Fantastic explanation. I am a medical student about to graduate from an American school. This is the only video on CZcams 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 CZcams 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.
Very clear explanation. I was able to follow step by step Thanks
You are very welcome. I'm glad
Well explained and appreciating
Thank you sir! Amazing explanation! No where near my professor in Biotech
Am Thomas from Ghana thank you very much ❤
Crystal clear explanation Sir..Thank you so much..
You are most welcome. I'm glad this video has helped you.
Thank u soo much it was too helpfull
Great! Thank you Dr. Mungli.
THANK YOU SOOOOOOOOOOOOOO MUCH !! PERFECT EXPLANATION
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.
thank you a bunch
Your welcome 🙏
Perfect demonstration
+Abdullah Abohimed : thank you
Thank you so much sir..very helpful
You are most welcome.
Thank you so much, this is really helpful
You are very welcome 🙏
Nice explaining
Clear as water thanks!
+Julia Chavez : Thank you. I'm glad this video helped you.
Very nice presentation Sir ! Greetings from Mauritius !
You are most welcome. Best wishes
Nice explanation sir
thank you
thank you so much sir
thank you so much!!
Thank you so much!! Very clear.
You are most welcome. I'm glad this video has been useful to you.
perfect!!!! exactly what i need!!!
+Erick :Thank you. I'm glad this video helped you.
Very informative
Really helpful, thank you!
You are very welcome. I'm glad the video helped you.
I love you and will never forget. Thank you!
amazing
Thank you Dr. Mungli!!!!!! :D
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
omg thanks a lot! that was so clear!
You are most welcome. I'm glad you found this video useful.
Thank you sir
Hello sir, what about HbE disease, heterozygous and homozygous???? Where will the bands form and mechanism????
NICE
sooo helpful thank you!!
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
Excellent explanation. How does alpha thalassemia present on Hb electrophoresis?
Can I get video on "electrophoresis" it's type medium apparatus application
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?
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
Tq sir
You are most welcome.
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 hemoglobin increase decrease what are the causes in our body.plz and me
thankyou.......:)
You are very welcome.
Hemoglobin loss of body .where are check about hemoglobin problems.
I am HbD trait an my wife HbE trait , so can possible any problem my baby
It it curable
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
is it dangerous
It depends on the disease.
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 presents 🇧🇩
Thank you
sir i am HbE does it mean thelesimia?
.
Hindushtani Ho Hindi me bolo