Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ana I, Coelho"'
Autor:
Minela Haskovic, Britt Derks, Liesbeth van der Ploeg, Jorn Trommelen, Jean Nyakayiru, Luc J. C. van Loon, Sabrina Mackinnon, Wyatt W. Yue, Roy W. A. Peake, Li Zha, Didem Demirbas, Wanshu Qi, Xiaoping Huang, Gerard T. Berry, Jelle Achten, Jörgen Bierau, M. Estela Rubio-Gozalbo, Ana I. Coelho
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
Abstract Background Classic galactosemia is a rare genetic metabolic disease with an unmet treatment need. Current standard of care fails to prevent chronically-debilitating brain and gonadal complications. Many mutations in the GALT gene responsible
Externí odkaz:
https://doaj.org/article/14f787f239734944a06747ee7ac1581c
Autor:
Jo Vanoevelen, Ana I. Coelho, M. Estela Rubio-Gozalbo, Jörgen Bierau, Laura K.M. Steinbusch, Minela Haskovic, Gerard T. Berry, Eduardo Villamor-Martinez, Luc J. I. Zimmermann
Publikováno v:
Journal of Inherited Metabolic Disease
Since the first description of galactosemia in 1908 and despite decades of research, the pathophysiology is complex and not yet fully elucidated. Galactosemia is an inborn error of carbohydrate metabolism caused by deficient activity of any of the ga
Autor:
Jörgen Bierau, Martijn Lindhout, M. Estela Rubio-Gozalbo, Fokje Zijlstra, Ana I. Coelho, Minela Haskovic, Raisa Veizaj, Dirk Lefeber, Rein Vos, Jo Vanoevelen
Publikováno v:
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, 43, 994-1001
Journal of Inherited Metabolic Disease, 43(5), 994-1001. Wiley
Journal of Inherited Metabolic Disease, 43, 5, pp. 994-1001
Journal of Inherited Metabolic Disease, 43, 994-1001
Journal of Inherited Metabolic Disease, 43(5), 994-1001. Wiley
Journal of Inherited Metabolic Disease, 43, 5, pp. 994-1001
Nucleotide sugars (NS) are fundamental molecules in life and play a key role in glycosylation reactions and signal conduction. Several pathways are involved in the synthesis of NS. The Leloir pathway, the main pathway for galactose metabolism, is cru
Autor:
Britt Delnoy, Minela Haskovic, Jo Vanoevelen, Laura K. M. Steinbusch, Esther Naomi Vos, Kèvin Knoops, Luc J. I. Zimmermann, Marek Noga, Dirk J. Lefeber, Paolo G. V. Martini, Ana I. Coelho, Maria Estela Rubio‐Gozalbo
Publikováno v:
Journal of Inherited Metabolic Disease, 45, 748-758
Journal of Inherited Metabolic Disease, 45(4), 748-758. Wiley
Journal of Inherited Metabolic Disease, 45, 4, pp. 748-758
Journal of Inherited Metabolic Disease, 45(4), 748-758. Wiley
Journal of Inherited Metabolic Disease, 45, 4, pp. 748-758
Contains fulltext : 282590.pdf (Publisher’s version ) (Open Access) Messenger RNA (mRNA) has emerged as a novel therapeutic approach for inborn errors of metabolism. Classic galactosemia (CG) is an inborn error of galactose metabolism caused by a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52e2f4c19e9e2710f907c35fdb0be565
http://hdl.handle.net/2066/282590
http://hdl.handle.net/2066/282590
Publikováno v:
Journal of Personalized Medicine
Journal of Personalized Medicine, Vol 11, Iss 75, p 75 (2021)
Journal of Personalized Medicine, Vol 11, Iss 75, p 75 (2021)
Type I (classic) galactosemia, galactose 1-phosphate uridylyltransferase (GALT)-deficiency is a hereditary disorder of galactose metabolism. The current therapeutic standard of care, a galactose-restricted diet, is effective in treating neonatal comp
Publikováno v:
Metabolism-Clinical and Experimental, 83, 188-196. W B Saunders Co-Elsevier Inc
Metabolism
Metabolism
Hereditary galactosemia is an inborn error of carbohydrate metabolism. Galactose is metabolized by Leloir pathway enzymes; galactokinase (GALK), galactose-1-phosphate uridylyltransferase (GALT) and UDP-galactose 4-epimerase (GALE). The defects in the
Autor:
Britt van Erven, M. Estela Rubio-Gozalbo, Gerard T. Berry, Xiaoping Huang, Ana I. Coelho, Jo Vanoevelen, Jörgen Bierau, Rein Vos
Publikováno v:
Journal of Inherited Metabolic Disease, 41(1), 117-127. Wiley
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease
Classic galactosemia is a genetic disorder of galactose metabolism, caused by severe deficiency of galactose-1-phosphate uridylyltransferase (GALT) enzyme activity due to mutations of the GALT gene. Its pathogenesis is still not fully elucidated, and
Autor:
Jörgen Bierau, Boris W. Kramer, Jelle Achten, Martijn Lindhout, Ana I. Coelho, M. Estela Rubio-Gozalbo
Publikováno v:
The Anatomical Record. 300:1570-1575
Classic galactosemia results from deficient activity of galactose-1-phosphate uridylyltransferase (GALT), a key enzyme of galactose metabolism. Despite early diagnosis and early postnatal therapeutic intervention, patients still develop neurologic an
Publikováno v:
Journal of Inherited Metabolic Disease
Classic galactosemia is a rare inherited disorder of galactose metabolism caused by deficient activity of galactose-1-phosphate uridylyltransferase (GALT), the second enzyme of the Leloir pathway. It presents in the newborn period as a life-threateni
Autor:
A Thijs, Patrícia Janeiro, Ina Knerr, Ana I. Coelho, Aurélie Hubert, Dirk Müller-Wieland, Philippe Labrune, D Ramadza, M T Forga, Isabel Rivera, Rein Vos, Saskia B. Wortmann, María L. Couce, Gerard T. Berry, Christel Tran, Elaine Murphy, Didem Demirbas, Roshni Vara, Charlotte Dawson, Janneke G. Langendonk, Katrin Õunap, Mendy M. Welsink-Karssies, M Haskovic, Eileen P. Treacy, Johannes Häberle, Matthias Gautschi, Annet M. Bosch, Stephanie Grunewald, Gepke Visser, Birute Burnyte, S Scholl-Buergi, David Cassiman, M. E. Rubio-Gozalbo, Susan E. Waisbren, Yuval Landau, François Eyskens, Karolina M. Stepien, Jorg Kotzka, H H Huidekoper, Michel Hochuli, Dorothea Möslinger, Terry G J Derks, M.S. de Vries
Publikováno v:
Orphanet journal of rare diseases, 14(1):86. BMC
Rubio-Gozalbo, M E; Haskovic, M; Bosch, A M; Burnyte, B; Coelho, A I; Cassiman, D; Couce, M L; Dawson, C; Demirbas, D; Derks, T; Eyskens, F; Forga, M T; Grunewald, S; Häberle, J; Hochuli, M; Hubert, A; Huidekoper, H H; Janeiro, P; Kotzka, J; Knerr, I; ... (2019). The natural history of classic galactosemia: lessons from the GalNet registry. Orphanet journal of rare diseases, 14(1), p. 86. BioMed Central 10.1186/s13023-019-1047-z
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Orphanet journal of rare diseases
Orphanet journal of rare diseases, London : BioMed Central Ltd., 2019, vol. 14, art. no 86, p. [1-11]
Orphanet journal of rare diseases, 14(1):86. BioMed Central
Orphanet journal of rare diseases, vol. 14, no. 1, pp. 86
Orphanet Journal of Rare Diseases, 14:86. BioMed Central Ltd.
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Orphanet Journal of Rare Diseases, 14:86. BioMed Central Ltd
Rubio-Gozalbo, M E, Haskovic, M, Bosch, A M, Burnyte, B, Coelho, A I, Cassiman, D, Couce, M L, Dawson, C, Demirbas, D, Derks, T, Eyskens, F, Forga, M T, Grunewald, S, Häberle, J, Hochuli, M, Hubert, A, Huidekoper, H H, Janeiro, P, Kotzka, J, Knerr, I, Labrune, P, Landau, Y E, Langendonk, J G, Möslinger, D, Müller-Wieland, D, Murphy, E, Õunap, K, Ramadza, D, Rivera, I A, Scholl-Buergi, S, Stepien, K M, Thijs, A, Tran, C, Vara, R, Visser, G, Vos, R, de Vries, M, Waisbren, S E, Welsink-Karssies, M M, Wortmann, S B, Gautschi, M, Treacy, E P & Berry, G T 2019, ' The natural history of classic galactosemia: Lessons from the GalNet registry ', Orphanet Journal of Rare Diseases, vol. 14, no. 1, 86 . https://doi.org/10.1186/s13023-019-1047-z
Orphanet Journal of Rare Diseases, 14(1). BioMed Central
Orphanet Journal of Rare Diseases, 14(1):86. BioMed Central
Rubio-Gozalbo, M E; Haskovic, M; Bosch, A M; Burnyte, B; Coelho, A I; Cassiman, D; Couce, M L; Dawson, C; Demirbas, D; Derks, T; Eyskens, F; Forga, M T; Grunewald, S; Häberle, J; Hochuli, M; Hubert, A; Huidekoper, H H; Janeiro, P; Kotzka, J; Knerr, I; ... (2019). The natural history of classic galactosemia: lessons from the GalNet registry. Orphanet journal of rare diseases, 14(1), p. 86. BioMed Central 10.1186/s13023-019-1047-z
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Orphanet journal of rare diseases
Orphanet journal of rare diseases, London : BioMed Central Ltd., 2019, vol. 14, art. no 86, p. [1-11]
Orphanet journal of rare diseases, 14(1):86. BioMed Central
Orphanet journal of rare diseases, vol. 14, no. 1, pp. 86
Orphanet Journal of Rare Diseases, 14:86. BioMed Central Ltd.
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Orphanet Journal of Rare Diseases, 14:86. BioMed Central Ltd
Rubio-Gozalbo, M E, Haskovic, M, Bosch, A M, Burnyte, B, Coelho, A I, Cassiman, D, Couce, M L, Dawson, C, Demirbas, D, Derks, T, Eyskens, F, Forga, M T, Grunewald, S, Häberle, J, Hochuli, M, Hubert, A, Huidekoper, H H, Janeiro, P, Kotzka, J, Knerr, I, Labrune, P, Landau, Y E, Langendonk, J G, Möslinger, D, Müller-Wieland, D, Murphy, E, Õunap, K, Ramadza, D, Rivera, I A, Scholl-Buergi, S, Stepien, K M, Thijs, A, Tran, C, Vara, R, Visser, G, Vos, R, de Vries, M, Waisbren, S E, Welsink-Karssies, M M, Wortmann, S B, Gautschi, M, Treacy, E P & Berry, G T 2019, ' The natural history of classic galactosemia: Lessons from the GalNet registry ', Orphanet Journal of Rare Diseases, vol. 14, no. 1, 86 . https://doi.org/10.1186/s13023-019-1047-z
Orphanet Journal of Rare Diseases, 14(1). BioMed Central
Orphanet Journal of Rare Diseases, 14(1):86. BioMed Central
Background: Classic galactosemia is a rare inborn error of carbohydrate metabolism, caused by a severe deficiency of the enzyme galactose-1-phosphate uridylyltransferase (GALT). A galactose-restricted diet has proven to be very effective to treat the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9621af2463fe452b8a626ef40cc6ee1a
https://research.rug.nl/en/publications/cec5aa55-6214-4b55-8fc1-1667be0be520
https://research.rug.nl/en/publications/cec5aa55-6214-4b55-8fc1-1667be0be520