- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1563-258X
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Progress in Rett Syndrome: from discovery to clinical trials ; volume:166 ; number:11-12 ; day:4 ; month:8 ; year:2016 ; pages:325-332 ; date:9.2016
Wiener medizinische Wochenschrift ; 166, Heft 11-12 (4.8.2016), 325-332, 9.2016
- Urheber
-
Percy, Alan K.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1007/s10354-016-0491-9
- URN
-
urn:nbn:de:1111-201609273741
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:46 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Percy, Alan K.
- SpringerLink (Online service)
Ähnliche Objekte (12)
MeCP2 mutations: progress towards understanding and treating Rett syndrome
Altered gut microbiota in Rett syndrome
Associations between genotype, phenotype and behaviours measured by the Rett syndrome behaviour questionnaire in Rett syndrome
Gait Initiation in Children with Rett Syndrome
Rett syndrome in Ireland: a demographic study
A perspective on “cure” for Rett syndrome
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
Key issues in Rett syndrome: emotional, behavioural and autonomic dysregulation (EBAD) - a target for clinical trials
I. Discovery and progress
Development of protein substitution therapy for Rett syndrome
A national survey of Rett syndrome: behavioural characteristics
Rett syndrome: a wide clinical and autonomic picture
MeCP2 mutations: progress towards understanding and treating Rett syndrome
Altered gut microbiota in Rett syndrome
Associations between genotype, phenotype and behaviours measured by the Rett syndrome behaviour questionnaire in Rett syndrome
Gait Initiation in Children with Rett Syndrome
Rett syndrome in Ireland: a demographic study
A perspective on “cure” for Rett syndrome
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
Key issues in Rett syndrome: emotional, behavioural and autonomic dysregulation (EBAD) - a target for clinical trials
I. Discovery and progress
Development of protein substitution therapy for Rett syndrome
A national survey of Rett syndrome: behavioural characteristics
Rett syndrome: a wide clinical and autonomic picture
MeCP2 mutations: progress towards understanding and treating Rett syndrome
Altered gut microbiota in Rett syndrome
Associations between genotype, phenotype and behaviours measured by the Rett syndrome behaviour questionnaire in Rett syndrome
Gait Initiation in Children with Rett Syndrome
Rett syndrome in Ireland: a demographic study
A perspective on “cure” for Rett syndrome
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
Key issues in Rett syndrome: emotional, behavioural and autonomic dysregulation (EBAD) - a target for clinical trials
I. Discovery and progress
Development of protein substitution therapy for Rett syndrome
A national survey of Rett syndrome: behavioural characteristics