Evaluation of Oxidative Stress in Cutaneous Leishmaniasis in Iraqi Patients von Al-Hattab, Mohammed K, Nahi, Noor H, Al-Kalidi, Jinan H

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Evaluation of lipid profile in patients with cherry angioma: A case–control study in Iraqi patients von Al-Hattab, Mohammed K, Gahlool, Ansaar H, Al-Kalidi, Jinan H

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Study of serum chitinase-3-like-1 protein (CHI3L1) and C-reactive protein (CRP) in patients suffering from chronic plaque psoriasis von Al-Saba, Ahmed, Shemran, Khawla, Al-Hattab, Mohammed

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The efficacy of intralesional vitamin D3 injection in the treatment of cutaneous warts: A clinical therapeutic trial study von Al‐Sabak, Haider, Al‐Hattab, Mohammed, Al‐Rammahi, Marwah, Al‐Dhalimi, Muhsin

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Effect of CoQ10 Administration to Psoriatic Iraqi Patients on Biological Therapy Upon Severity Index (PASI) and Quality of Life Index (DLQI) Before and After Therapy von Al-Oudah, Ghadah Ali, Sahib, Ahmed Salih, Al-Hattab, Mohammed K, Al-Ameedee, Ali Ameer

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Intelligent transportation systems for sustainable smart cities von Elassy, Mohamed, Al-Hattab, Mohammed, Takruri, Maen, Badawi, Sufian

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Evaluation of Serum Levels of Uric acid and Bilirubin in Iraqi Patients with Rosacea von Mohammad J. Al abdullah, Mohammed Al Hattab, Zahraa Jameel Abbas

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Study of serum chitinase-3-like-1 protein in patients suffering from chronic plaque psoriasis von Al-Saba, Ahmed, Shemran, Khawla, Al-Hattab, Mohammed

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VITAMIN D3 LEVEL AND ITS RECEPTOR OF PATIENTS WITH PSORIASIS: A CASE CONTROL STUDY von Mohammed Abd Al-Hussein Khalil

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Discoid lupus erythematosus in Iraqi patients: a clinical and histopathological study von Al-Hattab, Mohammed Kadhim, Al-Waiz, Makram

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Molecular and clinical spectra of FBXL4 deficiency von El‐Hattab, Ayman W., Dai, Hongzheng, Almannai, Mohammed, Wang, Julia, Faqeih, Eissa A., Al Asmari, Ali, Saleh, Mohammed A. M., Elamin, Mohammed A. O., Alfadhel, Majid, Alkuraya, Fowzan S., Hashem, Mais, Aldosary, Mazhor S., Almass, Rawan, Almutairi, Faten B., Alsagob, Maysoon, Al‐Owain, Mohammed, Al‐Sharfa, Shirin, Al‐Hassnan, Zuhair N., Rahbeeni, Zuhair, Al‐Muhaizea, Mohammed A., Makhseed, Nawal, Foskett, Gretchen K., Stevenson, David A., Gomez‐Ospina, Natalia, Lee, Chung, Boles, Richard G., Schrier Vergano, Samantha A., Wortmann, Saskia B., Sperl, Wolfgang, Opladen, Thomas, Hoffmann, Georg F., Hempel, Maja, Prokisch, Holger, Alhaddad, Bader, Mayr, Johannes A., Chan, Wenyaw, Kaya, Namik, Wong, Lee‐Jun C.

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Disorders of histone methylation: Molecular basis and clinical syndromes von Al Ojaimi, Mode, Banimortada, Bashar J., Othman, Amna, Riedhammer, Korbinian M., Almannai, Mohammed, El‐Hattab, Ayman W.

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El‐Hattab‐Alkuraya syndrome caused by biallelic WDR45B pathogenic variants: Further delineation of the phenotype and genotype von Almannai, Mohammed, Marafi, Dana, Abdel‐Salam, Ghada M. H., Zaki, Maha S., Duan, Ruizhi, Calame, Daniel, Herman, Isabella, Levesque, Felix, Elbendary, Hasnaa M., Hegazy, Ibrahim, Chung, Wendy K., Kavus, Haluk, Saeidi, Kolsoum, Maroofian, Reza, AlHashim, Aqeela, Al‐Otaibi, Ali, Al Madhi, Asma, Abou Al‐Seood, Hager M., Alasmari, Ali, Houlden, Henry, Gleeson, Joseph G., Hunter, Jill V., Posey, Jennifer E., Lupski, James R., El‐Hattab, Ayman W.

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Metabolic Seizures von Almannai, Mohammed, Al Mahmoud, Rabah A., Mekki, Mohammed, El-Hattab, Ayman W.

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Numerical simulation of a new heterostructure CIGS/GaSe solar cell system using SCAPS-1D software von Al-Hattab, Mohamed, Moudou, L'houcine, Khenfouch, Mohammed, Bajjou, Omar, Chrafih, Younes, Rahmani, Khalid

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Expanding the genetic heterogeneity of intellectual disability von Anazi, Shams, Maddirevula, Sateesh, Salpietro, Vincenzo, Asi, Yasmine T., Alsahli, Saud, Alhashem, Amal, Shamseldin, Hanan E., AlZahrani, Fatema, Patel, Nisha, Ibrahim, Niema, Abdulwahab, Firdous M., Hashem, Mais, Alhashmi, Nadia, Al Murshedi, Fathiya, Al Kindy, Adila, Alshaer, Ahmad, Rumayyan, Ahmed, Al Tala, Saeed, Kurdi, Wesam, Alsaman, Abdulaziz, Alasmari, Ali, Banu, Selina, Sultan, Tipu, Saleh, Mohammed M., Alkuraya, Hisham, Salih, Mustafa A., Aldhalaan, Hesham, Ben-Omran, Tawfeg, Al Musafri, Fatima, Ali, Rehab, Suleiman, Jehan, Tabarki, Brahim, El-Hattab, Ayman W., Bupp, Caleb, Alfadhel, Majid, Al Tassan, Nada, Monies, Dorota, Arold, Stefan T., Abouelhoda, Mohamed, Lashley, Tammaryn, Houlden, Henry, Faqeih, Eissa, Alkuraya, Fowzan S.

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ADAT3-related intellectual disability: Further delineation of the phenotype von El-Hattab, Ayman W., Saleh, Mohammed A., Hashem, Amal, Al-Owain, Mohammed, Asmari, Ali Al, Rabei, Hala, Abdelraouf, Hanem, Hashem, Mais, Alazami, Anas M., Patel, Nisha, Shaheen, Ranad, Faqeih, Eissa A., Alkuraya, Fowzan S.

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The determination of causality of drug induced liver injury in patients with COVID-19 clinical syndrome von Naseralallah, Lina Mohammad, Aboujabal, Bodoor Abdallah, Geryo, Nejat Mohamed, Al Boinin, Aisha, Al Hattab, Fatima, Akbar, Raza, Umer, Waseem, Abdul Jabbar, Layla, Danjuma, Mohammed I

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Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy von Harel, Tamar, Yesil, Gozde, Bayram, Yavuz, Coban-Akdemir, Zeynep, Charng, Wu-Lin, Karaca, Ender, Al Asmari, Ali, Eldomery, Mohammad K., Hunter, Jill V., Jhangiani, Shalini N., Rosenfeld, Jill A., Pehlivan, Davut, El-Hattab, Ayman W., Saleh, Mohammed A., LeDuc, Charles A., Muzny, Donna, Boerwinkle, Eric, Gibbs, Richard A., Chung, Wendy K., Yang, Yaping, Belmont, John W., Lupski, James R.

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A homozygous frame‐shift variant in PROSER1 is associated with developmental delay, hypotonia, genitourinary malformations, and distinctive facial features von Salah, Azza, Almannai, Mohammed, Al Ojaimi, Mode, Radefeldt, Mandy, Gulati, Nishtha, Iqbal, Maria, Alawbathani, Salem, Al‐Ali, Ruslan, Beetz, Christian, El‐Hattab, Ayman W.

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