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Paper Review Records

全部论文审稿周期

24 篇有效样本 · 按发表日期由新到旧排列
审稿天数=录用日期-收稿日期;保留 PDF/DOI/网页源链接

89 天

Associations Between Sensory Processing and Irritability in Prader–Willi Syndrome: Beyond Genetic Subtypes and Clinical Backgrounds

作者
Erina Nakane; Hiroyuki Ogata; Sohei Saima; Chuichi Kondo; Masaki Seki; Yuji Oto; Hiroshi Ihara展开收起
作者单位
1. Department of Psychiatry Dokkyo Medical University Saitama Medical Center Koshigaya Saitama Japan; 2. Department of Psychiatry Ikezawa Shinkeika Hospital Hanyuu Saitama Japan; 3. Department of Psychiatry Okute Hospital Mizunami Gifu Japan; 4. Department of Pediatrics Dokkyo Medical University Saitama Medical Center Koshigaya Saitama Japan展开收起
PDF源文件 DOI 网页
168 天

Vascular Abnormalities in Hypermobile Ehlers–Danlos Syndrome: A Retrospective Cohort Study

作者
Thomas Gehin; Malika Foy; Robert Carlier; Valentin Renault; Karelle Benistan展开收起
作者单位
1. AP‐HP, DMU Smart Imaging, Raymond Poincaré University Hospital Garches France; 2. AP‐HP, Ehlers‐Danlos Syndrome Referral Center, Raymond Poincaré University Hospital Garches France; 3. UR20261, PHARMAcoligo, Paris‐Saclay University, UVSQ Versailles France展开收起
PDF源文件 DOI 网页
51 天

Diagnostic Odyssey of Atypical Long‐Chain 3‐Hydroxyacyl‐ CoA Dehydrogenase Deficiency ( LCHADD ) Explained by Three Allelic Products From Two Pathogenic Variants

作者
Yutaka Furuta; Lynette C. Rives; T. Andrew Burrow; Thomas A. Cassini; Rory J. Tinker; Amy K. Robertson; Kimberly M. Ezell; Rizwan Hamid; Joy D. Cogan; John A. Phillips展开收起
作者单位
1. Division of Medical Genetics and Genomic Medicine, Department of Pediatrics Vanderbilt University Medical Center Nashville Tennessee USA; 2. Section of Genetics and Metabolism, Department of Pediatrics University of Arkansas for Medical Sciences, College of Medicine Little Rock Arkansas USA; 3. Department of Medical Genetics and Genomics Icahn School of Medicine at Mount Sinai New York New York USA展开收起
PDF源文件 DOI 网页
62 天

Early‐Onset Epileptic Encephalopathy and Neurodevelopmental Regression Associated With ST3GAL5 Deficiency

作者
Sabire Gokalp; Elif Guler; Mustafa Kilic展开收起
作者单位
1. Department of Pediatric Metabolic Disorders Etlik City Hospital, University of Health Science Ankara Türkiye展开收起
PDF源文件 DOI 网页
67 天

Resolution of Refractory Multifocal Atrial Tachycardia in C ostello Syndrome Using Trametinib: A Case Supporting MEK Inhibitors as Targeted, Specific Antiarrhythmic

作者
Vanina Taliercio; Annabelle Wilcox; Stacey Cole; Josue Flores Daboub; José E. Morales Moreno; Kasey G. Andrews; S. Yukiko Asaki; Thomas A. Pilcher; Martin Tristani‐Firouzi; Mary C. Niu; David Viskochil; Benjamin Hammond展开收起
作者单位
1. Department of Pediatrics, Division of Medical Genetics University of Utah Salt Lake City Utah USA; 2. Department of Pediatrics, Division of General Pediatrics University of Utah Salt Lake City Utah USA; 3. Department of Pediatrics, Division of Cardiology University of Utah Salt Lake City Utah USA展开收起
PDF源文件 DOI 网页
88 天

Response of an Infant With Presumed Multiple Acyl‐ CoA Dehydrogenase Deficiency ( MADD ) to Ketone Supplementation

作者
Yutaka Furuta; Kaitlyn N. Bloom; Jerry Vockley; Angela R. Grochowsky; Neena S. Agrawal; Ellen W. Strickler; Natalie N. Owen; Erica T. Gray; B. Lakshitha A. Perera; Eric R. Gamazon; Lynette C. Rives; Hua‐Chang Chen; Qi Liu; Rizwan Hamid; Joy D. Cogan; John A. Phillips; Thomas A. Cassini; Bryce A. Schuler展开收起
作者单位
1. Department of Pediatrics, Division of Medical Genetics and Genomic Medicine Vanderbilt University Medical Center Nashville Tennessee USA; 2. Department of Pediatrics, Division of Genetic and Genomic Medicine University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA; 3. Department of Medicine, Division of Genetic Medicine and Clinical Pharmacology Vanderbilt University Medical Center Nashville Tennessee USA; 4. Department of Biostatistics Vanderbilt University Medical Center Nashville Tennessee USA展开收起
PDF源文件 DOI 网页

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可以。先按 90 天时限做可行性筛选,同步查找无基金、无知名作者挂靠的典型论文案例,作为选刊依据。重点核对研究质量与期刊 scope。

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《融合机器学习与生命周期评价的城市污水处理碳排放预测与优化》

样本口径2026 年最近 5 篇有效论文样本

平均审稿62 天

中位数65 天

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