Correction to: Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2431
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Correction to: Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation ; volume:19 ; number:1 ; day:27 ; month:11 ; year:2019 ; pages:1 ; date:12.2019
BMC pediatrics ; 19, Heft 1 (27.11.2019), 1, 12.2019
- Creator
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Capozza, Manuela
Chinellato, Iolanda
Guarnieri, Vito
Iorgi, Natascia Di
Accadia, Maria
Traggiai, Cristina
Mattioli, Girolamo
Mauro, Antonio Di
Laforgia, Nicola
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12887-019-1850-7
- URN
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urn:nbn:de:101:1-2020032217590206376401
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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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
- Capozza, Manuela
- Chinellato, Iolanda
- Guarnieri, Vito
- Iorgi, Natascia Di
- Accadia, Maria
- Traggiai, Cristina
- Mattioli, Girolamo
- Mauro, Antonio Di
- Laforgia, Nicola
- SpringerLink (Online service)
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An Unusual Neonatal Presentation of Scimitar Syndrome
Brown Tumor Related to Secondary Hyperparathyroidism Leading to Spinal Cord Compression Syndrome
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Primary Hyperparathyroidism Presenting as Recurrent Pancreatitis Due to Parathyroid Adenoma
Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation
Novel TRPV6 variant linked with transient neonatal hyperparathyroidism
Unusual presentation of primary hyperparathyroidism: report of three cases
Neonatal Hypopituitarism: Unusual Presentation
Novel TRPV6 mutations in the spectrum of transient neonatal hyperparathyroidism
Primary hyperparathyroidism
An Unusual Neonatal Presentation of Scimitar Syndrome
Brown Tumor Related to Secondary Hyperparathyroidism Leading to Spinal Cord Compression Syndrome
Iranian neonatal diabetes mellitus due to mutation in PDX1 gene: a case report
Transient Neonatal Diabetes Mellitus in a Very Preterm Infant due to ABCC8 Mutation
Heterogeneous Presentation of Neonatal Hemochromatosis in Dichorionic Twins