Process Advantages of Direct CO2 to Methanol Synthesis von Marlin, Dana S., Sarron, Emeric, Sigurbjörnsson, Ómar

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A comprehensive comparative study on intelligence based optimization algorithms used for maximum power tracking in grid-PV systems von S, Marlin, Jebaseelan, Sundarsingh

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Spinal cord neural activity of patients with fibromyalgia and healthy controls during temporal summation of pain: an fMRI study von Staud, Roland, Boissoneault, Jeff, Lai, Song, Mejia, Marlin S., Ramanlal, Riddhi, Godfrey, Melyssa M., Stroman, Patrick W.

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Mutations in NALP12 cause hereditary periodic fever syndromes von Jéru, I, Duquesnoy, P, Fernandes-Alnemri, T, Cochet, E, Yu, J.W, Lackmy-Port-Lis, M, Grimprel, E, Landman-Parker, J, Hentgen, V, Marlin, S, McElreavey, K, Sarkisian, T, Grateau, G, Alnemri, E.S, Amselem, S

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Effects of blood extraction and ecophysiological experiments on stress in adult males of Liolaemus attenboroughi von Duran, Fernando, Medina, Marlin S, Ibargüengoytía, Nora R, Boretto, Jorgelina M

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Recurrent benign paroxysmal positional vertigo in two DFNB16 siblings: A CARE case report von Achard, S., Simon, F., Denoyelle, F., Marlin, S.

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Synergizing Design of Building Energy Performance Using Parametric Analysis, Dynamic Visualization, and Neural Network Modeling von Didwania, Srijan K., Agami Reddy, T., Addison, Marlin S.

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Myopia prevalence and risk factors in children von Theophanous, Christos, Modjtahedi, Bobeck S, Batech, Michael, Marlin, David S, Luong, Tiffany Q, Fong, Donald S

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Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutations von Elmaleh-Bergès, M, Baumann, C, Noël-Pétroff, N, Sekkal, A, Couloigner, V, Devriendt, K, Wilson, M, Marlin, S, Sebag, G, Pingault, V

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Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause von Petit, F., Escande, F., Jourdain, A.S., Porchet, N., Amiel, J., Doray, B., Delrue, M.A., Flori, E., Kim, C.A., Marlin, S., Robertson, S.P., Manouvrier-Hanu, S., Holder-Espinasse, M.

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SOX10 mutations mimic isolated hearing loss von Pingault, V., Faubert, E., Baral, V., Gherbi, S., Loundon, N., Couloigner, V., Denoyelle, F., Noël-Pétroff, N., Ducou Le Pointe, H., Elmaleh-Bergès, M., Bondurand, N., Marlin, S.

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Audiological phenotyping evaluation in KBG syndrome: Description of a multicenter review von Rhamati, L., Marcolla, A., Guerrot, A.M., Lerosey, Y., Goldenberg, A., Serey-Gaut, M., Rio, M., Cormier Daire, V., Baujat, G., Lyonnet, S., Rubinato, E., Jonard, L., Rondeau, S., Rouillon, I., Couloignier, V., Jacquemont, M.L., Dupin Deguine, D., Moutton, S., Vincent, M., Isidor, B., Ziegler, A., Marie, J.P., Marlin, S.

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Multi-image fusion: optimal decomposition strategy with heuristic-assisted non-subsampled shearlet transform for multimodal image fusion von Ravi, Jampani, Subbayamma, B. V., Kumar, P. Vijaya, Sriramam, Yadavalli S. S., Marlin, S., Sheeba, Adlin, Kumar, N. V. Phani Sai

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A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome von Nizon, M., Henry, M., Michot, C., Baumann, C., Bazin, A., Bessières, B., Blesson, S., Cordier-Alex, M.-P., David, A., Delahaye-Duriez, A., Delezoïde, A.-L., Dieux-Coeslier, A., Doco-Fenzy, M., Faivre, L., Goldenberg, A., Layet, V., Loget, P., Marlin, S., Martinovic, J., Odent, S., Pasquier, L., Plessis, G., Prieur, F., Putoux, A., Rio, M., Testard, H., Bonnefont, J.-P., Cormier-Daire, V.

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Complexation-Induced Translational Isomerism: Shuttling through Stepwise Competitive Binding von Marlin, Dana S., González Cabrera, Diego, Leigh, David A., Slawin, Alexandra M. Z.

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IgG4-Related Disease: A New Etiology Underlying Diffuse Intracranial Dilating Vasculopathy von Marlin, Evan S., Dornbos, David, Ikeda, Daniel S., Lehman, Norman L., Powers, Ciarán J.

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Impact of immunological state on eco-physiological variables in one of the southernmost lizards in the world von Duran, Fernando, Boretto, Jorgelina M, Fernández, Jimena B, Molina, Mora Ibáñez, Medina, Marlin S, Ibargüengoytía, Nora R

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RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa von Moore, A, Escudier, E, Roger, G, Tamalet, A, Pelosse, B, Marlin, S, Clément, A, Geremek, M, Delaisi, B, Bridoux, A-M, Coste, A, Witt, M, Duriez, B, Amselem, S

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Effect of Vitamin C, Thiamine, and Hydrocortisone on Ventilator- and Vasopressor-Free Days in Patients With Sepsis: The VICTAS Randomized Clinical Trial von Sevransky, Jonathan E, Rothman, Richard E, Hager, David N, Bernard, Gordon R, Brown, Samuel M, Buchman, Timothy G, Busse, Laurence W, Coopersmith, Craig M, DeWilde, Christine, Ely, E. Wesley, Eyzaguirre, Lindsay M, Fowler, Alpha A, Gaieski, David F, Gong, Michelle N, Hall, Alex, Hinson, Jeremiah S, Hooper, Michael H, Kelen, Gabor D, Khan, Akram, Levine, Mark A, Lewis, Roger J, Lindsell, Chris J, Marlin, Jessica S, McGlothlin, Anna, Moore, Brooks L, Nugent, Katherine L, Nwosu, Samuel, Polito, Carmen C, Rice, Todd W, Ricketts, Erin P, Rudolph, Caroline C, Sanfilippo, Fred, Viele, Kert, Martin, Greg S, Wright, David W

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A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impai... von del Castillo, F J, Rodríguez-Ballesteros, M, Álvarez, A, Hutchin, T, Leonardi, E, de Oliveira, C A, Azaiez, H, Brownstein, Z, Avenarius, M R, Marlin, S, Pandya, A, Shahin, H, Siemering, K R, Weil, D, Wuyts, W, Aguirre, L A, Martín, Y, Moreno-Pelayo, M A, Villamar, M, Avraham, K B, Dahl, H-H M, Kanaan, M, Nance, W E, Petit, C, Smith, R J H, Van Camp, G, Sartorato, E L, Murgia, A, Moreno, F, del Castillo, I

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