Anne Nørremølle
Associate Professor
Medical Genetics Program
Blegdamsvej 3
2200 København N.
- 2024
- Published
Generation of three isogenic gene-edited Huntington’s disease human embryonic stem cell lines with DOX-inducible NGN2 expression cassette in the AAVS1 safe locus
Duque Villegas, Luisana Carolina, Chandrasekaran, Abinaya, Flintholm Andersen, S. A., Nørremølle, Anne, Schmid, B., Pouladi, M. A. & Freude, Kristine, 2024, In: Stem Cell Research. 77, 6 p., 103408.Research output: Contribution to journal › Journal article › Research › peer-review
- 2023
- Published
The significance of mitochondrial haplogroups in preeclampsia risk
Wendelboe Olsen, K., Hedley, P. L., Hagen, C. M., Rode, L., Placing, S., Wøjdemann, K. R., Shalmi, A. C., Sundberg, K., Nørremølle, Anne, Tabor, Ann, Elson, J. L. & Christiansen, M., 2023, In: Pregnancy Hypertension. 34, p. 146-151 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2022
- Published
Progressive Mitochondrial Dysfunction of Striatal Synapses in R6/2 Mouse Model of Huntington's Disease
Petersen, M. H., Willert, C. W., Andersen, Jens Velde, Madsen, M., Waagepetersen, Helle S., Skotte, Niels Henning & Nørremølle, Anne, 2022, In: Journal of Huntington's disease. 11, 2, p. 121-140Research output: Contribution to journal › Journal article › Research › peer-review
- 2021
- Published
Nicotinamide Adenine Dinucleotide Phosphate Oxidases Are Everywhere in Brain Disease, but Not in Huntington’s Disease?
Duque Villegas, Luisana Carolina, Nørremølle, Anne, Freude, Kristine & Vilhardt, Frederik, 2021, In: Frontiers in Aging Neuroscience. 13, 20 p., 736734.Research output: Contribution to journal › Review › Research › peer-review
- 2020
- Published
Compromised IGF signaling causes caspase-6 activation in Huntington disease
Skotte, Niels Henning, Pouladi, M. A., Ehrnhoefer, D. E., Huynh, K., Qiu, X., Nielsen, S. M. B., Nielsen, T. T., Nørremølle, Anne & Hayden, M. R., 2020, In: Experimental Neurology. 332, 113396.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Investigating the feasibility of using assessment and explanatory feedback in desktop virtual reality simulations
Makransky, Guido, Mayer, R., Nørremølle, Anne, Cordoba, A. L., Wandall, J. & Bonde, M., 2020, In: Educational Technology Research and Development. 68, p. 293-317Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Paroxysmal Cranial Dyskinesia and Nail-Patella Syndrome Caused by a Novel Variant in the LMX1B Gene
Bech, S., Løkkegaard, Annemette, Nielsen, T. T., Nørremølle, Anne, Grønborg, S., Hasholt, Lis Frydenreich, Steffensen, G. K., Graehn, G., Olesen, J. H., Tommerup, Niels, Mang, Y., Bak, M., Nielsen, Jørgen Erik, Eiberg, Hans Rudolf Lytchoff & Hjermind, L. E., 2020, In: Movement Disorders. 35, 12, p. 2343-2347Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Serotonin transporter gene (SLC6A4) variation and sensory processing sensitivity—Comparison with other anxiety-related temperamental dimensions
Licht, C. L., Mortensen, Erik Lykke, Hjordt, L. V., Stenbæk, Dea Siggaard, Arentzen, T. E., Nørremølle, Anne & Knudsen, Gitte Moos, 2020, In: Molecular Genetics and Genomic Medicine. 8, 8, 10 p., e1352.Research output: Contribution to journal › Journal article › Research › peer-review
- 2019
- Published
Functional Differences between Synaptic Mitochondria from the Striatum and the Cerebral Cortex
Petersen, M. H., Willert, C. W., Andersen, Jens Velde, Waagepetersen, Helle S., Skotte, Niels Henning & Nørremølle, Anne, May 2019, In: Neuroscience. 406, p. 432-443 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Enhanced cerebral branched-chain amino acid metabolism in R6/2 mouse model of Huntington's disease
Andersen, Jens Velde, Skotte, Niels Henning, Aldana, Blanca, Nørremølle, Anne & Waagepetersen, Helle S., 2019, In: Cellular and Molecular Life Sciences. 76, 12, p. 2449-2461Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Ghrelin-mediated improvements in the metabolic phenotype in the R6/2 mouse model of Huntington's disease
Rudenko, Olga, Springer, C., Skov, Louise Julie, Madsen, A. N., Hasholt, Lis Frydenreich, Nørremølle, Anne & Holst, Birgitte, 2019, In: Journal of Neuroendocrinology. 31, 7 (SI), 14 p., e12699.Research output: Contribution to journal › Conference article › Research › peer-review
- Published
Haploinsufficiency of ARHGAP42 is associated with hypertension
Fjorder, A. S., Rasmussen, Malene Bøgehus, Mehrjouy, M. M., Nazaryan, Lusine, Hansen, C., Bak, M., Grarup, Niels, Nørremølle, Anne, Larsen, Lars Allan, drb459, drb459, Hansen, Torben, Tommerup, Niels & Bache, Iben, 2019, In: European Journal of Human Genetics. 27, 8, p. 1296-1303 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2018
- Published
The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease in 2 Danish families
Feldt-Rasmussen, Ulla, Hasholt, Lis Frydenreich, Ballegaard, Martin, Christiansen, M., Law, Ian, Lund, A., Nørremølle, Anne, Ravn, K., Rasmussen, A. K., Tuemer, Z., Bundgård, Henning & Wibrand, F., Feb 2018, In: Molecular Genetics and Metabolism. 123, 2, p. S44-S44 1 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Integrative Characterization of the R6/2 Mouse Model of Huntington's Disease Reveals Dysfunctional Astrocyte Metabolism
Skotte, Niels Henning, Andersen, Jens Velde, Santos, A., Aldana, Blanca, Willert, C. W., Nørremølle, Anne, Waagepetersen, Helle S. & Nielsen, Michael Lund, 2018, In: Cell Reports. 23, 7, p. 2211-2224 14 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Perturbations in the p53/miR-34a/SIRT1 pathway in the R6/2 Huntington's disease model
Reynolds, R. H., Petersen, M. H., Willert, C. W., Heinrich, M., Nymann, N., Dall, M., Treebak, Jonas Thue, Björkqvist, M., Silahtaroglu, Asli, Hasholt, Lis Frydenreich & Nørremølle, Anne, 2018, In: Molecular and Cellular Neuroscience. 88, p. 118-129Research output: Contribution to journal › Journal article › Research › peer-review
- 2017
- Published
TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3)
Rostgaard, N., Roos, P., Budtz-Joergensen, Esben, Johannsen, P., Waldemar, Gunhild, Nørremølle, Anne, Lindquist, S. G., Gydesen, S., Brown, J. M., Collinge, J., Isaacs, A. M., Nielsen, T. T., Nielsen, Jørgen Erik & FReJA collaboration, F. C., Nov 2017, In: Neurobiology of Aging. 59, p. 221.e1-221.e7 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The D313Y variant in the GLA gene–no evidence of a pathogenic role in Fabry disease
Hasholt, Lis Frydenreich, Ballegaard, Martin, Bundgård, Henning, Christiansen, M., Law, Ian, Lund, Allan Meldgaard, Nørremølle, Anne, Krogh Rasmussen, A., Ravn, K., Tümer, Asuman Zeynep, Wibrand, F. & Feldt-Rasmussen, Ulla, 2017, In: Scandinavian Journal of Clinical and Laboratory Investigation. 77, 8, p. 617-621 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2016
- Published
Liver function in Huntington's disease assessed by blood biochemical analyses in a clinical setting
Nielsen, S. M. B., Vinther-Jensen, T., Nielsen, Jørgen Erik, Nørremølle, Anne, Hasholt, Lis Frydenreich, Hjermind, L. E. & Josefsen, K., 15 Mar 2016, In: Journal of the Neurological Sciences. 362, p. 326-332 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genes
Vinther-Jensen, T., Nielsen, T. T., Budtz-Joergensen, Esben, Larsen, I. U., Hansen, M. M., Hasholt, Lis Frydenreich, Hjermind, L. E., Nielsen, J. E. & Nørremølle, Anne, Mar 2016, In: Clinical Genetics. 89, 3, p. 320-327 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Simulation based virtual learning environment in medical genetics counseling: an example of bridging the gap between theory and practice in medical education
Makransky, Guido, Bonde, M. T., Wulff, J. S. G., Wandall, J., Hood, M., Creed, P. A., Bache, Iben, Silahtaroglu, Asli & Nørremølle, Anne, Mar 2016, In: B M C Medical Education. 16, 1, p. 1-9 9 p., 98.Research output: Contribution to journal › Journal article › Research › peer-review
- 2015
- Published
A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease
Bečanović, K., Nørremølle, A., Neal, S. J., Kay, C., Collins, J. A., Arenillas, D., Lilja, T., Gaudenzi, G., Manoharan, S., Doty, C. N., Beck, J., Lahiri, N., Portales-Casamar, E., Warby, S. C., Connolly, C., De Souza, R. A. G., Tabrizi, S. J., Hermanson, O., Langbehn, D. R., Hayden, M. R. & 3 others, , Jun 2015, In: Nature Neuroscience. 18, 6, p. 807-816 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Progressive Impairment of Lactate-based Gluconeogenesis in the Huntington's Disease Mouse Model R6/2
Nielsen, S. M. B., Hasholt, Lis Frydenreich, Nørremølle, Anne & Josefsen, K. E., 20 Apr 2015, In: PLoS Currents. 7Research output: Contribution to journal › Conference abstract in journal › Research › peer-review
- 2014
- Published
A clinical classification acknowledging neuropsychiatric and cognitive impairment in Huntingtons disease
Vinther-Jensen, T., Larsen, I. U., Hjermind, L. E., Budtz-Joergensen, Esben, Nielsen, T. T., Nørremølle, Anne, Nielsen, Jørgen Erik & Vogel, Asmus, 17 Jul 2014, In: Orphanet Journal of Rare Diseases. 9, 1, p. 1-9 9 p., 114.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Central 5-HT4 receptor binding as biomarker of serotonergic tonus in humans: a [11C]SB207145 PET study
Haahr, M. E., Fisher, P. M., Jensen, C. G., Frøkjær, Vibe Gedsø, Mahon, B. M., Madsen, K., Baaré, W. F. C., Lehel, S., Nørremølle, Anne, Rabiner, E. A. & Knudsen, G. M., Apr 2014, In: Molecular Psychiatry. 19, 4, p. 427-32 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease
Petersen, M. H., Budtz-Joergensen, Esben, Sørensen, S. A., Nielsen, Jørgen Erik, Hjermind, L. E., Vinther-Jensen, T., Nielsen, S. M. B. & Nørremølle, Anne, 2014, In: Mitochondrion. 17, p. 14-21 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2013
- Published
Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model
Aidt, F. H., Nielsen, S. M. B., Kanters, Jørgen K., Pesta, D., Nielsen, T. T., Nørremølle, Anne, Hasholt, Lis Frydenreich, Christiansen, M. & Hagen, C. M., 2013, In: PLoS Currents. 5Research output: Contribution to journal › Journal article › Research › peer-review
- 2012
- Published
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion
Lee, J-M., Ramos, E. M., Lee, J-H., Gillis, T., Mysore, J. S., Hayden, M. R., Warby, S. C., Morrison, P., Nance, M., Ross, C. A., Margolis, R. L., Squitieri, F., Orobello, S., Di Donato, S., Gomez-Tortosa, E., Ayuso, C., Suchowersky, O., Trent, R. J. A., McCusker, E., Novelletto, A. & 22 others, , Mar 2012, In: Neurology. 78, 10, p. 690-5 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2011
- Published
Discrepancies in reporting the CAG repeat lengths for Huntington's disease
Quarrell, O. W., Handley, O., O'Donovan, K., Dumoulin, C., Ramos-Arroyo, M., Biunno, I., Bauer, P., Kline, M., Landwehrmeyer, G. B., Hjermind, L. E., Hasholt, Lis Frydenreich, Nørremølle, Anne, Nielsen, Jørgen Erik & European Huntington’s Disease Network, E. H. D. N., Aug 2011, In: European Journal of Human Genetics. 20, 1, p. 20-6 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders
Bech, S., Nørremølle, Anne, Winge, K., Hasholt, Lis Frydenreich, Tommerup, Niels, Svenstrup, K., Nielsen, Jørgen Erik & Hjermind, L. E., 1 Jun 2011, In: Parkinsonism & Related Disorders. 17, 5, p. 398-9 2 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY
Orth, M., Handley, O. J., Schwenke, C., Dunnett, S., Wild, E. J., Tabrizi, S. J., Landwehrmeyer, G. B., Hasholt, Lis Frydenreich, Hjermind, L. E., Nørremølle, Anne, Nielsen, Jørgen Erik & European Huntington's Disease Network, E. H. D. N., 2011, In: The Egyptian Journal of Neurology, Psychiatry, and Neurosurgery. 82, 12, p. 1409-12 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2010
- Published
Reduced gluconeogenesis and lactate clearance in Huntington's disease
Josefsen, K., Nielsen, S. M. B., Campos, A., Seifert, T., Hasholt, Lis Frydenreich, Nielsen, Jørgen Erik, Nørremølle, Anne, Skotte, Niels Henning, Secher, Niels H. & Quistorff, B., 1 Dec 2010, In: Neurobiology of Disease. 40, 3, p. 656-62 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Fabry disease mimicking hypertrophic cardiomyopathy: genetic screening needed for establishing the diagnosis in women
Havndrup, O., Christiansen, M., Stoevring, B., Jensen, M., Hoffman-Bang, J., Andersen, P. S., Hasholt, L., Nørremølle, A., Feldt-Rasmussen, U., Køber, L., Bundgaard, H., Havndrup, O., Christiansen, M., Stoevring, B., Jensen, M., Hofman-Bang, J., Andersen, P. S., Hasholt, L. F., Nørremølle, A., Feldt-Rasmussen, U. & 2 others, , 1 Jun 2010, In: European Journal of Heart Failure. 12, 6, p. 535-40 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation
Bech, S., Petersen, T., Nørremølle, Anne, Gjedde, Albert, Ehlers, L., Eiberg, Hans Rudolf Lytchoff, Hjermind, L. E., Hasholt, Lis Frydenreich, Lundorf, E. & Nielsen, Jørgen Erik, 2010, In: Parkinsonism & Related Disorders. 16, 1, p. 12-5 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2009
- Published
4p16.3 haplotype modifying age at onset of Huntington disease
Nørremølle, Anne, Budtz-Joergensen, Esben, Fenger, K., Nielsen, Jørgen Erik, Sørensen, S. A. & Hasholt, Lis Frydenreich, 2009, In: Clinical Genetics. 75, 3, p. 244-50 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Huntington's disease does not appear to increase the risk of diabetes mellitus
Boesgaard, T. W., Nielsen, T. T., Josefsen, K. E., Hansen, T., Jørgensen, T., Pedersen, O., Nørremølle, Anne, Nielsen, Jørgen Erik & Hasholt, Lis Frydenreich, 2009, In: Journal of Neuroendocrinology. 21, 9, p. 770-6 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia
Svenstrup, K., Bross, P., Koefoed, P., Hjermind, L. E., Eiberg, H., Born, A. P., Vissing, J., Gyllenborg, J., Nørremølle, A., Hasholt, L., Nielsen, J. E., Svenstrup, K., Bross, P., Koefoed, P., Hjermind, L. E., Eiberg, H., Born, A. P., Vissing, J., Gyllenborg, J., Nørremølle, A. & 2 others, , 2009, In: Journal of the Neurological Sciences. 284, 1-2, p. 90-5 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2008
- Published
A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment
Lindquist, S. G., Hasholt, Lis Frydenreich, Bahl, J. M. C., Heegaard, N. H. H., Andersen, B. B., Nørremølle, Anne, Stokholm, J., Schwartz, M., Batbayli, M., Laursen, H., Pardossi-Piquard, R., Chen, F., George-Hyslop, P. S., Waldemar, Gunhild & Nielsen, J. E., 2008, In: European Journal of Neurology. 15, 10, p. 1135-1139 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Impaired glucose tolerance in the R6/1 transgenic mouse model of Huntington's disease
Josefsen, K., Nielsen, M. D., Jorgensen, K. H., Bock, T., Nørremølle, Anne, Sørensen, S. A., Naver, B. & Hasholt, Lis Frydenreich, 2008, In: Journal of Neuroendocrinology. 20, 2, p. 165-172 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Inhibition of endoplasmic reticulum stress counteracts neuronal cell death and protein aggregation caused by N-terminal mutant huntingtin proteins
Reijonen, S., Putkonen, N., Nørremølle, Anne, Lindholm, D. & Korhonen, L., 2008, In: Experimental Cell Research. 314, 5, p. 950-960 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2006
- Published
Meiotic CAG repeat instability in spinocerebellar ataxia type 6: Maternally transmitted elongation in a presumed sporadic case
Lindquist, S. G., Nørremølle, Anne, Hjermind, L. E., Hasholt, Lis Frydenreich & Nielsen, J. E., 2006, In: Journal of the Neurological Sciences. 241, 1-2, p. 95-98 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
MicroRNAs in mammalian brain
Christensen, M., Bak, M., Silahtaroglu, A., Kloosterman, W., Skryapin, B., Nolting, D., Nørremølle, Anne, Lassen, A., Halsholm, L., Brosius, J., Tommerup, Niels, Plasterk, R. & Kauppinen, M. S., 2006, p. 1.Research output: Working paper › Research
- 2004
- Published
Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.
Nielsen, Jørgen Erik, Johnson, B., Koefoed, P., Scheuer, K. H., Grønbech-Jensen, M., Law, I., Krabbe, K., Nørremølle, Anne, Eiberg, Hans Rudolf Lytchoff, Søndergård, H., Dam, M., Rehfeld, J. F., Krarup, C., Paulson, Olaf B., Hasholt, Lis Frydenreich & Sørensen, S. A., 2004, In: European Journal of Neurology. 11, 12, p. 817-824 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Mosaicism of the CAG repeat sequence in the Huntington disease gene in a pair of monozygotic twins
Nørremølle, Anne, Hasholt, Lis Frydenreich, Petersen, C. B., Eiberg, Hans Rudolf Lytchoff, Hasselbalch, S. G., Gideon, P., Nielsen, J. E. & Sørensen, S. A., 2004, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 130, p. 154-159Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG4) using direct mutation detection
Nielsen, Jørgen Erik, Koefoed, P., Kjaergaard, S., Jensen, L. N., Nørremølle, Anne & Hasholt, Lis Frydenreich, 2004, In: Prenatal Diagnosis. 24, 5, p. 363-6 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2003
- Published
Antisense downregulation of mutant huntingtin in a cell model
Hasholt, Lis Frydenreich, Abell, K., Nørremølle, Anne, Nellemann, C., Fenger, K. & Sørensen, S. A., 2003, In: Journal of Gene Medicine. Vol. 5, p. 528-538Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cells exposed to a huntingtin fragment containing an expanded polyglutamine tract show no sign of ion channel formation: results arguing against the ion channel hypothesis.
Nørremølle, Anne, Grunnet, Morten, Hasholt, Lis Frydenreich & Sørensen, S. A., 2003, In: Journal of Neuroscience Research. 71, 1, p. 132-7 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Sekventering
Nørremølle, Anne, 2003, DNA og RNA. En håndbog. København: Gad, p. 161-180Research output: Chapter in Book/Report/Conference proceeding › Report chapter › Research
- 2000
- Published
Inhibition of Huntingtin synthesis by antisense oligodeoxynucleotides
Nellemann, C. L., Abell, K., Nørremølle, Anne, Løkkegaard, T., Naver, B., Röpke, C., Rygaard, J., Sørensen, S. A. & Hasholt, Lis Frydenreich, 2000, In: Molecular and Cellular Neuroscience. 16, p. 313-323Research output: Contribution to journal › Journal article › Research › peer-review
- 1996
- Published
Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family.
Nielsen, Jørgen Erik, Sørensen, S. A., Hasholt, Lis Frydenreich & Nørremølle, Anne, 1996, In: Movement Disorders. 11, 5, p. 533-541 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 1995
- Published
Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease
Nørremølle, Anne, Sørensen, S. A., Fenger, K. & Hasholt, L., 1995, In: Clinical Genetics. 47, p. 113-117Research output: Contribution to journal › Journal article › Research › peer-review
ID: 3886
Most downloads
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252
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Integrative Characterization of the R6/2 Mouse Model of Huntington's Disease Reveals Dysfunctional Astrocyte Metabolism
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
147
downloads
Serotonin transporter gene (SLC6A4) variation and sensory processing sensitivity—Comparison with other anxiety-related temperamental dimensions
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
22
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Nicotinamide Adenine Dinucleotide Phosphate Oxidases Are Everywhere in Brain Disease, but Not in Huntington’s Disease?
Research output: Contribution to journal › Review › Research › peer-review
Published