نتائج البحث - "E. Scudellaro"

1

Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26

المؤلفون: Giovanni Vazza, E. Scudellaro, Giulia Perini, Sabina Rampinelli, P. Peruzzi, Cinzia Bertolin, Andrea Vettori, G De Sanctis, Francesca Boaretto, Maria Luisa Mostacciuolo

المصدر: Molecular Psychiatry. 12:87-93

مصطلحات موضوعية: Genetic Markers, Male, NONPARAMETRIC LINKAGE ANALYSIS, Bipolar Disorder, Genotype, Genetic Linkage, Population, Single-nucleotide polymorphism, genome scan, SCHIZOAFFECTIVE DISORDER, SHARED SUSCEPTIBILITY, COMPLEX TRAITS, Chromosomes, Genetic determinism, Cellular and Molecular Neuroscience, Gene Frequency, Gene mapping, Genetic linkage, mental disorders, medicine, Humans, linkage analysis, Genetic Predisposition to Disease, Bipolar disorder, schizophrenia, bipolar disorder, gene mapping, Chromosome Mapping, Female, Follow-Up Studies, Italy, Schizophrenia, Chromosomes, Human, Pair 15, Genomics, education, Molecular Biology, Allele frequency, Genetics, education.field_of_study, Pair 15, medicine.disease, Psychiatry and Mental health, Genetic marker, Psychology, Human

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39ff8412bd06be105183e4ead3432ad4
https://doi.org/10.1038/sj.mp.4001895

Find this article in full text from ProQuest

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Familial epilepsy and developmental dysphasia: description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci

المؤلفون: Maria Luisa Mostacciuolo, Lilia Volpi, Patrizia Riguzzi, Maria Margherita Mancardi, D. Passarelli, S. Testoni, Guido Rubboli, Aldo Scabar, Erica Diani, E. Scudellaro, Giovanni Vazza, Carlo Alberto Tassinari, Federica Pinardi, Carlo Nobile, Roberto Michelucci, Valeria Vianello

المساهمون: Michelucci R, Scudellaro E, Testoni S, Passarelli D, Riguzzi P, Diani E, Vazza G, Vianello V, Scabar A, Mostacciuolo ML, Volpi L, Rubboli G, Pinardi F, Mancardi MM, Tassinari CA, Nobile C.

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::910874cda2b9c6762b761e5a1a16f00c
http://hdl.handle.net/11585/69157

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Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases

المؤلفون: Carlo Alberto Tassinari, Francesca Bisulli, Patrizia Avoni, Giuseppe d'Orsi, Salvatore Striano, Luca Vignatelli, Pasquale Striano, Irene Florindo, E. Scudellaro, Paolo Tinuper, Carlo Nobile, Roberto Michelucci, Agostino Baruzzi, Alessia Bagattin

المساهمون: BISULLI F, TINUPER P, AVONI P, STRIANO P, STRIANO S, D'ORSI G, VIGNATELLI L, BAGATTIN A, SCUDELLARO E, FLORINDO I, NOBILE C, TASSINARI CA, BARUZZI A., MICHELUCCI R., Bisulli, F, Tinuper, P, Avoni, P, Striano, P, Striano, Salvatore, D'Orsi, G, Vignatelli, L, Bagattin, A, Scudellaro, E, Florindo, I, Nobile, C, Tassinari, Ca, Baruzzi, A, Michelucci, R.

مصطلحات موضوعية: Adult, Male, etiology/genetics, Pediatrics, medicine.medical_specialty, Adolescent, Aura, DNA Mutational Analysis, Adolescent, Adult, Age of Onset, Auditory Perception, Child, DNA Mutational Analysis, Epilepsy, Partial, Sensory, diagnosis/genetics/psychology, Female, Genetic Predisposition to Disease, Humans, Male, Mutation, Perceptual Disorders, etiology/genetics, Prognosis, Proteins, genetics, Treatment Outcome, Temporal lobe, Central nervous system disease, Perceptual Disorders, Drug withdrawal, Epilepsy, Aphasia, medicine, Humans, Genetic Predisposition to Disease, genetics, Family history, Age of Onset, Child, Epilepsy, Partial, Sensory, diagnosis/genetics/psychology, Intracellular Signaling Peptides and Proteins, Proteins, medicine.disease, Prognosis, Surgery, Treatment Outcome, Mutation, Auditory Perception, Female, Neurology (clinical), Age of onset, medicine.symptom, Psychology