Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sadika Kadir"'
Autor:
Rafiqul Islam, Mohammed Ashraful Haque, Asif Imran, Tanveer Ahmed, S M Bazlul Karim, Sadika Kadir
Publikováno v:
Z H Sikder Women’s Medical College Journal. 3:20-23
The Kayser-Fleischer(K-F) ring is the hallmark of Wilson’s disease (WD). In most adults or older children, the diagnosis of Wilson’s disease may be made easily when K-Frings and low ceruloplasmin levels are present. In this study presence of K-F
Autor:
Mohammed Ashraful Haque, Nirupama Najim, Tamanna Begum, Shayma Chakravarty, Sadika Kadir, Anamika Roy, Tanvir Ahmeed
Publikováno v:
Z H Sikder Women’s Medical College Journal. 2:27-30
Wilson’s Disease is an autosomal recessive disorder of copper metabolism due to ATP7B gene defect. This defect result in progressive toxic accumulation of copper in liver, CNS, cornea, skeletal system and other organs. Clinical presentations of Wil
Autor:
Naima Sharmin Hoque, Ashraful Haque, Sadika Kadir, BH Nazma Yasmeen, Rafiqul Islam, Golam Nabi, Tamanna Begum
Publikováno v:
Northern International Medical College Journal. 10:397-399
Salmonella hepatitis is one of the atypical presentations of typhoid fever and can be defined as reversible involvement of liver during the course of typhoid fever. There have been more than 150 cases of salmonella hepatitis reported both in develope
Autor:
Sadika Kadir, Romela Yeasmin, Salina Nasrin, Rafiqul Islam, Khayerul Islam, Tamanna Begum, Asif Imran
Publikováno v:
Z H Sikder Women’s Medical College Journal. 1:6-9
This is a prospective observational study conducted in the department of Paediatrics from June to August 2019 during the time of dengue outbreak. All children age up to 14 years with either positive NSI antigen or serological Gg, IgM test Kit or ELIS
Autor:
Golam Sagir, Mahfuzur Rahman, Rafiqul Islam, Sadika Kadir, Aminul Hasanat, Mohammed Ashraful Haque, SK Sader Hossain
Publikováno v:
Journal of National Institute of Neurosciences Bangladesh. 4:82-86
Background: Surgical management of lower cervical spine injury is a very important issue among these patients. Objective: The purpose of the present study was todetermine the early neurological outcome of delayed anterior decompression and stabilizat
Autor:
Sarah Ambarin Chowdhury, Mahmudul Hasan, Sadika Kadir, Nmw Rahman, Mohammad Babul Miah, Fahmida Ferdou, Golam Nabi
Publikováno v:
Z H Sikder Women’s Medical College Journal. 1:29-31
Hypokalemic periodic paralysis (HKPP) is a rare genetic disorder with autosomal dominant inheritance and characterized by recurrent attacks of skeletal muscle weakness with associated hypokalemia which is precipitated by stress, cold, carbohydrate lo