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For: Čechová A, Altassan R, Borgel D, Bruneel A, Correia J, Girard M, Harroche A, Kiec-Wilk B, Mohnike K, Pascreau T, Pawliński Ł, Radenkovic S, Vuillaumier-Barrot S, Aldamiz-Echevarria L, Couce ML, Martins EG, Quelhas D, Morava E, de Lonlay P, Witters P, Honzík T. Consensus guideline for the diagnosis and management of mannose phosphate isomerase-congenital disorder of glycosylation. J Inherit Metab Dis 2020;43:671-93. [PMID: 32266963 DOI: 10.1002/jimd.12241] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Johnsen C, Edmondson AC. Manifestations and Management of Hepatic Dysfunction in Congenital Disorders of Glycosylation. Clin Liver Dis (Hoboken) 2021;18:54-66. [PMID: 34584669 DOI: 10.1002/cld.1105] [Reference Citation Analysis]
2 Starosta RT, Boyer S, Tahata S, Raymond K, Lee HE, Wolfe LA, Lam C, Edmondson AC, Schwartz IVD, Morava E. Liver manifestations in a cohort of 39 patients with congenital disorders of glycosylation: pin-pointing the characteristics of liver injury and proposing recommendations for follow-up. Orphanet J Rare Dis 2021;16:20. [PMID: 33413482 DOI: 10.1186/s13023-020-01630-2] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
3 Lipiński P, Bogdańska A, Socha P, Tylki-Szymańska A. Liver Involvement in Congenital Disorders of Glycosylation and Deglycosylation. Front Pediatr 2021;9:696918. [PMID: 34291020 DOI: 10.3389/fped.2021.696918] [Reference Citation Analysis]
4 Park JH, Marquardt T. Treatment Options in Congenital Disorders of Glycosylation. Front Genet 2021;12:735348. [PMID: 34567084 DOI: 10.3389/fgene.2021.735348] [Reference Citation Analysis]
5 Ondruskova N, Cechova A, Hansikova H, Honzik T, Jaeken J. Congenital disorders of glycosylation: Still "hot" in 2020. Biochim Biophys Acta Gen Subj 2021;1865:129751. [PMID: 32991969 DOI: 10.1016/j.bbagen.2020.129751] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
6 Sosicka P, Ng BG, Freeze HH. Chemical Therapies for Congenital Disorders of Glycosylation. ACS Chem Biol 2021. [PMID: 34788024 DOI: 10.1021/acschembio.1c00601] [Reference Citation Analysis]
7 Pajusalu S, Vals MA, Mihkla L, Šamarina U, Kahre T, Õunap K. The Estimated Prevalence of N-Linked Congenital Disorders of Glycosylation Across Various Populations Based on Allele Frequencies in General Population Databases. Front Genet 2021;12:719437. [PMID: 34447415 DOI: 10.3389/fgene.2021.719437] [Reference Citation Analysis]
8 Girard M, Douillard C, Debray D, Lacaille F, Schiff M, Vuillaumier-Barrot S, Dupré T, Fabre M, Damaj L, Kuster A, Torre S, Mention K, McLin V, Dobbelaere D, Borgel D, Bauchard E, Seta N, Bruneel A, De Lonlay P. Long term outcome of MPI-CDG patients on D-mannose therapy. J Inherit Metab Dis 2020;43:1360-9. [PMID: 33098580 DOI: 10.1002/jimd.12289] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
9 Lipiński P, Tylki-Szymańska A. Congenital Disorders of Glycosylation: What Clinicians Need to Know? Front Pediatr 2021;9:715151. [PMID: 34540767 DOI: 10.3389/fped.2021.715151] [Reference Citation Analysis]
10 Diamanti A, Calvitti G, Martinelli D, Santariga E, Capriati T, Bolasco G, Iughetti L, Pujia A, Knafelz D, Maggiore G. Etiology and Management of Pediatric Intestinal Failure: Focus on the Non-Digestive Causes. Nutrients 2021;13:786. [PMID: 33673586 DOI: 10.3390/nu13030786] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Mühlhausen C, Henneke L, Schlotawa L, Behme D, Grüneberg M, Gärtner J, Marquardt T. Mannose phosphate isomerase deficiency-congenital disorder of glycosylation (MPI-CDG) with cerebral venous sinus thrombosis as first and only presenting symptom: A rare but treatable cause of thrombophilia. JIMD Rep 2020;55:38-43. [PMID: 32905087 DOI: 10.1002/jmd2.12149] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
12 Abdel Ghaffar TY, Ng BG, Elsayed SM, El Naghi S, Helmy S, Mohammed N, El Hennawy A, Freeze HH. MPI-CDG from a hepatic perspective: Report of two Egyptian cases and review of literature. JIMD Rep 2020;56:20-6. [PMID: 33204592 DOI: 10.1002/jmd2.12159] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
13 Bogdańska A, Lipiński P, Szymańska-Rożek P, Jezela-Stanek A, Rokicki D, Socha P, Tylki-Szymańska A. Clinical, biochemical and molecular phenotype of congenital disorders of glycosylation: long-term follow-up. Orphanet J Rare Dis 2021;16:17. [PMID: 33407696 DOI: 10.1186/s13023-020-01657-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]