Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jalpa Pandya"'
Autor:
Amit C. Nathwani, Romuald Corbau, Petya Kalcheva, Emmaline Stotter, Erald Shehu, Jalpa Pandya, Fabrizio Comper, Clement Cocita, I-Mei Yu, Carlos Henrique Miranda, Natalie Northcott, Elisa Chisari, Rose Sheridan, Samantha Correia
Publikováno v:
Molecular Genetics and Metabolism. 132:S27-S28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8a97aad6f24912b4ed56ffb4911de33
https://doi.org/10.1016/j.ymgme.2020.12.047
https://doi.org/10.1016/j.ymgme.2020.12.047
Autor:
Natalie Northcott, Romuald Corbau, Ying Sun, Fabrizio Comper, Erald Shehu, Amit C. Nathwani, Rose Sheridan, Clement Cocita, Emmaline Stotter, Jalpa Pandya, I-Mei Yu, Jaminder Khinder, Petya Kalcheva, Samantha Correia, Benjamin Liou, Carlos Henrique Miranda, Elisa Chisari
Publikováno v:
Molecular Genetics and Metabolism. 132:S28-S29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aae5d07ac5b3f9fbd5e17732b5e3d979
https://doi.org/10.1016/j.ymgme.2020.12.050
https://doi.org/10.1016/j.ymgme.2020.12.050
Autor:
Venette Fannin, Natalie Northcott, Jaminder Khinder, Benjamin Liou, Elisa Chisari, Amit C. Nathwani, Miriam Canavese, Jalpa Pandya, Rachel Blackwood, Azadeh Kia, Romuald Corbau, Ying Sun, Rose Sheridan, Carlos Henrique Miranda, Allison P Dane
Publikováno v:
Molecular Genetics and Metabolism. 129:S110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da31d49f86bc22c8188f159463ddc8b7
https://doi.org/10.1016/j.ymgme.2019.11.283
https://doi.org/10.1016/j.ymgme.2019.11.283
Autor:
Olivier D. Christophe, Andreas Schulze, Elisa Chisari, Allison P Dane, Azadeh Kia, Jalpa Pandya, Maria Portillo, Fabrizio Comper, Renee Kober, Segen Negash, Cécile V. Denis, Jonathan H. Foley, Florian Sonntag, Hattie Ollerton, Samantha Correia, Jenny McIntosh, Jaminder Khinder, Rebecca Alade, Jey Jeyakumar, Clement Cocita, Caterina Casari, Romuald Corbau, Dodev Tihomir, Erald Shehu
Publikováno v:
Blood. 134:4638-4638
Background: Several first-generation gene therapies are currently in clinical trials for Haemophilia A. These trials have to date exhibited varying results including issues with large patient to patient variation in FVIII levels and lack of durabilit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::489ef7d4d8af0a5659b8f2114ee06f39
https://doi.org/10.1182/blood-2019-128490
https://doi.org/10.1182/blood-2019-128490
Autor:
Jalpa Pandya, Jey Jeyakumar, Rose Sheridan, Maria Portillo, Elisa Chisari, Miriam Canavese, Carlos Henrique Miranda, Clement Cocita, Amit C. Nathwani, Romuald Corbau, Jonathan H. Foley, Azadeh Kia, Allison P Dane, Jenny McIntosh
Publikováno v:
Blood. 134:3354-3354
Introduction: Gaucher disease (GD), one of the most common lysosomal storage disorders, is an autosomal recessive condition resulting from mutations in the GBA gene that codes for the b-glucocerebrosidase (GCase) enzyme. Over 90% of patients have typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ed9d03622a53774c9a13f35e51280bb
https://doi.org/10.1182/blood-2019-124280
https://doi.org/10.1182/blood-2019-124280