Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Wilfredo De Jesús Rojas"'
Autor:
Sonya J. Malavez-Cajigas, Fabiana I. Marini-Martinez, Mercedes Lacourt-Ventura, Karla J. Rosario-Pacheco, Natalia M. Ortiz-Perez, Bethzaly Velazquez-Perez, Wilfredo De Jesús-Rojas, Daniel S. Chertow, Jeffrey R. Strich, Marcos J. Ramos-Benítez
Publikováno v:
Heliyon, Vol 10, Iss 16, Pp e36386- (2024)
Neutrophil Extracellular Traps (NETs) present a paradoxical role in infectious diseases, contributing to both immunity and pathogenesis. The complex nature of this process necessitates further characterization to elucidate its clinical implications.
Externí odkaz:
https://doaj.org/article/2953a90a615f482497fcdba9c53ed978
Autor:
Hina Emanuel, Aravind Yadav, Julie C. Eapan, Maria Caldas-Vasquez, Tomika S. Harris, Katrina McBeth, Fatima Boricha, Janice John, Ivan G. Magana Ceballos., Giuseppe N. Colasurdo, Maria E. Tellez, Tina Reddy, Wilfredo De Jesús-Rojas, Ricardo A. Mosquera
Publikováno v:
Children, Vol 11, Iss 10, p 1171 (2024)
Background: In-home palivizumab administration programs (PH) have shown promise in reducing RSV-associated infections. These programs may be particularly beneficial for children with medical complexity (CMC) by limiting their exposure to healthcare-a
Externí odkaz:
https://doaj.org/article/5e5a6dfc4ba543be86c1bb7cc208d531
Autor:
Zachary J. Demetriou, José Muñiz-Hernández, Gabriel Rosario-Ortiz, Frances M. Quiñones, Gabriel Gonzalez-Diaz, Marcos J. Ramos-Benitez, Ricardo A. Mosquera, Wilfredo De Jesús-Rojas
Publikováno v:
Diagnostics, Vol 14, Iss 16, p 1814 (2024)
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder characterized by alterations in motile cilia function. The diagnosis of PCD is challenging due to the lack of standardized methods in clinical practice. High-speed video microscopy analysis
Externí odkaz:
https://doaj.org/article/e2fda1dc655f453f9ed7aaa35d30ba81
Autor:
Wilfredo De Jesús-Rojas, Zachary J. Demetriou, José Muñiz-Hernández, Gabriel Rosario-Ortiz, Frances M. Quiñones, Marcos J. Ramos-Benitez, Ricardo A. Mosquera
Publikováno v:
Cells, Vol 13, Iss 7, p 567 (2024)
Primary ciliary dyskinesia (PCD) is an inherited disorder that impairs motile cilia, essential for respiratory health, with a reported prevalence of 1 in 16,309 within Hispanic populations. Despite 70% of Puerto Rican patients having the RSPH4A [c.92
Externí odkaz:
https://doaj.org/article/d671d81613a84fea9484924b21c1568d
Autor:
Wilfredo De Jesús-Rojas, Luis Reyes-Peña, José Muñiz-Hernández, Patricia Quiles Ruiz de Porras, Jesús Meléndez-Montañez, Marcos J. Ramos-Benitez, Ricardo A. Mosquera
Publikováno v:
Diagnostics, Vol 13, Iss 13, p 2287 (2023)
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder that results from the dysfunction of motile cilia, which can cause chronic upper and lower respiratory infections leading to bronchiectasis. However, there is a need for additional t
Externí odkaz:
https://doaj.org/article/0d587eb5bc2943489a49bd0699364141
Publikováno v:
Children, Vol 10, Iss 2, p 280 (2023)
CFTR-related metabolic syndrome (CRMS) is a novel diagnosis due to widespread use of and advances in the newborn screening (NBS) process for cystic fibrosis (CF) in the United States of America, allowing for the diagnosis of asymptomatic children wit
Externí odkaz:
https://doaj.org/article/e5caaff8dc10499383326753d51f0126
Autor:
Wilfredo De Jesús-Rojas, José Muñiz-Hernández, Francisco Alvarado-Huerta, Jesús M. Meléndez-Montañez, Arnaldo J. Santos-López, Ricardo A. Mosquera
Publikováno v:
Diagnostics, Vol 12, Iss 5, p 1127 (2022)
Primary ciliary dyskinesia (PCD) has been linked to more than 50 genes that cause a spectrum of clinical symptoms, including newborn respiratory distress, sinopulmonary infections, and laterality abnormalities. Although the RSPH4A (c.921+3_6delAAGT)
Externí odkaz:
https://doaj.org/article/63bf01deb0af4fa09c68d92bd8f5acfa
Autor:
Mosquera, Wilfredo De Jesús-Rojas, Luis Reyes-Peña, José Muñiz-Hernández, Patricia Quiles Ruiz de Porras, Jesús Meléndez-Montañez, Marcos J. Ramos-Benitez, Ricardo A.
Publikováno v:
Diagnostics; Volume 13; Issue 13; Pages: 2287
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder that results from the dysfunction of motile cilia, which can cause chronic upper and lower respiratory infections leading to bronchiectasis. However, there is a need for additional t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::3129ee631a1486a56e8878176c20b691
Publikováno v:
Diagnostics, Vol 11, Iss 2, p 281 (2021)
Primary ciliary dyskinesia (PCD) is a rare, heterogeneous ciliopathy resulting in chronic oto-sino-pulmonary disease, bronchiectasis, newborn respiratory distress, and laterality defects. PCD diagnosis can be achieved by following diagnostic algorith
Externí odkaz:
https://doaj.org/article/d322377858bc47b58dc43fa3fddfda8b
Autor:
Wilfredo De Jesús-Rojas, Francisco Alvarado-Huerta, Jesús Meléndez-Montañez, José Muñiz-Hernández, Arnaldo Santos-López, Ricardo Mosquera
Publikováno v:
Advances in Respiratory Medicine; Volume 90; Issue 5; Pages: 399-406
Primary Ciliary Dyskinesia (PCD) is a rare genetic disease characterized by motile cilia dysfunction with a prevalence of 1 in 16,309 individuals in Hispanic populations. In Puerto Rico, the prevalence of PCD is unknown. Diagnosis of PCD in Puerto Ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed99604236d3e3389f55896bea986c2a