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Orphanet Journal of Rare Diseases 期刊封面 医学
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Review Cycle Records

Orphanet Journal of Rare Diseases

Springer SCIE OA
2026新锐 2区2025中科院 2区2025 JCR Q2
201.2平均天数
140中位天数
72最短天数
391最长天数
6622025发文量

Paper Review Records

全部论文审稿周期

11 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

278 天

Unlocking MENA’s potential in rare-disease precision medicine

作者Brahim Tabarki; Khalid Hundallah; Majid Alfadhel

作者单位1. Division of Pediatric Neurology, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia; 2. Medical Genomic Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud Bin Abdulaziz University for Health Sciences (KSAU-HS), Ministry of National Guard Health Affairs (MNG-HA), Riyadh, Saudi Arabia; 3. Genetics and Precision Medicine Department (GPM), King Abdullah Specialized Children’s Hospital (KASCH), King Abdulaziz Medical City, Ministry of National Guard Health Affairs (MNG-HA), Riyadh, Saudi Arabia; 4. King Salman Center for Disability Research, Riyadh, Saudi Arabia

PDF源文件 DOI 网页
139 天

Clinical and genetic landscape of neuronopathic gaucher disease in Ukraine: hepatosplenomegaly and diagnostic delay

作者Nataliia Samonenko; Nataliia Olkhovych; Olena Okhotnikova; Nataliia Gorovenko

作者单位1. Shupyk National Healthcare University of Ukraine, Kyiv, Ukraine; 2. National Children’s Specialized Hospital “Okhmatdyt”, Kyiv, Ukraine; 3. National Scientific Center “Institute of Cardiology, Clinical and Regenerative Medicine Named After M.D. Strazheska”, Kyiv, Ukraine

PDF源文件 DOI 网页
364 天

Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience

作者Sheng Yi; Qi Yang; Linlin Wang; Xunzhao Zhou; Shujie Zhang; Jiale Qian; Shang Yi; Jing Huang; Junjie Chen; Qiang Zhang; Fei Chen; Jiao Li; Shengkai Wei; Xiaofei Zhang; Qinle Zhang; Pingshan Pan; Zailong Qin; Jingsi Luo

作者单位1. Genetic and Metabolic Central Laboratory, Guangxi Birth Defects Research and Prevention Institute, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, China; 2. Guangxi Clinical Research Center for Birth Defects, Guangxi Clinical Research Center for Pediatric Diseases, Guangxi Key Laboratory of Reproductive Health and Birth Defects Prevention, Guangxi Key Laboratory of Precision Medicine for Genetic Diseases, Guangxi Key Laboratory of Birth Defects and Stem Cell Biobank, Guangxi Key Laboratory of Birth Defects Research and Prevention, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, China; 3. Department of Obstetrics, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, China; 4. Pediatrics Department, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, China; 5. Department of Radiology, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, China

PDF源文件 DOI 网页
234 天

Interventions targeting challenges experienced by individuals with Pitt Hopkins syndrome: a scoping review

作者Monika Dolik-Michno; Magnus Starbrink; Helena Wandin; Annika Jernberg Grönlund; Martha Gustavsson; Linn Johnels

作者单位1. Swedish National Center for Rett Syndrome and Related Disorders, Frösön, Sweden; 2. Oslo Metropolitan University, Oslo, Norway; 3. Department of Public Health and Caring Sciences, University of Uppsala, Uppsala, Sweden; 4. Department of Community Medicine and Rehabilitation, Umeå University, Umeå, Sweden; 5. Department of Women’s and Children’s Health, University of Uppsala, Uppsala, Sweden; 6. Department of Education and Special Education, University of Gothenburg, Gothenburg, Sweden; 7. Nationellt Center för Rett Syndrom & Närliggande Diagnoser, Frösön, Sweden

PDF源文件 DOI 网页
275 天

Psychological symptoms in individuals with Spinal Muscular Atrophy (SMA) and their caregivers – results from a nation-wide study in Germany

作者Justine Hussong; Berenike Leibrock; Tabea Huelle; Hannah Mattheus; Erik Landfeldt; Simone Thiele; Maggie C. Walter; Michael Zemlin; Eva Moehler; Ulrich Dillmann; Marina Flotats‑Bastardas

作者单位1. Department of Child and Adolescent Psychiatry, Saarland University, Homburg, Germany; 2. Department of Medicine, University of Saarland, Saarbruecken, Germany; 3. Clinical Psychology and Psychotherapy, Saarland University, Saarland, Germany; 4. IQVIA, Stockholm, Sweden; 5. Friedrich Baur Institute at the Department of Neurology, LMU University Hospital, LMU, Munich, Germany; 6. Department of General Pediatrics and Neonatology, Saarland University, Homburg, Germany; 7. Department of Neurology, Saarland University, Homburg, Germany; 8. Department of General Pediatrics and Neonatology, Division of Neuropaediatrics, Saarland University, Homburg, Germany

PDF源文件 DOI 网页
77 天

Aspiration and silent aspiration in Niemann-Pick disease type C1: longitudinal findings from the NIH natural history study

作者Beth I. Solomon; Andrea M. Munoz; Aiden Borruso; Ninet Sinaii; Nicole Farhat; Derek Alexander; Desiree A. Labor; An Dang Do; Forbes D. Porter

作者单位1. Speech-Language Pathology Section, Rehabilitation Medicine Department, Mark O. Hatfield Clinical Center, National Institutes of Health, Bethesda, USA; 2. Division of Translational Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, USA; 3. Biostatistics and Clinical Epidemiology Service, NIH Clinical Center, National Institutes of Health, Bethesda, USA

PDF源文件 DOI 网页
116 天

Transplantation as disease modifying therapy in the era of gene therapy medicinal products – health policy considerations

作者Margreet Wagenmakers; Anna Lehman; Caroline den Hoed; Laura van Dussen; Mirjam Langeveld; Sandra Sirrs

作者单位1. Department of Internal Medicine, Erasmus MC, Centre for Lysosomal and Metabolic Disease, University Medical Center Rotterdam, Rotterdam, The Netherlands; 2. Adult Metabolic Diseases Clinic, University of British Columbia, Vancouver, Canada; 3. Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands; 4. Department of Endocrinology and Metabolism, Amsterdam UMC, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, University of Amsterdam, Amsterdam, The Netherlands; 5. Division of Endocrinology, Department of Medicine, University of British Columbia, Vancouver, Canada

PDF源文件 DOI 网页
127 天

Expiratory phase lung mechanics in late-onset Pompe disease: a multicenter study using oscillometry to identify specific breathing abnormalities

作者Grazia Crescimanno; Oreste Marrone; Marta Lazzeri; Paolo Innocente Banfi; Agata Lax; Elena Compalati; Rosario Di Marco; Sabrina Planiscig; Paola Confalonieri; Fabrizio Seidita; Filippo Brighina; Marco Confalonieri

作者单位1. Institute for Biomedical Research and Innovation (IRIB), National Research Council, Palermo, Italy; 2. Departmental Unit of Neurophysiopathology, Regional Centre for Diagnosis and Treatment of Rare Neurological Diseases, AOUP Policlinico, University of Palermo, Palermo, Italy; 3. IRCCS Fondazione Don Gnocchi, Milano, Italy; 4. Functional Recovery and Rehabilitation, Ospedali Riuniti Villa Sofia- Cervello, Palermo, Italy; 5. Department of Pulmonology, University Hospital of Cattinara, Trieste, Italy; 6. AIGlico (Italian Glycogenosis Association), Assago, Italy

PDF源文件 DOI 网页
140 天

Assessment of cardiometabolic risk using single point insulin sensitivity estimator (SPISE) in pediatric Bardet–Biedl Syndrome: a pilot study

作者Tugce Kandemir; Melek Yildiz; Ummahan Tercan; Ozge Bayrak Demirel; Hasan Yanik; Volkan Karaman; Ayca Dilruba Aslanger; Aslı Derya Kardelen; Sukran Poyrazoglu; Feyza Darendeliler; Guven Toksoy; Firdevs Bas

作者单位1. Department of Pediatric Endocrinology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Türkiye; 2. Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Türkiye; 3. Department of Genetics, Institute of Graduate Studies in Health Sciences, Istanbul University, Istanbul, Türkiye

PDF源文件 DOI 网页
391 天

Management of patients with rare diseases in the Middle East: challenges & opportunities – insights from the Rare Advocacy Council

作者Agnès Farrugia; Ahmed Bahey; Ahmad Tarawah; Arwa Al Yamani; Carla Abou Selwan; Dania Mohty; Denis Wolfs; Dorica Dan; Hafiz Mosa Ali Malhan; Johan De Graaf; Stefan Živković; Yasser Wali; Youmna Ouraybi; Zakareya Al Kadhem; Nafisa Tawfiq; Lee Davelaar; Noha Mohamed Mahmoud Abdelbaky

作者单位1. Association Française Contre L’Amylose, Marseille, France; 2. Qatar Friends Hemophilia Group (QFHG), Doha, Qatar; 3. Pediatric Hematology-Oncology, King Salman Medical City, Madinah, Saudi Arabia; 4. Al Madinah Hereditary Blood Disorders Charity Society, Madinah, Saudi Arabia; 5. MENA Hematology League, Dubai, United Arab Emirates; 6. Hematology/Oncology/BMT Deputy Chairman of Saudi and Thalassemia and Sickle Cell Anemia Society, Riyadh, Saudi Arabia; 7. Saudi Association of Pediatric Hematology/Oncology Society (SAPHOS), Riyadh, Saudi Arabia; 8. Science PRO, Jal-el-dib, Lebanon; 9. King Faisal Specialist Hospital, Riyadh, Saudi Arabia; 10. Amyloidosis Association, Brussels, Belgium; 11. Romanian National Alliance for Rare Disease, Bucharest, Romania; 12. Adult Hematologist, Riyadh, Saudi Arabia; 13. Dutch Pituitary Foundation, Nijkerk, The Netherlands; 14. Endo-ERN European Reference Network on Rare Endocrine Conditions, Leiden, The Netherlands; 15. Department of Endocrinology, Leiden University Medical Center, Leiden, The Netherlands; 16. National Organization of Rare Diseases, Belgrade, Serbia; 17. Pediatric Hematology, College of Medicine and Health Sciences, Sultan Qaboos University, Board Member Omani Society of Hematology, Muscat, Oman; 18. Ana Fareed Health Consultancy for Patient Advocacy, Dubai, United Arab Emirates; 19. Bahrain Society for Sickle Cell Disease Patients Care, Manama, Bahrain; 20. UAE Rare Disease Society, Dubai, United Arab Emirates; 21. Emerging Markets, Global Policy & Public Affairs, Rare Diseases, Pfizer, Sydney, Australia; 22. Regional Patient Advocacy – Middle East, Pfizer, Cairo, Egypt

PDF源文件 DOI 网页

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样本口径2026 年最近 5 篇有效论文样本

平均审稿96.4 天

中位数77 天

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