Abacan MA[au] - Search Results

Year	Number of Results
2017	1
2018	1
2020	2
2021	4
2022	1
2023	1

1

Profile of hospital transplant ethics committees in the Philippines.

Abacan MA. Abacan MA. Dev World Bioeth. 2021 Sep;21(3):139-146. doi: 10.1111/dewb.12281. Epub 2020 Aug 5. Dev World Bioeth. 2021. PMID: 32761747

2

Successful Implementation of Expanded Newborn Screening in the Philippines Using Tandem Mass Spectrometry.

Padilla CD, Therrell BL Jr, Alcausin MMLB, Chiong MAD, Abacan MAR, Reyes MEL, Jomento CM, Dizon-Escoreal MTT, Canlas MAE, Abadingo ME, Posecion JEWC, Abarquez CG, Andal AP, Elizaga ALG, Halili-Mendoza BC, Otayza MPVK, Millington DS. Padilla CD, et al. Among authors: abacan mar. Int J Neonatal Screen. 2022 Jan 19;8(1):8. doi: 10.3390/ijns8010008. Int J Neonatal Screen. 2022. PMID: 35225931 Free PMC article.

3

A review of the clinical outcomes in idursulfase-treated and untreated Filipino patients with mucopolysaccharidosis type II: data from the local lysosomal storage disease registry.

Racoma MJC, Calibag MKKB, Cordero CP, Abacan MAR, Chiong MAD. Racoma MJC, et al. Among authors: abacan mar. Orphanet J Rare Dis. 2021 Jul 21;16(1):323. doi: 10.1186/s13023-021-01875-5. Orphanet J Rare Dis. 2021. PMID: 34289859 Free PMC article. Review.

4

Pregnancy in an adolescent with maple syrup urine disease: Case report.

Abadingo ME, Abacan MAR, Basas JRU, Padilla CD. Abadingo ME, et al. Among authors: abacan mar. Mol Genet Metab Rep. 2021 Mar 26;27:100745. doi: 10.1016/j.ymgmr.2021.100745. eCollection 2021 Jun. Mol Genet Metab Rep. 2021. PMID: 33868929 Free PMC article.

5

Maple syrup urine disease associated with nephrotic syndrome in a Filipino child.

Maceda EBG, Abadingo ME, Magbanua-Calalo CJ, Dator MA, Resontoc LPR, Castro-Hamoy L, Abacan MAR, Chiong MAD, Estrada SC. Maceda EBG, et al. Among authors: abacan mar. BMJ Case Rep. 2021 Jul 29;14(7):e242689. doi: 10.1136/bcr-2021-242689. BMJ Case Rep. 2021. PMID: 34326111

6

Genetic and clinical characteristics of Filipino patients with Gaucher disease.

Chiong MAD, Racoma MJC, Abacan MAR. Chiong MAD, et al. Among authors: abacan mar. Mol Genet Metab Rep. 2018 Apr 5;15:110-115. doi: 10.1016/j.ymgmr.2018.03.010. eCollection 2018 Jun. Mol Genet Metab Rep. 2018. PMID: 30023299 Free PMC article.

7

Clinical, biochemical and molecular characteristics of Filipino patients with mucopolysaccharidosis type II - Hunter syndrome.

Chiong MA, Canson DM, Abacan MA, Baluyot MM, Cordero CP, Silao CL. Chiong MA, et al. Among authors: abacan ma. Orphanet J Rare Dis. 2017 Jan 11;12(1):7. doi: 10.1186/s13023-016-0558-0. Orphanet J Rare Dis. 2017. PMID: 28077157 Free PMC article.

8

Novel NSDHL gene variant for congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome.

Maceda EBG, Kratz LE, Ramos VME, Abacan MAR. Maceda EBG, et al. Among authors: abacan mar. BMJ Case Rep. 2020 Nov 2;13(11):e236859. doi: 10.1136/bcr-2020-236859. BMJ Case Rep. 2020. PMID: 33139364 Free PMC article.

9

Carnitine-acylcarnitine Translocase Deficiency with c.199-10T>G Mutation in Two Filipino Neonates Detected through Parental Carrier Testing.

Carmona SMG, Abacan MAR, Alcausin MMLB. Carmona SMG, et al. Among authors: abacan mar. Int J Neonatal Screen. 2023 Jan 11;9(1):4. doi: 10.3390/ijns9010004. Int J Neonatal Screen. 2023. PMID: 36648771 Free PMC article.

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