Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Reem M. Alhammad"'
Autor:
Reem M. Alhammad, Marwa L. Alrehaili, Hana M. Albulaihe, Sultan S. Aljereish, Mohammed H. Alanazy
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Diagnosis of hereditary myopathy is often challenging owing to overlapping clinical phenotypes and muscle histopathological findings. This retrospective study aimed to identify the phenotypic and genotypic spectra of hereditary my
Externí odkaz:
https://doaj.org/article/b991048a56e54db0bb470d217acea376
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:
Reem M. Alhammad, MD, Roxanna S. Dronca, MD, Lisa A. Kottschade, CNP, Heidi J. Turner, BS, Nathan P. Staff, MD, PhD, Michelle L. Mauermann, MD, Jennifer A. Tracy, MD, Christopher J. Klein, MD
Publikováno v:
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, Vol 1, Iss 2, Pp 192-197 (2017)
Recently, guidelines have been outlined for management of immune-related adverse events occurring with immune checkpoint inhibitors in cancer, irrespective of affected organ systems. Increasingly, these complications have been recognized as including
Externí odkaz:
https://doaj.org/article/b370f541321d41759893f9a0cc1536f9