Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Felipe Cavagnaro"'
Autor:
Paola Krall, Jean Grandy, Lillian Bolte, Jennie Salgado, Felipe Cavagnaro, Claudia González, Jose Luis Guerrero
Publikováno v:
Journal of Rare Diseases Research & Treatment. 8:1-8
Background Cystinosis is a rare disease caused by CTNS gene defects. The main clinical presentations are nephropathic infantile cystinosis (NIC) and nephropathic juvenile cystinosis (NJC); both develop chronic kidney disease (CKD) and extrarenal comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1c562ec6f2734134ab1a66cca9fa529
https://doi.org/10.29245/2572-9411/2023/1.1208
https://doi.org/10.29245/2572-9411/2023/1.1208
Publikováno v:
Current Pediatrics Reports. 10:214-226
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::742f273dda0fec6c42b6dcb852f0a51e
https://doi.org/10.1007/s40124-022-00275-y
https://doi.org/10.1007/s40124-022-00275-y
Autor:
Alejandra Aird, Macarena Lagos, Alexander Vargas-Hernández, Jennifer E. Posey, Zeynep Coban-Akdemir, Shalini Jhangiani, Emily M. Mace, Anaid Reyes, Alejandra King, Felipe Cavagnaro, Lisa R. Forbes, Ivan K. Chinn, James R. Lupski, Jordan S. Orange, Maria Cecilia Poli
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Nuclear factor kappa-B subunit 2 (NF-κB2/p100/p52), encoded by NFKB2 (MIM: 164012) belongs to the NF-κB family of transcription factors that play a critical role in inflammation, immunity, cell proliferation, differentiation and survival. Heterozyg
Externí odkaz:
https://doaj.org/article/1eab47348551429cb8c5a97383b3954c
Autor:
Paola Krall, Jean Antoine Grandy Henríquez, Lillian Bolte, Jennie Salgado, Felipe Cavagnaro, Claudia Gonzalez, Jose Luis Guerrero
Cystinosis is a rare disease caused by CTNS gene defects. The main clinical presentations are nephropathic infantile cystinosis (NIC) and nephropathic juvenile cystinosis (NJC); both develop chronic kidney disease (CKD) and extrarenal complications.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c001ebddf37425707cd6271a4af9d3af
https://doi.org/10.21203/rs.3.rs-1717027/v1
https://doi.org/10.21203/rs.3.rs-1717027/v1
Autor:
Felipe Cavagnaro Santa María
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 71, Iss 6, Pp 329-331 (2014)
Externí odkaz:
https://doaj.org/article/44c7f751b3664e92be8b284a0ec7af82
Publikováno v:
Revista chilena de pediatria. 91(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa996aa11ba10dcfd597e0009145bec2
https://pubmed.ncbi.nlm.nih.gov/33861841
https://pubmed.ncbi.nlm.nih.gov/33861841
Autor:
Raina, Rupesh, Vijayvargiya, Nina, Kalra, Riti, Hui-Kim Yap, Nair, Nikhil, Alhasan, Khalid, Montini, Giovanni, Narang, Aarushi, McCulloch, Mignon, Bonilla-Felix, Melvin, Bagga, Arvind, Mok, Quen, de Sousa Tavares, Marcelo, Koch, Vera, Schaefer, Franz, Felipe, Cavagnaro, Bunchman, Tim, Sethi, Sidharth
Publikováno v:
Frontiers in Nephrology; 10/5/2022, Vol. 2, p1-8, 8p
Autor:
Felipe, Cavagnaro Sm
Publikováno v:
Revista chilena de pediatria. 91(3)
The premature newborn faces extrauterine conditions with some systems still immature, both ana tomically and physiologically. The kidney finishes developing at the end of the third trimester of pregnancy, so it is especially exposed to alter its norm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3cda2f1d79452d6e767d6040d0b24a0
https://pubmed.ncbi.nlm.nih.gov/32730511
https://pubmed.ncbi.nlm.nih.gov/32730511
Publikováno v:
Revista chilena de pediatría v.89 n.1 2018
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Resumen: Introducción: La hiperamonemia neonatal secundaria a errores congénitos del metabolismo es una entidad poco frecuente pero con una alta tasa de secuelas neurológicas y mortalidad. El manejo médico inicial es en muchas ocasiones insuficie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::630c28a72059cb93e4949bcf9609c724
https://doi.org/10.4067/s0370-41062018000100074
https://doi.org/10.4067/s0370-41062018000100074
Publikováno v:
Revista chilena de pediatría v.89 n.1 2018
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Henoch- Schonlein purpura (HSP) or IgA Vasculitis is the most common childhood vasculitis. The classic tetrad of signs and symptoms include palpable purpura, arthralgia, abdominal pain and renal disease. The occurrence of hemorrhagic bullae in childr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b714d876d6a546b18362e7753ca7eb93
https://doi.org/10.4067/s0370-41062018000100103
https://doi.org/10.4067/s0370-41062018000100103