Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

397 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
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.
397 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback