Arabic Automatic Speech Recognition: A Systematic Literature Review by Dhouib, Amira, Othman, Achraf, El Ghoul, Oussama, Khribi, Mohamed Koutheair, Al Sinani, Aisha

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A Novel Mutation Causing 17 - β - Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature by Mula-Abed , Waad-Allah S, Nahavandi , Nahid, Al-Kusaibi , Ghariba, Al-Azkawi , Hanan, Al-Kindi , Manal, Al-Sinani , Aisha

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Agammaglobulinaemia despite terminal B‐cell differentiation in a patient with a novel LRBA mutation by Al Sukaiti, Nashat, AbdelRahman, Khwater, AlShekaili, Jalila, Al Oraimi, Sumaya, Al Sinani, Aisha, Al Rahbi, Nasser, Cho, Vicky, Field, Matt, Cook, Matthew C

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A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population by Alzahrani, Ali S, Alswailem, Meshael, Abbas, Bassam Bin, Qasem, Ebtesam, Alsagheir, Afaf, Al Shidhani, Azza, Al Sinani, Aisha, Al Badi, Maryam, Al-Maqbali, Ali, Al Shawi, Manal, Albunyan, Abdulhameed, Bin Nafisah, Abdulghani, Shi, Yufei

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Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia [version 2; peer review: 3 approved, 1 approved with reservations] by Willows, Jamie, Al Badi, Maryam, Richardson, Chloe, Al Sinani, Aisha, Edwards, Noel, Rice, Sarah, Sayer, John A

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Inverted Presentation: Anal Bleeding as the Initial Manifestation of Pediatric Inverse Psoriasis: A Case Report by Al Sinani, Aisha

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Use of ambulatory glucose monitoring and analysis of ambulatory glucose profile in clinical practice for diabetes management; a position statement of the Arab Society of Paediatric... by Deeb, Asma, Muammar, Tawfik, Alsaffar, Hussain, Sedaghat, Sara, Al Hassani, Noura, Odeh, Rasha, Alkhayyat, Haya, Al Sinani, Aisha, Attia, Najya, Adhami, Sarah, Elbarbary, Nancy

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Hyperthyroidism Presenting as Jaundice in a Child by Al Lawati, Tawfiq Taki, Al Sinani, Aisha, Al Lawati, Fatma Ali Ramadhan

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Toward Closing the Training and Knowledge Gap in ICT Accessibility and Inclusive Design Harnessing Open Educational Resources by Khribi, Mohamed Koutheair, Othman, Achraf, Al-Sinani, Aisha

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A novel leprechaunism mutation, Cys807Arg, in an Arab infant: a rare cause of hypoglycaemia by Baqir, Zaineb S, Al-Lawati, Tawfiq T, Al Hussaini, Saniya O, Al-Sinani, Aisha, Al-Said, Khoula, Al-Rashdi, Ismail

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Agammaglobulinaemia despite terminal B-cell differentiation in a patient with a novel LRBA mutation by Al Sukaiti, Nashat, AbdelRahman, Khwater, AlShekaili, Jalila, Al Oraimi, Sumaya, Al Sinani, Aisha, Al Rahbi, Nasser, Cho, Vicky, Field, Matt, Cook, Matthew C

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A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature by Al-Sinani, Aisha, Mula-Abed, Waad-Allah S, Al-Kindi, Manal, Al-Kusaibi, Ghariba, Al-Azkawi, Hanan, Nahavandi, Nahid

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Disclosing the origin and diversity of Omani cattle by Mahgoub, Osman, Babiker, Hamza A., Kadim, I.T., Al-Kindi, Mohammed, Hassan, Salwa, Al-Marzooqi, W., Eltahir, Yasmin E., Al-Abri, M. A., Al-Khayat, Aisha, Al-Sinani, Kareema R., Hilal Al-Khanjari, Homoud, Costa, Vânia, Chen, Shanyuan, Beja-Pereira, Albano

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Prevalence of Celiac Disease in Omani Children with Type 1 Diabetes Mellitus: A Cross Sectional Study by Al-Hajri , Aisha, Al-Hasani , Said, Al-Zakwani , Ibrahim, Al-Naamani , Khalid, Sharef , Sharef Waadallah, Al-Sinani , Siham, Al-Yaarubi , Saif

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Disclosing the origin and diversity of O mani cattle by Mahgoub, Osman, Babiker, Hamza A., Kadim, I.T., Al‐Kindi, Mohammed, Hassan, Salwa, Al‐Marzooqi, W., Eltahir, Yasmin E., Al‐Abri, M. A., Al‐Khayat, Aisha, Al‐Sinani, Kareema R., Hilal Al‐Khanjari, Homoud, Costa, Vânia, Chen, Shanyuan, Beja‐Pereira, Albano

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Choledochal cysts in Omani children: A case series by Al-Sinani, Siham, Al Naamani, Khalid, Lutfi, Wafa, Al Hajri, Aisha

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