Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations.
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| Title: | Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations. |
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| Authors: | Vall-Palomar M; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain., Burballa C; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain., Claverie-Martín F; Unidad de Investigación, Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain., Meseguer A; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain.; Departament de Bioquímica I Biologia Molecular. Unitat de Bioquímica de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.; Red de Investigación Renal (REDINREN), Instituto Carlos III-FEDER, Madrid, Spain., Ariceta G; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain. gariceta@vhebron.net.; Servicio de Nefrología Pediátrica, Hospital Universitari Vall D'Hebron, 08035, Barcelona, Spain. gariceta@vhebron.net.; Departamento de Pediatría, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain. gariceta@vhebron.net. |
| Source: | Journal of nephrology [J Nephrol] 2021 Dec; Vol. 34 (6), pp. 2053-2062. Date of Electronic Publication: 2021 Apr 30. |
| Publication Type: | Journal Article; Multicenter Study |
| Journal Info: | Publisher: Springer Country of Publication: Italy NLM ID: 9012268 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1724-6059 (Electronic) Linking ISSN: 11218428 NLM ISO Abbreviation: J Nephrol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 33929692 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Vall-Palomar+M%22">Vall-Palomar M</searchLink>; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain.<br /><searchLink fieldCode="AU" term="%22Burballa+C%22">Burballa C</searchLink>; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain.<br /><searchLink fieldCode="AU" term="%22Claverie-Martín+F%22">Claverie-Martín F</searchLink>; Unidad de Investigación, Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain.<br /><searchLink fieldCode="AU" term="%22Meseguer+A%22">Meseguer A</searchLink>; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain.; Departament de Bioquímica I Biologia Molecular. Unitat de Bioquímica de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.; Red de Investigación Renal (REDINREN), Instituto Carlos III-FEDER, Madrid, Spain.<br /><searchLink fieldCode="AU" term="%22Ariceta+G%22">Ariceta G</searchLink>; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain. gariceta@vhebron.net.; Servicio de Nefrología Pediátrica, Hospital Universitari Vall D'Hebron, 08035, Barcelona, Spain. gariceta@vhebron.net.; Departamento de Pediatría, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain. gariceta@vhebron.net. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229012268%22">Journal of nephrology</searchLink> [J Nephrol] 2021 Dec; Vol. 34 (6), pp. 2053-2062. <i>Date of Electronic Publication: </i>2021 Apr 30. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Multicenter Study – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Springer%22">Springer </searchLink><i>Country of Publication: </i>Italy <i>NLM ID: </i>9012268 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1724-6059 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2211218428%22">11218428 </searchLink><i>NLM ISO Abbreviation: </i>J Nephrol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=33929692 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s40620-021-01054-6 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 2053 Titles: – TitleFull: Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Vall-Palomar M – PersonEntity: Name: NameFull: Burballa C – PersonEntity: Name: NameFull: Claverie-Martín F – PersonEntity: Name: NameFull: Meseguer A – PersonEntity: Name: NameFull: Ariceta G IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2021 Dec Type: published Y: 2021 Identifiers: – Type: issn-electronic Value: 1724-6059 Numbering: – Type: volume Value: 34 – Type: issue Value: 6 Titles: – TitleFull: Journal of nephrology Type: main |
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