Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2431
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation ; volume:18 ; number:1 ; day:30 ; month:10 ; year:2018 ; pages:1-7 ; date:12.2018
BMC pediatrics ; 18, Heft 1 (30.10.2018), 1-7, 12.2018
- Creator
-
Capozza, Manuela
Chinellato, Iolanda
Guarnieri, Vito
Di lorgi, Natascia
Accadia, Maria
Traggiai, Cristina
Mattioli, Girolamo
Di Mauro, Antonio
Laforgia, Nicola
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s12887-018-1319-0
- URN
-
urn:nbn:de:101:1-2018121822455805336509
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.0014, 9:59 AM CET
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
- Di lorgi, Natascia
- Accadia, Maria
- Traggiai, Cristina
- Mattioli, Girolamo
- Di Mauro, Antonio
- Laforgia, Nicola
- SpringerLink (Online service)
Other Objects (12)
Correction to: 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
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
Primary Hyperparathyroidism Presenting as Recurrent Pancreatitis Due to Parathyroid Adenoma
An Unusual Neonatal Presentation of Scimitar Syndrome
Heterogeneous Presentation of Neonatal Hemochromatosis in Dichorionic Twins
Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutation
Correction to: 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
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
Primary Hyperparathyroidism Presenting as Recurrent Pancreatitis Due to Parathyroid Adenoma
An Unusual Neonatal Presentation of Scimitar Syndrome
Heterogeneous Presentation of Neonatal Hemochromatosis in Dichorionic Twins
Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutation
Correction to: 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
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
Primary Hyperparathyroidism Presenting as Recurrent Pancreatitis Due to Parathyroid Adenoma
An Unusual Neonatal Presentation of Scimitar Syndrome
Heterogeneous Presentation of Neonatal Hemochromatosis in Dichorionic Twins