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Analysis of disease characteristics of a large patient cohort with congenital generalized lipodystrophy from the Middle East and North Africa.
Orphanet J Rare Dis. 2024 Mar 13;19(1):118. doi: 10.1186/s13023-024-03084-2.
Orphanet J Rare Dis. 2024.
PMID: 38481246
Free PMC article.
Burden of Illness of Type 2 Diabetes Mellitus in the Kingdom of Saudi Arabia: A Five-Year Longitudinal Study.
AlHarbi M, Othman A, Nahari AA, Al-Jedai AH, Cuadras D, Almalky F, AlAzmi F, Almudaiheem HY, AlShubrumi H, AlSwat H, AlSahafi H, Sindi K, Basaikh K, AlQahtani M, Lamotte M, Yahia M, Hassan ME, AlMutlaq M, AlRoaly M, AlZelaye S, AlGhamdi Z.
AlHarbi M, et al. Among authors: alzelaye s.
Adv Ther. 2024 Mar;41(3):1120-1150. doi: 10.1007/s12325-023-02772-y. Epub 2024 Jan 19.
Adv Ther. 2024.
PMID: 38240948
Free PMC article.
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Familial Screening for the Prevention of Rare Diseases: A Focus on Lipodystrophy in Southern Saudi Arabia.
Abuzenadah A, Alganmi N, AlQurashi R, Hawsa E, AlOtibi A, Hummadi A, Nahari AA, AlZelaye S, Aljuhani NR, Al-Attas M, Abusamra H, Turkistany S, Karim S, Mirza Z, Al-Qahtani M, Chaudhary A, Al Eissa MM.
Abuzenadah A, et al. Among authors: alzelaye s.
J Epidemiol Glob Health. 2024 Mar;14(1):162-168. doi: 10.1007/s44197-023-00182-5. Epub 2024 Jan 17.
J Epidemiol Glob Health. 2024.
PMID: 38231342
Free PMC article.
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A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families.
Shaikh AA, Shirah B, Alzelaye S.
Shaikh AA, et al. Among authors: alzelaye s.
Ann Pediatr Endocrinol Metab. 2020 Mar;25(1):42-45. doi: 10.6065/apem.2020.25.1.42. Epub 2020 Mar 31.
Ann Pediatr Endocrinol Metab. 2020.
PMID: 32252216
Free PMC article.
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Monies D, Abouelhoda M, Assoum M, Moghrabi N, Rafiullah R, Almontashiri N, Alowain M, Alzaidan H, Alsayed M, Subhani S, Cupler E, Faden M, Alhashem A, Qari A, Chedrawi A, Aldhalaan H, Kurdi W, Khan S, Rahbeeni Z, Alotaibi M, Goljan E, Elbardisy H, ElKalioby M, Shah Z, Alruwaili H, Jaafar A, Albar R, Akilan A, Tayeb H, Tahir A, Fawzy M, Nasr M, Makki S, Alfaifi A, Akleh H, Yamani S, Bubshait D, Mahnashi M, Basha T, Alsagheir A, Khaled MA, Alsaleem K, Almugbel M, Badawi M, Bashiri F, Bohlega S, Sulaiman R, Tous E, Ahmed S, Algoufi T, Al-Mousa H, Alaki E, Alhumaidi S, Alghamdi H, Alghamdi M, Sahly A, Nahrir S, Al-Ahmari A, Alkuraya H, Almehaidib A, Abanemai M, Alsohaibaini F, Alsaud B, Arnaout R, Abdel-Salam GMH, Aldhekri H, AlKhater S, Alqadi K, Alsabban E, Alshareef T, Awartani K, Banjar H, Alsahan N, Abosoudah I, Alashwal A, Aldekhail W, Alhajjar S, Al-Mayouf S, Alsemari A, Alshuaibi W, Altala S, Altalhi A, Baz S, Hamad M, Abalkhail T, Alenazi B, Alkaff A, Almohareb F, Al Mutairi F, Alsaleh M, Alsonbul A, Alzelaye S, Bahzad S, Manee AB, Jarrad O, Meriki N, Albeirouti B, Alqasmi A, AlBalwi M, Makhseed N, Hassan S, Salih I, Salih MA, Shaheen M, Sermin S, Shahrukh S, Hashmi S,…
See abstract for full author list ➔
Monies D, et al. Among authors: alzelaye s.
Am J Hum Genet. 2019 Oct 3;105(4):879. doi: 10.1016/j.ajhg.2019.09.019.
Am J Hum Genet. 2019.
PMID: 31585110
Free PMC article.
No abstract available.
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Monies D, Abouelhoda M, Assoum M, Moghrabi N, Rafiullah R, Almontashiri N, Alowain M, Alzaidan H, Alsayed M, Subhani S, Cupler E, Faden M, Alhashem A, Qari A, Chedrawi A, Aldhalaan H, Kurdi W, Khan S, Rahbeeni Z, Alotaibi M, Goljan E, Elbardisy H, ElKalioby M, Shah Z, Alruwaili H, Jaafar A, Albar R, Akilan A, Tayeb H, Tahir A, Fawzy M, Nasr M, Makki S, Alfaifi A, Akleh H, Yamani S, Bubshait D, Mahnashi M, Basha T, Alsagheir A, Abu Khaled M, Alsaleem K, Almugbel M, Badawi M, Bashiri F, Bohlega S, Sulaiman R, Tous E, Ahmed S, Algoufi T, Al-Mousa H, Alaki E, Alhumaidi S, Alghamdi H, Alghamdi M, Sahly A, Nahrir S, Al-Ahmari A, Alkuraya H, Almehaidib A, Abanemai M, Alsohaibaini F, Alsaud B, Arnaout R, Abdel-Salam GMH, Aldhekri H, AlKhater S, Alqadi K, Alsabban E, Alshareef T, Awartani K, Banjar H, Alsahan N, Abosoudah I, Alashwal A, Aldekhail W, Alhajjar S, Al-Mayouf S, Alsemari A, Alshuaibi W, Altala S, Altalhi A, Baz S, Hamad M, Abalkhail T, Alenazi B, Alkaff A, Almohareb F, Al Mutairi F, Alsaleh M, Alsonbul A, Alzelaye S, Bahzad S, Manee AB, Jarrad O, Meriki N, Albeirouti B, Alqasmi A, AlBalwi M, Makhseed N, Hassan S, Salih I, Salih MA, Shaheen M, Sermin S, Shahrukh S, Hashmi…
See abstract for full author list ➔
Monies D, et al. Among authors: alzelaye s.
Am J Hum Genet. 2019 Jun 6;104(6):1182-1201. doi: 10.1016/j.ajhg.2019.04.011. Epub 2019 May 23.
Am J Hum Genet. 2019.
PMID: 31130284
Free PMC article.
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