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For: Liu J, Peng Y, Zhou N, Liu X, Meng Q, Xu H, Zhao S. Combined methylmalonic acidemia and homocysteinemia presenting predominantly with late-onset diffuse lung disease: a case series of four patients. Orphanet J Rare Dis 2017;12:58. [PMID: 28327205 DOI: 10.1186/s13023-017-0610-8] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 2.6] [Reference Citation Analysis]
Number Citing Articles
1 Zhang C. Early Onset Predominantly Diffuse Lung Disease in an Infant of Combined Methylmalonic Acidemia With Hyperhomocysteinemia Cobalamin C Type. Indian Pediatr 2020;57:1079-81. [DOI: 10.1007/s13312-020-2045-x] [Reference Citation Analysis]
2 Liu J, Liu Z, Yan H, Li Y. Dandy-Walker malformation in methylmalonic acidemia: a rare case report. BMC Pediatr 2021;21:398. [PMID: 34511063 DOI: 10.1186/s12887-021-02874-y] [Reference Citation Analysis]
3 Chen M, Zhuang J, Yang J, Wang D, Yang Q. Atypical hemolytic uremic syndrome induced by CblC subtype of methylmalonic academia: A case report and literature review. Medicine (Baltimore) 2017;96:e8284. [PMID: 29068997 DOI: 10.1097/MD.0000000000008284] [Cited by in Crossref: 10] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Broomfield A, Kenth J, Bruce IA, Tan HL, Wilkinson S. Respiratory complications of metabolic disease in the paediatric population: A review of presentation, diagnosis and therapeutic options. Paediatr Respir Rev 2019;32:55-65. [PMID: 31101546 DOI: 10.1016/j.prrv.2019.04.004] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
5 Liu J, Tang X, Zhou C, Xu H, Yang H, He R, Li H, Zhao S. Cobalamin C deficiency presenting with diffuse alveolar hemorrhage and pulmonary microangiopathy. Pediatr Pulmonol 2020;55:1481-6. [PMID: 32293809 DOI: 10.1002/ppul.24781] [Reference Citation Analysis]
6 Liu Y, Yang L, Shuai R, Huang S, Zhang B, Han L, Sun K, Wu Y. Different Pattern of Cardiovascular Impairment in Methylmalonic Acidaemia Subtypes. Front Pediatr 2022;10:810495. [DOI: 10.3389/fped.2022.810495] [Reference Citation Analysis]
7 Gupta A, Kabra M, Gupta N. Combined Methylmalonic Aciduria and Homocystinuria Presenting as Pulmonary Hypertension. Indian J Pediatr 2021;88:1244-6. [PMID: 34510336 DOI: 10.1007/s12098-021-03938-8] [Reference Citation Analysis]
8 Zhang YN, Pi YL, Yan X, Li YQ, Qi ZJ, Zhang HF. Methylmalonic Acidemia Complicated by Homocystinuria Diseases: a Report of Three Cases. Adv Ther 2020;37:630-6. [PMID: 31758516 DOI: 10.1007/s12325-019-01149-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
9 Grandone E, Martinelli P, Villani M, Vecchione G, Fischetti L, Leccese A, Santacroce R, Corso G, Margaglione M. Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria. BMC Pregnancy Childbirth 2019;19:318. [PMID: 31470807 DOI: 10.1186/s12884-019-2474-5] [Reference Citation Analysis]
10 Zhou X, Cui Y, Han J. Methylmalonic acidemia: Current status and research priorities. Intractable Rare Dis Res 2018;7:73-8. [PMID: 29862147 DOI: 10.5582/irdr.2018.01026] [Cited by in Crossref: 16] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
11 Wiedemann A, Oussalah A, Lamireau N, Théron M, Julien M, Mergnac JP, Augay B, Deniaud P, Alix T, Frayssinoux M, Feillet F, Guéant JL. Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B12 metabolism: A meta-analysis. Cell Rep Med 2022;:100670. [PMID: 35764087 DOI: 10.1016/j.xcrm.2022.100670] [Reference Citation Analysis]
12 Yao Y, Shen K. Monogenic diseases in respiratory medicine: Clinical perspectives. Pediatr Investig 2017;1:27-31. [PMID: 32851215 DOI: 10.1002/ped4.12006] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
13 Tang X, Li H, Liu H, Xu H, Yang H, Liu J, Zhao S. Etiologic spectrum of interstitial lung diseases in Chinese children older than 2 years of age. Orphanet J Rare Dis 2020;15:25. [PMID: 31969166 DOI: 10.1186/s13023-019-1270-7] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
14 Zhu J, Wan S, Zhao X, Zhu B, Lv Y, Jiang H. Acute Lymphoblastic Leukemia in Combined Methylmalonic Acidemia and Homocysteinemia (cblC Type): A Case Report and Literature Review. Front Genet 2022;13:856552. [DOI: 10.3389/fgene.2022.856552] [Reference Citation Analysis]
15 Ramsay J, Morton J, Norris M, Kanungo S. Organic acid disorders. Ann Transl Med 2018;6:472. [PMID: 30740403 DOI: 10.21037/atm.2018.12.39] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
16 Broomfield AA, Padidela R, Wilkinson S. Pulmonary Manifestations of Endocrine and Metabolic Diseases in Children. Pediatr Clin North Am 2021;68:81-102. [PMID: 33228944 DOI: 10.1016/j.pcl.2020.09.011] [Reference Citation Analysis]