Lithium as a rescue therapy for regression and catatonia features in two SHANK3 patients with autism spectrum disorder: case reports
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-244X
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Lithium as a rescue therapy for regression and catatonia features in two SHANK3 patients with autism spectrum disorder: case reports ; volume:15 ; number:1 ; day:7 ; month:5 ; year:2015 ; pages:1-6 ; date:12.2015
BMC psychiatry ; 15, Heft 1 (7.5.2015), 1-6, 12.2015
- Creator
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Serret, Sylvie
- Contributor
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Thümmler, Susanne
Dor, Emmanuelle
Vesperini, Stephanie
Santos, Andreia
Askenazy, Florence
SpringerLink (Online service)
- DOI
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10.1186/s12888-015-0490-1
- URN
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urn:nbn:de:1111-2016110919904
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:49 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Serret, Sylvie
- Thümmler, Susanne
- Dor, Emmanuelle
- Vesperini, Stephanie
- Santos, Andreia
- Askenazy, Florence
- SpringerLink (Online service)
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Single-molecule fluorescence in-situ hybridization reveals that human SHANK3 mRNA expression varies during development and in autism-associated SHANK3 heterozygosity
Characterization of the structural and functional impact of autism-associated SHANK3 missense mutations
Sex differences in sleep deficits in mice with an autism-linked Shank3 mutation
Unravelling the role of SHANK3 mutations in targeted therapies for autism spectrum disorders
Autism-associated miR-873 regulates ARID1B, SHANK3 and NRXN2 involved in neurodevelopment
Disrupted extracellular matrix and cell cycle genes in autism-associated Shank3 deficiency are targeted by lithium
Disrupted extracellular matrix and cell cycle genes in autism-associated Shank3 deficiency are targeted by lithium
Transcriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant mice
Autism-associated gene shank3 is necessary for social contagion in zebrafish
The Role of Thioredoxin System in Shank3 Mouse Model of Autism
Disrupted Human–Dog Interbrain Neural Coupling in Autism‐Associated Shank3 Mutant Dogs
Association study of SHANK3 gene polymorphisms with autism in Chinese Han population
Single-molecule fluorescence in-situ hybridization reveals that human SHANK3 mRNA expression varies during development and in autism-associated SHANK3 heterozygosity
Characterization of the structural and functional impact of autism-associated SHANK3 missense mutations
Sex differences in sleep deficits in mice with an autism-linked Shank3 mutation
Unravelling the role of SHANK3 mutations in targeted therapies for autism spectrum disorders
Autism-associated miR-873 regulates ARID1B, SHANK3 and NRXN2 involved in neurodevelopment
Disrupted extracellular matrix and cell cycle genes in autism-associated Shank3 deficiency are targeted by lithium
Disrupted extracellular matrix and cell cycle genes in autism-associated Shank3 deficiency are targeted by lithium
Transcriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant mice
Autism-associated gene shank3 is necessary for social contagion in zebrafish
The Role of Thioredoxin System in Shank3 Mouse Model of Autism
Disrupted Human–Dog Interbrain Neural Coupling in Autism‐Associated Shank3 Mutant Dogs
Association study of SHANK3 gene polymorphisms with autism in Chinese Han population
Single-molecule fluorescence in-situ hybridization reveals that human SHANK3 mRNA expression varies during development and in autism-associated SHANK3 heterozygosity
Characterization of the structural and functional impact of autism-associated SHANK3 missense mutations
Sex differences in sleep deficits in mice with an autism-linked Shank3 mutation
Unravelling the role of SHANK3 mutations in targeted therapies for autism spectrum disorders