Hello again! I have to write about my study plan with the following: Goal of study, title or subject of research, and detailed study plan.
I've never done an study plan before so I'm not really sure if it's okay but I wrote a little draft about it. If it's too short please let me know. I hope you can help me with this essay as well and thanks for everything.
Currently in the research center where I work I have the opportunity to interact constantly with a doctor specialist in pulmonology, who always tells me about international conferences in which he has participated and the various research topics that have been presented in them. One of the topics that caught my attention was Cystic Fibrosis, a multisystem disease caused by the mutation of a gene on chromosome 7, which is quite frequent in our country due to the great variety and mixture of ethnicities that we present.
During my years of master's study I would like to develop this topic and contribute to the related advances presented. According to studies and reports presented by Korean researchers, I have noticed that there are not many articles about Cystic Fibrosis as it is a rare disease in the Asian community. However, I am convinced that it would be very useful to develop new studies to be able to reaffirm the knowledge about this disease, to improve them and to have more revisions of it for future projects. I would like to, with the guide and help of my professors, carry out a research work of descriptive type in which we can observe more clearly the clinical manifestations and other findings that allow us to diagnose this disease early as it can sometimes be camouflaged like any other one. Due to the low incidence of this disease in Korea, this work will be a challenge that will undoubtedly leave us satisfied once it is concluded and published in the scientific community, contributing to the Korean population with a more detailed study of this rare disease.
In addition, I would like to obtain more knowledge about the diagnostic methods of genetic study in Cystic Fibrosis in order to be able to implement them or to accommodate them in some way to my country and thus have the best technology for the diagnosis. This knowledge would be of great importance in my country that has a greater incidence of this disease, to have within reach a definitive diagnostic method that supports and confirms the clinical and radiological suspicions of our specialist doctors would be of great help to our entire community.
I've never done an study plan before so I'm not really sure if it's okay but I wrote a little draft about it. If it's too short please let me know. I hope you can help me with this essay as well and thanks for everything.
STUDY PLAN
Currently in the research center where I work I have the opportunity to interact constantly with a doctor specialist in pulmonology, who always tells me about international conferences in which he has participated and the various research topics that have been presented in them. One of the topics that caught my attention was Cystic Fibrosis, a multisystem disease caused by the mutation of a gene on chromosome 7, which is quite frequent in our country due to the great variety and mixture of ethnicities that we present.
During my years of master's study I would like to develop this topic and contribute to the related advances presented. According to studies and reports presented by Korean researchers, I have noticed that there are not many articles about Cystic Fibrosis as it is a rare disease in the Asian community. However, I am convinced that it would be very useful to develop new studies to be able to reaffirm the knowledge about this disease, to improve them and to have more revisions of it for future projects. I would like to, with the guide and help of my professors, carry out a research work of descriptive type in which we can observe more clearly the clinical manifestations and other findings that allow us to diagnose this disease early as it can sometimes be camouflaged like any other one. Due to the low incidence of this disease in Korea, this work will be a challenge that will undoubtedly leave us satisfied once it is concluded and published in the scientific community, contributing to the Korean population with a more detailed study of this rare disease.
In addition, I would like to obtain more knowledge about the diagnostic methods of genetic study in Cystic Fibrosis in order to be able to implement them or to accommodate them in some way to my country and thus have the best technology for the diagnosis. This knowledge would be of great importance in my country that has a greater incidence of this disease, to have within reach a definitive diagnostic method that supports and confirms the clinical and radiological suspicions of our specialist doctors would be of great help to our entire community.
