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1
المؤلفون: W. Lippross, B. Loss, J. H. Hansen, K. Becker, H. Muhle, A. Caliebe, M. Hitz, A. Uebing
المصدر: The Thoracic and Cardiovascular Surgeon.
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2Academic Journal
المؤلفون: R. C. Brown, B. Bellmann, H. Muhle, J. M. G. Davis, L. D. Maxim
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.573.6315; http://annhyg.oxfordjournals.org/content/49/4/295.full.pdf
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3Academic Journal
المؤلفون: R. C. Brown, B. Bellmann, H. Muhle, J. M. G. Davis, L. D. Maxim
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.606.6845; http://www.dkfg.de/pdf/studien/Brown-et-al-2005.pdf
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4Academic Journal
المؤلفون: B. Bellmann, O. Creutzenberg, C. Dasenbrock, H. Ernst, G. Pohlmann, H. Muhle
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.574.7832; http://toxsci.oxfordjournals.org/content/54/1/237.full.pdf
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5
المؤلفون: K.-D. Mibling, E. Carmona, G. Palubinskas, A. Ohndorf, Tobias Storch, S. Engelbrecht, Martin Habermeyer, S. Zimmermann, H. Muhle
المصدر: WHISPERS
مصطلحات موضوعية: Current (mathematics), 010504 meteorology & atmospheric sciences, Computer science, 0211 other engineering and technologies, Hyperspectral imaging, 02 engineering and technology, 01 natural sciences, Tree (data structure), Systems engineering, EnMAP, Satellite, Use case, Ground segment, 021101 geological & geomatics engineering, 0105 earth and related environmental sciences, Verification and validation
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6
المؤلفون: Holger Lerche, H. Muhle, N. Winter
المصدر: Zeitschrift für Epileptologie. 29:63-69
مصطلحات موضوعية: Pediatrics, Perinatology and Child Health, Neurology (clinical)
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7
المصدر: Zeitschrift für Epileptologie. 27:93-99
مصطلحات موضوعية: Pediatrics, Perinatology and Child Health, Neurology (clinical)
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8Academic Journal
المؤلفون: R. S. Møller, Y. G. Weber, L. L. Klitten, H. Trucks, H. Muhle, W. S. Kunz, H. C. Mefford, A. Franke, M. Kautza, P. Wolf, D. Dennig, S. Schreiber, I. M. Rückert, H. E. Wichmann, J. P. Ernst, C. Schurmann, H. J. Grabe, N. Tommerup, U. Stephani, H. Lerche, H. Hjalgrim, I. Helbig, T. Sander, F. Zimprich, M. Mörzinger, M. Feucht, A. Suls, S. Weckhuysen, L. Claes, L. Deprez, K. Smets, T. Van Dyck, T. Deconinck, P. De Jonghe, R. Velizarova, P. Dimova, M. Radionova, I. Tournev, D. Kancheva, R. Kaneva, A. Jordanova, D. B. Kjelgaard, A. E. Lehesjoki, A. Siren, S. Baulac, E. Leguern, S. Von Spiczak, P. Ostertag, M. Leber, C. Leu, M. R. Toliat, P. Nürnberg, A. Hempelmann, F. Rüschendorf, C. E. Elger, A. A. Kleefuß Lie, R. Surges, V. Gaus, D. Janz, B. Schmitz, K. M. Klein, P. S. Reif, W. H. Oertel, H. M. Hamer, F. Rosenow, F. Becker, C. Marini, R. Guerrini, D. Mei, V. Norci, F. Zara, P. Striano, A. Robbiano, M. Pezzella, A. Bianchi, A. Gambardella, P. Tinuper, A. La Neve, G. Capovilla, P. Vigliano, G. Crichiutti, F. Vanadia, A. Coppola, S. Striano, M. T. Giallonardo, S. Franceschetti, V. Belcastro, P. Benna, G. Coppola, A. De Palo, E. Ferlazzo, M. Vecchi, V. Martinelli, F. Bisulli, F. Beccaria, E. Del Giudice, M. Mancardi, G. Stranci, A. Scabar, G. Gobbi, I. Giordano, B. P. C. Koeleman, C. De Kovel, D. Lindhout, G. J. De Haan, U. Ozbeck, N. Bebek, B. Baykan, O. Ozdemir, S. Ugur, E. Kocasoy Orhan, E. Yücesan, N. Cine, A. Gokyigit, C. Gurses, G. Gul, Z. Yapici, C. Ozkara, H. Caglayan, O. Yalcin, D. Yalcin, D. Turkdogan, G. Dizdarer, K. Agan, A. Vignoli
المساهمون: R.S. Møller, Y.G. Weber, L.L. Klitten, H. Truck, H. Muhle, W.S. Kunz, H.C. Mefford, A. Franke, M. Kautza, P. Wolf, D. Dennig, S. Schreiber, I.-M. Rückert, H.-E. Wichmann, J.P. Ernst, C. Schurmann, H.J. Grabe, N. Tommerup, U. Stephani, H. Lerche, H. Hjalgrim, I. Helbig, T. Sander, F. Zimprich, M. Mörzinger, M. Feucht, A. Sul, S. Weckhuysen, L. Clae, L. Deprez, K. Smet, T. Van Dyck, T. Deconinck, P. De Jonghe, R. Velizarova, P. Dimova, M. Radionova, I. Tournev, D. Kancheva, R. Kaneva, A. Jordanova, D.B. Kjelgaard, A.-E. Lehesjoki, A. Siren, S. Baulac, E. Leguern, S. Von Spiczak, P. Ostertag, M. Leber, C. Leu, M.R. Toliat, P. Nürnberg, A. Hempelmann, F. Rüschendorf, C.E. Elger, A.A. Kleefuß-Lie, R. Surge, V. Gau, D. Janz, B. Schmitz, K.M. Klein, P.S. Reif, W.H. Oertel, H.M. Hamer, F. Rosenow, F. Becker, C. Marini, R. Guerrini, D. Mei, V. Norci, F. Zara, P. Striano, A. Robbiano, M. Pezzella, A. Bianchi, A. Gambardella, P. Tinuper, A. La Neve, G. Capovilla, P. Vigliano, G. Crichiutti, F. Vanadia, A. Vignoli, A. Coppola, S. Striano, M.T. Giallonardo, S. Franceschetti, V. Belcastro, P. Benna, G. Coppola, A. De Palo, E. Ferlazzo, M. Vecchi, V. Martinelli, F. Bisulli, F. Beccaria, E. Del Giudice, M. Mancardi, G. Stranci, A. Scabar
مصطلحات موضوعية: Adult, Age of Onset, Anticonvulsants, Case-Control Studies, Cell Adhesion Molecules, Neuronal, DNA Copy Number Variations, Electroencephalography, Epilepsy, Generalized, Exons, Family, Female, Fructose, Gene Deletion, Genotype, Human, Infant, Male, Microarray Analysis, Middle Aged, Nerve Tissue Proteins, Neuropsychological Tests, Odds Ratio, Pedigree, Triazines, Valproic Acid, Settore MED/39 - Neuropsichiatria Infantile, Settore MED/03 - Genetica Medica, Settore MED/26 - Neurologia
Relation: info:eu-repo/semantics/altIdentifier/pmid/23294455; info:eu-repo/semantics/altIdentifier/wos/WOS:000314750200008; volume:54; issue:2; firstpage:256; lastpage:264; numberofpages:9; journal:EPILEPSIA; http://hdl.handle.net/2434/223765; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84978024392
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9
المؤلفون: Moritz Tacke, Lucia Gerstl, Florian Heinen, Isabel Heukaeufer, Michaela Bonfert, Thomas Bast, Sonia Cornell, Bernd Axel Neubauer, Ingo Borggraefe, F.A.M. Baumeister, M. Baethmann, B. Schreiber-Gollwitzer, K. Bentele, C. Blank, J. Held, H.M. Blank, K. Liebrich, H. Bode, J. Braun, F. Bosch, R. Wagner, U. Brandl, K. Wetzel, K. Brockmann, C. Schlockwerder, P. Dahlem, I. Baudler, J.P. Ernst, H. Mayer, E. Feldmann, A. Pattber-Wolff, A. Fiedler, S. Sonnleitner, M. Gerigk, S. Heß, T. Feiereis, C. Hikel, H.G. Hoffmann, A. Rickeshenrich, M. Kieslich, R. Dewitz, M. Baz Bartels, J. Klepper, S. Kleuker, G. Kluger, A. Kirsch, H. Koch, U. Meerpohl, W. Koch, R. Korinthenberg, B. Stehle-Renner, I. Krois, A. Wegener, H. Kühne, C. Weiß, G. Kurlemann, U. Elkemann, M. Mandl, A. Friedl, U. Mause, M. Müller, P. Navratil, U. Iken, J. Opp, J. Walter, J. Penzien, V. Prietsch, B. Siegrist, A. Quattländer, D. Rating, G. Reuner, U. Schara, M.G. Shamdeen, H. Struchholz, A. Sprinz, H. Wendker-Magrabi, U. Stephani, H. Muhle, G. Carlsson, H.M. Straßburg, H. Ottensmeier, B. Töpke, K. Tatsek, R. Trollmann, E. Poida-Herzing, E. Tuschen-Hofstätter, M. Menschig, S. Waltz, A. Pickartz, G. Weber, T. Gehnen, F.U. Wien, J. Antemann, M. Wolff, E. Serra, T. Polster, H. Freitag, Ö Sönmez, K. Rheinhardt, M. Traus, A. Schröder, S. Hoovey, C. Navratil
المساهمون: Schara, Ulrike (Beitragende*r)
المصدر: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 20(6)
مصطلحات موضوعية: Male, Levetiracetam, Medizin, Thiazines, Child Behavior, Neuropsychological Tests, Verbal learning, 03 medical and health sciences, Executive Function, 0302 clinical medicine, Cognition, Double-Blind Method, Memory, 030225 pediatrics, medicine, Humans, Cognitive skill, Effects of sleep deprivation on cognitive performance, Neuropsychological assessment, Child, Language, Intelligence Tests, medicine.diagnostic_test, Kaufman Assessment Battery for Children, Neuropsychology, General Medicine, Epilepsy, Rolandic, Piracetam, Space Perception, Pediatrics, Perinatology and Child Health, Mental Recall, Anticonvulsants, Female, Neurology (clinical), Verbal memory, Psychology, 030217 neurology & neurosurgery, Psychomotor Performance, Clinical psychology
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10
المؤلفون: de Kovel, Carolien G.F., Brilstra, Eva H., van Kempen, Marjan J.A., van‘t Slot, Ruben, Nijman, Isaac J., Afawi, Zaid, De Jonghe, Peter, Djémié, Tania, Guerrini, Renzo, Hardies, Katia, Helbig, Ingo, Hendrickx, Rik, Kanaan, Moine, Kramer, Uri, Lehesjoki, Anna‐Elina E., Lemke, Johannes R., Marini, Carla, Mei, Davide, Møller, Rikke S., Pendziwiat, Manuela, Stamberger, Hannah, Suls, Arvid, Weckhuysen, Sarah, Koeleman, Bobby P.C., R, Balling, N, Barisic, S, Baulac, HS, Caglayan, DC, Craiu, C, Depienne, P, Gormley, H, Hjalgrim, D, Hoffman‐Zacharska, J, Jähn, KM, Klein, V, Komarek, E, LeGuern, H, Lerche, P, May, H, Muhle, D, Pal, A, Palotie, F, Rosenow, K, Selmer, JM, Serratosa, SM, Sisodiya, U, Stephani, K, Sterbova, P, Striano, T, Talvik, M, van Haelst, N, Verbeek, S, von Spiczak, YG, Weber
المساهمون: Other departments, Amsterdam Reproduction & Development (AR&D), Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, EuroEPINOMICS RES Consortium, Neuroscience Center, Research Programs Unit, Department of Medical and Clinical Genetics, Anna-Elina Lehesjoki / Principal Investigator, Research Programme for Molecular Neurology
المصدر: Molecular genetics and genomic medicine, 4(5), 568-580. John Wiley and Sons Inc.
Molecular Genetics and Genomic Medicine, 4(5), 568-580. John Wiley and Sons Inc.
de Kovel, C G F, Brilstra, E H, van Kempen, M J A, Van't Slot, R, Nijman, I J, Afawi, Z, De Jonghe, P, Djémié, T, Guerrini, R, Hardies, K, Helbig, I, Hendrickx, R, Kanaan, M, Kramer, U, Lehesjoki, A-E E, Lemke, J R, Marini, C, Mei, D, Møller, R S, Pendziwiat, M, Stamberger, H, Suls, A, Weckhuysen, S, Koeleman, B P C & EuroEPINOMICS RES Consortium 2016, ' Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients ', Molecular Genetics & Genomic Medicine, vol. 4, no. 5, pp. 568-580 . https://doi.org/10.1002/mgg3.235
EuroEPINOMICS RES Consortium 2016, ' Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients ', Molecular Genetics and Genomic Medicine, vol. 4, no. 5, pp. 568-580 . https://doi.org/10.1002/mgg3.235
Molecular genetics & genomic medicine
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, 4(5), 568. John Wiley and Sons Inc.مصطلحات موضوعية: 0301 basic medicine, Candidate gene, education, EEF1A2, Genomics, targeted panel sequencing, Biology, Frameshift mutation, loss-of-function, 03 medical and health sciences, Genotype, Journal Article, Genetics, De novo, HNRNPU, X‐linked, epileptic encephalopathy, loss‐of‐function, prioritization, recessive, Molecular Biology, Gene, Genetics (clinical), Loss function, X-linked, 3112 Neurosciences, Original Articles, Phenotype, 3. Good health, 030104 developmental biology, Original Article, Human medicine
وصف الملف: application/pdf; pdf; image/pdf
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11Academic Journal
المؤلفون: Epicure Consortium, C. Leu, C. G. F. De Kovel, F. Zara, P. Striano, M. Pezzella, A. Robbiano, A. Bianchi, F. Bisulli, A. Coppola, F. Beccaria, D. K. N. Trenite, D. Lindhout, V. Gaus, B. Schmitz, D. Janz, Y. G. Weber, F. Becker, H. Lerche, A. A. Kleefuss Lie, K. Hallman, W. S. Kunz, C. E. Elger, H. Muhle, U. Stephani, R. S. Møller, H. Hjalgrim, S. Mullen, I. E. Scheffer, S. F. Berkovic, K. V. Everett, M. R. Gardiner, C. Marini, R. Guerrini, A. E. Lehesjoki, A. Siren, R. Nabbout, S. Baulac, E. Leguern, J. M. Serratosa, F. Rosenow, M. Feucht, I. Unterberger, A. Covanis, A. Suls, S. Weckhuysen, R. Kaneva, H. Caglayan, D. Turkdogan, B. Baykan, N. Bebek, U. Ozbek, A. Hempelmann, H. Schulz, F. Ruschendorf, H. Trucks, P. Nurnberg, G. Avanzini, B. P. C. Koeleman, T. Sander, GIALLONARDO, Anna Teresa
المساهمون: Epicure, Consortium, C., Leu, C. G. F., De Kovel, F., Zara, P., Striano, M., Pezzella, A., Robbiano, A., Bianchi, F., Bisulli, A., Coppola, Giallonardo, Anna Teresa, F., Beccaria, D. K. N., Trenite, D., Lindhout, V., Gau, B., Schmitz, D., Janz, Y. G., Weber, F., Becker, H., Lerche, A. A., Kleefuss Lie, K., Hallman, W. S., Kunz, C. E., Elger, H., Muhle, U., Stephani, R. S., Møller, H., Hjalgrim, S., Mullen, I. E., Scheffer, S. F., Berkovic, K. V., Everett, M. R., Gardiner, C., Marini, R., Guerrini, A. E., Lehesjoki, A., Siren, R., Nabbout, S., Baulac, E., Leguern, J. M., Serratosa, F., Rosenow, M., Feucht, I., Unterberger, A., Covani, A., Sul, S., Weckhuysen, R., Kaneva, H., Caglayan, D., Turkdogan, B., Baykan, N., Bebek, U., Ozbek, A., Hempelmann, H., Schulz, F., Ruschendorf, H., Truck, P., Nurnberg, G., Avanzini, B. P. C., Koeleman, T., Sander
مصطلحات موضوعية: absence seizure, linkage analysi, genetic generalized epilepsy, myoclonic seizure, complex inheritance
وصف الملف: ELETTRONICO
Relation: info:eu-repo/semantics/altIdentifier/pmid/22242659; info:eu-repo/semantics/altIdentifier/wos/WOS:000299546100017; volume:53; issue:2; firstpage:308; lastpage:318; numberofpages:11; journal:EPILEPSIA; http://hdl.handle.net/11573/442818; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84856357672
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12Academic Journal
المؤلفون: E. P. I. C. U. R. E. Consortium, E. M. I. Net Consortium, M. Steffens, C. Leu, A. Ruppert, F. Zara, P. Striano, A. Robbiano, G. Capovilla, A. Gambardella, A. Bianchi, A. L. Neve, G. Crichiutti, C. G. F, D. K. Trenité, G. d. Haan, D. Lindhout, V. Gaus, B. Schmitz, D. Janz, Y. G. Weber, F. Becker, H. Lerche, B. J. Steinhoff, A. A. Kleefuß Lie, W. S. Kunz, R. Surges, C. E. Elger, H. Muhle, S. v. Spiczak, P. Ostertag, I. Helbig, U. Stephani, R. S. Møller, H. Hjalgrim, L. M. Dibbens, S. Bellows, K. Oliver, S. Mullen, I. E. Scheffer, S. F. Berkovic, K. V. Everett, M. R. Gardiner, C. Marini, R. Guerrini, A. Lehesjoki, A. Siren, M. Guipponi, A. Malafosse, P. Thomas, R. Nabbout, S. Baulac, E. Leguern, R. Guerrero, J. M. Serratosa, P. S. Reif, F. Rosenow, M. Mörzinger, M. Feucht, F. Zimprich, C. Kapser, C. J. Schankin, A. Suls, K. Smets, P. D. Jonghe, A. Jordanova, H. Caglayan, Z. Yapici, D. A. Yalcin, B. Baykan, N. Bebek, U. Ozbek, C. Gieger, H. Wichmann, T. Balschun, D. Ellinghaus, A. Franke, C. Meesters, T. Becker, T. F. Wienker, A. Hempelmann, H. Schulz, F. Rüschendorf, M. Leber, S. M. Pauck, H. Trucks, M. R. Toliat, P. Nürnberg, G. Avanzini, B. P. C, T. Sander, BISULLI, FRANCESCA, TINUPER, PAOLO
المساهمون: E. P. I. C. U. R. E. Consortium, E. M. I.Net Consortium, M. Steffen, C. Leu, A. Ruppert, F. Zara, P. Striano, A. Robbiano, G. Capovilla, P. Tinuper, A. Gambardella, A. Bianchi, A. L. Neve, G. Crichiutti, C. G. F, D. K. Trenité, G. d. Haan, D. Lindhout, V. Gau, B. Schmitz, D. Janz, Y. G. Weber, F. Becker, H. Lerche, B. J. Steinhoff, A. A. Kleefuß-Lie, W. S. Kunz, R. Surge, C. E. Elger, H. Muhle, S. v. Spiczak, P. Ostertag, I. Helbig, U. Stephani, R. S. Møller, H. Hjalgrim, L. M. Dibben, S. Bellow, K. Oliver, S. Mullen, I. E. Scheffer, S. F. Berkovic, K. V. Everett, M. R. Gardiner, C. Marini, R. Guerrini, A. Lehesjoki, A. Siren, M. Guipponi, A. Malafosse, P. Thoma, R. Nabbout, S. Baulac, E. Leguern, R. Guerrero, J. M. Serratosa, P. S. Reif, F. Rosenow, M. Mörzinger, M. Feucht, F. Zimprich, C. Kapser, C. J. Schankin, A. Sul, K. Smet, P. D. Jonghe, A. Jordanova, H. Caglayan, Z. Yapici, D. A. Yalcin, B. Baykan, N. Bebek, U. Ozbek, C. Gieger, H. Wichmann, T. Balschun, D. Ellinghau, A. Franke, C. Meester, T. Becker, T. F. Wienker, A. Hempelmann, H. Schulz, F. Rüschendorf, M. Leber, S. M. Pauck, H. Truck, M. R. Toliat, P. Nürnberg, G. Avanzini, B. P. C, T. Sander
مصطلحات موضوعية: Alleles, Epilepsy, Absence, genetics, Generalized, Genetic Predisposition to Disease, Genome-Wide Association Study, Homeodomain Protein, Humans, Myoclonic Epilepsy, Juvenile, NAV1.1 Voltage-Gated Sodium Channel, Protein-Serine-Threonine Kinase, Receptor, Muscarinic M3, Repressor Protein
وصف الملف: ELETTRONICO
Relation: info:eu-repo/semantics/altIdentifier/pmid/22949513; info:eu-repo/semantics/altIdentifier/wos/WOS:000311965600011; volume:21; issue:24; firstpage:5359; lastpage:5372; numberofpages:13; journal:HUMAN MOLECULAR GENETICS; http://hdl.handle.net/11585/145290; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84870312067; http://dx.doi.org/.1093/hmg/dds373
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المؤلفون: B, Fubini, A E, Aust, R E, Bolton, P J, Borm, J, Bruch, G, Ciapetti, K, Donaldson, Z, Elias, J, Gold, M C, Jaurand, A B, Kane, D, Lison, H, Muhle
المصدر: Alternatives to laboratory animals : ATLA. 26(5)
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14Academic Journal
المؤلفون: C. G. F, D. Pinto, U. Tauer, S. Lorenz, H. Muhle, C. Leu, B. A. Neubauer, A. Hempelmann, P. M. C, I. E. Scheffer, S. F. Berkovic, G. Rudolf, A. Siren, B. Baykan, T. Sander, D. Lindhout, D. G. Kasteleijn Nolst, U. Stephani, B. P. C., STRIANO, PASQUALE
المساهمون: C. G., F., D., Pinto, U., Tauer, S., Lorenz, H., Muhle, C., Leu, B. A., Neubauer, A., Hempelmann, P. M., C., I. E., Scheffer, S. F., Berkovic, G., Rudolf, Striano, Pasquale, A., Siren, B., Baykan, T., Sander, D., Lindhout, D. G., Kasteleijn Nolst, U., Stephani, B. P., C.
مصطلحات موضوعية: Chromosome Mapping, methods, Chromosome, Human, Pair 16, genetics, Pair 5, Pair 8, Epilepsy, Reflex, Female, Genetic Linkage, Genetic Predisposition to Disease, Genome, Humans, Male
وصف الملف: STAMPA
Relation: info:eu-repo/semantics/altIdentifier/pmid/20153606; info:eu-repo/semantics/altIdentifier/wos/WOS:000277872900015; volume:89; firstpage:286; lastpage:294; numberofpages:8; journal:EPILEPSY RESEARCH; http://hdl.handle.net/11567/314877; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-77951296253; http://dx.doi.org/10.1016/j.eplepsyres.2010.01.013
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المؤلفون: H. Muhle, Inge Mangelsdorf
المصدر: Toxicology Letters. :223-228
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Endpoint Determination, Pharmacology, Toxicology, medicine.disease_cause, Administration, Inhalation, Toxicity Tests, medicine, Animals, Humans, Toxicokinetics, Particle Size, Lung, Chronic toxicity, Carcinogen, Minerals, Inhalation, Chemistry, Asbestos, Dust, General Medicine, Silicon Dioxide, respiratory tract diseases, Toxicity, Particle size, Genotoxicity
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16
المؤلفون: B. Bellmann, H. Muhle
المصدر: The Annals of Occupational Hygiene. 39:655-660
مصطلحات موضوعية: Mineral Fibers, medicine.medical_specialty, Chromatography, Inhalation, Intratracheal instillation, Mineral wool, Public Health, Environmental and Occupational Health, Hypochlorite, General Medicine, Elimination kinetics, Rats, Surgery, chemistry.chemical_compound, Ashing, chemistry, Wool, medicine, Animals, Toxicokinetics, Tissue Distribution, Half-Life
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17Academic Journal
المؤلفون: LM Dibbens, S Mullen, I Helbig, HC Mefford, MA Bayly, S Bellows, C Leu, H Trucks, T Obermeier, M Wittig, A Franke, H Caglayan, Z Yapici, T Sander, EE Eichler, IE Scheffer, JC Mulley, SF Berkovic, P De Jonghe, A Suls, H Hjalgrim, JM Madsen, RS Møller, AE Lehesjoki, A Siren, V Gaus, D Janz, B Schmitz, CE Elger, K Hallmann, AA Kleefuß-Lie, WS Kunz, A Raabe, H Muhle, P Ostertag, S von Spiczak, U Stephani, H Lerche, YG Weber, P Striano, F Zara, C Marini, EH Brilstra, D Kastelijn-Nolst Trenité, BPC Koeleman, CGF de Kovel, D Lindhout, MEM Swinkels, O Yalcin, B Baykan, D Turkdogan, G Dizdarer, C Ozkara, Y Lee, J Müller-Quernheim, R Fölster-Holst, S Hofmann, A Nebel, S Schreiber, M Schürmann, E Rodriguez, S Weidinger, H Baurecht, BA Lie, KM Boberg, TH Karlsen
مصطلحات موضوعية: Uncategorised value
Relation: http://hdl.handle.net/10536/DRO/DU:30111755; https://figshare.com/articles/journal_contribution/Familial_and_sporadic_15q13_3_microdeletions_in_idiopathic_generalized_epilepsy_precedent_for_disorders_with_complex_inheritance/20804398
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المؤلفون: U, Volkmar, M, Groth-Malonek, J, Heinrichs, H, Muhle, M, Polsakiewicz, V, Knoop
المصدر: Plant biology (Stuttgart, Germany). 14(2)
مصطلحات موضوعية: Evolution, Molecular, Hepatophyta, Base Sequence, DNA, Plant, Molecular Sequence Data, Nucleic Acid Conformation, Sequence Analysis, DNA, DNA, Mitochondrial, Conserved Sequence, Introns, Phylogeny, Mitochondria
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19Academic Journal
المؤلفون: FUBINI, Bice, A. E. AUST, R. E. BOLTON, J. A. BORM, J. BRUCH, G. CIAPETTI, K. DONALDSON, Z. ELIAS, J. GOLD, M. C. JAURAND, A. B. KANE, D. LISON, H. MUHLE
المساهمون: B. FUBINI, A.E. AUST, R. E. BOLTON, J. A. BORM, J. BRUCH, G. CIAPETTI, K. DONALDSON, Z. ELIAS, J. GOLD, M. C. JAURAND, A. B. KANE, D. LISON, H. MUHLE
Relation: volume:26; firstpage:579; lastpage:617; journal:ATLA. ALTERNATIVES TO LABORATORY ANIMALS; http://hdl.handle.net/2318/4702
الاتاحة: http://hdl.handle.net/2318/4702
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20
المؤلفون: Andre Kleensang, Eberhard Schwinger, H. Muhle, Katja Lohmann-Hedrich, P. L. Kramer, Peter P. Pramstaller, Andreas Ziegler, Thora Lohnau, U. Stephani, Ana Djarmati, Inke R. König, A. Neumann, Christine Klein
المصدر: Neurology. 70(9)
مصطلحات موضوعية: Adult, Male, Adolescent, Genotype, Locus (genetics), Biology, Gene mutation, Genetic linkage, Restless Legs Syndrome, Humans, Genetic Predisposition to Disease, Child, Aged, Genes, Dominant, Genetics, Chromosome Aberrations, Models, Genetic, Haplotype, Family aggregation, Chromosome Mapping, Middle Aged, Complete linkage, Pedigree, Phenotype, Genetic marker, Child, Preschool, Microsatellite, Female, Neurology (clinical), Lod Score, Chromosomes, Human, Pair 9, Microsatellite Repeats