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Year | Number of Results |
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2004 | 1 |
2005 | 1 |
2021 | 2 |
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Page 1
Emergency medicine pharmacotherapy compromises accuracy of plasma creatinine determination by enzyme-based methods: real-world clinical evidence and implications for clinical practice.
Front Med (Lausanne). 2024 Jan 8;10:1236948. doi: 10.3389/fmed.2023.1236948. eCollection 2023.
Front Med (Lausanne). 2024.
PMID: 38259831
Free PMC article.
Novel mutations in TRPM6 gene associated with primary hypomagnesemia with secondary hypocalcemia. Case report.
Papez J, Starha J, Slaba K, Hubacek JA, Pecl J, Aulicka S, Urik M, Ceylaner S, Vesela P, Slaby O, Jabandziev P.
Papez J, et al. Among authors: starha j.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2021 Nov;165(4):454-457. doi: 10.5507/bp.2021.027. Epub 2021 May 18.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2021.
PMID: 34012148
Free article.
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Spindle Cell Hemangioma and Atypically Localized Juxtaglomerular Cell Tumor in a Patient with Hereditary BRIP1 Mutation: A Case Report.
Papez J, Starha J, Zerhau P, Pavlovska D, Jezova M, Jurencak T, Slaba K, Sterba M, Kerekes A, Merta T, Haluskova T, Palova H, Slaby O, Sterba J, Jabandziev P.
Papez J, et al. Among authors: starha j.
Genes (Basel). 2021 Feb 3;12(2):220. doi: 10.3390/genes12020220.
Genes (Basel). 2021.
PMID: 33546375
Free PMC article.
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Paroxysmal nocturnal hemoglobinuria in a girl with hemolysis and "hematuria".
Dolezel Z, Dostalkova D, Blatny J, Starha J, Gerykova H.
Dolezel Z, et al. Among authors: starha j.
Pediatr Nephrol. 2004 Oct;19(10):1177-9. doi: 10.1007/s00467-004-1563-4. Epub 2004 Jul 20.
Pediatr Nephrol. 2004.
PMID: 15278422
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Liddle syndrome caused by P616R mutation of the epithelial sodium channel beta subunit.
Ciechanowicz A, Dolezel Z, Placha G, Starha J, Góra J, Gaciong Z, Brodkiewicz A, Adler G.
Ciechanowicz A, et al. Among authors: starha j.
Pediatr Nephrol. 2005 Jun;20(6):837-8. doi: 10.1007/s00467-004-1793-5.
Pediatr Nephrol. 2005.
PMID: 15856328
No abstract available.
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