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

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Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy. A one-decade single-center experience von Badi, Maryam K. Al, Azkawi, Hanan S. Al, Yahyaei, Mouza S. Al, Mula-Abed, Waad A, Senani, Aisha M. Al

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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency von Yau, Mabel, Haider, Shozeb, Khattab, Ahmed, Ling, Chen, Mathew, Mehr, Zaidi, Samir, Bloch, Madison, Patel, Monica, Ewert, Sinead, Abdullah, Wafa, Toygar, Aysenur, Mudryi, Vitalii, Badi, Maryam Al, Alzubdi, Mouch, Wilson, Robert C., Azkawi, Hanan Said Al, Ozdemir, Hatice Nur, Abu-Amer, Wahid, Hertecant, Jozef, Razzaghy-Azar, Maryam, Funder, John W., Senani, Aisha Al, Sun, Li, Kim, Se-Min, Yuen, Tony, Zaidi, Mone, New, Maria I.

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Testosterone- and Cortisol-secreting Oncocytic Adrenocortical Adenoma in the Pediatric Age-group von Al Badi, Maryam K, Al-Alwan, Ibrahim, Al-Dubayee, Mohammed, Al-Anzi, Ayed, Al Turki, Maram S, Aloudah, Noura, Alsaad, Khaled O

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A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred von Yau, Mabel, Azkawi, Hanan Said Al, Haider, Shozeb, Khattab, Ahmed, Badi, Maryam Al, Abdullah, Wafa, Senani, Aisha Al, Wilson, Robert C., Yuen, Tony, Zaidi, Mone, New, Maria I.

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A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population von 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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Primary Hypothyroidism with Pituitary Hyperplasia in an Omani Girl von Abdallah Fadle, Wafa, Al Reesi, Ali, Al-Shabibi, Saud, Khamis Al-Badi, Maryam

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

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Deictic expressions and their contribution to create a viewpoint in discourse von Albadi, Mariam

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Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy von Al-Badi, Maryam K, Al-Azkawi, Hanan S, Al-Yahyaei, Mouza S, Mula-Abed, Waad A, Al-Senani, Aisha M

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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11ß- hydroxysteroid dehydrogenase type 2 deficiency von Yau, Mabel, Haider, Shozeb, Khattab, Ahmed, Ling, Chen, Mathew, Mehr, Zaidi, Samir, Bloch, Madison, Patel, Monica, Ewert, Sinead, Abdullah, Wafa, Toygar, Aysenur, Mudryi, Vitalii, Badi, Maryam Al, Alzubdi, Mouch, Wilson, Robert C, Al Azkawi, Hanan Said, Ozdemir, Hatice Nur, Abu-Amer, Wahid, Hertecant, Jozef, Razzaghy-Azar, Maryam, Funder, John W, Al Senani, Aisha, Sun, Li, Kim, Se-Min, Yuen, Tony, Zaidi, Mone, New, Maria I

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Higher serum alkaline phosphatase activity in infants born to vitamin D–deficient mothers von Al Alwan, Ibrahim, Al Badi, Maryam, Badri, Motasim, Tamimi, Waleed, Al Dubayee, Mohamed, Mughal, M. Zulf, Babiker, Amir

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Primary Hypothyroidism with Pituitary Hyperplasia in an Omani Girl von Abdallah Fadle, Wafa, Al Reesi, Ali, Al-Shabibi, Saud, Khamis Al-Badi, Maryam

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Prevalence and risk factors for SARS-CoV-2 infection and seroprevalence among clinical and non-clinical staff in a national healthcare system von Alishaq, Moza, Jeremijenko, Andrew, Al-Kanaani, Zeina, Nafady-Hego, Hanaa, Jboor, Diana H, Saba, Rosaline, Al-Ajmi, Jameela, Alansari, Nasser Asad, Thomas, Anil George, Fareh, Sameera Bihi, Vinoy, Suni, Nooh, Maryam, Alanzi, Nadya, Abou-Samra, Abdul-Badi, Butt, Adeel Ajwad

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An Unusual Presentation of Morphea: A Case Report von Al Badi, Asiya, Al-Khamisani, Maryam

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Comparison of demographic, clinical and laboratory characteristics between first and second COVID-19 waves in a secondary care hospital in Qatar: a retrospective study von Naushad, Vamanjore A, Purayil, Nishan K, Chandra, Prem, Saeed, Abazar Ahmad M, Radhakrishnan, Pradeep, Varikkodan, Irfan, Mathew, Joe V, Sirajudeen, Jaseem, Hammamy, Riyadh A, Badi, Ahmad M, Suliman, Aasir M, Badawi, Mohamed N, Arya, Saket, AlMotawa, Maryam, Al-Baker, Aisha, Alatom, Rania, Kartha, Anand

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Circulating microRNA signatures in patients with chronic Urticaria von Jerobin, Jayakumar, Ali, Ramzy Mohammed, Khalil, Sally, Ramanjaneya, Manjunath, Betahi, Ilham, Samra, Abdul Badi Abou, Al-Nesf, Maryam A

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Factors Affecting the Willingness to Undertake Premarital Screening Test Among Prospective Marital Individuals von Alkalbani, Ali, Alharrasi, Maryam, Achura, Susan, Al Badi, Ammar, Al Rumhi, Amjad, Alqassabi, Khalid, Almamari, Raya, Alomari, Omar

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Non-Ovarian Pelvic Cyst: Not Specific Enough von Al-Badi , Muna, Gowri , Vaidyanathan, Al-Ghafri , Wadha, Al-Shukri , Maryam

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Circulatory EVs as a predictor of chronic urticarial activity von Mohammed-Ali, Ramzy, Jerobin, Jayakumar, Khalil, Sally, Sivaraman, Siveen, Ramanjaneya, Manjunath, Betahi, Ilham, Badi Abou Samra, Abdul, Al-Nesf, Maryam

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