PubMed for id: 400954

Year	Number of Results
2004	1
2005	1
2009	1
2021	4
2022	294
2023	236
2024	1

1

Practice parameter: Evaluation of the child with microcephaly (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

Ashwal S, Michelson D, Plawner L, Dobyns WB; Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Ashwal S, et al. Neurology. 2009 Sep 15;73(11):887-97. doi: 10.1212/WNL.0b013e3181b783f7. Neurology. 2009. PMID: 19752457 Free PMC article.

2

Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors.

McConkie-Rosell A, Finucane B, Cronister A, Abrams L, Bennett RL, Pettersen BJ. McConkie-Rosell A, et al. J Genet Couns. 2005 Aug;14(4):249-70. doi: 10.1007/s10897-005-4802-x. J Genet Couns. 2005. PMID: 16047089

3

Practice parameter: diagnostic assessment of the child with cerebral palsy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

Ashwal S, Russman BS, Blasco PA, Miller G, Sandler A, Shevell M, Stevenson R; Quality Standards Subcommittee of the American Academy of Neurology; Practice Committee of the Child Neurology Society. Ashwal S, et al. Neurology. 2004 Mar 23;62(6):851-63. doi: 10.1212/01.wnl.0000117981.35364.1b. Neurology. 2004. PMID: 15037681

4

Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1^-/y mouse model of autism.

Bhaskaran AA, Gauvrit T, Vyas Y, Bony G, Ginger M, Frick A. Bhaskaran AA, et al. Nat Commun. 2023 Nov 30;14(1):7905. doi: 10.1038/s41467-023-43777-z. Nat Commun. 2023. PMID: 38036566 Free PMC article.

5

Foetal Akinesia Deformation Sequence: A Rare Lethal Entity.

Shafqat G, Fatima K, Hanif F. Shafqat G, et al. J Pak Med Assoc. 2023 Nov;73(11):2266-2268. doi: 10.47391/JPMA.8513. J Pak Med Assoc. 2023. PMID: 38013544 Free article.

6

Prolonged misdiagnosis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome: A case report.

Wang Y, Zhang W, Jiang X. Wang Y, et al. Medicine (Baltimore). 2023 Nov 24;102(47):e36008. doi: 10.1097/MD.0000000000036008. Medicine (Baltimore). 2023. PMID: 38013338 Free PMC article.

7

FMRP Enhances the Translation of 4EBP2 mRNA during Neuronal Differentiation.

Yu J, Woo Y, Kim H, An S, Park SK, Jang SK. Yu J, et al. Int J Mol Sci. 2023 Nov 14;24(22):16319. doi: 10.3390/ijms242216319. Int J Mol Sci. 2023. PMID: 38003508 Free PMC article.

8

[Analysis of clinical features and ATRX gene variants in a Chinese pedigree affected with X-linked alpha thalassemia mental retardation (ATR-X) syndrome].

Dong R, Yang Y, Guo H, Gao M, Lyu Y, Li Y, Yang X, Liu Y. Dong R, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Dec 10;40(12):1508-1511. doi: 10.3760/cma.j.cn511374-20210702-00565. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37994132 Chinese.

9

Retinoic acid regulation of homoeostatic synaptic plasticity and its relationship to cognitive disorders.

Moramarco F, McCaffery P. Moramarco F, et al. J Mol Endocrinol. 2023 Dec 6;72(1):e220177. doi: 10.1530/JME-22-0177. Print 2024 Jan 1. J Mol Endocrinol. 2023. PMID: 37930232

10

A Novel Neuroimaging Phenotype in the X-Linked Intellectual Disability with a Missense Mutation of CNKSR2 Gene.

Hosur B, Sinha R, Jain NK, Muthanna BA, Bansal V, Singh S, Kamila G. Hosur B, et al. Neurol India. 2023 Sep-Oct;71(5):980-983. doi: 10.4103/0028-3886.388124. Neurol India. 2023. PMID: 37929438

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