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For: Theodore M, Morava E. Congenital disorders of glycosylation: sweet news. Curr Opin Pediatr 2011;23:581-7. [PMID: 21970833 DOI: 10.1097/MOP.0b013e32834cd693] [Cited by in Crossref: 32] [Cited by in F6Publishing: 13] [Article Influence: 3.6] [Reference Citation Analysis]
Number Citing Articles
1 Rymen D, Peanne R, Millón MB, Race V, Sturiale L, Garozzo D, Mills P, Clayton P, Asteggiano CG, Quelhas D, Cansu A, Martins E, Nassogne MC, Gonçalves-Rocha M, Topaloglu H, Jaeken J, Foulquier F, Matthijs G. MAN1B1 deficiency: an unexpected CDG-II. PLoS Genet 2013;9:e1003989. [PMID: 24348268 DOI: 10.1371/journal.pgen.1003989] [Cited by in Crossref: 53] [Cited by in F6Publishing: 45] [Article Influence: 6.6] [Reference Citation Analysis]
2 Morava E. Galactose supplementation in phosphoglucomutase-1 deficiency; review and outlook for a novel treatable CDG. Mol Genet Metab 2014;112:275-9. [PMID: 24997537 DOI: 10.1016/j.ymgme.2014.06.002] [Cited by in Crossref: 55] [Cited by in F6Publishing: 46] [Article Influence: 7.9] [Reference Citation Analysis]
3 Scott K, Gadomski T, Kozicz T, Morava E. Congenital disorders of glycosylation: new defects and still counting. J Inherit Metab Dis 2014;37:609-17. [PMID: 24831587 DOI: 10.1007/s10545-014-9720-9] [Cited by in Crossref: 95] [Cited by in F6Publishing: 78] [Article Influence: 13.6] [Reference Citation Analysis]
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5 Iqbal Z, Shahzad M, Vissers LE, van Scherpenzeel M, Gilissen C, Razzaq A, Zahoor MY, Khan SN, Kleefstra T, Veltman JA, de Brouwer AP, Lefeber DJ, van Bokhoven H, Riazuddin S. A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype. Eur J Hum Genet 2013;21:844-9. [PMID: 23249953 DOI: 10.1038/ejhg.2012.257] [Cited by in Crossref: 17] [Cited by in F6Publishing: 12] [Article Influence: 1.9] [Reference Citation Analysis]
6 Thiel C, Meßner-Schmitt D, Hoffmann GF, Körner C. Screening for congenital disorders of glycosylation in the first weeks of life. J Inherit Metab Dis 2013;36:887-92. [PMID: 22991164 DOI: 10.1007/s10545-012-9531-9] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.7] [Reference Citation Analysis]
7 de Freitas C, Dos Reis V, Silva S, Videira PA, Morava E, Jaeken J. Public and patient involvement in needs assessment and social innovation: a people-centred approach to care and research for congenital disorders of glycosylation. BMC Health Serv Res 2017;17:682. [PMID: 28950866 DOI: 10.1186/s12913-017-2625-1] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
8 Parvaneh N, Quartier P, Rostami P, Casanova JL, de Lonlay P. Inborn errors of metabolism underlying primary immunodeficiencies. J Clin Immunol 2014;34:753-71. [PMID: 25081841 DOI: 10.1007/s10875-014-0076-6] [Cited by in Crossref: 16] [Cited by in F6Publishing: 10] [Article Influence: 2.3] [Reference Citation Analysis]
9 Witters P, Cassiman D, Morava E. Nutritional Therapies in Congenital Disorders of Glycosylation (CDG). Nutrients 2017;9:E1222. [PMID: 29112118 DOI: 10.3390/nu9111222] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 6.3] [Reference Citation Analysis]
10 Gupta VA, Kawahara G, Myers JA, Chen AT, Hall TE, Manzini MC, Currie PD, Zhou Y, Zon LI, Kunkel LM, Beggs AH. A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish. PLoS One 2012;7:e43794. [PMID: 22952766 DOI: 10.1371/journal.pone.0043794] [Cited by in Crossref: 32] [Cited by in F6Publishing: 27] [Article Influence: 3.6] [Reference Citation Analysis]
11 van de Loo KF, van Dongen L, Mohamed M, Gardeitchik T, Kouwenberg TW, Wortmann SB, Rodenburg RJ, Lefeber DJ, Morava E, Verhaak CM. Socio-emotional Problems in Children with CDG. JIMD Rep 2013;11:139-48. [PMID: 23733602 DOI: 10.1007/8904_2013_233] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
12 Heywood WE, Bliss E, Mills P, Yuzugulen J, Carreno G, Clayton PT, Muntoni F, Worthington VC, Torelli S, Sebire NJ, Mills K, Grunewald S. Global serum glycoform profiling for the investigation of dystroglycanopathies & Congenital Disorders of Glycosylation. Mol Genet Metab Rep 2016;7:55-62. [PMID: 27134828 DOI: 10.1016/j.ymgmr.2016.03.002] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.2] [Reference Citation Analysis]
13 de la Morena-Barrio ME, Hernández-Caselles T, Corral J, García-López R, Martínez-Martínez I, Pérez-Dueñas B, Altisent C, Sevivas T, Kristensen SR, Guillén-Navarro E, Miñano A, Vicente V, Jaeken J, Lozano ML. GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients. Orphanet J Rare Dis 2013;8:170. [PMID: 24139637 DOI: 10.1186/1750-1172-8-170] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 1.4] [Reference Citation Analysis]