Beyond gait and balance: urinary and bowel dysfunction in X-linked adrenoleukodystrophy
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Beyond gait and balance: urinary and bowel dysfunction in X-linked adrenoleukodystrophy ; volume:16 ; number:1 ; day:6 ; month:1 ; year:2021 ; pages:1-11 ; date:12.2021
Orphanet journal of rare diseases ; 16, Heft 1 (6.1.2021), 1-11, 12.2021
- Creator
-
Corre, Camille S.
Grant, Natalie
Sadjadi, Reza
Hayden, Douglas
Becker, Catherine
Gomery, Pablo
Eichler, Florian S.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13023-020-01596-1
- URN
-
urn:nbn:de:101:1-2021020723305463842135
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:37 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
- Corre, Camille S.
- Grant, Natalie
- Sadjadi, Reza
- Hayden, Douglas
- Becker, Catherine
- Gomery, Pablo
- Eichler, Florian S.
- SpringerLink (Online service)
Other Objects (12)
Easily misdiagnosed X-linked adrenoleukodystrophy
X-linked disorders with cerebellar dysgenesis
X-linked SCID with a rare mutation
X-linked inhibitor of apoptosis protein in intestinal homeostasis and the pathogenesis of inflammatory bowel disease
X-linked Hyper-IgM Syndrome with Bronchiectasis
X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
Germline mosaicism in X-linked periventricular nodular heterotopia
X-linked congenital adrenal hypoplasia: a case presentation
Optimising Gene Therapy for X-linked Retinitis Pigmentosa
Sporadic Case of Heterozygous X-Linked Alport Syndrome
Aspects of human genetics with special reference to X-linked disorders : selected papers from the Symposium on X-Linked Diseases
Easily misdiagnosed X-linked adrenoleukodystrophy
X-linked disorders with cerebellar dysgenesis
X-linked SCID with a rare mutation
X-linked inhibitor of apoptosis protein in intestinal homeostasis and the pathogenesis of inflammatory bowel disease
X-linked Hyper-IgM Syndrome with Bronchiectasis
X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
Germline mosaicism in X-linked periventricular nodular heterotopia
X-linked congenital adrenal hypoplasia: a case presentation
Optimising Gene Therapy for X-linked Retinitis Pigmentosa
Sporadic Case of Heterozygous X-Linked Alport Syndrome
Aspects of human genetics with special reference to X-linked disorders : selected papers from the Symposium on X-Linked Diseases
Easily misdiagnosed X-linked adrenoleukodystrophy
X-linked disorders with cerebellar dysgenesis
X-linked SCID with a rare mutation
X-linked inhibitor of apoptosis protein in intestinal homeostasis and the pathogenesis of inflammatory bowel disease
X-linked Hyper-IgM Syndrome with Bronchiectasis
X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
Germline mosaicism in X-linked periventricular nodular heterotopia
X-linked congenital adrenal hypoplasia: a case presentation
Optimising Gene Therapy for X-linked Retinitis Pigmentosa
Sporadic Case of Heterozygous X-Linked Alport Syndrome