Iino Y - Search Results

1

Hypercholesterolemia associated with splice-junction variation of inter-alpha-trypsin inhibitor heavy chain 4 (ITIH4) gene.

Fujita Y, Ezura Y, Emi M, Sato K, Takada D, Iino Y, Katayama Y, Takahashi K, Kamimura K, Bujo H, Saito Y. Fujita Y, et al. Among authors: iino y. J Hum Genet. 2004;49(1):24-28. doi: 10.1007/s10038-003-0101-8. Epub 2003 Dec 6. J Hum Genet. 2004. PMID: 14661079

2

Hypertriglyceridemia associated with amino acid variation Asn985Tyr of the RP1 gene.

Fujita Y, Ezura Y, Emi M, Ono S, Takada D, Takahashi K, Uemura K, Iino Y, Katayama Y, Bujo H, Saito Y. Fujita Y, et al. Among authors: iino y. J Hum Genet. 2003;48(6):305-308. doi: 10.1007/s10038-003-0029-z. Epub 2003 May 23. J Hum Genet. 2003. PMID: 12764676

3

Growth hormone receptor variant (L526I) modifies plasma HDL cholesterol phenotype in familial hypercholesterolemia: intra-familial association study in an eight-generation hyperlipidemic kindred.

Takada D, Ezura Y, Ono S, Iino Y, Katayama Y, Xin Y, Wu LL, Larringa-Shum S, Stephenson SH, Hunt SC, Hopkins PN, Emi M. Takada D, et al. Among authors: iino y. Am J Med Genet A. 2003 Aug 30;121A(2):136-40. doi: 10.1002/ajmg.a.20172. Am J Med Genet A. 2003. PMID: 12910492

4

Association of nucleotide variations in the apolipoprotein B48 receptor gene (APOB48R) with hypercholesterolemia.

Fujita Y, Ezura Y, Bujo H, Nakajima T, Takahashi K, Kamimura K, Iino Y, Katayama Y, Saito Y, Emi M. Fujita Y, et al. Among authors: iino y. J Hum Genet. 2005;50(4):203-209. doi: 10.1007/s10038-005-0240-1. Epub 2005 Apr 14. J Hum Genet. 2005. PMID: 15830122

5

Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred.

Takada D, Emi M, Ezura Y, Nobe Y, Kawamura K, Iino Y, Katayama Y, Xin Y, Wu LL, Larringa-Shum S, Stephenson SH, Hunt SC, Hopkins PN. Takada D, et al. Among authors: iino y. J Hum Genet. 2002;47(12):656-64. doi: 10.1007/s100380200101. J Hum Genet. 2002. PMID: 12522687

6

Apolipoprotein H variant modifies plasma triglyceride phenotype in familial hypercholesterolemia: a molecular study in an eight-generation hyperlipidemic family.

Takada D, Ezura Y, Ono S, Iino Y, Katayama Y, Xin Y, Wu LL, Larringa-Shum S, Stephenson SH, Hunt SC, Hopkins PN, Emi M. Takada D, et al. Among authors: iino y. J Atheroscler Thromb. 2003;10(2):79-84. doi: 10.5551/jat.10.79. J Atheroscler Thromb. 2003. PMID: 12740481 Free article.

7

Genetic association of low-density lipoprotein receptor-related protein 2 (LRP2) with plasma lipid levels.

Mii A, Nakajima T, Fujita Y, Iino Y, Kamimura K, Bujo H, Saito Y, Emi M, Katayama Y. Mii A, et al. Among authors: iino y. J Atheroscler Thromb. 2007 Dec;14(6):310-6. doi: 10.5551/jat.e494. Epub 2007 Dec 17. J Atheroscler Thromb. 2007. PMID: 18174661 Free article.

8

Membranous nephropathy complicated by renal cell carcinoma.

Fujita Y, Kashiwagi T, Takei H, Takada D, Kitamura H, Iino Y, Katayama Y. Fujita Y, et al. Among authors: iino y. Clin Exp Nephrol. 2004 Mar;8(1):59-62. doi: 10.1007/s10157-003-0261-z. Clin Exp Nephrol. 2004. PMID: 15067518 Review.

9

Severe thiamine deficiency resulted in Wernicke's encephalopathy in a chronic dialysis patient.

Ueda K, Takada D, Mii A, Tsuzuku Y, Saito SK, Kaneko T, Utsumi K, Iino Y, Katayama Y. Ueda K, et al. Among authors: iino y. Clin Exp Nephrol. 2006 Dec;10(4):290-3. doi: 10.1007/s10157-006-0440-9. Epub 2006 Dec 20. Clin Exp Nephrol. 2006. PMID: 17186335

10

Acute posterior leukoencephalopathy in a patient with nephrotic syndrome.

Utsumi K, Amemiya S, Iizuka M, Iino Y, Katayama Y. Utsumi K, et al. Among authors: iino y. Clin Exp Nephrol. 2003 Mar;7(1):63-6. doi: 10.1007/s101570300009. Clin Exp Nephrol. 2003. PMID: 14586746

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