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Year | Number of Results |
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2022 | 2 |
2023 | 1 |
2024 | 1 |
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Page 1
Cardiorenal Syndrome: Challenges in Everyday Clinical Practice and Key Points towards a Better Management.
J Clin Med. 2023 Jun 18;12(12):4121. doi: 10.3390/jcm12124121.
J Clin Med. 2023.
PMID: 37373813
Free PMC article.
Review.
The p.Pro482Ala Variant in the CNNM2 Gene Causes Severe Hypomagnesemia Amenable to Treatment with Spironolactone.
Petrakis I, Drosataki E, Stavrakaki I, Dermitzaki K, Lygerou D, Konidaki M, Pleros C, Kroustalakis N, Maragkou S, Androvitsanea A, Stylianou I, Zaganas I, Stylianou K.
Petrakis I, et al. Among authors: dermitzaki k.
Int J Mol Sci. 2022 Jun 30;23(13):7284. doi: 10.3390/ijms23137284.
Int J Mol Sci. 2022.
PMID: 35806288
Free PMC article.
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Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene.
Drosataki E, Maragkou S, Dermitzaki K, Stavrakaki I, Lygerou D, Latsoudis H, Pleros C, Petrakis I, Zaganas I, Stylianou K.
Drosataki E, et al. Among authors: dermitzaki k.
BMC Nephrol. 2022 May 12;23(1):182. doi: 10.1186/s12882-022-02812-9.
BMC Nephrol. 2022.
PMID: 35549682
Free PMC article.
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The Phenotypic Variability Associated with Hepatocyte Nuclear Factor 1B Genetic Defects Poses Challenges in Both Diagnosis and Therapy.
Petrakis I, Sfakiotaki M, Bitsori M, Drosataki E, Dermitzaki K, Pleros C, Androvitsanea A, Samonakis D, Sertedaki A, Xekouki P, Galanakis E, Stylianou K.
Petrakis I, et al. Among authors: dermitzaki k.
Int J Mol Sci. 2024 Apr 22;25(8):4552. doi: 10.3390/ijms25084552.
Int J Mol Sci. 2024.
PMID: 38674137
Free PMC article.
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