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Phenotype expression in familial combined hyperlipidemia.
Atherosclerosis. 1997 Sep;133(2):245-53. doi: 10.1016/s0021-9150(97)00134-2.
Atherosclerosis. 1997.
PMID: 9298685
No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families.
Pajukanta P, Porkka KV, Antikainen M, Taskinen MR, Perola M, Murtomäki-Repo S, Ehnholm S, Nuotio I, Suurinkeroinen L, Lahdenkari AT, Syvänen AC, Viikari JS, Ehnholm C, Peltonen L.
Pajukanta P, et al. Among authors: lahdenkari at.
Arterioscler Thromb Vasc Biol. 1997 May;17(5):841-50. doi: 10.1161/01.atv.17.5.841.
Arterioscler Thromb Vasc Biol. 1997.
PMID: 9157946
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Tissue expression of nephrin in human and pig.
Kuusniemi AM, Kestilä M, Patrakka J, Lahdenkari AT, Ruotsalainen V, Holmberg C, Karikoski R, Salonen R, Tryggvason K, Jalanko H.
Kuusniemi AM, et al. Among authors: lahdenkari at.
Pediatr Res. 2004 May;55(5):774-81. doi: 10.1203/01.PDR.0000117842.10241.2C. Epub 2004 Feb 5.
Pediatr Res. 2004.
PMID: 14764915
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Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).
Lahdenkari AT, Kestilä M, Holmberg C, Koskimies O, Jalanko H.
Lahdenkari AT, et al.
Kidney Int. 2004 May;65(5):1856-63. doi: 10.1111/j.1523-1755.2004.00583.x.
Kidney Int. 2004.
PMID: 15086927
Free article.
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Podocytes are firmly attached to glomerular basement membrane in kidneys with heavy proteinuria.
Lahdenkari AT, Lounatmaa K, Patrakka J, Holmberg C, Wartiovaara J, Kestilä M, Koskimies O, Jalanko H.
Lahdenkari AT, et al.
J Am Soc Nephrol. 2004 Oct;15(10):2611-8. doi: 10.1097/01.ASN.0000139478.03463.D9.
J Am Soc Nephrol. 2004.
PMID: 15466265
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Clinical features and outcome of childhood minimal change nephrotic syndrome: is genetics involved?
Lahdenkari AT, Suvanto M, Kajantie E, Koskimies O, Kestilä M, Jalanko H.
Lahdenkari AT, et al.
Pediatr Nephrol. 2005 Aug;20(8):1073-80. doi: 10.1007/s00467-005-1965-y. Epub 2005 Jun 21.
Pediatr Nephrol. 2005.
PMID: 15968559
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The number of podocyte slit diaphragms is decreased in minimal change nephrotic syndrome.
Patrakka J, Lahdenkari AT, Koskimies O, Holmberg C, Wartiovaara J, Jalanko H.
Patrakka J, et al. Among authors: lahdenkari at.
Pediatr Res. 2002 Sep;52(3):349-55. doi: 10.1203/00006450-200209000-00007.
Pediatr Res. 2002.
PMID: 12193666
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Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1).
Kuusniemi AM, Merenmies J, Lahdenkari AT, Holmberg C, Salmela K, Karikoski R, Rapola J, Jalanko H.
Kuusniemi AM, et al. Among authors: lahdenkari at.
Kidney Int. 2006 Oct;70(8):1423-31. doi: 10.1038/sj.ki.5001779. Epub 2006 Aug 30.
Kidney Int. 2006.
PMID: 16941028
Free article.
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