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

Year Number of Results
2002 3
2003 3
2004 1
2005 4
2006 7
2007 1
2008 3
2009 8
2010 5
2012 3
2013 3
2014 8
2015 5
2016 5
2017 9
2018 4
2019 4
2020 6
2021 4
2022 8
2023 8
2024 5

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91 results

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Page 1
Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
Canda E, Kalkan Uçar S, Çoker M. Canda E, et al. Among authors: coker m. Pediatric Health Med Ther. 2020 May 4;11:127-133. doi: 10.2147/PHMT.S198656. eCollection 2020. Pediatric Health Med Ther. 2020. PMID: 32440248 Free PMC article. Review.
Recommendations on phenylketonuria in Turkey.
Coşkun T, Çoker M, Mungan NÖ, Özel HG, Sivri HS. Coşkun T, et al. Among authors: coker m. Turk J Pediatr. 2022;64(3):413-434. doi: 10.24953/turkjped.2021.4098. Turk J Pediatr. 2022. PMID: 35899555 Free article.
Tetrahydrobiopterin deficiencies: Lesson from clinical experience.
Bozaci AE, Er E, Yazici H, Canda E, Kalkan Uçar S, Güvenc Saka M, Eraslan C, Onay H, Habif S, Thöny B, Coker M. Bozaci AE, et al. Among authors: coker m. JIMD Rep. 2021 Feb 1;59(1):42-51. doi: 10.1002/jmd2.12199. eCollection 2021 May. JIMD Rep. 2021. PMID: 33977029 Free PMC article.
Unique clinical presentations and follow-up outcomes from experience with congenital disorders of glycosylation: PMM2-PGM1-DPAGT1-MPI-POMT2-B3GALNT2-DPM1-SRD5A3-CDG.
Yoldas Celik M, Yazici H, Erdem F, Yuksel Yanbolu A, Aykut A, Durmaz A, Zeybek S, Canda E, Kalkan Ucar S, Coker M. Yoldas Celik M, et al. Among authors: coker m. J Pediatr Endocrinol Metab. 2023 Apr 13;36(6):530-538. doi: 10.1515/jpem-2022-0641. Print 2023 Jun 27. J Pediatr Endocrinol Metab. 2023. PMID: 37042760
Long-term follow-up of alkaptonuria patients: single center experience.
Bozaci AE, Yazici H, Canda E, Uçar SK, Guvenc MS, Berdeli A, Habif S, Coker M. Bozaci AE, et al. Among authors: coker m. J Pediatr Endocrinol Metab. 2022 Jun 6;35(7):913-923. doi: 10.1515/jpem-2022-0004. Print 2022 Jul 26. J Pediatr Endocrinol Metab. 2022. PMID: 35671204
An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study.
Steenweg ME, Jakobs C, Errami A, van Dooren SJ, Adeva Bartolomé MT, Aerssens P, Augoustides-Savvapoulou P, Baric I, Baumann M, Bonafé L, Chabrol B, Clarke JT, Clayton P, Coker M, Cooper S, Falik-Zaccai T, Gorman M, Hahn A, Hasanoglu A, King MD, de Klerk HB, Korman SH, Lee C, Meldgaard Lund A, Mejaski-Bosnjak V, Pascual-Castroviejo I, Raadhyaksha A, Rootwelt T, Roubertie A, Ruiz-Falco ML, Scalais E, Schimmel U, Seijo-Martinez M, Suri M, Sykut-Cegielska J, Trefz FK, Uziel G, Valayannopoulos V, Vianey-Saban C, Vlaho S, Vodopiutz J, Wajner M, Walter J, Walter-Derbort C, Yapici Z, Zafeiriou DI, Spreeuwenberg MD, Celli J, den Dunnen JT, van der Knaap MS, Salomons GS. Steenweg ME, et al. Among authors: coker m. Hum Mutat. 2010 Apr;31(4):380-90. doi: 10.1002/humu.21197. Hum Mutat. 2010. PMID: 20052767 Review.
Severe perinatal hypophosphatasia case with a novel mutation.
Yazici H, Canda E, Kalkan Ucar S, Coker M. Yazici H, et al. Among authors: coker m. Arch Argent Pediatr. 2022 Feb;120(1):e21-e24. doi: 10.5546/aap.2022.eng.e21. Epub 2022 Jan 1. Arch Argent Pediatr. 2022. PMID: 35068125 Free article. English, Spanish.
91 results