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For: Wasserstein M, Dionisi-Vici C, Giugliani R, Hwu WL, Lidove O, Lukacs Z, Mengel E, Mistry PK, Schuchman EH, McGovern M. Recommendations for clinical monitoring of patients with acid sphingomyelinase deficiency (ASMD). Mol Genet Metab 2019;126:98-105. [PMID: 30514648 DOI: 10.1016/j.ymgme.2018.11.014] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 3.8] [Reference Citation Analysis]
Number Citing Articles
1 Lidove O, Mauhin W, London J. Acid sphingomyelinase deficiency (Niemann‒Pick disease Type B) as an inflammatory disease. The Journal of Heart and Lung Transplantation 2019;38:583-4. [DOI: 10.1016/j.healun.2019.02.008] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
2 Wang NL, Lin J, Chen L, Lu Y, Xie XB, Abuduxikuer K, Wang JS. Neonatal cholestasis is an early liver manifestation of children with acid sphingomyelinase deficiency. BMC Gastroenterol 2022;22:227. [PMID: 35534800 DOI: 10.1186/s12876-022-02310-0] [Reference Citation Analysis]
3 Al-Eitan L, Alqa'qa' K, Amayreh W, Aljamal H, Khasawneh R, Al-Zoubi B, Okour I, Haddad A, Haddad Y, Haddad H. Novel mutations in the SMPD1 gene in Jordanian children with Acid sphingomyelinase deficiency (Niemann-Pick types A and B). Gene 2020;747:144683. [PMID: 32311413 DOI: 10.1016/j.gene.2020.144683] [Reference Citation Analysis]
4 Mauhin W, Levade T, Vanier MT, Froissart R, Lidove O. Prevalence of Cancer in Acid Sphingomyelinase Deficiency. J Clin Med 2021;10:5029. [PMID: 34768550 DOI: 10.3390/jcm10215029] [Reference Citation Analysis]
5 Evelina M, Roberto F, Caterina R, Federica D, Giovanni P, Vincenza G, Alberto B, Massimo S. ATHEROGENIC LIPID PROFILE IN PATIENTS WITH NIEMANN-PICK DISEASE TYPE B: WHAT TREATMENT STRATEGIES? Journal of Clinical Lipidology 2022. [DOI: 10.1016/j.jacl.2022.01.008] [Reference Citation Analysis]
6 Carubbi F, Barbato A, Burlina AB, Francini F, Mignani R, Pegoraro E, Landini L, De Danieli G, Bruni S, Strazzullo P; Italian Society of Human Nutrition Working Group on Nutrition in Lysosomal Storage Diseases. Nutrition in adult patients with selected lysosomal storage diseases. Nutr Metab Cardiovasc Dis 2021;31:733-44. [PMID: 33589321 DOI: 10.1016/j.numecd.2020.11.028] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Montgomery MK, Taddese AZ, Bayliss J, Nie S, Williamson NA, Watt MJ. Hexosaminidase A (HEXA) regulates hepatic sphingolipid and lipoprotein metabolism in mice. FASEB J 2021;35:e22046. [PMID: 34800307 DOI: 10.1096/fj.202101186R] [Reference Citation Analysis]
8 Capron T, Trigui Y, Gautier C, Puech B, Chanez P, Reynaud-Gaubert M. Respiratory impairment in Niemann-Pick B disease: Two case reports and review for the pulmonologist. Respir Med Res 2019;76:13-8. [PMID: 31254945 DOI: 10.1016/j.resmer.2019.05.001] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
9 Diaz GA, Jones SA, Scarpa M, Mengel KE, Giugliani R, Guffon N, Batsu I, Fraser PA, Li J, Zhang Q, Ortemann-Renon C. One-year results of a clinical trial of olipudase alfa enzyme replacement therapy in pediatric patients with acid sphingomyelinase deficiency. Genet Med 2021;23:1543-50. [PMID: 33875845 DOI: 10.1038/s41436-021-01156-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
10 Cassiman D, Libbrecht L, Meersseman W, Wilmer A. Case Report of Gastrointestinal Bleeding in an Adult with Chronic Visceral Acid Sphingomyelinase Deficiency. Case Rep Gastrointest Med 2019;2019:9613457. [PMID: 31080679 DOI: 10.1155/2019/9613457] [Reference Citation Analysis]
11 Bitencourt FV, Bender CV, Fiorini T, Gomes SC, Visioli F, Angst PDM. Periodontal condition and treatment in a patient with rare systemic condition: A case report for acid sphingomyelinase deficiency. Spec Care Dentist 2021;41:103-10. [PMID: 33179797 DOI: 10.1111/scd.12540] [Reference Citation Analysis]
12 Opoka L, Wyrostkiewicz D, Radwan-Rohrenschef P, Roży A, Tylki-Szymańska A, Tomkowski W, Szturmowicz M. Combined Emphysema and Interstitial Lung Disease as a Rare Presentation of Pulmonary Involvement in a Patient with Chronic Visceral Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Type B). Am J Case Rep 2020;21:e923394. [PMID: 32759889 DOI: 10.12659/AJCR.923394] [Reference Citation Analysis]
13 Nascimbeni F, Dionisi Vici C, Vespasiani Gentilucci U, Angelico F, Nobili V, Petta S, Valenti L; AISF Rare Diseases Committee. AISF update on the diagnosis and management of adult-onset lysosomal storage diseases with hepatic involvement. Dig Liver Dis 2020;52:359-67. [PMID: 31902560 DOI: 10.1016/j.dld.2019.12.005] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
14 Pinto C, Sousa D, Ghilas V, Dardis A, Scarpa M, Macedo MF. Acid Sphingomyelinase Deficiency: A Clinical and Immunological Perspective. Int J Mol Sci 2021;22:12870. [PMID: 34884674 DOI: 10.3390/ijms222312870] [Reference Citation Analysis]
15 Jones SA, McGovern M, Lidove O, Giugliani R, Mistry PK, Dionisi-Vici C, Munoz-Rojas MV, Nalysnyk L, Schecter AD, Wasserstein M. Clinical relevance of endpoints in clinical trials for acid sphingomyelinase deficiency enzyme replacement therapy. Mol Genet Metab 2020;131:116-23. [PMID: 32616389 DOI: 10.1016/j.ymgme.2020.06.008] [Reference Citation Analysis]
16 Johnson AA. Lipid Hydrolase Enzymes: Pragmatic Prolongevity Targets for Improved Human Healthspan? Rejuvenation Res 2020;23:107-21. [PMID: 31426688 DOI: 10.1089/rej.2019.2211] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]