Bassyouni H - Search Results

1

Biallelic mutations at PPARG cause a congenital, generalized lipodystrophy similar to the Berardinelli-Seip syndrome.

Dyment DA, Gibson WT, Huang L, Bassyouni H, Hegele RA, Innes AM. Dyment DA, et al. Among authors: bassyouni h. Eur J Med Genet. 2014 Sep;57(9):524-6. doi: 10.1016/j.ejmg.2014.06.006. Epub 2014 Jun 28. Eur J Med Genet. 2014. PMID: 24980513

2

Vitamin D-Binding Protein Deficiency and Homozygous Deletion of the GC Gene.

Henderson CM, Fink SL, Bassyouni H, Argiropoulos B, Brown L, Laha TJ, Jackson KJ, Lewkonia R, Ferreira P, Hoofnagle AN, Marcadier JL. Henderson CM, et al. Among authors: bassyouni h. N Engl J Med. 2019 Mar 21;380(12):1150-1157. doi: 10.1056/NEJMoa1807841. N Engl J Med. 2019. PMID: 30893535 Free PMC article.

3

Vitamin D-Binding Protein Deficiency and Homozygous Deletion of the GC Gene. Reply.

Bassyouni H, Lewkonia R, Marcadier JL. Bassyouni H, et al. N Engl J Med. 2019 Jun 27;380(26):2586-2587. doi: 10.1056/NEJMc1905282. N Engl J Med. 2019. PMID: 31242376 No abstract available.

4

Hepatocyte nuclear factor 4 inhibits the activity of site A from the rat apolipoprotein AI gene.

Murao K, Bassyouni H, Taylor AH, Wanke IE, Wong NC. Murao K, et al. Among authors: bassyouni h. Biochemistry. 1997 Jan 14;36(2):301-6. doi: 10.1021/bi9613943. Biochemistry. 1997. PMID: 9003181

5

Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients.

Sayed-Ahmed MM, El-Bassyouni HT, Afifi HH, Essawi ML, Taher MB, Gadelhak MI, Zaytoun RA, Abdelmonem AA, Elbagoury NM. Sayed-Ahmed MM, et al. Among authors: el bassyouni ht. J Mol Neurosci. 2024 Oct 28;74(4):102. doi: 10.1007/s12031-024-02279-3. J Mol Neurosci. 2024. PMID: 39467922 Free PMC article.

6

Potential biomarkers of ASD a target for future treatments: oxidative stress, chemokines, apoptotic, and methylation capacity.

Zaki M, Youness ER, Orban HA, Ahmed HM, Moustafa RSI, Alzaree FA, Ashaat EA, El-Bassyouni HT. Zaki M, et al. Among authors: el bassyouni ht. J Complement Integr Med. 2024 Jul 4. doi: 10.1515/jcim-2024-0145. Online ahead of print. J Complement Integr Med. 2024. PMID: 38960893

7

Altered expression of miR-17 and miR-148b in pediatric familial mediterranean fever patients.

Sokkar MF, Eldeen GN, Lotfy RS, Kobesiy MM, El-Bassyouni HT, Zarouk WA. Sokkar MF, et al. Among authors: el bassyouni ht. Clin Rheumatol. 2024 Aug;43(8):2661-2667. doi: 10.1007/s10067-024-07023-1. Epub 2024 Jun 15. Clin Rheumatol. 2024. PMID: 38879629

8

Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families.

El-Kamah GY, Mehrez MI, Taher MB, El-Bassyouni HT, Gaber KR, Amr KS. El-Kamah GY, et al. Among authors: el bassyouni ht. Genes (Basel). 2023 Apr 12;14(4):900. doi: 10.3390/genes14040900. Genes (Basel). 2023. PMID: 37107657 Free PMC article.

9

Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients.

Zekry ME, Sallam AM, AbdelHamid SG, Zarouk WA, El-Bassyouni HT, El-Mesallamy HO. Zekry ME, et al. Among authors: el bassyouni ht. Curr Issues Mol Biol. 2023 Jan 13;45(1):721-737. doi: 10.3390/cimb45010048. Curr Issues Mol Biol. 2023. PMID: 36661534 Free PMC article.

10

The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome.

Youness ER, Hashem SA, Hamed K, Khedr AA, Abdulhalim EN, Kamel SM, El-Bassyouni HT. Youness ER, et al. Among authors: el bassyouni ht. J Pediatr Endocrinol Metab. 2022 Dec 20;36(2):147-151. doi: 10.1515/jpem-2022-0482. Print 2023 Feb 23. J Pediatr Endocrinol Metab. 2022. PMID: 36530035

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