Phenotypic and molecular spectrum of pyridoxamine‐5′‐phosphate oxidase deficiency: A scoping review of 87 cases of pyridoxamine‐5′‐phosphate oxidase deficiency
Alghamdi, Malak, Bashiri, Fahad A., Abdelhakim, Marwa, Adly, Nouran, Jamjoom, Dima Z., Sumaily, Khalid M., Alghanem, Bandar, Arold, Stefan T.
Published in Clinical genetics (01.01.2021)
Published in Clinical genetics (01.01.2021)
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Journal Article
Association between morphine exposure and impaired brain development on term-equivalent age brain magnetic resonance imaging in very preterm infants
Al-Mouqdad, Mountasser M., Jamjoom, Dima Z., Huseynova, Roya, Khalil, Thanaa M., Asfour, Yasmeen S., Albeshri, Bushra A., Basodan, Nadia A., Assiri, Fuddah, Asfour, Suzan S.
Published in Scientific reports (16.03.2022)
Published in Scientific reports (16.03.2022)
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Journal Article
Association between acute kidney injury and brain injury on term-equivalent age brain magnetic resonance imaging in very preterm infants
Al-Mouqdad, Mountasser M., Jamjoom, Dima Z., Abdalgader, Ayman T., Ameen, Waleed S., Khalil, Thanaa M., Asfour, Yasmeen S., Al-Anazi, Maha R., Asfour, Suzan S.
Published in Pediatric nephrology (Berlin, West) (01.12.2022)
Published in Pediatric nephrology (Berlin, West) (01.12.2022)
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Journal Article
Case Report: A rare treatable metabolic syndrome (Brown-Vialetto-Van Laere syndrome) masquerading as chronic inflammatory demyelinating polyneuropathy from Saudi Arabia
Kentab, Amal Y, Alsalloum, Yara, Labani, Mai, Hudairi, Abrar, Hamad, Muddathir H, Jamjoom, Dima Z, Alwadei, Ali H, Alhammad, Reem M, Bashiri, Fahad A
Published in Frontiers in pediatrics (30.04.2024)
Published in Frontiers in pediatrics (30.04.2024)
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Journal Article
Genomic, Proteomic, and Phenotypic Spectrum of Novel O-Sialoglycoprotein Endopeptidase Variant in Four Affected Individuals With Galloway-Mowat Syndrome
Ali Alghamdi, Malak, Benabdelkamel, Hicham, Masood, Afshan, Saheb Sharif-Askari, Narjes, Hachim, Mahmood Y., Alsheikh, Hamad, Hamad, Muddathir H., Salih, Mustafa A., Bashiri, Fahad A., Alhasan, Khalid, Kashour, Tarek, Guatibonza Moreno, Pilar, Schröder, Sabine, Karageorgou, Vasiliki, Bertoli-Avella, Aida M., Alkhalidi, Hisham, Jamjoom, Dima Z., Alorainy, Ibrahim A., Alfadda, Assim A., Halwani, Rabih
Published in Frontiers in genetics (23.06.2022)
Published in Frontiers in genetics (23.06.2022)
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Journal Article
The association between petrous apex cephalocele and empty sella
Jamjoom, Dima Z., Alorainy, Ibrahim A.
Published in Surgical and radiologic anatomy (English ed.) (01.12.2015)
Published in Surgical and radiologic anatomy (English ed.) (01.12.2015)
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Journal Article
Hypermanganesemia with Dystonia Type 2: A Potentially Treatable Neurodegenerative Disorder: A Case Series in a Tertiary University Hospital
Alhasan, Khalid A, Alshuaibi, Walaa, Hamad, Muddathir H, Salim, Suha, Jamjoom, Dima Z, Alhashim, Aqeela H, AlGhamdi, Malak Ali, Kentab, Amal Y, Bashiri, Fahad A
Published in Children (Basel) (01.09.2022)
Published in Children (Basel) (01.09.2022)
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Journal Article
Succinic semialdehyde dehydrogenase deficiency presenting with central hypothyroidism
Alghamdi, Malak Ali, Alkhamis, Waleed H., Jamjoom, Dima Z., Al Khalifah, Reem, Alshammari, Nawaf Rahi, Alsumaili, Khalid, Arold, Stefan T.
Published in Clinical case reports (01.01.2021)
Published in Clinical case reports (01.01.2021)
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Journal Article
Case report: A late and isolated presentation of meningoencephalomyelitis uncovers a novel pathogenic variant in the CIITA gene
Alosaimi, Mohammed F., Hamad, Muddathir H., AlShammari, Muneera J., Jamjoom, Dima Z., Musibeeh, Najd S.
Published in Frontiers in pediatrics (29.09.2023)
Published in Frontiers in pediatrics (29.09.2023)
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Journal Article
Effect of interferon treatment on hearing of patients with chronic hepatitis C
Hagr, Abdulrahman, Jamjoom, Dima, Sanai, Faisal M, Al Hamoudi, Waleed, Abdo, Ayman A, Al-Arfaj, Ahmed
Published in Saudi journal of gastroenterology (01.03.2011)
Published in Saudi journal of gastroenterology (01.03.2011)
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Journal Article
Expanding the phenotype and the genotype of Stromme syndrome: A novel variant of the CENPF gene and literature review
Alghamdi, Malak, Alkhamis, Waleed H., Bashiri, Fahad A., Jamjoom, Dima, Al-Nafisah, Ghada, Tahir, Asma, Abdouelhoda, Mohamed
Published in European journal of medical genetics (01.05.2020)
Published in European journal of medical genetics (01.05.2020)
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Journal Article
Proceedings of the 13th International Newborn Brain Conference: Neuro-imaging studies: Virtual conference, February 10th-12th 2022
Abramsky, Ramy, Acosta, Rebeka, Acosta Izquierdo, Laura, Albeshri, Bushra, Almouqdad, Mountasser, Asfour, Yasmeen, Asfour, Suzan, Austin, Topun, Bach, Ashley, Barkovich, Jim, Beare, Richard, Ben Fadel, Nadya, Berger, Angelika, Blanco, Borja, Boomsma, Martijn, Bora, Samudragupta, Boswinkel, Vivian, Chin, Theresa, Collins-Jones, Liam, Cooper, Robert, Dagur, Gautam, Davila, Jorge, de Vries, Linda, Shesrao, Laxmikant, Deshmukh, Dovjak, Gregor, Edwards, Andrea, El-Dib, Mohamed, Elshibiny, Hoda, Eshel, Dafna, Eshel, Ron, Ferriero, Donna, Gano, Dawn, Girvan, Olivia, Glass, Hannah, Goeral, Katharina, Golan, Agneta, Gurvitz, Michelle, Inder, Terrie, Jamjoom, Dima, Kadom, Nadja, Kasprian, Gregor, Khalil, Thanaa, Klebermass-Schrehof, Katrin, Kleinmahon, Jake, Krüse-Ruijter, Martine, Lambing, Hannah, Lee, Sarah, Leemans, Alexander, Leijser, Lara, Lemyre, Brigitte, Li, Yi, Maltais-Bilodeau, Camille, Marks, Kyla, McCulloch, Charles, Milla, Sarah, Miller, Elka, Mishra, Aradhana, Mitsakakis, Nicholas, Mohammad, Khorshid, Tollenaer, Susanne Mulder-de, Munster, Chelsea, Nijboer, Jacqueline, Nijboer-Oosterveld, Jacqueline, Nijholt, Ingrid, Novoa, Rosa, Ortinau, Cynthia, Porter, Emma, Prayer, Daniela, Reddy, Deepti, Redpath, Stephanie, Rogers, Elizabeth, Schmidbauer, Victor, Scott, James, Sewell, Elizabeth, Shany, Eilon, Shelef, Ilan, Singh, Elizabeth, Slump, Cornelis, Steele, Tina, Szakmar, Eniko, Tax, Chantal, Thiim, Kirsten, Uchitel, Julie, van Osch, Jochen, van Wezel-Meijler, Gerda, Verschuur, Anouk, Wu-Smit, Mei-Nga, Yang, Edward, Zein, Hussein
Published in Journal of neonatal-perinatal medicine (12.04.2022)
Published in Journal of neonatal-perinatal medicine (12.04.2022)
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Journal Article
Case Report: A rare treatable metabolic syndrome (Brown-Vialetto-Van Laere syndrome) masquerading as chronic inflammatory demyelinating polyneuropathy from Saudi Arabia
Kentab, Amal Y, Alsalloum, Yara, Labani, Mai, Hudairi, Abrar, Hamad, Muddathir H, Jamjoom, Dima Z, Alwadei, Ali H, Alhammad, Reem M, Bashiri, Fahad A
Published in Frontiers in pediatrics (01.01.2024)
Published in Frontiers in pediatrics (01.01.2024)
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