El-Harouni AA - Search Results

1

Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs).

Essawi ML, Al-Attribi GM, Gaber KR, El-Harouni AA. Essawi ML, et al. Among authors: el harouni aa. Gene. 2012 Nov 1;509(1):120-3. doi: 10.1016/j.gene.2012.07.085. Epub 2012 Aug 17. Gene. 2012. PMID: 22921322

2

Screening of dystrophin gene deletions in Egyptian patients with DMD/BMD muscular dystrophies.

Effat LK, El-Harouni AA, Amr KS, El-Minisi TI, Abdel Meguid N, El-Awady M. Effat LK, et al. Dis Markers. 2000;16(3-4):125-9. doi: 10.1155/2000/437372. Dis Markers. 2000. PMID: 11381192 Free PMC article.

3

The milder phenotype of the dystrophin gene double deletions.

El-Harouni AA, Amr KS, Effat LK, Eassawi ML, Ismail S, Gad YZ, El-Awady MK. El-Harouni AA, et al. Acta Neurol Scand. 2003 Jun;107(6):400-4. doi: 10.1034/j.1600-0404.2003.00072.x. Acta Neurol Scand. 2003. PMID: 12757471

4

Review of literature: genes related to postaxial polydactyly.

Verma PK, El-Harouni AA. Verma PK, et al. Among authors: el harouni aa. Front Pediatr. 2015 Feb 11;3:8. doi: 10.3389/fped.2015.00008. eCollection 2015. Front Pediatr. 2015. PMID: 25717468 Free PMC article. Review.

5

The most encountered groups of genetic disorders in Giza Governorate, Egypt.

Afifi HH, El-Ruby MO, El-Bassyouni HT, Ismail SI, Aglan MS, El-Harouni AA, Mazen IM, Zaki MS, Bassiouni RI, Hosny LA, El-Kamah GY, El-Kotoury AI, Ashour AM, Abdel-Salam GM, El-Gammal MA, Hamed K, Kamal RM, El-Nekhely I, Temtamy SA. Afifi HH, et al. Among authors: el harouni aa. Bratisl Lek Listy. 2010;111(2):62-9. Bratisl Lek Listy. 2010. PMID: 20429316

6

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.

Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG; Greater Middle East Variome Consortium; Alkuraya FS, Casanova JL, Gleeson JG. Scott EM, et al. Nat Genet. 2016 Sep;48(9):1071-6. doi: 10.1038/ng.3592. Epub 2016 Jul 18. Nat Genet. 2016. PMID: 27428751 Free PMC article.

7

First comprehensive in silico analysis of the functional and structural consequences of SNPs in human GalNAc-T1 gene.

Mohamoud HS, Hussain MR, El-Harouni AA, Shaik NA, Qasmi ZU, Merican AF, Baig M, Anwar Y, Asfour H, Bondagji N, Al-Aama JY. Mohamoud HS, et al. Among authors: el harouni aa. Comput Math Methods Med. 2014;2014:904052. doi: 10.1155/2014/904052. Epub 2014 Mar 4. Comput Math Methods Med. 2014. PMID: 24723968 Free PMC article.

8

Congenital heart defects in Down syndrome patients from western Saudi Arabia.

Al-Aama JY, Bondagji NS, El-Harouni AA. Al-Aama JY, et al. Among authors: el harouni aa. Saudi Med J. 2012 Nov;33(11):1211-5. Saudi Med J. 2012. PMID: 23147879

9

Pluripotent Stem Cell-Derived Hematopoietic Progenitors Are Unable to Downregulate Key Epithelial-Mesenchymal Transition-Associated miRNAs.

Meader E, Barta T, Melguizo-Sanchis D, Tilgner K, Montaner D, El-Harouni AA, Armstrong L, Lako M. Meader E, et al. Among authors: el harouni aa. Stem Cells. 2018 Jan;36(1):55-64. doi: 10.1002/stem.2724. Epub 2017 Oct 27. Stem Cells. 2018. PMID: 29047185 Free PMC article.

10

Identification of miRNA-mRNA-TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches.

Shaik NA, Nasser K, Mohammed A, Mujalli A, Obaid AA, El-Harouni AA, Elango R, Banaganapalli B. Shaik NA, et al. Among authors: el harouni aa. PLoS One. 2022 Oct 20;17(10):e0271262. doi: 10.1371/journal.pone.0271262. eCollection 2022. PLoS One. 2022. PMID: 36264868 Free PMC article.

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