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Structural analysis of a missense mutation (Val414Phe) in the catalytic core domain of the factor XIII(A) subunit.
Aslam S, Yee VC, Narayanan S, Duraisamy G, Standen GR. Aslam S, et al. Br J Haematol. 1997 Aug;98(2):346-52. doi: 10.1046/j.1365-2141.1997.2263043.x. Br J Haematol. 1997. PMID: 9266932
Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H gene.
Aslam S, Standen GR. Aslam S, et al. Postgrad Med J. 1997 Sep;73(863):573-4. doi: 10.1136/pgmj.73.863.573. Postgrad Med J. 1997. PMID: 9373599 Free PMC article.
Prenatal diagnosis in factor XIII-A deficiency.
Killick CJ, Barton CJ, Aslam S, Standen G. Killick CJ, et al. Among authors: aslam s. Arch Dis Child Fetal Neonatal Ed. 1999 May;80(3):F238-9. doi: 10.1136/fn.80.3.f238. Arch Dis Child Fetal Neonatal Ed. 1999. PMID: 10212091 Free PMC article.
Molecular analysis of six factor XIII-A-deficient families in Southern Pakistan.
Aslam S, Standen GR, Khurshid M, Bilwani F. Aslam S, et al. Br J Haematol. 2000 May;109(2):463. doi: 10.1046/j.1365-2141.2000.01998.x. Br J Haematol. 2000. PMID: 10877543 No abstract available.
Factor XIII(A) subunit deficiency due to a homozygous 13-base pair deletion in exon 3 of the A subunit gene.
Aslam S, Bowen DJ, Mandalaki T, Gialeraki R, Standen GR. Aslam S, et al. Am J Hematol. 1996 Oct;53(2):77-80. doi: 10.1002/(SICI)1096-8652(199610)53:2<77::AID-AJH4>3.0.CO;2-0. Am J Hematol. 1996. PMID: 8892731
Factor XIIIA Calgary: a candidate missense mutation (Leu667Pro) in the beta barrel 2 domain of the factor XIIIA subunit.
Aslam S, Poon MC, Yee VC, Bowen DJ, Standen GR. Aslam S, et al. Br J Haematol. 1995 Oct;91(2):452-7. doi: 10.1111/j.1365-2141.1995.tb05321.x. Br J Haematol. 1995. PMID: 8547093
A novel insertion mutation (1286insC) in exon 9 of the factor XIII-A subunit gene.
Aslam S, Standen GR, Bruce LJ, Gialeraki R, Mandalaki T. Aslam S, et al. Blood Coagul Fibrinolysis. 1998 Jul;9(5):441-3. doi: 10.1097/00001721-199807000-00007. Blood Coagul Fibrinolysis. 1998. PMID: 9712293
Molecular analysis in factor XIIIA deficiency.
Aslam S, Standen GR. Aslam S, et al. Thromb Haemost. 1995 May;73(5):895. Thromb Haemost. 1995. PMID: 7482425 No abstract available.
Haemoperitoneum due to ruptured ovarian cyst in a 13-year-old girl with factor V deficiency- A case report.
Aslam SL, Fareeduddin M. Aslam SL, et al. J Pak Med Assoc. 2017 Feb;67(2):314-315. J Pak Med Assoc. 2017. PMID: 28138193
Recurrent thrombosis in a patient with pseudohomozygous activated protein C resistance and homozygosity for MTHFR gene polymorphism C677T.
Standen G, Morse C, Aslam S, Bowron A. Standen G, et al. Among authors: aslam s. Thromb Haemost. 1999 Apr;81(4):663-4. Thromb Haemost. 1999. PMID: 10235461 No abstract available.
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