Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Tricia Bhatti"'
Autor:
Julia A Baran, Mya Bojarsky, Stephen Halada, Julio C Ricarte-Filho, Amber Isaza, Aime T Franco, Lea F Surrey, Tricia Bhatti, Zubair Baloch, N Scott Adzick, Sogol Mostoufi-Moab, Ken Kazahaya, Andrew J Bauer
Publikováno v:
European Thyroid Journal, Vol 13, Iss 4, Pp 1-12 (2024)
Objective: The American Thyroid Association (ATA) Pediatric Guidelines recommend selective, prophylactic central neck dissection (pCND) for patients with papillary thyroid carcinoma (PTC) based on tumor focality, tumor size, and the surgeon’s exper
Externí odkaz:
https://doaj.org/article/1dee72f56ad7449c8c2d8e08d1d9773c
Autor:
Robyn T. Sussman, Jo Lynne Rokita, Kevin Huang, Pichai Raman, Komal S. Rathi, Daniel Martinez, Kristopher R. Bosse, Maria Lane, Lori S. Hart, Tricia Bhatti, Bruce Pawel, John M. Maris
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
We developed a computational pipeline designed to use RNA sequencing (n = 136) and gene expression profiling (n = 250) data from neuroblastoma tumors to identify cell surface proteins predicted to be highly expressed in MYCN amplified neuroblastomas
Externí odkaz:
https://doaj.org/article/92b8399491b14034a7ca4fb04570dc8f
Autor:
Kara E Boodhansingh, Zhongying Yang, Changhong Li, Pan Chen, Katherine Lord, Susan A Becker, Lisa J States, N Scott Adzick, Tricia Bhatti, Show-Ling Shyng, Arupa Ganguly, Charles A Stanley, Diva D De Leon
Publikováno v:
European Journal of Endocrinology. 187:301-313
Objective Congenital hyperinsulinism (HI) is the most common cause of persistent hypoglycemia in children. In addition to typical focal or diffuse HI, some cases with diazoxide-unresponsive congenital HI have atypical pancreatic histology termed Loca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7033f1f22538ed7c7ccb84c7c0be3b42
https://doi.org/10.1530/eje-21-1095
https://doi.org/10.1530/eje-21-1095
Autor:
Mohamed M. Elsingergy, Bernarda Viteri, Hansel J. Otero, Tricia Bhatti, Tatiana Morales, Timothy P. L. Roberts, Sandra Amaral, Erum Hartung, Suraj D. Serai
Publikováno v:
Pediatric Transplantation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c9a7ed46375ad62b14dfedaa1bf7806
https://doi.org/10.1111/petr.14540
https://doi.org/10.1111/petr.14540
Autor:
Kara E. Boodhansingh, Elizabeth Rosenfeld, Katherine Lord, N. Scott Adzick, Tricia Bhatti, Arupa Ganguly, Diva D. De Leon, Charles A. Stanley
Publikováno v:
Hormone Research in Paediatrics. 95:492-498
Introduction: The hyperinsulinemia-hyperammonemia syndrome (HIHA) is the second most common cause of congenital hyperinsulinism and is caused by activating heterozygous missense mutations in GLUD1. In the majority of HIHA cases, the GLUD1 mutation is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52d4b797c184a3f1ac8022e7fa6f414a
https://doi.org/10.1159/000526203
https://doi.org/10.1159/000526203
Autor:
Sameer Mittal, John Weaver, Aznive Aghababian, Rebecca Edwins, Karl Godlewski, Katherine Fischer, Sharmayne Siu, Denise Gruccio, Jason Van Batavia, Arun Srinivasan, Christopher Long, Vaneeta Bamba, Vandana Batra, Tricia Bhatti, Thomas Kolon
Publikováno v:
Journal of Pediatric Urology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b16cda1c18191e6040110aeb7379ac8b
https://doi.org/10.1016/j.jpurol.2022.12.012
https://doi.org/10.1016/j.jpurol.2022.12.012
Autor:
Chelsi Flippo, Vipula Kolli, Melissa Andrew, Seth Berger, Tricia Bhatti, Alison M Boyce, Daniel Casella, Michael T Collins, Emmanuèle Délot, Joseph Devaney, Stephen M Hewitt, Thomas Kolon, Ashwini Mallappa, Perrin C White, Deborah P Merke, Andrew Dauber
Publikováno v:
J Endocr Soc
Context Autosomal dominant and rarely de novo gain-of-function variants in the LHCGR gene are associated with precocious male puberty, while somatic LHCGR variants have been found in isolated Leydig cell adenomas and Leydig cell hyperplasia. Bilatera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b22264b1da6a571e4780ba5b7a88822c
https://europepmc.org/articles/PMC9469925/
https://europepmc.org/articles/PMC9469925/
Autor:
Stacey K. Mardekian, Danielle Fortuna, Allan Nix, Tricia Bhatti, Clayton A. Wiley, Adam Flanders, Jacqueline Urtecho, Jennifer Sloane, Jowairiyya Ahmad, Mark T. Curtis
Publikováno v:
International Journal of Infectious Diseases, Vol 36, Iss C, Pp 6-8 (2015)
Human parechovirus (HPeV) belongs to the Picornaviridae family of RNA viruses. HPeV infections can be asymptomatic, lead to mild respiratory and/or gastrointestinal symptoms, or less frequently cause severe diseases such as sepsis, meningitis, enceph
Externí odkaz:
https://doaj.org/article/a45ac36b1ce9420b9a0a5e6ee24ddbbe
Autor:
Julia A. Baran, Stephen Halada, Andrew J. Bauer, Julio C. Ricarte-Filho, Amber Isaza, Lea F. Surrey, Cindy McGrath, Tricia Bhatti, Jalal Jalaly, Sogol Mostoufi-Moab, Aime T. Franco, N. Scott Adzick, Ken Kazahaya, Anne Marie Cahill, Zubair Baloch
Publikováno v:
Hormone research in paediatrics. 95(5)
Introduction: The diagnostic utility of molecular profiling for the evaluation of indeterminate pediatric thyroid nodules is unclear. We aimed to assess pediatric cases with indeterminate thyroid fine-needle aspiration (FNA) alongside clinicopatholog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd0be3747aadc51027c16e26637fb495
https://pubmed.ncbi.nlm.nih.gov/35871517
https://pubmed.ncbi.nlm.nih.gov/35871517
Autor:
Alyssa L. Ritter, Jessica Gold, Hiroshi Hayashi, Amanda M. Ackermann, Stephanie Hanke, Cara Skraban, Sanmati Cuddapah, Elizabeth Bhoj, Dong Li, Yukiko Kuroda, Jessica Wen, Ryojun Takeda, Audrey Bibb, Salima El Chehadeh, Amélie Piton, Jeanine Ohl, Mary K. Kukolich, Keisuke Nagasaki, Kohji Kato, Tomoo Ogi, Tricia Bhatti, Pierre Russo, Bryan Krock, Jill R. Murrell, Jennifer A. Sullivan, Vandana Shashi, Nicholas Stong, Hakon Hakonarson, Kentaro Sawano, Erin Torti, Rebecca Willaert, Yue Si, William Ross Wilcox, Katrine Verena Wirgenes, Kristian Thomassen, Katherine Carlotti, Angelika Erwin, Joanna Lazier, Thorsten Marquardt, Miao He, Andrew C. Edmondson, Kosuke Izumi
Publikováno v:
Genet Med
PURPOSE: This study aimed to describe the phenotypic and molecular characteristics of ARCN1-related syndrome. METHODS: Patients with ARCN1 variants were identified, and clinician researchers were connected using GeneMatcher and physician referrals. C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d86f4d63eea8ccc80eff372d25a1e057
https://europepmc.org/articles/PMC9923403/
https://europepmc.org/articles/PMC9923403/