Records 1 - 5
| Important roles of the human leukocyte antigen class I and II molecules and their associated genes in the autoimmune coagulation factor XIII deficiency via whole-exome sequencing analysis.
PloS one 2021 16 (9): e0257322.
Osaki Tsukasa, Souri Masayoshi, Ichinose Akita
| Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations.
Blood cells, molecules & diseases 2016 Mar 57 81-4.
Shanbhag Sharda, Ghosh Kanjaksha, Shetty Shrima
| Central nervous system bleeding in pediatric patients with factor XIII deficiency: a study on 23 new cases.
Hematology (Amsterdam, Netherlands) 2015 Mar 20 (2): 112-8.
Naderi Majid, Alizadeh Shaban, Kazemi Ahmad, Tabibian Shadi, Zaker Farhad, Bamedi Taregh, Kashani Khatib Zahra, Dorgalaleh Akb
| Association between expression of MMP-2 and MMP-9 genes and pathogenesis of intracranial hemorrhage in severe coagulation factor XIII deficiency.
Hematology (Amsterdam, Netherlands) 2014 Dec .
Naderi Majid, Younesi Mohammad Reza, Dorgalaleh Akbar, Alizadeh Shaban, Kazemi Ahmad, Tabibian Sha
| A common F13A1 intron 1 variant IVS1+12(A) is associated with mild FXIII deficiency in Caucasian population.
Annals of hematology 2013 Jul 92 (7): 975-9.
Ivaskevicius Vytautas, Biswas Arijit, Thomas Anne, Lyonga Sophie, Rott Hannelore, Halimeh Susan, Kappert Guenther, Klammroth Robert, Scholz Ute, Eberl Wolfgang, Harbrecht Ursula, Gnida Christine, Hertfelder Hans-Joerg, Marquardt Natascha, Oldenburg Johann