Holding versus seeing pathology. Three-dimensional printing of the bony pelvis for preoperative planning of a complex pelvis fracture: A case report

Por Sanghavi, Parang S, Jankharia, Bhavin G
Publicado no Indian J Radiol Imaging (2016)

A novel, multidisciplinary clinic for complex visual problems in older people

Por Han, R C, Jefferis, J M, Taylor, J P, Archibald, N K, Clarke, M P
Publicado em 2012

Extraordinary virtual multidisciplinary team meetings – a novel forum for the coordinated care...

Por Aston, Stephen J, Reade, Sophie, Petersen, Barbara, Ward, Charlotte, Duffy, Anthony, Nsutebu, Emmanuel
Publicado no Future Healthc J (2018)

A Novel ELP2 Compound Heterozygous Mutation in a Boy with Severe Intellectual Disability, Spastic...

Por Turkyilmaz, Ayberk, Sager, Gunes
Publicado no Mol Syndromol (2020)

A novel mutation in the succinate dehydrogenase subunit D gene in siblings with the hereditary paraganglioma–pheochromocytoma syndrome

Por Prasad, Chaithra, Oakley, Gerard J, Yip, Linwah, Coyne, Christopher, Rangaswamy, Balasubramanya, Dixit, Sanjay B
Publicado no SAGE Open Med Case Rep (2014)

Surgical approaches to complex vascular lesions: the use of virtual reality and stereoscopic analysis as a tool for resident and student education

Por Agarwal, Nitin, Schmitt, Paul J, Sukul, Vishad, Prestigiacomo, Charles J
Publicado no BMJ Case Rep (2012)

Interdental papilla regeneration around implants: A novel window technique (2 years follow-up)

Por Lambodharan, R., Balaji, V. R.
Publicado no J Pharm Bioallied Sci (2015)

Familial hypertriglyceridaemia and type 2 diabetes in pregnancy: prevention of acute pancreatitis with diet control and omega-3 fatty acids

Por Ong, Melissa, Jerreat, Lynne, Hameed, Aisha
Publicado no BMJ Case Rep (2019)

Preputial Graft Ureteroplasty for the Treatment of Complex Ureteral Stricture: A New Surgical Technique and Review of Literature

Por Onal, Bulent, Gultekin, Mehmet Hamza, Simsekoglu, Muhammed Fatih
Publicado no J Endourol Case Rep (2018)

Transarterial catheter embolisation for an unusual cause of upper gastrointestinal haemorrhage

Por Shelmerdine, Susan Cheng, Ameli-Renani, Seyed, Lynch, Jeremy Oliver, Gonsalves, Michael
Publicado no BMJ Case Rep (2015)

Complex Chromosomal Rearrangements in B-Cell Lymphoma: Evidence of Chromoanagenesis? A Case Report

Por Ortega, Veronica, Chaubey, Alka, Mendiola, Christina, Ehman, William, Vadlamudi, Kumari, Dupont, Barbara, Velagaleti, Gopalrao
Publicado no Neoplasia (2016)

Novel t(7;10)(p22;p24) along with NPM1 mutation in patient with relapsed acute myeloid leukemia

Por Sarojam, Santhi, Raveendran, Sureshkumar, Narayanan, Geetha, Sreedharan, Hariharan
Publicado no Ann Saudi Med (2013)

Cerebral Cavernous Malformation: A Portuguese Family with a Novel CCM1 Mutation

Por Marto, João Pedro, Gil, Inês, Calado, Sofia, Viana-Baptista, Miguel
Publicado no Case Rep Neurol (2016)

Consensus Molecular Subtypes (CMS) in Metastatic Colorectal Cancer - Personalized Medicine Decision

Por Rebersek, Martina
Publicado no Radiol Oncol (2020)

Transdisciplinary translational science and the case of preterm birth

Por Stevenson, D K, Shaw, G M, Wise, P H, Norton, M E, Druzin, M L, Valantine, H A, McFarland, D A
Publicado em 2013

Translational approaches to the biology of Autism: false dawn or a new era?

Por Ecker, C, Spooren, W, Murphy, D G M
Publicado em 2013

Three-dimensional printing in surgical planning: A case of aortopulmonary window with interrupted aortic arch

Por Moore, Ryan A, Wallen, William Jack, Riggs, Kyle W, Morales, David LS
Publicado no Ann Pediatr Cardiol (2018)

Unifying themes in complex systems new research volume IIIB Proceedings from the Third International Conference on Complex Systems /

Por International Conference on Complex Systems, Minai, Ali A, Bar-yam, Yanner, International Conference on Complex Systems
Publicado em 2006

Expanded genetic insight and clinical experience of DNMT1-complex disorder

Por Bi, Hongyan, Hojo, Kaori, Watanabe, Masashi, Yee, Christina, Maski, Kiran, Saba, Sadaf, Graff-Radford, Jonathan, Machulda, Mary M., St Louis, Erik K., Humes, Ilona Spitsyna, Flanagan, Eoin P., Nicolau, Stefan, Jones, David T., Patterson, Marc C., Kotagal, Suresh, Raz, Yael, Niu, Zhiyv, Li, Jun, Klein, Christopher J.
Publicado no Neurol Genet (2020)

Origination of an X-Linked Testes Chimeric Gene by Illegitimate Recombination in Drosophila

Por Arguello, J. Roman, Chen, Ying, Yang, Shuang, Wang, Wen, Long, Manyuan
Publicado em 2006