Thomas MM - Search Results

1

Growth charts of Down syndrome in Egypt: a study of 434 children 0-36 months of age.

Afifi HH, Aglan MS, Zaki ME, Thomas MM, Tosson AM. Afifi HH, et al. Among authors: thomas mm. Am J Med Genet A. 2012 Nov;158A(11):2647-55. doi: 10.1002/ajmg.a.35468. Epub 2012 Jul 18. Am J Med Genet A. 2012. PMID: 22811286

2

Gómez-López-hernández syndrome versus rhombencephalosynapsis spectrum: a rare co-occurrence with bipartite parietal bone.

Abdel-Salam GM, Abdel-Hadi S, Thomas MM, Eid OM, Ali MM, Afifi HH. Abdel-Salam GM, et al. Among authors: thomas mm. Am J Med Genet A. 2014 Feb;164A(2):480-3. doi: 10.1002/ajmg.a.36276. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311025

3

De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features.

Afifi HH, Fukai R, Miyake N, Gamal El Din AA, Eid MM, Eid OM, Thomas MM, El-Badry TH, Tosson AM, Abdel-Salam GM, Matsumoto N. Afifi HH, et al. Among authors: thomas mm. Am J Med Genet A. 2015 Oct;167A(10):2418-24. doi: 10.1002/ajmg.a.37185. Epub 2015 May 31. Am J Med Genet A. 2015. PMID: 26033841

4

Oxidative Stress -a Phenotypic Hallmark of Fanconi Anemia and Down Syndrome: The Effect of Antioxidants.

El-Bassyouni HT, Afifi HH, Eid MM, Kamal RM, El-Gebali HH, El-Saeed G, Thomas MM, Abdel-Maksoud SA. El-Bassyouni HT, et al. Among authors: thomas mm. Ann Med Health Sci Res. 2015 May-Jun;5(3):205-12. doi: 10.4103/2141-9248.157511. Ann Med Health Sci Res. 2015. PMID: 26097763 Free PMC article.

5

Detection and Quantification of Free Radicals in Peroxisomal Disorders: A Comparative Study with Oxidative Stress Parameters.

Abd-Elmaksoud SA, El-Bassyouni H, Afifi H, Thomas MM, Ibrahim AA, Shalaby A, Hamid TA, Hamid NA, El-Ghobary H. Abd-Elmaksoud SA, et al. Among authors: thomas mm. J Clin Diagn Res. 2015 Nov;9(11):SC17-20. doi: 10.7860/JCDR/2015/15629.6788. Epub 2015 Nov 1. J Clin Diagn Res. 2015. PMID: 26674249 Free PMC article.

6

Quality of Life Outcomes in a Pediatric Thalassemia Population in Egypt.

Adam S, Afifi H, Thomas M, Magdy P, El-Kamah G. Adam S, et al. Hemoglobin. 2017 Jan;41(1):16-20. doi: 10.1080/03630269.2017.1312434. Epub 2017 Apr 25. Hemoglobin. 2017. PMID: 28440111

7

Mutation in the SLC29A3 Gene in an Egyptian Patient with H Syndrome: A Case Report and Review of Literature.

El-Bassyouni HT, Thomas MM, Tosson AMS. El-Bassyouni HT, et al. Among authors: thomas mm. J Pediatr Genet. 2020 Jun;9(2):109-113. doi: 10.1055/s-0039-1697900. Epub 2019 Sep 30. J Pediatr Genet. 2020. PMID: 32341814 Free PMC article.

8

Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year Study.

Afifi HH, Gaber KR, Thomas MM, Taher MB, Tosson AMS. Afifi HH, et al. Among authors: thomas mm. Am J Perinatol. 2022 Nov;39(15):1659-1667. doi: 10.1055/s-0041-1724002. Epub 2021 Feb 26. Am J Perinatol. 2022. PMID: 33636738

9

First Report of Two Egyptian Patients with Desbuquois Dysplasia due to Homozygous CANT1 Mutations.

Thomas MM, Ashaat EA, Otaify GA, Ismail S, Essawi ML, Abdel-Hamid MS, Hassan HA, Alsaiedi SA, Aglan M, El Ruby MO, Temtamy S. Thomas MM, et al. Mol Syndromol. 2021 Aug;12(5):279-288. doi: 10.1159/000516607. Epub 2021 Jul 22. Mol Syndromol. 2021. PMID: 34602954 Free PMC article.

10

Importance of TREC and KREC as molecular markers for immunological evaluation of down syndrome children.

Eissa E, Afifi HH, Abo-Shanab AM, Thomas MM, Taher MB, Kandil R, Kholoussi NM. Eissa E, et al. Among authors: thomas mm. Sci Rep. 2023 Sep 18;13(1):15445. doi: 10.1038/s41598-023-42370-0. Sci Rep. 2023. PMID: 37723211 Free PMC article.

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