Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Dima Z. Jamjoom"'
Autor:
Amal Y. Kentab, Yara Alsalloum, Mai Labani, Abrar Hudairi, Muddathir H. Hamad, Dima Z. Jamjoom, Ali H. Alwadei, Reem M. Alhammad, Fahad A. Bashiri
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundBrown-Vialetto-Van Laere (BVVL) syndrome is an extremely rare autosomal recessive progressive motoneuron disease that is caused by a defect in the riboflavin transporter genes SLC52A2 and SLC52A3. BVVL syndrome has a variable age of present
Externí odkaz:
https://doaj.org/article/64720140ac684806ac89d179edf0e67f
Autor:
Mohammed F. Alosaimi, Muddathir H. Hamad, Muneera J. AlShammari, Dima Z. Jamjoom, Najd S. Musibeeh
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundBare lymphocyte syndrome type II (BLS II) is a rare form of severe combined immunodeficiency caused by mutations in the CIITA gene, which regulates major histocompatibility complex class II (MHC II) expression.ObjectiveWe report the case of
Externí odkaz:
https://doaj.org/article/be525d4acb7141f99081288a0f3fbb89
Autor:
Mountasser M. Al-Mouqdad, Dima Z. Jamjoom, Roya Huseynova, Thanaa M. Khalil, Yasmeen S. Asfour, Bushra A. Albeshri, Nadia A. Basodan, Fuddah Assiri, Suzan S. Asfour
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-10 (2022)
Abstract To investigate the relationship between morphine exposure in the first week of life and brain injury on term-equivalent age magnetic resonance imaging (MRI) in very preterm infants. A retrospective study included 106 infants with a birth wei
Externí odkaz:
https://doaj.org/article/123d34bfccc048be95ce51c086c099a7
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Epidermoid cysts are benign congenital extra-axial lesions commonly found in the posterior fossa. These lesions have a characteristic imaging appearance on computed tomography (CT) scan and magnetic resonance imaging (MRI), but occasionally
Externí odkaz:
https://doaj.org/article/f0f8cee069304ecb98fbdc48dd3545fb
Autor:
Malak Ali Alghamdi, Hicham Benabdelkamel, Afshan Masood, Narjes Saheb Sharif-Askari, Mahmood Y. Hachim, Hamad Alsheikh, Muddathir H. Hamad, Mustafa A. Salih, Fahad A. Bashiri, Khalid Alhasan, Tarek Kashour, Pilar Guatibonza Moreno, Sabine Schröder, Vasiliki Karageorgou, Aida M. Bertoli-Avella, Hisham Alkhalidi, Dima Z. Jamjoom, Ibrahim A. Alorainy, Assim A. Alfadda, Rabih Halwani
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Galloway-Mowat syndrome is a rare autosomal recessive disease characterized by a unique combination of renal and neurological manifestations, including early-onset steroid-resistant nephrotic syndrome, microcephaly, psychomotor delay, and gyral abnor
Externí odkaz:
https://doaj.org/article/8db6644c11c4473ea480bba4e547fa50
Autor:
Malak Ali Alghamdi, Waleed H. Alkhamis, Dima Z. Jamjoom, Reem Al Khalifah, Nawaf Rahi Alshammari, Khalid Alsumaili, Stefan T. Arold
Publikováno v:
Clinical Case Reports, Vol 9, Iss 1, Pp 229-235 (2021)
Abstract Central hypothyroidism might be another clinical sign of SSADH deficiency which prompts urinary organic acid screening for GHB in central hypothyroidism patients. Studies on GABA and thyroid hormone interaction might be a concept of a new th
Externí odkaz:
https://doaj.org/article/efa06ea84b33463e9b1c0fb0ddd86c7c
Autor:
Nasser Waleed Alobida, Aseel O. Doubi, Mohammed Alswayyed, Dima Z. Jamjoom, Khalid Al-Qahtani
Publikováno v:
Acta Oto-Laryngologica Case Reports, Vol 5, Iss 1, Pp 69-73 (2020)
Parapharyngeal space (PPS) tumors are a rare entity and account for less than 1% of all head and neck tumors. Although they exhibit a benign behavior, malignant neoplasms may arise from any of the structure contained in the space. Differential diagno
Externí odkaz:
https://doaj.org/article/a4e8acf25d13440680de2631c2719441
Autor:
Khalid A. Alhasan, Walaa Alshuaibi, Muddathir H. Hamad, Suha Salim, Dima Z. Jamjoom, Aqeela H. Alhashim, Malak Ali AlGhamdi, Amal Y. Kentab, Fahad A. Bashiri
Publikováno v:
Children, Vol 9, Iss 9, p 1335 (2022)
Importance: Hypermanganesemia with dystonia type 2 is a rare autosomal recessive neurodegenerative disorder characterized by the loss of previously acquired milestones, dystonia, parkinsonian features, a high serum manganese level, and characteristic
Externí odkaz:
https://doaj.org/article/d7de030f5995434a943fbef7d4dc8554
Autor:
Mountasser M. Al-Mouqdad, Dima Z. Jamjoom, Ayman T. Abdalgader, Waleed S. Ameen, Thanaa M. Khalil, Yasmeen S. Asfour, Maha R. Al-Anazi, Suzan S. Asfour
Publikováno v:
Pediatric Nephrology. 37:3235-3242
Autor:
Malak Alghamdi, Waleed H. Alkhamis, Stefan T. Arold, Reem Al Khalifah, Nawaf Rahi Alshammari, Dima Z. Jamjoom, Khalid Alsumaili
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 1, Pp 229-235 (2021)
Clinical Case Reports, Vol 9, Iss 1, Pp 229-235 (2021)
Central hypothyroidism might be another clinical sign of SSADH deficiency which prompts urinary organic acid screening for GHB in central hypothyroidism patients. Studies on GABA and thyroid hormone interaction might be a concept of a new therapy.