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

Development of national biobank for lysosomal storage disorders in India- a step towards advancing research and precision medicine

印度建立溶酶体贮积症国家生物样本库——迈向研究和精准医疗的一步

Sheth, Jayesh; Nair, Aadhira; Bhavsar, Riddhi; Kamate, Mahesh; Gowda, Vykuntaraju K; Bavdekar, Ashish; Kadam, Sandeep; Nampoothiri, Sheela; Datar, Chaitanya; Panigrahi, Inusha; Kaur, Anupriya; Shah, Siddharth; Mehta, Sanjeev; Jagadeesan, Sujatha; Suresh, Indrani; Prabha, C Ratna; Kapoor, Seema; Bajaj, Shruti; Devi, Radha Rama; Prajapati, Ashka; Godbole, Koumudi; Patel, Harsh; Luhar, Zulfiqar; Shah, Raju C; Iyer, Anand; Bijarnia-Mahay, Sunita; Puri, Ratna; Muranjan, Mamta; Shah, Ami; Magar, Suvarna; Gupta, Neerja; Tayade, Naresh; Kabra, Madhulika; Jalan, Anil; Solanki, Dhaval; Dalal, Ashwin; Sheth, Frenny; Sheth, Harsh

Hypertension Treatment Cascade in Rural Delhi: Prevalence, Awareness, Treatment, and Control Among Adults

德里农村地区高血压治疗级联:成人患病率、知晓率、治疗率和控制率

Antony, S; Muranjan, M; Gogtay, N J; Furqan, Swaleha; Yadav, Geeta

Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia

248名印度骨骼发育不良患者的遗传和等位基因异质性

Jacob, Prince; Singh, Swati; Bhavani, Gandham SriLakshmi; Gowrishankar, Kalpana; Narayanan, Dhanya Lakshmi; Nampoothiri, Sheela; Patil, S J; Soni, J P; Muranjan, Mamta; Kapoor, Seema; Dhingra, Bhavna; Bhat, Ballambattu Vishnu; Bajaj, Shruti; Banerjee, Amrita; Mamadapur, Mahabaleshwar; Hariharan, Sankar V; Kamath, Nutan; Shenoy, Rathika D; Suri, Deepti; Shukla, Anju; Dalal, Ashwin; Phadke, Shubha R; Nishimura, Gen; Mortier, Geert; Shah, Hitesh; Girisha, Katta M

Prenatal diagnosis of rare genetic disorders: fourteen years' experience of a tertiary genetic centre from India

罕见遗传疾病的产前诊断:印度一家三级遗传中心十四年的经验

Sheth, Jayesh; Dhondekar, Tejasvi; Ajagekar, Manali; Datar, Chaitanya; Kher, Archana; Trivedi, Jigish; Thakkar, Swati; Gandhi, Ajit; Soni, Meenakshi; Chaudhary, Mayank; Banker, Manish; Jalan, Anil; Muranjan, Mamta; Munshi, Sujal; Munshi, Ami; Pandya, Mili; Shah, Jhanvi; Nair, Aadhira; Bhavsar, Riddhi; Sheth, Frenny; Sheth, Harsh

Biallelic Variants in LRRC45 Impair Ciliogenesis and Cause a Severe Neurological Disorder.

LRRC45 的双等位基因变异会损害纤毛发生并导致严重的神经系统疾病

Radhakrishnan Periyasamy, Quadri Neha, Erger Florian, Fuhrmann Nico, Geist Otilia-Maria, Netzer Christian, Khyriem Ibakordor, Muranjan Mamta, Udani Vrajesh, Yeole Mayuri, Mascarenhas Selinda, Limaye Sanket, Siddiqui Shahyan, Upadhyai Priyanka, Shukla Anju

Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre

印度罕见遗传病的负担:三级医疗中心二十二年的经验

Jayesh Sheth, Aadhira Nair, Frenny Sheth, Manali Ajagekar, Tejasvi Dhondekar, Inusha Panigrahi, Ashish Bavdekar, Sheela Nampoothiri, Chaitanya Datar, Ajit Gandhi, Mamta Muranjan, Anupriya Kaur, Manisha Desai, Mehul Mistri, Chitra Patel, Premal Naik, Maulin Shah, Koumudi Godbole, Seema Kapoor, Neerja

A Clinical Suspicion of Quetiapine-Induced Psychosis: A Case Report and Literature Review

喹硫平诱发精神病的临床疑似病例报告及文献综述

Michael J Valentine,Ankur Kayastha,Takara R Newsome-Cuby,Anh Thu N Nguyen,Riley G Fisher,Hanh M Pham,Saif A Meimon,Alexander Phu,Connor A Parry,Joshua J Nelson,Ethan C Hayes,Sunita Muranjan

In vitro evaluation of fenfluramine and norfenfluramine as victims of drug interactions

芬氟拉明和去甲芬氟拉明药物相互作用的体外评价

Parthena Martin, Maciej Czerwiński, Pallavi B Limaye, Seema Muranjan, Brian W Ogilvie, Steven Smith, Brooks Boyd

Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1

印度戊二酸尿症1型患者的临床特征、分子谱和预后

Tamhankar, Parag M; Vasudevan, Lakshmi; Kondurkar, Pratima; Niazi, Sarfaraj; Christopher, Rita; Solanki, Dhaval; Dholakia, Pooja; Muranjan, Mamta; Kamate, Mahesh; Kalane, Umesh; Sheth, Jayesh; Tamhankar, Vasundhara; Gulati, Reena; Vasikarla, Madhavi; Danda, Sumita; Naushad, Shaik M; Girisha, Katta M; Patil, Shekhar

Bilateral idiopathic temporal bone meningoencephaloceles - An unusual presentation

双侧特发性颞骨脑膜脑膨出——一种罕见的临床表现

Muranjan, S N; Singhal, D D; Shah, S H; Shah, A K