Мукополисахаридоза (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Мукополисахаридоза" in Serbian language version.

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archive.org

Malm G, Lund AM, Mansson JE, Heiberg A (новембар 2008). „Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence”. Acta Paediatr. 97 (11): 1577—81. PMID 18681890. doi:10.1111/j.1651-2227.2008.00965.x. . „Medline”. .

doi.org

Murphy, A. M.; Lambert, D; Treacy, E. P.; O'Meara, A.; Lynch, S. A. (јануар 2009). „Incidence and prevalence of mucopolysaccharidosis type 1 in the Irish republic”. Arch Dis Child. 94 (1): 52—4. PMID 18463126. doi:10.1136/adc.2007.135772.
Malm G, Lund AM, Mansson JE, Heiberg A (новембар 2008). „Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence”. Acta Paediatr. 97 (11): 1577—81. PMID 18681890. doi:10.1111/j.1651-2227.2008.00965.x. . „Medline”. .
McKusick, V. A., Howell, R. R., Hussels, I. E., Neufeld, E. F., Stevenson, R. E (1972). „Allelism, nonallelism and genetic compounds among the mucopolysaccharidoses.”. Lancet. 299 (7758): 993—996. PMID 4112371. doi:10.1016/S0140-6736(72)91159-2. , 1972.
Fan X, Tkachyova I, Sinha A, Rigat B, Mahuran D (2011). „Characterization of the biosynthesis, processing and kinetic mechanism of action of the enzyme deficient in mucopolysaccharidosis IIIC.”. PLOS ONE. 6 (9): e24951. Bibcode:2011PLoSO...624951F. PMC 3177862 . PMID 21957468. doi:10.1371/journal.pone.0024951 .
Ouesleti S, Brunel V, Ben Turkia H, Dranguet H, Miled A, Miladi N; et al. (новембар 2011). „Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patients”. Clin Chim Acta. 412 (23–24): 2326—2331. PMID 21910976. doi:10.1016/j.cca.2011.08.032. . 412(23-24):2326-31.
Valstar MJ, Neijs S, Bruggenwirth HT, Olmer R, Ruijter GJ, Wevers RA; et al. (децембар 2010). „Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlations”. Ann Neurol. 68 (6): 876—87. PMID 21061399. doi:10.1002/ana.22092. .
Sanfilippo, Sylvester J.; Podosin, Robert; Langer, Leonard; Good, Robert A. (1963). „Mental retardation associated with acid mucopolysacchariduria (heparitin sulfate type)”. J. Pediat. 63 (4): 837—838. doi:10.1016/S0022-3476(63)80279-6.

harvard.edu

adsabs.harvard.edu

Fan X, Tkachyova I, Sinha A, Rigat B, Mahuran D (2011). „Characterization of the biosynthesis, processing and kinetic mechanism of action of the enzyme deficient in mucopolysaccharidosis IIIC.”. PLOS ONE. 6 (9): e24951. Bibcode:2011PLoSO...624951F. PMC 3177862 . PMID 21957468. doi:10.1371/journal.pone.0024951 .

medscape.com

emedicine.medscape.com

Germaine L, Defendi (28. 10. 2024). „Background, Hunter Syndrome (Mucopolysaccharidosis Type II)”. emedicine.medscape.com. Приступљено 16. 6. 2018.
Germaine L Defendi, Sanfilippo Syndrome (Mucopolysaccharidosis Type III) Меdscape
„Pediatric Syphilis”. emedicine.medscape.com/article/969023. 12. 12. 2022. Приступљено 22. 6. 2018.
Curto, Lynne Ierardi (8. 10. 2024). „Sphingomyelinase Deficiency”. emedicine.medscape.com, article/951564. Приступљено 22. 6. 2018.

reference.medscape.com

Malm G, Lund AM, Mansson JE, Heiberg A (новембар 2008). „Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence”. Acta Paediatr. 97 (11): 1577—81. PMID 18681890. doi:10.1111/j.1651-2227.2008.00965.x. . „Medline”. .

nih.gov

ncbi.nlm.nih.gov

Murphy, A. M.; Lambert, D; Treacy, E. P.; O'Meara, A.; Lynch, S. A. (јануар 2009). „Incidence and prevalence of mucopolysaccharidosis type 1 in the Irish republic”. Arch Dis Child. 94 (1): 52—4. PMID 18463126. doi:10.1136/adc.2007.135772.
Malm G, Lund AM, Mansson JE, Heiberg A (новембар 2008). „Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence”. Acta Paediatr. 97 (11): 1577—81. PMID 18681890. doi:10.1111/j.1651-2227.2008.00965.x. . „Medline”. .
McKusick, V. A., Howell, R. R., Hussels, I. E., Neufeld, E. F., Stevenson, R. E (1972). „Allelism, nonallelism and genetic compounds among the mucopolysaccharidoses.”. Lancet. 299 (7758): 993—996. PMID 4112371. doi:10.1016/S0140-6736(72)91159-2. , 1972.
Zhang, W. M.; Shi, H. P.; Meng, Y.; Li, B. T.; Qiu, Z. Q.; Liu, J. T. (јун 2008). „Postnatal and prenatal diagnosis of mucopolysaccharidosis type III (Sanfilippo syndrome)”. Zhonghua Er Ke Za Zhi. 46 (6): 407—10. PMID 19099774.
Fan X, Tkachyova I, Sinha A, Rigat B, Mahuran D (2011). „Characterization of the biosynthesis, processing and kinetic mechanism of action of the enzyme deficient in mucopolysaccharidosis IIIC.”. PLOS ONE. 6 (9): e24951. Bibcode:2011PLoSO...624951F. PMC 3177862 . PMID 21957468. doi:10.1371/journal.pone.0024951 .
Ouesleti S, Brunel V, Ben Turkia H, Dranguet H, Miled A, Miladi N; et al. (новембар 2011). „Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patients”. Clin Chim Acta. 412 (23–24): 2326—2331. PMID 21910976. doi:10.1016/j.cca.2011.08.032. . 412(23-24):2326-31.
Valstar MJ, Neijs S, Bruggenwirth HT, Olmer R, Ruijter GJ, Wevers RA; et al. (децембар 2010). „Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlations”. Ann Neurol. 68 (6): 876—87. PMID 21061399. doi:10.1002/ana.22092. .

ninds.nih.gov

„Mucopolysaccharidoses Face Sheet”. Архивирано из оригинала 18. 08. 2016. г. Приступљено 21. 06. 2018. National Institute of Neurological Disorders and Stroke 15. 11. 2017.

web.archive.org

„Mucopolysaccharidoses Face Sheet”. Архивирано из оригинала 18. 08. 2016. г. Приступљено 21. 06. 2018. National Institute of Neurological Disorders and Stroke 15. 11. 2017.