Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Adriana M. Montano"'
Autor:
Adriana M. Montano, Agnieszka Różdżyńska-Świątkowska, Agnieszka Jurecka, Antonio Nino Ramirez, Lin Zhang, Raymond Y. Wang, Paul Harmatz
Publikováno v:
Molecular Genetics and Metabolism. 132:S72
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8adf25924baad61676dd342709578aa0
https://doi.org/10.1016/j.ymgme.2020.12.167
https://doi.org/10.1016/j.ymgme.2020.12.167
Autor:
Adriana M. Montaño, Agnieszka Różdżyńska-Świątkowska, Agnieszka Jurecka, Antonio Nino Ramirez, Lin Zhang, Deborah Marsden, Raymond Y. Wang, Paul Harmatz
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 36, Iss , Pp 100987- (2023)
Objective: This study assessed growth patterns in patients with mucopolysaccharidosis (MPS) VII before enzyme replacement therapy. Methods: Height, weight, and body mass index (BMI) measurements and Z-scores from patients from three clinical studies
Externí odkaz:
https://doaj.org/article/68199889bc9745e98000b49f745e7638
Autor:
Michael Flanagan, Isha Pathak, Qi Gan, Linda Winter, Ryan Emnet, Salem Akel, Adriana M. Montaño
Publikováno v:
Stem Cell Research & Therapy, Vol 12, Iss 1, Pp 1-15 (2021)
Abstract Background Mucopolysaccharidosis IVA (Morquio A syndrome) is a lysosomal storage disease caused by the deficiency of enzyme N-acetylgalactosamine-6-sulfate sulfatase (GALNS), which results in the accumulation of the glycosaminoglycans (GAGs)
Externí odkaz:
https://doaj.org/article/726e1a7edffd48e9bad9c093cd83e3c2
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-10 (2021)
Abstract Background Mucopolysaccharidoses (MPS) are rare, inherited lysosomal storage disorders characterized by progressive multiorgan involvement. Previous studies on incidence and prevalence of MPS mainly focused on countries other than the United
Externí odkaz:
https://doaj.org/article/47a8bd86f0bc421ba6a0c88b4076d177
Autor:
Michael Flanagan, Qi Gan, Saahil Sheth, Rachel Schafer, Samuel Ruesing, Linda E. Winter, Karoly Toth, Silviya P. Zustiak, Adriana M. Montaño
Publikováno v:
Pharmaceuticals, Vol 16, Iss 7, p 931 (2023)
Morquio A disease is a genetic disorder resulting in N-acetylgalactosamine-6-sulfate sulfatase (GALNS) deficiency, and patients are currently treated with enzyme replacement therapy via weekly intravenous enzyme infusions. A means of sustained enzyme
Externí odkaz:
https://doaj.org/article/691a9fc5717e47bbbcfa0a2a77ce3452
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Cardiovascular disease (CVD) in Mucopolysaccharidosis Type IVA (Morquio A), signified by valvular disease and cardiac hypertrophy, is the second leading cause of death and remains untouched by current therapies. Enzyme replacement therapy (ERT) is th
Externí odkaz:
https://doaj.org/article/fb67f276dbe54b9fb028095bad7a5ca2
Autor:
Raymond Y. Wang, Kyle D. Rudser, Donald R. Dengel, Nicholas Evanoff, Julia Steinberger, Nina Movsesyan, Robert Garrett, Katherine Christensen, Deborah Boylan, Stephen R. Braddock, Marwan Shinawi, Qi Gan, Adriana M. Montaño
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Cardiovascular disease frequently causes morbidity and mortality in mucopolysaccharidoses (MPS); however, cardiovascular anatomy and dysfunction in MPS IVA (Morquio A disease) is not well described. Consequently, the study aimed t
Externí odkaz:
https://doaj.org/article/86c21a6f386d4ecdb984bab4aa309028
Autor:
Shunji Tomatsu, Tsutomu Shimada, Robert W. Mason, Adriana M. Montaño, Joan Kelly, William A. LaMarr, Francyne Kubaski, Roberto Giugliani, Aratrik Guha, Eriko Yasuda, William Mackenzie, Seiji Yamaguchi, Yasuyuki Suzuki, Tadao Orii
Publikováno v:
Metabolites, Vol 4, Iss 3, Pp 655-679 (2014)
Mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders caused by deficiency of the lysosomal enzymes essential for catabolism of glycosaminoglycans (GAGs). Accumulation of undegraded GAGs results in dysfunction of multiple organs, res
Externí odkaz:
https://doaj.org/article/f1c6d7024dc24975b8e510fd50856ea4
Autor:
Jonathan P. Hintze, Shunji Tomatsu, Tadashi Fujii, Adriana M. Montaño, Seiji Yamaguchi, Yasuyuki Suzuki, Masaru Fukushi, Takeshi Ishimaru, Tadao Orii
Publikováno v:
Biomarker Insights, Vol 2011, Iss 6, Pp 69-78 (2011)
Externí odkaz:
https://doaj.org/article/ea048576f73b422f9eb7281ce0facf3e