Zobrazeno 1 - 10
of 15
pro vyhledávání: '"A. J. M. Van Unnik"'
Autor:
I. S. van Maurik, E. D. Bakker, A. A. J. M. van Unnik, H. M. Broulikova, M. D. Zwan, E. van de Giessen, J. Berkhof, F. H. Bouwman, J. E. Bosmans, W. M. van der Flier
Publikováno v:
Alzheimer’s Research & Therapy, Vol 15, Iss 1, Pp 1-7 (2023)
Abstract Background To estimate the perceived value of additional testing with amyloid-PET in Euros in healthy participants acting as analogue patients with mild cognitive impairment (MCI). Methods One thousand four hundred thirty-one healthy partici
Externí odkaz:
https://doaj.org/article/0d57021efbd34e12bdccd24683ff5a3f
Autor:
Christina A. Hulsbergen-van de Kaa, Leen van Leuven, Max M. van Noesel, Ernst J. M. Speel, Ronald R. de Krijger, Sandra M.H. Claessen, Ad J M van Unnik, Frieda van der Ham
Publikováno v:
Modern Pathology, 20, 11, pp. 1191-9
Modern Pathology, 20, 1191-9
Modern Pathology, 20, 1191-1199. Nature Publishing Group
Modern Pathology, 20, 1191-9
Modern Pathology, 20, 1191-1199. Nature Publishing Group
Contains fulltext : 53430.pdf (Publisher’s version ) (Closed access) Pleuropulmonary blastomas are rare malignant intrathoracic tumors of early childhood. They appear as a pulmonary- and/or pleural-based mass and their pathogenesis and relationship
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b639c6cca40f41a0fd2ce01e96ec6a2
https://doi.org/10.1038/modpathol.3800953
https://doi.org/10.1038/modpathol.3800953
Autor:
A. J. M. Van Unnik, J C van der Linden, P.A. Voûte, Chris J.L.M. Meijer, Liliane C. D. Wijnaendts
Publikováno v:
Current Diagnostic Pathology. 3:137-142
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14f4f2512fbe7e757c080373d54a198d
https://doi.org/10.1016/s0968-6053(05)80011-0
https://doi.org/10.1016/s0968-6053(05)80011-0
Autor:
David M. Parham, Frank Gonzalez-Crussi, Dieter Harms, Andrea O. Cavazzana, Timothy J. Triche, Harold M. Maurer, Henry B. Marsden, Bruce L Webber, Hiroyuki Shimada, Vito Ninfo, Lina Asmar, A. J. M. van Unnik, William A. Newton, Dietmar Schmidt, Maria C. Tsokos, Herbert M. Reiman, Nancy E. Sachs, Mohan Beltangady, Ala B. Hamoudi, Edmund A. Gehan
Publikováno v:
Cancer. 76:1073-1085
Background. There is a need to develop a single prognostically significant classification of rhabdomyosarcomas (RMS) and other related tumors of children, adolescents, and young adults which would be a current guide for their diagnosis, allow valid c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::795cf569f9d012a54d796f72a761f5b2
https://doi.org/10.1002/1097-0142(19950915)76:6<1073::aid-cncr2820760624>3.0.co
https://doi.org/10.1002/1097-0142(19950915)76:6<1073::aid-cncr2820760624>3.0.co
Autor:
A. J. M. Van Unnik, P.A. Voûte, Chris J.L.M. Meijer, Jan P. A. Baak, M. Brinkhuis, J.C. van der Linden, L.C.D. Wijnaendts
Publikováno v:
Virchows Archiv. 425:611-616
Although peripheral primitive neuroectodermal tumour (pPNET) and extra-osseous Ewing's sarcoma (EES) are thought to be closely related neoplasms, their clinical behaviour differs considerably. To determine the clinical relevance of the Schmidt classi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df22caf7c6a1bf37e6df79f7f201cfac
https://doi.org/10.1007/bf00199351
https://doi.org/10.1007/bf00199351
Autor:
Andrea O. Cavazzana, Adrian J. M. Van Unnik, Mohan S. Beltangady, Dieter Harms, Dietmar Schmidt, William A. Newton, Ala B. Hamoudi, Edmund A. Gehan, Herbert M. Reiman, Frank Gonzales-Crussi, Hiroyuki Shimada, Henry B Marsden, Vito Ninfo, Timothy J. Triche, Maria Tsokos, Harold M. Maurer, David M. Parham, Lina Asmar, Bruce Webber, Nancy Sachs
Publikováno v:
Cancer. 74:2579-2588
Background. An International Pathology study was conducted to measure the agreement demonstrated among and within groups of pathologists involved in the categorization of childhood rhabdomyosarcoma according to four pathology classifications. Data co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73038f392fd1505a0963c5b3864040a0
https://doi.org/10.1002/1097-0142(19941101)74:9<2579::aid-cncr2820740928>3.0.co
https://doi.org/10.1002/1097-0142(19941101)74:9<2579::aid-cncr2820740928>3.0.co
Autor:
P.A. Voûte, Chris J.L.M. Meijer, J. F. M. Delemarre, L.C.D. Wijnaendts, J.C. van der Linden, A. J. M. Van Unnik
Publikováno v:
Histopathology. 24:303-309
Rhabdomyosarcoma represents a large group of soft tissue sarcomas displaying heterogeneous histopathological features. In addition to their histopathological classification, the variable expression of a number of histopathological features may contri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::748a943767a60b7076ccbfa2f5af0063
https://doi.org/10.1111/j.1365-2559.1994.tb00530.x
https://doi.org/10.1111/j.1365-2559.1994.tb00530.x
Autor:
C. J. L. M. Meijer, Liliane C. D. Wijnaendts, J C van der Linden, P. J. Van Diest, P.A. Voûte, A. J. M. Van Unnik, J. F. M. Delemarre
Publikováno v:
Journal of Clinical Pathology. 46:948-952
AIM--To determine whether DNA ploidy patterns and S phase fraction offer prognostic information in patients with rhabdomyosarcoma (RMS). METHODS--DNA flow cytometry was performed on formalin fixed, paraffin wax embedded samples from primary tumours,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e997c320d98c07667cb010a5ecfaa65
https://doi.org/10.1136/jcp.46.10.948
https://doi.org/10.1136/jcp.46.10.948
Autor:
François Deméocq, H. Basil Marsden, Françoise Flamant, Marie-José Terrier-Lacombe, Jacques Otten, Jacques Valayer, P.A. Voûte, Adriaan J. M. Van Unnik, C Behar, Annie Babin-Boilletot, Jean-Michel Zucker
Publikováno v:
Medical and Pediatric Oncology. 21:634-639
Primary intrahepatic malignant nonepithelial tumors are very rare in children and account for 2% of all malignant mesenchymatous tumors under the age of 15 years. Clinical presentation, radiologic features, and histologic types are not unequivocal. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9105f39c804c93770acb3c474859eb60
https://doi.org/10.1002/mpo.2950210905
https://doi.org/10.1002/mpo.2950210905
Autor:
José Sanchez de Toledo, H. Basil Marsden, Adrian J. M. Van Unnik, Hélène Martelli, Michael C. Stevens, Jean Louis Habrand, Marie José Terrier-Lacombe, Nathalie Bouvet, Annie Rey, Richard D. Spicer, Caroline Ellershaw, Odile Oberlin, Françoise Flamant, David Spooner
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 23(12)
Purpose To improve outcome for children with nonmetastatic rhabdomyosarcoma and to reduce systematic use of local therapy. Patients and Methods Five hundred three previously untreated patients aged from birth to 18 years, recruited between 1989 and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac85fa721da6d17897a9fcd4fce52071
https://pubmed.ncbi.nlm.nih.gov/15728222
https://pubmed.ncbi.nlm.nih.gov/15728222