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Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).
Feldmann J, Callebaut I, Raposo G, Certain S, Bacq D, Dumont C, Lambert N, Ouachée-Chardin M, Chedeville G, Tamary H, Minard-Colin V, Vilmer E, Blanche S, Le Deist F, Fischer A, de Saint Basile G. Feldmann J, et al. Among authors: tamary h. Cell. 2003 Nov 14;115(4):461-73. doi: 10.1016/s0092-8674(03)00855-9. Cell. 2003. PMID: 14622600 Free article.
Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations.
Thalhammer J, Kindle G, Nieters A, Rusch S, Seppänen MRJ, Fischer A, Grimbacher B, Edgar D, Buckland M, Mahlaoui N, Ehl S; European Society for Immunodeficiencies Registry Working Party. Thalhammer J, et al. J Allergy Clin Immunol. 2021 Nov;148(5):1332-1341.e5. doi: 10.1016/j.jaci.2021.04.015. Epub 2021 Apr 23. J Allergy Clin Immunol. 2021. PMID: 33895260 Free article.
Red cell transfusions in neonatal care.
Tamary H, Tamary H, Sivota L, Magan X, Orlin X. Tamary H, et al. Vox Sang. 2001 Feb;80(2):132. Vox Sang. 2001. PMID: 11348554 No abstract available.
Red cell transfusions in neonatal care.
Engelfriet CP, Reesink HW, Strauss RG, Modi N, Murray N, Maier RF, Obladen M, van Kaam AH, Martin-Vega C, Castella D, Almar J, Martell M, De Felice C, Tamary H, Sivota L, Magan X, Orlin X, Naples ML, Bednarek FJ. Engelfriet CP, et al. Among authors: tamary h. Vox Sang. 2001 Feb;80(2):122-33. Vox Sang. 2001. PMID: 11378968 No abstract available.
Triallelic and epigenetic-like inheritance in human disorders of telomerase.
Collopy LC, Walne AJ, Cardoso S, de la Fuente J, Mohamed M, Toriello H, Tamary H, Ling AJ, Lloyd T, Kassam R, Tummala H, Vulliamy TJ, Dokal I. Collopy LC, et al. Among authors: tamary h. Blood. 2015 Jul 9;126(2):176-84. doi: 10.1182/blood-2015-03-633388. Epub 2015 May 29. Blood. 2015. PMID: 26024875 Free PMC article.
Diagnosis, treatment, and surveillance of Diamond-Blackfan anaemia syndrome: international consensus statement.
Wlodarski MW, Vlachos A, Farrar JE, Da Costa LM, Kattamis A, Dianzani I, Belendez C, Unal S, Tamary H, Pasauliene R, Pospisilova D, de la Fuente J, Iskander D, Wolfe L, Liu JM, Shimamura A, Albrecht K, Lausen B, Bechensteen AG, Tedgard U, Puzik A, Quarello P, Ramenghi U, Bartels M, Hengartner H, Farah RA, Al Saleh M, Hamidieh AA, Yang W, Ito E, Kook H, Ovsyannikova G, Kager L, Gleizes PE, Dalle JH, Strahm B, Niemeyer CM, Lipton JM, Leblanc TM; international Diamond-Blackfan anaemia syndrome guideline panel. Wlodarski MW, et al. Among authors: tamary h. Lancet Haematol. 2024 May;11(5):e368-e382. doi: 10.1016/S2352-3026(24)00063-2. Lancet Haematol. 2024. PMID: 38697731 Review.
Symptomatic corpus luteum hemorrhage in adolescent females with ITP.
Yelak A, From A, Gilad O, Brik Simon D, Rubin S, Cohen M, Amarilyo G, Levin C, Bakry D, Izraeli S, Tamary H, Yacobovich J, Steinberg-Shemer O. Yelak A, et al. Among authors: tamary h. Eur J Pediatr. 2024 Apr 11. doi: 10.1007/s00431-024-05560-0. Online ahead of print. Eur J Pediatr. 2024. PMID: 38602530
Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.
Yeshareem L, Yacobovich J, Lebel A, Noy-Lotan S, Dgany O, Krasnov T, Berger Pinto G, Oniashvili N, Mardoukh J, Bielorai B, Laor R, Mandel-Shorer N, Ben Barak A, Levin C, Asleh M, Miskin H, Revel-Vilk S, Levin D, Benish M, Zuckerman T, Wolach O, Pazgal I, Brik Simon D, Gilad O, Yanir AD, Goldberg TA, Izraeli S, Tamary H, Steinberg-Shemer O. Yeshareem L, et al. Among authors: tamary h. Eur J Haematol. 2024 Apr 11. doi: 10.1111/ejh.14197. Online ahead of print. Eur J Haematol. 2024. PMID: 38600884
185 results