64 A case series of two adolescent diabetic siblings due to novel mutation in CFAP126 von Arshad, Kashan, Sommayya Aftab, Aamir Naseem, Anjum, Muhammad Nadeem, Saeed, Anjum

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28 Frequency and risk factors of lipohypertrophy in children and adolescent with type 1 diabetes in a single tertiary care centre von Arshad, Kashan, Naseem, Aamir, Aftab, Sommayya, Ayesha, Hina

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Frequency and Associated Factors of Lipohypertrophy in Children and Adolescent with Type 1 Diabetes in a Single Tertiary Care Centre: Frequency and Associated Factors of Lipohypert... von Arshad, Kashan, Naseem, Aamir, Sommayya Aftab, Syed Saddam Hussain

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Corticosterone Methyl Oxidase Type 1 (CMO1) Deficiency Due to CYP11B2 Mutation: Two Case Reports von Ur Rehman, Saad, Aftab, Sommayya, Naseem, Aamir, Saeed, Anjum, Cheema, Huma Arshad

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Aromatase deficiency due to novel CYP19A1 mutation: a rare cause of maternal and fetal virilization von Naseem, Aamir, Zahid, Muhammad, Arshad, Kashan, Hussain, Syed Saddam, Aftab, Sommayya, Saeed, Anjum, Cheema, Huma Arshad

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A National Survey on Congenital Hypothyroidism Newborn Screening in Pakistan von Khan, Sabeen Abid, Aftab, Sommayya, Khan, Yasir Naqi, Yasir, Mehrunnisa, Arshad, Kashan, Mehak, Noor ul Ain, Rehman, Syed Kaleem ur, Faiztalpur, Abida, Bahar, Shazia, Abdul Razzaq, Ayesha, Habibullah, Sajjad, Naseem, Aamir, Hussain, Syed Saddam, Sattar, Hina, Usman, Mohammed, Ayub, Aqeela, Waris, Rehmana, Butt, Taeed Ahmed

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Corticosterone Methyl Oxidase Type 1 (CMO1) Deficiency Due to CYP11B2 Mutation: Two Case Reports von Ur Rehman, Saad, Aftab, Sommayya, Naseem, Aamir, Saeed, Anjum, Cheema, Huma Arshad

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