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The clinical characteristics and quality of life of 248 pediatric and adult patients with Congenital Adrenal Hyperplasia.
Shafaay EA, Aldriweesh MA, Aljahdali GL, Babiker A, Alomar AO, Alharbi KM, Aldalaan H, Alenazi A, Alangari AS, Alsagheir A, Adriaansen BPH, Claahsen-van der Grinten HL, Al Alwan I. Shafaay EA, et al. Among authors: alsagheir a. Front Endocrinol (Lausanne). 2023 Jun 6;14:1122435. doi: 10.3389/fendo.2023.1122435. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37347111 Free PMC article.
Outcome of COVID19 in Patients With Osteogenesis Imperfecta: A Retrospective Multicenter Study in Saudi Arabia.
Alshukairi AN, Doar H, Al-Sagheir A, Bahasan MA, Sultan AA, Al Hroub MK, Itani D, Khalid I, Saeedi MF, Bakhamis S, Layqah L, Almutairi AA, Saifullah M, Hefni L, Al-Omari A, Alraddadi BM, Baharoon SA. Alshukairi AN, et al. Front Endocrinol (Lausanne). 2022 Jan 13;12:800376. doi: 10.3389/fendo.2021.800376. eCollection 2021. Front Endocrinol (Lausanne). 2022. PMID: 35095767 Free PMC article.
Experience of X-linked hypophosphatemic rickets in the Gulf Cooperation Council countries: case series.
Al-Juraibah F, Al Shaikh A, Al-Sagheir A, Babiker A, Al Nuaimi A, Al Enezi A, Mikhail GS, Mundi HA, Penninckx HK, Mustafa H, Al Ameri M, Al-Dubayee M, Ali NS, Fawzy N, Al Shammari S, Fiad T. Al-Juraibah F, et al. Endocrinol Diabetes Metab Case Rep. 2024 Apr 11;2024(2):23-0098. doi: 10.1530/EDM-23-0098. Print 2024 Apr 1. Endocrinol Diabetes Metab Case Rep. 2024. PMID: 38614130 Free PMC article.
Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis.
Zou M, Alzahrani AS, Al-Odaib A, Alqahtani MA, Babiker O, Al-Rijjal RA, BinEssa HA, Kattan WE, Al-Enezi AF, Al Qarni A, Al-Faham MSA, Baitei EY, Alsagheir A, Meyer BF, Shi Y. Zou M, et al. Among authors: alsagheir a. J Clin Endocrinol Metab. 2018 May 1;103(5):1889-1898. doi: 10.1210/jc.2017-02202. J Clin Endocrinol Metab. 2018. PMID: 29546359
Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation.
Faiyaz-Ul-Haque M, AlDhalaan W, AlAshwal A, Bin-Abbas BS, AlSagheir A, Alotaiby M, Rafiq Z, Zaidi SHE. Faiyaz-Ul-Haque M, et al. Among authors: alsagheir a. J Pediatr Endocrinol Metab. 2018 Aug 28;31(8):861-868. doi: 10.1515/jpem-2017-0312. J Pediatr Endocrinol Metab. 2018. PMID: 29949513 Free article.
Analysis of disease characteristics of a large patient cohort with congenital generalized lipodystrophy from the Middle East and North Africa.
Al Yaarubi S, Alsagheir A, Al Shidhani A, Alzelaye S, Alghazir N, Brema I, Alsaffar H, Al Dubayee M, Alshahrani A, Abdelmeguid Y, Omar OM, Attia N, Al Amiri E, Al Jubeh J, Algethami A, Alkhayyat H, Haleem A, Al Yahyaei M, Khochtali I, Babli S, Nugud A, Thalange N, Albalushi S, Hergli N, Deeb A, Alfadhel M. Al Yaarubi S, et al. Among authors: alsagheir a. 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.
68 results