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1
المؤلفون: Carolina Putotto, Marta Unolt, Caterina Lambiase, Flaminia Marchetti, Silvia Anaclerio, Alessandra Favoriti, Giancarlo Tancredi, Gioia Mastromoro, Flaminia Pugnaloni, Natascia Liberati, Enrica De Luca, Luigi Tarani, Daniela De Canditiis, Viviana Caputo, Laura Bernardini, Maria Cristina Digilio, Bruno Marino, Paolo Versacci
المصدر: European Journal of Medical Genetics. 66:104651
مصطلحات موضوعية: Genetics, General Medicine, Genetics (clinical)
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2
المؤلفون: Claudio Colonnese, Alessandra Morano, Marco Ceccanti, Antonino Buzzanca, Massimo Biondi, Antonio Pizzuti, Martina Fanella, Marianna Frascarelli, Alfredo Berardelli, Carlo Di Bonaventura, Caterina Lambiase, Alessandro Viganò, Jinane Fattouch, Natascia Liberati, Fabio Di Fabio, Marta Unolt, Tommaso Accinni, Anna Teresa Giallonardo
مصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, Psychosis, Parkinson's disease, Adolescent, 22q11.2 deletion syndrome, left-handedness, myoclonic epilepsy, schizophrenia, Epilepsies, Myoclonic, Functional Laterality, Young Adult, Epilepsy, Parkinsonian Disorders, Genetic model, DiGeorge Syndrome, Genetics, medicine, Humans, Genetic Predisposition to Disease, Genetics (clinical), business.industry, Parkinsonism, Middle Aged, medicine.disease, Phenotype, Schizophrenia, Myoclonic epilepsy, Female, Juvenile myoclonic epilepsy, business
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3
المؤلفون: Luigi Tarani, Natascia Liberati, Giovanni Parlapiano Marco Fiore, Giovanna Coriale, Mauro Ceccanti
المصدر: Il Pediatra (Milano) aprile 2019 (2019): 54-58.
info:cnr-pdr/source/autori:Luigi Tarani, Natascia Liberati, Giovanni Parlapiano Marco Fiore, Giovanna Coriale, Mauro Ceccanti/titolo:Il pediatra e la sindrome feto-alcolica./doi:/rivista:Il Pediatra (Milano)/anno:2019/pagina_da:54-58/pagina_a:/intervallo_pagine:54-58/volume:aprile 2019مصطلحات موضوعية: FASD
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4
المؤلفون: Antonio Greco, Mauro Ceccanti, Diego De Angelis, Marco Fiore, Luigi Tarani, Valentina Carito, Silvia Ottombrino, Ginevra Micangeli, Natascia Liberati, Debora Rasio
المصدر: Biomedical Reviews (Varna. Online) 29 (2018): 37–46. doi:10.14748/bmr.v29.5848
info:cnr-pdr/source/autori:Tarani L, Micangeli G, Rasio D, Ottombrino S, Liberati N, De Angelis D, Carito V, Greco A, Ceccanti M, Fiore M/titolo:CLINICAL AND GENETIC APPROACH TO THE DYSMORPHIC CHILD/doi:10.14748%2Fbmr.v29.5848/rivista:Biomedical Reviews (Varna. Online)/anno:2018/pagina_da:37/pagina_a:46/intervallo_pagine:37–46/volume:29مصطلحات موضوعية: medicine.medical_specialty, treatment, Genetic syndromes, diagnosis, business.industry, birth defect, 05 social sciences, pediatrician, General Medicine, Multidisciplinary team, medicine.disease, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, Social integration, Malformative syndrome, Medicine, 0501 psychology and cognitive sciences, genetic syndrome, 050102 behavioral science & comparative psychology, business, Intensive care medicine, Rare disease, 030217 neurology & neurosurgery
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5Academic Journal
المؤلفون: ZICARI, Anna Maria, TARANI, Luigi, PAPETTI, LAURA, NICITA, Francesco, DUSE, MARZIA, Daniela Perotti, Natascia Liberati, Alberto Spalice, Guglielmo Salvatori, Federica Guaraldi
المساهمون: Zicari, Anna Maria, Tarani, Luigi, Daniela, Perotti, Papetti, Laura, Nicita, Francesco, Natascia, Liberati, Alberto, Spalice, Guglielmo, Salvatori, Federica, Guaraldi, Duse, Marzia
مصطلحات موضوعية: bone displasia, bone dysplasia, cranial sclerosi, horan-beighton syndrome, osteopathia striata, wtx
وصف الملف: ELETTRONICO
Relation: info:eu-repo/semantics/altIdentifier/pmid/22716240; info:eu-repo/semantics/altIdentifier/wos/WOS:000307394400001; volume:38; issue:1; firstpage:27; numberofpages:6; journal:THE ITALIAN JOURNAL OF PEDIATRICS; http://hdl.handle.net/11573/455876; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84862337902; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000307394400001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a; http://www.scopus.com/inward/record.url?eid=2-s2.0-84862337902&partnerID=65&md5=8f4eb64953e943da6296b5a622540a12
الاتاحة: http://hdl.handle.net/11573/455876
https://doi.org/10.1186/1824-7288-38-27
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000307394400001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a
http://www.scopus.com/inward/record.url?eid=2-s2.0-84862337902&partnerID=65&md5=8f4eb64953e943da6296b5a622540a12 -
6Academic Journal
المؤلفون: RAMIERI, VALERIO, TARANI, Luigi, COSTANTINO, Francesco, BASILE, EMANUELA, RINNA, CLAUDIO, CASCONE, PIERO, COLLORIDI, Fiorenza, Natascia Liberati
المساهمون: Ramieri, Valerio, Tarani, Luigi, Costantino, Francesco, Basile, Emanuela, Natascia, Liberati, Rinna, Claudio, Cascone, Piero, Colloridi, Fiorenza
مصطلحات موضوعية: microcephaly, cleft palate, blepharophimosis-ptosis-epicanthus inversus syndrome, interstitial deletion, 3q, bpe, contiguous gene syndrome
وصف الملف: ELETTRONICO
Relation: info:eu-repo/semantics/altIdentifier/pmid/22067867; info:eu-repo/semantics/altIdentifier/wos/WOS:000297741900054; volume:22; issue:6; firstpage:2124; lastpage:2128; numberofpages:5; journal:THE JOURNAL OF CRANIOFACIAL SURGERY; http://hdl.handle.net/11573/354493; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-82955214542; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000297741900054&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a; http://www.scopus.com/inward/record.url?eid=2-s2.0-82955214542&partnerID=65&md5=777b7caa5d36fb8c06b4e3a8c1f00c72
الاتاحة: http://hdl.handle.net/11573/354493
https://doi.org/10.1097/scs.0b013e3182323cdf
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000297741900054&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a
http://www.scopus.com/inward/record.url?eid=2-s2.0-82955214542&partnerID=65&md5=777b7caa5d36fb8c06b4e3a8c1f00c72 -
7
المؤلفون: Leonardo Pimpolari, Fiorenza Colloridi, Natascia Liberati, Francesca Mancini, Michela Martini, Chiara Mattiucci, Richard C. Semelka, Chiara Mancini, Giovanni Parlapiano, Luigi Tarani
المصدر: Text-Atlas of Skeletal Age Determination: MRI of the Hand and Wrist in Children
مصطلحات موضوعية: età ossea, genetica, crescita, Pathology, medicine.medical_specialty, Skeletal maturation, business.industry, Medicine, Disease, business
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8
المؤلفون: Piero Cascone, Þ Francesco Costantino, Luigi Tarani, Natascia Liberati, Þ Emanuela Basile, Valerio Ramieri, Claudio Rinna, Fiorenza Colloridi
مصطلحات موضوعية: Male, medicine.medical_specialty, Pediatrics, Clinodactyly, bpes, Dwarfism, Contiguous gene syndrome, Diagnosis, Differential, Dandy–Walker syndrome, Hypotelorism, medicine, contiguous gene syndrome, Humans, Abnormalities, Multiple, microcephaly, cleft palate, blepharophimosis-ptosis-epicanthus inversus syndrome, interstitial deletion, 3q, In Situ Hybridization, Fluorescence, Pierre Robin Syndrome, business.industry, Facies, Infant, General Medicine, Syndrome, medicine.disease, Blepharophimosis, Surgery, Palpebral fissure, Seckel syndrome, Otorhinolaryngology, Malformative syndrome, Chromosomes, Human, Pair 3, medicine.symptom, Chromosome Deletion, business, Dandy-Walker Syndrome
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9
المؤلفون: Luigi Tarani, Natascia Liberati, Costantino F, Enrico Properzi, Alberto Spalice, Del Balzo F, Patrizia D'Eufemia
المصدر: Pediatric Reports, Vol 2, Iss 1, Pp e8-e8 (2010)
Pediatric Reports
Volume 2
Issue 1مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, media_common.quotation_subject, lcsh:Medicine, Case Report, Hypoglycemia, Vertigo, medicine, Girl, media_common, Foramen magnum, biology, business.industry, Chiari type I malformation, lcsh:R, Syncope (genus), lcsh:RJ1-570, lcsh:Pediatrics, Chiari type i malformation, medicine.disease, biology.organism_classification, nervous system diseases, medicine.anatomical_structure, Causal association, embryonic structures, Steatosis, business
وصف الملف: application/pdf
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10
المؤلفون: Michela Martini, Francesca Mancini, Leonardo Pimpolari, Chiara Mancini, Luigi Tarani, Giovanni Parlapiano, Natascia Liberati, Fiorenza Colloridi
المصدر: Italian Journal of Pediatrics
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Pediatrics, medicine.medical_specialty, Cornelia de Lange Syndrome, business.industry, medicine.disease, Short stature, Idiopathic short stature, CHARGE syndrome, Costello syndrome, Turner syndrome, Meeting Abstract, medicine, Noonan syndrome, medicine.symptom, business, Kabuki syndrome
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11
المؤلفون: Paolo Radice, Angelo Selicorni, Natascia Liberati, Luigi Tarani, Sara Ciceri, Daniela Perotti, Elisa Cattaneo
المصدر: World Journal of Medical Genetics. 4:34
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Cranial sclerosis, medicine, Wilms' tumor, Biology, medicine.disease, Gene, Osteopathia striata
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12Academic Journal
المؤلفون: Luigi Tarani, Francesca Del Balzo, Francesco Costantino, Enrico Properzi, Natascia Liberati, Alberto Spalice
المساهمون: The Pennsylvania State University CiteSeerX Archives
المصدر: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/b4/4d/Pediatr_Rep_2010_Jun_18_2(1)_e8.tar.gz
وصف الملف: application/zip