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Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.
Clin Genet. 2017 Nov;92(5):517-527. doi: 10.1111/cge.13077. Epub 2017 Sep 25.
Clin Genet. 2017.
PMID: 28632965
The Alport nephropathy: clinicopathological correlations.
White RH, Raafat F, Milford DV, Komianou F, Moghal NE.
White RH, et al. Among authors: komianou f.
Pediatr Nephrol. 2005 Jul;20(7):897-903. doi: 10.1007/s00467-005-1955-0. Epub 2005 Apr 26.
Pediatr Nephrol. 2005.
PMID: 15856312
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A novel point mutation in the DNA-binding domain (DBD) of the human glucocorticoid receptor causes primary generalized glucocorticoid resistance by disrupting the hydrophobic structure of its DBD.
Roberts ML, Kino T, Nicolaides NC, Hurt DE, Katsantoni E, Sertedaki A, Komianou F, Kassiou K, Chrousos GP, Charmandari E.
Roberts ML, et al. Among authors: komianou f.
J Clin Endocrinol Metab. 2013 Apr;98(4):E790-5. doi: 10.1210/jc.2012-3549. Epub 2013 Feb 20.
J Clin Endocrinol Metab. 2013.
PMID: 23426617
Free PMC article.
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Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms' tumor 1 (WT1) gene.
Megremis S, Mitsioni A, Fylaktou I, Tzeli SK, Komianou F, Stefanidis CJ, Kanavakis E, Traeger-Synodinos J.
Megremis S, et al. Among authors: komianou f.
Eur J Pediatr. 2011 Dec;170(12):1529-34. doi: 10.1007/s00431-011-1450-5. Epub 2011 Apr 16.
Eur J Pediatr. 2011.
PMID: 21499692
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A new SLC12A3 founder mutation (p.Val647Met) in Gitelman's syndrome patients of Roma ancestry.
Gil-Peña H, Coto E, Santos F, Espino M, Cea Crespo JM, Chantzopoulos G, Komianou F, Gómez J, Alonso B, Iglesias S, Treard C, Vargas-Poussou R; Renaltube Group.
Gil-Peña H, et al. Among authors: komianou f.
Nefrologia. 2017 Jul-Aug;37(4):423-428. doi: 10.1016/j.nefro.2017.01.007. Epub 2017 Mar 18.
Nefrologia. 2017.
PMID: 28325561
Free article.
English, Spanish.
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Psychomotor development in congenital hypothyroidism. The Greek screening programme.
Komianou F, Makaronis G, Lambadaridis J, Sarafidou E, Vrachni F, Mengreli C, Pantelakis S.
Komianou F, et al.
Eur J Pediatr. 1988 Apr;147(3):275-8. doi: 10.1007/BF00442694.
Eur J Pediatr. 1988.
PMID: 3391222
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Human gene mutations. Gene symbol: SLC3A1. Disease: cystinuria.
Dedoussis G, Louzou E, Michelekakis H, Komianou F, di Perna M, Bisceglia L.
Dedoussis G, et al. Among authors: komianou f.
Hum Genet. 2007 Sep;122(2):215.
Hum Genet. 2007.
PMID: 18386384
No abstract available.
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Human gene mutations. Gene symbol: SLC7A9. Disease: cystinuria.
Louizou E, Michelakakis H, Komianou F, Di Perna M, Bisceglia L, Dedoussis G.
Louizou E, et al. Among authors: komianou f.
Hum Genet. 2007 Sep;122(2):214.
Hum Genet. 2007.
PMID: 18386380
No abstract available.
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