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

Exploring challenges and opportunities in paediatric bereavement care: a qualitative study from a tertiary care hospital in Pakistan

探索儿童丧亲关怀中的挑战与机遇:一项来自巴基斯坦三级医院的定性研究

Hussain, Hawra; Altaf, Sadaf; Khalid, Ayesha; Hashmi, Syed Muhammad Irtiza; Rehman, Naveed; Bharuchi, Vardah; Rahman, Fatima; Shafi, Aamena; Syed, Areeba; Fadoo, Zehra; Mushtaq, Naureen; Resham, Shahzadi

Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder

一种进行性RBL2相关神经发育障碍的临床和遗传特征

Aughey, Gabriel N; Cali, Elisa; Maroofian, Reza; Zaki, Maha S; Pagnamenta, Alistair T; Ali, Zafar; Abdulllah, Uzma; Rahman, Fatima; Menzies, Lara; Shafique, Anum; Suri, Mohnish; Roze, Emmanuel; Aguennouz, Mohammed; Ghizlane, Zouiri; Saadi, Saadia Maryam; Fatima, Ambrin; Cheema, Huma Arshad; Anjum, Muhammad Nadeem; Morel, Godelieve; Robin, Stephanie; McFarland, Robert; Altunoglu, Umut; Kraus, Verena; Shoukier, Moneef; Murphy, David; Flemming, Kristina; Yttervik, Hilde; Rhouda, Hajar; Lesca, Gaetan; Chatron, Nicolas; Rossi, Massimiliano; Murtaza, Bibi Nazia; Ur Rehman, Mujaddad; Lord, Jenny; Giacopuzzi, Edoardo; Hayat, Azam; Siraj, Muhammad; Shervin Badv, Reza; Seo, Go Hun; Beetz, Christian; Kayserili, Hülya; Krioulie, Yamna; Chung, Wendy K; Naz, Sadaf; Maqbool, Shazia; Chandler, Kate E; Kershaw, Christopher J; Wright, Thomas; Banka, Siddharth; Gleeson, Joseph G; Taylor, Jenny C; Efthymiou, Stephanie; Baig, Shahid Mahmood; Severino, Mariasavina; Jepson, James E C; Houlden, Henry

SLK is mutated in individuals with a neurodevelopmental disorder.

SLK基因突变与神经发育障碍有关

Alabdi Lama, Altuwaijri Norah, Zhu Jun-Yi, Efthymiou Stephanie, Lee Hangnoh, Duan Jianli, Salem Israa, Yu Piao, Abdullah Nor Linda, Alzahrani Fatema, Xu Qing, Felemban Mashael M, Alfaifi Abdullah, Rahman Fatima, Christoforou Marilena, Maqbool Shazia, Martinez-Agosto Julian A, Alsaif Hessa S, Hashem Mais, Helaby Rana, Alsulaiman Ahood, Maroofian Reza, Houlden Henry, Arold Stefan T, Ibrahim Leena A, Han Zhe, Alkuraya Fowzan S

Multiomic profiling reveals timing of menopause predicts prefrontal cortex aging and cognitive function

多组学分析揭示更年期时间可预测前额叶皮层衰老和认知功能

Gunter-Rahman, Fatima; Adams, Charleen D; Raju, Ravikiran M; Zhang, Yu; Lee, Eunjung Alice; Messerlian, Carmen

Corrigendum: Characterizing the immune response to Mycobacterium tuberculosis: a comprehensive narrative review and implications in disease relapse

更正:结核分枝杆菌免疫反应的特征:一项全面的叙述性综述及其对疾病复发的影响

Rahman, Fatima

Spike specific IgG3 and nucleocapsid IgG response in serum serve as distinguishing immunological markers between SARS-CoV-2 infection and vaccination

血清中针对刺突蛋白特异性IgG3和核衣壳蛋白IgG的反应可作为区分SARS-CoV-2感染和疫苗接种的免疫学标志物。

Akhtar, Marjahan; Islam, Md Rashedul; Khaton, Fatema; Rahman, Fatima; Sami, Tausif Adnan; Tauheed, Imam; Ahmed, Tasnuva; Akter, Afroza; Khan, Ishtiakul Islam; Khan, Zahid Hasan; Kumar Biswas, Prasanta; Ryan, Edward T; Banu, Sayera; Shirin, Tahmina; Chowdhury, Fahima; Khan, Ashraful Islam; Bhuiyan, Taufiqur Rahman; Qadri, Firdausi

Bi-allelic MYMX variants cause a syndromic congenital myopathy with recognizable facial palsy, growth restriction, and dysmorphism

双等位基因MYMX变异会导致一种综合征性先天性肌病,其特征为明显的面瘫、生长受限和畸形。

Rahman, Fatima; Marsili, Luisa; Pasquetti, Domizia; Rad, Aboulfazl; Nadeem Anjum, Muhammad; Oprea, Gabriela; Cheema, Huma Arshad; Vona, Barbara; Augusto Alves, Cesar; Houlden, Henry; Maqbool, Shazia; Efthymiou, Stephanie; Smol, Thomas; Maroofian, Reza

Hypoxia in extravillous trophoblasts links maternal obesity and offspring neurobehavior

滋养层细胞外缺氧与母体肥胖和子代神经行为有关

Gunter-Rahman, Fatima; Mallett, Shayna; White, Frédérique; Jacques, Pierre-Étienne; Raju, Ravikiran M; Hivert, Marie-France; Lee, Eunjung Alice

Diabetes Prediction Using Feature Selection Algorithms and Boosting-Based Machine Learning Classifiers

基于特征选择算法和基于提升算法的机器学习分类器进行糖尿病预测

Rahman, Fatima; Hossain, Sheyum; Tiang, Jun-Jiat; Nahid, Abdullah-Al

The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders

遗传性糖基磷脂酰肌醇缺乏症的临床和遗传谱

Sidpra, Jai; Sudhakar, Sniya; Biswas, Asthik; Massey, Flavia; Turchetti, Valentina; Lau, Tracy; Cook, Edward; Alvi, Javeria Raza; Elbendary, Hasnaa M; Jewell, Jerry L; Riva, Antonella; Orsini, Alessandro; Vignoli, Aglaia; Federico, Zara; Rosenblum, Jessica; Schoonjans, An-Sofie; de Wachter, Matthias; Delgado Alvarez, Ignacio; Felipe-Rucián, Ana; Haridy, Nourelhoda A; Haider, Shahzad; Zaman, Mashaya; Banu, Selina; Anwaar, Najwa; Rahman, Fatima; Maqbool, Shazia; Yadav, Rashmi; Salpietro, Vincenzo; Maroofian, Reza; Patel, Rajan; Radhakrishnan, Rupa; Prabhu, Sanjay P; Lichtenbelt, Klaske; Stewart, Helen; Murakami, Yoshiko; Löbel, Ulrike; D'Arco, Felice; Wakeling, Emma; Jones, Wendy; Hay, Eleanor; Bhate, Sanjay; Jacques, Thomas S; Mirsky, David M; Whitehead, Matthew T; Zaki, Maha S; Sultan, Tipu; Striano, Pasquale; Jansen, Anna C; Lequin, Maarten; de Vries, Linda S; Severino, Mariasavina; Edmondson, Andrew C; Menzies, Lara; Campeau, Philippe M; Houlden, Henry; McTague, Amy; Efthymiou, Stephanie; Mankad, Kshitij