Al-Thani G - Search Results

1

Microscale thermophoresis as a powerful growing analytical technique for the investigation of biomolecular interaction and the determination of binding parameters.

El Deeb S, Al-Harrasi A, Khan A, Al-Broumi M, Al-Thani G, Alomairi M, Elumalai P, Sayed RA, Ibrahim AE. El Deeb S, et al. Among authors: al thani g. Methods Appl Fluoresc. 2022 Jul 28;10(4). doi: 10.1088/2050-6120/ac82a6. Methods Appl Fluoresc. 2022. PMID: 35856854 Review.

2

Toxic Elemental Impurities in Herbal Weight Loss Supplements; A Study Using ICP-OES Microwave-Assisted Digestion.

Al-Thani G, Ibrahim AE, Alomairi M, Salman BI, Hegazy MM, Al-Harrasi A, El Deeb S. Al-Thani G, et al. Toxics. 2023 Mar 16;11(3):272. doi: 10.3390/toxics11030272. Toxics. 2023. PMID: 36977037 Free PMC article.

3

Comparative analysis of heavy metal content of unregulated facial whitening creams and branded facial whitening creams.

Arputhanantham SS, Al-Thani GSS, Al Amri RMS, Hossain MA. Arputhanantham SS, et al. Among authors: al thani gss. Toxicol Rep. 2024 Mar 5;12:326-330. doi: 10.1016/j.toxrep.2023.10.011. eCollection 2024 Jun. Toxicol Rep. 2024. PMID: 38516207 Free PMC article.

4

Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families.

Faiyaz-Ul-Haque M, Zaidi SH, Wahab AA, Eltohami A, Al-Mureikhi MS, Al-Thani G, Peltekova VD, Tsui LC, Teebi AS. Faiyaz-Ul-Haque M, et al. Among authors: al thani g. Clin Genet. 2008 Aug;74(2):189-93. doi: 10.1111/j.1399-0004.2008.01049.x. Epub 2008 Jun 28. Clin Genet. 2008. PMID: 18565096 No abstract available.

5

Outcome of congenital hydronephrosis in qatar.

Saad TS, Al-Zamer J, Al-Thani GM, Al-Khateeb D, Salman M. Saad TS, et al. Among authors: al thani gm. Saudi J Kidney Dis Transpl. 1998 Oct-Dec;9(4):430-4. Saudi J Kidney Dis Transpl. 1998. PMID: 18408313

6

Implementation of extended neonatal screening and a metabolic unit in the State of Qatar: developing and optimizing strategies in cooperation with the Neonatal Screening Center in Heidelberg.

Lindner M, Abdoh G, Fang-Hoffmann J, Shabeck N, Al-Sayrafi M, Al-Janahi M, Ho S, Abdelrahman MO, Ben-Omran T, Bener A, Schulze A, Al-Rifai H, Al-Thani G, Hoffmann GF. Lindner M, et al. Among authors: al thani g. J Inherit Metab Dis. 2007 Aug;30(4):522-9. doi: 10.1007/s10545-007-0553-7. Epub 2007 May 12. J Inherit Metab Dis. 2007. PMID: 17510756

7

A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type.

Faiyaz-Ul-Haque M, Zaidi SH, Al-Ali M, Al-Mureikhi MS, Kennedy S, Al-Thani G, Tsui LC, Teebi AS. Faiyaz-Ul-Haque M, et al. Among authors: al thani g. Am J Med Genet A. 2004 Jul 1;128A(1):39-45. doi: 10.1002/ajmg.a.30005. Am J Med Genet A. 2004. PMID: 15211654

8

Rare CFTR mutation 1525-1G>A in a Pakistani patient.

Wahab A, Al Thani G, Dawod ST, Kambouris M, Al Hamed M. Wahab A, et al. Among authors: al thani g. J Trop Pediatr. 2004 Apr;50(2):120-2. doi: 10.1093/tropej/50.2.120. J Trop Pediatr. 2004. PMID: 15088804

9

Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V).

Abdul Wahab A, Al Thani G, Dawod ST, Kambouris M, Al Hamed M. Abdul Wahab A, et al. Among authors: al thani g. J Trop Pediatr. 2001 Apr;47(2):110-2. doi: 10.1093/tropej/47.2.110. J Trop Pediatr. 2001. PMID: 11336127

10

Cystic fibrosis in a large kindred family in Qatar.

Abdul Wahab A, Dawod ST, al Thani G. Abdul Wahab A, et al. Among authors: al thani g. Ann Trop Paediatr. 2000 Sep;20(3):203-7. doi: 10.1080/02724936.2000.11748135. Ann Trop Paediatr. 2000. PMID: 11064773

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