Title : Treatment of Traumatic Optic Neuropathy (TON) with Megadose Methylprednisolone (MDMP)- Pros and Cons |
|
---|---|
Published by -Jalalabad Medical Journal | PDF Page : 3-4 |
DOI : | |
Abstract :
Traumatic optic neuropathy (TON) is a condition in which there is severe impairment of vision due to acute injury to the optic nerve as a result of ocular trauma or head injury. More..... |
|
Title : Efficacy and Tolerability of Amlodipine-Valsartan Compared to Amlodipine-Atenolol Combinations in Hypertensive Patients: A Prospective Comparative Study |
|
---|---|
Published by -Jalalabad Medical Journal | PDF Page : 5-12 |
DOI : | |
Abstract :
Amlodipine-valsartan and amlodipine-atenolol combination therapies may be used in patients where blood pressure is not adequately controlled on either component monotherapy or as initial therapy in patients who are likely to need multiple drug More..... |
|
Title : Knowledge, Attitude and Practise Regarding Hepatitis B among Preclinical Medical Students and Their Vaccination Status at a Private Medical College in Sylhet |
|
Published by -Jalalabad Medical Journal | PDF Page : 13-22 |
DOI : | |
Abstract :
Hepatitis B is a worldwide disease that affects millions of people. Vaccination and preventive knowledge are crucial for all, especially health care professionals. This study was aimed at evaluating the hepatitis B vaccination status of precli More..... |
|
Title : Feeding Practice during Infancy: A Hospital Based Study |
|
Published by -Jalalabad Medical Journal | PDF Page : 23-30 |
DOI : | |
Abstract :
Optimal infant feeding practises are crucial for the nutritional status, growth, development, and ultimately the survival of infants and young children. Proper feeding of infants can reduce childhood mortality and morbidity significantly. This More..... |
|
Title : Marfan Syndrome: A Case Report |
|
---|---|
Published by -Jalalabad Medical Journal | PDF Page : 31-34 |
DOI : | |
Abstract :
Marfan syndrome is a rare autosomal dominant, multisystem connective tissue disease, caused by mutation in the extra cellular matrix protein fibrillin-1 gene located on chromosome 15. It has variable phenotypic expression with a reported incid More..... |
|