Found: 52
Select item for more details and to access through your institution.
Characterization of cornea donors at a tissue center in the city of Medellin, Colombia.
- Published in:
- Cell & Tissue Banking, 2024, v. 25, n. 2, p. 619, doi. 10.1007/s10561-023-10124-x
- By:
- Publication type:
- Article
Incidencia del Síndrome Confusional (delirio) en un Hospital Universitario Latinoamericano.
- Published in:
- Revista Colombiana de Psiquiatria, 2024, v. 53, n. 1, p. 41, doi. 10.1016/j.rcp.2022.01.001
- By:
- Publication type:
- Article
Organic cation transporter 2 contributes to SSRI antidepressant efficacy by controlling tryptophan availability in the brain.
- Published in:
- Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-023-02596-y
- By:
- Publication type:
- Article
Updated consensus guidelines on the management of Phelan–McDermid syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 8, p. 2015, doi. 10.1002/ajmg.a.63312
- By:
- Publication type:
- Article
Decidir la vida que queremos: aportes de organizaciones culturales a la promoción de la salud mental.
- Published in:
- Revista CES Psicologia, 2023, v. 16, n. 2, p. 62, doi. 10.21615/cesp.6478
- By:
- Publication type:
- Article
Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 625, doi. 10.1093/hmg/ddab280
- By:
- Publication type:
- Article
Usos, retos y perspectivas de las técnicas visuales en la investigación en salud pública.
- Published in:
- Revista Salud UIS, 2022, v. 54, n. 1, p. 1, doi. 10.18273/saluduis.54.e:22008
- By:
- Publication type:
- Article
Psychiatric illness and regression in individuals with Phelan-McDermid syndrome.
- Published in:
- Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s11689-020-9309-6
- By:
- Publication type:
- Article
Clinical and neurocognitive issues associated with Bosch‐Boonstra‐Schaaf optic atrophy syndrome: A case study.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 1, p. 213, doi. 10.1002/ajmg.a.61409
- By:
- Publication type:
- Article
Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature.
- Published in:
- Molecular Autism, 2019, v. 10, n. 1, p. 1, doi. 10.1186/s13229-019-0291-3
- By:
- Publication type:
- Article
Viral vector‐mediated Cre recombinase expression in substantia nigra induces lesions of the nigrostriatal pathway associated with perturbations of dopamine‐related behaviors and hallmarks of programmed cell death.
- Published in:
- Journal of Neurochemistry, 2019, v. 150, n. 3, p. 330, doi. 10.1111/jnc.14684
- By:
- Publication type:
- Article
La adolescencia en contexto: Representaciones Sociales en adolescentes de Medellín y Armenia, Colombia.
- Published in:
- Psicogente, 2019, v. 22, n. 42, p. 1, doi. 10.17081/psico.22.42.3471
- By:
- Publication type:
- Article
Salud mental de la niñez: significados y abordajes de profesionales en Medellín, Colombia.
- Published in:
- Revista CES Psicologia, 2019, v. 12, n. 2, p. 51, doi. 10.21615/cesp.12.2.5
- By:
- Publication type:
- Article
Rigor in science and science reporting: updated guidelines for submissions to Molecular Autism.
- Published in:
- 2019
- By:
- Publication type:
- Editorial
Del control al apoyo: representaciones sociales sobre adultos significativos en adolescentes de Medellín.
- Published in:
- Revista Katharsis, 2019, n. 27, p. 26, doi. 10.25057/25005731.1113
- By:
- Publication type:
- Article
Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by <italic>SHANK3</italic> point mutations.
- Published in:
- Molecular Autism, 2018, v. 9, n. 1, p. N.PAG, doi. 10.1186/s13229-018-0205-9
- By:
- Publication type:
- Article
Propiedad intelectual en el sistema universitario de investigación.
- Published in:
- Estudios de Derecho, 2016, v. 73, n. 162, p. 51, doi. 10.17533/udea.esde.v73n162a03
- By:
- Publication type:
- Article
The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 3, p. 377, doi. 10.1002/ajmg.b.32416
- By:
- Publication type:
- Article
Representaciones sociales sobre salud mental en un grupo de profesionales en la ciudad de Medellín: análisis prototípico y categorial.
- Published in:
- Revista CES Psicologia, 2014, v. 7, n. 2, p. 96
- By:
- Publication type:
- Article
Heterozygous FA2H mutations in autism spectrum disorders.
- Published in:
- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-124
- By:
- Publication type:
- Article
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
- Published in:
- Molecular Autism, 2013, v. 4, n. 1, p. 1, doi. 10.1186/2040-2392-4-18
- By:
- Publication type:
- Article
Characterization of <i>SLITRK1</i> Variation in Obsessive-Compulsive Disorder.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070376
- By:
- Publication type:
- Article
SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders.
- Published in:
- Molecular Autism, 2013, v. 4, n. 1, p. 1, doi. 10.1186/2040-2392-4-17
- By:
- Publication type:
- Article
Network Topologies and Convergent Aetiologies Arising from Deletions and Duplications Observed in Individuals with Autism.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003523
- By:
- Publication type:
- Article
Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 5, p. 540, doi. 10.1038/ejhg.2011.244
- By:
- Publication type:
- Article
Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 5, p. 594, doi. 10.1038/ejhg.2012.32
- By:
- Publication type:
- Article
FACTORES DE RIESGO PARA DIABETES GESTACIONAL EN POBLACIÓN OBSTÉTRICA EN TRES INSTITUCIONES DE MEDELLÍN, COLOMBIA. ESTUDIO DE CASOS Y CONTROLES.
- Published in:
- Revista Colombiana de Obstetricia y Ginecologia, 2012, v. 63, n. 2, p. 114, doi. 10.18597/rcog.187
- By:
- Publication type:
- Article
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 2, p. 1, doi. 10.1371/journal.pgen.1002521
- By:
- Publication type:
- Article
Optimizing the phenotyping of rodent ASD models: enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological, electrophysiological, neurological, and behavioral features.
- Published in:
- Molecular Autism, 2012, v. 3, n. 1, p. 1, doi. 10.1186/2040-2392-3-1
- By:
- Publication type:
- Article
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.
- Published in:
- Molecular Autism, 2012, v. 3, n. 1, p. 5, doi. 10.1186/2040-2392-3-5
- By:
- Publication type:
- Article
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3.
- Published in:
- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 124, doi. 10.1007/s11689-011-9076-5
- By:
- Publication type:
- Article
Clinical utility gene card for: Deletion 22q13 syndrome.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 4, p. 1, doi. 10.1038/ejhg.2010.193
- By:
- Publication type:
- Article
Cuerpo, comercio sexual, amor e identidad. Significados construidos por mujeres que practicaron la prostitución.
- Published in:
- Revista CES Psicologia, 2011, v. 4, n. 1, p. 32
- By:
- Publication type:
- Article
Search for copy number variants in chromosomes15q11-q13 and 22q11.2 in obsessive compulsivedisorder.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 100, doi. 10.1186/1471-2350-11-100
- By:
- Publication type:
- Article
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 108, doi. 10.1186/1471-2350-11-108
- By:
- Publication type:
- Article
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region.
- Published in:
- Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-5
- By:
- Publication type:
- Article
An investigation of ribosomal protein L10 gene in autism spectrum disorders.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2350-10-7
- By:
- Publication type:
- Article
Parallel Loss of Hippocampal LTD and Cognitive Flexibility in a Genetic Model of Hyperdopaminergia.
- Published in:
- Neuropsychopharmacology, 2007, v. 32, n. 10, p. 2108, doi. 10.1038/sj.npp.1301354
- By:
- Publication type:
- Article
Mutation analysis of the NSD1 gene in patients with autismspectrum disorders and macrocephaly.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 68, doi. 10.1186/1471-2350-8-68
- By:
- Publication type:
- Article
Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder
- Published in:
- European Psychiatry, 2007, v. 22, n. 1, p. 32, doi. 10.1016/j.eurpsy.2006.05.002
- By:
- Publication type:
- Article
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 25, doi. 10.1038/ng1933
- By:
- Publication type:
- Article
Exploratory analysis of obsessive compulsive symptom dimensions in children and adolescents: a Prospective follow-up study.
- Published in:
- BMC Psychiatry, 2006, v. 6, p. 1, doi. 10.1186/1471-244X-6-1
- By:
- Publication type:
- Article
Platelet Serotonergic Markers as Endophenotypes for Obsessive-Compulsive Disorder.
- Published in:
- Neuropsychopharmacology, 2005, v. 30, n. 8, p. 1539, doi. 10.1038/sj.npp.1300752
- By:
- Publication type:
- Article
The reinforcing effects of chronic d-amphetamine and morphine are impaired in a line of memory-deficient mice overexpressing calcineurin.
- Published in:
- European Journal of Neuroscience, 2005, v. 21, n. 11, p. 3089, doi. 10.1111/j.1460-9568.2005.04132.x
- By:
- Publication type:
- Article
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
- Published in:
- Nature Genetics, 2003, v. 34, n. 1, p. 27
- By:
- Publication type:
- Article
Hypolocomotor effects of acute and daily d-amphetamine in mice lacking the dopamine transporter.
- Published in:
- Psychopharmacology, 2001, v. 159, n. 1, p. 2, doi. 10.1007/s002130100901
- By:
- Publication type:
- Article
Increased rewarding properties of morphine in dopamine-transporter knockout mice.
- Published in:
- European Journal of Neuroscience, 2000, v. 12, n. 5, p. 1827, doi. 10.1046/j.1460-9568.2000.00063.x
- By:
- Publication type:
- Article
Repeated Administration of the Neurotensin Receptor Antagonist SR 48692 Differentially Regulates Mesocortical and Mesolimbic Dopaminergic Systems.
- Published in:
- Journal of Neurochemistry, 1998, v. 71, n. 3, p. 1158, doi. 10.1046/j.1471-4159.1998.71031158.x
- By:
- Publication type:
- Article
Use of Nonpeptide Antagonists to Explore the Physiological Roles of Neurotensin.
- Published in:
- Annals of the New York Academy of Sciences, 1997, v. 814, n. 1, p. 125, doi. 10.1111/j.1749-6632.1997.tb46151.x
- By:
- Publication type:
- Article
Endogenous Neurotensin Regulates Hypothalamic-Pituitary-Adrenal Axis Activity and Peptidergic Neurons in the Rat Hypothalamic Paraventricular Nucleus.
- Published in:
- Journal of Neuroendocrinology, 1997, v. 9, n. 4, p. 263, doi. 10.1046/j.1365-2826.1997.00581.x
- By:
- Publication type:
- Article