Couce ML - Search Results

1

Gene Therapy for Neuronopathic Mucopolysaccharidoses: State of the Art.

de Castro MJ, Del Toro M, Giugliani R, Couce ML. de Castro MJ, et al. Among authors: couce ml. Int J Mol Sci. 2021 Aug 25;22(17):9200. doi: 10.3390/ijms22179200. Int J Mol Sci. 2021. PMID: 34502108 Free PMC article. Review.

2

Proteomic Analysis in Morquio A Cells Treated with Immobilized Enzymatic Replacement Therapy on Nanostructured Lipid Systems.

Álvarez JV, Bravo SB, García-Vence M, De Castro MJ, Luzardo A, Colón C, Tomatsu S, Otero-Espinar FJ, Couce ML. Álvarez JV, et al. Among authors: couce ml. Int J Mol Sci. 2019 Sep 18;20(18):4610. doi: 10.3390/ijms20184610. Int J Mol Sci. 2019. PMID: 31540344 Free PMC article.

3

Bone Status in Patients with Phenylketonuria: A Systematic Review.

de Castro MJ, de Lamas C, Sánchez-Pintos P, González-Lamuño D, Couce ML. de Castro MJ, et al. Among authors: couce ml. Nutrients. 2020 Jul 20;12(7):2154. doi: 10.3390/nu12072154. Nutrients. 2020. PMID: 32698408 Free PMC article.

4

Rapid Phenotype-Driven Gene Sequencing with the NeoSeq Panel: A Diagnostic Tool for Critically Ill Newborns with Suspected Genetic Disease.

de Castro MJ, González-Vioque E, Barbosa-Gouveia S, Salguero E, Rite S, López-Suárez O, Pérez-Muñuzuri A, Couce ML. de Castro MJ, et al. Among authors: couce ml. J Clin Med. 2020 Jul 23;9(8):2362. doi: 10.3390/jcm9082362. J Clin Med. 2020. PMID: 32718099 Free PMC article.

5

Tyrosinemia type 1 in Spain: mutational analysis, treatment and long-term outcome.

Couce ML, Dalmau J, del Toro M, Pintos-Morell G, Aldámiz-Echevarría L; Spanish Working Group on Tyrosinemia type 1. Couce ML, et al. Pediatr Int. 2011 Dec;53(6):985-9. doi: 10.1111/j.1442-200X.2011.03427.x. Pediatr Int. 2011. PMID: 21752152

6

Effects of LC-PUFA Supplementation in Patients with Phenylketonuria: A Systematic Review of Controlled Trials.

Couce ML, de Castro MJ, de Lamas C, Leis R. Couce ML, et al. Nutrients. 2019 Jul 6;11(7):1537. doi: 10.3390/nu11071537. Nutrients. 2019. PMID: 31284588 Free PMC article.

7

Rapid Molecular Diagnosis of Genetically Inherited Neuromuscular Disorders Using Next-Generation Sequencing Technologies.

Barbosa-Gouveia S, Vázquez-Mosquera ME, González-Vioque E, Hermida-Ameijeiras Á, Sánchez-Pintos P, de Castro MJ, León SR, Gil-Fournier B, Domínguez-González C, Camacho Salas A, Negrão L, Fineza I, Laranjeira F, Couce ML. Barbosa-Gouveia S, et al. Among authors: couce ml. J Clin Med. 2022 May 12;11(10):2750. doi: 10.3390/jcm11102750. J Clin Med. 2022. PMID: 35628876 Free PMC article.

8

Effects of Dairy Product Consumption on Height and Bone Mineral Content in Children: A Systematic Review of Controlled Trials.

de Lamas C, de Castro MJ, Gil-Campos M, Gil Á, Couce ML, Leis R. de Lamas C, et al. Among authors: couce ml. Adv Nutr. 2019 May 1;10(suppl_2):S88-S96. doi: 10.1093/advances/nmy096. Adv Nutr. 2019. PMID: 31089738 Free PMC article.

9

Longitudinal Natural History of Pediatric Subjects Affected with Mucopolysaccharidosis IIIB.

Okur I, Ezgu F, Giugliani R, Muschol N, Koehn A, Amartino H, Harmatz P, de Castro Lopez MJ, Couce ML, Lin SP, Batzios S, Cleary M, Solano M, Peters H, Lee J, Nestrasil I, Shaywitz AJ, Maricich SM, Kuca B, Kovalchin J, Zanelli E. Okur I, et al. Among authors: couce ml. J Pediatr. 2022 Oct;249:50-58.e2. doi: 10.1016/j.jpeds.2022.06.005. Epub 2022 Jun 13. J Pediatr. 2022. PMID: 35709957 Free article.

10

Mucopolysaccharidosis IVA: Diagnosis, Treatment, and Management.

Sawamoto K, Álvarez González JV, Piechnik M, Otero FJ, Couce ML, Suzuki Y, Tomatsu S. Sawamoto K, et al. Among authors: couce ml. Int J Mol Sci. 2020 Feb 23;21(4):1517. doi: 10.3390/ijms21041517. Int J Mol Sci. 2020. PMID: 32102177 Free PMC article. Review.

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