Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Souza, Carolina F.M."'
Autor:
dos Santos, Bruna B., Colonetti, Karina, Nalin, Tatiéle, de Oliveira, Bibiana M., de Souza, Carolina F.M., Spritzer, Poli Mara, Schwartz, Ida V.D.
Publikováno v:
In Nutrition November-December 2022 103-104
Autor:
Eisengart, Julie B., Rudser, Kyle D., Xue, Yong, Orchard, Paul, Miller, Weston, Lund, Troy, Van der Ploeg, Ans, Mercer, Jean, Jones, Simon, Mengel, Karl Eugen, Gökce, Seyfullah, Guffon, Nathalie, Giugliani, Roberto, de Souza, Carolina F.M., Shapiro, Elsa G., Whitley, Chester B.
Publikováno v:
In Genetics in Medicine November 2018 20(11):1423-1429
Publikováno v:
In The Pediatric Clinics of North America April 2018 65(2):247-265
Autor:
Bravo, Heydy, Neto, Eurico Camargo, Schulte, Jaqueline, Pereira, Jamile, Filho, Claudio Sampaio, Bittencourt, Fernanda, Sebastião, Fernanda, Bender, Fernanda, de Magalhães, Ana Paula Scholz, Guidobono, Régis, Trapp, Franciele Barbosa, Michelin-Tirelli, Kristiane, Souza, Carolina F.M., Rojas Málaga, Diana, Pasqualim, Gabriela, Brusius-Facchin, Ana Carolina, Giugliani, Roberto
Publikováno v:
In Molecular Genetics and Metabolism Reports September 2017 12:92-97
Autor:
Jacques, Carlos Eduardo Diaz, Donida, Bruna, Mescka, Caroline P., Rodrigues, Daiane G.B., Marchetti, Desirèe P., Bitencourt, Fernanda H., Burin, Maira G., de Souza, Carolina F.M., Giugliani, Roberto, Vargas, Carmen Regla
Publikováno v:
In BBA - Molecular Basis of Disease September 2016 1862(9):1608-1616
Autor:
Santos, Berenice L., de Souza, Carolina F.M., Schuler‐Faccini, Lavinia, Refosco, Lilia, Epifanio, Matias, Nalin, Tatiele, Vieira, Sandra M.G., Schwartz, Ida V.D.
Publikováno v:
In Jornal de Pediatria (Versao en Portugues) November-December 2014 90(6):572-579
Autor:
Vargas Carmen R., Barschak Alethéa G., Coelho Daniella M., Furlanetto Vivian, Souza Carolina F.M. de, Karam Simone M., Jardim Laura, Wajner Moacir, Giugliani Roberto
Publikováno v:
Genetics and Molecular Biology, Vol 23, Iss 4, Pp 697-701 (2000)
X-Linked adrenoleukodystrophy (X-ALD) is a hereditary disorder of the peroxisomal metabolism biochemically characterized by the accumulation of very long chain fatty acids (VLCFA) in tissues and biological fluids. The major accumulated acids are hexa
Externí odkaz:
https://doaj.org/article/3c15492ecff843baa10e28fe250c054b
Autor:
Schwartz, Ida V.D., Silva, Thiago O., Poswar, Fabiano O., Souza, Carolina F.M., Giugliani, Roberto
Publikováno v:
In Molecular Genetics and Metabolism February 2021 132(2):S98-S98
Autor:
Schwartz, Ida V.D., Randon, Dévora N., Ferraro, Lethicia C., de Souza, Carolina F.M., Horovitz, Dafne D.G., de Sá, Natan M., Brunoni, Decio
Publikováno v:
In Molecular Genetics and Metabolism February 2021 132(2):S97-S98
Autor:
Bender, Claubia Viegas, Visioli, Fernanda, Giugliani, Roberto, De Souza, Carolina F.M., Da Silveira, Heraldo L.D., John, Angela B., Rados, Pantelis V., Cavagni, Juliano, Souza, Natalia
Publikováno v:
In Molecular Genetics and Metabolism February 2021 132(2):S20-S20