PubMed for id: 341396

Year	Number of Results
1994	1
1997	1
2000	1
2002	1
2005	6
2006	23
2007	38
2008	51
2009	35
2010	38
2011	41
2012	32
2013	34
2014	39
2015	36
2016	32
2017	26
2018	23
2019	36
2020	42
2021	35
2022	19
2023	15

1

Cerebellar and frontal lobe hypoplasia in fetuses with trisomy 21: usefulness as combined US markers.

Winter TC, Ostrovsky AA, Komarniski CA, Uhrich SB. Winter TC, et al. Radiology. 2000 Feb;214(2):533-8. doi: 10.1148/radiology.214.2.r00fe40533. Radiology. 2000. PMID: 10671607

2

Brachycephaly and frontal lobe hypoplasia in fetuses with trisomy 21 at 11 + 0 to 13 + 6 weeks.

Borenstein M, Dagklis T, Csapo B, Sotiriadis A, Nicolaides KH. Borenstein M, et al. Ultrasound Obstet Gynecol. 2006 Dec;28(7):870-5. doi: 10.1002/uog.3858. Ultrasound Obstet Gynecol. 2006. PMID: 17086579 Free article.

3

MRI in Smith-Lemli-Opitz syndrome type I.

Trasimeni G, Di Biasi C, Iannilli M, Orlandi L, Boscherini B, Balducci R, Gualdi GF. Trasimeni G, et al. Childs Nerv Syst. 1997 Jan;13(1):47-9. doi: 10.1007/s003810050039. Childs Nerv Syst. 1997. PMID: 9083702

4

Frontal brain expansion during development using MRI and endocasts: relation to microcephaly and Homo floresiensis.

Vannucci RC, Barron TF, Holloway RL. Vannucci RC, et al. Anat Rec (Hoboken). 2013 Apr;296(4):630-7. doi: 10.1002/ar.22663. Epub 2013 Feb 13. Anat Rec (Hoboken). 2013. PMID: 23408553 Free article.

5

Extramuscular manifestations in children with severe congenital myopathy due to ACTA1 gene mutations.

Saito Y, Komaki H, Hattori A, Takeuchi F, Sasaki M, Kawabata K, Mitsuhashi S, Tominaga K, Hayashi YK, Nowak KJ, Laing NG, Nonaka I, Nishino I. Saito Y, et al. Neuromuscul Disord. 2011 Jul;21(7):489-93. doi: 10.1016/j.nmd.2011.03.004. Epub 2011 Apr 21. Neuromuscul Disord. 2011. PMID: 21514153

6

Neuropathological analysis of an adult case of the Cornelia de Lange syndrome.

Vuilleumier N, Kövari E, Michon A, Hof PR, Mentenopoulos G, Giannakopoulos P, Bouras C. Vuilleumier N, et al. Acta Neuropathol. 2002 Sep;104(3):327-32. doi: 10.1007/s00401-002-0562-4. Epub 2002 May 30. Acta Neuropathol. 2002. PMID: 12172920

7

Two cases of glutaric aciduria type 1: clinical and neuropathological findings.

Kimura S, Hara M, Nezu A, Osaka H, Yamazaki S, Saitoh K. Kimura S, et al. J Neurol Sci. 1994 May;123(1-2):38-43. doi: 10.1016/0022-510x(94)90201-1. J Neurol Sci. 1994. PMID: 8064319

8

Prefrontal cortex-specific Dcc deletion induces schizophrenia-related behavioral phenotypes and fail to be rescued by olanzapine treatment.

Sun J, Cong Q, Sun T, Xi S, Liu Y, Zeng R, Wang J, Zhang W, Gao J, Qian J, Qin S. Sun J, et al. Eur J Pharmacol. 2023 Oct 5;956:175940. doi: 10.1016/j.ejphar.2023.175940. Epub 2023 Aug 2. Eur J Pharmacol. 2023. PMID: 37541362

9

Arihisa W, Kondo T, Yamaguchi K, Matsumoto J, Nakanishi H, Kunii Y, Akatsu H, Hino M, Hashizume Y, Sato S, Sato S, Niwa SI, Yabe H, Sasaki T, Shigenobu S, Setou M. Arihisa W, et al. Neuropsychopharmacol Rep. 2023 Sep;43(3):403-413. doi: 10.1002/npr2.12368. Epub 2023 Jul 27. Neuropsychopharmacol Rep. 2023. PMID: 37498306 Free PMC article.

10

Synergistic, long-term effects of glutamate dehydrogenase 1 deficiency and mild stress on cognitive function and mPFC gene and miRNA expression.

Asraf K, Zaidan H, Natoor B, Gaisler-Salomon I. Asraf K, et al. Transl Psychiatry. 2023 Jul 7;13(1):248. doi: 10.1038/s41398-023-02534-y. Transl Psychiatry. 2023. PMID: 37419882 Free PMC article.

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