Cerebral sinuses thrombosis prior to the diagnosis of acute lymphoblastic leukemia in a child: A case report von Sherief, Laila M, Zakaria, Marwa, Soliman, Basma K, Kamal, Naglaa M, Alharthi, Sultan A, Abosabie, Sara AS, Abdelazeem, Mahmoud

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Cerebral sinuses thrombosis prior to the diagnosis of acute lymphoblastic leukemia in a child: A case report von Sherief, Laila M, Zakaria, Marwa, Soliman, Basma K, Kamal, Naglaa M, Alharthi, Sultan A, Abosabie, Sara As, Abdelazeem, Mahmoud

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Vertebral artery dissection aneurysm in a pediatric patient: A rare case with unusual clinical manifestations, diagnostic, and management challenges von Oshi, Mohammed A. M., Aljabri, Mohammed Fahad, Alotaibi, Saad, Alzahrani, Yahea, Alfaifi, Jaber, Abosabie, Salma A. S., Abosabie, Sara A., Algethami, Samaher S., Younes, Alaa E., Almanjoomi, Raid K., Babkour, Bashar, Kamal, Naglaa M.

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Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation von Bakkar, Ayman A, Alsaedi, Abdulaziz, Kamal, Naglaa M, Althobaiti, Enad, Aboulkhair, Lujain A, Almalki, Abdullah M, Alsalmi, Shaima A, Alharthi, Qaydah, Abosabie, Sara A, Abosabie, Salma AS

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An Unusual Case of Headache in a Child: Idiopathic Intracranial Hypertension with Diagnostic Challenge von Alqahtani, Youssef Ali M, Aljabri, Mohammed Fahad, Oshi, Mohammed Ahmed Mohammed, Kamal, Naglaa M, Elhaj, Waleed, Abosabie, Sara A, Abosabie, Salma AS

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Pediatric myelin oligodendrocyte glycoprotein antibody associated disease—Asymmetric papilledema and elevated ICP are two of the chameleons: A case report von Alqahtani, Youssef, Oshi, Mohammed, Kamal, Naglaa M., Aljabri, Mohammed, Abosabie, Salma, Elhaj, Waleed, Abosabie, Sara A

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Renal angina index in critically ill children as an applicable and reliable tool in the prediction of severe acute kidney injury: Two tertiary centers' prospective observational st... von Soliman, Ahmed S A, Al-Ghamdi, Hamdan S, Abukhatwah, Mohamed W, Kamal, Nagla M, Dabour, Shaheen A, Elgendy, Soha A, Alfaifi, Jaber, Abukhatwah, Omar M W, Abosabie, Salma A S, Abosabie, Sara A, Oshi, Mohammed A M, Althobaity, Jwaher, Sakr Sherbiny, Hanan, Al-Juaid, Futun A, Rahman, Eman G Abdel

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First report of SYNE1 arthrogryposis multiplex congenita from Saudi Arabia with a novel mutation: a case report von Kamal, Naglaa M., Alzeky, AlaaEddin M., Omair, Maher R., Attar, Ruwayd A., Alotaibi, Abdullah M., Safar, Abdullah, Alosaimi, Nawal S., Abosabie, Sara A. S.

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Progressive myoclonic ataxia and developmental/epileptic encephalopathy associated with a novel homozygous mutation in TCN2 gene von Oshi, Mohammed Ahmed Mohammed, Alfaifi, Jaber, Alqahtani, Youssef Ali M., Aljabri, Mohammed Fahad, Kamal, Naglaa M., Althopaity, Jwaher, Althobaiti, Khalid A., Almalki, Abdullah M., Abosabie, Salma A. S., Abosabie, Sara A., Sherbiny, Hanan Sakr, Almanjoomi, Saif K., Abdallah, Enas A. A.

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Unraveling Alström syndrome: Homozygous mutation c.2729C>G in ALMS1 gene across an extended family von Abosabie, Salma A. S., Abosabie, Sara A., Alfaifi, Jaber, Alqahtani, Youssef A., Shati, Ayed A., Alotaibi, Najmah A., Alghamdi, Ohoud A., Alotaibi, Ghadi N., Baabdullah, Abdulrahman A., Kabrah, Lama K., Kamal, Naglaa M., Oshi, Mohammed A. M., Abdallah, Enas A. A.

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Progressive myoclonic ataxia and developmental/epileptic encephalopathy associated with a novel homozygous mutation in TCN 2 gene von Oshi, Mohammed Ahmed Mohammed, Alfaifi, Jaber, Alqahtani, Youssef Ali M., Aljabri, Mohammed Fahad, Kamal, Naglaa M., Althopaity, Jwaher, Althobaiti, Khalid A., Almalki, Abdullah M., Abosabie, Salma A. S., Abosabie, Sara A., Sherbiny, Hanan Sakr, Almanjoomi, Saif K., Abdallah, Enas A. A.

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An Unusual Case of Headache in a Child: Idiopathic Intracranial Hypertension with Diagnostic Challenge von Alqahtani, Youssef Ali M, Aljabri, Mohammed Fahad, Oshi, Mohammed Ahmed Mohammed, Kamal, Naglaa M, Elhaj, Waleed, Abosabie, Sara A, Abosabie, Salma As

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