These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
150 related articles for article (PubMed ID: 9385378)
21. Five novel mutations of GALNS in Korean patients with mucopolysaccharidosis IVA. Park HD; Ko AR; Ki CS; Lee SY; Kim JW; Cho SY; Kim SH; Park SW; Sohn YB; Jin DK Am J Med Genet A; 2013 Mar; 161A(3):509-17. PubMed ID: 23401410 [TBL] [Abstract][Full Text] [Related]
22. Mucopolysaccharidosis IVA: screening and identification of mutations of the N-acetylgalactosamine-6-sulfate sulfatase gene. Ogawa T; Tomatsu S; Fukuda S; Yamagishi A; Rezvi GM; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orü T Hum Mol Genet; 1995 Mar; 4(3):341-9. PubMed ID: 7795586 [TBL] [Abstract][Full Text] [Related]
23. The GALNS p.P77R variant is a probable Gujarati-Indian founder mutation causing Mucopolysaccharidosis IVA syndrome. Sheth H; Naik P; Shah M; Bhavsar R; Nair A; Sheth F; Sheth J BMC Genomics; 2022 Jun; 23(1):458. PubMed ID: 35729508 [TBL] [Abstract][Full Text] [Related]
24. Clinical, biochemical and genetic profiles of patients with mucopolysaccharidosis type IVA (Morquio A syndrome) in Malaysia: the first national natural history cohort study. Leong HY; Abdul Azize NA; Chew HB; Keng WT; Thong MK; Mohd Khalid MKN; Hung LC; Mohamed Zainudin N; Ramlee A; Md Haniffa MA; Yakob Y; Ngu LH Orphanet J Rare Dis; 2019 Jun; 14(1):143. PubMed ID: 31200731 [TBL] [Abstract][Full Text] [Related]
25. Investigation of GALNS variants and genotype-phenotype correlations in a large cohort of patients with mucopolysaccharidosis type IVA. Yi M; Wang Y; Gao X; Han L; Qiu W; Gu X; Maegawa GHB; Zhang H J Inherit Metab Dis; 2022 May; 45(3):593-604. PubMed ID: 35212421 [TBL] [Abstract][Full Text] [Related]
26. Mutations and polymorphisms in N-acetylgalactosamine-6-sulfate sulfatase gene in Turkish Morquio A patients. Khedhiri S; Chkioua L; Elcioglu N; Laradi S; Miled A Pathol Biol (Paris); 2014 Feb; 62(1):38-40. PubMed ID: 24411403 [TBL] [Abstract][Full Text] [Related]
27. Mucopolysaccharidosis IVA: submicroscopic deletion of 16q24.3 and a novel R386C mutation of N-acetylgalactosamine-6-sulfate sulfatase gene in a classical Morquio disease. Fukuda S; Tomatsu S; Masuno M; Ogawa T; Yamagishi A; Rezvi GM; Sukegawa K; Shimozawa N; Suzuki Y; Kondo N; Imaizumi K; Kuroki Y; Okabe T; Orii T Hum Mutat; 1996; 7(2):123-34. PubMed ID: 8829629 [TBL] [Abstract][Full Text] [Related]
28. Development of MPS IVA mouse (Galnstm(hC79S.mC76S)slu) tolerant to human N-acetylgalactosamine-6-sulfate sulfatase. Tomatsu S; Gutierrez M; Nishioka T; Yamada M; Yamada M; Tosaka Y; Grubb JH; Montaño AM; Vieira MB; Trandafirescu GG; Peña OM; Yamaguchi S; Orii KO; Orii T; Noguchi A; Laybauer L Hum Mol Genet; 2005 Nov; 14(22):3321-35. PubMed ID: 16219627 [TBL] [Abstract][Full Text] [Related]
29. Mucopolysaccharidosis type IVA: common double deletion in the N-acetylgalactosamine-6-sulfatase gene (GALNS). Hori T; Tomatsu S; Nakashima Y; Uchiyama A; Fukuda S; Sukegawa K; Shimozawa N; Suzuki Y; Kondo N; Horiuchi T Genomics; 1995 Apr; 26(3):535-42. PubMed ID: 7607677 [TBL] [Abstract][Full Text] [Related]
30. Murine model (Galns(tm(C76S)slu)) of MPS IVA with missense mutation at the active site cysteine conserved among sulfatase proteins. Tomatsu S; Vogler C; Montaño AM; Gutierrez M; Oikawa H; Dung VC; Orii T; Noguchi A; Sly WS Mol Genet Metab; 2007 Jul; 91(3):251-8. PubMed ID: 17498992 [TBL] [Abstract][Full Text] [Related]
31. Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variants. Zanetti A; D'Avanzo F; AlSayed M; Brusius-Facchin AC; Chien YH; Giugliani R; Izzo E; Kasper DC; Lin HY; Lin SP; Pollard L; Singh A; Tonin R; Wood T; Morrone A; Tomanin R Hum Mutat; 2021 Nov; 42(11):1384-1398. PubMed ID: 34387910 [TBL] [Abstract][Full Text] [Related]
32. Effect of 'attenuated' mutations in mucopolysaccharidosis IVA on molecular phenotypes of N-acetylgalactosamine-6-sulfate sulfatase. Montaño AM; Sukegawa K; Kato Z; Carrozzo R; Di Natale P; Christensen E; Orii KO; Orii T; Kondo N; Tomatsu S J Inherit Metab Dis; 2007 Oct; 30(5):758-67. PubMed ID: 17876718 [TBL] [Abstract][Full Text] [Related]
33. Identification of 31 novel mutations in the N-acetylgalactosamine-6-sulfatase gene reveals excessive allelic heterogeneity among patients with Morquio A syndrome. Bunge S; Kleijer WJ; Tylki-Szymanska A; Steglich C; Beck M; Tomatsu S; Fukuda S; Poorthuis BJ; Czartoryska B; Orii T; Gal A Hum Mutat; 1997; 10(3):223-32. PubMed ID: 9298823 [TBL] [Abstract][Full Text] [Related]
34. Molecular characterization of mucopolysaccharidosis type IVA patients in the Andean region of Colombia. Pachajoa H; Acosta MA; Alméciga-Díaz CJ; Ariza Y; Diaz-Ordoñez L; Caicedo-Herrera G; Cuartas D; Nastasi-Catanese JA; Ramírez-Montaño D; Silva YK; Moreno L; Satizabal J; Garcia N; Montoya J; Prada C; Porras G; Velasco H; Candelo E Am J Med Genet C Semin Med Genet; 2021 Sep; 187(3):388-395. PubMed ID: 34542925 [TBL] [Abstract][Full Text] [Related]
36. Mucopolysaccharidosis IVA within Tunisian patients: Confirmation of the two novel GALNS gene mutations. Khedhiri S; Chkioua L; Bouzidi H; Dandana A; Ferchichi S; Ben Turkia H; Miled A; Laradi S Pathol Biol (Paris); 2012 Jun; 60(3):190-2. PubMed ID: 22078177 [TBL] [Abstract][Full Text] [Related]
37. A novel splicing variant in GALNS in mucopolysaccharidosis IVA and the necessity of re-evaluating primer sequences. Kim SM; Noh ES; Park JH; Park HD; Lee SY; Jang JH; Cho SY Ann Hum Genet; 2022 Nov; 86(6):361-368. PubMed ID: 36000290 [TBL] [Abstract][Full Text] [Related]
38. Mucopolysaccharidosis IVA: four new exonic mutations in patients with N-acetylgalactosamine-6-sulfate sulfatase deficiency. Tomatsu S; Fukuda S; Yamagishi A; Cooper A; Wraith JF; Hori T; Kato Z; Yamada N; Isogai K; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orii T Am J Hum Genet; 1996 May; 58(5):950-62. PubMed ID: 8651279 [TBL] [Abstract][Full Text] [Related]
39. Identification of a common mutation in mucopolysaccharidosis IVA: correlation among genotype, phenotype, and keratan sulfate. Tomatsu S; Dieter T; Schwartz IV; Sarmient P; Giugliani R; Barrera LA; Guelbert N; Kremer R; Repetto GM; Gutierrez MA; Nishioka T; Serrato OP; Montaño AM; Yamaguchi S; Noguchi A J Hum Genet; 2004; 49(9):490-494. PubMed ID: 15309681 [TBL] [Abstract][Full Text] [Related]
40. Generation of an induced pluripotent stem cell line (TRNDi005-A) from a Mucopolysaccharidosis Type IVA (MPS IVA) patient carrying compound heterozygous p.R61W and p.WT405del mutations in the GALNS gene. Li R; Baskfield A; Beers J; Zou J; Liu C; Alméciga-Díaz CJ; Zheng W Stem Cell Res; 2019 Apr; 36():101408. PubMed ID: 30797135 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]