Tosson AMS - Search Results

1

The Effect of Anti-inflammatory Diet and Vitamin D Supplementation on the Amelioration of the Clinical Status and Cognitive functions of Familial Mediterranean Fever Patients.

Kazem Y, Zarouk WA, Hamed K, Tosson AMS, Essa HA, El-Bassyouni HT. Kazem Y, et al. Among authors: tosson ams. Kobe J Med Sci. 2021 Feb 15;66(5):E159-E165. Kobe J Med Sci. 2021. PMID: 34001682 Free PMC article.

2

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: tosson ams. 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.

3

Coenzyme Q10 and pro-inflammatory markers in children with Down syndrome: clinical and biochemical aspects.

Zaki ME, El-Bassyouni HT, Tosson AM, Youness E, Hussein J. Zaki ME, et al. J Pediatr (Rio J). 2017 Jan-Feb;93(1):100-104. doi: 10.1016/j.jped.2016.04.012. Epub 2016 Oct 19. J Pediatr (Rio J). 2017. PMID: 27770619 Free article.

4

Early Detection and Management of Prader-Willi Syndrome in Egyptian Patients.

El-Bassyouni HT, Hassan N, Mahfouz I, Abd-Elnaby AE, Mostafa MI, Tosson AMS. El-Bassyouni HT, et al. Among authors: tosson ams. J Pediatr Genet. 2019 Dec;8(4):179-186. doi: 10.1055/s-0039-1695042. Epub 2019 Aug 4. J Pediatr Genet. 2019. PMID: 31687254 Free PMC article.

5

Clinical, Biochemical, and Molecular Characterization of Metachromatic Leukodystrophy Among Egyptian Pediatric Patients: Expansion of the ARSA Mutational Spectrum.

Amr K, Fateen E, Mansour L, Tosson AM, Zaki MS, Salam GMA, Mohamed AN, El-Bassyouni HT. Amr K, et al. J Mol Neurosci. 2021 May;71(5):1112-1130. doi: 10.1007/s12031-020-01734-1. Epub 2020 Nov 13. J Mol Neurosci. 2021. PMID: 33185815

6

Lipoid proteinosis: A clinical and molecular study in Egyptian patients.

Afifi HH, Amr KS, Tosson AMS, Hassan TA, Mehrez MI, El-Kamah GY. Afifi HH, et al. Among authors: tosson ams. Gene. 2017 Sep 10;628:308-314. doi: 10.1016/j.gene.2017.07.026. Epub 2017 Jul 15. Gene. 2017. PMID: 28720532

7

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. 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

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: tosson ams. 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

Evaluation of serum and salivary C-reactive protein for diagnosis of late-onset neonatal sepsis: A single center cross-sectional study.

Tosson AMS, Koptan D, Abdel Aal R, Abd Elhady M. Tosson AMS, et al. J Pediatr (Rio J). 2021 Nov-Dec;97(6):623-628. doi: 10.1016/j.jped.2021.01.004. Epub 2021 Feb 11. J Pediatr (Rio J). 2021. PMID: 33582092 Free PMC article.

10

Expanding the mutation and clinical spectrum of Roberts syndrome.

Afifi HH, Abdel-Salam GM, Eid MM, Tosson AM, Shousha WG, Abdel Azeem AA, Farag MK, Mehrez MI, Gaber KR. Afifi HH, et al. Congenit Anom (Kyoto). 2016 Jul;56(4):154-62. doi: 10.1111/cga.12151. Congenit Anom (Kyoto). 2016. PMID: 26710928

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