Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

376 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Stroke: a modern history.
Kelly MA. Kelly MA. Am J Ther. 2011 Jan;18(1):51-6. doi: 10.1097/MJT.0b013e3181e13a0b. Am J Ther. 2011. PMID: 20634683 Review.
Alcohol as a risk factor for stroke.
Gorelick PB, Kelly MA. Gorelick PB, et al. Among authors: kelly ma. Heart Dis Stroke. 1992 Sep-Oct;1(5):255-8. Heart Dis Stroke. 1992. PMID: 1344115 No abstract available.
The role of drugs in the etiology of stroke.
Kelly MA, Gorelick PB, Mirza D. Kelly MA, et al. Clin Neuropharmacol. 1992 Aug;15(4):249-75. doi: 10.1097/00002826-199208000-00001. Clin Neuropharmacol. 1992. PMID: 1516072 Review.
Pioglitazone and Risk for Bone Fracture: Safety Data From a Randomized Clinical Trial.
Viscoli CM, Inzucchi SE, Young LH, Insogna KL, Conwit R, Furie KL, Gorman M, Kelly MA, Lovejoy AM, Kernan WN; IRIS Trial Investigators. Viscoli CM, et al. Among authors: kelly ma. J Clin Endocrinol Metab. 2017 Mar 1;102(3):914-922. doi: 10.1210/jc.2016-3237. J Clin Endocrinol Metab. 2017. PMID: 27935736 Free PMC article. Clinical Trial.
A de novo variant in PAK2 detected in an individual with Knobloch type 2 syndrome.
Werren EA, Kalsner L, Ewald J, Peracchio M, King C, Vats P, Audano PA, Robinson PN, Adams MD, Kelly MA, Matson AP. Werren EA, et al. Among authors: kelly ma. bioRxiv [Preprint]. 2024 Apr 22:2024.04.18.590108. doi: 10.1101/2024.04.18.590108. bioRxiv. 2024. PMID: 38712026 Free PMC article. Preprint.
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly.
Herbst C, Bothe V, Wegler M, Axer-Schaefer S, Audebert-Bellanger S, Gecz J, Cogne B, Feldman HB, Horn AHC, Hurst ACE, Kelly MA, Kruer MC, Kurolap A, Laquerriere A, Li M, Mark PR, Morawski M, Nizon M, Pastinen T, Polster T, Saugier-Veber P, SeSong J, Sticht H, Stieler JT, Thifffault I, van Eyk CL, Marcorelles P, Vezain-Mouchard M, Abou Jamra R, Oppermann H. Herbst C, et al. Among authors: kelly ma. Hum Genet. 2024 Mar;143(3):455-469. doi: 10.1007/s00439-024-02655-4. Epub 2024 Mar 25. Hum Genet. 2024. PMID: 38526744 Free PMC article.
376 results