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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 2
2008 1
2009 1
2010 6
2011 2
2012 1
2016 2
2017 1
2018 1
2020 1
2022 1
2023 1
2024 2

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21 results

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Page 1
Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study.
Hägele P, Staus P, Scheible R, Uhlmann A, Heeg M, Klemann C, Maccari ME, Ritterbusch H, Armstrong M, Cutcutache I, Elliott KS, von Bernuth H, Leahy TR, Leyh J, Holzinger D, Lehmberg K, Svec P, Masjosthusmann K, Hambleton S, Jakob M, Sparber-Sauer M, Kager L, Puzik A, Wolkewitz M, Lorenz MR, Schwarz K, Speckmann C, Rensing-Ehl A, Ehl S; ALPID study group. Hägele P, et al. Lancet Haematol. 2024 Feb;11(2):e114-e126. doi: 10.1016/S2352-3026(23)00362-9. Lancet Haematol. 2024. PMID: 38302222
Lemierre Syndrome in Adolescent with Active Ulcerative Colitis.
Unić J, Kovačić M, Jakovljević G, Batoš AT, Grmoja T, Hojsak I. Unić J, et al. Among authors: jakovljevic g. Pediatr Gastroenterol Hepatol Nutr. 2018 Jul;21(3):214-217. doi: 10.5223/pghn.2018.21.3.214. Epub 2018 Jun 28. Pediatr Gastroenterol Hepatol Nutr. 2018. PMID: 29992123 Free PMC article.
Contraception-related deep venous thrombosis and pulmonary embolism in a 17-Year-old girl heterozygous for factor V leiden, prothrombin G20210A mutation, MTHFR C677T and homozygous for PAI-1 mutation: report of a family with multiple genetic risk factors and review of the literature.
Lenicek Krleza J, Jakovljevic G, Bronic A, Coen Herak D, Bonevski A, Stepan-Giljevic J, Roic G. Lenicek Krleza J, et al. Among authors: jakovljevic g. Pathophysiol Haemost Thromb. 2010;37(1):24-9. doi: 10.1159/000319051. Epub 2010 Jul 20. Pathophysiol Haemost Thromb. 2010. PMID: 20664190 Review.
Mast-cell sarcoma of the tibia.
Brcić L, Vuletić LB, Stepan J, Bonevski A, Jakovljević G, Gasparov S, Marjanović K, Seiwerth S. Brcić L, et al. Among authors: jakovljevic g. J Clin Pathol. 2007 Apr;60(4):424-5. doi: 10.1136/jcp.2006.040857. J Clin Pathol. 2007. PMID: 17405977 Free PMC article.
Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D.
Meeths M, Chiang SC, Wood SM, Entesarian M, Schlums H, Bang B, Nordenskjöld E, Björklund C, Jakovljevic G, Jazbec J, Hasle H, Holmqvist BM, Rajic L, Pfeifer S, Rosthøj S, Sabel M, Salmi TT, Stokland T, Winiarski J, Ljunggren HG, Fadeel B, Nordenskjöld M, Henter JI, Bryceson YT. Meeths M, et al. Among authors: jakovljevic g. Blood. 2011 Nov 24;118(22):5783-93. doi: 10.1182/blood-2011-07-369090. Epub 2011 Sep 19. Blood. 2011. PMID: 21931115 Free article.
21 results