- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
0973-7693
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Fanconi-Bickel Syndrome - Mutation in SLC2A2 Gene ; volume:81 ; number:11 ; day:10 ; month:6 ; year:2014 ; pages:1237-1239 ; date:11.2014
Indian journal of pediatrics ; 81, Heft 11 (10.6.2014), 1237-1239, 11.2014
- Creator
-
Kehar, Mohit
- Contributor
-
Bijarnia, Sunita
Ellard, Sian
Houghton, Jayne
Saxena, Renu
Verma, I. C.
Wadhwa, Nishant
SpringerLink (Online service)
- DOI
-
10.1007/s12098-014-1487-3
- URN
-
urn:nbn:de:1111-2016080112375
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:53 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
- Kehar, Mohit
- Bijarnia, Sunita
- Ellard, Sian
- Houghton, Jayne
- Saxena, Renu
- Verma, I. C.
- Wadhwa, Nishant
- SpringerLink (Online service)
Other Objects (12)
Fanconi-Bickel syndrome in two Palestinian children: marked phenotypic variability with identical mutation
Fanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese children
Pediatric metanephric adenoma with Fanconi–Bickel syndrome: a case report and review of literature
Repurposing SGLT2 inhibitors: treatment of renal proximal tubulopathy in Fanconi‐Bickel syndrome with empagliflozin
Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome
Fanconi–Bickel syndrome in a Ugandan child – diagnostic challenges in resource-limited settings: a case report
Acute Lymphoblastic Leukemia Presenting as Fanconi Syndrome
Importance about use of high-throughput sequencing in pediatric: case report of a patient with Fanconi-Bickel syndrome
Acquired Fanconi syndrome in patients with Legionella pneumonia
De novo HNF4A-associated atypical Fanconi renal tubulopathy syndrome
Fainting Fanconi syndrome clarified by proxy: a case report
Fanconi, Aimé
Fanconi-Bickel syndrome in two Palestinian children: marked phenotypic variability with identical mutation
Fanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese children
Pediatric metanephric adenoma with Fanconi–Bickel syndrome: a case report and review of literature
Repurposing SGLT2 inhibitors: treatment of renal proximal tubulopathy in Fanconi‐Bickel syndrome with empagliflozin
Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome
Fanconi–Bickel syndrome in a Ugandan child – diagnostic challenges in resource-limited settings: a case report
Acute Lymphoblastic Leukemia Presenting as Fanconi Syndrome
Importance about use of high-throughput sequencing in pediatric: case report of a patient with Fanconi-Bickel syndrome
Acquired Fanconi syndrome in patients with Legionella pneumonia
De novo HNF4A-associated atypical Fanconi renal tubulopathy syndrome
Fainting Fanconi syndrome clarified by proxy: a case report
Fanconi, Aimé
Fanconi-Bickel syndrome in two Palestinian children: marked phenotypic variability with identical mutation
Fanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese children
Pediatric metanephric adenoma with Fanconi–Bickel syndrome: a case report and review of literature
Repurposing SGLT2 inhibitors: treatment of renal proximal tubulopathy in Fanconi‐Bickel syndrome with empagliflozin
Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome
Fanconi–Bickel syndrome in a Ugandan child – diagnostic challenges in resource-limited settings: a case report
Acute Lymphoblastic Leukemia Presenting as Fanconi Syndrome
Importance about use of high-throughput sequencing in pediatric: case report of a patient with Fanconi-Bickel syndrome
Acquired Fanconi syndrome in patients with Legionella pneumonia
De novo HNF4A-associated atypical Fanconi renal tubulopathy syndrome
Fainting Fanconi syndrome clarified by proxy: a case report