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Pediatric Blood & Cancer, ISSN 1545-5009, 01/2019, Volume 66, Issue 1, pp. e27500 - n/a
From 2009 to 2018, 10 consecutive patients with Wilms tumors and bilateral nephroblastomatosis, who had completed standard therapy, were provided a maintenance... 
nephroblastomatosis | chemotherapy | Wilms tumor | PEDIATRICS | ONCOLOGY | HEMATOLOGY | Chemotherapy | Nephroblastoma | Cancer | Tumors | Index Medicus
Journal Article
Journal Article
ISSN 1552-4825, 2016
Wilms tumor and nephroblastomatosis are associated with syndromic conditions including hemihyperplasia. Hemihyperplasia is genetically heterogeneous and may be... 
hemihypertrophy | nephroblastomatosis | PIK3CA-related overgrowth | CLOVES | Wilms tumor | lipoma | hemihyperplasia | somatic mutation
Journal Article
Fetal & Pediatric Pathology, ISSN 1551-3815, 6/2015, Volume 34, Issue 3, pp. 190 - 196
Journal Article
Pediatric Hematology/Oncology and Immunopathology, ISSN 1726-1708, 2015, Volume 14, Issue 4, pp. 37 - 43
Journal Article
Pediatric Hematology and Oncology, ISSN 0888-0018, 11/2018, Volume 35, Issue 3, pp. 218 - 224
Although the fate of nephrogenic rests varies, they are known to be precursors of Wilms tumour. Thus, nephrogenic rests require adequate treatment to prevent... 
Wilms tumour | retinoic acid | 13-cis retinoic acid | nephroblastomatosis | nephrogenic rest | MANAGEMENT | NEPHROGENIC RESTS | CANCER | CHEMOTHERAPY | ONCOLOGY | HIGH-RISK | PEDIATRICS | HEMATOLOGY
Journal Article
Onkourologiâ, ISSN 1726-9776, 08/2014, Volume 5, Issue 4, pp. 19 - 24
Some nontumor processes can resemble renal tumors both clinically and morphologically. Malformations in the kidneys can lead to that the latter preserve... 
treatment | nephroblastomatosis | morphology | children | diagnosis | bilateral nephroblastoma
Journal Article
Advances In Anatomic Pathology, ISSN 1072-4109, 05/2014, Volume 21, Issue 3, pp. 166 - 173
Journal Article
Journal of pediatric surgery, ISSN 0022-3468, 5/2011, Volume 46, Issue 5, pp. 983 - 988
Diffuse hyperplasticperilobarnephroblastomatosis (DHPLN) is a rare precursor lesion of Wilms tumor (WT). Because of the increased risk to develop WT in either... 
laparoscopy | nephron-sparing surgery | nephroblastomatosis | Wilms tumor
Journal Article
Journal Article
Clinical Genetics, ISSN 0009-9163, 05/2018, Volume 93, Issue 5, pp. 1075 - 1080
Congenital lipomatous overgrowth with vascular, epidermal, and skeletal (CLOVES) anomalies and Klippel‐Trenaunay (KTS) syndromes are caused by somatic... 
SNPs | CLOVES syndrome | PIK3CA | somatic mutation | Wilms tumor | DIAGNOSIS | PIK3CA MUTATION | WILMS-TUMOR | MALFORMATIONS | PATHWAY | KLIPPEL-TRENAUNAY-SYNDROME | GENETICS & HEREDITY | 4TH PATIENT | NEPHROBLASTOMATOSIS | ACTIVATING MUTATIONS | MARMORATA-TELANGIECTATICA-CONGENITA | Gene mutations | DNA | Genetic aspects | Urine | Polymerase chain reaction | Mutation | Deoxyribonucleic acid--DNA | Alleles | Tumors
Journal Article
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 12/2017, Volume 64, Issue 12, pp. e26684 - n/a
Journal Article
European Radiology, ISSN 0938-7994, 6/2016, Volume 26, Issue 6, pp. 1665 - 1669
Journal Article