koren, Michael Bennett, Luci Zalman, Haya Palmor
Publikováno v:
European Journal of Haematology. 97:137-144
UNLABELLED Hereditary sequence variants in globin genes are usually silent and are rarer in α-globin chains than β-globin chains. Some may lead to an unstable protein with a hemolytic or thalassemic phenotype. Hb Taybe is an unstable α-chain hemog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99d57ba7a043a96bd7ef96fcf408230a
https://doi.org/10.1111/ejh.12694
https://doi.org/10.1111/ejh.12694
Autor:
Tanya Krasnov, Hannah Tamary, Achiya Z. Amir, Orly Dgany, Michael Bennett, Peretz Resnitzky, Alain Berrebi, Ronit Mor-Cohen
Publikováno v:
Acta Haematologica. 125:202-207
Objective: Congenital dyserythropoietic anemia (CDA) is characterized by ineffective erythropoiesis, binuclearity of erythroid precursors and secondary hemochromatosis. Recently, the gene mutated in CDA type II (CDA II), SEC23B, was identified. All I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e201e99c6cb0e7fe74617f8a9bd81ff4
https://doi.org/10.1159/000322948
https://doi.org/10.1159/000322948
Publikováno v:
British Journal of Haematology. 120:774-781
We report eight new patients with de novo acute basophilic leukaemia (ABL) diagnosed by electron microscopy (EM) in 184 patients with poorly differentiated AML who were selected for ultrastructural analysis between the years 1989 and 2002. Morphology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9489a9267d05d93cf8d7631574d41cf
https://doi.org/10.1046/j.1365-2141.2003.04167.x
https://doi.org/10.1046/j.1365-2141.2003.04167.x
Publikováno v:
American Journal of Hematology. 70:72-76
We describe a new case of congenital dyserythropoietic anemia (CDA) type III. This least common type of CDA was diagnosed at the age of 59 in a 70-year-old woman who suffered from a young age from mild macrocytic anemia, while the long follow up sinc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cb73dfca1ade07de8c0472f4556f994
https://doi.org/10.1002/ajh.10086
https://doi.org/10.1002/ajh.10086
Publikováno v:
Leukemia & Lymphoma. 49:2203-2205
AML-M2 is a common subtype of acute myeloid leukemia (AML), usually associated with translocation t(8;21) and often accompanied by eosinophilia [1]. Bone marrow (BM) basophilia is a rarely encounte...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81995e6f140d80f067b9572c8353514f
https://doi.org/10.1080/10428190802258949
https://doi.org/10.1080/10428190802258949
Publikováno v:
British Journal of Haematology. 103:729-739
We investigated the electronmicroscopic (EM) features and cellular lysozyme (LZ) content in 16 cases of acute promyelocytic leukaemia (APL): 11 cases of the hypergranular form (M3) and five cases of the microgranular variant (M3-V). The main EM featu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c0a5eb60f6b3cdef63153ca6bdec627
https://doi.org/10.1046/j.1365-2141.1998.01065.x
https://doi.org/10.1046/j.1365-2141.1998.01065.x
Publikováno v:
British Journal of Haematology. 137:381-383
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f61565a691d8d6398f39d007ef97883b
https://doi.org/10.1111/j.1365-2141.2007.06579.x
https://doi.org/10.1111/j.1365-2141.2007.06579.x
Publikováno v:
Leukemia & Lymphoma. 48:434-436
Ribosome-lamella complexes (RLCs) are rarely found intracytoplasmic organelles intimately associated with the rough endoplasmic reticulum (RER). RLCs have been observed in different conditions but ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e24cc70a2c7f043e04fbdd5a8bbf5be4
https://doi.org/10.1080/10428190601078837
https://doi.org/10.1080/10428190601078837