1. Cancer risk in relatives of patients with a primary disorder of lymphocyte cytotoxicity: a retrospective cohort study. Issue 12 (December 2015) Authors: Löfstedt, Alexandra; Chiang, Samuel C C; Onelöv, Erik; Bryceson, Yenan T; Meeths, Marie; Henter, Jan-Inge Journal: Lancet Issue: Volume 2:Issue 12(2015) Page Start: e536 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chondrodysplasia and growth failure in children after early hematopoietic stem cell transplantation for non‐oncologic disorders. Issue 2 (4th January 2021) Authors: 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... Journal: American journal of medical genetics Issue: Volume 185:Issue 2(2021) Page Start: 517 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Diagnostic challenges for a novel SH2D1A mutation associated with X‐linked lymphoproliferative disease. Issue 4 (29th January 2020) Authors: 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 Journal: Pediatric blood & cancer Issue: Volume 67:Issue 4(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetics and pathophysiology of haemophagocytic lymphohistiocytosis. (12th July 2021) Authors: Meeths, Marie; Bryceson, Yenan T. Journal: Acta pædiatrica Issue: Volume 110:Number 11(2021) Page Start: 2903 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3. Issue 5 (19th January 2011) Authors: 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 Journal: Journal of medical genetics Issue: Volume 48:Issue 5(2011) Page Start: 343 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Haploinsufficiency of UNC13D increases the risk of lymphoma. Issue 11 (13th February 2019) Authors: Löfstedt, Alexandra; Ahlm, Clas; Tesi, Bianca; Bergdahl, Ingvar A.; Nordenskjöld, Magnus; Bryceson, Yenan T.; Henter, Jan‐Inge; Meeths, Marie Journal: Cancer Issue: Volume 125:Issue 11(2019) Page Start: 1848 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Hematopoietic stem cell transplantation of an adolescent with neurological manifestations of homozygous missense PRF1 mutation. Issue 12 (11th August 2014) Authors: Hussein, Ayad Ahmed; Hamadah, Tuka; Qandeel, Monther; Sughayer, Maher; Amarin, Rula; Mansour, Asem; Chiang, Samuel C.; Al‐Zaben, Abdulhadi; Meeths, Marie; Bryceson, Yenan T. Journal: Pediatric blood & cancer Issue: Volume 61:Issue 12(2014:Dec.) Page Start: 2313 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Incidence and clinical presentation of primary hemophagocytic lymphohistiocytosis in Sweden. Issue 2 (8th November 2014) Authors: Meeths, Marie; Horne, AnnaCarin; Sabel, Magnus; Bryceson, Yenan T.; Henter, Jan‐Inge Journal: Pediatric blood & cancer Issue: Volume 62:Issue 2(2015:Feb.) Page Start: 346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel deep intronic and missense UNC13D mutations in familial haemophagocytic lymphohistiocytosis type 3. (14th May 2013) Authors: Entesarian, Miriam; Chiang, Samuel C. C.; Schlums, Heinrich; Meeths, Marie; Chan, Mei‐Yoke; Mya, Soe‐Nwe; Soh, Shui‐Yen; Nordenskjöld, Magnus; Henter, Jan‐Inge; Bryceson, Yenan T. Journal: British journal of haematology Issue: Volume 162:Number 3(2013:Aug.) Page Start: 415 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations. Issue 12 (16th July 2015) Authors: 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 Journal: Pediatric blood & cancer Issue: Volume 62:Issue 12(2015:Dec.) Page Start: 2094 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗