- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1880-6562
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Novel TRPV6 mutations in the spectrum of transient neonatal hyperparathyroidism ; volume:70 ; number:1 ; day:9 ; month:7 ; year:2020 ; pages:1-10 ; date:12.2020
The journal of physiological sciences ; 70, Heft 1 (9.7.2020), 1-10, 12.2020
- Creator
-
Suzuki, Yoshiro
Sawada, Hirotake
Tokumasu, Tomoko
Suzuki, Shigeru
Ninomiya, Shinsuke
Shirai, Masaru
Mukai, Tokuo
Saito, Claire T.
Nishimura, Gen
Tominaga, Makoto
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s12576-020-00761-2
- URN
-
urn:nbn:de:101:1-2020090719584263304511
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:58 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
- Suzuki, Yoshiro
- Sawada, Hirotake
- Tokumasu, Tomoko
- Suzuki, Shigeru
- Ninomiya, Shinsuke
- Shirai, Masaru
- Mukai, Tokuo
- Saito, Claire T.
- Nishimura, Gen
- Tominaga, Makoto
- SpringerLink (Online service)
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Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation
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Novel TRPV6 variant linked with transient neonatal hyperparathyroidism
Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57
Primary hyperparathyroidism
Clinical Predictors of Transient versus Persistent Neonatal Hyperinsulinism
Neonatal hyperinsulinism in transient and classical forms of tyrosinemia
Hyperparathyroidism-Jaw Tumor Syndrome
Heterozygous FA2H mutations in autism spectrum disorders
Transient hypercortisolism and symptomatic hyperthyroidism associated to primary hyperparathyroidism in an elderly patient: case report and literature review
Autosomal dominant transmission of transient neonatal lactic acidosis: a case report
Seronegative Maternal Ocular Myasthenia Gravis and Delayed Transient Neonatal Myasthenia Gravis
Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation
Persistent hyperparathyroidism after preemptive kidney transplantation
Novel TRPV6 variant linked with transient neonatal hyperparathyroidism
Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57
Primary hyperparathyroidism
Clinical Predictors of Transient versus Persistent Neonatal Hyperinsulinism
Neonatal hyperinsulinism in transient and classical forms of tyrosinemia
Hyperparathyroidism-Jaw Tumor Syndrome
Heterozygous FA2H mutations in autism spectrum disorders
Transient hypercortisolism and symptomatic hyperthyroidism associated to primary hyperparathyroidism in an elderly patient: case report and literature review
Autosomal dominant transmission of transient neonatal lactic acidosis: a case report
Seronegative Maternal Ocular Myasthenia Gravis and Delayed Transient Neonatal Myasthenia Gravis
Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation