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Year Number of Results
1972 2
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163 results

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Page 1
Did you mean halabi ma[au] (14 results)?
Evaluating different pain lowering medications during intrauterine device insertion: a systematic review and network meta-analysis.
Samy A, Abbas AM, Mahmoud M, Taher A, Awad MH, El Husseiny T, Hussein M, Ramadan M, Shalaby MA, El Sharkawy M, Hatem D, Alaa-El-Din Wali A, Abd-El-Fatah SM, Hussein AH, Haggag H. Samy A, et al. Among authors: shalaby ma. Fertil Steril. 2019 Mar;111(3):553-561.e4. doi: 10.1016/j.fertnstert.2018.11.012. Epub 2019 Jan 2. Fertil Steril. 2019. PMID: 30611553 Free article.
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome.
Mansour B, Lemberg K, Schneider R, Saida K, Elmubarak I, Yu S, Yousef K, Nicolas Frank C, Riedhammer KM, Zahoor MY, Kolvenbach CM, Merz LM, Mertens ND, Bao A, Salmanullah D, Kalkar G, Hölzel S, Zion E, Marchuk D, Lomjansook K, Braun A, Franken GAC, Eid LA, Awad HSH, Al Saffar M, Soliman NA, Nabhan MM, Kari JA, El Desoky S, Shalaby MA, Ooda S, Fathy HM, Mane S, Shril S, Somers MJG, Buerger F, Hildebrandt F. Mansour B, et al. Among authors: shalaby ma. Pediatr Nephrol. 2026 Jun;41(6):1663-1675. doi: 10.1007/s00467-026-07151-7. Epub 2026 Jan 23. Pediatr Nephrol. 2026. PMID: 41575523
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.
Merz LM, Kolvenbach CM, Wang C, Mertens ND, Seltzsam S, Mansour B, Zheng B, Schneider S, Schierbaum L, Hölzel S, Salmanullah D, Pantel D, Kalkar G, Connaughton DM, Mann N, Wu CW, Kause F, Nakayama M, Dai R, Schneider R, Buerger F, Nicolas-Frank C, Yousef K, Lemberg K, Saida K, Yu S, Elmubarak I, Franken GAC, Lomjansook K, Braun A, Bauer SB, Rodig NM, Somers MJG, Traum AZ, Stein DR, Daga A, Baum MA, Daouk GH, Awad HS, Eid LA, El Desoky S, Shalaby MA, Kari JA, Ooda S, Fathy HM, Soliman NA, Nabhan M, Abdelrahman S, Hilger AC, Mane SM, Ferguson MA, Tasic V, Shril S, Hildebrandt F. Merz LM, et al. Among authors: shalaby ma. Genet Med. 2025 Jul;27(7):101432. doi: 10.1016/j.gim.2025.101432. Epub 2025 Apr 11. Genet Med. 2025. PMID: 40223730 Free PMC article.
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment.
Buerger F, Salmanullah D, Liang L, Gauntner V, Krueger K, Qi J, Normand J, Sharma V, Ranga A, Rubin A, Ball D, Hong S, Lemberg K, Saida K, Merz LM, Sever S, Issac B, Ma Q, Sun L, Billing AM, Demir F, Rinschen MM, Reusch B, Beck BB, Guerrero-Castillo S; Nephrotic Syndrome Study Network (NEPTUNE); Gomez AC, McNulty MT, Sampson MG, Al-Hamed MH, Saleh MM, Shalaby MA, Kari JA, Fawcett JP, Hildebrandt F, Majmundar AJ. Buerger F, et al. Among authors: shalaby ma. Nat Commun. 2025 Nov 27;16(1):10654. doi: 10.1038/s41467-025-65663-6. Nat Commun. 2025. PMID: 41309577 Free PMC article.
Exome Sequencing in Saudi Arabian Pediatric Kidney Disease Single-Center Cohort.
Lemberg K, Shalaby MA, Zion E, Saida K, Yousef K, Schneider R, Mertens ND, Mansour B, Kolvenbach CM, Merz LM, Riedhammer KM, Braun A, Hölzel S, Yu S, Lomjansook K, Kalkar G, Marchuk D, Elmubarak I, Franken GAC, Shril S, El Desoky S, Kari JA, Buerger F, Hildebrandt F. Lemberg K, et al. Among authors: shalaby ma. Kidney Int Rep. 2025 Jul 14;10(10):3564-3577. doi: 10.1016/j.ekir.2025.07.011. eCollection 2025 Oct. Kidney Int Rep. 2025. PMID: 41141495 Free PMC article.
Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome.
Schneider R, Shril S, Buerger F, Deutsch K, Yousef K, Frank CN, Onuchic-Whitford AC, Kitzler TM, Mao Y, Klämbt V, Zahoor MY, Lemberg K, Majmundar AJ, Mansour B, Saida K, Seltzsam S, Kolvenbach CM, Merz LM, Mertens ND, Hermle T, Mann N, Pantel D, Halawi AA, Bao A, Schierbaum L, Schneider S, Salmanullah D, Ben-Dov IZ, Sagiv I, Eid LA, Awad HSH, Al Saffar M, Soliman NA, Nabhan MM, Kari JA, El Desoky S, Shalaby MA, Ooda S, Fathy HM, Mane S, Lifton RP, Somers MJG, Hildebrandt F. Schneider R, et al. Among authors: shalaby ma. Genes Dis. 2024 Mar 28;12(2):101280. doi: 10.1016/j.gendis.2024.101280. eCollection 2025 Mar. Genes Dis. 2024. PMID: 39584075 Free PMC article. No abstract available.
Recessive CHRM5 variant as a potential cause of neurogenic bladder.
Schneider S, Schierbaum L, Burger WAC, Seltzsam S, Wang C, Zheng B, Wu CW, Nakayama M, Connaughton DM, Mann N, Shalaby MA, Kari JA, ElDesoky S, Tasic V, Eid LA, Shril S, Thal DM, Hildebrandt F. Schneider S, et al. Among authors: shalaby ma. Am J Med Genet A. 2023 Aug;191(8):2083-2091. doi: 10.1002/ajmg.a.63241. Epub 2023 May 22. Am J Med Genet A. 2023. PMID: 37213061 Free PMC article.
163 results