First report of SYNE1 arthrogryposis multiplex congenita from Saudi Arabia with a novel mutation: a case report by 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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Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation by 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 by 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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Cerebral sinuses thrombosis prior to the diagnosis of acute lymphoblastic leukemia in a child: A case report by Sherief, Laila M, Zakaria, Marwa, Soliman, Basma K, Kamal, Naglaa M, Alharthi, Sultan A, Abosabie, Sara AS, Abdelazeem, Mahmoud

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

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Vertebral artery dissection aneurysm in a pediatric patient: A rare case with unusual clinical manifestations, diagnostic, and management challenges by 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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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... by 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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Progressive myoclonic ataxia and developmental/epileptic encephalopathy associated with a novel homozygous mutation in TCN2 gene by 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 by 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 by 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 by 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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Cerebral sinuses thrombosis prior to the diagnosis of acute lymphoblastic leukemia in a child: A case report by Sherief, Laila M, Zakaria, Marwa, Soliman, Basma K, Kamal, Naglaa M, Alharthi, Sultan A, Abosabie, Sara As, Abdelazeem, Mahmoud

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