Distrofia neuroaxonal infantil (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Distrofia neuroaxonal infantil" in Spanish language version.

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1clinicaltrials.gov

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cell.com

Bellen, Hugo J.; Wang, Liping; Lin, Wen-Wen; Zuo, Zhongyuan; Tan, Kai Li; Mao, Dongxue; Chen, Kuchuan; Lee, Pei-Tseng et al. (2 de octubre de 2018). «Phospholipase PLA2G6, a Parkinsonism-Associated Gene, Affects Vps26 and Vps35, Retromer Function, and Ceramide Levels, Similar to α-Synuclein Gain». Cell Metabolism (en inglés) 28 (4): 605-618.e6. ISSN 1550-4131. PMID 29909971. doi:10.1016/j.cmet.2018.05.019.

clinicaltrials.gov

Retrotope, Inc. (6 de octubre de 2021). A Prospective Open-label Study to Assess Efficacy and Safety of RT001 in Subjects With Infantile Neuroaxonal Dystrophy (NCT03570931). clinicaltrials.gov. Consultado el 9 de marzo de 2022.

doi.org

dx.doi.org

«Schindler disease: the molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes an infantile neuroaxonal dystrophy». J. Clin. Invest. 86 (5): 1752-6. November 1990. PMC 296929. PMID 2243144. doi:10.1172/JCI114901.
Bellen, Hugo J.; Wang, Liping; Lin, Wen-Wen; Zuo, Zhongyuan; Tan, Kai Li; Mao, Dongxue; Chen, Kuchuan; Lee, Pei-Tseng et al. (2 de octubre de 2018). «Phospholipase PLA2G6, a Parkinsonism-Associated Gene, Affects Vps26 and Vps35, Retromer Function, and Ceramide Levels, Similar to α-Synuclein Gain». Cell Metabolism (en inglés) 28 (4): 605-618.e6. ISSN 1550-4131. PMID 29909971. doi:10.1016/j.cmet.2018.05.019.

issn.org

portal.issn.org

Bellen, Hugo J.; Wang, Liping; Lin, Wen-Wen; Zuo, Zhongyuan; Tan, Kai Li; Mao, Dongxue; Chen, Kuchuan; Lee, Pei-Tseng et al. (2 de octubre de 2018). «Phospholipase PLA2G6, a Parkinsonism-Associated Gene, Affects Vps26 and Vps35, Retromer Function, and Ceramide Levels, Similar to α-Synuclein Gain». Cell Metabolism (en inglés) 28 (4): 605-618.e6. ISSN 1550-4131. PMID 29909971. doi:10.1016/j.cmet.2018.05.019.

nih.gov

ncbi.nlm.nih.gov

«Schindler disease: the molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes an infantile neuroaxonal dystrophy». J. Clin. Invest. 86 (5): 1752-6. November 1990. PMC 296929. PMID 2243144. doi:10.1172/JCI114901.
Bellen, Hugo J.; Wang, Liping; Lin, Wen-Wen; Zuo, Zhongyuan; Tan, Kai Li; Mao, Dongxue; Chen, Kuchuan; Lee, Pei-Tseng et al. (2 de octubre de 2018). «Phospholipase PLA2G6, a Parkinsonism-Associated Gene, Affects Vps26 and Vps35, Retromer Function, and Ceramide Levels, Similar to α-Synuclein Gain». Cell Metabolism (en inglés) 28 (4): 605-618.e6. ISSN 1550-4131. PMID 29909971. doi:10.1016/j.cmet.2018.05.019.

orpha.net

RESERVADOS, INSERM US14 -- TODOS LOS DERECHOS. «Orphanet: Infantile neuroaxonal dystrophy». www.orpha.net. Consultado el 11 de marzo de 2022.