Found: 20
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Evidence for dopaminergic denervation in classical galactosemia.
- Published in:
- 2017
- By:
- Publication type:
- case study
G303V tau mutation presenting with progressive supranuclear palsy-like features.
- Published in:
- Movement Disorders, 2012, v. 27, n. 4, p. 581, doi. 10.1002/mds.24060
- By:
- Publication type:
- Article
Torsional nystagmus induced by subthalamic nucleus stimulation.
- Published in:
- Movement Disorders, 2008, v. 23, n. 11, p. 1621, doi. 10.1002/mds.22151
- By:
- Publication type:
- Article
Noradrenaline and Movement Initiation Disorders in Parkinson's Disease: A Pharmacological Functional MRI Study with Clonidine.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 17, p. 2640, doi. 10.3390/cells11172640
- By:
- Publication type:
- Article
Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide the Forest?
- Published in:
- Journal of Autism & Developmental Disorders, 2018, v. 48, n. 8, p. 2886, doi. 10.1007/s10803-018-3552-7
- By:
- Publication type:
- Article
Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 14, p. 3533, doi. 10.3390/ijms20143533
- By:
- Publication type:
- Article
Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
The Almirall European Headache Awards 2009.
- Published in:
- Journal of Headache & Pain, 2010, v. 11, n. 3, p. 207, doi. 10.1007/s10194-010-0209-0
- By:
- Publication type:
- Article
Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-019-0946-0
- By:
- Publication type:
- Article
A Functional Magnetic Resonance Imaging Study of Pathophysiological Changes Responsible for Mirror Movements in Parkinson’s Disease.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066910
- By:
- Publication type:
- Article
Relationships between Cognitive Functions and Driving Behavior in Parkinson's Disease.
- Published in:
- European Neurology, 2012, v. 68, n. 2, p. 98, doi. 10.1159/000338264
- By:
- Publication type:
- Article
Behavioral disturbance and treatment strategies in Smith-Magenis syndrome.
- Published in:
- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0330-x
- By:
- Publication type:
- Article
Behavioral disturbance and treatment strategies in Smith-Magenis syndrome.
- Published in:
- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0330-x
- By:
- Publication type:
- Article
Computer-based cognitive remediation program for the treatment of behavioral problems in children with intellectual disability: the «COGNITUS & MOI» study protocol for a randomized controlled trial.
- Published in:
- BMC Psychiatry, 2018, v. 18, n. 1, p. N.PAG, doi. 10.1186/s12888-018-1810-z
- By:
- Publication type:
- Article
Acute paraplegia due to spinal arteriovenous fistula in two patients with hereditary hemorrhagic telangiectasia.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p.
- Published in:
- BMC Medical Genetics, 2014, v. 15, n. 1, p. 59, doi. 10.1186/s12881-014-0132-3
- By:
- Publication type:
- Article
Do the effects measured by intraoperative and postoperative STN macrostimulation in Parkinson’s disease match?
- Published in:
- Journal of Neurology, 2010, v. 257, n. 9, p. 1453, doi. 10.1007/s00415-010-5543-2
- By:
- Publication type:
- Article
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature.
- Published in:
- Human Mutation, 2020, v. 41, n. 1, p. 69, doi. 10.1002/humu.23915
- By:
- Publication type:
- Article
Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review.
- Published in:
- BMC Psychiatry, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12888-021-03342-8
- By:
- Publication type:
- Article
Subthreshold social cognitive deficits may be a key to distinguish 22q11.2DS from schizophrenia.
- Published in:
- Early Intervention in Psychiatry, 2019, v. 13, n. 2, p. 304, doi. 10.1111/eip.12557
- By:
- Publication type:
- Article