- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Rett syndrome: a wide clinical and autonomic picture ; volume:11 ; number:1 ; day:29 ; month:9 ; year:2016 ; pages:1-16 ; date:12.2016
Orphanet journal of rare diseases ; 11, Heft 1 (29.9.2016), 1-16, 12.2016
- Creator
-
Pini, G.
- Contributor
-
Bigoni, S.
Congiu, L.
Romanelli, A. M.
Scusa, M. F.
Di Marco, P.
Benincasa, A.
Morescalchi, P.
Ferlini, A.
Bianchi, F.
Tropea, D.
Zappella, M.
SpringerLink (Online service)
- DOI
-
10.1186/s13023-016-0499-7
- URN
-
urn:nbn:de:1111-2016110426433
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:52 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Pini, G.
- Bigoni, S.
- Congiu, L.
- Romanelli, A. M.
- Scusa, M. F.
- Di Marco, P.
- Benincasa, A.
- Morescalchi, P.
- Ferlini, A.
- Bianchi, F.
- Tropea, D.
- Zappella, M.
- SpringerLink (Online service)
Other Objects (12)
Autonomic breathing abnormalities in Rett syndrome: caregiver perspectives in an international database study
Variant of Rett Syndrome and CDKL5 Gene: Clinical and Autonomic Description of 10 Cases
Key issues in Rett syndrome: emotional, behavioural and autonomic dysregulation (EBAD) - a target for clinical trials
VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia
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
Characterizing the journey of Rett syndrome among females in the United States: a real-world evidence study using the Rett syndrome natural history study database
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
Development of protein substitution therapy for Rett syndrome
Autonomic breathing abnormalities in Rett syndrome: caregiver perspectives in an international database study
Variant of Rett Syndrome and CDKL5 Gene: Clinical and Autonomic Description of 10 Cases
Key issues in Rett syndrome: emotional, behavioural and autonomic dysregulation (EBAD) - a target for clinical trials
VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia
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
Characterizing the journey of Rett syndrome among females in the United States: a real-world evidence study using the Rett syndrome natural history study database
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
Development of protein substitution therapy for Rett syndrome
Autonomic breathing abnormalities in Rett syndrome: caregiver perspectives in an international database study
Variant of Rett Syndrome and CDKL5 Gene: Clinical and Autonomic Description of 10 Cases
Key issues in Rett syndrome: emotional, behavioural and autonomic dysregulation (EBAD) - a target for clinical trials
VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia
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
Characterizing the journey of Rett syndrome among females in the United States: a real-world evidence study using the Rett syndrome natural history study database
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation