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

Phenotypic Evolution in Fabry Disease: Our Experience in Indian Cohort

法布里病表型演变:我们在印度队列中的经验

Dave, Usha; Kadali, Srilatha; Hussain, Tajamul; Radhika, Ananthaneni; Patel, Sagar; Patel, Nirav; Naushad, Shaik Mohammad

The role of TLR7 agonists in modulating COVID-19 severity in subjects with loss-of-function TLR7 variants

TLR7激动剂在调节TLR7功能缺失变异体患者COVID-19严重程度中的作用

Naushad, Shaik Mohammad; Mandadapu, Gowtham; Ramaiah, Mekala Janaki; Almajhdi, Fahad N; Hussain, Tajamul

The rs1991517 polymorphism is a genetic risk factor for congenital hypothyroidism.

rs1991517 多态性是先天性甲状腺功能减退症的遗传风险因素

Kollati Yedukondalu, Akella Radha Rama Devi, Naushad Shaik Mohammad, Thalla Maunika, Reddy G Bhanuprakash, Dirisala Vijaya R

Adaptive Neuro-Fuzzy Inference System-Based Exploration of the Interrelationships of 25-Hydroxyvitamin D, Calcium, Phosphorus with Parathyroid Hormone Production

基于自适应神经模糊推理系统的25-羟基维生素D、钙、磷与甲状旁腺激素生成相互关系的研究

Mohan, Iyyapu Krishna; Khan, Siraj Ahmed; Shiva Krishna, D; Vijaya Bhaskar, M; Sai Baba, K S S; Hussain, Tajamul; Alrokayan, Salman A; Naushad, Shaik Mohammad

Identification and in Silico Characterization of a Novel CASK c.2546T>C (p.V849A) Mutation in a Male Infant with Pontocerebellar Hypoplasia

在一名患有脑桥小脑发育不全的男性婴儿中鉴定并进行计算机模拟表征一种新的CASK c.2546T>C (p.V849A)突变

Rama Devi, Akella Radha; Lingappa, Lokesh; Naushad, Shaik Mohammad

Acute Gaucher Disease-Like Condition in an Indian Infant with a Novel Biallelic Mutation in the Prosaposin Gene

印度一名婴儿出现急性戈谢病样症状,其前蛋白酶基因存在一种新的双等位基因突变

Radha Rama Devi, Akella; Kadali, Srilatha; Radhika, Ananthaneni; Singh, Vineeta; Kumar, M Aravind; Reddy, Gummadi Maheshwar; Naushad, Shaik Mohammad

Artificial neural network model for predicting the bioavailability of tacrolimus in patients with renal transplantation

用于预测肾移植患者他克莫司生物利用度的神经网络人工模型

Thishya, Kalluri; Vattam, Kiran Kumar; Naushad, Shaik Mohammad; Raju, Shree Bhushan; Kutala, Vijay Kumar