日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Major Histocompatibility Complex Class II Deficiency due to a Novel Mutation in RFXANK in a Child of Mexican Descent

一名墨西哥裔儿童因RFXANK基因新突变导致主要组织相容性复合体II类缺陷

Clarridge, Katherine; Leitenberg, David; Loechelt, Brett; Picard, Capuchine; Keller, Michael

Screening and Monitoring for Infectious Complications When Immunosuppressive Agents Are Studied in the Treatment of Autoimmune Disorders

在研究使用免疫抑制剂治疗自身免疫性疾病时,应筛查和监测感染并发症

Loechelt, Brett J; Green, Michael; Gottlieb, Peter A; Blumberg, Emily; Weinberg, Adriana; Quinlan, Scott; Baden, Lindsey R

Systemic injection of CD34(+)-enriched human cord blood cells modulates poststroke neural and glial response in a sex-dependent manner in CD1 mice

系统性注射富含 CD34+ 的人类脐带血细胞可调控 CD1 小鼠中风后神经和神经胶质反应,且这种调节方式存在性别依赖性

Shilpa D Kadam, HuiGen Chen, Geoffrey J Markowitz, Saba Raja, Shanu George, Tatayana Verina, Elisabeth Shotwell, Brett Loechelt, Michael V Johnston, Naynesh Kamani, Ali Fatemi, Anne M Comi

Transplantation outcomes for severe combined immunodeficiency, 2000-2009

2000-2009年重症联合免疫缺陷患者的移植结果

Pai, Sung-Yun; Logan, Brent R; Griffith, Linda M; Buckley, Rebecca H; Parrott, Roberta E; Dvorak, Christopher C; Kapoor, Neena; Hanson, Imelda C; Filipovich, Alexandra H; Jyonouchi, Soma; Sullivan, Kathleen E; Small, Trudy N; Burroughs, Lauri; Skoda-Smith, Suzanne; Haight, Ann E; Grizzle, Audrey; Pulsipher, Michael A; Chan, Ka Wah; Fuleihan, Ramsay L; Haddad, Elie; Loechelt, Brett; Aquino, Victor M; Gillio, Alfred; Davis, Jeffrey; Knutsen, Alan; Smith, Angela R; Moore, Theodore B; Schroeder, Marlis L; Goldman, Frederick D; Connelly, James A; Porteus, Matthew H; Xiang, Qun; Shearer, William T; Fleisher, Thomas A; Kohn, Donald B; Puck, Jennifer M; Notarangelo, Luigi D; Cowan, Morton J; O'Reilly, Richard J

Epstein-Barr and other herpesvirus infections in patients with early onset type 1 diabetes treated with daclizumab and mycophenolate mofetil

接受达克珠单抗和吗替麦考酚酯治疗的早期发病型 1 型糖尿病患者发生 Epstein-Barr 病毒和其他疱疹病毒感染的风险增加

Loechelt, Brett J; Boulware, David; Green, Michael; Baden, Lindsey R; Gottlieb, Peter; Krause-Steinrauf, Heidi; Weinberg, Adriana

The natural history of children with severe combined immunodeficiency: baseline features of the first fifty patients of the primary immune deficiency treatment consortium prospective study 6901

重症联合免疫缺陷患儿的自然病程:原发性免疫缺陷治疗联盟前瞻性研究 6901 中前 50 例患者的基线特征

Dvorak, Christopher C; Cowan, Morton J; Logan, Brent R; Notarangelo, Luigi D; Griffith, Linda M; Puck, Jennifer M; Kohn, Donald B; Shearer, William T; O'Reilly, Richard J; Fleisher, Thomas A; Pai, Sung-Yun; Hanson, I Celine; Pulsipher, Michael A; Fuleihan, Ramsay; Filipovich, Alexandra; Goldman, Frederick; Kapoor, Neena; Small, Trudy; Smith, Angela; Chan, Ka-Wah; Cuvelier, Geoff; Heimall, Jennifer; Knutsen, Alan; Loechelt, Brett; Moore, Theodore; Buckley, Rebecca H

Complex management of a patient with a contiguous Xp11.4 gene deletion involving ornithine transcarbamylase: a role for detailed molecular analysis in complex presentations of classical diseases

对一位患有累及鸟氨酸转氨甲酰酶的连续性Xp11.4基因缺失的患者进行复杂管理:详细分子分析在经典疾病复杂表现中的作用

Deardorff, Matthew A; Gaddipati, Himabindu; Kaplan, Paige; Sanchez-Lara, Pedro A; Sondheimer, Neal; Spinner, Nancy B; Hakonarson, Hakon; Ficicioglu, Can; Ganesh, Jaya; Markello, Thomas; Loechelt, Brett; Zand, Dina J; Yudkoff, Marc; Lichter-Konecki, Uta

Intravascular extension of Wilms tumor

肾母细胞瘤的血管内延伸

Shamberger, R C; Ritchey, M L; Haase, G M; Bergemann, T L; Loechelt-Yoshioka, T; Breslow, N E; Green, D M