Phytochemicals of Conocarpus spp. as a Natural and Safe Source of Phenolic Compounds and Antioxidants von Afifi, Hanan S., Al Marzooqi, Hassan M., Tabbaa, Mohammad J., Arran, Ahmed A.

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Importance of TREC and KREC as molecular markers for immunological evaluation of down syndrome children von Eissa, Eman, Afifi, Hanan H., Abo-Shanab, Assem M., Thomas, Manal M., Taher, Mohamed B., Kandil, Rania, Kholoussi, Naglaa M.

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The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration von Abdel-Salam, Ghada, Thoenes, Michaela, Afifi, Hanan H, Körber, Friederike, Swan, Daniel, Bolz, Hanno Jörn

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Honey Bee Products: Preclinical and Clinical Studies of Their Anti-inflammatory and Immunomodulatory Properties von El-Seedi, Hesham R, Eid, Nehal, Abd El-Wahed, Aida A, Rateb, Mostafa E, Afifi, Hanan S, Algethami, Ahmed F, Zhao, Chao, Al Naggar, Yahya, Alsharif, Sultan M, Tahir, Haroon Elrasheid, Xu, Baojun, Wang, Kai, Khalifa, Shaden A M

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Expanding the phenotypic spectrum and clinical severity associated with WLS gene von Abdel-Salam, Ghada M H, Afifi, Hanan H, Abdel-Hamid, Mohamed S, Ahmed, Nermeen E B, Taher, Mohamed B, El-Kamah, Ghada, Thiele, Holger, Nürnberg, Peter N, Bolz, Hanno J

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Anti-Viral and Immunomodulatory Properties of Propolis: Chemical Diversity, Pharmacological Properties, Preclinical and Clinical Applications, and In Silico Potential against SARS-... von Yosri, Nermeen, Abd El-Wahed, Aida A., Ghonaim, Reem, Khattab, Omar M., Sabry, Aya, Ibrahim, Mahmoud A. A., Moustafa, Mahmoud F., Guo, Zhiming, Zou, Xiaobo, Algethami, Ahmed F. M., Masry, Saad H. D., AlAjmi, Mohamed F., Afifi, Hanan S., Khalifa, Shaden A. M., El-Seedi, Hesham R.

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Mutations in ANTXR1 Cause GAPO Syndrome von Stránecký, Viktor, Hoischen, Alexander, Hartmannová, Hana, Zaki, Maha S., Chaudhary, Amit, Zudaire, Enrique, Nosková, Lenka, Barešová, Veronika, Přistoupilová, Anna, Hodaňová, Kateřina, Sovová, Jana, Hůlková, Helena, Piherová, Lenka, Hehir-Kwa, Jayne Y., de Silva, Deepthi, Senanayake, Manouri P., Farrag, Sameh, Zeman, Jiří, Martásek, Pavel, Baxová, Alice, Afifi, Hanan H., St. Croix, Brad, Brunner, Han G., Temtamy, Samia, Kmoch, Stanislav

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Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients von Sayed-Ahmed, Mohammed M., El-Bassyouni, Hala T., Afifi, Hanan H., Essawi, Mona L., Taher, Mohamed B., Gadelhak, Mohamed I., Zaytoun, Rehab A., Abdelmonem, Ahmed A., Elbagoury, Nagham M.

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Optimizing extraction conditions of crude fiber, phenolic compounds, flavonoids and antioxidant activity of date seed powder von Afifi, Hanan S., Hashim, Isameldin B., Altubji, Sabreen I.

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Magnetic resonance imaging of developmental facial paresis: a spectrum of complex anomalies von Mohammad, Shaimaa Abdelsattar, Abdelaziz, Tougan Taha, Gadelhak, Mohamed I., Afifi, Hanan H., Abdel-Salam, Ghada M. H.

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Further Evidence of a Continuum in the Clinical Spectrum of Dominant PIEZO2-Related Disorders and Implications in Cerebellar Anomalies von Abdel-Salam, Ghada M.H., Afifi, Hanan H., Saleem, Sahar N., Gadelhak, Mohamed I., El-Serafy, Manar A., Sayed, Inas S.M., Abdel-Hamid, Mohamed S.

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Synthesis of Cyclobutane Analogue 4: Preparation of Purine and Pyrimidine Carbocyclic Nucleoside Derivatives von Hasaneen, Noha, Ebead, Abdelaziz, Hassan, Murtaza, Afifi, Hanan, Hunter, Howard, Lee-Ruff, Edward, El-Gohary, Nadia S, Maarouf, Azza R, El-Emam, Ali A

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Lipoid proteinosis: A clinical and molecular study in Egyptian patients von Afifi, Hanan H., Amr, Khalda S., Tosson, Angie M.S., Hassan, Tarak A., Mehrez, Mennat I., El-Kamah, Ghada Y.

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Lenz–Majewski syndrome in a patient from Egypt von Afifi, Hanan H., Abdel‐Hamid, Mohamed S., Mehrez, Mennat I., El‐Kamah, Ghada, Abdel‐Salam, Ghada M. H.

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Quantitative assessment and genomic profiling of Campylobacter dynamics in poultry processing: a case study in the United Arab Emirates integrated abattoir system von Habib, Ihab, Mohamed, Mohamed-Yousif Ibrahim, Lakshmi, Glindya Bhagya, Al Marzooqi, Hassan Mohamed, Afifi, Hanan Sobhy, Shehata, Mohamed Gamal, Khan, Mushtaq, Ghazawi, Akela, Abdalla, Afra, Anes, Febin

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Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation von Abdel‐Salam, Ghada M. H., Sayed, Inas S. M., Afifi, Hanan H., Abdel‐Ghafar, Sherif F., Abouzaid, Maha R., Ismail, Samira I., Aglan, Mona S., Issa, Mahmoud Y., EL‐Bassyouni, Hala T., El‐Kamah, Ghada, Effat, Laila K., Eid, Maha, Zaki, Maha S., Temtamy, Samia A., Abdel‐Hamid, Mohamed S.

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Distinct Ocular Expression in Infants and Children With Down Syndrome in Cairo, Egypt: Myopia and Heart Disease von Afifi, Hanan H, Abdel Azeem, Amira A, El-Bassyouni, Hala T, Gheith, Moataz E, Rizk, Akmal, Bateman, J. Bronwyn

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Clinical features of SMARCA2 duplication overlap with Coffin-Siris syndrome von Miyake, Noriko, Abdel-Salam, Ghada, Yamagata, Takanori, Eid, Maha M., Osaka, Hitoshi, Okamoto, Nobuhiko, Mohamed, Amal M., Ikeda, Takahiro, Afifi, Hanan H., Piard, Juliette, van Maldergem, Lionel, Mizuguchi, Takeshi, Miyatake, Satoko, Tsurusaki, Yoshinori, Matsumoto, Naomichi

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Mutation in WDR4 impairs tRNA m7G46 methylation and causes a distinct form of microcephalic primordial dwarfism von Shaheen, Ranad, Abdel-Salam, Ghada M H, Guy, Michael P., Alomar, Rana, Abdel-Hamid, Mohamed S., Afifi, Hanan H., Ismail, Samira I., Emam, Bayoumi A., Phizicky, Eric M., Alkuraya, Fowzan S.

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De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder von Afifi, Hanan H., Abdel‐Hamid, Mohamed S., Eid, Maha M., Mostafa, Inas S., Abdel‐Salam, Ghada M.H.

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