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

Contrasting low- and high-resolution features for HER2 scoring using deep learning

利用深度学习对比低分辨率和高分辨率特征进行HER2评分

Chauhan, Ekansh; Sharma, Anila; Sharma, Amit; Nishadham, Vikas; Padariya, Karan Vrajlal; Ghughtyal, Asha; Kumar, Ankur; Gupta, Gurudutt; Mehta, Anurag; Jawahar, C V; Vinod, P K

GNE Myopathy: Genotype - Phenotype Correlation and Disease Progression in an Indian Cohort

GNE肌病:印度人群中基因型-表型相关性及疾病进展

Baskar, Dipti; Reddy, Nishanth; Preethish-Kumar, Veeramani; Polavarapu, Kiran; Nishadham, Vikas; Vengalil, Seena; Nashi, Saraswati; Sanka, Sai Bhargava; Bardhan, Mainak; Huddar, Akshata; Unnikrishnan, Gopikrishnan; Harikrishna, Ganaraja Valakunja; Gunasekaran, Swetha; Thomas, Priya Treesa; Keerthipriya, Muddasu Suhasini; Girija, Manu Santhappan; Arunachal, Gautham; Anjanappa, Ram Murthy; Nishino, Ichizo; Pogoryelova, Oksana; Lochmuller, Hanns; Nalini, Atchayaram

A Novel Mutation in Frabin (FGD4) Causing a Mild Phenotype of CMT4H in an Indian Patient

印度患者中发现 Frabin (FGD4) 基因的新突变导致 CMT4H 的轻型表型

Nishadham, Vikas; Santhoshkumar, Rashmi; Nashi, Saraswati; Vengalil, Seena; Bardhan, Mainak; Polavarapu, Kiran; Sanka, Sai Bhargava; Anjanappa, Ram Murthy; Kulanthaivelu, Karthik; Saini, Jitender; Chickabasaviah, Yasha T; Nalini, Atchayaram

Qualitative and Quantitative Electrocardiogram Parameters in a Large Cohort of Children with Duchenne Muscle Dystrophy in Comparison with Age-Matched Healthy Subjects: A Study from South India

南印度一项研究比较了杜氏肌营养不良症患儿与年龄匹配的健康受试者的心电图定性和定量参数。

Girija, Manu S; Menon, Deepak; Polavarapu, Kiran; Preethish-Kumar, Veeramani; Vengalil, Seena; Nashi, Saraswati; Keertipriya, Madassu; Bardhan, Mainak; Thomas, Priya T; Kiran, Valasani R; Nishadham, Vikas; Sadasivan, Arun; Huddar, Akshata; Unnikrishnan, Gopi K; Inbaraj, Ganagarajan; Krishnamurthy, Arjun; Kramer, Boris W; Sathyaprabha, Talakad N; Nalini, Atchayaram

Cardiac MRI in Duchenne and Becker Muscular Dystrophy

杜氏肌营养不良症和贝克尔肌营养不良症的心脏磁共振成像

Girija, Manu Santhappan; Menon, Deepak; Polavarapu, Kiran; Preethish-Kumar, Veeramani; Vengalil, Seena; Nashi, Saraswati; Keertipriya, Madassu; Bardhan, Mainak; Thomas, Priya Treesa; Kiran, Valasani Ravi; Nishadham, Vikas; Sadasivan, Arun; Huddar, Akshata; Unnikrishnan, Gopi Krishnan; Barthur, Ashita; Nalini, Atchayaram

Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia

晚发性小脑共济失调中FGF14 GAA重复序列深部内含子扩增

Pellerin, David; Danzi, Matt C; Wilke, Carlo; Renaud, Mathilde; Fazal, Sarah; Dicaire, Marie-Josée; Scriba, Carolin K; Ashton, Catherine; Yanick, Christopher; Beijer, Danique; Rebelo, Adriana; Rocca, Clarissa; Jaunmuktane, Zane; Sonnen, Joshua A; Larivière, Roxanne; Genís, David; Molina Porcel, Laura; Choquet, Karine; Sakalla, Rawan; Provost, Sylvie; Robertson, Rebecca; Allard-Chamard, Xavier; Tétreault, Martine; Reiling, Sarah J; Nagy, Sara; Nishadham, Vikas; Purushottam, Meera; Vengalil, Seena; Bardhan, Mainak; Nalini, Atchayaram; Chen, Zhongbo; Mathieu, Jean; Massie, Rami; Chalk, Colin H; Lafontaine, Anne-Louise; Evoy, François; Rioux, Marie-France; Ragoussis, Jiannis; Boycott, Kym M; Dubé, Marie-Pierre; Duquette, Antoine; Houlden, Henry; Ravenscroft, Gianina; Laing, Nigel G; Lamont, Phillipa J; Saporta, Mario A; Schüle, Rebecca; Schöls, Ludger; La Piana, Roberta; Synofzik, Matthis; Zuchner, Stephan; Brais, Bernard

Phenotype Genotype Characterization of FKRP-related Muscular Dystrophy among Indian Patients

印度患者 FKRP 相关肌营养不良症的表型基因型特征

Gopikrishnan Unnikrishnan, Kiran Polavarapu, Mainak Bardhan, Saraswati Nashi, Seena Vengalil, Veeramani Preethish-Kumar, Ravi Kiran Valasani, Akshata Huddar, Vikas Nishadham, Bevinahalli Nanjegowda Nandeesh, Atchayaram Nalini