المؤلفون: AlHargan, Aljouhra^{Aff1, Aff2}, AlMuhaizea, Mohammed A.^{Aff3, Aff4}, Almass, Rawan, Alwadei, Ali H., Daghestani, Maha, Arold, Stefan T.^{Aff7, Aff8, Aff9}, Kaya, Namik^{Aff1, IDs4143902300234z_cor7}

المصدر: Human Genome Variation. 10(1)

المؤلفون: AlMuhaizea, Mohammed^{Aff1, Aff2}, AlMass, Rawan, AlHargan, Aljouhra, AlBader, Anoud, Medico Salsench, Eva, Howaidi, Jude, Ihinger, Jacie, Karachunski, Peter, Begtrup, Amber, Segura Castell, Monica, Bauer, Peter, Bertoli-Avella, Aida, Kaya, Ibrahim H., AlSufayan, Jumanah, AlQuait, Laila, Chedrawi, Aziza, Arold, Stefan T.^{Aff9, Aff10}, Colak, Dilek, Barakat, Tahsin Stefan^Aff4, Kaya, Namik^Aff3

المصدر: Acta Neuropathologica: Pathology and Mechanisms of Neurological Disease. 139(4):791-794

المؤلفون: Perenthaler, Elena, Nikoncuk, Anita, Yousefi, Soheil, Berdowski, Woutje M., Alsagob, Maysoon, Capo, Ivan, van der Linde, Herma C., van den Berg, Paul, Jacobs, Edwin H., Putar, Darija, Ghazvini, Mehrnaz, Aronica, Eleonora^{Aff5, Aff6}, van IJcken, Wilfred F. J., de Valk, Walter G., Medici-van den Herik, Evita, van Slegtenhorst, Marjon, Brick, Lauren, Kozenko, Mariya, Kohler, Jennefer N., Bernstein, Jonathan A., Monaghan, Kristin G., Begtrup, Amber, Torene, Rebecca, Al Futaisi, Amna, Al Murshedi, Fathiya, Mani, Renjith, Al Azri, Faisal, Kamsteeg, Erik-Jan, Mojarrad, Majid^{Aff17, Aff18, Aff19}, Eslahi, Atieh^{Aff17, Aff20}, Khazaei, Zaynab, Darmiyan, Fateme Massinaei, Doosti, Mohammad, Karimiani, Ehsan Ghayoor^{Aff23, Aff24}, Vandrovcova, Jana, Zafar, Faisal, Rana, Nuzhat, Kandaswamy, Krishna K., Hertecant, Jozef, Bauer, Peter, AlMuhaizea, Mohammed A., Salih, Mustafa A., Aldosary, Mazhor, Almass, Rawan, Al-Quait, Laila, Qubbaj, Wafa, Coskun, Serdar, Alahmadi, Khaled O., Hamad, Muddathir H. A., Alwadaee, Salem, Awartani, Khalid, Dababo, Anas M., Almohanna, Futwan, Colak, Dilek, Dehghani, Mohammadreza^{Aff36, Aff37}, Mehrjardi, Mohammad Yahya Vahidi, Gunel, Murat, Ercan-Sencicek, A. Gulhan^{Aff39, Aff40}, Passi, Gouri Rao, Cheema, Huma Arshad, Efthymiou, Stephanie, Houlden, Henry, Bertoli-Avella, Aida M., Brooks, Alice S., Retterer, Kyle, Maroofian, Reza, Kaya, Namik, van Ham, Tjakko J., Barakat, Tahsin Stefan^Aff1

المصدر: Acta Neuropathologica: Pathology and Mechanisms of Neurological Disease. 139(3):415-442

المؤلفون: Albakheet, AlBandary, Almuallami, Duaa, Almass, Rawan, Qari, Alya, Kenana, Rosan, AlQudairy, Hanan, Huma, Rozeena, Binomar, Hadeel, Wakil, Salma Majid, Alowain, Mohammad, Colak, Dilek, Kaya, Namik, AlSayed, Moeenaldeen D.

المصدر: Clinical Dysmorphology; Apr2024, Vol. 33 Issue 2, p55-62, 8p

المؤلفون: Albakheet, AlBandary, Almuallami, Duaa, Almass, Rawan, Qari, Alya, Kenana, Rosan, AlQudairy, Hanan, Huma, Rozeena, Binomar, Hadeel, Wakil, Salma Majid, Alowain, Mohammad, Colak, Dilek, Kaya, Namik, AlSayed, Moeenaldeen D.

المصدر: Clinical Dysmorphology; April 2024, Vol. 33 Issue: 2 p55-62, 8p

المؤلفون: Al-Muhaizea, Mohammad A.^{Aff1, Aff2}, AlMutairi, Faten, Almass, Rawan, AlHarthi, Safinaz, Aldosary, Mazhor S., Alsagob, Maysoon, AlOdaib, Ali, Colak, Dilek, Kaya, Namik^Aff3

المصدر: The Cerebellum. 17(3):276-285

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المؤلفون: Scala, Marcello, Wortmann, Saskia B., Kaya, Namik, Stellingwerff, Menno D., Pistorio, Angela, Glamuzina, Emma, van Karnebeek, Clara D., Skrypnyk, Cristina, Iwanicka-Pronicka, Katarzyna, Piekutowska-Abramczuk, Dorota, Ciara, Elżbieta, Tort, Frederic, Sheidley, Beth, Poduri, Annapurna, Jayakar, Parul, Jayakar, Anuj, Upadia, Jariya, Walano, Nicolette, Haack, Tobias B., Prokisch, Holger, Aldhalaan, Hesham, Karimiani, Ehsan G., Yildiz, Yilmaz, Ceylan, Ahmet C., Santiago-Sim, Teresa, Dameron, Amy, Yang, Hui, Toosi, Mehran B., Ashrafzadeh, Farah, Akhondian, Javad, Imannezhad, Shima, Mirzadeh, Hanieh S., Maqbool, Shazia, Farid, Aisha, Al-Muhaizea, Mohamed A., Alshwameen, Meznah O., Aldowsari, Lama, Alsagob, Maysoon, Alyousef, Ashwaq, AlMass, Rawan, AlHargan, Aljouhra, Alwadei, Ali H., AlRasheed, Maha M., Colak, Dilek, Alqudairy, Hanan, Khan, Sameena, Lines, Matthew A., García Cazorla, M. Ángeles, Ribes, Antonia, Morava, Eva, Bibi, Farah, Haider, Shahzad, Ferla, Matteo P., Taylor, Jenny C., Alsaif, Hessa S., Firdous, Abdulwahab, Hashem, Mais, Shashkin, Chingiz, Koneev, Kairgali, Kaiyrzhanov, Rauan, Efthymiou, Stephanie, Genomics, Queen Square, Schmitt-Mechelke, Thomas, Ziegler, Andreas, Issa, Mahmoud Y., Elbendary, Hasnaa M., Striano, Pasquale, Alkuraya, Fowzan S., Zaki, Maha S., Gleeson, Joseph G., Barakat, Tahsin Stefan, Bierau, Jorgen, van der Knaap, Marjo S., Maroofian, Reza, Houlden, Henry

المصدر: Scala , M , Wortmann , S B , Kaya , N , Stellingwerff , M D , Pistorio , A , Glamuzina , E , van Karnebeek , C D , Skrypnyk , C , Iwanicka-Pronicka , K , Piekutowska-Abramczuk , D , Ciara , E , Tort , F , Sheidley , B , Poduri , A , Jayakar , P , Jayakar , A , Upadia , J , Walano , N , Haack , T B , Prokisch , H , Aldhalaan , H , Karimiani , E G , Yildiz , Y , Ceylan , A C , Santiago-Sim , T , Dameron , A , Yang , H , Toosi , M B , Ashrafzadeh , F , Akhondian , J , Imannezhad , S , Mirzadeh , H S , Maqbool , S , Farid , A , Al-Muhaizea , M A , Alshwameen , M O , Aldowsari , L , Alsagob , M , Alyousef , A , AlMass , R , AlHargan , A , Alwadei , A H , AlRasheed , M M , Colak , D , Alqudairy , H , Khan , S , Lines , M A , García Cazorla , M Á , Ribes , A , Morava , E , Bibi , F , Haider , S , Ferla , M P , Taylor , J C , Alsaif , H S , Firdous , A , Hashem , M , Shashkin , C , Koneev , K , Kaiyrzhanov , R , Efthymiou , S , Genomics , Q S , Schmitt-Mechelke , T , Ziegler , A , Issa , M Y , Elbendary , H M , Striano , P , Alkuraya , F S , Zaki , M S , Gleeson , J G , Barakat , T S , Bierau , J , van der Knaap , M S , Maroofian , R & Houlden , H 2022 , ' Clinico-radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiency ' , Human Mutation , vol. 43 , no. 3 , pp. 403-419 .

مصطلحات الفهرس: article

URL: https://pure.eur.nl/en/publications/8f44f678-de01-492d-b764-468bcda6b382

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