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Long-term enzyme-replacement therapy (ERT) with alglucosidase alfa: Evolution of two siblings with juvenile late-onset Pompe disease.
J Neurol Sci. 2015 Nov 15; 358(1-2):459-60.JN

Authors+Show Affiliations

Department of Paediatrics, University Hospital Doctor Peset, Valencia, Spain; University of Valencia, Spain. Electronic address: jbretonmar@gmail.com.Department of Paediatrics, University Hospital Doctor Peset, Valencia, Spain.

Pub Type(s)

Case Reports
Letter
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

26279333

Citation

Rafael Bretón Martínez, J, and Andrés Cánovas Martínez. "Long-term Enzyme-replacement Therapy (ERT) With Alglucosidase Alfa: Evolution of Two Siblings With Juvenile Late-onset Pompe Disease." Journal of the Neurological Sciences, vol. 358, no. 1-2, 2015, pp. 459-60.
Rafael Bretón Martínez J, Martínez AC. Long-term enzyme-replacement therapy (ERT) with alglucosidase alfa: Evolution of two siblings with juvenile late-onset Pompe disease. J Neurol Sci. 2015;358(1-2):459-60.
Rafael Bretón Martínez, J., & Martínez, A. C. (2015). Long-term enzyme-replacement therapy (ERT) with alglucosidase alfa: Evolution of two siblings with juvenile late-onset Pompe disease. Journal of the Neurological Sciences, 358(1-2), 459-60. https://doi.org/10.1016/j.jns.2015.08.007
Rafael Bretón Martínez J, Martínez AC. Long-term Enzyme-replacement Therapy (ERT) With Alglucosidase Alfa: Evolution of Two Siblings With Juvenile Late-onset Pompe Disease. J Neurol Sci. 2015 Nov 15;358(1-2):459-60. PubMed PMID: 26279333.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Long-term enzyme-replacement therapy (ERT) with alglucosidase alfa: Evolution of two siblings with juvenile late-onset Pompe disease. AU - Rafael Bretón Martínez,J, AU - Martínez,Andrés Cánovas, Y1 - 2015/08/07/ PY - 2015/06/11/received PY - 2015/07/14/revised PY - 2015/08/05/accepted PY - 2015/8/18/entrez PY - 2015/8/19/pubmed PY - 2016/9/16/medline KW - Enzyme-replacement therapy KW - Juvenile late-onset Pompe disease KW - Late-onset Pompe disease KW - Pompe disease SP - 459 EP - 60 JF - Journal of the neurological sciences JO - J. Neurol. Sci. VL - 358 IS - 1-2 SN - 1878-5883 UR - https://www.unboundmedicine.com/medline/citation/26279333/Long_term_enzyme_replacement_therapy__ERT__with_alglucosidase_alfa:_Evolution_of_two_siblings_with_juvenile_late_onset_Pompe_disease_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0022-510X(15)00500-6 DB - PRIME DP - Unbound Medicine ER -