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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1961 1
1979 1
1983 1
1984 1
1986 1
1989 1
1993 1
1995 1
1996 1
2000 2
2003 1
2004 1
2013 3
2016 1
2019 1
2020 2
2021 4
2022 1
2023 1
2024 0

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24 results

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Page 1
Paratesticular rhabdomyosarcoma: a rare case report from Syria.
Sabbagh A, Hamza A, Sukkari MW, Fattal A, Chammout A, Ayoub K, Al-Hadid I. Sabbagh A, et al. Among authors: fattal a. Ann Med Surg (Lond). 2023 Apr 3;85(5):1928-1931. doi: 10.1097/MS9.0000000000000461. eCollection 2023 May. Ann Med Surg (Lond). 2023. PMID: 37228919 Free PMC article.
Falls in hospital: a case-control study.
de Groot GCL, Al-Fattal A, Sandven I. de Groot GCL, et al. Among authors: al fattal a. Scand J Caring Sci. 2020 Jun;34(2):332-339. doi: 10.1111/scs.12733. Epub 2019 Jul 11. Scand J Caring Sci. 2020. PMID: 31294860 Free PMC article.
A biomechanical approach to second-molar intrusion.
Uribe F, Janakiraman N, Fattal AN, Padala S, Nanda R. Uribe F, et al. Among authors: fattal an. J Clin Orthod. 2013 Oct;47(10):608-13. J Clin Orthod. 2013. PMID: 24225168 No abstract available.
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy.
Yechieli M, Gulsuner S, Ben-Pazi H, Fattal A, Aran A, Kuzminsky A, Sagi L, Guttman D, Schneebaum Sender N, Gross-Tsur V, Klopstock T, Walsh T, Renbaum P, Zeligson S, Shemer Meiri L, Lev D, Shmueli D, Blumkin L, Lahad A, King MC, Levy EL, Segel R. Yechieli M, et al. Among authors: fattal a. J Med Genet. 2022 Aug;59(8):759-767. doi: 10.1136/jmedgenet-2021-107884. Epub 2021 Jul 28. J Med Genet. 2022. PMID: 34321325
De novo mutations in the X-linked TFE3 gene cause intellectual disability with pigmentary mosaicism and storage disorder-like features.
Lehalle D, Vabres P, Sorlin A, Bierhals T, Avila M, Carmignac V, Chevarin M, Torti E, Abe Y, Bartolomaeus T, Clayton-Smith J, Cogné B, Cusco I, Duplomb L, De Bont E, Duffourd Y, Duijkers F, Elpeleg O, Fattal A, Geneviève D, Guillen Sacoto MJ, Guimier A, Harris DJ, Hempel M, Isidor B, Jouan T, Kuentz P, Koshimizu E, Lichtenbelt K, Loik Ramey V, Maik M, Miyakate S, Murakami Y, Pasquier L, Pedro H, Simone L, Sondergaard-Schatz K, St-Onge J, Thevenon J, Valenzuela I, Abou Jamra R, van Gassen K, van Haelst MM, van Koningsbruggen S, Verdura E, Whelan Habela C, Zacher P, Rivière JB, Thauvin-Robinet C, Betschinger J, Faivre L. Lehalle D, et al. Among authors: fattal a. J Med Genet. 2020 Dec;57(12):808-819. doi: 10.1136/jmedgenet-2019-106508. Epub 2020 May 14. J Med Genet. 2020. PMID: 32409512
[New tool to detect delirium and cognitive impairment].
Evensen S, Forr T, Al-Fattal A, de Groot C, Lønne G, Gjevjon ER, Berg GV, Bergh S. Evensen S, et al. Among authors: al fattal a. Tidsskr Nor Laegeforen. 2016 Feb 23;136(4):299-300. doi: 10.4045/tidsskr.15.1334. eCollection 2016 Feb 23. Tidsskr Nor Laegeforen. 2016. PMID: 26905842 Free article. Norwegian. No abstract available.
24 results