Genotype-Phenotype Correlation of a Rare Transthyretin Variant Causing Amyloidosis von Chaudhary, Ammar G., AlReefi, Fadi M., Abou Zahr, Riad G., Elzeftawy, Hossam A., Alghamdi, Saleh S., Bushnag, Areej A., Al-Maghrabi, Jaudah A., Abumansour, Iman S.

Volltext

Genotype-Phenotype Correlation of a Rare Transthyretin Variant Causing AmyloidosisNovel Teaching Points von Ammar G. Chaudhary, MBChB, FRCPC, Fadi M. AlReefi, MD, Riad G. Abou Zahr, MD, FSCMR, Hossam A. Elzeftawy, MD, Saleh S. Alghamdi, MD, Areej A. Bushnag, MD, Jaudah A. Al-Maghrabi, MD, MSc, FRCPC, Iman S. Abumansour, MD

Volltext

Genotype-Phenotype Correlation of a Rare Transthyretin Variant Causing Amyloidosis von Chaudhary, Ammar G, AlReefi, Fadi M, Abou Zahr, Riad G, Elzeftawy, Hossam A, Alghamdi, Saleh S, Bushnag, Areej A, Al-Maghrabi, Jaudah A, Abumansour, Iman S

Volltext

Society for Cardiovascular Magnetic Resonance 2022 Cases of SCMR case series von Johnson, Jason N., Pouraliakbar, Hamidreza, Mahdavi, Mohammad, Ranjbar, Abdolmohammad, Pfirman, Kristopher, Mehra, Vishal, Ahmed, Shahzad, Ba-Atiyah, Wejdan, Galal, Mohammed Omar, Zahr, Riad Abou, Hussain, Nasir, Tadikamalla, Raghu R., Farah, Victor, Dzelebdzic, Sanja, Muniz, Juan Carlos, Lee, Marc, Williams, Jason, Lee, Simon, Aggarwal, Sachin K., Clark, Daniel E., Hughes, Sean G., Ganigara, Madhusudan, Nagiub, Mohamed, Hussain, Tarique, Kwok, Cecilia, Lim, Han S., Nolan, Mark, Kikuchi, Daniel S., Goulbourne, Clive A., Sahu, Anurag, Sievers, Berge, Sievers, Berk, Sievers, Burkhard, Garg, Rimmy, Armas, Carlos Requena, Paleru, Vijayasree, Agarwal, Ritu, Rajagopal, Rengarajan, Bhagirath, Pranav, Kozor, Rebecca, Aneja, Ashish, Tunks, Robert, Chen, Sylvia S.M.

Volltext