Gross Hematuria Caused by Intravesical Migration of a Forgotten Intrauterine Device: A Case Report and Literature Review von Salih, Mohammed Abdulaziz, Tefera, Alemayehu Tegegne, Gebrehiwot, Fitsum Gebreegziabher, Mideksa, Adugna Getachew, Halala, Nebiyou Samuel, Gebreselassie, Kaleab Habtemichael

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GLI3‐related polydactyly: a review von Al‐Qattan, M.M., Shamseldin, H.E., Salih, M.A., Alkuraya, F.S.

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Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy von Ramadan, W., Patel, N., Anazi, S., Kentab, A.Y., Bashiri, F.A., Hamad, M.H., Jad, L., Salih, M.A., Alsaif, H., Hashem, M., Faqeih, E., Shamseddin, H.E., Alkuraya, F.S.

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Climate of Online e-Learning During COVID-19 Pandemic in a Saudi Medical School: Students’ Perspective von Salih, Karimeldin MA, Elnour, Suaad, Mohammed, Nahid, Alkhushayl, Abdullah M., Alghamdi, Ali A, Eljack, Ibrahim A., Al-Faifi, Jaber, Ibrahim, Mutasim E

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Congenital Microcephaly with a Simplified Gyral Pattern: Associated Findings and Their Significance von ADACHI, Y, PODURI, A, KAWAGUCH, A, YOON, G, SALIH, M. A, YAMASHITA, F, WALSH, C. A, BARKOVICH, A. J

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Pellagra-like condition is xeroderma pigmentosum/Cockayne syndrome complex and niacin confers clinical benefit von Hijazi, H., Salih, M.A., Hamad, M.H.A., Hassan, H.H., Salih, S.B.M., Mohamed, K.A., Mukhtar, M.M., Karrar, Z.A., Ansari, S., Ibrahim, N., Alkuraya, F.S.

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Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report von AMIN, MUTAZ, BAKHIT, YOUSUF, KOKO, MAHMOUD, IBRAHIM, MOHAMED OSAMA MIRGAHNI, SALIH, MA, IBRAHIM, MUNTASER, SEIDI, OSHEIK A

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Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations von Yahia, Ashraf, Hamed, Ahlam A. A., Mohamed, Inaam N., Elseed, Maha A., Salih, Mustafa A., El-sadig, Sarah M., Siddig, Hassab Elrasoul, Nasreldien, Ali Elsir Musa, Abdullah, Mohamed Ahmed, Elzubair, Maha, Omer, Farouk Yassen, Bakhiet, Aisha Motwakil, Abubaker, Rayan, Abozar, Fatima, Adil, Rawaa, Emad, Sara, Musallam, Mhammed Alhassan, Eltazi, Isra Z. M., Omer, Zulfa, Malik, Hiba, Mohamed, Mayada O. E., Elhassan, Ali A., Mohamed, Eman O. E., Ahmed, Ahmed K. M. A., Ahmed, Elhami A. A., Eltaraifee, Esraa, Hussein, Bidour K., Abd Allah, Amal S. I., Salah, Lina, Nimir, Mohamed, Tag Elseed, Omnia M., Elhassan, Tasneem E. A., Elbashier, Abubakr, Alfadul, Esraa S. A., Fadul, Moneeb, Ali, Khalil F., Taha, Shaimaa Omer M. A., Bushara, Elfatih E., Amin, Mutaz, Koko, Mahmoud, Ibrahim, Muntaser E., Ahmed, Ammar E., Elsayed, Liena E. O., Stevanin, Giovanni

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Clinical characterization of the HOXA1 syndrome BSAS variant von BOSLEY, T. M, SALIH, M. A, ALORAINY, I. A, OYSTRECK, D. T, NESTER, M, ABU-AMERO, K. K, TISCHFIELD, M. A, ENGLE, E. C

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Association of Adverse Childhood Experiences and Resilience With Obesity, High Blood Pressure, and Parental Report of Behavioral Health Symptoms in Children: A Cross Sectional Stud... von Hall, Ashleigh, West, Xandria, Brown, Marilyn, Hall, Erin, Kim, Ella, Leib, Alexa, Mergaman, Paige, Salih, Zanaib, Aronoff, Stephen

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Measurement of the educational environment in MBBS teaching program, according to DREEM in College of Medicine, University of Bahri, Khartoum, Sudan von Salih, Karimeldin MA, Idris, Muawia EA, Elfaki, Omer A, Osman, Nasir MN, Nour, Saada M, Elsidig, Hind A, Toam, Rahamatalla M, Elfakey, Walyeldin E.M

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Assessment of Treatment of Community Acquired Severe Pneumonia by Two Different Antibiotics von Salih, Karimeldin Ma, Bilal, Jalal Ali, Eldouch, Widad, Abdin, Ali

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NPHP4 mutation is linked to cerebello-oculo-renal syndrome and male infertility von Alazami, A.M., Alshammari, M.J., Baig, M., Salih, M.A., Hassan, H.H., Alkuraya, F.S.

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The Salih Ataxia Mutation Impairs Rubicon Endosomal Localization von Assoum, M., Salih, M. A., Drouot, N., Hnia, K., Martelli, A., Koenig, M.

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Expanding the clinical spectrum and allelic heterogeneity in van den Ende-Gupta syndrome von Patel, N., Salih, M.A., Alshammari, M.J., Abdulwahhab, F., Adly, N., Alzahrani, F., Elgamal, E.A., Elkhashab, H.Y., Al-Qattan, M., Alkuraya, F.S.

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Unraveling the MRI‐Based Microstructural Signatures Behind Primary Progressive and Relapsing–Remitting Multiple Sclerosis Phenotypes von Boscolo Galazzo, Ilaria, Brusini, Lorenza, Akinci, Muge, Cruciani, Federica, Pitteri, Marco, Ziccardi, Stefano, Bajrami, Albulena, Castellaro, Marco, Salih, Ahmed M.A., Pizzini, Francesca B., Jovicich, Jorge, Calabrese, Massimiliano, Menegaz, Gloria

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Oral Liposome Vaccines Containing Cyprinid herpesvirus 3 (CyHv3) and Aeromonas hydrophila Antigen for the Immunization of Common Carp Cyprinus carpio von Al-Zaini, Sundus Oun Ali, Al-Bayati, Mohanad A., Khazaal, Khazaal Abbas, Salih, Salma Talib

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IFNG and IFNGR1 gene polymorphisms and susceptibility to post-kala-azar dermal leishmaniasis in Sudan von Salih, M A, Ibrahim, M E, Blackwell, J M, Miller, E N, Khalil, E A G, ElHassan, A M, Musa, A M, Mohamed, H S

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Évolution historique du travail social en turquie: De la République à nos jours von Güzel,Bekir

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Genetic investigation of 93 families with microphthalmia or posterior microphthalmos von Patel, N., Khan, A.O., Alsahli, S., Abdel‐Salam, G., Nowilaty, S.R., Mansour, A.M., Nabil, A., Al‐Owain, M., Sogati, S., Salih, M.A., Kamal, A.M., Alsharif, H., Alsaif, H.S., Alzahrani, S.S., Abdulwahab, F., Ibrahim, N., Hashem, M., Faquih, T., Shah, Z.A., Abouelhoda, M., Monies, D., Dasouki, M., Shaheen, R., Wakil, S.M., Aldahmesh, M.A., Alkuraya, F.S.

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