المؤلفون: Cugurullo, Francesca

المساهمون: Dessole, Salvatore

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, MED/40 Ginecologia e ostetricia

وصف الملف: 830901/application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______1389::9fd4a11b1cdcbe5551937e9e19516445Test
http://eprints.uniss.it/11852Test/

المؤلفون: PISCOPO, CARMELO

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities

وصف الملف: text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_______152::1817b186a1e96bbf0ae9715cb889d158Test
http://www.fedoa.unina.it/12223Test/

المؤلفون: Ruggiero, Lucia

مصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities

وصف الملف: text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_______152::7dfd541f62de3835d10a077e65237192Test
http://www.fedoa.unina.it/12139Test/

المؤلفون: Antenora, Antonella

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities

وصف الملف: text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_______152::9034c0814f94c7da1b73317b74357f13Test
http://www.fedoa.unina.it/12162Test/

المؤلفون: HOPPS, Eugenia, MONTANA, Maria, CANINO, Baldassare, CALANDRINO, Vincenzo, LUCIDO, Daniela, LO PRESTI, Rosalia, CAIMI, Gregorio

المساهمون: Hopps, E, Montana, M, Canino, B, Calandrino, V, Lucido, D, Lo Presti, R, Caimi, G

مصطلحات موضوعية: erythrocyte membrane, hereditary spherocytosis, hereditary elliptocytosis, acanthocytosis, Settore MED/09 - Medicina Interna

العلاقة: ispartofbook:Atti del XXXVI Congresso della Società Italiana di Patologia Vascolare; Congresso Nazionale SIAPAV; issue:62 (suppl. 1); firstpage:88; lastpage:89; numberofpages:2; journal:MINERVA CARDIOANGIOLOGICA; http://hdl.handle.net/10447/105359Test

الإتاحة: http://hdl.handle.net/10447/105359Test

المؤلفون: MACCARONI, ELENA

المساهمون: Maccaroni, Elena, BERARDI, ROSSANA

مصطلحات موضوعية: ovarian cancer, BRCA, hereditary, germline mutation, Settore MED/06 - Oncologia Medica

العلاقة: http://hdl.handle.net/11566/252973Test

الإتاحة: http://hdl.handle.net/11566/252973Test

العنوان البديل: Rare diseases and the child's family: a study of a case. (English)

المؤلفون: Cotichelli, Giordano

المصدر: Children's Nurses: Italian Journal of Pediatric Nursing Science / Infermieri dei Bambini: Giornale Italiano di Scienze Infermieristiche Pediatriche; inverno2012/2013, Vol. 4 Issue 4, p133-135, 3p

مصطلحات موضوعية: GENETIC disorders, PSYCHOLOGICAL adaptation, CASE studies, QUALITATIVE research, FAMILY relations, HEREDITARY central nervous system demyelinating diseases, PSYCHOLOGY

المؤلفون: Santorelli, Marco

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, endocrine system, embryonic structures

وصف الملف: text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_______152::330ebff45b5b5c4ba49645648818065aTest
http://www.fedoa.unina.it/11054Test/

المؤلفون: Cinzia Zanatta, M. Marzaro, F. Zoppellaro, Vittorina Ghirardo, Marco Gasparella, Carlo Benetton, M. Ferro

المصدر: La Pediatria Medica e Chirurgica, Vol 38, Iss 2 (2016)

مصطلحات موضوعية: Male, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Bowel obstruction, Meckel’s diverticulum, Pediatric surgery, Phytobezoar, Bezoars, Child, Humans, Intestinal Obstruction, Meckel Diverticulum, Pediatrics, Perinatology and Child Health, Surgery, lcsh:Surgery, digestive system, Pediatrics, 03 medical and health sciences, 0302 clinical medicine, medicine, otorhinolaryngologic diseases, Meckel's diverticulum, Hepatic diverticulum, business.industry, lcsh:RJ1-570, lcsh:Pediatrics, lcsh:RD1-811, Perinatology and Child Health, medicine.disease, digestive system diseases, surgical procedures, operative, 030220 oncology & carcinogenesis, 030211 gastroenterology & hepatology, Radiology, business, Diverticulum

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d30ff42da07454e96036e9807386eebTest
http://hdl.handle.net/11577/3300083Test

المؤلفون: Graziano, Antonino, Giorgio Maria Paolo Graziano, Marco Cavallaro ISSN 2455 2968

مصطلحات موضوعية: Difficult problem, medicine.medical_specialty, business.industry, General surgery, Mutation (genetic algorithm), medicine, Autosomal dominant trait, Hereditary familial adenomatous polyposis treatment, Disease, Bioinformatics, medicine.disease, business, Familial adenomatous polyposis

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbd10ddf78ffa0f30c3d8d746dace9d2Test
http://hdl.handle.net/20.500.11769/17784Test