Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Janaina Nogueira"'
Autor:
Janaina Nogueira Anderson, Zineb Ammous, Yasemen Eroglu, Erick Hernandez, James Heubi, Ryan Himes, Sirish Palle
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-13 (2021)
Abstract Background Zellweger spectrum disorders (ZSDs) are a rare, heterogenous group of autosomal recessively inherited disorders characterized by reduced peroxisomes numbers, impaired peroxisomal formation, and/or defective peroxisomal functioning
Externí odkaz:
https://doaj.org/article/a45a422967144db6a090a288c29189f1
Autor:
Dana M. H. Dykes, Sean R. Moore, D. Brent Polk, Michael J. Rosen, Marcia L. Wills, Brian Morris, Jeanine S. Maclin, Janaina Nogueira, Avi Katz, Tracey E. Hunley, Judith Pugh, Shehzad Saeed
Publikováno v:
Case Reports in Pediatrics, Vol 2012 (2012)
Mycophenolate mofetil (MMF) is an immunosuppressive medication utilized in the management of both autoimmune and solid organ transplant patients. Diarrhea is a common gastrointestinal side effect of MMF, but more severe forms of GI symptoms are descr
Externí odkaz:
https://doaj.org/article/b0b0e9376994423887b49d1b269fad24
Autor:
Regina Brostolin, Marta1 brosto@ucdb.br, Maia Carvalho, Janaina Nogueira1 janaina.maia@ufms.br
Publikováno v:
Interações. Jan-Mar2023, Vol. 24 Issue 1, p343-356. 14p.
Publikováno v:
Interações (Campo Grande), Volume: 24, Issue: 1, Pages: 343-356, Published: 26 JUN 2023
Resumo A região do Pantanal sul-mato-grossense, por meio da implantação de suas escolas-fazenda, abre possibilidades para investigações e, nesse contexto, emerge este texto, que apresenta um recorte de uma pesquisa de doutoramento. A investigaç
Autor:
Anderson, Janaina Nogueira1 (AUTHOR) nogueirj@musc.edu, Ammous, Zineb2 (AUTHOR), Eroglu, Yasemen3 (AUTHOR), Hernandez, Erick4 (AUTHOR), Heubi, James5 (AUTHOR), Himes, Ryan6 (AUTHOR), Palle, Sirish7 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 9/14/2021, Vol. 16 Issue 1, p1-13. 13p.
Publikováno v:
ACG Case Reports Journal; Feb2024, Vol. 11 Issue 2, p1-3, 3p
Autor:
Janaina Nogueira, Meghan Sullivan, Sirish Palle, Charina M. Ramirez, Gregory M. Enns, Zineb Ammous, Ryan Himes
Publikováno v:
Molecular Genetics and Metabolism. 134:217-222
Peroxisome Biogenesis Disorders-Zellweger spectrum disorder (PBD-ZSD) is a rare, autosomal recessive peroxisome biogenesis disorder that presents with variable symptoms. In patients with PBD-ZSD, pathogenic variants in the PEX family of genes disrupt
Autor:
Ana Flávia Soares de Oliveira, Janaina Nogueira da Silva, Daniela Freitas Borges, Emerson Carlos Guimarães, Ayonara Cristina da Silva, Aurea Messias de Jesus
Publikováno v:
Engenharia em foco v.5 ISBN: 9786581028756
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b1e9aabc414a9b10e86a6bdbb0521bb
https://doi.org/10.35587/brj.ed.0001930
https://doi.org/10.35587/brj.ed.0001930
Autor:
Edward P. Acosta, Megan Smith, Hector H. Gutierrez, Luz Helena Gutierrez Sanchez, Kevin J. Ryan, Jennifer S. Guimbellot, Janaina Nogueira Anderson, Kim W. Benner
Publikováno v:
J Cyst Fibros
The CFTR modulator combination elexacaftor/tezacaftor/ivacaftor (ETI) is a genetic mutation-targeted treatment in cystic fibrosis that results in profound improvements in clinical outcomes. Each of the compounds are substrates of CYP3A4/5, the cytoch
Autor:
Kevin J. Ryan, J. Natt, Latona Kersh, Zhongyu Liu, Jennifer S. Guimbellot, Edward P. Acosta, Janaina Nogueira Anderson
Publikováno v:
Journal of Cystic Fibrosis. 20:S86-S87