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

Year Number of Results
1997 2
1998 2
1999 2
2000 5
2001 5
2002 9
2003 8
2004 4
2005 14
2006 6
2007 6
2008 6
2009 8
2010 6
2011 5
2012 6
2013 11
2014 6
2015 7
2016 6
2017 4
2018 4
2019 4
2020 7
2021 12
2022 5
2023 2
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Search Results

140 results
Results by year
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Page 1
Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy.
Wong HH, Seet SH, Maier M, Gurel A, Traspas RM, Lee C, Zhang S, Talim B, Loh AYT, Chia CY, Teoh TS, Sng D, Rensvold J, Unal S, Shishkova E, Cepni E, Nathan FM, Sirota FL, Liang C, Yarali N, Simsek-Kiper PO, Mitani T, Ceylaner S, Arman-Bilir O, Mbarek H, Gumruk F, Efthymiou S, Uğurlu Çi Men D, Georgiadou D, Sotiropoulou K, Houlden H, Paul F, Pehlivan D, Lainé C, Chai G, Ali NA, Choo SC, Keng SS, Boisson B, Yılmaz E, Xue S, Coon JJ, Ly TTN, Gilani N, Hasbini D, Kayserili H, Zaki MS, Isfort RJ, Ordonez N, Tripolszki K, Bauer P, Rezaei N, Seyedpour S, Khotaei GT, Bascom CC, Maroofian R, Chaabouni M, Alsubhi A, Eyaid W, Işıkay S, Gleeson JG, Lupski JR, Casanova JL, Pagliarini DJ, Akarsu NA, Maurer-Stroh S, Cetinkaya A, Bertoli-Avella A, Mathuru AS, Ho L, Bard FA, Reversade B. Wong HH, et al. Among authors: talim b. Am J Hum Genet. 2021 Jul 1;108(7):1301-1317. doi: 10.1016/j.ajhg.2021.05.003. Epub 2021 May 25. Am J Hum Genet. 2021. PMID: 34038740 Free PMC article.
Prenatal Diagnosis of Merosin-Deficient Muscular Dystrophy.
Fadiloglu E, Ozten G, Unal C, Talim B, Topaloglu H, Beksac MS. Fadiloglu E, et al. Among authors: talim b. Fetal Pediatr Pathol. 2018 Dec;37(6):418-423. doi: 10.1080/15513815.2018.1520944. Epub 2018 Oct 25. Fetal Pediatr Pathol. 2018. PMID: 30358464
Lissencephaly type II.
Topaloğlu H, Talim B. Topaloğlu H, et al. Among authors: talim b. Handb Clin Neurol. 2008;87:219-34. doi: 10.1016/S0072-9752(07)87014-X. Handb Clin Neurol. 2008. PMID: 18809028 No abstract available.
Milk of calcium: A rare manifestation of juvenile dermatomyositis.
Yildirim DG, Akdulum İ, Talim B, Demir E, Buyan N, Bakkaloğlu SA. Yildirim DG, et al. Among authors: talim b. Arch Rheumatol. 2020 Dec 10;36(2):302-304. doi: 10.46497/ArchRheumatol.2021.8197. eCollection 2021 Jun. Arch Rheumatol. 2020. PMID: 34527937 Free PMC article. No abstract available.
Calpain-3 mutations in Turkey.
Balci B, Aurino S, Haliloglu G, Talim B, Erdem S, Akcören Z, Tan E, Caglar M, Richard I, Nigro V, Topaloglu H, Dincer P. Balci B, et al. Among authors: talim b. Eur J Pediatr. 2006 May;165(5):293-8. doi: 10.1007/s00431-005-0046-3. Epub 2006 Jan 13. Eur J Pediatr. 2006. PMID: 16411092
A Rare Pediatric Case of Severe Rhabdomyolysis Owing to Dual Infection.
Akıncı Göktaş Ö, Bektaş Ö, Öz Tunçer G, Birsin Özçakar Z, Talim B, Tuba Eminoğlu F, Teber S. Akıncı Göktaş Ö, et al. Among authors: talim b. Klin Padiatr. 2022 Mar;234(2):119-122. doi: 10.1055/a-1486-7186. Epub 2021 Jul 16. Klin Padiatr. 2022. PMID: 35255503 English.
Inflammatory milieu of muscle biopsies in juvenile dermatomyositis.
Sag E, Kale G, Haliloglu G, Bilginer Y, Akcoren Z, Orhan D, Gucer S, Topaloglu H, Ozen S, Talim B. Sag E, et al. Among authors: talim b. Rheumatol Int. 2021 Jan;41(1):77-85. doi: 10.1007/s00296-020-04735-w. Epub 2020 Oct 26. Rheumatol Int. 2021. PMID: 33106894
140 results