Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mahfuj-Ul Anwar"'
Autor:
Md Mahfuj Ul Anwar, Sajeda Afrin, Md Shakhawat Hossain, Shah Md Sarwer Jahan, Md Mahfuzer Rahman
Publikováno v:
Journal of Rangpur Medical College. 8:33-39
Background: Stroke is a leading cause of death and disability globally and particularly in low and middle-income countries, and the burden is increasing. To prevent complications and permanent defects in stroke, early diagnosis is the key that can ea
Autor:
Md Helal Miah, Md Ahad Bakas, Md Kamal Hossein, Tahmina Begum, Md Shafiul Alam, Md Jahangir Kabir, Abu Said Md Rahenur Mondol, Md Ruhul Amin Sarkar, Md Mahfuj Ul Anwar, Shah Md Sarwer Jahan, Md Mahfuzer Rahman
Publikováno v:
Journal of Rangpur Medical College. 8:72-75
We report an isoniazid-induced encephalopathy in a man with chronic renal failure. Drug-induced encephalopathy is a common side effect of many drugs. Isoniazid (INH), a first-line drug for tuberculosis, can cause encephalopathy in patients with chron
Autor:
Abu Said Md Rahenur Mondol, Tanzina Zaman, Md Mahfuj Ul Anwar, Md Helal Miah, Md Al Fatah Al Adiluzzaman, Akter Banu, Shah Md Sarwer Jahan, Md Mahfuzer Rahman
Publikováno v:
Journal of Rangpur Medical College. 8:3-10
Background: Hypertension is a growing issue of public health problem of the adult population in both developed as well as developing world, is a serious medical condition that significantly increases the risks of heart, brain, kidney, and other disea
Publikováno v:
Journal of Rangpur Medical College. 7:69-72
Bangladesh is an example of a highly populous, agricultural country where melioidosis may be a significantly underdiagnosed cause of infection and death. Melioidosis is caused by a highly pathogenic, soil-borne, Gram-negative bacterium, Burkholderia
Autor:
Md Shakhawat Hossain, Md Mahfuj Ul Anwar, Maknunnahar, Md Abdul Motin, Md Shafiul Alam, Jimma Hossain, Md Naushad Ali, Abu Hena Md Shohel Rana
Publikováno v:
Journal of Rangpur Medical College. 7:63-68
Eating disorders are common and frequently missed behavioral disorders associated with significant physical, mental and social morbidity and mortality. Among psychiatric illness, mortality rate of anorexia nervosa and bulimia nervosa is about 10% and
Autor:
Mahfuzer Rahman, Md. Golam Rabbani, Akter Banu, Mohsina Akter, A S M Shafiujjaman, Mahfuj-ul Anwar, Md Jahangir Kabir, Md. Abul Kalam Azad, Md. Kamrul Hasan
Publikováno v:
Haematology Journal of Bangladesh. 6:30-37
Hereditary angioedema (HAE) is a rare disease that is characterised by recurrent episodes of angioedema in absence of urticaria or pruritus. It usually affects skin and the mucosa of the upper respiratory tract and the gastrointestinal tracts. It is
Autor:
Mahfuj-Ul Anwar, Sajeda Afrin, ASM Rahenur Mondol, Mohammad Nurul Islam Khan, Narayan Chandra Sarkar, Kamruzzaman Sarkar, Shah Sarwer Jahan, Moni Rani, Ratindra Nath Mondal
Publikováno v:
Journal of Obesity and Diabetes. :9-14
Background: Stroke is a leading cause of mortality and disability worldwide. To prevent complications and permanent defects, early diagnosis, distinguishing the type and risk factor of stroke is crucial. Methodology: It was a hospital based cross sec
Autor:
Akter Banu, Md Mahfuzer Rahman, Md Mahfuj Ul Anwar, Raihan Ahmed, Md Abul Kalam Azad, Jahangir Kabir, Anis Ahmed, Devendranath Sarkar, Shah Md Sarwer Jahan, MA Ohab, Shafiul Alam, Md Ashraful Haque, AKM Shaheduzzaman, Md Mokhlesur Rahman, Shariful Islam Mondol, Md Kamruzzaman Sarkar, Md Helal Miah, Rahenur Mondol, Md Golam Rabbani, Prosanto Kumar Pondit, Narayan Chandro Sarkar, Md Ruhul Amin Sarkar, Abul Kalam Azad, Md Al Fatah Al Adiluzzaman, Priobrata Karmakar, Probal Sutradhar, Md Abdullah Al Mamoon, Firoz Mondol, ASM Shafiujjaman
Publikováno v:
Bangladesh Journal of Neuroscience. 35:95-103
Congenital myasthenic syndromes (CMS) comprise a heterogeneous group of rare inherited diseases in which the neuromuscular transmission in the motor plate is compromised by one or more genetic pathophysiological specific mechanisms are characterized
Publikováno v:
Journal of Medicine. 2017, Vol. 18 Issue 2, p75-79. 5p.