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1Academic Journal
المؤلفون: Francesco Weiss, Margherita Barbuti, Giulia Carignani, Alba Calderone, Ferruccio Santini, Icro Maremmani, Giulio Perugi
المصدر: Journal of Clinical Medicine; Volume 9; Issue 8; Pages: 2344
مصطلحات موضوعية: psychiatric obesity, emotional dysregulation, executive dysfunction, bipolarity, affective temperaments, food addiction
وصف الملف: application/pdf
Relation: Mental Health; https://dx.doi.org/10.3390/jcm9082344
الاتاحة: https://doi.org/10.3390/jcm9082344
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2
المؤلفون: Margherita Barbuti, Giulia Carignani, Francesco Weiss, Alba Calderone, Paola Fierabracci, Guido Salvetti, Giulia Menculini, Alfonso Tortorella, Ferruccio Santini, Giulio Perugi
مصطلحات موضوعية: Bariatric surgery, Weight loss, Binge eating disorder, Mood disorders, Emotional dysregulation, Obesity
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3
المؤلفون: Guido Salvetti, Margherita Barbuti, A Calderone, Giulia Carignani, Giulio E. Brancati, Francesco Weiss, Giulio Perugi, Paola Fierabracci, Ferruccio Santini
المصدر: Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity. 27:1021-1027
مصطلحات موضوعية: medicine.medical_specialty, Bariatric Surgery, Comorbidity, Body Mass Index, Feeding and Eating Disorders, 03 medical and health sciences, 0302 clinical medicine, Binge-eating disorder, Prevalence, medicine, Humans, Obesity, 030212 general & internal medicine, Bipolar disorder, Depressive Disorder, Major, Binge eating, business.industry, Panic disorder, medicine.disease, Surgery, Psychiatry and Mental health, Clinical Psychology, Eating disorders, Cross-Sectional Studies, Mood disorders, Major depressive disorder, Female, medicine.symptom, business, 030217 neurology & neurosurgery
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4
المؤلفون: Francesco Weiss, Ferruccio Santini, Giulia Carignani, Giulio Perugi, Margherita Barbuti, A Calderone
المصدر: Journal of affective disorders. 279
مصطلحات موضوعية: Impulsivity, Bariatric surgery, Emotional dysregulation, Mood disorders, Obesity, Comorbidity, Humans, Retrospective Studies, Binge-Eating Disorder, Mood Disorders, 03 medical and health sciences, 0302 clinical medicine, Binge-eating disorder, medicine, business.industry, Panic disorder, medicine.disease, 030227 psychiatry, Psychiatry and Mental health, Clinical Psychology, Eating disorders, Mood, medicine.symptom, business, 030217 neurology & neurosurgery, Clinical psychology
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5
المؤلفون: Alessandra Rufa, Alessandra Renieri, Antonio Federico, Maria Antonietta Mencarelli, Francesca Mari, Giulia Carignani, Chiara Fallerini, Alessandro Rossi, Giorgio Capoccitti, Caterina Lo Rizzo, Fabio Giannini, Anna Maria Pinto
المصدر: Journal of the Neurological Sciences. 359:409-417
مصطلحات موضوعية: Adult, Dynamins, Male, Sporadic next generation sequencing technology, DNA Mutational Analysis, Biology, Custom panel, DNA sequencing, GTP Phosphohydrolases, Mitochondrial Proteins, Dynamin II, symbols.namesake, Locus heterogeneity, medicine, Humans, Inheritance Patterns, Hereditary motor and sensory neuropathies, Sanger sequencing, Genetics, Genetic heterogeneity, Low-cost diagnosis, High-Throughput Nucleotide Sequencing, Middle Aged, medicine.disease, DNM2, Neurology, Mutation, Mutation (genetic algorithm), symbols, Mendelian inheritance, Female, Neurology (clinical), Hereditary Sensory and Motor Neuropathy
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6
المؤلفون: Marina Vascotto, Margherita Baldassarri, Pietro Rubegni, Giulia Carignani, Francesca Mari, Ranuccio Nuti, Joussef Hayek, Alessandra Renieri, Joris Vermeesch, Elena Pretegiani, Carla Caffarelli, Livia Garavelli, Angelo Selicorni, Maria Teresa Dotti, Francesca Cristofoli, Chiara Di Marco, Paola Cianci, Salvatore Grosso, Caterina Lo Rizzo, Maria Antonietta Mencarelli, Michele Fimiani, Paolo Balestri, Chiara Fallerini, Laura Dosa, Annabella Marozza, R. Vivarelli
المصدر: Brain and Development. 37:527-536
مصطلحات موضوعية: Male, Pediatrics, Chromosomal Proteins, Non-Histone, SMARCB1, Hypotrichosis, Cohort Studies, SMARCA2, Intellectual disability, Missense mutation, Coffin-Siris syndrome, Low frontal hairline, Child, BAF-complex, ARID1B, Nicolaides-Baraitser syndrome, High-Throughput Nucleotide Sequencing, SMARCB1 Protein, General Medicine, DNA-Binding Proteins, Nicolaides–Baraitser syndrome, Child, Preschool, Cohort, Female, Hand Deformities, Congenital, Adult, medicine.medical_specialty, Adolescent, Foot Deformities, Congenital, Micrognathism, Developmental Neuroscience, Intellectual Disability, medicine, Humans, Abnormalities, Multiple, Sparse hair, Psychiatry, Coffin–Siris syndrome, Genetic Association Studies, business.industry, Facies, Infant, medicine.disease, Face, Pediatrics, Perinatology and Child Health, Neurology (clinical), business, Neck, Transcription Factors
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7
المؤلفون: Giulia Carignani, Maria Antonietta Mencarelli, Paolo Toti, Francesca Mari, Chiara Di Marco, Francesca Ariani, Daniela Galimberti, Annabella Marozza, Serena Somma, Theodora Hadjistilianou, Ilaria Meloni, Pietro Piu, Caterina Lo Rizzo, Sonia De Francesco, Valentina Imperatore, Sara Amitrano, Laura Dosa, Francesco Cetta, Alessandra Renieri
المصدر: European Journal of Human Genetics. 23:1523-1530
مصطلحات موضوعية: Adult, Male, Heterozygote, Adolescent, Genetics (clinical), Genetics, Genetic counseling, Germline mosaicism, Biology, Retinoblastoma Protein, Article, Deep sequencing, DNA sequencing, Germline mutation, medicine, Humans, Allele, Child, Alleles, Germ-Line Mutation, Mosaicism, Retinoblastoma, Sporadic Retinoblastoma, High-Throughput Nucleotide Sequencing, medicine.disease, eye diseases, Child, Preschool, Female
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8
المؤلفون: Thomas Wieland, Guido M. Kukuk, Dagmar Wieczorek, Anne Dieux-Coeslier, Alessandra Renieri, Jessica Becker, Tim M. Strom, Julia K. Ehret, Beate Albrecht, Mohnish Suri, Kirsten Cremer, Alexander M. Zink, Joris Andrieux, Nicola Dennert, Giulia Carignani, Hermann-Josef Lüdecke, Hartmut Engels, Eva Wohlleber
مصطلحات موضوعية: Male, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Medizin, SOX2, 030105 genetics & heredity, Biology, Polymorphism, Single Nucleotide, Microphthalmia, genotype first, intellectual disability, microdeletion, whole exome sequencing, Genetics, Genetics (clinical), 03 medical and health sciences, symbols.namesake, Intellectual disability, Genotype, medicine, Humans, Point Mutation, Exome, Eye Abnormalities, Registries, Genetic Association Studies, Exome sequencing, Sequence Deletion, Sanger sequencing, Comparative Genomic Hybridization, Anophthalmia, SOXB1 Transcription Factors, Infant, Newborn, Brain, Facies, High-Throughput Nucleotide Sequencing, medicine.disease, Magnetic Resonance Imaging, eye diseases, Phenotype, Child, Preschool, symbols, Female, sense organs, Comparative genomic hybridization