BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 12644929)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome.
    Zhang Q; Si N; Liu Y; Zhang D; Wang R; Zhang Y; Wang S; Liu X; Deng X; Ma Y; Ge P; Zhao J; Zhang X
    Gene; 2017 Sep; 628():103-108. PubMed ID: 28710038
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic analysis of a 12-year-old boy with X-linked ichthyosis in association with sclerosing glomerulonephritis.
    Song Y; Chen J; Yi Z; Dang X; Cheng D; Wu X; Tan Y
    Mol Med Rep; 2013 Oct; 8(4):1183-7. PubMed ID: 23939749
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 116(3):456-8. PubMed ID: 11231321
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray.
    Hand JL; Runke CK; Hodge JC
    J Am Acad Dermatol; 2015 Apr; 72(4):617-27. PubMed ID: 25659225
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked ichthyosis and Crigler-Najjar syndrome I: Coexistence in a male patient with two copy number variable regions of 2q37.1 and Xp22.3.
    Bai J; Qu Y; Cao Y; Li Y; Zhang W; Jin Y; Wang H; Song F
    Mol Med Rep; 2016 Feb; 13(2):1135-40. PubMed ID: 26676689
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series.
    Rodrigo-Nicolás B; Bueno-Martínez E; Martín-Santiago A; Cañueto J; Vicente A; Torrelo A; Noguera-Morel L; Duat-Rodríguez A; Jorge-Finnigan C; Palacios-Álvarez I; García-Hernández JL; Sebaratnam DF; González-Sarmiento R; Hernández-Martín A
    Br J Dermatol; 2018 Oct; 179(4):933-939. PubMed ID: 29901853
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.
    Kent L; Emerton J; Bhadravathi V; Weisblatt E; Pasco G; Willatt LR; McMahon R; Yates JR
    J Med Genet; 2008 Aug; 45(8):519-24. PubMed ID: 18413370
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A study of the steroid sulfatase gene in families with X-linked ichthyosis using polymerase chain reaction.
    Nomura K; Nakano H; Umeki K; Harada K; Kon A; Tamai K; Sawamura D; Hashimoto I
    Acta Derm Venereol; 1995 Sep; 75(5):340-2. PubMed ID: 8615047
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations.
    Ramesh R; Chen H; Kukula A; Wakeling EL; Rustin MH; McLean WH
    J Dermatol Sci; 2011 Dec; 64(3):159-62. PubMed ID: 21945601
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 527(2):578-83. PubMed ID: 23791652
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank.
    Brcic L; Underwood JF; Kendall KM; Caseras X; Kirov G; Davies W
    J Med Genet; 2020 Oct; 57(10):692-698. PubMed ID: 32139392
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of a novel partial deletion of
    Williams D; Onyia O; Chung DD; Kirakosyan A; Hovakimyan A; Payne C; Moshirfar M; Aldave AJ
    Mol Vis; 2023; 29():25-30. PubMed ID: 37287641
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked ichthyosis: Clinical and molecular findings in 35 Italian patients.
    Diociaiuti A; Angioni A; Pisaneschi E; Alesi V; Zambruno G; Novelli A; El Hachem M
    Exp Dermatol; 2019 Oct; 28(10):1156-1163. PubMed ID: 29672931
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel missense mutation of the STS gene in two siblings with X-linked ichthyosis, complicated by short stature, bone density reduction, epilepsy, and cryptorchidism.
    Ohyama A; Nakano H; Imanishi Y; Seto T; Tsuruta D; Fukai K
    Clin Exp Dermatol; 2019 Jan; 44(1):78-79. PubMed ID: 30221377
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.