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

Year Number of Results
2004 2
2005 3
2006 2
2007 2
2009 1
2011 1
2014 2
2015 1
2017 2
2018 2
2019 5
2020 2
2024 0

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23 results

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Page 1
Image-guided phenotyping of ovariectomized mice: altered functional connectivity, cognition, myelination, and dopaminergic functionality.
Anckaerts C, van Gastel J, Leysen V, Hinz R, Azmi A, Simoens P, Shah D, Kara F, Langbeen A, Bols P, Laloux C, Prevot V, Verhoye M, Maudsley S, Van der Linden A. Anckaerts C, et al. Among authors: azmi a. Neurobiol Aging. 2019 Feb;74:77-89. doi: 10.1016/j.neurobiolaging.2018.10.012. Epub 2018 Oct 17. Neurobiol Aging. 2019. PMID: 30439596
PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease.
Juneja M, Azmi A, Baets J, Roos A, Jennings MJ, Saveri P, Pisciotta C, Bernard-Marissal N, Schneider BL, Verfaillie C, Chrast R, Seeman P, Hahn AF, de Jonghe P, Maudsley S, Horvath R, Pareyson D, Timmerman V. Juneja M, et al. Among authors: azmi a. J Neurol Neurosurg Psychiatry. 2018 Aug;89(8):870-878. doi: 10.1136/jnnp-2017-317562. Epub 2018 Feb 15. J Neurol Neurosurg Psychiatry. 2018. PMID: 29449460
Altered learning, memory, and social behavior in type 1 taste receptor subunit 3 knock-out mice are associated with neuronal dysfunction.
Martin B, Wang R, Cong WN, Daimon CM, Wu WW, Ni B, Becker KG, Lehrmann E, Wood WH 3rd, Zhang Y, Etienne H, van Gastel J, Azmi A, Janssens J, Maudsley S. Martin B, et al. Among authors: azmi a. J Biol Chem. 2017 Jul 7;292(27):11508-11530. doi: 10.1074/jbc.M116.773820. Epub 2017 May 18. J Biol Chem. 2017. PMID: 28522608 Free PMC article.
Genomic deletion of GIT2 induces a premature age-related thymic dysfunction and systemic immune system disruption.
Siddiqui S, Lustig A, Carter A, Sankar M, Daimon CM, Premont RT, Etienne H, van Gastel J, Azmi A, Janssens J, Becker KG, Zhang Y, Wood W, Lehrmann E, Martin JG, Martin B, Taub DD, Maudsley S. Siddiqui S, et al. Among authors: azmi a. Aging (Albany NY). 2017 Mar 4;9(3):706-740. doi: 10.18632/aging.101185. Aging (Albany NY). 2017. PMID: 28260693 Free PMC article.
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.
Hardies K, de Kovel CG, Weckhuysen S, Asselbergh B, Geuens T, Deconinck T, Azmi A, May P, Brilstra E, Becker F, Barisic N, Craiu D, Braun KP, Lal D, Thiele H, Schubert J, Weber Y, van 't Slot R, Nürnberg P, Balling R, Timmerman V, Lerche H, Maudsley S, Helbig I, Suls A, Koeleman BP, De Jonghe P; autosomal recessive working group of the EuroEPINOMICS RES Consortium. Hardies K, et al. Among authors: azmi a. Brain. 2015 Nov;138(Pt 11):3238-50. doi: 10.1093/brain/awv263. Epub 2015 Sep 17. Brain. 2015. PMID: 26384929
23 results