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    C

    Children''s Hospital Central California

    EST. 1949
    511论文总数
    1.1万引用总数

    Valley Children's Hospital (VCH), formerly Children's Hospital Central California is a stand-alone, pediatric acute care children's teaching hospital located in Madera County, California. The hospital has 358 pediatric beds and is affiliated the Stanford University School of Medicine. The hospital is a member of Valley Children's Healthcare and is one of only two children's hospitals in the network, servicing approximately 1.3 million children and adolescents in their coverage area. The hospital provides comprehensive pediatric specialties and subspecialties to infants, children, teens, and young adults aged 0–21 throughout Madera County, Fresno, and California. Valley Children's also sometimes treats adults that require pediatric care.Valley Children's also features the largest ACS verified Level 2 Pediatric Trauma Center in the region, the only Level IV NICU in the Central Valley, and the only provider of pediatric extracorporeal life support (ECLS) for their service area. Valley Children's is one of the largest providers of pediatric health services in California and in the country. The hospital is adjacent to the Ronald McDonald House of the Central Valley.

    论文量&引用量时间轴

    机构学者

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    Samuel David
    Samuel David
    Department of Anatomy and Cell Biology, Faculty of Medicine and Health Sciences, McGill University
    论文:13引用:0H-index:0
    Karen Sofia Fernandez
    Karen Sofia Fernandez
    Valley Children's Hospital
    论文:12引用:0H-index:0
    Valerie Larouche
    Valerie Larouche
    Ctr Mere Enfant Soleil, Univ Laval
    论文:10引用:0H-index:0
    Alyssa Reddy
    Alyssa Reddy
    University of California
    论文:10引用:0H-index:0
    Mary Anne Tablizo
    Mary Anne Tablizo
    Pediatrics Department, Stanford University
    论文:9引用:0H-index:0
    Nalin Gupta
    Nalin Gupta
    Department of Neurological Surgery and Brain Tumor Research Center, University of California, San Francisco
    论文:8引用:0H-index:0
    Melyssa Aronson
    Melyssa Aronson
    Department of Molecular Genetics, University of Toronto
    论文:7引用:0H-index:0
    Michael Henrickson
    Michael Henrickson
    College of Medicine, University of Cincinnati
    论文:7引用:0H-index:0
    Bruce Crooks
    Bruce Crooks
    Department of Hematology/Oncology, IWK Health Centre
    论文:7引用:0H-index:0

    论文(511)

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    1Treat-to-Target Strategies and Early Biologic Initiation in Polyarticular Juvenile Idiopathic Arthritis: Translating Evidence into Clinical Practice
    Jyothi Ranga Patri, Sastry Chamarthi, Venkata Sushma Chamarthi

    Juvenile idiopathic arthritis (JIA) is among the most prevalent chronic inflammatory rheumatic diseases in children. Over the past two decades, the treatment landscape has evolved significantly with the introduction of biologic disease-modifying antirheumatic drugs and the adoption of treat-to-target strategies aimed at achieving clinically inactive disease. Early initiation of biologic therapies can facilitate rapid disease control and improve long-term outcomes. However, the implementation and integration of newer treatments within the current healthcare system are often hindered by insurance authorization requirements, high costs, and variability in clinical practice. This review evaluates current evidence-based approaches supporting the treat-to-target strategy and early biologic intervention in polyarticular JIA. Additionally, it discusses the practical challenges of translating evidence into routine clinical care and proposes sustainable strategies to optimize treatment outcomes while addressing existing knowledge and practice gaps.

    2026Rheumato(2026)
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    2A 14-Year-old Female Presenting with Cough and Dyspnea.
    Jeffrey Ni, Bassel Al Horany, Bhavishya Devireddy, Caroline Uchechi Adanma Okorie
    2026Clinical pediatrics(2026)
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    3National Trends and Comorbidities Associated with Pediatric Sleep Apnea-related Hospitalizations in the United States, 2012-2019
    A. Sunny, A. Suresh, F. Dapaah-Siakwan
    2026AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE(2026)
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    4Outcomes and Surgical Management of Malignant Rhabdoid Tumor of the Kidney: A Report from the Pediatric Surgical Oncology Research Collaborative.
    Hannah N Rinehardt,Elisabeth T Tracy, Anghela Paredes, Catherine Beckhorn,Harold J Leraas, Joseph Fusco,Katlyn G McKay, Nelly-Ange T Kontchou,Zachary J Kastenberg, David W Hoyt, Jonathan Roach, Emily K Myers,

    PURPOSE:Malignant rhabdoid tumor of the kidney (MRTK) is a rare, aggressive tumor seen in young children. The optimal timing of resection for locally advanced tumors is not well-defined. The purpose of this study is to evaluate modern oncologic outcomes and the impact of surgical timing. METHODS:A multicenter retrospective review was performed by institutions participating in the Pediatric Surgical Oncology Research Collaborative. Children younger than 21 years old with MRTK diagnosed between 2000 and 2022 were included. RESULTS:Sixty-nine patients were identified with MRTK and met the inclusion criteria. Median age of diagnosis was 10.1 months. Overall survival (OS) at 1, 5, and 10 years was 49%, 32%, and 19%, respectively. Patients with local Stage III disease who underwent upfront resection (n = 18) compared to those who had delayed resection after NAT (n = 15) had a similar OS, median OS greater than 60 months versus 14.6 months, respectively; p = 0.396. The surgical timing groups were balanced in terms of the presence of metastasis, length of follow-up, and tumor characteristics. There was one occurrence of primary intraoperative tumor spill and two occurrences of organ injury in the upfront resection group compared to none in the delayed resection group. CONCLUSION:MRTK carries a poor prognosis despite multimodal treatment. Histologic diagnosis may not be confirmed at presentation, and MRTK cannot be reliably distinguished from Wilms tumor on imaging alone. As overall survival is similar, the decision regarding surgical timing in locally advanced tumors should be individualized based on perceived resectability, balancing the risk of intraoperative complications against the possibility of tumor progression during neoadjuvant therapy.

    2026Pediatric blood & cancer(2026)
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    5Good Enough: when to Avoid Perfection and Accept Adequate Surgery Results in Pediatric Hand Surgery.
    Alex J Davit, Kelsi N Krakauer, Aaron J Berger,Michael G Galvez

    Pediatric hand surgery frequently requires precise surgical reconstruction of the upper limb to prevent worsening deformity. However, there is a balance of achieving a perfect radiologic film of the planned surgery and causing inadvertent harm from performing overly aggressive surgery. Precise K-wire placement and immobilization are important for optimal results; however, surgery that is too invasive results in several downsides, including loss of reduction, poor bony healing, loss of blood supply, growth plate failure, and scar contractures from poor wound healing. Here, we review this important concept of "Good Enough" to accept completely adequate results over unattainable perfection in pediatric hand surgery.

    2026The Journal of hand surgery(2026)
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    合作机构(100)

    加州大学旧金山分校合作论文 44
    费城儿童医院合作论文 30
    斯坦福大学合作论文 29
    华盛顿大学合作论文 29
    Children''s Hospital of Los Angeles合作论文 26
    密歇根大学合作论文 19
    加利福尼亚大学戴维斯分校合作论文 16
    威斯康星医学院合作论文 16
    Children''s Hospital Colorado合作论文 16
    贝勒医学院合作论文 16

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