Page last updated: 2024-09-04

cinacalcet and Infant, Newborn, Diseases

cinacalcet has been researched along with Infant, Newborn, Diseases in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's5 (71.43)24.3611
2020's2 (28.57)2.80

Authors

AuthorsStudies
Demir, S; Dilek, E; Gürkan, H; İnan, M; Kökenli, F; Özgüç Çömlek, F; Sezer, A1
Ata, P; Bereket, A; Bilgen, H; Eltan, M; Gulcan-Kersin, S; Kirkgoz, T; Ozek, E; Rzayev, T; Turan, S1
Accadia, M; Capozza, M; Chinellato, I; Di Lorgi, N; Di Mauro, A; Guarnieri, V; Laforgia, N; Mattioli, G; Traggiai, C1
Huang, L; Sun, X; Tao, Y; Wu, J; Yang, F1
Domínguez Quintero, ML; Ferrer Castillo, MT; García Soblechero, E; González Fuentes, C; Jiménez Crespo, B1
Gannon, AW; Levine, MA; Monk, HM1
Abali, S; Altuncu, E; Atay, Z; Bereket, A; Canaff, L; Cole, DE; Haliloglu, B; Hendy, GN; Ozdogan, T; Turan, S; Vilaça, T; Wong, BY1

Reviews

2 review(s) available for cinacalcet and Infant, Newborn, Diseases

ArticleYear
Novel homozygous inactivating mutation of the calcium-sensing receptor gene in neonatal severe hyperparathyroidism responding to cinacalcet therapy: A case report and literature review.
    Medicine, 2018, Volume: 97, Issue:45

    Topics: Calcimimetic Agents; Calcium; Cinacalcet; Female; Genetic Testing; Homozygote; Humans; Hyperparathyroidism, Primary; Infant; Infant, Newborn; Infant, Newborn, Diseases; Mutation; Parathyroid Hormone; Receptors, Calcium-Sensing

2018
Cinacalcet monotherapy in neonatal severe hyperparathyroidism: a case study and review.
    The Journal of clinical endocrinology and metabolism, 2014, Volume: 99, Issue:1

    Topics: Cinacalcet; Humans; Hyperparathyroidism; Infant, Newborn; Infant, Newborn, Diseases; Male; Naphthalenes; Receptors, Calcium-Sensing; Severity of Illness Index; Treatment Outcome

2014

Other Studies

5 other study(ies) available for cinacalcet and Infant, Newborn, Diseases

ArticleYear
The efficiency of cinacalcet treatment in delaying parathyroidectomy in a case with neonatal severe hyperparathyroidism caused by homozygous mutation in the CASR gene.
    Pediatric endocrinology, diabetes, and metabolism, 2022, Volume: 28, Issue:2

    Topics: Calcium; Cinacalcet; Humans; Hypercalcemia; Hyperparathyroidism, Primary; Infant, Newborn; Infant, Newborn, Diseases; Male; Mutation; Parathyroidectomy; Receptors, Calcium-Sensing

2022
Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation.
    Hormone research in paediatrics, 2020, Volume: 93, Issue:5

    Topics: Calcimimetic Agents; Cinacalcet; Female; Humans; Hyperparathyroidism, Primary; Infant, Newborn; Infant, Newborn, Diseases; Receptors, Calcium-Sensing

2020
Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation.
    BMC pediatrics, 2018, 10-30, Volume: 18, Issue:1

    Topics: Bone Density Conservation Agents; Calcimimetic Agents; Cinacalcet; Clodronic Acid; Diphosphonates; Female; Fluid Therapy; Furosemide; Genes, Recessive; Homozygote; Humans; Hyperparathyroidism, Primary; Infant, Newborn; Infant, Newborn, Diseases; Mutation; Parathyroidectomy; Receptors, Calcium-Sensing

2018
Neonatal hypercalcemia due to a homozygous mutation in the calcium-sensing receptor: failure of cinacalcet.
    Neonatology, 2013, Volume: 104, Issue:2

    Topics: Calcimimetic Agents; Cinacalcet; DNA Mutational Analysis; Drug Resistance; Exons; Genetic Predisposition to Disease; Homozygote; Humans; Hypercalcemia; Hyperparathyroidism, Primary; Infant, Newborn; Infant, Newborn, Diseases; Male; Naphthalenes; Phenotype; Receptors, Calcium-Sensing; Sequence Deletion; Treatment Failure

2013
Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism-lack of effect of cinacalcet.
    Bone, 2014, Volume: 64

    Topics: Cinacalcet; Female; Homozygote; Humans; Hyperparathyroidism; Infant, Newborn; Infant, Newborn, Diseases; Male; Mutation; Naphthalenes; Pedigree; Receptors, Calcium-Sensing

2014