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

Year Number of Results
1996 3
1997 6
1998 2
1999 2
2001 1
2002 4
2003 2
2004 1
2005 1
2007 7
2008 4
2009 4
2010 6
2011 6
2012 6
2013 6
2014 8
2015 8
2016 4
2017 5
2018 4
2019 4
2020 6
2021 5
2022 3
2023 5
2024 1

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103 results

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Page 1
Clinical implications of the glucokinase impaired function - GCK MODY today.
Hulín J, Škopková M, Valkovičová T, Mikulajová S, Rosoľanková M, Papcun P, Gašperíková D, Staník J. Hulín J, et al. Among authors: gasperikova d. Physiol Res. 2020 Dec 22;69(6):995-1011. doi: 10.33549/physiolres.934487. Epub 2020 Nov 2. Physiol Res. 2020. PMID: 33129248 Free PMC article. Review.
Molecular-genetic aspects of familial hypercholesterolemia.
Gabcova-Balaziova D, Stanikova D, Vohnout B, Huckova M, Stanik J, Klimes I, Raslova K, Gasperikova D. Gabcova-Balaziova D, et al. Among authors: gasperikova d. Endocr Regul. 2015 Jul;49(3):164-81. doi: 10.4149/endo_2015_03_164. Endocr Regul. 2015. PMID: 26238499 Review.
Novel insights into genetics and clinics of the HNF1A-MODY.
Valkovicova T, Skopkova M, Stanik J, Gasperikova D. Valkovicova T, et al. Among authors: gasperikova d. Endocr Regul. 2019 Apr 1;53(2):110-134. doi: 10.2478/enr-2019-0013. Endocr Regul. 2019. PMID: 31517624 Free article. Review.
Variants influencing age at diagnosis of HNF1A-MODY.
Ludwig-Słomczyńska AH, Seweryn MT, Radkowski P, Kapusta P, Machlowska J, Pruhova S, Gasperikova D, Bellanne-Chantelot C, Hattersley A, Kandasamy B, Letourneau-Freiberg L, Philipson L, Doria A, Wołkow PP, Małecki MT, Klupa T. Ludwig-Słomczyńska AH, et al. Among authors: gasperikova d. Mol Med. 2022 Sep 14;28(1):113. doi: 10.1186/s10020-022-00542-0. Mol Med. 2022. PMID: 36104811 Free PMC article.
Mitochondria and mitochondrial disorders: an overview update.
Rambani V, Hromnikova D, Gasperikova D, Skopkova M. Rambani V, et al. Among authors: gasperikova d. Endocr Regul. 2022 Jul 13;56(3):232-248. doi: 10.2478/enr-2022-0025. Endocr Regul. 2022. PMID: 35843711 Free article.
Hereditary bilateral sudden sensorineural hearing loss.
Varga L, Jovankovicova A, Huckova M, Demesova L, Gasperikova D, Sebova I, Profant M. Varga L, et al. Among authors: gasperikova d. Bratisl Lek Listy. 2019;120(9):699-702. doi: 10.4149/BLL_2019_118. Bratisl Lek Listy. 2019. PMID: 31475558
103 results