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Trastorno por déficit de atención/hiperactividad y hábitos de vida en niños y adolescentes.
- Published in:
- Actas Espanolas de Psiquiatria, 2019, v. 47, n. 4, p. 158
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- Publication type:
- Article
Consenso Delphi sobre el Trastorno por Déficit de Atención e Hiperactividad (TDAH): valoración por un panel de expertos.
- Published in:
- Actas Espanolas de Psiquiatria, 2016, v. 44, n. 6, p. 231
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- Publication type:
- Article
Expert Recommendation: contributions to clinical practice of the new prodrug lisdexamfetamine dimesylate (LDX) in the treatment of attention deficit hyperactivity disorder (ADHD).
- Published in:
- Actas Espanolas de Psiquiatria, 2014, v. 42, p. 1
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- Publication type:
- Article
Habilidades sociales y de liderazgo en el trastorno por déficit de atención/ hiperactividad: relación con las capacidades cognitivo-atencionales.
- Published in:
- Actas Espanolas de Psiquiatria, 2012, v. 40, n. 3, p. 136
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- Publication type:
- Article
Trastorno por déficit de atención/ hiperactividad y su relación con las habilidades sociales y de liderazgo evaluadas a través de un sistema de evaluación de la conducta de niños y adolescentes (BASC).
- Published in:
- Actas Espanolas de Psiquiatria, 2011, v. 39, n. 6, p. 339
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- Publication type:
- Article
Bi-Allelic c.1746G>T; p.Leu582= Variants in TUBGCP4 in a Boy with Autism: Clinical Data and Literature Review.
- Published in:
- Molecular Syndromology, 2022, v. 13, n. 2, p. 165, doi. 10.1159/000519365
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- Publication type:
- Article
Neuroimaging Findings in Patients with EBF3 Mutations: Report of Two Cases.
- Published in:
- Molecular Syndromology, 2021, v. 12, n. 3, p. 186, doi. 10.1159/000513583
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- Publication type:
- Article
Prenatal Diagnosis of Frontonasal Dysplasia Associated With Bilateral Periventricular Nodular Heterotopia.
- Published in:
- Journal of Child Neurology, 2014, v. 29, n. 10, p. NP122, doi. 10.1177/0883073813508316
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- Publication type:
- Article
Broadening the clinical spectrum: molecular mechanisms and new phenotypes of ANO3-dystonia.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 6, p. 1982, doi. 10.1093/brain/awad412
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- Publication type:
- Article
Clinical and cognitive response to extended-release methylphenidate (Medikinet®) in attention deficit/hyperactivity disorder: Efficacy evaluation.
- Published in:
- Advances in Therapy, 2009, v. 26, n. 12, p. 1097, doi. 10.1007/s12325-009-0083-9
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- Publication type:
- Article
A Novel Loss-of-Function SEMA3E Mutation in a Patient with Severe Intellectual Disability and Cognitive Regression.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 10, p. 5632, doi. 10.3390/ijms23105632
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- Publication type:
- Article
High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA Studies.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 13, p. 3358, doi. 10.3390/ijms20133358
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- Publication type:
- Article
Cingulate Cortical Thickness and Dopamine Transporter ( DAT1) Genotype in Children and Adolescents With ADHD.
- Published in:
- 2018
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- Publication type:
- journal article
Efficacy of Atomoxetine for the Treatment of ADHD Symptoms in Patients With Pervasive Developmental Disorders: A Prospective, Open-Label Study.
- Published in:
- Journal of Attention Disorders, 2013, v. 17, n. 6, p. 497, doi. 10.1177/1087054711423626
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- Publication type:
- Article
Bilateral, wide-spread, mechanical pain sensitivity in children with frequent episodic tension-type headache suggesting impairment in central nociceptive processing.
- Published in:
- Cephalalgia, 2010, v. 30, n. 9, p. 1049, doi. 10.1177/0333102410362806
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- Publication type:
- Article
Tatton‐Brown–Rahman syndrome: Novel pathogenic variants and new neuroimaging findings.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 2, p. 211, doi. 10.1002/ajmg.a.63434
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- Publication type:
- Article
The variability of SMARCA4‐related Coffin–Siris syndrome: Do nonsense candidate variants add to milder phenotypes?
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 9, p. 2058, doi. 10.1002/ajmg.a.61732
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- Publication type:
- Article
Cerebral palsy, epilepsy, and severe intellectual disability in a patient with 3q29 microduplication syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 8, p. 2043, doi. 10.1002/ajmg.a.36559
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- Publication type:
- Article
Microduplication 10q24.31 in a Spanish girl with scoliosis and myopathy: The critical role of LBX.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 8, p. 2074, doi. 10.1002/ajmg.a.36589
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- Publication type:
- Article
Craniosynostosis, psychomotor retardation, and facial dysmorphic features in a Spanish patient with a 4q27q28.3 deletion.
- Published in:
- Child's Nervous System, 2014, v. 30, n. 12, p. 2157, doi. 10.1007/s00381-014-2474-8
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- Publication type:
- Article
Síndrome cerebeloso cognitivo afectivo tras cerebelitis aguda.
- Published in:
- Revista Pediatría de Atención Primaria, 2023, v. 25, n. 97, p. 49
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- Publication type:
- Article
Selective Inhibitory Control in Middle Childhood.
- Published in:
- International Journal of Environmental Research & Public Health, 2021, v. 18, n. 12, p. 6300, doi. 10.3390/ijerph18126300
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- Publication type:
- Article
PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1615, doi. 10.1038/ejhg.2015.51
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- Publication type:
- Article
Evaluating Internet Information on Attention- Deficit/Hyperactivity Disorder (ADHD) Treatment: Parent and Expert Perspectives.
- Published in:
- Education for Health: Change in Learning & Practice, 2013, v. 26, n. 1, p. 48, doi. 10.4103/1357-6283.112801
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- Publication type:
- Article
Functional and structural deficiencies of Gemin5 variants associated with neurological disorders.
- Published in:
- Life Science Alliance, 2022, v. 5, n. 7, p. 1, doi. 10.26508/lsa.202201403
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- Publication type:
- Article
TRASTORNO POR DÉFICIT DE ATENCIÓN/HIPERACTIVIDAD. HÁBITOS DE ESTUDIO.
- Published in:
- Revista Medicina, 2019, v. 79, n. Suppl1, p. 57
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- Publication type:
- Article
The development of selective stopping: Qualitative and quantitative changes from childhood to early adulthood.
- Published in:
- Developmental Science, 2022, v. 25, n. 5, p. 1, doi. 10.1111/desc.13210
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- Publication type:
- Article
Developmental epileptic encephalopathy in DLG4‐related synaptopathy.
- Published in:
- Epilepsia (Series 4), 2024, v. 65, n. 4, p. 1029, doi. 10.1111/epi.17876
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- Publication type:
- Article
Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy.
- Published in:
- Frontiers in Cell & Developmental Biology, 2024, p. 1, doi. 10.3389/fcell.2024.1321282
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- Publication type:
- Article
Tenorio syndrome: Description of 14 novel cases and review of the clinical and molecular features.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 4, p. 405, doi. 10.1111/cge.14020
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- Publication type:
- Article
A novel human Cdh1 mutation impairs anaphase promoting complex/cyclosome activity resulting in microcephaly, psychomotor retardation, and epilepsy.
- Published in:
- Journal of Neurochemistry, 2019, v. 151, n. 1, p. 103, doi. 10.1111/jnc.14828
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- Publication type:
- Article
GENÉTICA DEL TDAH EN LA PRÁCTICA CLÍNICA.
- Published in:
- Medicina (Buenos Aires), 2024, v. 84, p. 26
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- Publication type:
- Article
EL IMPACTO DEL TDAH SOBRE LA LECTURA.
- Published in:
- Medicina (Buenos Aires), 2023, v. 83, p. 22
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- Publication type:
- Article
DÉFICITS NEUROPSICOLÓGICOS, INTENSIDAD SINTOMÁTICA Y REPERCUSIÓN FUNCIONAL EN EL TRASTORNO POR DÉFICIT DE ATENCIÓN CON HIPERACTIVIDAD.
- Published in:
- Medicina (Buenos Aires), 2022, v. 82, p. 23
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- Publication type:
- Article
ESTUDIOS GENÉTICOS Y NEURODESARROLLO. DE LA UTILIDAD AL MODELO GENÉTICO.
- Published in:
- Medicina (Buenos Aires), 2020, v. 80, p. 26
- By:
- Publication type:
- Article
TRASTORNO POR DÉFICIT DE ATENCIÓN/HIPERACTIVIDAD. HÁBITOS DE ESTUDIO.
- Published in:
- Medicina (Buenos Aires), 2019, v. 79, p. 57
- By:
- Publication type:
- Article
Identification and functional analysis of two new de novo KCNMA1 variants associated with Liang–Wang syndrome.
- Published in:
- Acta Physiologica, 2022, v. 235, n. 1, p. 1, doi. 10.1111/apha.13800
- By:
- Publication type:
- Article
ESTUDIOS GENÉTICOS Y NEURODESARROLLO. DE LA UTILIDAD AL MODELO GENÉTICO.
- Published in:
- Revista Medicina, 2020, v. 80, p. 26
- By:
- Publication type:
- Article
In Utero Diagnosis of PHACE Syndrome by Fetal Magnetic Resonance Imaging (MRI).
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Clinical Response to Methylphenidate in a Patient With Self-Induced Photosensitive Epilepsy.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Schizencephaly: Pre- and Postnatal Magnetic Resonance Imaging.
- Published in:
- Journal of Child Neurology, 2010, v. 25, n. 8, p. 1020, doi. 10.1177/0883073809355821
- By:
- Publication type:
- Article
Meralgia Paresthetica in the Pediatric Population: A Propos of 2 Cases.
- Published in:
- Journal of Child Neurology, 2010, v. 25, n. 1, p. 110
- By:
- Publication type:
- Article
Deleterious de novo variants of X‐linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita.
- Published in:
- Human Mutation, 2019, v. 40, n. 12, p. 2270, doi. 10.1002/humu.23841
- By:
- Publication type:
- Article
Trastorno por déficit de atención/hiperactividad en el adulto.
- Published in:
- Kranion, 2020, v. 15, n. 1, p. 5
- By:
- Publication type:
- Article
Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Health care and societal costs of the management of children and adolescents with attention-deficit/hyperactivity disorder in Spain: a descriptive analysis.
- Published in:
- BMC Psychiatry, 2018, v. 18, p. 1, doi. 10.1186/s12888-017-1581-y
- By:
- Publication type:
- Article