1817 is Paracervical Block Useful to Decrease Pain During in Office? von Lederer, MH, Grady, MM, Timmons, D, Palin, H, Carugno, JA

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Mutation Spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and Genotype-Phenotype Correlations in Warburg Micro Syndrome and Martsolf Syndrome von Handley, Mark T., Morris-Rosendahl, Deborah J., Brown, Stephen, Macdonald, Fiona, Hardy, Carol, Bem, Danai, Carpanini, Sarah M., Borck, Guntram, Martorell, Loreto, Izzi, Claudia, Faravelli, Francesca, Accorsi, Patrizia, Pinelli, Lorenzo, Basel-Vanagaite, Lina, Peretz, Gabriela, Abdel-Salam, Ghada M.H., Zaki, Maha S., Jansen, Anna, Mowat, David, Glass, Ian, Stewart, Helen, Mancini, Grazia, Lederer, Damien, Roscioli, Tony, Giuliano, Fabienne, Plomp, Astrid S., Rolfs, Arndt, Graham, John M., Seemanova, Eva, Poo, Pilar, García-Cazorla, Àngels, Edery, Patrick, Jackson, Ian J., Maher, Eamonn R., Aligianis, Irene A.

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Idiopathic pulmonary fibrosis is associated with common genetic variants and limited rare variants von Peljto, AL, Walts, AD, Cardwell, J, Powers, J, Corte, TJ, Dickinson, JL, Glaspole, I, Moodley, YP, Vasakova, MK, Bendstrup, E, Borie, R, Crestani, B, Bonella, F, Costabel, U, Gudmundsson, G, Donnelly, SC, Henry, MT, Kennedy, MP, McCarthy, C, O'Reilly, KMA, Poletti, V, Puppo, F, Tomassetti, S, Luzzi, V, Kokturk, N, Mogulkoc, N, Fiddler, CA, Hirani, N, Jenkins, G, Maher, TM, Molyneaux, PL, Parfrey, H, Blackwell, TS, Jackson, PD, Nathan, SD, Porteous, MK, Brown, KK, Christie, JD, Collard, HR, Eickelberg, O, Foster, EE, Glassberg, M, Kass, D, Kropski, JA, Lederer, D, Linderholm, AL, Loyd, J, Mathai, SK, Montesi, SB, Noth, I, Oldham, JM, Palmisciano, AJ, Reichner, CA, Rojas, M, Roman, J, Schluger, N, Shea, BS, Swigris, JJ, Wolters, PJ, Zhang, Y, Prele, CMA, Enghelmayer, JI, Otaola, M, Ryerson, CJ, Salinas, M, Sterclova, M, Gebremariam, TH, Myllärniemi, M, Carbone, R, Furusawa, H, Hirose, M, Inoue, Y, Miyazaki, Y, Ohta, K, Ohta, S, Okamoto, T, Kim, DS, Pardo, A, Selman, M, Aranda, AU, Park, MS, Park, JS, Song, JW, Molina-Molina, M, Planas-Cerezales, L, Westergren-Thorsson, G, Smith, AV, Rich, SS, Oelsner, EC, Barr, RG, Rotter, JI, O'Connor, G, Vasan, RS, Cho, MH, Schwarz, MI, Steele, MP, Lee, JS, Yang, IV, Fingerlin, TE, Schwartz, DA

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Overlap of genetic risk between interstitial lung abnormalities and idiopathic pulmonary fibrosis von Hobbs, BD, Putman, RK, Araki, T, Nishino, M, Gudmundsson, G, Gudnason, V, Eiriksdottir, G, Zilhao Nogueira, NR, Dupuis, J, Xu, H, O'Connor, GT, Manichaikul, A, Nguyen, J, Podolanczuk, AJ, Madahar, P, Rotter, JI, Lederer, DJ, Barr, RG, Rich, SS, Ampleford, EJ, Ortega, VE, Peters, SP, O'Neal, WK, Newell, JD, Bleecker, ER, Meyers, DA, Allen, RJ, Oldham, JM, Ma, S-F, Noth, I, Jenkins, RG, Maher, TM, Hubbard, RB, Wain, LV, Fingerlin, TE, Schwartz, DA, Washko, GR, Rosas, IO, Silverman, EK, Hatabu, H, Cho, MH, Hunninghake, GM, COPDGene Investigators, ECLIPSE Investigators, SPIROMICS Research Group, and UK ILD Consortium

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Genome-wide association study of susceptibility to idiopathic pulmonary fibrosis von Allen, RJ, Guillen-Guio, B, Oldham, JM, Ma, S-F, Dressen, A, Paynton, ML, Kraven, LM, Obeidat, M, Li, X, Ng, M, Braybrooke, R, Molina-Molina, M, Hobbs, BD, Putman, RK, Sakornsakolpat, P, Booth, HL, Fahy, WA, Hart, SP, Hill, MR, Hirani, N, Hubbard, RB, McAnulty, RJ, Millar, AB, Navaratnam, V, Oballa, E, Parfrey, H, Saini, G, Whyte, MKB, Zhang, Y, Kaminski, N, Adegunsoye, A, Strek, ME, Neighbors, M, Sheng, XR, Gudmundsson, G, Gudnason, V, Hatabu, H, Lederer, DJ, Manichaikul, A, Newell Jr., JD, O'Connor, GT, Ortega, VE, Xu, H, Fingerlin, TE, Bossé, Y, Hao, K, Joubert, P, Nickle, DC, Sin, DD, Timens, W, Furniss, D, Morris, AP, Zondervan, K, Hall, IP, Sayers, I, Tobin, MD, Maher, TM, Cho, MH, Hunninghake, GM, Schwartz, DA, Yaspan, BL, Molyneaux, PL, Flores, C, Noth, I, Jenkins, RG, Wain, LV

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Resequencing study confirms host defense and cell senescence gene variants contribute to the risk of idiopathic pulmonary fibrosis von Moore, C, Yang, IV, Powers, J, Bishop, M, Russell, P, Vestal, B, Cardwell, J, Markin, CR, Steele, MP, Lee, J, Brown, KK, Loyd, JE, Crapo, JD, Silverman, EK, Cho, MH, James, JA, Guthridge, JM, Cogan, JD, Kropski, JA, Swigris, JJ, Bair, C, Soon Kim, D, Ji, W, Kim, H, Maier, LA, Pacheco, KA, Hirani, N, Poon, AS, Li, F, Braybrooke, R, Saini, G, Maher, TM, Molyneaux, PL, Saunders, P, Zhang, Y, Gibson, KF, Kass, DJ, Rojas, M, Sembrat, J, Wolters, PJ, O'Riordan, T, Strek, ME, Noth, I, Ma, S-F, Porteous, MK, Kreider, ME, Patel, NB, Inoue, Y, Akagawa, S, Eickelberg, O, Fernandez, IE, Behr, J, Mogulkoc, N, Glaspole, I, Tomassetti, S, Ravaglia, C, Poletti, V, Crestani, B, Borie, R, Kannengiesser, C, Parfrey, H, Fiddler, C, Rassl, D, Gudmundsson, G, Lederer, DJ, Podolanczuk, AJ, Bendstrup, E, Danchel, V, Henry, MT, Keane, MP, Doran, P, Vašáková, M, Sterclova, M, Ryerson, CJ, Wilcox, PG, Okamoto, T, Furusawa, H, Laurent, G, Baltic, S, Prele, C, Moodley, Y, Shea, BS, Ohta, K, Narumoto, O, Nathan, SD, Venuto, DC, Woldehanna, ML, Kokturk, N, De Andrade, JA, Luckhardt, T, Kulkarni, T, Bonella, F, Donnelly, SC, McElroy, A, Armstrong, ME, Aranda, A, Carbone, RG, Beckman, KB, Fingerlin, TE, Schwartz, DA

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Mutation Spectrum in RAB 3 GAP 1 , RAB 3 GAP 2 , and RAB 18 and Genotype-Phenotype Correlations in Warburg Micro Syndrome and Martsolf Syndrome von Handley, Mark T., Morris-Rosendahl, Deborah J., Brown, Stephen, Macdonald, Fiona, Hardy, Carol, Bem, Danai, Carpanini, Sarah M., Borck, Guntram, Martorell, Loreto, Izzi, Claudia, Faravelli, Francesca, Accorsi, Patrizia, Pinelli, Lorenzo, Basel-Vanagaite, Lina, Peretz, Gabriela, Abdel-Salam, Ghada M.H., Zaki, Maha S., Jansen, Anna, Mowat, David, Glass, Ian, Stewart, Helen, Mancini, Grazia, Lederer, Damien, Roscioli, Tony, Giuliano, Fabienne, Plomp, Astrid S., Rolfs, Arndt, Graham, John M., Seemanova, Eva, Poo, Pilar, García-Cazorla, Àngels, Edery, Patrick, Jackson, Ian J., Maher, Eamonn R., Aligianis, Irene A.

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Both CD80 and CD86 co-stimulatory molecules regulate allergic pulmonary inflammation von Mark, D A, Donovan, C E, De Sanctis, G T, Krinzman, S J, Kobzik, L, Linsley, P S, Sayegh, M H, Lederer, J, Perkins, D L, Finn, P W

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Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition von Palmer, EE, Pusch, M, Picollo, A, Forwood, C, Nguyen, MH, Suckow, V, Gibbons, J, Hoff, A, Sigfrid, L, Megarbane, A, Nizon, M, Cogné, B, Beneteau, C, Alkuraya, FS, Chedrawi, A, Hashem, MO, Stamberger, H, Weckhuysen, S, Vanlander, A, Ceulemans, B, Rajagopalan, S, Nunn, K, Arpin, S, Raynaud, M, Motter, CS, Ward-Melver, C, Janssens, K, Meuwissen, M, Beysen, D, Dikow, N, Grimmel, M, Haack, TB, Clement, E, McTague, A, Hunt, D, Townshend, S, Ward, M, Richards, LJ, Simons, C, Costain, G, Dupuis, L, Mendoza-Londono, R, Dudding-Byth, T, Boyle, J, Saunders, C, Fleming, E, El Chehadeh, S, Spitz, MA, Piton, A, Gerard, B, Abi Warde, MT, Rea, G, McKenna, C, Douzgou, S, Banka, S, Akman, C, Bain, JM, Sands, TT, Wilson, GN, Silvertooth, EJ, Miller, L, Lederer, D, Sachdev, R, Macintosh, R, Monestier, O, Karadurmus, D, Collins, F, Carter, M, Rohena, L, Willemsen, MH, Ockeloen, CW, Pfundt, R, Kroft, SD, Field, M, Laranjeira, FER, Fortuna, AM, Soares, AR, Michaud, V, Naudion, S, Golla, S, Weaver, DD, Bird, LM, Friedman, J, Clowes, V, Joss, S, Pölsler, L, Campeau, PM, Blazo, M, Bijlsma, EK, Rosenfeld, JA, Beetz, C, Powis, Z, McWalter, K, Brandt, T, Torti, E, Mathot, M, Mohammad, SS, Armstrong, R, Kalscheuer, VM

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Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis von Allen, RJ, Guillen-Guio, B, Oldham, JM, Ma, S-F, Dressen, A, Paynton, ML, Kraven, LM, Obeidat, M, Li, X, Ng, M, Braybrooke, R, Molina-Molina, M, Hobbs, BD, Putman, RK, Sakornsakolpat, P, Booth, HL, Fahy, WA, Hart, SP, Hill, MR, Hirani, N, Hubbard, RB, McAnulty, RJ, Millar, AB, Navaratnam, V, Oballa, E, Parfrey, H, Saini, G, Whyte, MKB, Zhang, Y, Kaminski, N, Adegunsoye, A, Strek, ME, Neighbors, M, Sheng, XR, Gudmundsson, G, Gudnason, V, Hatabu, H, Lederer, DJ, Manichaikul, A, Newell, JD, O'Connor, GT, Ortega, VE, Xu, H, Fingerlin, TE, Bossé, Y, Hao, K, Joubert, P, Nickle, DC, Sin, DD, Timens, W, Furniss, D, Morris, AP, Zondervan, K, Hall, IP, Sayers, I, Tobin, MD, Maher, TM, Cho, MH, Hunninghake, GM, Schwartz, DA, Yaspan, BL, Molyneaux, PL, Flores, C, Noth, I, Jenkins, RG, Wain, LV

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