FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN OMAN: FROM NON-EXISTENCE TO MOLECULAR CHARACTERIZATION

被引:0
|
作者
Elshinawy, Mohamed [1 ]
El-beshlawi, Ismail [1 ]
AlNuaimi, Mohammed [1 ]
AlDhuhli, Ahmed [1 ]
Alrawas, Abdulhakim [1 ]
Wali, Yasser [1 ]
机构
[1] Sultan Qaboos Univ Hosp, Muscat, Oman
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页码:1045 / 1045
页数:1
相关论文
共 50 条
  • [21] Clonal dissemination of T-lymphocytes in scid mice from familial hemophagocytic lymphohistiocytosis
    Ishii, E
    Yoshida, N
    Kimura, N
    Fujimoto, J
    Mizutani, S
    Sako, M
    Hibi, S
    Nagano, M
    Yoshida, T
    Mori, T
    Kiyokawa, N
    Mohri, S
    Tanaka, T
    Miyazaki, S
    Hara, T
    MEDICAL AND PEDIATRIC ONCOLOGY, 1999, 32 (03): : 201 - 208
  • [22] MONOALLELIC VARIANTS IN GENES RELATED TO FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS: REPORT FROM THE ITALIAN REGISTRY
    Vinas, L.
    Coniglio, M. L.
    Balasco, D.
    Fotzi, I.
    Favre, C.
    Arico, M.
    Sieni, E.
    HAEMATOLOGICA, 2017, 102 : 287 - 287
  • [23] Pantanal in the eyes of the media: from non-existence to paradise
    Bigatao, Rosiney
    CORDIS-REVISTA ELETRONICA DE HISTORIA SOCIAL DA CIDADE, 2009, (3-4):
  • [24] Monoallelic Mutations in Genes Related to Familial Hemophagocytic Lymphohistiocytosis (FHL): Report from the Italian Registry
    Sieni, Elena
    Coniglio, Maria Luisa
    Vinas, Laura
    Micalizzi, Concetta
    Todesco, Alessandra
    Timeus, Fabio
    Rizzari, Carmelo
    Pierani, Paolo
    De Fusco, Carmen
    MariaMura, Rosa
    Fotzi, Ilaria
    Arica, Maurizio
    Favre, Claudio
    PEDIATRIC BLOOD & CANCER, 2017, 64 : S36 - S37
  • [25] Treatment of familial hemophagocytic lymphohistiocytosis with bone marrow transplantation from HLA genetically nonidentical donors
    Jabado, N
    deGraeffMeeder, ER
    CavazzanaCalvo, M
    Haddad, E
    LeDeist, F
    Benkerrou, M
    Dufourcq, R
    Caillat, S
    Blanche, S
    Fischer, A
    BLOOD, 1997, 90 (12) : 4743 - 4748
  • [26] Genetic characterization of non-familial hemophagocytic lymphohistiocytosis patients: monogenic defects in HAVCR2, TNFRSF9 and MADD genes
    Batlle-Maso, Laura
    Franco-Jarava, Clara
    Vinas-Gimenez, Laura
    Garcia-Prat, Marina
    Parra-Martinez, Alba
    Diaz-de-Heredia, Cristina
    Cueto-Gonzalez, Anna Maria
    Codina-Sola, Marta
    Campos, Berta
    Tizzano, Eduardo
    Riviere, Jacques G.
    Soler-Palacin, Pere
    Alsina, Laia
    Martinez-Gallo, Monica
    Casals, Ferran
    Colobran, Roger
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 437 - 438
  • [27] Mutations affecting mRNA splicing are the most common molecular defect in patients with familial hemophagocytic lymphohistiocytosis type 3
    Santoro, Alessandra
    Cannella, Sonia
    Trizzino, Antonino
    Bruno, Giuseppa
    De Fusco, Carmen
    Notarangelo, Luigi D.
    Pende, Daniela
    Griffiths, Gillian M.
    Arico, Maurizio
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 (07): : 1086 - 1090
  • [28] The Evolution Of Pretence: From Intentional Availability To Intentional Non-Existence
    Gomez, Juan-Carlos
    MIND & LANGUAGE, 2008, 23 (05) : 586 - 606
  • [29] Characterization of a large UNC13D gene duplication in a patient with familial hemophagocytic lymphohistiocytosis type 3
    Hiejima, Eitaro
    Shibata, Hirofumi
    Yasumi, Takahiro
    Shimodera, Saeko
    Hori, Masayuki
    Izawa, Kazushi
    Kawai, Tomoki
    Matsuoka, Masaki
    Kojima, Yasuko
    Ohara, Akira
    Nishikomori, Ryuta
    Ohara, Osamu
    Heike, Toshio
    CLINICAL IMMUNOLOGY, 2018, 191 : 63 - 66
  • [30] First characterization of platelet secretion defect in patients with familial hemophagocytic lymphohistiocytosis type 3 (FHL-3)
    Nakamura, Lea
    Bertling, Anne
    Brodde, Martin F.
    zur Stadt, Udo
    Schulz, Ansgar S.
    Ammann, Sandra
    Sandrock-Lang, Kirstin
    Beutel, Karin
    Zieger, Barbara
    Kehrel, Beate E.
    BLOOD, 2015, 125 (02) : 412 - 414