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B. Weijs(4)Asirvatham Samuel J SJ(3)Alan S. Go, MD(3)
Charlotte Eitel, MD(3)Ayman A. Hussein, MD(3)Berenfeld Omer O(2)
Caputo M(2)Chao TF(2)Chen Peng-Sheng PS(2)
Andrade JG(2)Akira Fukui, MD(2)Albert Nancy M NM(2)
Ajay K Jain(2)Cook G Elliott GE(2)Botto GL(2)
Casella M(2)Bokeriia L A LA(2)Antonio Hernández-Madrid(2)
Christian Sohns(2)Bengt Zöller(2)Badger Troy J TJ(2)
Charlotte Eitel(2)Blanke Philipp P(2)Anné Wim W(2)
Chamberlain AM(2)Chamorro A A(1)Andrikopoulos G(1)
cas V.A. Boersma, MD, PhD(1)Aakriti Gupta(1)Boll Stefanie S(1)
Badge Ravi R(1)Burashnikov Alexander A(1)Cohen-Lehman Janna J(1)
Crotti Lia L(1)Cao H(1)Clare Teresa Oliver-Williams(1)
Creswell Lawrence L LL(1)Chung Tommy T(1)Benussi Stefano S(1)
Ariansen Inger I(1)Beukema Rypko P RP(1)Alexander Samol(1)
Alsheikh-Ali Alawi A AA(1)Copie X X(1)Biffi Mauro M(1)
Bhuriya Rohit R(1)Chugh Aman A(1)Andreas Goette1(1)
Anand N. Ganesan, MBBS, PhD(1)Aguadé-Bruix Santiago S(1)


Literature Related to Simha V V [Author]
1
  • Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations.


    Authors : Subramanyam L L; Simha V V; Garg A A;

    Affiliations : Department of Internal Medicine, Division of Nutrition and Metabolic Diseases, Center for Human Nutrition, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, USA.

    Journal : N/A   (2009)

    Related Links: Pubmed | Publisher website


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