Harvard Catalyst Profiles

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Aloysius Romero Domingo, M.D.

Concepts

This page shows the publications Aloysius Domingo has written about Male.
Connection Strength

0.092
  1. Evidence of TAF1 dysfunction in peripheral models of X-linked dystonia-parkinsonism. Cell Mol Life Sci. 2016 08; 73(16):3205-15.
    View in: PubMed
    Score: 0.011
  2. New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3). Eur J Hum Genet. 2015 Oct; 23(10):1334-40.
    View in: PubMed
    Score: 0.010
  3. X-linked agammaglobulinemia with hearing impairment, dystonia-parkinsonism, and progressive neurodegeneration. J Neurol. 2014 Nov; 261(11):2225-7.
    View in: PubMed
    Score: 0.010
  4. Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism. Nat Commun. 2021 05 28; 12(1):3216.
    View in: PubMed
    Score: 0.004
  5. Imaging gradual neurodegeneration in a basal ganglia model disease. Ann Neurol. 2019 10; 86(4):517-526.
    View in: PubMed
    Score: 0.003
  6. A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism. Ann Neurol. 2019 06; 85(6):812-822.
    View in: PubMed
    Score: 0.003
  7. Association of Pallidal Neurostimulation and Outcome Predictors With X-linked Dystonia Parkinsonism. JAMA Neurol. 2019 02 01; 76(2):211-216.
    View in: PubMed
    Score: 0.003
  8. Eye movement deficits in X-linked dystonia-parkinsonism are related to striatal degeneration. Parkinsonism Relat Disord. 2019 04; 61:170-178.
    View in: PubMed
    Score: 0.003
  9. Basal ganglia and cerebellar pathology in X-linked dystonia-parkinsonism. Brain. 2018 10 01; 141(10):2995-3008.
    View in: PubMed
    Score: 0.003
  10. The Basal Ganglia Striosomes Affect the Modulation of Conflicts by Subliminal Information-Evidence from X-Linked Dystonia Parkinsonism. Cereb Cortex. 2018 07 01; 28(7):2243-2252.
    View in: PubMed
    Score: 0.003
  11. Genome editing in induced pluripotent stem cells rescues TAF1 levels in X-linked dystonia-parkinsonism. Mov Disord. 2018 07; 33(7):1108-1118.
    View in: PubMed
    Score: 0.003
  12. Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly. Cell. 2018 02 22; 172(5):897-909.e21.
    View in: PubMed
    Score: 0.003
  13. Increased insula-putamen connectivity in X-linked dystonia-parkinsonism. Neuroimage Clin. 2018; 17:835-846.
    View in: PubMed
    Score: 0.003
  14. Screening study of TUBB4A in isolated dystonia. Parkinsonism Relat Disord. 2017 Aug; 41:118-120.
    View in: PubMed
    Score: 0.003
  15. Dysfunctions in striatal microstructure can enhance perceptual decision making through deficits in predictive coding. Brain Struct Funct. 2017 Nov; 222(8):3807-3817.
    View in: PubMed
    Score: 0.003
  16. Sonographic alteration of substantia nigra is related to parkinsonism-predominant course of X-linked dystonia-parkinsonism. Parkinsonism Relat Disord. 2017 04; 37:43-49.
    View in: PubMed
    Score: 0.003
  17. Striosomal dysfunction affects behavioral adaptation but not impulsivity-Evidence from X-linked dystonia-parkinsonism. Mov Disord. 2017 04; 32(4):576-584.
    View in: PubMed
    Score: 0.003
  18. Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases. J Pediatr. 2017 02; 181:306-308.e1.
    View in: PubMed
    Score: 0.003
  19. Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia. Mov Disord. 2016 12; 31(12):1929-1931.
    View in: PubMed
    Score: 0.003
  20. Neuroanatomical changes extend beyond striatal atrophy in X-linked dystonia parkinsonism. Parkinsonism Relat Disord. 2016 10; 31:91-97.
    View in: PubMed
    Score: 0.003
  21. RAB39B mutations are a rare finding in Parkinson disease patients. Parkinsonism Relat Disord. 2016 Feb; 23:116-7.
    View in: PubMed
    Score: 0.003
  22. Neurophysiological fingerprints of X-linked dystonia-parkinsonism: A model basal ganglia disease. Mov Disord. 2015 May; 30(6):873-5.
    View in: PubMed
    Score: 0.003
  23. Mutations in GNAL: a novel cause of craniocervical dystonia. JAMA Neurol. 2014 Apr; 71(4):490-4.
    View in: PubMed
    Score: 0.002
  24. Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice. Nat Genet. 2013 Sep; 45(9):1077-82.
    View in: PubMed
    Score: 0.002
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.

Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.