Zobrazeno 1 - 10
of 149
pro vyhledávání: '"Rasheed Gbadegesin"'
Autor:
Yask Gupta, David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon Lane, Chen Wang, Juntao Ke, Gina Jin, Benjamin Wooden, Andrea L. Knob, Tze Y. Lim, Gerald B. Appel, Kinsie Huggins, Lili Liu, Adele Mitrotti, Megan C. Stangl, Andrew Bomback, Rik Westland, Monica Bodria, Maddalena Marasa, Ning Shang, David J. Cohen, Russell J. Crew, William Morello, Pietro Canetta, Jai Radhakrishnan, Jeremiah Martino, Qingxue Liu, Wendy K. Chung, Angelica Espinoza, Yuan Luo, Wei-Qi Wei, Qiping Feng, Chunhua Weng, Yilu Fang, Iftikhar J. Kullo, Mohammadreza Naderian, Nita Limdi, Marguerite R. Irvin, Hemant Tiwari, Sumit Mohan, Maya Rao, Geoffrey K. Dube, Ninad S. Chaudhary, Orlando M. Gutiérrez, Suzanne E. Judd, Mary Cushman, Leslie A. Lange, Ethan M. Lange, Daniel L. Bivona, Miguel Verbitsky, Cheryl A. Winkler, Jeffrey B. Kopp, Dominick Santoriello, Ibrahim Batal, Sérgio Veloso Brant Pinheiro, Eduardo Araújo Oliveira, Ana Cristina Simoes e Silva, Isabella Pisani, Enrico Fiaccadori, Fangming Lin, Loreto Gesualdo, Antonio Amoroso, Gian Marco Ghiggeri, Vivette D. D’Agati, Riccardo Magistroni, Eimear E. Kenny, Ruth J. F. Loos, Giovanni Montini, Friedhelm Hildebrandt, Dirk S. Paul, Slavé Petrovski, David B. Goldstein, Matthias Kretzler, Rasheed Gbadegesin, Ali G. Gharavi, Krzysztof Kiryluk, Matthew G. Sampson, Martin R. Pollak, Simone Sanna-Cherchi
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-8 (2023)
Abstract African Americans have a significantly higher risk of developing chronic kidney disease, especially focal segmental glomerulosclerosis -, than European Americans. Two coding variants (G1 and G2) in the APOL1 gene play a major role in this di
Externí odkaz:
https://doaj.org/article/9f6233ad88a44f828fd1c0264b712139
Autor:
Rasheed Gbadegesin, Elena Martinelli, Yask Gupta, David J. Friedman, Matthew G. Sampson, Martin R. Pollak, Simone Sanna-Cherchi
Publikováno v:
Glomerular Diseases, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/dd831a1b969e4e1db739ae72e4490e11
Autor:
Michelle N. Rheault, Sandra Amaral, Margret Bock, Eileen Tsai Chambers, Blanche Chavers, Mireile El Ters, Rouba Garro, Rasheed Gbadegesin, Amit Govil, Lyndsay Harshman, Hatem Amer, David K. Hooper, Ajay K. Israni, Samy Riad, Junichiro Sageshima, Ron Shapiro, Michael Seifert, Jodi Smith, Randall Sung, Christie P. Thomas, Qi Wang, Priya S. Verghese
Publikováno v:
Frontiers in Nephrology, Vol 3 (2023)
BackgroundFocal segmental glomerulosclerosis (FSGS) is a common cause of end-stage kidney disease requiring kidney transplantation and can recur in the allograft in 30-80% of recipients resulting in reduced graft survival. Plasmapheresis has shown ef
Externí odkaz:
https://doaj.org/article/bacc39cbba8e4ab09a1ad3f137ad1b59
Autor:
Debbie S. Gipson, Chia-shi Wang, Eloise Salmon, Rasheed Gbadegesin, Abhijit Naik, Simone Sanna-Cherchi, Alessia Fornoni, Matthias Kretzler, Sandra Merscher, Paul Hoover, Kelley Kidwell, Moin Saleem, Leonardo Riella, Lawrence Holzman, Annette Jackson, Opeyemi Olabisi, Paolo Cravedi, Benjamin Solomon Freedman, Jonathan Himmelfarb, Marina Vivarelli, Jennifer Harder, Jon Klein, George Burke, Michelle Rheault, Cathie Spino, Hailey E. Desmond, Howard Trachtman
Publikováno v:
Glomerular Diseases, Pp 1-1 (2023)
Since it was first described more than 50 years ago, recurrence of FSGS in kidney allografts has frustrated the transplant community. This rare condition is associated with considerable morbidity, and it is the most common cause of graft loss in pati
Externí odkaz:
https://doaj.org/article/9bd7d704a73d447f997a7ecb9b5f8d94
Autor:
Reshma Jagsi, T. DeLene Beeland, Kevin Sia, Lauren A. Szczygiel, Matthew R. Allen, Vineet M. Arora, Megan Bair-Merritt, Melissa D. Bauman, Hillary R. Bogner, Gail Daumit, Esa Davis, Angela Fagerlin, Daniel E. Ford, Rasheed Gbadegesin, Kathy Griendling, Katherine Hartmann, S. Susan Hedayati, Rebecca D. Jackson, Susan Matulevicius, Michael J. Mugavero, Eric J. Nehl, Tuhina Neogi, Judith G. Regensteiner, Michael A. Rubin, Doris Rubio, Kanakadurga Singer, Brownsyne Tucker Edmonds, Anna Volerman, Sandra Laney, Carrie Patton, Sindy Escobar Alvarez
Publikováno v:
The Journal of Clinical Investigation, Vol 132, Iss 23 (2022)
Externí odkaz:
https://doaj.org/article/e5734f6762c448b791bcb147d3f38391
Autor:
Brandon M. Lane, Megan Chryst-Stangl, Guanghong Wu, Mohamed Shalaby, Sherif El Desoky, Claire C. Middleton, Kinsie Huggins, Amika Sood, Alejandro Ochoa, Andrew F. Malone, Ricardo Vancini, Sara E. Miller, Gentzon Hall, So Young Kim, David N. Howell, Jameela A. Kari, Rasheed Gbadegesin
Publikováno v:
JCI Insight, Vol 7, Iss 2 (2022)
We performed next-generation sequencing in patients with familial steroid-sensitive nephrotic syndrome (SSNS) and identified a homozygous segregating variant (p.H310Y) in the gene encoding clavesin-1 (CLVS1) in a consanguineous family with 3 affected
Externí odkaz:
https://doaj.org/article/e471d6c0a2dc49eb9ee43cce30adda9e
Autor:
Rachel Wine, Jovanka Vasilevska-Ristovska, Tonny Banh, Janae Knott, Damien Noone, Rasheed Gbadegesin, Titilayo O. Ilori, Henrietta U. Okafor, Francis Furia, Ifeoma Ulasi, Adaobi U. Solarin, Christopher Esezobor, Anthony Batte, Yemi Raji, Timothy O. Olanrewaju, Uzoamaka Muoneke, Adewale E. Adetunji, Vincent Boima, Oluwatoyin Amira, Charlotte Osafo, Georgette Guemkam, Samuel Ajayi, Muhammad A. Makusidi, Emmanuel A. Anigilaje, Paschal Ruggajo, Adanze O. Asinobi, Adebowale D. Ademola, Rulan S. Parekh
Publikováno v:
Global Epidemiology, Vol 3, Iss , Pp 100061- (2021)
Summary: Background: Childhood nephrotic syndrome, if left untreated, leads to progressive kidney disease or death. We quantified the prevalence of steroid-sensitive nephrotic syndrome, steroid-resistant nephrotic syndrome, and histological types as
Externí odkaz:
https://doaj.org/article/2a697d0392f344a5b5f613f2ab7e869d
Autor:
Brian I. Shaw, MD, Alejandro Ochoa, PhD, Cliburn Chan, MD, Chloe Nobuhara, BS, Rasheed Gbadegesin, MD, Annette M. Jackson, PhD, Eileen T. Chambers, MD
Publikováno v:
Transplantation Direct, Vol 7, Iss 10, p e748 (2021)
Background. Recurrent focal segmental glomerulosclerosis (FSGS) after kidney transplantation accounts for the majority of allograft failures in children with primary FSGS. Although current research focuses on FSGS pathophysiology, a common etiology a
Externí odkaz:
https://doaj.org/article/2a83091c688240ec8f472bfbc61473d8
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0239300 (2020)
BackgroundRecent reports from small studies in West Africa suggest that Black children may have high rate of steroid sensitivity nephrotic syndrome (SSNS) contrary to long held knowledge. Herein, we determined the proportion of children with idiopath
Externí odkaz:
https://doaj.org/article/0e57d1b21be345cc8b49c18830a5ef41
Autor:
Kyle W. Freischlag, Vivian Chen, Shashi K. Nagaraj, Annabelle N. Chua, Dongfeng Chen, Delbert R. Wigfall, John W. Foreman, Rasheed Gbadegesin, Deepak Vikraman, Eileen T. Chambers
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Background: Currently, there is no standardized approach for determining psychosocial readiness in pediatric transplantation. We examined the utility of the Psychosocial Assessment of Candidates for Transplantation (PACT) to identify pediatric kidney
Externí odkaz:
https://doaj.org/article/cc24796b041746e198695f1a7621d694