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51

Common variants in the ARC gene are not associated with cognitive abilities

Myrum, Craig, Giddaluru, Sudheer, Jacobsen, Kaya, Espeseth, Thomas, Nyberg, Lars, Lundervold, Astri J., Haavik, Jan, Nilsson, Lars-Göran, Reinvang, Ivar, Steen, Vidar M., Johansson, Stefan, Wibrand, K

Journal:

Brain and Behavior

Year:

2015

Language:

english

File:

PDF, 222 KB

english, 2015

52

CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria

Saunders, Carol, Smith, Laurie, Wibrand, Flemming, Ravn, Kirstine, Bross, Peter, Thiffault, Isabelle, Christensen, Mette, Atherton, Andrea, Farrow, Emily, Miller, Neil, Kingsmore, Stephen F., Ostergaa

Journal:

The American Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 726 KB

english, 2015

53

Opening of Glibenclamide-Sensitive K+Channels in Follicular Cells Promotes Xenopus Oocyte Maturation

Flemming Wibrand, Eric Honore and Michel Lazdunski

Journal:

Proceedings of the National Academy of Sciences

Year:

1992

Language:

english

File:

PDF, 891 KB

english, 1992

54

31P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathy

Tina Dysgaard Jeppesen, Bjørn Quistorff, Flemming Wibrand, John Vissing

Journal:

Journal of Neurology

Year:

2007

Language:

english

File:

PDF, 242 KB

english, 2007

55

The D313Y variant in the GLA gene – no evidence of a pathogenic role in Fabry disease

Hasholt, Lis, Ballegaard, Martin, Bundgaard, Henning, Christiansen, Michael, Law, Ian, Lund, Allan M., Norremolle, Anne, Krogh Rasmussen, Ase, Ravn, Kirstine, Tumer, Zeynep, Wibrand, Flemming, Feldt-R

Journal:

Scandinavian Journal of Clinical & Laboratory Investigation

Year:

2017

Language:

english

File:

PDF, 956 KB

english, 2017

56

A novel mitochondrial mutation m.8989G>C associated with neuropathy, ataxia, retinitis pigmentosa — The NARP syndrome

Duno, Morten, Wibrand, Flemming, Baggesen, Kirsten, Rosenberg, Thomas, Kjaer, Niels, Frederiksen, Anja L.

Journal:

Year:

2013

Language:

english

File:

PDF, 596 KB

english, 2013

57

A novel de novo mutation of the mitochondrial tRNAlys gene mt.8340G>A associated with pure myopathy

Jeppesen, Tina Dysgaard, Duno, Morten, Risom, Lotte, Wibrand, Flemming, Rafiq, Jabin, Krag, Thomas, Jakobsen, Johannes, Andersen, Henning, Vissing, John

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 963 KB

english, 2014

58

A microplate-based enzymatic assay for the simultaneous determination of phenylalanine and tyrosine in serum

Flemming Wibrand

Journal:

Clinica Chimica Acta

Year:

2004

Language:

english

File:

PDF, 299 KB

english, 2004

59

PKR Inhibition Rescues Memory Deficit and ATF4 Overexpression in ApoE 4 Human Replacement Mice

Segev, Y., Barrera, I., Ounallah-Saad, H., Wibrand, K., Sporild, I., Livne, A., Rosenberg, T., David, O., Mints, M., Bramham, C. R., Rosenblum, K.

Journal:

Journal of Neuroscience

Year:

2015

Language:

english

File:

PDF, 758 KB

english, 2015

60

Clinical presentation and mutations in Danish patients with Wilson disease

Møller, Lisbeth Birk, Horn, Nina, Jeppesen, Tina Dysgaard, Vissing, John, Wibrand, Flemming, Jennum, Poul, Ott, Peter

Journal:

European Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 333 KB

english, 2011

61

Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect

Hana Antonicka, Elsebet Østergaard, Florin Sasarman, Woranontee Weraarpachai, Flemming Wibrand, Anne Marie B. Pedersen, Richard J. Rodenburg, Marjo S. van der Knaap, Jan A.M. Smeitink, Zofia M. Chrzan

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 1.01 MB

english, 2010

62

A Patient With Pyruvate Carboxylase Deficiency and Nemaline Rods on Muscle Biopsy

Unal, O., Orhan, D., Ostergaard, E., Tokatli, A., Dursun, A., Ozturk-Hismi, B., Coskun, T., Wibrand, F., Kalkanoglu-Sivri, H. S.

Journal:

Journal of Child Neurology

Year:

2013

Language:

english

File:

PDF, 186 KB

english, 2013

63

Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome

Ostergaard, E., Rodenburg, R. J., van den Brand, M., Thomsen, L. L., Duno, M., Batbayli, M., Wibrand, F., Nijtmans, L.

Journal:

Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 234 KB

english, 2011

64

Acylcarnitine profiles in mitochondrial myopathies

Vissing, C., Christensen, M., Dunø, M., Wibrand, F., Olesen, J., Vissing, J.

Journal:

Neuromuscular Disorders

Year:

2015

Language:

english

File:

PDF, 205 KB

english, 2015

65

PAICS deficiency, a new defect of de novo purine synthesis resulting in multiple congenital anomalies and fatal outcome

Pelet, Anna, Skopova, Vaclava, Steuerwald, Ulrike, Baresova, Veronika, Zarhrate, Mohammed, Plaza, Jean-Marc, Hnizda, Ales, Krijt, Matyas, Souckova, Olga, Wibrand, Flemming, Andorsdóttir, Guðrið, Joens

Journal:

Human Molecular Genetics

Year:

2019

Language:

english

File:

PDF, 2.21 MB

english, 2019

66

Erratum to: The Arc of synaptic memory

Clive R. Bramham, Maria N. Alme, Margarethe Bittins, Sjoukje D. Kuipers, Rajeevkumar R. Nair, Balagopal Pai, Debabrata Panja, Manja Schubert, Jonathan Soule, Adrian Tiron, Karin Wibrand

Journal:

Experimental Brain Research

Year:

2011

Language:

english

File:

PDF, 85 KB

english, 2011

67

Reconstitution of the lactate carrier from rat skeletal-muscle sarcolemma

Wibrand, F, Juel, C

Journal:

Biochemical Journal

Year:

1994

Language:

english

File:

PDF, 1.13 MB

english, 1994

68

Cover Image, Volume 528, Issue 11

Adden, Andrea, Wibrand, Sara, Pfeiffer, Keram, Warrant, Eric, Heinze, Stanley

Journal:

The Journal of Comparative Neurology

Year:

2020

File:

PDF, 35.37 MB

2020

69

S.08.03 Arc/Arg3.1 synthesis and control of LTp consolidation in the adult dentate gyrus in vivo

C. Bramham, D. Panja, A. Tiron, R. Nair, K. Wibrand, S. Kuipers

Journal:

European Neuropsychopharmacology

Year:

2009

Language:

english

File:

PDF, 103 KB

english, 2009

70

Muscle Phenotype and Mutation Load in 51 Persons With the 3243A>G Mitochondrial DNA Mutation

Jeppesen, Tina D., Schwartz, Marianne, Frederiksen, Anja L., Wibrand, Flemming, Olsen, David B., Vissing, John

Journal:

Archives of Neurology

Year:

2006

Language:

english

File:

PDF, 163 KB

english, 2006

71

Multiple mtDNA deletions with features of MNGIE

Vissing, J., Ravn, K., Danielsen, E.R., Duno, M., Wibrand, F., Wevers, R.A., Schwartz, M.

Journal:

Year:

2002

Language:

english

File:

PDF, 180 KB

english, 2002

72

Opening of glibenclamide-sensitive K+ channels in follicular cells promotes Xenopus oocyte maturation.

Wibrand, F., Honore, E., Lazdunski, M.

Journal:

Proceedings of the National Academy of Sciences

Year:

1992

Language:

english

File:

PDF, 998 KB

english, 1992

73

Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene

Flemming Wibrand, Kirstine Ravn, Marianne Schwartz, Thomas Rosenberg, Nina Horn, John Vissing

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 8.52 MB

english, 2001

74

Linker histone H1M transcripts mark the developing germ line in zebrafish

Karin Wibrand, Lisbeth Charlotte Olsen

Journal:

Mechanisms of Development

Year:

2002

Language:

english

File:

PDF, 145 KB

english, 2002

75

G.P.115 Recurrent myoglobinuria and deranged acyl-carnitines due to mutation of the COII gene of mtDNA

Vissing, C.R., Duno, M., Wibrand, F., Vissing, J.

Journal:

Neuromuscular Disorders

Year:

2012

Language:

english

File:

PDF, 47 KB

english, 2012

76

Four novelPDHA1mutations in pyruvate dehydrogenase deficiency

Ostergaard, E., Moller, L. Birk, Kalkanoglu-Sivri, H. Serap, Dursun, A., Kibaek, M., Thelle, T., Christensen, E., Duno, M., Wibrand, F.

Journal:

Journal of Inherited Metabolic Disease

Year:

2009

Language:

english

File:

PDF, 270 KB

english, 2009

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