Zobrazeno 1 - 10
of 186
pro vyhledávání: '"Ronald Jaffe"'
Autor:
Mylarappa Ningappa, Juhoon So, Joseph Glessner, Chethan Ashokkumar, Sarangarajan Ranganathan, Jun Min, Brandon W Higgs, Qing Sun, Kimberly Haberman, Lori Schmitt, Silvia Vilarinho, Pramod K Mistry, Gerard Vockley, Anil Dhawan, George K Gittes, Hakon Hakonarson, Ronald Jaffe, Shankar Subramaniam, Donghun Shin, Rakesh Sindhi
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0138381 (2015)
Altered extrahepatic bile ducts, gut, and cardiovascular anomalies constitute the variable phenotype of biliary atresia (BA).To identify potential susceptibility loci, Caucasian children, normal (controls) and with BA (cases) at two US centers were c
Externí odkaz:
https://doaj.org/article/4cadd2774c32437fbb86d6068f14a00d
Autor:
M. Whitehead, Eli L. Diamond, M. L. Sulis, Brian Harding, Jennifer Picarsic, Y. Fellig, T. Pettit, Mariarita Santi, K. Shekdar, Mark Fluchel, Bret C. Mobley, Ronald Jaffe, G. Goldstein, T. Pysher, Holly Zhou, Lea F. Surrey, P. M. Sharples, M. Weintraub
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-13 (2019)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
The family of juvenile xanthogranuloma family neoplasms (JXG) with ERK-pathway mutations are now classified within the “L” (Langerhans) group, which includes Langerhans cell histiocytosis (LCH) and Erdheim Chester disease (ECD). Although theBRAFV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a67a9cab636aa83117f711265603fa15
http://link.springer.com/article/10.1186/s40478-019-0811-6
http://link.springer.com/article/10.1186/s40478-019-0811-6
Autor:
Aleksandar Rajkovic, Cristina Quesada-Candela, Svetlana A. Yatsenko, Stefan Kostadinov, Stacy Beck, Judith L. Yanowitz, Ronald Jaffe, Devereux N. Saller
Publikováno v:
Prenat Diagn
ObjectivesTo investigate the incidence of chromosomal abnormalities in the products of conception (POC) of patients with spontaneous miscarriages (SM) and with recurrent pregnancy losses (RPL), and to determine biological mechanisms contributing to R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18475da71d3a1a06af2aec35b2e7e8b4
https://doi.org/10.1101/2020.07.01.20144535
https://doi.org/10.1101/2020.07.01.20144535
Publikováno v:
International Journal of Surgical Pathology. 27:176-180
Proteinaceous lymphadenopathy (PLD) is a poorly defined, underreported pathological entity of uncertain etiology characterized by massive deposition of amorphous, eosinophilic, and periodic acid-Schiff–positive material involving lymph nodes, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca3e0c7235012e889cd8ee457b2ab6e4
https://doi.org/10.1177/1066896918802024
https://doi.org/10.1177/1066896918802024
Autor:
Pamela Kachmar, Qing Sun, Brittany Boehm, Tara Hartle, Amanda Brown, Mylarappa Ningappa, George V. Mazariegos, Sarangarajan Ranganathan, Chethan Ashokkumar, Patricia Harris, Adriana Zeevi, Ronald Jaffe, Lisa Remaley, Paula Stanley, Geoffrey Bond, Samantha Levy, Nicole Jativa, Megan Nicely, Brandon W. Higgs, Jaimie White, Kyle Soltys, Katie Dirling, Rakesh Sindhi, Lindsay OʼToole, Tamara Fazzolare
Publikováno v:
Transplantation. 101:131-140
Background Allospecific CD154+T-cytotoxic memory cells (CD154+TcM) predict acute cellular rejection after liver transplantation (LTx) or intestine transplantation (ITx) in small cohorts of children and can enhance immunosuppression management, but aw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76bf210fceaaf46fab8ffe565cbde0af
https://doi.org/10.1097/tp.0000000000001076
https://doi.org/10.1097/tp.0000000000001076
Autor:
Jean Donadieu, Eric D. Jacobsen, Carlos Rodriguez-Galindo, Oussama Abla, Zdenka Krenova, Sheila Weitzman, Ronald Jaffe, Benjamin H. Durham, Jean-François Emile, Fleur Cohen-Aubart, Kenneth L. McClain, Julien Haroche, James A. Whitlock, Carl E. Allen, Jorge Braier, Jennifer Picarsic, Frédéric Charlotte, Eli L. Diamond
Publikováno v:
Blood. 131(26)
Rosai-Dorfman-Destombes disease (RDD) is a rare non–Langerhans cell histiocytosis characterized by accumulation of activated histiocytes within affected tissues. RDD, which now belongs to the R group of the 2016 revised histiocytosis classification
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6811cca67844bbe6ef5b976fc9b238ee
https://pubmed.ncbi.nlm.nih.gov/29720485
https://pubmed.ncbi.nlm.nih.gov/29720485
Autor:
Jonhan Ho, Amanda Hernandez, Sara E. Monaco, Jennifer Picarsic, Arthur C. Huen, William T. Johnson, Parth Patel, Ronald Jaffe, Lisa M. Grandinetti, Stanley M. Marks
Publikováno v:
Journal of Cutaneous Pathology. 43:270-275
Langerhans cell histocytosis (LCH) and Erdheim-Chester disease are two rare histiocytic disorders. Their occurrence in the same patient is more infrequent, but has been described. We report a case of a 38-year-old woman who presented with a diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2120a07c90de51bbc951b050df84ac1
https://doi.org/10.1111/cup.12636
https://doi.org/10.1111/cup.12636
Autor:
Yosuke Miyashita, Agnieszka Swiatecka-Urban, Johannes Hofer, Heidi Griffiths, Michael L. Moritz, Tennille N. Webb, Riha Bhatt, Ronald Jaffe
Publikováno v:
International journal of medical and pharmaceutical case reports
Background Hemolytic-uremic syndrome (HUS) presents with hemolytic anemia, thrombocytopenia, and thrombotic microangiopathy of the kidney and usually results from Shiga-toxin induced activation of the alternative complement pathway. Gastroenteritis i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::827e6fac59a151e67c90da425ff1a740
http://europepmc.org/articles/PMC4849479
http://europepmc.org/articles/PMC4849479
Autor:
Kudakwashe R. Chikwava, R. Maarten Egeler, Jennifer Picarsic, Ronald Jaffe, Kathleen Patterson
Publikováno v:
Pediatric and Developmental Pathology. 18:127-138
Thymic involvement by Langerhans cell histiocytosis (LCH) has been described mainly in isolated case reports. A description of the histopathologic patterns of LCH proliferations in the thymus, together with therapeutic implications, has not, to our k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bf6544f813f90507027c7bc4d83fe59
https://doi.org/10.2350/15-01-1593-oa.1
https://doi.org/10.2350/15-01-1593-oa.1
Autor:
Jennifer Picarsic, Ronald Jaffe
Publikováno v:
Histiocytic Disorders ISBN: 9783319596310
The pathology of histiocytic disorders and neoplasms of the macrophage-dendritic cell lineages is heterogeneous and may have overlapping features, all the while made more difficult by their rarity. The morphologic features together with immunophenoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac44444840e37c6d6d78e9e7f6ff3c0c
https://doi.org/10.1007/978-3-319-59632-7_1
https://doi.org/10.1007/978-3-319-59632-7_1