Adenosine deaminase 2 deficiency with a novel variant of CECR1 gene mutation: Responding to tumor necrosis factor antagonist therapy von Al Mosawi, Zakiya, Abduljawad, Hiba, Busehail, Maryam, Al Moosawi, Barrak

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Juvenile eosinophilic fasciitis presenting with polyarthritis and koebner's phenomenon von Al Mosawi, Zakiya, Al Hammadi, Muneera, Karim Ebrahim, Batool, George, Sara

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Renal manifestations in hypocomplementic urticarial vasculitis syndrome : is it a distinct pathology ? von al-Hirmi, Badriyah, al-Musawi, Zakiyah, Muhammad, Dina

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Kikuchi-Fujimoto Disease: Eleven Pediatric Cases and Literature Review von Mosawi, Zakiya Al, Ebrahim, Batool, Baik, Salwa, Madan, Wafa, Aljufairi, Eman

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Hypocomplementemic Urticarial Vasculitis Syndrome in an 8-Year-Old Boy: A Case Report and Review of Literature von Al Hermi , Badriya Ebrahim Ahmed, Al Mosawi , Zakiya Saleh Adnan

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Dramatic Response of Familial Majeed Syndrome to Interleukin-1 Antagonist Therapy: Case report von Mosawi, Zakiya Al, Madan, Wafa, Moosawi, Barrak Al, Wadaei, Sayed Al, Naser, Husain, Ali, Fuad

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A splice site mutation confirms the role of LPIN2 in Majeed syndrome von Al‐Mosawi, Zakiya S., Al‐Saad, Khulood K., Ijadi‐Maghsoodi, Roya, El‐Shanti, Hatem I., Ferguson, Polly J.

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Pediatric-onset Behçet Disease in Bahrain: Report of Nine Cases and Literature Review von Al Mosawi, Zakiya Saleh, Madan, Wafa, Fareed, Eman

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Juvenile systemic lupus erythematosus in Bahrain: A tertiary referral center experience von AL-MOSAWI, Zakiya, AL-HERMI, Badriya E, AL-SAAD, Khulood K, FARID, Eman M, MAKKI, Hussain A

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Renal manifestations in hypocomplementic urticarial vasculitis syndrome: Is it a distinct pathology? von AlHermi, Badriya, Al Mosawi, Zakiya, Mohammed, Deena

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Hypocomplementemic Urticarial Vasculitis Syndrome in an 8-year-old Boy: A Case Report and Review of Literature von Al Mosawi, Zakiya Saleh Adnan, Al Hermi, Badriya Ebrahim Ahmed

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