Suppr超能文献

相似文献

1
Updated consensus guidelines on the management of Phelan-McDermid syndrome.
Am J Med Genet A. 2023 Aug;191(8):2015-2044. doi: 10.1002/ajmg.a.63312. Epub 2023 Jul 1.
2
Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome.
J Neurodev Disord. 2024 May 10;16(1):25. doi: 10.1186/s11689-024-09541-0.
4
Gait Abnormalities in Children with Phelan-McDermid Syndrome.
J Child Neurol. 2023 Dec;38(13-14):665-671. doi: 10.1177/08830738231204395. Epub 2023 Oct 18.
5
Phenotypic variation in neural sensory processing by deletion size, age, and sex in Phelan-McDermid syndrome.
J Neurodev Disord. 2025 Aug 25;17(1):51. doi: 10.1186/s11689-025-09642-4.
6
Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome.
Mol Autism. 2022 Apr 8;13(1):17. doi: 10.1186/s13229-022-00493-7.
7
[Clinical and genetic analysis of four patients with Phelan-McDermid syndrome due to variants of SHANK gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2025 May 10;42(5):563-567. doi: 10.3760/cma.j.cn511374-20250213-00074.
8
Phelan-McDermid syndrome in a Chinese pediatric patient: A case report - new heterozygous mutations lead to PMS.
Medicine (Baltimore). 2025 Sep 5;104(36):e44114. doi: 10.1097/MD.0000000000044114.
9
Psychometric Study of the Social Responsiveness Scale in Phelan-McDermid Syndrome.
Autism Res. 2020 Aug;13(8):1383-1396. doi: 10.1002/aur.2299. Epub 2020 May 14.
10
The Black Book of Psychotropic Dosing and Monitoring.
Psychopharmacol Bull. 2024 Jul 8;54(3):8-59.

引用本文的文献

1
Phelan-McDermid syndrome in a Chinese pediatric patient: A case report - new heterozygous mutations lead to PMS.
Medicine (Baltimore). 2025 Sep 5;104(36):e44114. doi: 10.1097/MD.0000000000044114.
4
Psychopharmacology in children with genetic disorders of epigenetic and chromatin regulation.
J Neurodev Disord. 2025 Apr 24;17(1):21. doi: 10.1186/s11689-025-09605-9.
5
Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome.
Orphanet J Rare Dis. 2025 Mar 18;20(1):132. doi: 10.1186/s13023-025-03598-3.
6
Diagnosis and treatment of bipolar disorder in Phelan-McDermid syndrome: A case report and review of literature.
World J Psychiatry. 2025 Feb 19;15(2):101948. doi: 10.5498/wjp.v15.i2.101948.
8
A roadmap for SHANK3-related Epilepsy Research: recommendations from the 2023 strategic planning workshop.
Ther Adv Rare Dis. 2024 Sep 5;5:26330040241273464. doi: 10.1177/26330040241273464. eCollection 2024 Jan-Dec.
9
Aortic Root Dilation and Genotype Associations in Phelan-McDermid Syndrome.
Am J Med Genet A. 2025 Jan;197(1):e63872. doi: 10.1002/ajmg.a.63872. Epub 2024 Sep 11.
10
Adult syndromology: challenges, opportunities and perspectives: .
Med Genet. 2024 Jun 6;36(2):95-102. doi: 10.1515/medgen-2024-2023. eCollection 2024 Jun.

本文引用的文献

1
Sleep and Phelan-McDermid Syndrome: Lessons from the International Registry and the scientific literature.
Mol Genet Genomic Med. 2022 Oct;10(10):e2035. doi: 10.1002/mgg3.2035. Epub 2022 Aug 23.
2
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18.
3
Sensory processing and adaptive behavior in Phelan-McDermid syndrome: a cross-sectional study.
Eur J Pediatr. 2022 Aug;181(8):3141-3152. doi: 10.1007/s00431-022-04564-y. Epub 2022 Jul 15.
4
Variability in Phelan-McDermid Syndrome in a Cohort of 210 Individuals.
Front Genet. 2022 Apr 12;13:652454. doi: 10.3389/fgene.2022.652454. eCollection 2022.
5
Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome.
Mol Autism. 2022 Apr 8;13(1):17. doi: 10.1186/s13229-022-00493-7.
6
Phelan-McDermid syndrome: a classification system after 30 years of experience.
Orphanet J Rare Dis. 2022 Jan 29;17(1):27. doi: 10.1186/s13023-022-02180-5.
7
Parent-reported measure of repetitive behavior in Phelan-McDermid syndrome.
J Neurodev Disord. 2021 Nov 5;13(1):53. doi: 10.1186/s11689-021-09398-7.
8
A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome.
Mol Autism. 2021 Sep 30;12(1):62. doi: 10.1186/s13229-021-00459-1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验