Mo A - Search Results

1

Child Neurology: Recurrent Brainstem Strokes and Aphthous Ulcers in a Child With Mutations in the ADA2 Gene.

Mo A, Donatelli S, Benson LA, Lee PY, Rivkin MJ. Mo A, et al. Neurology. 2021 Oct 4;97(14):696-699. doi: 10.1212/WNL.0000000000012271. Neurology. 2021. PMID: 34039731 No abstract available.

2

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15.

Saffari A, Kellner M, Jordan C, Rosengarten H, Mo A, Zhang B, Strelko O, Neuser S, Davis MY, Yoshikura N, Futamura N, Takeuchi T, Nabatame S, Ishiura H, Tsuji S, Aldeen HS, Cali E, Rocca C, Houlden H, Efthymiou S, Assmann B, Yoon G, Trombetta BA, Kivisäkk P, Eichler F, Nan H, Takiyama Y, Tessa A, Santorelli FM, Sahin M, Blackstone C, Yang E, Schüle R, Ebrahimi-Fakhari D. Saffari A, et al. Among authors: mo a. Brain. 2023 May 2;146(5):2003-2015. doi: 10.1093/brain/awac391. Brain. 2023. PMID: 36315648 Free PMC article.

3

Neurodevelopmental profile of HIVEP2-related disorder.

Mo A, Snyder LG, Babington O, Chung WK, Sahin M, Srivastava S. Mo A, et al. Dev Med Child Neurol. 2022 May;64(5):654-661. doi: 10.1111/dmcn.15100. Epub 2021 Oct 26. Dev Med Child Neurol. 2022. PMID: 34704275 Free PMC article.

4

Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST.

Mo A, Saffari A, Kellner M, Döbler-Neumann M, Jordan C, Srivastava S, Zhang B, Sahin M, Fink JK, Smith L, Posey JE, Alter KE, Toro C, Blackstone C, Soldatos AG, Christie M, Schüle R, Ebrahimi-Fakhari D. Mo A, et al. Mov Disord. 2022 Dec;37(12):2440-2446. doi: 10.1002/mds.29225. Epub 2022 Sep 14. Mov Disord. 2022. PMID: 36103453 Free PMC article.

5

Upper motor neuron signs and early onset gait abnormalities in young children with bi-allelic VWA1 variants.

Gable DL, Mo A, Estrella E, Saffari A, Ghosh PS, Ebrahimi-Fakhari D. Gable DL, et al. Among authors: mo a. Am J Med Genet A. 2022 Dec;188(12):3531-3534. doi: 10.1002/ajmg.a.62953. Epub 2022 Aug 17. Am J Med Genet A. 2022. PMID: 35975723

6

Age, CAG repeat length, and clinical progression in Huntington's disease.

Rosenblatt A, Kumar BV, Mo A, Welsh CS, Margolis RL, Ross CA. Rosenblatt A, et al. Among authors: mo a. Mov Disord. 2012 Feb;27(2):272-6. doi: 10.1002/mds.24024. Epub 2011 Dec 15. Mov Disord. 2012. PMID: 22173986

7

Cellular resolution maps of X chromosome inactivation: implications for neural development, function, and disease.

Wu H, Luo J, Yu H, Rattner A, Mo A, Wang Y, Smallwood PM, Erlanger B, Wheelan SJ, Nathans J. Wu H, et al. Among authors: mo a. Neuron. 2014 Jan 8;81(1):103-19. doi: 10.1016/j.neuron.2013.10.051. Neuron. 2014. PMID: 24411735 Free PMC article.

8

Epigenomic Signatures of Neuronal Diversity in the Mammalian Brain.

Mo A, Mukamel EA, Davis FP, Luo C, Henry GL, Picard S, Urich MA, Nery JR, Sejnowski TJ, Lister R, Eddy SR, Ecker JR, Nathans J. Mo A, et al. Neuron. 2015 Jun 17;86(6):1369-84. doi: 10.1016/j.neuron.2015.05.018. Neuron. 2015. PMID: 26087164 Free PMC article.

9

Epigenomic landscapes of retinal rods and cones.

Mo A, Luo C, Davis FP, Mukamel EA, Henry GL, Nery JR, Urich MA, Picard S, Lister R, Eddy SR, Beer MA, Ecker JR, Nathans J. Mo A, et al. Elife. 2016 Mar 7;5:e11613. doi: 10.7554/eLife.11613. Elife. 2016. PMID: 26949250 Free PMC article.

10

Patient With Post-operative Recurrent Pancreatic Cancer Treated With Cone Beam Computed Tomography-Guided Stereotactic Adaptive Radiotherapy: A Case Report.

Forghani F, D'Souza A, Laugeman E, Mo A, Samson PP, Kim H. Forghani F, et al. Among authors: mo a. Cureus. 2024 Dec 7;16(12):e75284. doi: 10.7759/cureus.75284. eCollection 2024 Dec. Cureus. 2024. PMID: 39764328 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

323 results

Search Page

Filters