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1.

Malignancy-associated hemophagocytic lymphohistiocytosis in Sweden: incidence, clinical characteristics, and survival.

Löfstedt, Alexandra; Jädersten, Martin; Meeths, Marie; Henter, Jan-Inge.

Blood ; 143(3): 233-242, 2024 Jan 18.

Artículo en Inglés | MEDLINE | ID: mdl-37595287

2.

Rubella vaccine-induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicity.

Groß, Miriam; Speckmann, Carsten; May, Annette; Gajardo-Carrasco, Tania; Wustrau, Katharina; Maier, Sarah Lena; Panning, Marcus; Huzly, Daniela; Agaimy, Abbas; Bryceson, Yenan T; Choo, Sharon; Chow, C W; Dückers, Gregor; Fasth, Anders; Fraitag, Sylvie; Gräwe, Katja; Haxelmans, Sabine; Holzinger, Dirk; Hudowenz, Ole; Hübschen, Judith M; Khurana, Claudia; Kienle, Korbinian; Klifa, Roman; Korn, Klaus; Kutzner, Heinz; Lämmermann, Tim; Ledig, Svea; Lipsker, Dan; Meeths, Marie; Naumann-Bartsch, Nora; Rascon, Jelena; Schänzer, Anne; Seidl, Maximilian; Tesi, Bianca; Vauloup-Fellous, Christelle; Vollmer-Kary, Beate; Warnatz, Klaus; Wehr, Claudia; Neven, Bénédicte; Vargas, Pablo; Sepulveda, Fernando E; Lehmberg, Kai; Schmitt-Graeff, Annette; Ehl, Stephan.

J Allergy Clin Immunol ; 149(1): 388-399.e4, 2022 01.

Artículo en Inglés | MEDLINE | ID: mdl-34033843

3.

Chondrodysplasia and growth failure in children after early hematopoietic stem cell transplantation for non-oncologic disorders.

Botto, Lorenzo D; Meeths, Marie; Campos-Xavier, Belinda; Bergamaschi, Rosalba; Mazzanti, Laura; Scarano, Emanuela; Finocchi, Andrea; Cancrini, Caterina; Zirn, Birgit; Kühnle, Ingrid; Kramm, Christof Maria; Alanay, Yasemin; Jones, Wendy D; Irving, Melita; Sabir, Ataf; Henter, Jan-Inge; Borgström, Birgit; Nordgren, Ann; Hammarsjö, Anna; Putti, Caterina; Mozzato, Chiara; Zuccarello, Daniela; Nishimura, Gen; Bonafè, Luisa; Grigelioniene, Giedre; Unger, Sheila; Superti-Furga, Andrea.

Am J Med Genet A ; 185(2): 517-527, 2021 02.

Artículo en Inglés | MEDLINE | ID: mdl-33398909

4.

Genetics and pathophysiology of haemophagocytic lymphohistiocytosis.

Meeths, Marie; Bryceson, Yenan T.

Acta Paediatr ; 110(11): 2903-2911, 2021 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-34192386

5.

Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score.

Tesch, Victoria Katharina; Abolhassani, Hassan; Shadur, Bella; Zobel, Joachim; Mareika, Yuliya; Sharapova, Svetlana; Karakoc-Aydiner, Elif; Rivière, Jacques G; Garcia-Prat, Marina; Moes, Nicolette; Haerynck, Filomeen; Gonzales-Granado, Luis I; Santos Pérez, Juan Luis; Mukhina, Anna; Shcherbina, Anna; Aghamohammadi, Asghar; Hammarström, Lennart; Dogu, Figen; Haskologlu, Sule; Ikinciogullari, Aydan I; Köstel Bal, Sevgi; Baris, Safa; Kilic, Sara Sebnem; Karaca, Neslihan Edeer; Kutukculer, Necil; Girschick, Hermann; Kolios, Antonios; Keles, Sevgi; Uygun, Vedat; Stepensky, Polina; Worth, Austen; van Montfrans, Joris M; Peters, Anke M J; Meyts, Isabelle; Adeli, Mehdi; Marzollo, Antonio; Padem, Nurcicek; Khojah, Amer M; Chavoshzadeh, Zahra; Avbelj Stefanija, Magdalena; Bakhtiar, Shahrzad; Florkin, Benoit; Meeths, Marie; Gamez, Laura; Grimbacher, Bodo; Seppänen, Mikko R J; Lankester, Arjan; Gennery, Andrew R; Seidel, Markus G.

J Allergy Clin Immunol ; 145(5): 1452-1463, 2020 05.

Artículo en Inglés | MEDLINE | ID: mdl-31887391

6.

Diagnostic challenges for a novel SH2D1A mutation associated with X-linked lymphoproliferative disease.

Torralba-Raga, Lamberto; Tesi, Bianca; Chiang, Samuel C C; Schlums, Heinrich; Nordenskjöld, Magnus; Horne, AnnaCarin; Henter, Jan-Inge; Meeths, Marie; Abdelhaleem, Mohamed; Weitzman, Sheila; Bryceson, Yenan.

Pediatr Blood Cancer ; 67(4): e28184, 2020 04.

Artículo en Inglés | MEDLINE | ID: mdl-31994322

7.

Haploinsufficiency of UNC13D increases the risk of lymphoma.

Löfstedt, Alexandra; Ahlm, Clas; Tesi, Bianca; Bergdahl, Ingvar A; Nordenskjöld, Magnus; Bryceson, Yenan T; Henter, Jan-Inge; Meeths, Marie.

Cancer ; 125(11): 1848-1854, 2019 06 01.

Artículo en Inglés | MEDLINE | ID: mdl-30758854

8.

Successful Hematopoietic Stem Cell Transplantation in a Patient with LPS-Responsive Beige-Like Anchor (LRBA) Gene Mutation.

Tesi, Bianca; Priftakis, Peter; Lindgren, Fredrik; Chiang, Samuel C C; Kartalis, Nikolaos; Löfstedt, Alexandra; Lörinc, Esther; Henter, Jan-Inge; Winiarski, Jacek; Bryceson, Yenan T; Meeths, Marie.

J Clin Immunol ; 36(5): 480-9, 2016 07.

Artículo en Inglés | MEDLINE | ID: mdl-27146671

9.

Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production.

Chiang, Samuel C C; Theorell, Jakob; Entesarian, Miriam; Meeths, Marie; Mastafa, Monika; Al-Herz, Waleed; Frisk, Per; Gilmour, Kimberly C; Ifversen, Marianne; Langenskiöld, Cecilia; Machaczka, Maciej; Naqvi, Ahmed; Payne, Jeanette; Perez-Martinez, Antonio; Sabel, Magnus; Unal, Ekrem; Unal, Sule; Winiarski, Jacek; Nordenskjöld, Magnus; Ljunggren, Hans-Gustaf; Henter, Jan-Inge; Bryceson, Yenan T.

Blood ; 121(8): 1345-56, 2013 Feb 21.

Artículo en Inglés | MEDLINE | ID: mdl-23287865

10.

Incidence and clinical presentation of primary hemophagocytic lymphohistiocytosis in Sweden.

Meeths, Marie; Horne, AnnaCarin; Sabel, Magnus; Bryceson, Yenan T; Henter, Jan-Inge.

Pediatr Blood Cancer ; 62(2): 346-352, 2015 02.

Artículo en Inglés | MEDLINE | ID: mdl-25382070

11.

Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations.

Tesi, Bianca; Chiang, Samuel C C; El-Ghoneimy, Dalia; Hussein, Ayad Ahmed; Langenskiöld, Cecilia; Wali, Rabia; Fadoo, Zehra; Silva, João Pinho; Lecumberri, Ramón; Unal, Sule; Nordenskjöld, Magnus; Bryceson, Yenan T; Henter, Jan-Inge; Meeths, Marie.

Pediatr Blood Cancer ; 62(12): 2094-100, 2015 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-26184781

12.

Pathophysiology and spectrum of diseases caused by defects in lymphocyte cytotoxicity.

Meeths, Marie; Chiang, Samuel C C; Löfstedt, Alexandra; Müller, Martha-Lena; Tesi, Bianca; Henter, Jan-Inge; Bryceson, Yenan T.

Exp Cell Res ; 325(1): 10-7, 2014 Jul 01.

Artículo en Inglés | MEDLINE | ID: mdl-24680986

13.

Hematopoietic stem cell transplantation of an adolescent with neurological manifestations of homozygous missense PRF1 mutation.

Hussein, Ayad Ahmed; Hamadah, Tuka; Qandeel, Monther; Sughayer, Maher; Amarin, Rula; Mansour, Asem; Chiang, Samuel C; Al-Zaben, Abdulhadi; Meeths, Marie; Bryceson, Yenan T.

Pediatr Blood Cancer ; 61(12): 2313-5, 2014 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-25110876

14.

Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation.

Seidel, Markus G; Böhm, Katrin; Dogu, Figen; Worth, Austen; Thrasher, Adrian; Florkin, Benoit; Ikinciogullari, Aydan; Peters, Anke; Bakhtiar, Shahrzad; Meeths, Marie; Stepensky, Polina; Meyts, Isabelle; Sharapova, Svetlana O; Gámez-Díaz, Laura; Hammarström, Lennart; Ehl, Stephan; Grimbacher, Bodo; Gennery, Andrew R.

J Allergy Clin Immunol ; 141(2): 770-775.e1, 2018 02.

Artículo en Inglés | MEDLINE | ID: mdl-28502825

15.

A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentation.

Tesi, Bianca; Rascon, Jelena; Chiang, Samuel C C; Burnyte, Birute; Löfstedt, Alexandra; Fasth, Anders; Heizmann, Miriam; Juozapaite, Sandra; Kiudeliene, Rosita; Kvedaraite, Egle; Miseviciene, Valdone; Muleviciene, Audrone; Müller, Martha-Lena; Nordenskjöld, Magnus; Matuzeviciene, Reda; Samaitiene, Ruta; Speckmann, Carsten; Stankeviciene, Sigita; Zekas, Vytautas; Voss, Matthias; Ehl, Stephan; Vaiciene-Magistris, Nerija; Henter, Jan-Inge; Meeths, Marie; Bryceson, Yenan T.

J Allergy Clin Immunol ; 142(1): 317-321.e8, 2018 07.

Artículo en Inglés | MEDLINE | ID: mdl-29522846

16.

HLH susceptibility: genetic lesions add up.

Meeths, Marie; Bryceson, Yenan T.

Blood ; 127(17): 2051-2, 2016 04 28.

Artículo en Inglés | MEDLINE | ID: mdl-27127299

17.

Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D.

Meeths, Marie; Chiang, Samuel C C; Wood, Stephanie M; Entesarian, Miriam; Schlums, Heinrich; Bang, Benedicte; Nordenskjöld, Edvard; Björklund, Caroline; Jakovljevic, Gordana; Jazbec, Janez; Hasle, Henrik; Holmqvist, Britt-Marie; Rajic, Ljubica; Pfeifer, Susan; Rosthøj, Steen; Sabel, Magnus; Salmi, Toivo T; Stokland, Tore; Winiarski, Jacek; Ljunggren, Hans-Gustaf; Fadeel, Bengt; Nordenskjöld, Magnus; Henter, Jan-Inge; Bryceson, Yenan T.

Blood ; 118(22): 5783-93, 2011 Nov 24.

Artículo en Inglés | MEDLINE | ID: mdl-21931115

18.

Development of classical Hodgkin's lymphoma in an adult with biallelic STXBP2 mutations.

Machaczka, Maciej; Klimkowska, Monika; Chiang, Samuel C C; Meeths, Marie; Müller, Martha-Lena; Gustafsson, Britt; Henter, Jan-Inge; Bryceson, Yenan T.

Haematologica ; 98(5): 760-4, 2013 May.

Artículo en Inglés | MEDLINE | ID: mdl-23100279

19.

Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2.

Meeths, Marie; Entesarian, Miriam; Al-Herz, Waleed; Chiang, Samuel C C; Wood, Stephanie M; Al-Ateeqi, Wafa; Almazan, Francisco; Boelens, Jaap J; Hasle, Henrik; Ifversen, Marianne; Lund, Bendik; van den Berg, J Merlijn; Gustafsson, Britt; Hjelmqvist, Hans; Nordenskjöld, Magnus; Bryceson, Yenan T; Henter, Jan-Inge.

Blood ; 116(15): 2635-43, 2010 Oct 14.

Artículo en Inglés | MEDLINE | ID: mdl-20558610

20.

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3.

Sieni, Elena; Cetica, Valentina; Santoro, Alessandra; Beutel, Karin; Mastrodicasa, Elena; Meeths, Marie; Ciambotti, Benedetta; Brugnolo, Francesca; zur Stadt, Udo; Pende, Daniela; Moretta, Lorenzo; Griffiths, Gillian M; Henter, Jan-Inge; Janka, Gritta; Aricò, Maurizio.

J Med Genet ; 48(5): 343-52, 2011 May.

Artículo en Inglés | MEDLINE | ID: mdl-21248318

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