Cargando…

PTH infusion ameliorates seizures in autosomal dominant hypocalcemia type 1

Detalles Bibliográficos
Autores principales:	Sastre, Ana, Valentino, Kevin, Hannan, Fadil M., Lines, Kate E., Gluck, Anna K., Stevenson, Mark, Ryalls, Michael, Pullen, Debbie, Buck, Jackie, Sankar, Sailesh, Allgrove, Jeremy, Thakker, Rajesh V., Gevers, Evelien F.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614858/ https://www.ncbi.nlm.nih.gov/pubmed/34233101 http://dx.doi.org/10.1056/NEJMc2034981

Ejemplares similares

Calcilytic NPSP795 Increases Plasma Calcium and PTH in an Autosomal Dominant Hypocalcemia Type 1 Mouse Model
por: Hannan, Fadil M, et al.
Publicado: (2020)

Autosomal Dominant Hypocalcemia Type 1 (ADH1) Associated With Myoclonus and Intracerebral Calcifications
por: Elston, Marianne S, et al.
Publicado: (2022)

Activating Mutations of the G-protein Subunit α (11) Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2
por: Gorvin, Caroline M, et al.
Publicado: (2019)

SAT218 Refractory Hypocalcemia From Combined Autosomal Dominant Hypocalcemia Type 2 And Postsurgical Hypoparathyroidism
por: Sonmez Ince, Melda, et al.
Publicado: (2023)

Familial Hypocalciuric Hypercalcemia Type 1 and Autosomal-Dominant Hypocalcemia Type 1: Prevalence in a Large Healthcare Population
por: Dershem, Ridge, et al.
Publicado: (2020)

The Calcilytic Agent NPS 2143 Rectifies Hypocalcemia in a Mouse Model With an Activating Calcium-Sensing Receptor (CaSR) Mutation: Relevance to Autosomal Dominant Hypocalcemia Type 1 (ADH1)
por: Hannan, Fadil M., et al.
Publicado: (2015)

PTH Gradient as a Predictor of Post Thyroidectomy Hypocalcemia
por: Garg, Surabhi, et al.
Publicado: (2021)

PTH after Thyroidectomy as a Predictor of Post-Operative Hypocalcemia
por: Metere, Alessio, et al.
Publicado: (2021)

Hypocalcemia after thyroidectomy: iPTH levels and iPTH decline are predictive? Retrospective cohort study()
por: Cannizzaro, Matteo Angelo, et al.
Publicado: (2018)

Identification of a G‐Protein Subunit‐α11 Gain‐of‐Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2)
por: Piret, Sian E, et al.
Publicado: (2016)

Rare Case of Severe Hypocalcemia Due to PTH Resistance Related to Diet Pill
por: Katkar, Rujuta Baban, et al.
Publicado: (2021)

Effectiveness of an i-PTH Measurement in Predicting Post Thyroidectomy Hypocalcemia: Prospective Controlled Study
por: Kim, Jin Pyeong, et al.
Publicado: (2013)

Autosomal Dominant Hypocalcemia (Hypoparathyroidism) Types 1 and 2
por: Roszko, Kelly L., et al.
Publicado: (2016)

Hypocalcemia in COVID-19 is associated with low vitamin D levels and impaired compensatory PTH response
por: di Filippo, Luigi, et al.
Publicado: (2021)

Autosomal Dominant Hypocalcemia Type 1: A Systematic Review
por: Roszko, Kelly L, et al.
Publicado: (2022)

Autosomal Dominant Hypocalcemia Type 1 and Neonatal Focal Seizures
por: Teleanu, Raluca Ioana, et al.
Publicado: (2023)

Low serum iPTH at the end of surgery is the earliest predictor of postoperative hypocalcemia after total thyroidectomy
por: Lalos, Alexandros, et al.
Publicado: (2023)

Intractable Generalized Epilepsy and Autosomal Dominant Hypocalcemia: A Case Report
por: Rossi, Gian C., et al.
Publicado: (2019)

Gα(11) mutation in mice causes hypocalcemia rectifiable by calcilytic therapy
por: Gorvin, Caroline M., et al.
Publicado: (2017)

Short-Term PTH(1-34) Therapy in Children to Correct Severe Hypocalcemia and Hyperphosphatemia due to Hypoparathyroidism: Two Case Studies
por: Mishra, Pooja E., et al.
Publicado: (2016)

Subcutaneous Infusion of rhPTH(1-34) During Pregnancy and Nursing in a Woman With Autosomal Dominant Hypoparathyroidism 1
por: Shulman, Dorothy
Publicado: (2022)

Differential parathyroid and kidney Ca(2+)-sensing receptor activation in autosomal dominant hypocalcemia 1
por: van Megen, Wouter H., et al.
Publicado: (2022)

Autosomal dominant hypocalcemia with a novel CASR mutation: a case study and literature review
por: Wu, Yingying, et al.
Publicado: (2022)

SAT-036 Extracellular Domain Calcium-Sensing Receptor (CaSR) Mutations Leading to Hypercalcemic and Hypocalcemic Disorders Cluster at the Homodimeric Interface
por: Olesen, Mie, et al.
Publicado: (2019)

Hypocalcemia After Completion Thyroidectomy for Papillary Thyroid Carcinoma
por: Bumber, Boris, et al.
Publicado: (2020)

Disorders of the calcium-sensing receptor and partner proteins: insights into the molecular basis of calcium homeostasis
por: Hannan, Fadil M, et al.
Publicado: (2016)

Autosomal Dominant Hypocalcemia Caused by an Activating Mutation of the Calcium-Sensing Receptor Gene: The First Case Report in Korea
por: Kim, Mi Yeon, et al.
Publicado: (2010)

Animal models of pituitary neoplasia
por: Lines, K.E., et al.
Publicado: (2016)

Control of PTH secretion by the TRPC1 ion channel
por: Onopiuk, Marta, et al.
Publicado: (2020)

OR07-06 The Roles of GNAQ and GNA11 in Calcium-Sensing Receptor (CaSR) Signalling
por: Gluck, Anna K, et al.
Publicado: (2020)

The Unusual Suspect: Hypocalcemia in Preeclampsia After Magnesium Infusion
por: Abdulhadi, Basma, et al.
Publicado: (2021)

Optimization of PTH/PTHrP Hybrid Peptides to Derive a Long‐Acting PTH Analog (LA‐PTH)
por: Noda, Hiroshi, et al.
Publicado: (2020)

Identification and Functional Characterization of a Novel Mutation in the Human Calcium-Sensing Receptor That Co-Segregates With Autosomal-Dominant Hypocalcemia
por: Rasmussen, Anne Qvist, et al.
Publicado: (2018)

SAT-347 Diagnosis of Autosomal Dominant Hypocalcemia Type 1 Following the Initiation of Imatinib for Treatment of Chronic Myeloid Leukemia
por: Jones-Ryan, Madeline L, et al.
Publicado: (2020)

Autosomal Dominant Hypocalcemia With Atypical Urine Findings Accompanied by Novel CaSR Gene Mutation and VitD Deficiency
por: Tsuji, Tomoya, et al.
Publicado: (2020)

Genetics of Monogenic Disorders of Calcium and Bone Metabolism
por: Newey, Paul J, et al.
Publicado: (2022)

Lip Tremor in Hypocalcemia
por: Kumar, Niraj, et al.
Publicado: (2020)

Hypocalcemia Induced Bronchospasm
por: Kumari, Aneeta, et al.
Publicado: (2022)

Autosomal dominant hypocalcemia with Bartter syndrome due to a novel activating mutation of calcium sensing receptor, Y829C
por: Choi, Keun Hee, et al.
Publicado: (2015)

Hypercalcemic Disorders in Children
por: Stokes, Victoria J, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_gdj43c8kfrah03st8visusmtd8