Cited by

• Detection of alloimmunization in Glanzmann Thrombasthenia and Bernard-Soulier Syndrome: Data from a Brazilian Center.

  Gabe C, Ziza KC, Durazzo N, Pagani FM, Oliveira VB, Conrado MAV, Dezan MR, Mendrone A Jr, Villaça PR, Dinardo CL, Rocha V. Gabe C, et al. Hematol Transfus Cell Ther. 2023 Jul;45 Suppl 2(Suppl 2):S101-S107. doi: 10.1016/j.htct.2022.06.005. Epub 2022 Jul 20. Hematol Transfus Cell Ther. 2023. PMID: 36114116 Free PMC article.
• Progressive skeletal defects caused by Kindlin3 deficiency, a model of autosomal recessive osteopetrosis in humans.

  Dudiki T, Nascimento DW, Childs LS, Kareti S, Androjna C, Zhevlakova I, Byzova TV. Dudiki T, et al. Bone. 2022 Jul;160:116397. doi: 10.1016/j.bone.2022.116397. Epub 2022 Mar 25. Bone. 2022. PMID: 35342016 Free PMC article.
• Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations.

  Zafarghandi Motlagh F, Fallah MS, Bagherian H, Shirzadeh T, Ghasri S, Dabbagh S, Jamali M, Salehi Z, Abiri M, Zeinali S. Zafarghandi Motlagh F, et al. Orphanet J Rare Dis. 2019 Apr 27;14(1):87. doi: 10.1186/s13023-019-1042-4. Orphanet J Rare Dis. 2019. PMID: 31029159 Free PMC article.
• Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients.

  Owaidah T, Saleh M, Baz B, Abdulaziz B, Alzahrani H, Tarawah A, Almusa A, AlNounou R, AbaAlkhail H, Al-Numair N, Altahan R, Abouelhoda M, Alamoudi T, Monies D, Jabaan A, Al Tassan N. Owaidah T, et al. NPJ Genom Med. 2019 Feb 14;4:4. doi: 10.1038/s41525-019-0079-6. eCollection 2019. NPJ Genom Med. 2019. PMID: 30792900 Free PMC article.
• Menstrual and obstetrical bleeding in women with inherited platelet receptor defects-A systematic review.

  Punt MC, Schuitema PCE, Bloemenkamp KWM, Kremer Hovinga ICL, van Galen KPM. Punt MC, et al. Haemophilia. 2020 Mar;26(2):216-227. doi: 10.1111/hae.13927. Epub 2020 Jan 31. Haemophilia. 2020. PMID: 32004416 Free PMC article.