Výsledky vyhledávání - "Azza Abd El Moneim"

Akademický článek

Effect of soft tissue thickness on accuracy of conventional and digital implant impression techniques

Autor: Eman Mostafa Awad, Mohamed Maamoun ElSheikh, Azza Abd el moneim El-Segai

Publikováno v: BMC Oral Health, Vol 24, Iss 1, Pp 1-10 (2024)

Abstract Background Placing implants deep sub-gingivally may affect the accuracy of implant impression techniques and the fit of final restoration. Purpose The aim of this in-vitro study was to evaluate the effect of soft tissue thickness on accuracy

Externí odkaz: https://doaj.org/article/d083c695d8e84fe59ab465e8658fc0e9

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Akademický článek

P699: Identification of a novel pathogenic variant in SERPINH1 associated with a presentation of osteogenesis imperfecta: Case study

Autor: Val Zvereff, Azza Abd El Moneim Attia, Amal Al Tenaiji, Sana Islam, Anushree Dileep, Shalini Behl

Publikováno v: Genetics in Medicine Open, Vol 2, Iss , Pp 101603- (2024)

Externí odkaz: https://doaj.org/article/a5129763cb254c0f936e80f6dc661b23

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Akademický článek

Shedding light on the phenotypic–genotypic correlation of rare treatable and potentially treatable pediatric movement disorders

Autor: Dina Amin Saleh, Azza Abd El Moneim Attia

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-16 (2022)

Abstract Background Advances in genetic science have led to the identification of many rare treatable pediatric movements disorders (MDs). We explored the phenotypic–genotypic spectrum of pediatric patients presenting with MDs. By this, we aimed at

Externí odkaz: https://doaj.org/article/40d49acc00c245c89117ba8e421b241c

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Akademický článek

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Akademický článek

Shedding light on the phenotypic–genotypic correlation of rare treatable and potentially treatable pediatric movement disorders.

Autor: Saleh, Dina Amin^1,2 (AUTHOR) dina_pediatric@yahoo.com, Attia, Azza Abd El Moneim³ (AUTHOR)

Publikováno v: Egyptian Journal of Medical Human Genetics. 4/3/2022, Vol. 23 Issue 1, p1-16. 16p.

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Effects of RTTN gene mutations and the need for complementary cDNA analysis for some transcripts: case report

Autor: Dina A Amin, Afshin PourMirza, Mohamed Issa Tawil, Azza Abd El Moneim Attia

Publikováno v: QJM: An International Journal of Medicine. 114

RTTN is a gene coding for Rotatin protein which has been localized at ciliary body and centriole of human fibroblasts. Its exact function in human is not well identified. However, it is thought to play important role in maintenance of normal structur

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::21f9103512b79d6d6429903ec9792d00
https://doi.org/10.1093/qjmed/hcab099.001

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