Abo El Fotoh WMM - Search Results

1

A66G and C524T polymorphisms of methionine synthase reductase gene are linked to the development of acyanotic congenital heart diseases in Egyptian children.

Hassan FM, Khattab AA, Abo El Fotoh WMM, Zidan RS. Hassan FM, et al. Among authors: abo el fotoh wmm. Gene. 2017 Sep 20;629:59-63. doi: 10.1016/j.gene.2017.07.081. Epub 2017 Aug 2. Gene. 2017. PMID: 28778621

2

The genetic variant "C588T" of GABARG2 is linked to childhood idiopathic generalized epilepsy and resistance to antiepileptic drugs.

Abou El Ella SS, Tawfik MA, Abo El Fotoh WMM, Soliman OAM. Abou El Ella SS, et al. Among authors: abo el fotoh wmm. Seizure. 2018 Aug;60:39-43. doi: 10.1016/j.seizure.2018.06.004. Epub 2018 Jun 6. Seizure. 2018. PMID: 29894917 Free article.

3

The Genetic Variants of IKZF1 Gene Linked with the Growing Risk of Childhood Acute Lymphoblastic Leukaemia.

Tayel SI, El-Hefnway SM, Abo El-Fotoh WMM, El-Zayat RS. Tayel SI, et al. Among authors: abo el fotoh wmm. Curr Mol Med. 2019;19(1):32-39. doi: 10.2174/1566524019666190219123900. Curr Mol Med. 2019. PMID: 30806315

4

The potential implication of SCN1A and CYP3A5 genetic variants on antiepileptic drug resistance among Egyptian epileptic children.

Abo El Fotoh WM, Abd El Naby SA, Habib MS, ALrefai AA, Kasemy ZA. Abo El Fotoh WM, et al. Seizure. 2016 Oct;41:75-80. doi: 10.1016/j.seizure.2016.07.005. Epub 2016 Jul 26. Seizure. 2016. PMID: 27498208 Free article.

5

Genetic Variants and Haplotypes of Tryptophan Hydroxylase 2 and Reelin Genes May Be Linked with Attention Deficit Hyperactivity Disorder in Egyptian Children.

Abo El Fotoh WMM, Bayomy NR, Kasemy ZA, Barain AM, Shalaby BM, Abd El Naby SA. Abo El Fotoh WMM, et al. ACS Chem Neurosci. 2020 Jul 15;11(14):2094-2103. doi: 10.1021/acschemneuro.0c00136. Epub 2020 Jun 26. ACS Chem Neurosci. 2020. PMID: 32530273

6

Children with Down syndrome: association of Bcl-I polymorphism of nuclear receptor subfamily 3 group C member 1 gene with obesity.

Abo El-Fotoh WMM, Bahbah HMN, Elaithy MAE, Ahmed RKR, Bayomy NR. Abo El-Fotoh WMM, et al. Pediatr Res. 2022 Jul;92(1):216-224. doi: 10.1038/s41390-021-01711-3. Epub 2021 Aug 25. Pediatr Res. 2022. PMID: 34433889

7

Establishment of blood pressure nomograms representative for Egyptian children and adolescents: a cross-sectional study.

El-Shafie AM, El-Gendy FM, Allhony DM, Abo El Fotoh WMM, Omar ZA, Samir MA, Bahbah WA, Abd El Naby SA, El Zayat RS, Abd El Hady NMS, El Gazar BA, Zannoun MA, Kasemy ZA, El-Bazzar AN, Abd El-Fattah MAE, Abd El-Monsef AA, Kairallah AM, Raafet HM, Baz GM, Salah AG, Galab WS. El-Shafie AM, et al. Among authors: abo el fotoh wmm. BMJ Open. 2018 Jul 25;8(7):e020609. doi: 10.1136/bmjopen-2017-020609. BMJ Open. 2018. PMID: 30049691 Free PMC article. Clinical Trial.

8

Screening for developmental delay in preschool-aged children using parent-completed Ages and Stages Questionnaires: additional insights into child development.

Abo El Elella SS, Tawfik MAM, Abo El Fotoh WMM, Barseem NF. Abo El Elella SS, et al. Among authors: abo el fotoh wmm. Postgrad Med J. 2017 Oct;93(1104):597-602. doi: 10.1136/postgradmedj-2016-134694. Epub 2017 Apr 13. Postgrad Med J. 2017. PMID: 28408725

9

Serum Neutrophil Gelatinase-Associated Lipocalin: A Diagnostic Marker in Pediatric Sepsis.

Saleh NY, Abo El Fotoh WMM, El-Hawy MA. Saleh NY, et al. Among authors: el hawy ma, abo el fotoh wmm. Pediatr Crit Care Med. 2017 Jun;18(6):e245-e252. doi: 10.1097/PCC.0000000000001186. Pediatr Crit Care Med. 2017. PMID: 28445241 Clinical Trial.

10

The potential role of incorporating real-time PCR and DNA sequencing for amplification and detection of 16S rRNA gene signatures in neonatal sepsis.

Midan DA, Abo El Fotoh WMM, El Shalakany AH. Midan DA, et al. Among authors: abo el fotoh wmm, el shalakany ah. J Matern Fetal Neonatal Med. 2017 Jun;30(12):1476-1483. doi: 10.1080/14767058.2016.1219994. Epub 2016 Aug 23. J Matern Fetal Neonatal Med. 2017. PMID: 27484181

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