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Pediatric Diabetes
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August 31, 2012
Good practice recommendations on paediatric training programmes for health care professionals in the EU
Sheridan Waldron, Imre Rurik, Laszlo Madacsy, et al.
Bone
|
October 27, 2019
Juvenile Paget's disease with compound heterozygous mutations in TNFRSF11B presenting with recurrent clavicular fractures and a mild skeletal phenotype
Dorit Naot, Louise C Wilson, Jeremy Allgrove, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 14, 2010
A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism
Samantha M Mirczuk, Michael R Bowl, M Andrew Nesbit, et al.
Bone
|
May 1, 2025
Rebound hypercalcaemia timing is associated with cumulative weight-based denosumab dose for central giant cell granuloma treatment in children despite a dose weaning regimen
Alexander D Chesover, Jeremy Allgrove, Alistair Calder, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 14, 2024
Eiken syndrome with parathyroid hormone resistance due to a novel parathyroid hormone receptor type 1 mutation: clinical features and functional analysis
Alistair D Calder, Jeremy Allgrove, Jakob Höppner, et al.
Archives of Disease in Childhood
|
November 9, 2021
Non-collagen pathogenic variants resulting in the osteogenesis imperfecta phenotype in children: a single-country observational cohort study
Patrick Thornley, Nicholas Bishop, Duncan Baker, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 1, 2020
Case report: a 10-year-old girl with primary hypoparathyroidism and systemic lupus erythematosus
Hanna Borysewicz-Sańczyk, Beata Sawicka, Justyna Michalak, et al.
Pediatric Diabetes
|
July 22, 2014
ISPAD Clinical Practice Consensus Guidelines 2014. Diabetic ketoacidosis and hyperglycemic hyperosmolar state
Joseph I Wolfsdorf, Jeremy Allgrove, Maria E Craig, et al.
European Journal of Pediatrics
|
January 4, 2014
Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times
Alex Habel, Richard Herriot, Dinakantha Kumararatne, et al.
The New England Journal of Medicine
|
July 7, 2021
PTH Infusion for Seizures in Autosomal Dominant Hypocalcemia Type 1
Ana Sastre, Kevin Valentino, Fadil M Hannan, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
Pediatric Diabetes
|
August 31, 2012
Good practice recommendations on paediatric training programmes for health care professionals in the EU
Sheridan Waldron, Imre Rurik, Laszlo Madacsy, et al.
Bone
|
October 27, 2019
Juvenile Paget's disease with compound heterozygous mutations in TNFRSF11B presenting with recurrent clavicular fractures and a mild skeletal phenotype
Dorit Naot, Louise C Wilson, Jeremy Allgrove, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 14, 2010
A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism
Samantha M Mirczuk, Michael R Bowl, M Andrew Nesbit, et al.
Bone
|
May 1, 2025
Rebound hypercalcaemia timing is associated with cumulative weight-based denosumab dose for central giant cell granuloma treatment in children despite a dose weaning regimen
Alexander D Chesover, Jeremy Allgrove, Alistair Calder, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 14, 2024
Eiken syndrome with parathyroid hormone resistance due to a novel parathyroid hormone receptor type 1 mutation: clinical features and functional analysis
Alistair D Calder, Jeremy Allgrove, Jakob Höppner, et al.
Archives of Disease in Childhood
|
November 9, 2021
Non-collagen pathogenic variants resulting in the osteogenesis imperfecta phenotype in children: a single-country observational cohort study
Patrick Thornley, Nicholas Bishop, Duncan Baker, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 1, 2020
Case report: a 10-year-old girl with primary hypoparathyroidism and systemic lupus erythematosus
Hanna Borysewicz-Sańczyk, Beata Sawicka, Justyna Michalak, et al.
Pediatric Diabetes
|
July 22, 2014
ISPAD Clinical Practice Consensus Guidelines 2014. Diabetic ketoacidosis and hyperglycemic hyperosmolar state
Joseph I Wolfsdorf, Jeremy Allgrove, Maria E Craig, et al.
European Journal of Pediatrics
|
January 4, 2014
Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times
Alex Habel, Richard Herriot, Dinakantha Kumararatne, et al.
The New England Journal of Medicine
|
July 7, 2021
PTH Infusion for Seizures in Autosomal Dominant Hypocalcemia Type 1
Ana Sastre, Kevin Valentino, Fadil M Hannan, et al.
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of 4