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Glanzmann thrombasthenia in Pakistan: molecular analysis and identification of novel mutations.
Published in:
Clinical Genetics, 2016, v. 89, n. 2, p. 187, doi. 10.1111/cge.12622
By:
- Haghighi, A.;
- Borhany, M.;
- Ghazi, A.;
- Edwards, N.;
- Tabaksert, A.;
- Fatima, N.;
- Shamsi, T.S.;
- Sayer, J.A.
Publication type:
Article
Acute blood transfusion reactions in a tertiary care hospital in Pakistan ‐ an initiative towards haemovigilance.
Published in:
Transfusion Medicine, 2019, v. 29, n. 4, p. 275, doi. 10.1111/tme.12541
By:
- Borhany, M.;
- Anwar, N.;
- Tariq, H.;
- Fatima, N.;
- Arshad, A.;
- Naseer, I.;
- Shamsi, T.
Publication type:
Article
Frequency and reasons of donor deferral prior to blood donation process: a single centre experience.
Published in:
Transfusion Medicine, 2017, v. 27, n. 1, p. 10, doi. 10.1111/tme.12368
By:
- Khurram, S.;
- Borhany, M.;
- Anwar, N.;
- Naseer, I.;
- Boota, S.;
- Mirza, I.;
- Nadeem, M.;
- Shamsi, T.
Publication type:
Article
Red cell alloimmunisation in regularly transfused beta thalassemia patients in Pakistan.
Published in:
Transfusion Medicine, 2015, v. 25, n. 2, p. 106, doi. 10.1111/tme.12196
By:
- Zaidi, U.;
- Borhany, M.;
- Ansari, S.;
- Parveen, S.;
- Boota, S.;
- Shamim, I.;
- Zahid, D.;
- Shamsi, T.
Publication type:
Article
Two new double mutant alleles of the F7 gene and a literature review on alleles with two mutations in FVII deficiency.
Published in:
Haemophilia, 2016, v. 22, n. 4, p. e304, doi. 10.1111/hae.12897
By:
- Giansily‐Blaizot, M.;
- Kolaitis, N.;
- Borhany, M.;
- Moulis, G.;
- Guillot, O.;
- Shamsi, T.
Publication type:
Article
A new report of FVII-inhibitor in a patient suffering from severe congenital FVII deficiency.
Published in:
Haemophilia, 2015, v. 21, n. 4, p. e336, doi. 10.1111/hae.12708
By:
- Borhany, M.;
- Delbes, C.;
- Giansily‐Blaizot, M.;
- Zubair, M.;
- Ahmed, M. S.;
- Fatima, N.;
- Shamsi, T.
Publication type:
Article
Identification of two novel missense mutations causing severe factor XIII deficiency.
Published in:
Haemophilia, 2015, v. 21, n. 3, p. e253, doi. 10.1111/hae.12663
By:
- Handrkova, H.;
- Borhany, M.;
- Schroeder, V.;
- Fatima, N.;
- Hussain, A.;
- Shamsi, T.;
- Kohler, H. P.
Publication type:
Article
Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.
Published in:
Haemophilia, 2014, v. 20, n. 4, p. 568, doi. 10.1111/hae.12340
By:
- BORHANY, M.;
- HANDRKOVA, H.;
- CAIRO, A.;
- SCHROEDER, V.;
- FATIMA, N.;
- NAZ, A.;
- AMANAT, S.;
- SHAMSI, T.;
- PEYVANDI, F.;
- KOHLER, H. P.
Publication type:
Article
Genotype and phenotype relationships in 10 Pakistani unrelated patients with inherited factor VII deficiency.
Published in:
Haemophilia, 2013, v. 19, n. 6, p. 893, doi. 10.1111/hae.12186
By:
- Borhany, M.;
- Boijout, H.;
- Pellequer, J.‐L.;
- Shamsi, T.;
- Moulis, G.;
- Aguilar‐Martinez, P.;
- Schved, J.‐F.;
- Giansily‐Blaizot, M.
Publication type:
Article
Pattern of bleeding and response to therapy in Glanzmann thrombasthenia.
Published in:
Haemophilia, 2012, v. 18, n. 6, p. e423, doi. 10.1111/hae.12017
By:
- Borhany, M.;
- Fatima, H.;
- Naz, A.;
- Patel, H.;
- Shamsi, T.
Publication type:
Article

Found: 10