Yes! I now record on an iPad, which allows me to write. It also doesn't have a fan, which caused a little bit of background noise when I was recording on a computer.
We have here Five Autosomal Recessive Diseases of Lysosomal Storage Disorders (Pathology of Metabolism and Degeneration Types) and one particular to Pediatric Males: 1) Tay-Sachs Disease, 2) Niemann Pick, 3) Krabbe, 4)Fabry's Disease (XLR), 5) Gauchers Disease and 6) Metachromatic Lipodystrophy and they all have their respective Enzyme Deficiency, namely and respectively Hexoaminidase (Ganglioside Buildup), Sphingomyelinase (Sphingomyelin), Galactocerebrosidase (Galactocerebroside), Alpha Galactosidase (Ceramide Trihexoside) and Arylsulfatase A (Sulfatides)....Give me a point now. MD Paul Bolin, du bist ausgezeichnet!
I wonder why this channel doesn’t have more subscribers … amazing!! Easy to understand and quick to the point ❤ thank you so much
thank you so much for such an amazing talent in explaining
You made this topic easy ,thanks
Yay, Dr Bolin finally got himself a new mic....congratulations
Yes! I now record on an iPad, which allows me to write. It also doesn't have a fan, which caused a little bit of background noise when I was recording on a computer.
We have here Five Autosomal Recessive Diseases of Lysosomal Storage Disorders (Pathology of Metabolism and Degeneration Types) and one particular to Pediatric Males: 1) Tay-Sachs Disease, 2) Niemann Pick, 3) Krabbe, 4)Fabry's Disease (XLR), 5) Gauchers Disease and 6) Metachromatic Lipodystrophy and they all have their respective Enzyme Deficiency, namely and respectively Hexoaminidase (Ganglioside Buildup), Sphingomyelinase (Sphingomyelin), Galactocerebrosidase (Galactocerebroside), Alpha Galactosidase (Ceramide Trihexoside) and Arylsulfatase A (Sulfatides)....Give me a point now. MD Paul Bolin, du bist ausgezeichnet!
Insightful
Thanks
thank you so much for this! it is greatly appreciated
Thank you sir❤️❤️❤️
Thank you sir may Allah bless you