يعرض 1 - 10 نتائج من 30 نتيجة بحث عن '"Hassib, Nehal F."', وقت الاستعلام: 1.14s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Brachyolmia, dental anomalies and short stature (DASS):Phenotype and genotype analyses of Egyptian and Pakistani patients

    المؤلفون: Nawaz, Hamed, Parveen, Asia, Khan, Sher Alam, Zalan, Abul Khair, Khan, Muhammad Adnan, Muhammad, Noor, Hassib, Nehal F., Mostafa, Mostafa I., Elhossini, Rasha M., Roshdy, Nehal Nabil, Ullah, Asmat, Arif, Amina, Khan, Saadullah, Ammerpohl, Ole, Wasif, Naveed

    المصدر: Nawaz , H , Parveen , A , Khan , S A , Zalan , A K , Khan , M A , Muhammad , N , Hassib , N F , Mostafa , M I , Elhossini , R M , Roshdy , N N , Ullah , A , Arif , A , Khan , S , Ammerpohl , O & Wasif , N 2024 , ' Brachyolmia, dental anomalies and short stature (DASS) : Phenotype and genotype analyses of Egyptian and Pakistani patients ' , Heliyon , vol. 10 , no. 1 , e23688 . https://doi.org/10.1016/j.heliyon.2023.e23688Test

    مصطلحات موضوعية: Amelogenesis imperfecta, Brachyolmia, Exome sequencing, Frameshift variants, Hearing impairment, Homozygous splice acceptor site, LTBP3

    العلاقة: https://pure.au.dk/portal/en/publications/f4b2684e-d017-4f86-b55b-69ef17b224b7Test

    الإتاحة: https://doi.org/10.1016/j.heliyon.2023.e23688Test
    https://pure.au.dk/portal/en/publications/f4b2684e-d017-4f86-b55b-69ef17b224b7Test
    http://www.scopus.com/inward/record.url?scp=85180281967&partnerID=8YFLogxKTest

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  2. 2
    دورية أكاديمية
    Deleterious variants in WNT10A, EDAR, and EDA causing isolated and syndromic tooth agenesis: a structural perspective from molecular dynamics simulations

    المؤلفون: Parveen, Asia, Khan, Sher Alam, Mirza, Muhammad Usman, Bashir, Hina, Arshad, Fatima, Iqbal, Maria, Ahmad, Waseem, Wahab, Ahsan, Fiaz, Amal, Naz, Sidra, Ashraf, Fareeha, Mobeen, Tayyaba, Aziz, Salman, Ahmed, Syed Shoaib, Muhammad, Noor, Hassib, Nehal F., Mostafa, Mostafa I., Gaboon, Nagwa E., Gul, Roquyya, Khan, Saadullah, Froeyen, Matheus, Shoaib, Muhammad, Wasif, Naveed

    مصطلحات موضوعية: Hypodontia/oligodontia, Hypohidrotic ectodermal dysplasia, WNT10A, EDAR, EDA, Exome sequencing, MD simulations, DDC 610 / Medicine & health, Ectodermal dysplasia, Genetics, Tooth abnormalities, Odontodysplasia, Ektodermaldysplasie, Oligodontie

    وصف الملف: application/pdf

    العلاقة: https://www.mdpi.com/1422-0067/20/21/5282/s1Test; http://dx.doi.org/10.18725/OPARU-47807Test; https://oparu.uni-ulm.de/xmlui/123456789/47883Test; http://nbn-resolving.de/urn:nbn:de:bsz:289-oparu-47883-7Test

    الإتاحة: https://doi.org/10.18725/OPARU-47807Test
    https://oparu.uni-ulm.de/xmlui/123456789/47883Test
    http://nbn-resolving.de/urn:nbn:de:bsz:289-oparu-47883-7Test

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  3. 3
    دورية أكاديمية
    Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling.

    المؤلفون: Hassib, Nehal F.1,2 (AUTHOR) nounih@hotmail.com, Mehrez, Mennat1 (AUTHOR), Mostafa, Mostafa I.1 (AUTHOR), Abdel-Hamid, Mohamed S.3 (AUTHOR)

    المصدر: Clinical Oral Investigations. May2024, Vol. 28 Issue 5, p1-8. 8p.


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  4. 4
    دورية أكاديمية
    Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature

    المؤلفون: Elaraby, Nesma M., Ahmed, Hoda A., Ashaat, Neveen A., Tawfik, Sameh, Ahmed, Mahmoud K. H., Hassib, Nehal F., Ashaat, Engy A.

    المساهمون: National Research Centre Egypt

    المصدر: Journal of Molecular Neuroscience ; volume 72, issue 11, page 2242-2251 ; ISSN 0895-8696 1559-1166

    مصطلحات موضوعية: Cellular and Molecular Neuroscience, General Medicine

    الإتاحة: https://doi.org/10.1007/s12031-022-02074-yTest

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  5. 5
    دورية أكاديمية
    A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.

    المؤلفون: Elhossini, Rasha M., Sayed, Inas M., Hellal, Usama Saad, Mahmoud, Sarah A. M., Aglan, Mona S., Hassib, Nehal F., Abdel‐Hamid, Mohamed S.

    المصدر: American Journal of Medical Genetics. Part A; Jan2024, Vol. 194 Issue 1, p39-45, 7p


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  6. 6
    دورية أكاديمية
    A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management

    المؤلفون: Elhossini, Rasha M., Sayed, Inas M., Hellal, Usama Saad, Mahmoud, Sarah A. M., Aglan, Mona S., Hassib, Nehal F., Abdel‐Hamid, Mohamed S.

    المساهمون: Science and Technology Development Fund

    المصدر: American Journal of Medical Genetics Part A ; volume 194, issue 1, page 39-45 ; ISSN 1552-4825 1552-4833

    الإتاحة: https://doi.org/10.1002/ajmg.a.63415Test

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  7. 7
    دورية أكاديمية
    Bruck syndrome in 13 new patients: Identification of five novel FKBP10 and PLOD2 variants and further expansion of the phenotypic spectrum

    المؤلفون: Otaify, Ghada A., Abdel‐Hamid, Mohamed S., Hassib, Nehal F., Elhossini, Rasha M., Abdel‐Ghafar, Sherif F., Aglan, Mona S.

    المساهمون: Science and Technology Development Fund

    المصدر: American Journal of Medical Genetics Part A ; volume 188, issue 6, page 1815-1825 ; ISSN 1552-4825 1552-4833

    الإتاحة: https://doi.org/10.1002/ajmg.a.62718Test

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  8. 8
    دورية أكاديمية
    Atypical Case of Amelogenesis Imperfecta and Generalized Impacted Dentitions: Dental Management and Follow Ups.

    المؤلفون: Hassib, Nehal F.1 nounih@hotmail.com, Hellal, Usama S.1, Mostafa, Mostafa I.1

    المصدر: Middle East Journal of Medical Genetics. Jan2023, Vol. 12 Issue 1, p1-4. 4p.


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  9. 9
    دورية أكاديمية
    Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene.

    المؤلفون: Elaraby, Nesma M., Ahmed, Hoda A., Ashaat, Neveen A., Tawfik, Sameh, Ahmed, Mahmoud K. H., Hassib, Nehal F., Ashaat, Engy A.

    المصدر: Journal of Molecular Neuroscience; Jun2024, Vol. 74 Issue 2, p1-1, 1p


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  10. 10
    دورية أكاديمية
    Gene mutations of the three ectodysplasin pathway key players (EDA, EDAR, and EDARADD) account for more than 60% of Egyptian ectodermal dysplasia: A report of seven novel mutations

    المؤلفون: Ahmed, Hoda A., El-Kamah, Ghada Y., Rabie, Eman, Mostafa, Mostafa I., Abouzaid, Maha R., Hassib, Nehal F., Mehrez, Mennat I., Abdel-Kader, Mohamed A., Mohsen, Yasmine H., Zada, Suher K., Amr, Khalda S., Sayed, Inas S.M.

    المصدر: Faculty Journal Articles

    مصطلحات موضوعية: Ectodermal eysplasia, Ectodysplasin A, EDA, EDAR, EDARADD, Hypodontia, Hypohidrotic ectodermal eysplasia, Oligodontia, WNT10A

    العلاقة: https://fount.aucegypt.edu/faculty_journal_articles/2418Test

    الإتاحة: https://doi.org/10.3390/genes12091389Test
    https://fount.aucegypt.edu/faculty_journal_articles/2418Test

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