Gastrostomy for infants with severe epidermolysis bullosa simplex in neonatal intensive care
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Gastrostomy for infants with severe epidermolysis bullosa simplex in neonatal intensive care ; volume:16 ; number:1 ; day:11 ; month:6 ; year:2021 ; pages:1-3 ; date:12.2021
Orphanet journal of rare diseases ; 16, Heft 1 (11.6.2021), 1-3, 12.2021
- Creator
-
Marro, M.
Smet, S. De
Caldari, D.
Lambe, C.
Leclerc-Mercier, S.
Chiaverini, C.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13023-021-01896-0
- URN
-
urn:nbn:de:101:1-2021100308074684104503
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:33 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
- Marro, M.
- Smet, S. De
- Caldari, D.
- Lambe, C.
- Leclerc-Mercier, S.
- Chiaverini, C.
- SpringerLink (Online service)
Other Objects (12)
Molekulargenetische und klinische Analysen bei der Epidermolysis Bullosa Simplex
Epidermolysis bullosa hereditaria
Epidermolysis bullosa hereditaria
Epidermolysis bullosa hereditaria
Inherited epidermolysis bullosa
A Sporadic Neonatal Case of Epidermolysis Bullosa Simplex Generalized Intermediate with KRT5 and KRT14 Gene Mutations
Seltene Form der Epidermolysis bullosa simplex mit homozygoter Mutation im Gen EXPH5
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Krankheitsverarbeitung bei Epidermolysis bullosa hereditaria
Clinical aspects of epidermolysis bullosa : findings of the Freiburg epidermolysis bullosa registry 2003-2011
Molekulargenetische und klinische Analysen bei der Epidermolysis Bullosa Simplex
Epidermolysis bullosa hereditaria
Epidermolysis bullosa hereditaria
Epidermolysis bullosa hereditaria
Inherited epidermolysis bullosa
A Sporadic Neonatal Case of Epidermolysis Bullosa Simplex Generalized Intermediate with KRT5 and KRT14 Gene Mutations
Seltene Form der Epidermolysis bullosa simplex mit homozygoter Mutation im Gen EXPH5
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Krankheitsverarbeitung bei Epidermolysis bullosa hereditaria
Clinical aspects of epidermolysis bullosa : findings of the Freiburg epidermolysis bullosa registry 2003-2011
Molekulargenetische und klinische Analysen bei der Epidermolysis Bullosa Simplex
Epidermolysis bullosa hereditaria
Epidermolysis bullosa hereditaria
Epidermolysis bullosa hereditaria
Inherited epidermolysis bullosa
A Sporadic Neonatal Case of Epidermolysis Bullosa Simplex Generalized Intermediate with KRT5 and KRT14 Gene Mutations
Seltene Form der Epidermolysis bullosa simplex mit homozygoter Mutation im Gen EXPH5
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Krankheitsverarbeitung bei Epidermolysis bullosa hereditaria