Imaging of Traumatic Neurovascular Injury von Stallmeyer, M.J.B., Morales, Robert E., Flanders, Adam E.

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Quantitative MRI studies for assessment of multiple sclerosis von Pannizzo, F., Stallmeyer, M. J. B., Friedman, J., Jennis, R. J., Zabriskie, J., Plank, C., Zimmerman, R., Whalen, J. P., Cahill, P. T.

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Report of a scalp arteriovenous malformation spontaneously hemorrhaging into a preauricular sinus von Winkler, Andrew A, Stallmeyer, M J B, Le, Thomas T

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Carotid Trauma: Bluntly von Schofield, Deborah L., Stallmeyer, M.J.B.

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Facet blocks and sacroiliac joint injections von Stallmeyer, M.J.B., Ortiz, A.Orlando

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Antithrombotic therapy and outcomes of cervical arterial dissection in the trauma patient: a case series von Hinson, Holly E, Stallmeyer, M Jb, Furuno, Jon P, Yarbrough, Karen L, Cole, John W

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Substructure of the flagellar basal body of Salmonella typhimurium von Sosinsky, Gina E., Francis, Noreen R., Stallmeyer, M.J.B., DeRosier, David J.

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Quantitation of normal canine hippocampus formation volume: Correlation of MRI with gross histology von Vullo, Thomas, Deo-Narine, Vishnu, Stallmeyer, M.JoAnn B., Gomez, Daniel G., Cahill, Patrick T.

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Image reconstruction of the flagellar basal body of Salmonella typhimurium von Stallmeyer, M.J.Bernadette, Aizawa, Shin-Ichi, Macnab, Robert M., DeRosier, David J.

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Image reconstruction of the flagellar basal body of Caulobacter crescentus von Stallmeyer, M.J.Bernadette, Hahnenberger, Karen M., Sosinsky, Gina E., Shapiro, Lucy, DeRosier, David J.

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Patient Evaluation and Selection von Stallmeyer, M. J. B., Zoarski, Gregg H.

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Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes von Wyrwoll, M J, van Walree, E S, Hamer, G, Rotte, N, Motazacker, M M, Meijers-Heijboer, H, Alders, M, Meißner, A, Kaminsky, E, Wöste, M, Krallmann, C, Kliesch, S, Hunt, T J, Clark, A T, Silber, S, Stallmeyer, B, Friedrich, C, van Pelt, A M M, Mathijssen, I B, Tüttelmann, F

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The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans von Wyrwoll, Margot J., Gaasbeek, Channah M., Golubickaite, Ieva, Stakaitis, Rytis, Oud, Manon S., Nagirnaja, Liina, Dion, Camille, Sindi, Emad B., Leitch, Harry G., Jayasena, Channa N., Sironen, Anu, Dicke, Ann-Kristin, Rotte, Nadja, Stallmeyer, Birgit, Kliesch, Sabine, Grangeiro, Carlos H.P., Araujo, Thaís F., Lasko, Paul, D’Hauwers, Kathleen, Smits, Roos M., Ramos, Liliana, Xavier, Miguel J., Conrad, Don F., Almstrup, Kristian, Veltman, Joris A., Tüttelmann, Frank, van der Heijden, Godfried W.

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The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans von Wyrwoll, MJ, Gaasbeek, CM, Golubickaite, I, Stakaitis, R, Oud, MS, Nagirnaja, L, Dion, C, Sindi, EB, Leitch, HG, Jayasena, CN, Sironen, A, Dicke, A-K, Rotte, N, Stallmeyer, B, Kliesch, S, Grangeiro, CHP, Araujo, TF, Lasko, P, Genetics of Male Infertility Initiative (GEMINI) consortium, D'Hauwers, K, Smits, RM, Ramos, L, Xavier, MJ, Conrad, DF, Almstrup, K, Veltman, JA, Tüttelmann, F, Van der Heijden, GW

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, R, Lahrouchi, N, Tadros, R, Kyndt, F, Glinge, C, Postema, Pg, Amin, As, Nannenberg, Ea, Ware, Js, Whiffin, N, Mazzarotto, F, Škorić-Milosavljević, D, Krijger, C, Arbelo, E, Babuty, D, Barajas-Martinez, H, Beckmann, Bm, Bézieau, S, Bos, Jm, Breckpot, J, Campuzano, O, Castelletti, S, Celen, C, Clauss, S, Corveleyn, A, Crotti, L, Dagradi, F, de Asmundis, C, Denjoy, I, Dittmann, S, Ellinor, Pt, Ortuño, Cg, Giustetto, C, Gourraud, Jb, Hazeki, D, Horie, M, Ishikawa, T, Itoh, H, Kaneko, Y, Kanters, Jk, Kimoto, H, Kotta, Mc, Krapels, Ipc, Kurabayashi, M, Lazarte, J, Leenhardt, A, Loeys, Bl, Lundin, C, Makiyama, T, Mansourati, J, Martins, Rp, Mazzanti, A, Mörner, S, Napolitano, C, Ohkubo, K, Papadakis, M, Rudic, B, Molina, Ms, Sacher, F, Sahin, H, Sarquella-Brugada, G, Sebastiano, R, Sharma, S, Sheppard, Mn, Shimamoto, K, Shoemaker, Mb, Stallmeyer, B, Steinfurt, J, Tanaka, Y, Tester, Dj, Usuda, K, van der Zwaag, Pa, van Dooren, S, van Laer, L, Winbo, A, Winkel, Bg, Yamagata, K, Zumhagen, S, Volders, Pga, Lubitz, Sa, Antzelevitch, C, Platonov, Pg, Odening, Ke, Roden, Dm, Roberts, Jd, Skinner, Jr, Tfelt-Hansen, J, van den Berg, Mp, Olesen, Ms, Lambiase, Pd, Borggrefe, M, Hayashi, K, Rydberg, A, Nakajima, T, Yoshinaga, M, Saenen, Jb, Kääb, S, Brugada, P, Robyns, T, Giachino, Df

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, Charlotte, Postema, Pieter G, Amin, Ahmad S, Nannenberg, Eline A, Ware, James S, Whiffin, Nicola, Mazzarotto, Francesco, Skoric-Milosavljevic, Doris, Krijger, Christian, Arbelo, Elena, Babuty, Dominique, Barajas-Martinez, Hector, Beckmann, Britt M, Bezieau, Stephane, Bos, J. Martijn, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Celen, Candan, Clauss, Sebastian, Corveleyn, Anniek, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Dittmann, Sven, Ellinor, Patrick T, Ortuno, Cristina Gil, Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jorgen K, Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid P.C, Kurabayashi, Masahiko, Lazarte, Julieta, Leenhardt, Antoine, Loeys, Bart L, Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Martins, Raphael P, Mazzanti, Andrea, Morner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Sabater Molina, Maria, Sacher, Frederic, Sahin, Hatice, Sarquella-Brugada, Georgia, Sebastiano, Regina, Sharma, Sanjay, Sheppard, Mary N, Shimamoto, Keiko, Shoemaker, M. Benjamin, Stallmeyer, Birgit, Steinfurt, Johannes, Tanaka, Yuji, Tester, David J, Usuda, Keisuke, van der Zwaag, Paul A, Van Dooren, Sonia, Van Laer, Lut, Winbo, Annika, Winkel, Bo G, Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul G.A, Lubitz, Steven A, Antzelevitch, Charles, Platonov, Pyotr G, Odening, Katja E, Roden, Dan M, Roberts, Jason D, Skinner, Jonathan R, Tfelt-Hansen, Jacob, van den Berg, Maarten P, Olesen, Morten S, Lambiase, Pier D, Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan B, Kaeaeb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela F

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A Novel Keratinocyte Mitogen: Regulation of Leptin and its Functional Receptor in Skin Repair von Stallmeyer, Birgit, Kämpfer, Heiko, Pfeilschifter, Josef, Frank, Stefan, Podda, Maurizio, Kaufmann, Roland

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Sodium permeable and "hypersensitive" TREK-1 channels cause ventricular tachycardia von Decher, N, Ortiz-Bonnin, B, Friedrich, C, Schewe, M, Kiper, AK, Rinné, S, Seemann, G, Peyronnet, R, Zumhagen, S, Bustos, D, Kockskämper, J, Kohl, P, Just, S, González, W, Baukrowitz, T, Stallmeyer, B, Schulze-Bahr, E

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Regulation of eNOS in Normal and Diabetes-Impaired Skin Repair: Implications for Tissue Regeneration von Stallmeyer, Birgit, Anhold, Manuel, Wetzler, Christian, Kahlina, Kornelija, Pfeilschifter, Josef, Frank, Stefan

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Human Molybdopterin Synthase Gene: Genomic Structure and Mutations in Molybdenum Cofactor Deficiency Type B von Reiss, J., Dorche, C., Stallmeyer, B., Mendel, R.R., Cohen, N., Zabot, M.T.

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