Starha J - Search Results

1

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.

2

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.

3

Juxtaglomerular cell tumor--a rare cause of secondary hypertension.

Dolezel Z, Starha J, Pavlovsky Z, Skotakova J, Dostalkova D. Dolezel Z, et al. Among authors: starha j. Bratisl Lek Listy. 2010;111(12):653-5. Bratisl Lek Listy. 2010. PMID: 21384734

4

[Diagnosis of acute pyelonephritis in childhood: comparison of ultrasonographic examination and renal scintigraphy using 99mTc DMSA].

Dolezel Z, Mach V, Kopecna L, Starha J, Dostalkova D. Dolezel Z, et al. Among authors: starha j. Bratisl Lek Listy. 2000;101(9):495-8. Bratisl Lek Listy. 2000. PMID: 11187052 Czech.

5

Is it possible to influence the mortality in children with hemolytic uremic syndrome?

Dolezel Z, Kopecna L, Starha J, Dostalkova D. Dolezel Z, et al. Among authors: starha j. Bratisl Lek Listy. 2001;102(2):59-65. Bratisl Lek Listy. 2001. PMID: 11396125 Czech, English.

6

Secondary pseudohypoaldosteronism in an infant with pyelonephritis.

Dolezel Z, Starha J, Novotna D, Dostalkova D. Dolezel Z, et al. Among authors: starha j. Bratisl Lek Listy. 2004;105(12):435-7. Bratisl Lek Listy. 2004. PMID: 15777077

7

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

8

The analysis of the risks for the development of tumour lysis syndrome in children.

Kopecna L, Dolezel Z, Osvaldova Z, Starha J, Hrstkova H. Kopecna L, et al. Among authors: starha j. Bratisl Lek Listy. 2002;103(6):206-9. Bratisl Lek Listy. 2002. PMID: 12448566

9

The rare cause of hypokalaemia.

Dolezel Z, Kopecna L, Starha J. Dolezel Z, et al. Among authors: starha j. Nephrol Dial Transplant. 2000 Sep;15(9):1475-6. doi: 10.1093/ndt/15.9.1475. Nephrol Dial Transplant. 2000. PMID: 10978416 No abstract available.

10

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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