Molecular Analysis of Phenylketonuria in Denmark: 99% of the Mutations Detected by Denaturing Gradient Gel Electrophoresis von Guldberg, Per, Henriksen, Karen Friis, Güttler, Flemming

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MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation patte... von Nielsen, J B, Henriksen, K F, Hansen, C, Silahtaroglu, A, Schwartz, M, Tommerup, N

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Good Clinical Practice is now Obligatory in Academic Clinical Drug Research in the European Union von Jørgensen, Annette, Bach, Karin Friis, Friis, Karen

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Conformational entropy in molecular recognition of intrinsically disordered proteins von Skriver, Karen, Theisen, Frederik Friis, Kragelund, Birthe B.

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Characterization of Diarrheagenic Enteroaggregative Escherichia coli in Danish Adults-Antibiotic Treatment Does Not Reduce Duration of Diarrhea von Hebbelstrup Jensen, Betina, Adler Sørensen, Camilla, Hebbelstrup Rye Rasmussen, Stig, Rejkjær Holm, Dorthe, Friis-Møller, Alice, Engberg, Jørgen, Mirsepasi-Lauridsen, Hengameh C, Struve, Carsten, Hammerum, Anette M, Porsbo, Lone Jannok, Petersen, Randi Føns, Petersen, Andreas Munk, Krogfelt, Karen Angeliki

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Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B von Halgren, C, Kjaergaard, S, Bak, M, Hansen, C, El-Schich, Z, Anderson, CM, Henriksen, KF, Hjalgrim, H, Kirchhoff, M, Bijlsma, EK, Nielsen, M, den Hollander, NS, Ruivenkamp, CAL, Isidor, B, Le Caignec, C, Zannolli, R, Mucciolo, M, Renieri, A, Mari, F, Anderlid, B-M, Andrieux, J, Dieux, A, Tommerup, N, Bache, I

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Silver resistance: an alarming public health concern? von Jakobsen, Lotte, Andersen, Anders S, Friis-Møller, Alice, Jørgensen, Bo, Krogfelt, Karen A, Frimodt-Møller, Niels

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Disease-Specific Enteric Microbiome Dysbiosis in Inflammatory Bowel Disease von Mirsepasi-Lauridsen, Hengameh Chloé, Vrankx, Katleen, Engberg, Jørgen, Friis-Møller, Alice, Brynskov, Jørn, Nordgaard-Lassen, Inge, Petersen, Andreas Munk, Krogfelt, Karen Angeliki

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E. coli Outer Membrane Protein C Antibodies in Active and Inactive Inflammatory Bowel Diseases von Petersen, Andreas M, Schou, Christian, Engberg, Jørgen H, Friis-Møller, Alice, Mirsepasi, Hengameh, Nordgaard-Lassen, Inge, Krogfelt, Karen A

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Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation von Gilling, Mette, Lind-Thomsen, Allan, Mang, Yuan, Bak, Mads, Møller, Morten, Ullmann, Reinhard, Kristoffersson, Ulf, Kalscheuer, Vera M, Henriksen, Karen Friis, Bugge, Merete, Tümer, Zeynep, Tommerup, Niels

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A 3.2Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia von GILLING, Mette, LAURITSEN, Marlene Briciet, ROSENBERG, Thomas, BRØNDUM-NIELSEN, Karen, COTTERILL, Rodney M. J, LUNDSTEEN, Claes, ROJERS, Hans-Hilger, ULLMANN, Reinhard, BACHE, Iben, TÜMER, Zeynep, TOMMERUP, Niels, MØLLER, Morten, HENRIKSEN, Karen Friis, VICENTE, Astrid, OLIVEIRA, Guiomar, CINTIN, Christina, EIBERG, Hans, ANDERSEN, Paal Skyt, MORS, Ole

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Identification of novel genes regulated in the developing human ventral mesencephalon von Jørgensen, Jesper Roland, Juliusson, Bengt, Henriksen, Karen Friis, Hansen, Claus, Knudsen, Steen, Petersen, Thomas Nordahl, Blom, Nikolaj, Seiger, Åke, Wahlberg, Lars U.

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A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia von Gilling, Mette, Lauritsen, Marlene Briciet, Møller, Morten, Henriksen, Karen Friis, Vicente, Astrid, Oliveira, Guiomar, Cintin, Christina, Eiberg, Hans, Andersen, Paal Skyt, Mors, Ole, Rosenberg, Thomas, Brøndum-Nielsen, Karen, Cotterill, Rodney M J, Lundsteen, Claes, Ropers, Hans-Hilger, Ullmann, Reinhard, Bache, Iben, Tümer, Zeynep, Tommerup, Niels

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Karen Friis

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A Molecular Survey of Phenylketonuria in Iceland: Identification of a Founding Mutation and Evidence of Predominant Norse Settlement von Guldberg, Per, Zschocke, Johannes, Dagbjartsson, Atli, Henriksen, Karen Friis, Güttler, Flemming

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Post-Transjugular Intrahepatic Portosystemic Shunt (TIPS) Hepatic Encephalopathy-A Review of the Past Decade's Literature Focusing on Incidence, Risk Factors, and Prophylaxis von Friis, Karina Holm, Thomsen, Karen Louise, Laleman, Wim, Montagnese, Sara, Vilstrup, Hendrik, Lauridsen, Mette Munk

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Post-Transjugular Intrahepatic Portosystemic Shunt (TIPS) Hepatic Encephalopathy-A Review of the Past Decade's Literature Focusing on Incidence, Risk Factors, and Prophylaxis von Friis, Karina Holm, Thomsen, Karen Louise, Laleman, Wim, Montagnese, Sara, Vilstrup, Hendrik, Lauridsen, Mette Munk

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Phenylalanine hydroxylase deficiency in a population in Germany: Mutational profile and nine novel mutations von Guldberg, Per, Mallmann, Rudolf, Henriksen, Karen Friis, Güttler, Flemming

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Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland von Guldberg, P, Henriksen, K F, Sipilä, I, Güttler, F, de la Chapelle, A

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PCR-based screening of YAC clones without DNA extraction von Hansen, Claus, Henriksen, Karen Friis, Rendtorff, Nanna Dahl, Moestrup, Soren Kragh, Tommerup, Niels

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