Quiz. Osteoblastic osteosarcoma of high grade malignancy.

Sudanese A , Femino F , Sangiorgi L
La Chirurgia Degli Organi Di Movimento 78 ( 3) 195 -198

1993
Additional methods of diagnosis in the histopathology of the musculoskeletal system.

Molendini L , Benassi Ms , Sollazzo Mr , Picci P
La Chirurgia Degli Organi Di Movimento 80 ( 4) 417 -426

1995
Register of primary malignant tumors of the bone at the Rizzoli Orthopaedic Institute in Bologna.

Caldora P , Zavatta M , Picci P , Sangiorgi L
La Chirurgia Degli Organi Di Movimento 79 ( 3) 303 -308

1994
Fibro-osseous pseudotumor of the digits: description of a case.

Bacchini P , Sangiorgi L , Bueno A , Calista F
La Chirurgia Degli Organi Di Movimento 81 ( 1) 69 -72

1996
Ebstein's anomaly in a child with osteogenesis imperfecta type I.

Paolo Versacci , Mauro Celli , Patrizia D'Eufemia , Anna Zambrano
Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases 8 ( 2) 50 -51

2
2011
Child abuse and osteogenesis imperfecta: how can they be still misdiagnosed? A case report.

Marta Palombaro , Mauro Celli , Patrizia D'Eufemia , Anna Zambrano
Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases 9 ( 3) 195 -197

3
2012
Outcomes of Temporary Hemiepiphyseal Stapling for Correcting Genu Valgum in Children with Multiple Osteochondromas: A Single Institution Study.

Diego Antonioli , Giovanni Gallone , Paola Zarantonello , Stefano Stallone
Children today 8 ( 4) 287

2021
COL1-Related Disorders: Case Report and Review of Overlapping Syndromes.

Maria Gnoli , Margherita Maioli , Elena Pedrini , Cecilia Giunta
Frontiers in Genetics 12 640558 -640558

8
2021
Clinical, Histological, and Molecular Features of Solitary Fibrous Tumor of Bone: A Single Institution Retrospective Review.

Angelo Paolo Dei Tos , Katia Scotlandi , Marco Gambarotti , Elena Pedrini
Cancers 13 ( 10) 2470

2021
Imaging of Congenital Skeletal Disorders.

Alberto Bazzocchi , Giuseppe Guglielmi , Giovanni Trisolino , Luca Sangiorgi
Seminars in Musculoskeletal Radiology 25 ( 1) 22 -38

2021
The European Registry for Rare Bone and Mineral Conditions (EuRR-Bone): First year experience of the use of an e-reporting tool

Ana Luisa Priego Zurita , Agnès Linglart , Inês Alves , Renata Simona Auriemma
Bone reports 14 100849

2021
Stromal stem cells and platelet-rich plasma improve bone allograft integration.

Enrico Lucarelli , Milena Fini , Amira Beccheroni , Gianluca Giavaresi
Clinical Orthopaedics and Related Research 435 ( 435) 62 -68

116
2005
Establishing the first pan-European Registry for rare bone and mineral disorders: EuRR-Bone

Corinna Grasemann , Marina Mordenti , Inês Alves , Rebecca Skarberg
Bone reports 13 100318

2020
Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?

Mauro Bozzola , Chiara Gertosio , Maria Gnoli , Federico Baronio
Italian Journal of Pediatrics 41 ( 1) 53 -53

4
2015
Models of Autonomy and Coordination: Integrating Subjective and Objective Approaches in Agent Development Frameworks

Stefano Mariani , Andrea Omicini , Luca Sangiorgi
intelligent distributed computing 570 69 -79

4
2015
Validation of a new multiple osteochondromas classification through Switching Neural Networks.

Marina Mordenti , Enrico Ferrari , Elena Pedrini , Nicola Fabbri
American Journal of Medical Genetics Part A 161 ( 3) 556 -560

16
2013
Nosology and classification of genetic skeletal disorders: 2015 revision

Luisa Bonafe , Valerie Cormier-Daire , Christine Hall , Ralph Lachman
American Journal of Medical Genetics Part A 167 ( 12) 2869 -2892

348
2015
Disease Registry: A Tool for European Cross-Border Medicine

Luca Sangiorgi , Marina Mordenti
New Perspectives in Medical Records 141 -152

2
2017
The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanks

Chiara Baldo , Lorena Casareto , Alessandra Renieri , Giuseppe Merla
Orphanet Journal of Rare Diseases 11 ( 1) 1 -8

26
2016