183 related articles for article (PubMed ID: 35495149)
1. Acute Lymphoblastic Leukemia in Combined Methylmalonic Acidemia and Homocysteinemia (cblC Type): A Case Report and Literature Review.
Zhu J; Wan S; Zhao X; Zhu B; Lv Y; Jiang H
Front Genet; 2022; 13():856552. PubMed ID: 35495149
[No Abstract] [Full Text] [Related]
2. Case report: An asymptomatic mother with an inborn error of cobalamin metabolism (cblC) detected through high homocysteine levels during prenatal diagnosis.
Liu YP; He RX; Chen ZH; Kang LL; Song JQ; Liu Y; Shi CY; Chen JY; Dong H; Zhang Y; Li MQ; Jin Y; Qin J; Yang YL
Front Nutr; 2023; 10():1124387. PubMed ID: 37252234
[TBL] [Abstract][Full Text] [Related]
3. Atypical hemolytic uremic syndrome induced by CblC subtype of methylmalonic academia: A case report and literature review.
Chen M; Zhuang J; Yang J; Wang D; Yang Q
Medicine (Baltimore); 2017 Oct; 96(43):e8284. PubMed ID: 29068997
[TBL] [Abstract][Full Text] [Related]
4. Proteinuria as a presenting sign of combined methylmalonic acidemia and homocysteinemia: case report.
Chen RY; Li XZ; Lin Q; Zhu Y; Shen YY; Xu QY; Zhu XM; Chen LQ; Wu HY; Chen XQ
BMC Med Genet; 2020 Sep; 21(1):183. PubMed ID: 32957924
[TBL] [Abstract][Full Text] [Related]
5. Case Report: A Case of Late-Onset Combined Methylmalonic Acidemia and Hyperhomocysteinemia Induced by a Vegetarian Diet.
Xu B; Zhang L; Chen Q; Wang Y; Peng Y; Tang H
Front Pediatr; 2022; 10():896177. PubMed ID: 35903162
[TBL] [Abstract][Full Text] [Related]
6. Clinical presentation, gene analysis and outcomes in young patients with early-treated combined methylmalonic acidemia and homocysteinemia (cblC type) in Shandong province, China.
Han B; Cao Z; Tian L; Zou H; Yang L; Zhu W; Liu Y
Brain Dev; 2016 May; 38(5):491-7. PubMed ID: 26563984
[TBL] [Abstract][Full Text] [Related]
7. [Pulmonary arterial hypertension as leading manifestation of methylmalonic aciduria: clinical characteristics and gene testing in 15 cases].
Liu XQ; Yan H; Qiu JX; Zhang CY; Qi JG; Zhang X; Xiao HJ; Yang YL; Chen YH; Du JB
Beijing Da Xue Xue Bao Yi Xue Ban; 2017 Oct; 49(5):768-777. PubMed ID: 29045954
[TBL] [Abstract][Full Text] [Related]
8. Case Report: A Case of Adult Methylmalonic Acidemia With Bilateral Cerebellar Lesions Caused by a New Mutation in
Wang S; Wang X; Xi J; Yang W; Zhu M
Front Neurol; 2022; 13():935604. PubMed ID: 35865640
[TBL] [Abstract][Full Text] [Related]
9. Clinical, biochemical, and molecular analysis of combined methylmalonic acidemia and hyperhomocysteinemia (cblC type) in China.
Wang F; Han L; Yang Y; Gu X; Ye J; Qiu W; Zhang H; Zhang Y; Gao X; Wang Y
J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S435-42. PubMed ID: 20924684
[TBL] [Abstract][Full Text] [Related]
10. [Analysis of gene mutations in Chinese patients with methylmalonic acidemia and homocysteinemia].
Wang F; Han LS; Hu YH; Yang YL; Ye J; Qiu WJ; Zhang YF; Gao XL; Wang Y; Gu XF
Zhonghua Er Ke Za Zhi; 2009 Mar; 47(3):189-93. PubMed ID: 19573432
[TBL] [Abstract][Full Text] [Related]
11. [Analysis of propionylcarnitine in blood and methylmalonic acid in urine of 162 patients with methylmalonic acidemia].
Wu SN; Han LS; Ye J; Qiu WJ; Zhang HW; Gao XL; Wang Y; Li XY; Xu H; Gu XF
Zhonghua Yi Xue Za Zhi; 2013 Feb; 93(8):561-5. PubMed ID: 23663331
[TBL] [Abstract][Full Text] [Related]
12. Treatable cause of hereditary spastic paraplegia: eight cases of combined homocysteinaemia with methylmalonic aciduria.
Wei Y; Zhou Y; Yuan J; Ni J; Qian M; Cui L; Peng B
J Neurol; 2019 Oct; 266(10):2434-2439. PubMed ID: 31203424
[TBL] [Abstract][Full Text] [Related]
13. Clinical features and outcomes of patients with cblC type methylmalonic acidemia carrying gene c.609G>A mutation.
Yu Y; Ling S; Shuai R; Qiu W; Zhang H; Liang L; Ji W; Liu Y; Gu X; Han L
Zhejiang Da Xue Xue Bao Yi Xue Ban; 2021 Aug; 50(4):436-443. PubMed ID: 34704411
[TBL] [Abstract][Full Text] [Related]
14. Methylmalonic acid levels in serum, exosomes, and urine and its association with cblC type methylmalonic acidemia-induced cognitive impairment.
Sun S; Jin H; Rong Y; Song W; Li Q
Front Neurol; 2022; 13():1090958. PubMed ID: 36582607
[TBL] [Abstract][Full Text] [Related]
15. Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type.
Chen T; Liang L; Zhang H; Ye J; Qiu W; Xiao B; Zhu H; Wang L; Xu F; Gong Z; Gu X; Han L
Orphanet J Rare Dis; 2021 Mar; 16(1):125. PubMed ID: 33691766
[TBL] [Abstract][Full Text] [Related]
16. [Heterogeneous phenotypes, genotypes, treatment and prevention of 1 003 patients with methylmalonic acidemia in the mainland of China].
Liu Y; Liu YP; Zhang Y; Song JQ; Zheng H; Dong H; Ma YY; Wu TF; Wang Q; Li XY; Ding Y; Li DX; Jin Y; Li MQ; Wang ZX; Yuan Y; Li HX; Qin J; Yang YL
Zhonghua Er Ke Za Zhi; 2018 Jun; 56(6):414-420. PubMed ID: 29886603
[No Abstract] [Full Text] [Related]
17. [Analysis of clinical phenotypes and MMACHC gene variants in 65 children with Methylmalonic acidemia and homocysteinemia].
Chen C; Zhang Y; Ge L; Liu L; Zhang X; Mei S; Luo S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Sep; 40(9):1086-1092. PubMed ID: 37643953
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of combined methylmalonic acidemia and homocystinuria cobalamin C type using clinical exome sequencing and targeted gene analysis.
Hwang N; Jang JH; Cho EH; Choi R; Choi SJ; Park HD
Mol Genet Genomic Med; 2021 Nov; 9(11):e1838. PubMed ID: 34655177
[TBL] [Abstract][Full Text] [Related]
19. Rare cause of coronary artery ectasia in children: A case report of methylmalonic acidemia with hyperhomocysteinemia.
Juan T; Chao-Ying C; Hua-Rong L; Ling W
Front Pediatr; 2022; 10():917734. PubMed ID: 35935352
[TBL] [Abstract][Full Text] [Related]
20. Clinical characteristics and genotype analysis of five infants with cblX type of methylmalonic acidemia.
Wang F; Liang L; Ling S; Yu Y; Chen T; Xu F; Gong Z; Han L
Zhejiang Da Xue Xue Bao Yi Xue Ban; 2022 Jun; 51(3):298-305. PubMed ID: 36207831
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
