Tam A - Search Results

1

Functional connectivity subtypes associate robustly with ASD diagnosis.

Urchs SGW, Tam A, Orban P, Moreau C, Benhajali Y, Nguyen HD, Evans AC, Bellec P. Urchs SGW, et al. Among authors: tam a. Elife. 2022 Nov 29;11:e56257. doi: 10.7554/eLife.56257. Elife. 2022. PMID: 36444973 Free PMC article.

2

Assessment of white matter hyperintensity severity using multimodal magnetic resonance imaging.

Parent O, Bussy A, Devenyi GA, Dai A, Costantino M, Tullo S, Salaciak A, Bedford S, Farzin S, Béland ML, Valiquette V, Villeneuve S, Poirier J, Tardif CL, Dadar M; PREVENT-AD Research Group; Chakravarty MM. Parent O, et al. Brain Commun. 2023 Oct 19;5(6):fcad279. doi: 10.1093/braincomms/fcad279. eCollection 2023. Brain Commun. 2023. PMID: 37953840 Free PMC article.

3

Insulin-like growth factor binding protein-2 in at-risk adults and autopsy-confirmed Alzheimer brains.

Quesnel MJ, Labonté A, Picard C, Zetterberg H, Blennow K, Brinkmalm A, Villeneuve S, Poirier J; Alzheimer’s Disease Neuroimaging Initiative; PREVENT-AD Research Group. Quesnel MJ, et al. Brain. 2024 May 3;147(5):1680-1695. doi: 10.1093/brain/awad398. Brain. 2024. PMID: 37992295 Free PMC article.

4

Blended phenotype of TECPR2-associated hereditary sensory-autonomic neuropathy and Temple syndrome.

Zubair U, Yang K, Schierbaum L, Tam A, Battaglia N, Rong J, Quiroz V, Ebrahimi-Fakhari D. Zubair U, et al. Among authors: tam a. Ann Clin Transl Neurol. 2025 Jan 14. doi: 10.1002/acn3.52293. Online ahead of print. Ann Clin Transl Neurol. 2025. PMID: 39807687 Free article.

5

Critical role for Transglutaminase 2 in scleroderma skin fibrosis and in the development of dermal sclerosis in a mouse model of scleroderma.

Tam AYY, Khan K, Xu S, Bergin M, Huang L, Arroyo Colon E, Cheng D, Verderio EA, Ong V, Denton CP, Atkinson J, Johnson TS, Abraham DJ. Tam AYY, et al. Arthritis Rheumatol. 2025 Jan 12. doi: 10.1002/art.43104. Online ahead of print. Arthritis Rheumatol. 2025. PMID: 39800950

6

Results of a Global Survey on the State of Interventional Radiology 2024.

Guan JJ, Elhakim T, Matsumoto MM, McKeon T, Laage-Gaupp F, Iqbal S, Patel PJ, Pereira P, Tam AL, Binkert C, Sofocleous CT. Guan JJ, et al. Among authors: tam al. J Vasc Interv Radiol. 2025 Jan 8:S1051-0443(25)00002-8. doi: 10.1016/j.jvir.2024.12.594. Online ahead of print. J Vasc Interv Radiol. 2025. PMID: 39793699

7

Endovascular interventions in cancer patients with compromise of the mediastinal vasculature: a review.

Yevich S, Cardenas N, Sheth R, Kuban J, Patel M, Shah K, Pal K, Chen SR, Tam A. Yevich S, et al. Among authors: tam a. Mediastinum. 2024 May 17;8:45. doi: 10.21037/med-22-43. eCollection 2024. Mediastinum. 2024. PMID: 39781200 Free PMC article. Review.

8

Expanding molecular and clinical spectrum of CPT1C-associated hereditary spastic paraplegia (SPG73)-a case series.

Brooks AK, Quiroz V, Schierbaum L, Tam A, Alecu JE, Ebrahimi-Fakhari D. Brooks AK, et al. Among authors: tam a. Ann Clin Transl Neurol. 2024 Dec 29. doi: 10.1002/acn3.52288. Online ahead of print. Ann Clin Transl Neurol. 2024. PMID: 39737739 Free article.

9

Quantitative natural history modeling of HPDL-related disease based on cross-sectional data reveals genotype-phenotype correlations.

Alecu JE, Tam A, Richter S, Quiroz V, Schierbaum L, Saffari A, Ebrahimi-Fakhari D. Alecu JE, et al. Among authors: tam a. Genet Med. 2024 Dec 24:101349. doi: 10.1016/j.gim.2024.101349. Online ahead of print. Genet Med. 2024. PMID: 39731469

10

STUB1-Associated Autosomal-Recessive Spinocerebellar Ataxia Type 16 (SCAR16) Presenting with Gordon-Holmes Syndrome Caused by Maternal Uniparental Isodisomy.

Agianda HAP, Tam A, Kunta A, Zubair U, Saffari A, Rong J, Crough M, Srouji R, Quiroz V, Yang K, Schierbaum L, Ebrahimi-Fakhari D. Agianda HAP, et al. Among authors: tam a. Mov Disord Clin Pract. 2024 Dec 27. doi: 10.1002/mdc3.14322. Online ahead of print. Mov Disord Clin Pract. 2024. PMID: 39728009 No abstract available.

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