Formative evaluation of a prototype system for automated analysis of mass spectrometry data von Fananapazir, N, Li, M, Spentzos, D, Aliferis, C F

Volltext

A study of the pen motif in the Bahá'í writings von MILANI, K, FANANAPAZIR, N

Volltext

Association of pancreatic fat content with type II diabetes mellitus von Nadarajah, C., Fananapazir, G., Cui, E., Gichoya, J., Thayalan, N., Asare-Sawiri, M., Menias, C.O., Sandrasegaran, K.

Volltext

Synthetic dual-energy CT reconstruction from single-energy CT Using artificial intelligence von Jeong, Jiwoong, Wentland, Andrew, Mastrodicasa, Domenico, Fananapazir, Ghaneh, Wang, Adam, Banerjee, Imon, Patel, Bhavik N.

Volltext

Consensus report from the 9 th International Forum for Liver Magnetic Resonance Imaging: applications of gadoxetic acid-enhanced imaging von Koh, Dow-Mu, Ba-Ssalamah, Ahmed, Brancatelli, Giuseppe, Fananapazir, Ghaneh, Fiel, M Isabel, Goshima, Satoshi, Ju, Sheng-Hong, Kartalis, Nikolaos, Kudo, Masatoshi, Lee, Jeong Min, Murakami, Takamichi, Seidensticker, Max, Sirlin, Claude B, Tan, Cher Heng, Wang, Jin, Yoon, Jeong Hee, Zeng, Mengsu, Zhou, Jian, Taouli, Bachir

Volltext

Acquired cystic disease subtype renal cell carcinoma (ACD-RCC): prevalence and imaging features at a single institution von Carnahan, Molly B., Kunzelman, Jacqueline, Kawashima, Akira, Patel, Bhavik N., Menias, Christine O., Fananapazir, Ghaneh

Volltext

Long-term results of dual-chamber (DDD) pacing in obstructive hypertrophic cardiomyopathy : evidence for progressive symptomatic and hemodynamic improvement and reduction of left v... von LAMEH FANANAPAZIR, EPSTEIN, N. D, CURIEL, R. V, PANZA, J. A, TRIPODI, D, MCAREAVEY, D

Volltext

Inherited and de novo Mutations in the Cardiac Actin Gene Cause Hypertrophic Cardiomyopathy von Olson, Timothy M, Doan, Thao P, Kishimoto, Nina Y, Whitby, Frank G, Ackerman, Michael J, Fananapazir, Lameh

Volltext

Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37 von Ahmed, Zubair M., Morell, Robert J., Riazuddin, Saima, Gropman, Andrea, Shaukat, Shahzad, Ahmad, Mussaber M., Mohiddin, Saidi A., Fananapazir, Lameh, Caruso, Rafael C., Husnain, Tayyab, Khan, Shaheen N., Riazuddin, Sheikh, Griffith, Andrew J., Friedman, Thomas B., Wilcox, Edward R.

Volltext

Molecular and phenotypic effects of heterozygous, homozygous, and compound heterozygote myosin heavy-chain mutations von Alpert, Norman R, Mohiddin, Saidi A, Tripodi, Dorothy, Jacobson-Hatzell, Jacqueline, Vaughn-Whitley, Kelly, Brosseau, Christine, Warshaw, David M, Fananapazir, Lameh

Volltext

Skeletal muscle expression and abnormal function of β-myosin in hypertrophic cardiomyopathy von CUDA, G, LAMEH FANANAPAZIR, WEN-SI ZHU, SELLERS, J. R, EPSTEIN, N. D

Volltext

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle von Poetter, Karl, Jiang, He, Hassanzadeh, Shahin, Master, Stephen R, Chang, Anthony, Dalakas, Marinos C, Rayment, Ivan, Sellers, James R, Fananapazir, Lameh, Epstein, Neal D

Volltext

Missense Mutations in the β-Myosin Heavy-Chain Gene Cause Central Core Disease in Hypertrophic Cardiomyopathy von Fananapazir, Lameh, Dalakas, Marinos C., Cyran, Francis, Cohn, Gabriel, Epstein, Neal D.

Volltext

Structural Interpretation of the Mutations in the β-Cardiac Myosin that have been Implicated in Familial Hypertrophic Cardiomyopathy von Rayment, Ivan, Holden, Hazel M., Sellers, James R., Fananapazir, Lameh, Epstein, Neal D.

Volltext

Multicenter randomized study of anticoagulation guided by remote rhythm monitoring in patients with implantable cardioverter-defibrillator and CRT-D devices: Rationale, design, and... von IP, John, WALDO, Albert L, HALPERIN, Jonathan L, LIP, Gregory Y. H, ROTHWELL, Peter M, MARTIN, David T, BERSOHN, Malcolm M, CHOUCAIR, Wassim K, AKAR, Joseph G, WATHEN, Mark S, ROHANI, Pooyan

Volltext

Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis von Dobson-Stone, C, Danek, A, Rampoldi, L, Hardie, R J, Chalmers, R M, Wood, N W, Bohlega, S, Dotti, M T, Federico, A, Shizuka, M, Tanaka, M, Watanabe, M, Ikeda, Y, Brin, M, Goldfarb, L G, Karp, B I, Mohiddin, S, Fananapazir, L, Storch, A, Fryer, A E, Maddison, P, Sibon, I, Trevisol-Bittencourt, P C, Singer, C, Caballero, I R, Aasly, J O, Schmierer, K, Dengler, R, Hiersemenzel, L-P, Zeviani, M, Meiner, V, Lossos, A, Johnson, S, Mercado, F C, Sorrentino, G, Dupré, N, Rouleau, G A, Volkmann, J, Arpa, J, Lees, A, Geraud, G, Chouinard, S, Németh, A, Monaco, A P

Volltext

Genotype-phenotype correlations in hypertrophic cardiomyopathy : insights provided by comparisons of kindreds with distinct and identical β-myosin heavy chain gene mutations von FANANAPAZIR, L, EPSTEIN, N. D

Volltext

Hypertrophic cardiomyopathy caused by a novel α-tropomyosin mutation (V95A) is associated with mild cardiac phenotype, abnormal calcium binding to troponin, abnormal myosin cycling... von KARIBE, Akihiko, TOBACMAN, Larry S, FANANAPAZIR, Lameh, STRAND, James, BUTTERS, Carol, BACK, Nick, BACHINSKI, Linda L, ARAI, Andrew E, ORTIZ, Anne, ROBERTS, Robert, HOMSHER, Earl

Volltext

The in vitro motility activity of beta-cardiac myosin depends on the nature of the beta-myosin heavy chain gene mutation in hypertrophic cardiomyopathy von Cuda, G, Fananapazir, L, Epstein, N D, Sellers, J R

Volltext

Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy von Lankford, E B, Epstein, N D, Fananapazir, L, Sweeney, H L

Volltext