Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Shayla Imam Kanta"'
Autor:
Shaoli Sarker, Tamannyat Binte Eshaque, Anjana Soorajkumar, Nasna Nassir, Binte Zehra, Shayla Imam Kanta, Md Atikur Rahaman, Amirul Islam, Shimu Akter, Mohammad Kawsar Ali, Rabeya Akter Mim, K. M. Furkan Uddin, Mohammod Shah Jahan Chowdhury, Nusrat Shams, Md. Abdul Baqui, Elaine T. Lim, Hosneara Akter, Marc Woodbury-Smith, Mohammed Uddin
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Duchenne muscular dystrophy (DMD) is a severe rare neuromuscular disorder caused by mutations in the X-linked dystrophin gene. Several mutations have been identified, yet the full mutational spectrum, and their phenotypic consequences, will
Externí odkaz:
https://doaj.org/article/b12c0b69d34d43fc96da4a42d0764a7d
Autor:
Hosneara Akter, Muhammad Mizanur Rahman, Shaoli Sarker, Mohammed Basiruzzaman, Md. Mazharul Islam, Md. Atikur Rahaman, Md. Ashiquir Rahaman, Tamannyat Binte Eshaque, Nushrat Jahan Dity, Shouvik Sarker, Md. Robed Amin, Mohammad Monir Hossain, Maksuda Lopa, Nargis Jahan, Shafaat Hossain, Amirul Islam, Ashaduzzaman Mondol, Md Omar Faruk, Narayan Saha, Gopen kumar Kundu, Shayla Imam Kanta, Rezaul Karim Kazal, Kanij Fatema, Md. Ashrafur Rahman, Maruf Hasan, Md. Abid Hossain Mollah, Md. Ismail Hosen, Noushad Karuvantevida, Ghausia Begum, Binte Zehra, Nasna Nassir, A. H. M. Nurun Nabi, K. M. Furkan Uddin, Mohammed Uddin
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Copy number variations (CNVs) play a critical role in the pathogenesis of neurodevelopmental disorders (NDD) among children. In this study, we aim to identify clinically relevant CNVs, genes and their phenotypic characteristics in an et
Externí odkaz:
https://doaj.org/article/990779ba5a7e42dc992125e6354c08cc
Publikováno v:
Dhaka Shishu (Children) Hospital Journal. 37:45-50
Background: Febrile seizure is one of the most common diseases in early childhood. The impact of early-life Febrile Seizure on the developing brain is an important issue to detect. Objectives: To observe the neurodevelopment of children suffering fro
Autor:
AZM Mosiul Azam, Humaira Rafiqa Quaderi, Shaoli Sarker, Shayla Imam Kanta, Suraj Chandra Majumdar
Publikováno v:
SAS Journal of Medicine. 7:447-452
Introduction: Outpatient services usually cost less, because you don't need to stay overnight. Staff members at outpatient centers are well trained in the service they provide. Neurodevelopmental Disorders (NDDs) are a heterogeneous group of conditio
Publikováno v:
Scholars Journal of Applied Medical Sciences. 9:794-798
Introduction: A majority of neonates present with histories of brain insult in the antenatal, natal and post-natal periods. Identification, appropriate assessment and intervention are crucial for best neurodevelopmental outcomes. In DSH the Pediatric
Publikováno v:
Dhaka Shishu (Children) Hospital Journal. 35:48-54
Background: Epilepsy is the most common conditions encountered in most paediatric neurology clinics in many parts of the developing world. It is important to understand the sociodemographic profile of children with epilepsy and also to recognize the
Publikováno v:
Northern International Medical College Journal. 11:411-414
Background : The optimal response to antiepileptic treatment is the control of seizures. In different studies, it has been shown that childhood epilepsy presents with a variable course, and approximately one-third of epilepsy experience alternating r
Autor:
Muhammad Mizanur Rahman, Hosneara Akter, Md. Ashiquir Rahaman, Md. Abid Hossain Mollah, Nushrat Jahan Dity, A.H.M. Nurun Nabi, Ashaduzzaman Mondol, Md. Robed Amin, Mohammed Basiruzzaman, Ghausia Begum, Maruf Hasan, Rezaul Karim Kazal, Narayan Saha, Gopenkumar Kundu, Md. Atikur Rahaman, Md. Ismail Hosen, Zehra Binte Ashraf, Amirul Islam, Maksuda Lopa, Shayla Imam Kanta, Mazharul M. Islam, Nargis Jahan, Mohammed Uddin, Shaoli Sarker, Md. Ashrafur Rahman, Shouvik Sarker, Omar Faruk, Tamannyat Binte Eshaque, Shafaat Hossain, K. M. Furkan Uddin, Noushad Karuvantevida, Monir Hossain, Nasna Nassir, Kanij Fatema
Background: Copy number variations (CNVs) play a critical role into the pathogenesis of neurodevelopmental disorders (NDD) among children. In this study, we aim to identify clinically relevant CNVs, genes and their phenotypic characteristics in an et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe1434565d248ccaf955acafc2020fd2
https://doi.org/10.21203/rs.3.rs-948388/v1
https://doi.org/10.21203/rs.3.rs-948388/v1