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Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c.
Brunkhorst M, Brunkhorst L, Martens H, Papizh S, Besouw M, Grasemann C, Turan S, Sikora P, Chromek M, Cornelissen E, Fila M, Lilien M, Allgrove J, Neuhaus TJ, Eltan M, Espinosa L, Schnabel D, Gokce I, González-Rodríguez JD, Khandelwal P, Keijzer-Veen MG, Lechner F, Szczepańska M, Zaniew M, Bacchetta J, Emma F, Haffner D. Brunkhorst M, et al. Among authors: turan s. Kidney Int. 2024 Oct 24:S0085-2538(24)00727-0. doi: 10.1016/j.kint.2024.08.035. Online ahead of print. Kidney Int. 2024. PMID: 39461557 Free article.
A global survey on the use of the international classification of diseases codes for metabolic dysfunction-associated fatty liver disease.
Zhang H, Targher G, Byrne CD, Kim SU, Wong VW, Valenti L, Glickman M, Ponce J, Mantzoros CS, Crespo J, Gronbaek H, Yang W, Eslam M, Wong RJ, Machado MV, Yu ML, Ghanem OM, Okanoue T, Liu JF, Lee YH, Xu XY, Pan Q, Sui M, Lonardo A, Yilmaz Y, Zhu LY, Moreno C, Miele L, Lupsor-Platon M, Zhao L, LaMasters TL, Gish RG, Zhang H, Nedelcu M, Chan WK, Xia MF, Bril F, Shi JP, Datz C, Romeo S, Sun J, Liu D, Sookoian S, Mao YM, Méndez-Sánchez N, Wang XY, Pyrsopoulos NT, Fan JG, Fouad Y, Sun DQ, Giannini C, Chai J, Xia ZF, Jun DW, Li GJ, Treeprasertsuk S, Li YX, Cheung TT, Zhang F, Goh GB, Furuhashi M, Seto WK, Huang H, Di Sessa A, Li QH, Cholongitas E, Zhang L, Silveira TR, Sebastiani G, Adams LA, Chen W, Qi X, Rankovic I, De Ledinghen V, Lv WJ, Hamaguchi M, Kassir R, Müller-Wieland D, Romero-Gomez M, Xu Y, Xu YC, Chen SY, Kermansaravi M, Kuchay MS, Lefere S, Parmar C, Lip GYH, Liu CJ, Åberg F, Lau G, George J, Sarin SK, Zhou JY, Zheng MH; MAFLD ICD-11 coding collaborators. Zhang H, et al. Hepatol Int. 2024 Aug;18(4):1178-1201. doi: 10.1007/s12072-024-10702-5. Epub 2024 Jun 15. Hepatol Int. 2024. PMID: 38878111
Global burden of disease attributable to metabolic risk factors in adolescents and young adults aged 15-39, 1990-2021.
Zhou XD, Chen QF, Targher G, Byrne CD, Mantzoros CS, Zhang H, Lonardo A, Lip GYH, Porta G, Misra A, Robertson AG, Luo F, Alisi A, Yang W, El-Shabrawi M, Al Momani H, Somers VK, Katsouras CS, Méndez-Sánchez N, Lefere S, Szepietowski O, Sung KC, Hui Ng NB, Valenti L, Lee WS, Pik-Shan Kong A, Kızılkaya MC, Ocama P, Ali A, Viveiros O, Ryan JD, Toro-Huamanchumo CJ, Perera N, Ataya K, Yen Kok KY, Gracia-Sancho J, Sharara AI, Prasad A, Oviedo RJ, Ospanov O, Ruiz-Úcar E, Alswat K, Abbas SI, Abdelbaki TN, Wong YJ, Fouad Y, Shapiro MD, Bacopoulou F, Sookoian S, Kehar M, Chan WK, Treeprasertsuk S, Adams L, Turan S, Zuluaga M, Pirola CJ, Thaher O, Molina GA, Jumaev NA, Al-Busafi SA, Opio CK, Lim-Loo MC, Adithya Lesmana CR, Kamani L, Zheng MH. Zhou XD, et al. Among authors: turan s. Clin Nutr. 2024 Nov 14;43(12):391-404. doi: 10.1016/j.clnu.2024.11.016. Online ahead of print. Clin Nutr. 2024. PMID: 39579593
C19orf12 gene mutation with neuropsychiatric symptoms: a case report.
Yıldırım İ, Altunç AT, Gür E, Hacikurteş G, Usta Sağlam NG, Kızıltan G, Turan Ş. Yıldırım İ, et al. Among authors: turan s. Neurocase. 2024 Nov 10:1-3. doi: 10.1080/13554794.2024.2426822. Online ahead of print. Neurocase. 2024. PMID: 39523449
Evaluation of Growth Characteristics and Final Heights of Cases Diagnosed with Noonan Syndrome on GH Treatment.
Şıklar Z, Berberoğlu M, Kızılcan Çetin S, Yıldız M, Turan S, Darcan Ş, Çetinkaya S, Hatipoğlu N, Yıldırım R, Demir K, Vermezoğlu Ö, Yavaş Abalı Z, Özalp Kızılay D, Görkem Erdoğan N, Şiraz ÜG, Orbak Z, Özgen İT, Bideci A, Selver Eklioğlu B, Karakılıç Özturan E, Tarçın G, Bereket A, Darendeliler F. Şıklar Z, et al. Among authors: turan s. J Clin Res Pediatr Endocrinol. 2024 Oct 8. doi: 10.4274/jcrpe.galenos.2024.2024-7-3. Online ahead of print. J Clin Res Pediatr Endocrinol. 2024. PMID: 39377546 Free article.
576 results