Similar articles for PMID: 24234586

Year	Number of Results
1974	2
1975	2
1976	6
1977	2
1978	1
1980	1
1981	1
1982	1
1983	1
1986	1
1994	3
1995	1
1996	1
2000	1
2004	1
2005	3
2007	2
2008	1
2009	2
2010	4
2011	4
2012	2
2013	6
2014	13
2015	7
2016	6
2017	5
2018	6
2019	5
2020	15
2021	6
2022	4
2023	2
2024	1

1

Radiological and clinical characterization of the lysosomal storage disorders: non-lipid disorders.

Parker EI, Xing M, Moreno-De-Luca A, Harmouche E, Terk MR. Parker EI, et al. Br J Radiol. 2014 Jan;87(1033):20130467. doi: 10.1259/bjr.20130467. Epub 2013 Nov 14. Br J Radiol. 2014. PMID: 24234586 Free PMC article. Review.

2

[Mucopolysaccharide storage diseases. II. Possibilities and problems in diagnostic typing as seen in patients in a pediatric hospital].

Hässler A, Kirchner M, Friedrich H, Machill G. Hässler A, et al. Kinderarztl Prax. 1980 Sep;48(9):455-70. Kinderarztl Prax. 1980. PMID: 6776332 German. No abstract available.

3

Lysosomal storage disorders in Thailand: the Siriraj experience.

Wasant P, Wattanaweeradej S, Raksadawan N, Kolodny EH. Wasant P, et al. Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:54-8. Southeast Asian J Trop Med Public Health. 1995. PMID: 8629143

4

Hurler-like disorders in infancy.

Kelly TE. Kelly TE. Clin Perinatol. 1976 Mar;3(1):115-32. Clin Perinatol. 1976. PMID: 821689 Review. No abstract available.

5

Otorhinolaryngological manifestations in 61 patients with mucopolysaccharidosis.

Murgasova L, Jurovcik M, Jesina P, Malinova V, Bloomfield M, Zeman J, Magner M. Murgasova L, et al. Int J Pediatr Otorhinolaryngol. 2020 Aug;135:110137. doi: 10.1016/j.ijporl.2020.110137. Epub 2020 May 27. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32502916

6

[Mucopolysaccharidoses].

Kopyść Z, Gura C, Ryzko J. Kopyść Z, et al. Pediatr Pol. 1976 Jun;51(6):735-47. Pediatr Pol. 1976. PMID: 821035 Review. Polish. No abstract available.

7

[Mucopolysaccharidosis].

Gajdos A. Gajdos A. Nouv Presse Med. 1977 May 14;6(20):1745-6. Nouv Presse Med. 1977. PMID: 141039 French. No abstract available.

8

[Clinical, roentgenological and biochemical differential diagnosis of mucopolysaccharidosis I, II, III and IV I. Clinical and roentgeno-morphological differentiation].

Weisenbach J, Kapcsányi I, Klujber L, Várady S, Szász E. Weisenbach J, et al. Orv Hetil. 1975 May 18;116(20):1143-7. Orv Hetil. 1975. PMID: 806050 Hungarian. No abstract available.

9

Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III.

de Ruijter J, de Ru MH, Wagemans T, Ijlst L, Lund AM, Orchard PJ, Schaefer GB, Wijburg FA, van Vlies N. de Ruijter J, et al. Mol Genet Metab. 2012 Dec;107(4):705-10. doi: 10.1016/j.ymgme.2012.09.024. Epub 2012 Sep 28. Mol Genet Metab. 2012. PMID: 23084433

10

Assay of heparan-N-sulfamidase in dried leukocytes impregnated in filter paper: a new tool for the identification of mucopolisaccharidosis IIIA and potentially other lysosomal disorders.

Civallero G, De Mari J, Viapiana Camelier M, Burin M, Giugliani R. Civallero G, et al. Mol Genet Metab. 2013 Apr;108(4):267-8. doi: 10.1016/j.ymgme.2013.02.001. Mol Genet Metab. 2013. PMID: 23485107

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