Fantastic explanation. I am a medical student about to graduate from an American school. This is the only video on UA-cam I found that actually explains the high yield findings of Hgb electrophoresis without going into intense, unnecessary detail. This is FANTASTIC for medical students preparing for boards.
Thank you Blake Briggs. I'm glad this video has been helpful to you. kindly refer this channel to your friends who are preparing for step-1 so that they will get benefited from this channel in whatever the little way it can be while they prepare for step-1
Thank you so much Doc. I am a 3rd year medical student and was so confused about how this worked. This is the only video that explained it clearly in English
+Shivanand Nelogal : thank you, I'm glad this video has helped you. I'm surprised, how do you known I'm Kannadiga! It's true I'm from Sandur, Bellary district.
sir you have updated very well sir I have completed my biochemistry paper with main help of you Sir thanks for all the uploaded videos sir....once again 1000 thanks so much sir....
That's excellent... I would like to see the electrophoresis for Hbs/beta thalassemia disease where there is tow mutation involving the hemoglobin synthesis causing both diseases at the same time...
+DrAbKaN : thank you, I'm glad this video has helped you. Since the disease you have asked is not a high yield area for exams so I generally do not teach.
Hi,this is Dr.Sanjay Zadgaonkar from Jabalpur,your video explains most of the things very nicely.I wish to know as a clinician how frequent is association of alpha or beta thalassemia with sickle cell trait/anemia.Secondly if I request for Hb electrophoresis to a lab, is Hb-H detected/tested & reported routinely & what is its position in relation to cathode/anode & other Hb bands as explained in the above diagram.Thanking you.Dr.Sanjay
Thank you for the information.... I'm also suffering from Haemoglobin e disease.. Is there any food restrictions?...can I eat vegetables n fish rich in iron
Amar husband ar E Beta Thalassemia and Amar HB E Trait, Please bolen vaia , Amra baby nile ki babyr Kono khoti hobe?HB E Trait ki Thalassemia bahok na rogi? Naki ar konotie na?
Sir, I and my wife both are ''beta thalassaemia carrier'' Can we have other disorder like 'sickle cell carrier', 'sickle cell disease', 'HBSC carrier', 'HBSC disease' simultaneously with this ? Answer us please.
Fantastic explanation. I am a medical student about to graduate from an American school. This is the only video on UA-cam I found that actually explains the high yield findings of Hgb electrophoresis without going into intense, unnecessary detail. This is FANTASTIC for medical students preparing for boards.
Thank you Blake Briggs. I'm glad this video has been helpful to you. kindly refer this channel to your friends who are preparing for step-1 so that they will get benefited from this channel in whatever the little way it can be while they prepare for step-1
Thank you so much Doc. I am a 3rd year medical student and was so confused about how this worked. This is the only video that explained it clearly in English
I’m glad video helped you to understand the concept.
Dr. Mungli you beautiful man! Thank you for the help, that was amazing.
very nice explanation sir.thank you.Proud kannadiga.proud of you!
I am from Ranebennur,Haveri dist
+Shivanand Nelogal : thank you, I'm glad this video has helped you. I'm surprised, how do you known I'm Kannadiga! It's true I'm from Sandur, Bellary district.
sir you have updated very well sir I have completed my biochemistry paper with main help of you Sir thanks for all the uploaded videos sir....once again 1000 thanks so much sir....
You are most welcome Vigneshwar. I'm glad my videos partly helped you to understand this subject and to do well in your exams.
That's excellent...
I would like to see the electrophoresis for Hbs/beta thalassemia disease where there is tow mutation involving the hemoglobin synthesis causing both diseases at the same time...
+DrAbKaN : thank you, I'm glad this video has helped you. Since the disease you have asked is not a high yield area for exams so I generally do not teach.
Great! Thank you Dr. Mungli.
Thank you sir! Amazing explanation! No where near my professor in Biotech
Am Thomas from Ghana thank you very much ❤
Very clear explanation. I was able to follow step by step Thanks
You are very welcome. I'm glad
THANK YOU SOOOOOOOOOOOOOO MUCH !! PERFECT EXPLANATION
Well explained and appreciating
Crystal clear explanation Sir..Thank you so much..
You are most welcome. I'm glad this video has helped you.
Hi,this is Dr.Sanjay Zadgaonkar from Jabalpur,your video explains most of the things very nicely.I wish to know as a clinician how frequent is association of alpha or beta thalassemia with sickle cell trait/anemia.Secondly if I request for Hb electrophoresis to a lab, is Hb-H detected/tested & reported routinely & what is its position in relation to cathode/anode & other Hb bands as explained in the above diagram.Thanking you.Dr.Sanjay
Very nice presentation Sir ! Greetings from Mauritius !
You are most welcome. Best wishes
Hello sir, what about HbE disease, heterozygous and homozygous???? Where will the bands form and mechanism????
Thank you for the information.... I'm also suffering from Haemoglobin e disease.. Is there any food restrictions?...can I eat vegetables n fish rich in iron
Thank you so much sir..very helpful
You are most welcome.
Perfect demonstration
+Abdullah Abohimed : thank you
Excellent explanation. How does alpha thalassemia present on Hb electrophoresis?
Thank u soo much it was too helpfull
What about HBH? what do you see then?
Thank you so much, this is really helpful
You are very welcome 🙏
hello doc, it is cure or no? Because my son and daughter like this,, hemoglobin not normal all blood 👇
Sir I have hemoglobin d disease with no physical issues, living a normal life, I want to know is it similar to thallasemia carrier?
Thank you so much!! Very clear.
You are most welcome. I'm glad this video has been useful to you.
Amar husband ar E Beta Thalassemia and Amar HB E Trait, Please bolen vaia , Amra baby nile ki babyr Kono khoti hobe?HB E Trait ki Thalassemia bahok na rogi? Naki ar konotie na?
I have Hbsc disease but there are very few doctors who knows about E trait.... I'm taking folic acid 5mg/day.... Is it enough or I need more
Nice explaining
Can I get video on "electrophoresis" it's type medium apparatus application
Nice explanation sir
Clear as water thanks!
+Julia Chavez : Thank you. I'm glad this video helped you.
perfect!!!! exactly what i need!!!
+Erick :Thank you. I'm glad this video helped you.
Really helpful, thank you!
You are very welcome. I'm glad the video helped you.
thank you so much sir
thank you so much!!
Thank you Dr. Mungli!!!!!! :D
omg thanks a lot! that was so clear!
You are most welcome. I'm glad you found this video useful.
thank you a bunch
Your welcome 🙏
Sir hemoglobin increase decrease what are the causes in our body.plz and me
thank you
Very informative
I love you and will never forget. Thank you!
sooo helpful thank you!!
amazing
I am HbD trait an my wife HbE trait , so can possible any problem my baby
Thank you sir
Sir i am sickal s trait my wife is normal can trait after age 45 tairn into sickal call dises plese tall me abut sir ji
Sir, I and my wife both are ''beta thalassaemia carrier''
Can we have other disorder like 'sickle cell carrier', 'sickle cell disease', 'HBSC carrier', 'HBSC disease' simultaneously with this ?
Answer us please.
Not necessarily. However, to be 100 sure you can get genetic testing done for the carrier status for these diseases.
NICE
Hemoglobin loss of body .where are check about hemoglobin problems.
is it dangerous
It depends on the disease.
It it curable
sir i am HbE does it mean thelesimia?
.
thankyou.......:)
You are very welcome.
Tq sir
You are most welcome.
Nice presents 🇧🇩
Thank you
Hindushtani Ho Hindi me bolo