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Year | Number of Results |
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2016 | 1 |
2018 | 1 |
2019 | 1 |
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2023 | 1 |
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Page 1
Management of pseudohypoparathyroidism.
Curr Opin Pediatr. 2019 Aug;31(4):537-549. doi: 10.1097/MOP.0000000000000783.
Curr Opin Pediatr. 2019.
PMID: 31145125
Free PMC article.
Review.
Aberrant Bone Regulation in Albright Hereditary Osteodystrophy dueto Gnas Inactivation: Mechanisms and Translational Implications.
McMullan P, Germain-Lee EL.
McMullan P, et al.
Curr Osteoporos Rep. 2022 Feb;20(1):78-89. doi: 10.1007/s11914-022-00719-w. Epub 2022 Feb 28.
Curr Osteoporos Rep. 2022.
PMID: 35226254
Review.
Item in Clipboard
Parental Origin of Gsα Inactivation Differentially Affects Bone Remodeling in a Mouse Model of Albright Hereditary Osteodystrophy.
McMullan P, Maye P, Yang Q, Rowe DW, Germain-Lee EL.
McMullan P, et al.
JBMR Plus. 2021 Nov 16;6(1):e10570. doi: 10.1002/jbm4.10570. eCollection 2022 Jan.
JBMR Plus. 2021.
PMID: 35079678
Free PMC article.
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Prevalence of Chiari malformation type 1 is increased in pseudohypoparathyroidism type 1A and associated with aberrant bone development.
Krishnan N, McMullan P, Yang Q, Buscarello AN, Germain-Lee EL.
Krishnan N, et al.
PLoS One. 2023 Jan 20;18(1):e0280463. doi: 10.1371/journal.pone.0280463. eCollection 2023.
PLoS One. 2023.
PMID: 36662765
Free PMC article.
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Anomalous Putamen Volume in Children With Complex Motor Stereotypies.
Mahone EM, Crocetti D, Tochen L, Kline T, Mostofsky SH, Singer HS.
Mahone EM, et al.
Pediatr Neurol. 2016 Dec;65:59-63. doi: 10.1016/j.pediatrneurol.2016.08.023. Epub 2016 Sep 8.
Pediatr Neurol. 2016.
PMID: 27751663
Free PMC article.
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Ossifications in Albright Hereditary Osteodystrophy: Role of Genotype, Inheritance, Sex, Age, Hormonal Status, and BMI.
Salemi P, Skalamera Olson JM, Dickson LE, Germain-Lee EL.
Salemi P, et al.
J Clin Endocrinol Metab. 2018 Jan 1;103(1):158-168. doi: 10.1210/jc.2017-00860.
J Clin Endocrinol Metab. 2018.
PMID: 29059381
Free PMC article.
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