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Journal Abstract Search

278 related items for PubMed ID: 17468528

  • 1. Nephrotic syndrome with X-linked ichthyosis, Kallmann Syndrome and unilateral renal agenesis.
    Krishnamurthy S, Kapoor S, Yadav S.
    Indian Pediatr; 2007 Apr; 44(4):301-3. PubMed ID: 17468528
    [Abstract] [Full Text] [Related]

  • 2. Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency-x-linked recessive ichthyosis: a case report and review of literature.
    Mishra K, Batra VV, Basu S, Rath B, Saxena R.
    Eur J Pediatr; 2012 May; 171(5):847-50. PubMed ID: 22419362
    [Abstract] [Full Text] [Related]

  • 3. The detection of steroid sulfatase gene deletion (STS) in Egyptian males with X-linked ichthyosis.
    Abdel-Hamed MF, Hussein HA, Helmy NA, Elsaie ML.
    J Drugs Dermatol; 2010 Oct; 9(10):1192-6. PubMed ID: 20941942
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  • 4. End-stage renal failure in a child with X-linked ichthyosis.
    Matsukura H, Fuchizawa T, Ohtsuki A, Higashiyama H, Higuchi O, Higuchi A, Miyawaki T.
    Pediatr Nephrol; 2003 Mar; 18(3):297-300. PubMed ID: 12644929
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  • 5. [Investigation of steroid sulfatase gene in two pedigrees with X-linked ichthyosis].
    Liu A, Xiao SX, Tan SS, Jiao T, Liu Y, Li XL, Zhou SN.
    Di Yi Jun Yi Da Xue Xue Bao; 2005 Aug; 25(8):1023-5. PubMed ID: 16109567
    [Abstract] [Full Text] [Related]

  • 6. Atypical X-linked ichthyosis in a patient with a large deletion involving the steroid sulfatase (STS) gene.
    Gonzalez-Huerta L, Mendiola-Jimenez J, Del Moral-Stevenel M, Rivera-Vega M, Cuevas-Covarrubias S.
    Int J Dermatol; 2009 Feb; 48(2):142-4. PubMed ID: 19200188
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  • 7. Novel homozygous deletion of segmental KAL1 and entire STS cause Kallmann syndrome and X-linked ichthyosis in a Chinese family.
    Xu H, Li Z, Wang T, Wang S, Liu J, Wang DW.
    Andrologia; 2015 Dec; 47(10):1160-5. PubMed ID: 25597551
    [Abstract] [Full Text] [Related]

  • 8. Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation.
    Ben Khelifa H, Soyah N, Ben-Abdallah-Bouhjar I, Gritly R, Sanlaville D, Elghezal H, Saad A, Mougou-Zerelli S.
    Gene; 2013 Sep 25; 527(2):578-83. PubMed ID: 23791652
    [Abstract] [Full Text] [Related]

  • 9. Analysis of the STS gene in 40 patients with recessive X-linked ichthyosis: a high frequency of partial deletions in a Spanish population.
    Cañueto J, Ciria S, Hernández-Martín A, Unamuno P, González-Sarmiento R.
    J Eur Acad Dermatol Venereol; 2010 Oct 25; 24(10):1226-9. PubMed ID: 20236202
    [Abstract] [Full Text] [Related]

  • 10. X-linked ichthyosis with hypogonadism: not always Kallmann's syndrome.
    Quinton R, Schofield JK, Duke VM, Bouloux PM, Buchanan CR, Leigh IM, Wood DF.
    Clin Exp Dermatol; 1997 Jul 25; 22(4):201-4. PubMed ID: 9499614
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  • 12. X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studies.
    Robledo R, Melis P, Schillinger E, Casciano I, Balazs I, Rinaldi A, Siniscalco M, Filippi G.
    Am J Med Genet; 1995 Nov 06; 59(2):143-8. PubMed ID: 8588575
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  • 13. Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene.
    Maya-Núñez G, Cuevas-Covarrubias S, Zenteno JC, Ulloa-Aguirre A, Kofman-Alfaro S, Méndez JP.
    Clin Endocrinol (Oxf); 1998 Jun 06; 48(6):713-8. PubMed ID: 9713559
    [Abstract] [Full Text] [Related]

  • 14. Detection of the STS gene in a family with X-linked recessive ichthyosis.
    Wang N, An K, Liu H, Fu X, Yu G, Yu Y, Tian H, Zhang F.
    Indian J Dermatol Venereol Leprol; 2013 Jun 06; 79(2):268. PubMed ID: 23442483
    [No Abstract] [Full Text] [Related]

  • 15. [Two cases of X-linked ichthyosis associated with myopathies].
    Ishikawa Y, Imai T, Kameda K, Okabe M, Nagaoka M, Minami R.
    Rinsho Shinkeigaku; 1990 Aug 06; 30(8):855-9. PubMed ID: 2253421
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  • 17. Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis.
    Winge MC, Hoppe T, Liedén A, Nordenskjöld M, Vahlquist A, Wahlgren CF, Törmä H, Bradley M, Berne B.
    J Dermatol Sci; 2011 Jul 06; 63(1):62-4. PubMed ID: 21530180
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  • 20. Deletion of exons 1-5 of the STS gene causing X-linked ichthyosis.
    Valdes-Flores M, Kofman-Alfaro SH, Vaca AL, Cuevas-Covarrubias SA.
    J Invest Dermatol; 2001 Mar 06; 116(3):456-8. PubMed ID: 11231321
    [Abstract] [Full Text] [Related]

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