Sfoglia per Autore  

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Mostrati risultati da 1 a 16 di 16
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
"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 2021 Giacometti, CinziaBellan, ElenaAmbrosi, AlessandroDei Tos, Angelo PaoloLudwig, Kathrin + PLACENTA - -
Photosensitive epilepsy and long QT: expanding Timothy syndrome phenotype 2019 Po' C.Zordan R.Cerutti A.Sartori S.Trevisson E.Ludwig K.Castaldi B.Salviati L.Leoni L.Toldo I. + CLINICAL NEUROPHYSIOLOGY - -
BCOR-CCNB3 undifferentiated sarcoma-does immunohistochemistry help in the identification? 2017 Ludwig K.Alaggio R.Guzzardo V. + PEDIATRIC AND DEVELOPMENTAL PATHOLOGY - -
Diagnostic utility of cyclin D1 in the diagnosis of small round blue cell tumors in children and adolescents: beware of cyclin D1 expression in clear cell sarcoma of the kidney and CIC-DUX4 fusion–positive sarcomas. Comment on Magro et al (2016)—reply 2017 Ludwig K.Alaggio R. + HUMAN PATHOLOGY - -
Recurrent BCOR Internal Tandem Duplication and YWHAE-NUTM2B Fusions in Soft Tissue Undifferentiated Round Cell Sarcoma of Infancy: Overlapping Genetic Features With Clear Cell Sarcoma of Kidney 2016 LUDWIG, KATHRINZIN, ANGELICAALAGGIO, RITA + THE AMERICAN JOURNAL OF SURGICAL PATHOLOGY - -
Anti-Glypican 3, a Novel Ancillary Maker in the Histological Assessment of Hirschsprung's Disease 2016 LUDWIG, KATHRINVOLPE, ANDREASANTORO, LUISAMidrio, PaolaGAMBA, PIERGIORGIOALAGGIO, RITA + JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION - -
Molecular Cytogenetics Detect an Unbalanced t(2;13)(q36;q14) and PAX3-FOXO1 Fusion in Rhabdomyosarcoma With Mixed Embryonal/Alveolar Features 2015 ZIN, ANGELICABISOGNO, GIANNILUDWIG, KATHRIN + PEDIATRIC BLOOD & CANCER - -
Omental mesenteric myxoid hamartoma, a subtype of inflammatory myofibroblastic tumor? Considerations based on the histopathological evaluation of four cases 2015 LUDWIG, KATHRINALAGGIO, RITADALL'IGNA, MARTINA + VIRCHOWS ARCHIV - -
Ichthyosis and Kallmann syndrome: Not always a contiguous gene syndrome 2015 TREVISSON, EVALUDWIG, KATHRINRenzo ManaraCLEMENTI, MAURIZIOSALVIATI, LEONARDO + JOURNAL OF DERMATOLOGICAL SCIENCE - -
"Double Trouble" or an Amplification of the Triploidy Phenotype? 2013 LUDWIG, KATHRINPizzi MFASSAN, MATTEOSALMASO, ROBERTORUGGE, MASSIMO + FETAL AND PEDIATRIC PATHOLOGY - -
Apert Syndrome with Fused Thalami. 2012 LUDWIG, KATHRINSALMASO, ROBERTOManara RCOSMI, ERICHRUGGE, MASSIMO + FETAL AND PEDIATRIC PATHOLOGY - -
Congenital pulmonary airway malformation (CPAM) [congenital cystic adenomatoid malformation] associated with tracheoesophageal fistula and agensesis of the corpus callosum. 2012 PIZZI, MARCOFASSAN, MATTEOLUDWIG, KATHRINCASSINA, MATTEOSALMASO, ROBERTO + FETAL AND PEDIATRIC PATHOLOGY - -
Human epithelial growth factor receptor 2 (HER2) status in primary and metastatic esophagogastric junction adenocarcinomas. 2012 FASSAN, MATTEOLUDWIG, KATHRINPIZZI, MARCOGUZZARDO, VINCENZAZANINOTTO, GIOVANNIRUOL, ARTUROGIACOMELLI, LUCAANCONA, ERMANNORUGGE, MASSIMO + HUMAN PATHOLOGY - -
Cervical follicular dendritic cell sarcoma: a case report and review of the literature 2011 Pizzi, MLudwig, KAltavilla, G + INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY - -
PDCD4 nuclear loss inversely correlates with miR-21 levels in colon carcinogenesis. 2011 FASSAN, MATTEOPIZZI MMESCOLI, CLAUDIALUDWIG, KATHRINPUCCIARELLI, SALVATORERUGGE, MASSIMO + VIRCHOWS ARCHIV - -
Association of intra-uterine exposure to drugs with congenital defects: the thalidomide effect 2007 CLEMENTI, MAURIZIOLUDWIG, KATHRINANDRISANI, ALESSANDRA - - Congenital Diseases and the Environment
Mostrati risultati da 1 a 16 di 16
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