المؤلفون: Orsini, Alessandro, Santangelo, Andrea, Carmignani, Alessandra, Camporeale, Anna, Massart, Francesco, Tyutyusheva, Nina, Peroni, Diego Giampietro, Foiadelli, Thomas, Ferretti, Alessandro, Toschi, Benedetta, Romano, Silvia, Bonuccelli, Alice

المساهمون: Orsini, Alessandro, Santangelo, Andrea, Carmignani, Alessandra, Camporeale, Anna, Massart, Francesco, Tyutyusheva, Nina, Peroni, Diego Giampietro, Foiadelli, Thoma, Ferretti, Alessandro, Toschi, Benedetta, Romano, Silvia, Bonuccelli, Alice

مصطلحات موضوعية: AP-4, ERF, epilepsy, AP-4 deficiency syndrome, ERF-related craniosynostosi, hereditary spastic paraparesis

Relation: volume:15; issue:4; journal:GENES; https://hdl.handle.net/11573/1707356

الاتاحة: https://hdl.handle.net/11573/1707356
https://doi.org/10.3390/genes15040436

المؤلفون: Fabrizio Chirico, Giuseppe Colella, Antonio Cortese, Pierfrancesco Bove, Romolo Fragola, Luigi Rugge, Giovanni Audino, Nicola Sgaramella, Gianpaolo Tartaro

المساهمون: Chirico, Fabrizio, Colella, Giuseppe, Cortese, Antonio, Bove, Pierfrancesco, Fragola, Romolo, Rugge, Luigi, Audino, Giovanni, Sgaramella, Nicola, Tartaro, Gianpaolo

مصطلحات موضوعية: facial reconstruction, craniosynostosi, facial trauma, post‐surgical facial sequelae, hyaluronic acid filler, facial plastic surgery, craniomaxillofacial surgery, reconstructive surgery, surgical oncology, non‐surgical approach

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000688596000001; volume:11; issue:16; journal:APPLIED SCIENCES; https://hdl.handle.net/11573/1695728; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85113234117

الاتاحة: https://hdl.handle.net/11573/1695728
https://doi.org/10.3390/app11167507

المؤلفون: BELTRAMI, BENEDETTA, Prada E., Tolva G., Scuvera G., Silipigni R., Graziani D., Bulfamante G., Gervasini C., Marchisio P., Milani D.

المساهمون: B. Beltrami, E. Prada, G. Tolva, G. Scuvera, R. Silipigni, D. Graziani, G. Bulfamante, C. Gervasini, P. Marchisio, D. Milani

مصطلحات موضوعية: 9q22.3 microdeletion syndrome, craniosynostosi, Gorlin syndrome, PTCH1, Settore MED/38 - Pediatria Generale e Specialistica, Settore MED/08 - Anatomia Patologica

Relation: info:eu-repo/semantics/altIdentifier/pmid/31578813; info:eu-repo/semantics/altIdentifier/wos/WOS:000488559100001; volume:8; issue:1; firstpage:1; lastpage:4; numberofpages:4; journal:MOLECULAR GENETICS & GENOMIC MEDICINE; http://hdl.handle.net/2434/700050; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85073931676

الاتاحة: http://hdl.handle.net/2434/700050
https://doi.org/10.1002/mgg3.987

المؤلفون: Uhl, Jean Francois, Sufianov, Albert, Ruiz, Camillo, Iakimov, Yuri, Mogorron, Huerta Jose, Encarnacion Ramirez, Manuel, Prat, Guillermo, Lorea, Barbara, Baldoncini, Matias, Goncharov, Evgeniy, Ramirez, Issael, Céspedes, José Rafael Cerda, Nurmukhametov, Renat, Montemurro, Nicola

المساهمون: Uhl, Jean Francoi, Sufianov, Albert, Ruiz, Camillo, Iakimov, Yuri, Mogorron, Huerta Jose, Encarnacion Ramirez, Manuel, Prat, Guillermo, Lorea, Barbara, Baldoncini, Matia, Goncharov, Evgeniy, Ramirez, Issael, Céspedes, José Rafael Cerda, Nurmukhametov, Renat, Montemurro, Nicola

مصطلحات موضوعية: 3D modeling, 3D printed model, 3D printing, cranioplasty, craniosynostosi, neurosurgery, simulation, surgical education

Relation: info:eu-repo/semantics/altIdentifier/pmid/37371373; info:eu-repo/semantics/altIdentifier/wos/WOS:001014290100001; volume:13; issue:6; journal:BRAIN SCIENCES; https://hdl.handle.net/11568/1223495; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85163773895

الاتاحة: https://hdl.handle.net/11568/1223495
https://doi.org/10.3390/brainsci13060894

المؤلفون: Lugli L., Rossi C., Ceccarelli P. L., Calabrese O., Bedetti L., Miselli F., Bianchini M. A., Iughetti L., Berardi A.

المساهمون: Lugli, L., Rossi, C., Ceccarelli, P. L., Calabrese, O., Bedetti, L., Miselli, F., Bianchini, M. A., Iughetti, L., Berardi, A.

مصطلحات موضوعية: Ciliopathie, Craniosynostosi, SALL1, Townes-Brocks syndrome

Relation: info:eu-repo/semantics/altIdentifier/pmid/36252910; info:eu-repo/semantics/altIdentifier/wos/WOS:000912962000006; volume:65; issue:12; firstpage:1; lastpage:4; journal:EUROPEAN JOURNAL OF MEDICAL GENETICS; https://hdl.handle.net/11380/1301169; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85140054282

الاتاحة: https://hdl.handle.net/11380/1301169
https://doi.org/10.1016/j.ejmg.2022.104642

المؤلفون: Pogliani L. M., Zuccotti G. V., Reggiori M., Erbetta A., Lacerenza M., Prada F., Furlanetto M., Vetrano I. G., Valentini L. G.

المساهمون: L.M. Pogliani, G.V. Zuccotti, M. Reggiori, A. Erbetta, M. Lacerenza, F. Prada, M. Furlanetto, I.G. Vetrano, L.G. Valentini

مصطلحات موضوعية: computerized tomography, cranial suture, cranial ultrasound, craniosynostosi, infants, Settore MED/27 - Neurochirurgia, Settore MED/38 - Pediatria Generale e Specialistica

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000826496100001; firstpage:1; lastpage:9; numberofpages:9; journal:ULTRASCHALL IN DER MEDIZIN; https://hdl.handle.net/2434/945349; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85134521268; https://www.thieme-connect.de/products/ejournals/html/10.1055/a-1820-8101

الاتاحة: https://hdl.handle.net/2434/945349
https://doi.org/10.1055/a-1820-8101
https://www.thieme-connect.de/products/ejournals/html/10.1055/a-1820-8101

المؤلفون: Santoro, Claudia, Riccio, Simona, Palladino, Federica, Aliberti, Ferdinando, Carotenuto, Marco, Zanobio, Mariateresa, Peduto, Cristina, Nigro, Vincenzo, Perrotta, Silverio, Piluso, Giulio

المساهمون: Santoro, Claudia, Riccio, Simona, Palladino, Federica, Aliberti, Ferdinando, Carotenuto, Marco, Zanobio, Mariateresa, Peduto, Cristina, Nigro, Vincenzo, Perrotta, Silverio, Piluso, Giulio

مصطلحات موضوعية: 17q11.2 microdeletion, MEIS2, bicoronal craniosynostosi, NF1, concurrent genetic disorder, exome sequencing

Relation: info:eu-repo/semantics/altIdentifier/pmid/33722742; info:eu-repo/semantics/altIdentifier/wos/WOS:000640911400005; firstpage:104190; journal:EUROPEAN JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11591/447268; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85102777873

الاتاحة: http://hdl.handle.net/11591/447268
https://doi.org/10.1016/j.ejmg.2021.104190

المؤلفون: Vimercati, Antonella, Olivieri, Claudiana, Dellino, Miriam, Gentile, Mattia, Tinelli, Raffaele, Cicinelli, Ettore

المساهمون: Vimercati, Antonella, Olivieri, Claudiana, Dellino, Miriam, Gentile, Mattia, Tinelli, Raffaele, Cicinelli, Ettore

مصطلحات موضوعية: Craniosynostosi, FGFR 1, FGFR 2, Pfeiffer syndrome, cloverleaf skull, prenatal diagnosis

Relation: info:eu-repo/semantics/altIdentifier/pmid/34182859; info:eu-repo/semantics/altIdentifier/wos/WOS:000667551500001; firstpage:1-4; lastpage:4; journal:THE JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE; http://hdl.handle.net/11586/371911; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85142364259

الاتاحة: http://hdl.handle.net/11586/371911
https://doi.org/10.1080/14767058.2021.1937984

المؤلفون: Maspero C, Giannini L, Galbiati G, Kairyte L, Farronato G

المساهمون: C. Maspero, L. Giannini, G. Galbiati, L. Kairyte, G. Farronato

مصطلحات موضوعية: Crouzon Syndrome, Craniosynostosi, FGFR 2, Settore MED/28 - Malattie Odontostomatologiche

Relation: volume:16; issue:2; firstpage:72; lastpage:80; numberofpages:9; journal:STOMATOLOGIJA; http://hdl.handle.net/2434/699238; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84930810281

الاتاحة: http://hdl.handle.net/2434/699238

المؤلفون: Balestrino A., Secci F., Piatelli G., Morana G., Pavanello M., Pacetti M., Cama A., Consales A.

المساهمون: Balestrino, A., Secci, F., Piatelli, G., Morana, G., Pavanello, M., Pacetti, M., Cama, A., Consales, A.

مصطلحات موضوعية: Bilateral lambdoid, Craniosynostosi, Mercedes−Benz syndrome, Multisutural craniosynostosi, Sagittal synostosy, Skull remodeling

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/31009784; info:eu-repo/semantics/altIdentifier/wos/WOS:000475895100145; volume:128; firstpage:77; lastpage:82; numberofpages:6; journal:WORLD NEUROSURGERY; http://hdl.handle.net/11567/984297; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85066245885

الاتاحة: http://hdl.handle.net/11567/984297
https://doi.org/10.1016/j.wneu.2019.04.117

المؤلفون: Accogli A., Scala M., Pavanello M., Severino M., Gandolfo C., De Marco P., Musacchia F., Torella A., Pinelli M., Nigro V., Capra V.

المساهمون: Accogli, A., Scala, M., Pavanello, M., Severino, M., Gandolfo, C., De Marco, P., Musacchia, F., Torella, A., Pinelli, M., Nigro, V., Capra, V.

مصطلحات موضوعية: cranio-cervical junction anomaly, craniosynostosi, dysgyria, RASopathie, sinus pericranii, TRAF7, Brain, Human, Skull, Tumor Necrosis Factor Receptor-Associated Peptides and Protein, Craniosynostose, Neurodevelopmental Disorder

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000535571700001; volume:112; issue:14; firstpage:1085; lastpage:1092; numberofpages:8; journal:BIRTH DEFECTS RESEARCH; http://hdl.handle.net/11588/873448; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85085543520

الاتاحة: http://hdl.handle.net/11588/873448
https://doi.org/10.1002/bdr2.1711

المؤلفون: Di Pietro, Lorena, Barba, Marta, Lattanzi, Wanda

المساهمون: Cuellar, Araceli, Bala, Krithi, Di Pietro, Lorena, Barba, Marta, Yagnik, Garima, Liu, Jia Lie, Stevens, Christina, Hur, David J, Ingersoll, Roxann G, Justice, Cristina M, Drissi, Hicham, Kim, Jinoh, Lattanzi, Wanda, Boyadjiev, Simeon A

مصطلحات موضوعية: Birth defect, Craniofacial, Mesenchymal stromal cell, Nonsyndromic craniosynostosi, Osteogenesi, RUNX2, Settore BIO/13 - BIOLOGIA APPLICATA

Relation: info:eu-repo/semantics/altIdentifier/pmid/32360898; info:eu-repo/semantics/altIdentifier/wos/WOS:000547005800017; issue:Apr 30; firstpage:1; lastpage:8; numberofpages:8; issueyear:2020; journal:BONE; http://hdl.handle.net/10807/152658; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85086393241

الاتاحة: http://hdl.handle.net/10807/152658
https://doi.org/10.1016/j.bone.2020.115395

المؤلفون: Patrizia De Marco, Marco Pavanello, Michele Pinelli, Andrea Accogli, Marcello Scala, Valeria Capra, Annalaura Torella, Mariasavina Severino, Carlo Gandolfo, Vincenzo Nigro, Francesco Musacchia

المساهمون: Accogli, A., Scala, M., Pavanello, M., Severino, M., Gandolfo, C., De Marco, P., Musacchia, F., Torella, A., Pinelli, M., Nigro, V., Capra, V., Accogli, Andrea, Scala, Marcello, Pavanello, Marco, Severino, Mariasavina, Gandolfo, Carlo, De Marco, Patrizia, Musacchia, Francesco, Torella, Annalaura, Pinelli, Michele, Nigro, Vincenzo, Capra, Valeria

مصطلحات موضوعية: 0301 basic medicine, Embryology, Pathology, medicine.medical_specialty, Health, Toxicology and Mutagenesis, Tumor Necrosis Factor Receptor-Associated Peptides and Protein, 030105 genetics & heredity, Toxicology, Germline, Craniosynostosis, Craniosynostoses, 03 medical and health sciences, Neurodevelopmental disorder, Neurodevelopmental Disorder, RASopathie, medicine, Humans, Missense mutation, Craniofacial, Sinus pericranii, cranio-cervical junction anomaly, Craniosynostose, business.industry, Skull, Sinus Pericranii, Brain, medicine.disease, Phenotype, Tumor Necrosis Factor Receptor-Associated Peptides and Proteins, craniosynostosi, 030104 developmental biology, medicine.anatomical_structure, Neurodevelopmental Disorders, Pediatrics, Perinatology and Child Health, dysgyria, business, Developmental Biology, TRAF7, Human

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dc337dbf3946fd87bcbd2f8d5f5b024
http://hdl.handle.net/11588/873448

المؤلفون: Mazzeo AT, Bolzon M, Telamoni G

المساهمون: Mazzeo, At, Bolzon, M, Telamoni, G

مصطلحات موضوعية: craniosynostosi, perioperative, anesthesia

Relation: info:eu-repo/semantics/altIdentifier/isbn/9789386293565; ispartofbook:Tenets of Craniosynostosis; firstpage:1; lastpage:22; numberofpages:22; http://hdl.handle.net/11570/3149579

الاتاحة: http://hdl.handle.net/11570/3149579

المؤلفون: Unolt M., Kammoun M., Nowakowska B., Graham G. E., Crowley T. B., Hestand M. S., Demaerel W., Geremek M., Emanuel B. S., Zackai E. H., Vermeesch J. R., McDonald-McGinn D.

المساهمون: Unolt, M., Kammoun, M., Nowakowska, B., Graham, G. E., Crowley, T. B., Hestand, M. S., Demaerel, W., Geremek, M., Emanuel, B. S., Zackai, E. H., Vermeesch, J. R., McDonald-McGinn, D.

مصطلحات موضوعية: 22q11.2 deletion syndrome, CDC45 gene, craniosynostosi, next-generation sequencing, rare nonsynonymous variants

Relation: info:eu-repo/semantics/altIdentifier/pmid/31474763; info:eu-repo/semantics/altIdentifier/wos/WOS:000510866200011; journal:GENETICS IN MEDICINE; http://hdl.handle.net/11573/1344396; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85071488378

الاتاحة: http://hdl.handle.net/11573/1344396
https://doi.org/10.1038/s41436-019-0645-4

المؤلفون: Saletti V., Vigano I., Melloni G., Pantaleoni C., Vetrano I. G., Valentini L. G.

المساهمون: V. Saletti, I. Vigano, G. Melloni, C. Pantaleoni, I.G. Vetrano, L.G. Valentini

مصطلحات موضوعية: Chiari I malformation, chromosomal rearrangement, craniosynostosi, genetic syndrome, PTENopathie, RASopathies, Settore MED/27 - Neurochirurgia, Settore MED/03 - Genetica Medica, Settore MED/39 - Neuropsichiatria Infantile

Relation: info:eu-repo/semantics/altIdentifier/pmid/31363831; info:eu-repo/semantics/altIdentifier/wos/WOS:000486225100013; volume:35; issue:10; firstpage:1727; lastpage:1739; numberofpages:13; journal:CHILDS NERVOUS SYSTEM; https://hdl.handle.net/2434/946178; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85069917164

الاتاحة: https://hdl.handle.net/2434/946178
https://doi.org/10.1007/s00381-019-04319-5

المؤلفون: Dentici, Maria Lisa, Barresi, Sabina, Niceta, Marcello, Pantaleoni, Francesca, Pizzi, Simone, Dallapiccola, Bruno, Tartaglia, Marco, Digilio, Maria Cristina

المساهمون: Dentici, Maria Lisa, Barresi, Sabina, Niceta, Marcello, Pantaleoni, Francesca, Pizzi, Simone, Dallapiccola, Bruno, Tartaglia, Marco, Digilio, Maria Cristina

مصطلحات موضوعية: craniosynostosi, exome, HNRNPK, Kabuki syndrome, nodular heterotopia, polydactyly, Genetic, Genetics (clinical)

Relation: info:eu-repo/semantics/altIdentifier/pmid/28374925; info:eu-repo/semantics/altIdentifier/wos/WOS:000423373900031; volume:93; issue:2; firstpage:401; lastpage:407; numberofpages:7; journal:CLINICAL GENETICS; http://hdl.handle.net/11573/1078696; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85018282135; http://www.blackwellpublishing.com/aims.asp?ref=0009-9163?site=1

الاتاحة: http://hdl.handle.net/11573/1078696
https://doi.org/10.1111/cge.13029
http://www.blackwellpublishing.com/aims.asp?ref=0009-9163?site=1

المؤلفون: Messi M., Luzi M., Consorti G.

المساهمون: Messi, M., Luzi, M., Consorti, G.

مصطلحات موضوعية: Craniofacial malformation, craniosynostosi, one-wing technique, plagiocephaly, supraorbital bar

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000430788700073; volume:29; issue:1; firstpage:167; lastpage:169; numberofpages:3; journal:THE JOURNAL OF CRANIOFACIAL SURGERY; https://hdl.handle.net/11566/331739; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85039701181

الاتاحة: https://hdl.handle.net/11566/331739
https://doi.org/10.1097/SCS.0000000000004047

المؤلفون: Barba, Marta, Di Pietro, Lorena, Massimi, Luca, Geloso, Maria Concetta, Frassanito, Paolo, Caldarelli, Massimo, Michetti, Fabrizio, Di Rocco, Concezio, Arcovito, Alessandro, Parolini, Ornella, Tamburrini, Gianpiero, Bernardini, Camilla, Lattanzi, Wanda

المساهمون: Barba, Marta, Di Pietro, Lorena, Massimi, Luca, Geloso, Maria Concetta, Frassanito, Paolo, Caldarelli, Massimo, Michetti, Fabrizio, Della Longa, Stefano, Romitti, Paul A., Di Rocco, Concezio, Arcovito, Alessandro, Parolini, Ornella, Tamburrini, Gianpiero, Bernardini, Camilla, Boyadjiev, Simeon A., Lattanzi, Wanda

مصطلحات موضوعية: BBS9, Gene expression signature, Innovative biotechnologie, Mesenchymal stromal cell, Nonsyndromic craniosynostosi, Primary cilium, Endocrinology, Diabetes and Metabolism, Physiology, Histology, Settore BIO/13 - BIOLOGIA APPLICATA

Relation: info:eu-repo/semantics/altIdentifier/pmid/29674126; info:eu-repo/semantics/altIdentifier/wos/WOS:000434371100008; volume:112; issue:112; firstpage:58; lastpage:70; numberofpages:13; issueyear:2018; journal:BONE; http://hdl.handle.net/10807/120120; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85045762056; www.elsevier.com/locate/bone

الاتاحة: http://hdl.handle.net/10807/120120
https://doi.org/10.1016/j.bone.2018.04.013

المؤلفون: Lattanzi W.

المساهمون: Lee, E., Le, T., Zhu, Y., Elakis, G., Turner, A., Lo, W., Venselaar, H., Verrenkamp, C. -A., Snow, N., Mowat, D., Kirk, E. P., Sachdev, R., Smith, J., Brown, N. J., Wallis, M., Barnett, C., Mckenzie, F., Freckmann, M. -L., Collins, F., Chopra, M., Gregersen, N., Hayes, I., Rajagopalan, S., Tan, T. Y., Stark, Z., Savarirayan, R., Yeung, A., Ades, L., Gattas, M., Gibson, K., Gabbett, M., Amor, D. J., Lattanzi, Wanda, Boyd, S., Haan, E., Gianoutsos, M., Cox, T. C., Buckley, M. F., Roscioli, T.

مصطلحات موضوعية: coronal, craniosynostosi, EFNB1, panel, TCF12, Australia, Basic Helix-Loop-Helix Transcription Factor, Cohort Studie, Cranial Suture, Craniosynostose, DNA-Binding Protein, Ephrin-B1, Female, Fibroblast Growth Factor 10, Genetic Testing, High-Throughput Nucleotide Sequencing, Human, Male, New Zealand, Nuclear Protein, Prospective Studie, Receptor, Fibroblast Growth Factor, Type 1, Repressor Protein, Retrospective Studie, Transcription Factor, Twist-Related Protein 1, Settore BIO/13 - BIOLOGIA APPLICATA

Relation: info:eu-repo/semantics/altIdentifier/pmid/29215649; info:eu-repo/semantics/altIdentifier/wos/WOS:000445531800020; volume:20; issue:9; firstpage:1061; lastpage:1068; numberofpages:8; issueyear:2018; journal:GENETICS IN MEDICINE; http://hdl.handle.net/10807/152979; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85053737381

الاتاحة: http://hdl.handle.net/10807/152979
https://doi.org/10.1038/gim.2017.214