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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
2008 2
2018 1
2020 2
2021 1
2022 2
2023 1

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Page 1
Mucha-Habermann disease: a pediatric case report and proposal of a risk score.
Blohm ME, Ebenebe CU, Rau C, Escherich C, Johannsen J, Escherich G, Driemeyer J, Nagel PD, Kobbe R, Lütgehetmann M, Lennartz M, Booken N, Schneider SW, Singer D. Blohm ME, et al. Among authors: driemeyer j. Int J Dermatol. 2022 Apr;61(4):401-409. doi: 10.1111/ijd.15770. Epub 2021 Jul 20. Int J Dermatol. 2022. PMID: 34287852 Review.
Training-induced brain structure changes in the elderly.
Boyke J, Driemeyer J, Gaser C, Büchel C, May A. Boyke J, et al. Among authors: driemeyer j. J Neurosci. 2008 Jul 9;28(28):7031-5. doi: 10.1523/JNEUROSCI.0742-08.2008. J Neurosci. 2008. PMID: 18614670 Free PMC article.
Structural deficits in key domains of Shank2 lead to alterations in postsynaptic nanoclusters and to a neurodevelopmental disorder in humans.
Hassani Nia F, Woike D, Bento I, Niebling S, Tibbe D, Schulz K, Hirnet D, Skiba M, Hönck HH, Veith K, Günther C, Scholz T, Bierhals T, Driemeyer J, Bend R, Failla AV, Lohr C, Alai MG, Kreienkamp HJ. Hassani Nia F, et al. Among authors: driemeyer j. Mol Psychiatry. 2022 Nov 30. doi: 10.1038/s41380-022-01882-3. Online ahead of print. Mol Psychiatry. 2022. PMID: 36450866
Changes in gray matter induced by learning--revisited.
Driemeyer J, Boyke J, Gaser C, Büchel C, May A. Driemeyer J, et al. PLoS One. 2008 Jul 23;3(7):e2669. doi: 10.1371/journal.pone.0002669. PLoS One. 2008. PMID: 18648501 Free PMC article.
Multimodal lipid-lowering treatment in pediatric patients with homozygous familial hypercholesterolemia-target attainment requires further increase of intensity.
Klaus G, Taylan C, Büscher R, Schmitt CP, Pape L, Oh J, Driemeyer J, Galiano M, König J, Schürfeld C, Spitthöver R, Schaefer JR, Weber LT, Heibges A, Klingel R. Klaus G, et al. Among authors: driemeyer j. Pediatr Nephrol. 2018 Jul;33(7):1199-1208. doi: 10.1007/s00467-018-3906-6. Epub 2018 Mar 3. Pediatr Nephrol. 2018. PMID: 29502162
Practice of lipoprotein apheresis and short-term efficacy in children with homozygous familial hypercholesterolemia: Data from an international registry.
Luirink IK, Hutten BA, Greber-Platzer S, Kolovou GD, Dann EJ, de Ferranti SD, Taylan C, Bruckert E, Saheb S, Oh J, Driemeyer J, Farnier M, Pape L, Schmitt CP, Novoa FJ, Maeser M, Masana L, Shahrani A, Wiegman A, Groothoff JW. Luirink IK, et al. Among authors: driemeyer j. Atherosclerosis. 2020 Apr;299:24-31. doi: 10.1016/j.atherosclerosis.2020.01.031. Epub 2020 Feb 18. Atherosclerosis. 2020. PMID: 32199148
Cardiovascular Outcome of Pediatric Patients With Bi-Allelic (Homozygous) Familial Hypercholesterolemia Before and After Initiation of Multimodal Lipid Lowering Therapy Including Lipoprotein Apheresis.
Taylan C, Driemeyer J, Schmitt CP, Pape L, Büscher R, Galiano M, König J, Schürfeld C, Spitthöver R, Versen A, Koziolek M, Marsen TA, Stein H, Schaefer JR, Heibges A, Klingel R, Oh J, Weber LT, Klaus G. Taylan C, et al. Among authors: driemeyer j. Am J Cardiol. 2020 Dec 1;136:38-48. doi: 10.1016/j.amjcard.2020.09.015. Epub 2020 Sep 16. Am J Cardiol. 2020. PMID: 32946862