Recurrent BCOR internal tandem duplication and YWHAE-NUTM2B fusions in soft tissue undifferentiated round cell sarcoma of infancy: overlapping genetic features with clear cell … YC Kao, YS Sung, L Zhang, SC Huang, P Argani, CT Chung, NS Graf, ... The American journal of surgical pathology 40 (8), 1009-1020, 2016 | 186 | 2016 |
Novel TMEM67 mutations and genotype‐phenotype correlates in meckelin‐related ciliopathies M Iannicelli, F Brancati, S Mougou‐Zerelli, A Mazzotta, S Thomas, ... Human mutation 31 (5), E1319-E1331, 2010 | 110 | 2010 |
PDCD4 nuclear loss inversely correlates with miR-21 levels in colon carcinogenesis M Fassan, M Pizzi, L Giacomelli, C Mescoli, K Ludwig, S Pucciarelli, ... Virchows Archiv 458, 413-419, 2011 | 91 | 2011 |
PDCD4/miR-21 dysregulation in inflammatory bowel disease-associated carcinogenesis K Ludwig, M Fassan, C Mescoli, M Pizzi, M Balistreri, L Albertoni, ... Virchows Archiv 462, 57-63, 2013 | 82 | 2013 |
Rare uterine cancer: carcinosarcomas. Review from histology to treatment G Artioli, J Wabersich, K Ludwig, MP Gardiman, L Borgato, F Garbin Critical reviews in oncology/hematology 94 (1), 98-104, 2015 | 69 | 2015 |
BCOR-CCNB3 undifferentiated sarcoma—does immunohistochemistry help in the identification? K Ludwig, R Alaggio, A Zin, M Peron, V Guzzardo, S Benini, A Righi, ... Pediatric and Developmental Pathology 20 (4), 321-329, 2017 | 42 | 2017 |
Oral-facial-digital syndrome type VI: is C5orf42 really the major gene? M Romani, F Mancini, A Micalizzi, A Poretti, E Miccinilli, P Accorsi, E Avola, ... Human genetics 134, 123-126, 2015 | 39 | 2015 |
Human epithelial growth factor receptor 2 (HER2) status in primary and metastatic esophagogastric junction adenocarcinomas M Fassan, K Ludwig, M Pizzi, C Castoro, V Guzzardo, M Balistreri, ... Human pathology 43 (8), 1206-1212, 2012 | 36 | 2012 |
Recessive spondylocarpotarsal synostosis syndrome due to compound heterozygosity for variants in MYH3 SR Cameron-Christie, CF Wells, M Simon, M Wessels, CZN Tang, W Wei, ... The American Journal of Human Genetics 102 (6), 1115-1125, 2018 | 27 | 2018 |
Endometrial Polyps in Women Affected by Levothyroxine‐Treated Hypothyroidism—Histological Features, Immunohistochemical Findings, and Possible Explanation of Etiopathogenic … C Saccardi, S Gizzo, K Ludwig, M Guido, M Scarton, M Gangemi, R Tinelli, ... BioMed Research International 2013 (1), 503419, 2013 | 22 | 2013 |
Dandy-Walker malformation masking the molar tooth sign: an illustrative case with magnetic resonance imaging follow-up S Sartori, K Ludwig, M Fortuna, C Marzocchi, M Calderone, I Toldo, ... Journal of child neurology 25 (11), 1419-1422, 2010 | 17 | 2010 |
Pentalogy of cantrell with complete ectopia cordis in a fetus with asplenia K Ludwig, R Salmaso, E Cosmi, L Iaria, A De Luca, K Margiotti, V Citton, ... Pediatric and Developmental Pathology 15 (6), 495-498, 2012 | 12 | 2012 |
Cervical follicular dendritic cell sarcoma: a case report and review of the literature M Pizzi, K Ludwig, G Palazzolo, G Busatto, C Rettore, G Altavilla International journal of immunopathology and pharmacology 24 (2), 539-544, 2011 | 12 | 2011 |
The impact of single nucleotide polymorphisms of the thrombin activatable fibrinolysis inhibitor (TAFI) gene on TAFI antigen levels in healthy children and pediatric oncology … R Knoefler, K Ludwig, H Kostka, E Kuhlisch, G Siegert, M Suttorp Seminars in thrombosis and hemostasis 29 (06), 575-584, 2003 | 12 | 2003 |
Apert syndrome with fused thalami K Ludwig, R Salmaso, R Manara, E Cosmi, M Baldi, M Rugge Fetal and Pediatric Pathology 31 (6), 410-414, 2012 | 10 | 2012 |
Congenital anomalies of the tubular gastrointestinal tract K Ludwig, D De Bartolo, A Salerno, G Ingravallo, G Cazzato, C Giacometti, ... Pathologica 114 (1), 40, 2022 | 9 | 2022 |
The anatomy and histology of the liver and biliary tract M Guido, S Sarcognato, D Sacchi, K Ludwig Pediatric Hepatology and Liver Transplantation, 41-55, 2019 | 8 | 2019 |
“While there is p57, there is hope.” The past and the present of diagnosis in first trimester abortions: diagnostic dilemmas and algorithmic approaches. A review C Giacometti, E Bellan, A Ambrosi, AP Dei Tos, M Cassaro, K Ludwig Placenta 116, 31-37, 2021 | 7 | 2021 |
Molecular Cytogenetics Detect an Unbalanced t(2;13)(q36;q14) and PAX3–FOXO1 Fusion in Rhabdomyosarcoma With Mixed Embryonal/Alveolar Features R La Starza, V Nofrini, T Pierini, V Pierini, A Zin, G Bisogno, C Cerri, ... Pediatric Blood & Cancer 62 (12), 2238-2241, 2015 | 7 | 2015 |
Congenital anomalies of the gastrointestinal tract: the liver, extrahepatic biliary tree and pancreas K Ludwig, L Santoro, G Ingravallo, G Cazzato, C Giacometti, P Dall’Igna Pathologica 114 (1), 55, 2022 | 6 | 2022 |