Peter Adamson
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Explore the profile of Peter Adamson including associated specialties, affiliations and a list of published articles.
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70
Citations
1999
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Recent Articles
1.
Goshtasbi K, Best C, Powers B, Ching H, Pastorek N, Altman D, et al.
Facial Plast Surg Aesthet Med
. 2025 Jan;
PMID: 39812574
Various large language models (LLMs) can provide human-level medical discussions, but they have not been compared regarding rhinoplasty knowledge. To compare the leading LLMs in answering complex rhinoplasty consultation questions...
2.
de Rojas T, Chiodin D, Pearson A, Heenen D, Adamson P, Caron H, et al.
Clin Pharmacol Ther
. 2023 Oct;
115(1):36-41.
PMID: 37885401
Better therapies for childhood cancer remain an unmet need to improve the dismal prognosis of certain malignancies and to reduce the burden of toxicity. Rescuing discontinued or shelved drugs for...
3.
Russell S, Drack A, Cideciyan A, Jacobson S, Leroy B, Van Cauwenbergh C, et al.
Nat Med
. 2022 Apr;
28(5):1014-1021.
PMID: 35379979
CEP290-associated Leber congenital amaurosis type 10 (LCA10) is a retinal disease resulting in childhood blindness. Sepofarsen is an RNA antisense oligonucleotide targeting the c.2991+1655A>G variant in the CEP290 gene to...
4.
Adamson P, Janney C, Chen J, Panchbhavi V
J Orthop Case Rep
. 2021 Jun;
11(2):63-66.
PMID: 34141673
Introduction: First metatarsal phalangeal joint (MTPJ) arthroplasty has a high failure rate due to aseptic loosening, which leads to bone loss. The salvage procedure is conversion to an arthrodesis, but...
5.
Dulla K, Slijkerman R, van Diepen H, Albert S, Dona M, Beumer W, et al.
Mol Ther
. 2021 Apr;
29(8):2441-2455.
PMID: 33895329
Mutations in USH2A are among the most common causes of syndromic and non-syndromic retinitis pigmentosa (RP). The two most recurrent mutations in USH2A, c.2299delG and c.2276G > T, both reside...
6.
Adamson P, Peters W, Janney C, Panchbhavi V
J Orthop
. 2020 Apr;
21:203-206.
PMID: 32273657
Background: This study evaluates the safety of foot and ankle outpatient surgeries at a freestanding ambulatory surgery centers. Methods: A total of 1352 cases were evaluated for adverse events in...
7.
Pearson A, Scobie N, Norga K, Ligas F, Chiodin D, Burke A, et al.
Eur J Cancer
. 2019 Feb;
110:74-85.
PMID: 30772656
Paediatric Strategy Forums have been created by the multistakeholder organisation, ACCELERATE, and the European Medicines Agency to facilitate dialogue between all relevant stakeholders and suggest strategies in critical areas of...
8.
Cideciyan A, Jacobson S, Drack A, Ho A, Charng J, Garafalo A, et al.
Nat Med
. 2018 Dec;
25(2):225-228.
PMID: 30559420
Photoreceptor ciliopathies constitute the most common molecular mechanism of the childhood blindness Leber congenital amaurosis. Ten patients with Leber congenital amaurosis carrying the c.2991+1655A>G allele in the ciliopathy gene centrosomal...
9.
Adamson P, Kunzler D, Janney C, Panchbhavi V
Cureus
. 2018 Oct;
10(8):e3159.
PMID: 30357075
Lisfranc injuries are typically treated in the acute setting with open reduction and internal fixation (ORIF). The type of hardware that provides the best fixation for these injuries has not...
10.
Dulla K, Aguila M, Lane A, Jovanovic K, Parfitt D, Schulkens I, et al.
Mol Ther Nucleic Acids
. 2018 Aug;
12:730-740.
PMID: 30114557
Leber congenital amaurosis type 10 (LCA10) is a severe inherited retinal dystrophy associated with mutations in CEP290. The deep intronic c.2991+1655A>G mutation in CEP290 is the most common mutation in...