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Combined immunotherapy with controlled interleukin-12 gene therapy and immune checkpoint blockade in recurrent glioblastoma: An open-label, multi-institutional phase I trial.
Chiocca EA, Gelb AB, Chen CC, Rao G, Reardon DA, Wen PY, Bi WL, Peruzzi P, Amidei C, Triggs D, Seften L, Park G, Grant J, Truman K, Buck JY, Hadar N, Demars N, Miao J, Estupinan T, Loewy J, Chadha K, Tringali J, Cooper L, Lukas RV. Chiocca EA, et al. Among authors: hadar n. Neuro Oncol. 2022 Jun 1;24(6):951-963. doi: 10.1093/neuonc/noab271. Neuro Oncol. 2022. PMID: 34850166 Free PMC article. Clinical Trial.
A ciliopathy combining Joubert syndrome and Oro-Facial-Digital syndrome caused by bi-allelic 5'-UTR loss-of-function CEP83 variant.
Jean MM, Yunis A, Elbaz-Biton T, Dolgin V, Narkis G, Michaelovsky A, Eskin-Schwartz M, Tsitrina AA, Agam N, Poleg T, Safran A, Freund O, Hadar N, Levy D, Shelef I, El Amour K, Flusser H, Birk OS. Jean MM, et al. Among authors: hadar n. NPJ Genom Med. 2025 Oct 10;10(1):66. doi: 10.1038/s41525-025-00514-3. NPJ Genom Med. 2025. PMID: 41073425 Free PMC article.
Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula Ancestry.
Agam N, Wormser O, Biller A, Hadar N, Dolgin V, Freund O, Jean MM, Safran A, Poleg T, Kanengisser-Pines B, Kebesch-Assi R, Mazor-Oring M, Cohen-Zontag O, Zmudjak-Olevson M, Ben-Menachem S, Ben-Ruby D, Shlomovitz O, Vivante A, Dekel B, Birk OS, Schreiber R. Agam N, et al. Among authors: hadar n. Am J Kidney Dis. 2025 Dec;86(6):730-739.e1. doi: 10.1053/j.ajkd.2025.06.011. Epub 2025 Aug 13. Am J Kidney Dis. 2025. PMID: 40816622
Early-Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1B.
Poleg T, Hadar N, Kristal E, Roberts NY, Dolgin V, Aminov I, Safran A, Agam N, Jean M, Freund O, Sheridan EG, Poulter JA, Thompson ML, Algoos Y, Al-Qahtani S, AlAbdi L, Maddirevula S, Hartill V, Houlden H, Maroofian R, Nahum A, Birk OS. Poleg T, et al. Among authors: hadar n. Mov Disord. 2025 Sep;40(9):1874-1882. doi: 10.1002/mds.30249. Epub 2025 Jun 10. Mov Disord. 2025. PMID: 40492975 Free PMC article.
Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney Failure.
Chowers G, Ben-Ruby D, Atias-Varon D, Shlomovitz O, Slabodnik-Kaner K, Kagan M, Avayou S, Romanjuk E, Rogachev B, Haviv YS, Birk OS, Hadar N, Bathish Y, Barshack I, Volkov A, Avivi C, Pavlovsky A, Haskin O, Simon AJ, Glick-Saar E, Ostrovsky A, Assi M, Schreiber R, Levin D, Yagil Y, Awawdeh M, Skorecki K, Dominissini D, Shnaider A, Vivante A. Chowers G, et al. Among authors: hadar n. Kidney Int Rep. 2025 Jan 20;10(4):1274-1278. doi: 10.1016/j.ekir.2025.01.019. eCollection 2025 Apr. Kidney Int Rep. 2025. PMID: 40303201 Free PMC article. No abstract available.
52 results