GAIXOTASUN ARRAROEN IKERKETA
University of Paris-Saclay
Gif-sur-Yvette, FranciaUniversity of Paris-Saclay-ko ikertzaileekin lankidetzan egindako argitalpenak (11)
2023
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Growth patterns and outcomes of growth hormone therapy in patients with acrodysostosis
Journal of Endocrinological Investigation, Vol. 46, Núm. 8, pp. 1673-1684
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Recombinant growth hormone improves growth and adult height in patients with maternal inactivating GNAS mutations
European journal of endocrinology, Vol. 189, Núm. 1, pp. 123-131
2021
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Inactivating PTH/PTHrP signaling disorders (iPPSDs): Evaluation of the new classification in a multicenter large series of 544 molecularly characterized patients
European Journal of Endocrinology, Vol. 184, Núm. 2, pp. 311-320
2020
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Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients
Hormone Research in Paediatrics, Vol. 93, Núm. 3, pp. 182-196
2018
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Diagnosis and management of pseudohypoparathyroidism and related disorders: First international Consensus Statement
Nature Reviews Endocrinology, Vol. 14, Núm. 8, pp. 476-500
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Genetic and Epigenetic Defects at the GNAS Locus Lead to Distinct Patterns of Skeletal Growth but Similar Early-Onset Obesity
Journal of Bone and Mineral Research, Vol. 33, Núm. 8, pp. 1480-1488
2017
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Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3
Human Molecular Genetics, Vol. 26, Núm. 20, pp. 3883-3894
2016
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From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network
European Journal of Endocrinology, Vol. 175, Núm. 6, pp. P1-P17
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Report of two novel mutations in PTHLH associated with brachydactyly type E and literature review
American Journal of Medical Genetics, Part A, Vol. 170, Núm. 3, pp. 734-742
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The prevalence of GNAS deficiency-related diseases in a large cohort of patients characterized by the EuroPHP network
Journal of Clinical Endocrinology and Metabolism, Vol. 101, Núm. 10, pp. 3657-3668
2013
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Clinical utility gene card for: Pseudohypoparathyroidism
European Journal of Human Genetics, Vol. 21, Núm. 6