BLOOD DIFFERENTIALS AND WHOLE EXOME SEQUENCING (WES) OF PATIENTS WITH JUVENILE DERMATOMYOSITIS (JDM)

被引：0
|
作者：
Zhou, Danlei
Coss, Samantha
Aziz, Rabheh Abdul
Miller, Katherine
Al Ahmed, Ohoud
Sivaraman, Vidya
Akoghlanian, Shoghik
Oberle, Edward
Drew, Joanne
Driest, Kyla
Ardoin, Stacy P.
Spencer, Charles
Yu, Chack-Yung
机构：
[1] Nationwide Childrens Hosp, Abigail Wexner Res Inst, Columbus, OH USA
[2] Nationwide Childrens Hosp, Div Rheumatol, Columbus, OH USA
[3] Univ Buffalo, New York, NY USA
来源：
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY | 2024年 / 42卷 / 02期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P-79
引用
收藏
页码：528 / 528
页数：1
相关论文
共 50 条
  • [21] Whole exome sequencing (WES) reveals novel therapeutic targets in cervical cancer
    Lopez, S.
    Han, C.
    Altwerger, G.
    Menderes, G.
    Zammataro, L.
    Bellone, S.
    Bianchi, A.
    Zeybek, B.
    Ratner, E. S.
    Schwartz, P. E.
    Santin, A. D.
    GYNECOLOGIC ONCOLOGY, 2019, 154 : 61 - 62
  • [22] Whole Exome Sequencing (WES) in unravelling complex cases of bicuspid aortic valve
    Morgante, Ginevra
    Bonati, Maria Teresa
    Faletra, Flavio
    Morgan, Anna
    Rubinato, Elisa
    Feresin, Agnese
    Luglio, Agnese
    Spedicati, Beatrice
    Girotto, Giorgia
    Gasparini, Paolo
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 144 - 144
  • [23] Variations in the medical management of juvenile dermatomyositis (JDM) patients enrolled in the NIAMS JDM research registry.
    Chin, L
    Ramsey-Goldman, R
    Shamiyeh, E
    Chang, RW
    Dyer, AR
    Lipton, RB
    Pachman, LM
    ARTHRITIS AND RHEUMATISM, 2002, 46 (09): : S490 - S490
  • [24] Whole exome sequencing in systemic juvenile idiopathic arthritis
    Moghaddas F.
    De Nardo D.
    Baker P.
    Gordon L.
    Sadedin S.
    Oshlack A.
    Akikusa J.
    Allen R.
    Munro J.
    Ellis J.
    Masters S.
    Pediatric Rheumatology, 13 (Suppl 1)
  • [25] Unique Neurologic Disorders with Unique Genetic Alterations Revealed by Whole Exome Sequencing (WES)
    Clark, G. D.
    ANNALS OF NEUROLOGY, 2013, 74 : S165 - S165
  • [26] Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders
    Rosell, Allyn McConkie
    Pena, Loren D. M.
    Schoch, Kelly
    Spillmann, Rebecca
    Sullivan, Jennifer
    Hooper, Stephen R.
    Jiang, Yong-Hui
    Mathey-Andrews, Nicolas
    Goldstein, David B.
    Shashi, Vandana
    JOURNAL OF GENETIC COUNSELING, 2016, 25 (05) : 1019 - 1031
  • [27] Prognosis Determined by Tumor Mutational Burden (TMB) Using Whole Exome Sequencing (WES)
    Fernandez, E.
    Eng, K.
    Sboner, A.
    Elemento, O.
    Song, W.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2018, 20 (06): : 1013 - 1013
  • [28] The Challenges, limitations and uncertainties of whole exome sequencing (WES) for hereditary ocular disorders.
    Ortube, Maria Carolina
    Strom, Samuel P.
    Martinez, Ariadna
    Gorin, Michael
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2014, 55 (13)
  • [29] FEASIBILITY OF PROSPECTIVE WHOLE-EXOME SEQUENCING (WES) IN PEDIATRIC MEDULLOBLASTOMA PATIENTS ON THE HEAD START 4 PROTOCOL
    Graham, Richard
    Bell, Erica Hlavin
    Webb, Amy
    Jannu, Asha Jacob
    Timmers, Cynthia
    McElroy, Joseph
    Becker, Aline
    Guo, Yingshi
    Dhall, Girish
    Finlay, Jonathan
    Chakravarti, Arnab
    NEURO-ONCOLOGY, 2018, 20 : 201 - 201
  • [30] Whole-Exome Sequencing (WES) results of 50 patients with chronic kidney diseases: a perspective of Alport syndrome
    Yavas, Cuneyd
    Un, Cemal
    Celebi, Evrim
    Gezdirici, Alper
    Dogan, Mustafa
    Ili, Ezgi Gokpinar
    Dogan, Tunay
    Ozgenturk, Nehir Ozdemir
    REVISTA DA ASSOCIACAO MEDICA BRASILEIRA, 2022, 68 (09): : 1282 - 1287
12345