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A B7-H3-Targeted CD28 Bispecific Antibody Enhances the Activity of Anti-PD-1 and CD3 T-cell Engager Immunotherapies.
Moore GL, Zeng VG, Diaz JE, Bonzon C, Avery KN, Rashid R, Qi J, Nam DH, Jacinto J, Dragovich MA, Kim YK, Balcazar KP, Bakhit CG, Eivazi A, Nguyen H, Muchhal US, Szymkowski DE, Desjarlais JR, Hedvat M. Moore GL, et al. Mol Cancer Ther. 2025 Mar 4;24(3):331-344. doi: 10.1158/1535-7163.MCT-24-0327. Mol Cancer Ther. 2025. PMID: 39301613 Free PMC article.
Abstracts of the Australasian Association for Academic Primary Care (AAAPC) Annual Research Conference.
[No authors listed] [No authors listed] Aust J Prim Health. 2024 Aug 15;30(4):PYv30n4abs. doi: 10.1071/PYv30n4abs. Aust J Prim Health. 2024. PMID: 41122907 Free article.
Australian Journal of Primary Health30, PYv30n4abs. doi:10.1071/PYv30n4abs To cite individual abstracts use the following format: Bakhit M et al. (2024) 3. Cardiovascular disease risk communication and prevention: a meta-analysis [Conference abstract]. ...
Australian Journal of Primary Health30, PYv30n4abs. doi:10.1071/PYv30n4abs To cite individual abstracts use the following format: Bakhit
Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment.
Kaheel H, Breß A, Hassan MA, Shah AA, Amin M, Bakhit YHY, Kniper M. Kaheel H, et al. BMC Ear Nose Throat Disord. 2018 May 21;18:7. doi: 10.1186/s12901-018-0055-2. eCollection 2018. BMC Ear Nose Throat Disord. 2018. PMID: 29942192 Free PMC article.
METHODS: We carried out PCR, restriction enzyme based screening, and sequencing of 337 subjects (including 132 patients diagnosed clinically with hereditary deafness) from 54 families from Syria for m.1555A > G mitochondrial mutation. RESULTS: Mitochondrial m.155 …
METHODS: We carried out PCR, restriction enzyme based screening, and sequencing of 337 subjects (including 132 patients diagnosed clinically …
Hybrid Closed-Loop Therapy in Adults With Type 1 Diabetes and Above-Target HbA1c: A Real-world Observational Study.
Crabtree TSJ, Griffin TP, Yap YW, Narendran P, Gallen G, Furlong N, Cranston I, Chakera A, Philbey C, Karamat MA, Saraf S, Kamaruddin S, Gurnell E, Chapman A, Hussain S, Elliott J, Leelarathna L, Ryder REJ, Hammond P, Lumb A, Choudhary P, Wilmot EG; ABCD Closed-Loop Audit Contributors. Crabtree TSJ, et al. Diabetes Care. 2023 Oct 1;46(10):1831-1838. doi: 10.2337/dc23-0635. Diabetes Care. 2023. PMID: 37566697 Free PMC article.
A Ruptured Spetzler and Martin Grade V Arteriovenous Malformation in a Child Treated With Radiotherapy Followed by Embolization: A Case Report and Literature Review.
Iwatate K, Kikuchi Y, Sato S, Bakhit M, Hyodo A. Iwatate K, et al. Cureus. 2021 Jul 24;13(7):e16605. doi: 10.7759/cureus.16605. eCollection 2021 Jul. Cureus. 2021. PMID: 34430185 Free PMC article.
Treatment of ruptured high-grade Spetzler-Martin (S&M) arteriovenous malformation (AVM) is challenging and requires a multidisciplinary treatment approach. ...
Treatment of ruptured high-grade Spetzler-Martin (S&M) arteriovenous malformation (AVM) is challenging and requires a multidiscip …
Clinical Characteristics and Renal Outcomes in Patients with IgM Nephropathy: A Retrospective Single-Center Study.
Albakr RB, Sandokji IA, Asfina KN, Bakhit A, Alnaeim N, Albacker AB, Husain S. Albakr RB, et al. Int J Gen Med. 2025 Aug 29;18:4923-4939. doi: 10.2147/IJGM.S541794. eCollection 2025. Int J Gen Med. 2025. PMID: 40909909 Free PMC article.
BACKGROUND: Defining immunoglobulin M (IgM) nephropathy as a discrete clinical disorder remains controversial, with limited documentation in Saudi Arabian patients. ...
BACKGROUND: Defining immunoglobulin M (IgM) nephropathy as a discrete clinical disorder remains controversial, with limited documenta …