PubMed for id: 82895

Year	Number of Results
1981	1
1987	2
1990	1
1993	1
1998	2
2003	1
2004	1
2014	1
2015	1
2021	2
2022	2
2024	0

1

One-step separation of Cu, Fe, Zn and Cd and isotope ratio analysis by MC-ICP-MS for geological samples.

Li HT, Li X, Li M, Guo W, Jin LL, Zhu ZL, Hou QY, Hu SH. Li HT, et al. Anal Methods. 2022 Jul 21;14(28):2782-2792. doi: 10.1039/d2ay00559j. Anal Methods. 2022. PMID: 35815347

2

A new phenotype of aldolase a deficiency in a 14 year-old boy with epilepsy and rhabdomyolysis - case report.

Santoro L, Pjetraj D, Velmishi V, Campana C, Catassi C, Dionisi-Vici C, Maiorana A. Santoro L, et al. Ital J Pediatr. 2022 Mar 4;48(1):39. doi: 10.1186/s13052-022-01228-3. Ital J Pediatr. 2022. PMID: 35246226 Free PMC article.

3

Glycogen storage disease type XII; an ultra rare cause of hemolytic anemia and rhabdomyolysis: one new case report.

Kara E, Kor D, Bulut FD, Hergüner Ö, Ceylaner S, Köşeci B, Burgaç E, Mungan NÖ. Kara E, et al. J Pediatr Endocrinol Metab. 2021 Jun 28;34(10):1335-1339. doi: 10.1515/jpem-2021-0258. Print 2021 Oct 26. J Pediatr Endocrinol Metab. 2021. PMID: 34171939

4

Aldolase A deficiency: Report of new cases and literature review.

Papadopoulos C, Svingou M, Kekou K, Vergnaud S, Xirou S, Niotakis G, Papadimas GK. Papadopoulos C, et al. Mol Genet Metab Rep. 2021 Feb 23;27:100730. doi: 10.1016/j.ymgmr.2021.100730. eCollection 2021 Jun. Mol Genet Metab Rep. 2021. PMID: 33665120 Free PMC article.

5

Acute rhabdomyolysis and inflammation.

Hamel Y, Mamoune A, Mauvais FX, Habarou F, Lallement L, Romero NB, Ottolenghi C, de Lonlay P. Hamel Y, et al. J Inherit Metab Dis. 2015 Jul;38(4):621-8. doi: 10.1007/s10545-015-9827-7. Epub 2015 Mar 17. J Inherit Metab Dis. 2015. PMID: 25778939 Review.

6

A thermolabile aldolase A mutant causes fever-induced recurrent rhabdomyolysis without hemolytic anemia.

Mamoune A, Bahuau M, Hamel Y, Serre V, Pelosi M, Habarou F, Nguyen Morel MA, Boisson B, Vergnaud S, Viou MT, Nonnenmacher L, Piraud M, Nusbaum P, Vamecq J, Romero N, Ottolenghi C, Casanova JL, de Lonlay P. Mamoune A, et al. PLoS Genet. 2014 Nov 13;10(11):e1004711. doi: 10.1371/journal.pgen.1004711. eCollection 2014 Nov. PLoS Genet. 2014. PMID: 25392908 Free PMC article.

7

[Extractive chromatograph on-line preconcentration flow injection flame atomic absorption spectrometric determination of trace silver in geological samples].

Yuan Y, Guo X. Yuan Y, et al. Guang Pu Xue Yu Guang Pu Fen Xi. 1998 Oct;18(5):593-6. Guang Pu Xue Yu Guang Pu Fen Xi. 1998. PMID: 15825375 Chinese.

8

Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr).

Yao DC, Tolan DR, Murray MF, Harris DJ, Darras BT, Geva A, Neufeld EJ. Yao DC, et al. Blood. 2004 Mar 15;103(6):2401-3. doi: 10.1182/blood-2003-09-3160. Epub 2003 Nov 13. Blood. 2004. PMID: 14615364 Free article.

9

Glycogen storage diseases of muscle.

DiMauro S, Bruno C. DiMauro S, et al. Curr Opin Neurol. 1998 Oct;11(5):477-84. doi: 10.1097/00019052-199810000-00010. Curr Opin Neurol. 1998. PMID: 9847997 Review.

10

[Anesthesia for a patient with red cell aldolase deficiency].

Kiriyama T, Wakamatsu M, Furuta M, Kato H, Ono K. Kiriyama T, et al. Masui. 1993 May;42(5):750-2. Masui. 1993. PMID: 8515555 Japanese.

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