Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome

Cited by (275)

Items 101–200 of 275

1. Pediatric renal tumors
   Robert C. Shamberger · 1999 · Seminars in Surgical Oncology
2. Disruption of a Novel Imprinted Zinc-Finger Gene, ZNF215, in Beckwith-Wiedemann Syndrome
   Marielle M. Alders, Andy Ryan, Matt Hodges · 2000 · The American Journal of Human Genetics
3. Malignant adrenal tumors
   Frederick J. Rescorla · 2006 · Seminars in Pediatric Surgery
4. From the Archives of the AFIP
   Geoffrey A. Agrons, Gael J. Lonergan, Glenn E. Dickey · 1999 · Radiographics
5. RENAL FINDINGS ON RADIOLOGICAL FOLLOWUP OF PATIENTS WITH BECKWITH-WIEDEMANN SYNDROME
   Joseph G. Borer, Martin A. Kaefer, Carol E. Barnewolt, Ellen Roy Elias, Nedda Hobbs, ALAN B. RETIC, Craig Andrew Peters · 1999 · The Journal of Urology
6. Screening for Wilms Tumor in High-Risk Individuals
   Carol L. Clericuzio, Carey Johnson · 1995 · Hematology/Oncology Clinics of North America
7. Genetic testing and tumor surveillance for children with cancer predisposition syndromes
   Aarati Rao, Jennifer Rothman, Kim E. Nichols · 2008 · Current Opinion in Pediatrics
8. Pancreatoblastoma associated with incomplete Beckwith-Wiedemann syndrome: case report and review of the literature
   Rosa Muguerza, Alberto Rodríguez, Emilia Formigo · 2005 · Journal of Pediatric Surgery
9. Brain abnormalities in patients with Beckwith–Wiedemann syndrome
   Kate Gardiner, David A. Chitayat, Sanaa Choufani, Cheryl T. Shuman, Susan E. Blaser, Deborah Terespolsky, Sandra A. Farrell, Rosemary E. Reiss, Shoshana J. Wodak, Shuye Pu et al. · 2012 · American Journal of Medical Genetics Part A
10. Pediatric Urologic Oncology
    Gwen M. Grimsby, Michael L. Ritchey · 2012 · Pediatric Clinics of North America
11. Follow-up and Risk of Tumors in Overgrowth Syndromes
    Ricardo Gracia Bouthelier, Pablo Daniel Lapunzina · 2005 · Journal of Pediatric Endocrinology and Metabolism
12. Syndromes and Disorders Associated with Omphalocele (I): Beckwith–Wiedemann Syndrome
    Chih‐Ping Chen · 2007 · Taiwanese Journal of Obstetrics and Gynecology
13. Apparent postnatal onset of some manifestations of the Wiedemann‐Beckwith syndrome
    David A. Chitayat, Avi Rothchild, Emily W. Y. Ling · 1990 · American Journal of Medical Genetics
14. Simpson—Golabi—Behmel syndrome: Disproportionate fetal overgrowth and elevated maternal serum alpha‐fetoprotein
    R Hughes-Benzie, John Tolmie, Margaret B. McNay · 1994 · Prenatal Diagnosis
15. Cytogenetic study of malignant triton tumor: a case report
    Mary H. Haddadin, Anita L. Hawkins, Patricia P. Long · 2003 · Cancer Genetics and Cytogenetics
16. Inherited cancer in children: practical/ethical problems and challenges
    Marc D. Tischkowitz, Elisabeth M. Rosser · 2004 · European Journal of Cancer
17. Role of the Pathologist in the Diagnosis of Hereditary Non‐Polyposis Colorectal Cancer
    Jeremy R. Jass · 2004 · Disease Markers
18. New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome
    Adam C. Smith, Tamar N. Rubin, Cheryl Shuman · 2006 · Cytogenetic and Genome Research
19. Molecular Genetics and Cytogenetics of Sarcomas
    Russell P. Kruzelock, Marc F. Hansen · 1995 · Hematology/Oncology Clinics of North America
20. Beckwith-Wiedemann Syndrome, Tumorigenesis and Imprinting
    Claudine Junien · 1992 · Springer eBooks
21. Incidence of Abdominal Tumors in Syndromic and Idiopathic Hemihypertrophy/Isolated Hemihyperplasia
    Molly Dempsey, David C. Wilkes, Alec C. Stall · 2012 · Journal of Pediatric Orthopaedics
22. GENETIC PREDISPOSITION TO CANCER AND FAMILIAL CANCER SYNDROMES
    Susan Quesnel, David M. Malkin · 1997 · Pediatric Clinics of North America
23. Aberrant expression of the tumour suppressor gene p53 is very frequent in Wilms' tumours
    Nicholas Robert Lemoine, Christine M. Hughes, John Kenneth Cowell · 1992 · The Journal of Pathology
24. Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann—Beckwith syndrome
    Nicholas K. Hayward, Melissa Helen Little, R.H. Mortimer, W.M. Clouston, Peter J. Smith · 1988 · Cancer Genetics and Cytogenetics
25. Insulin-like Growth Factor Binding Proteins as Mediators of IGF-I Effects on Colon Cancer Cell Proliferation
    N. P. Michell, S. Dent, Michael J. S. Langman · 1997 · Growth Factors
26. Genomic Imprinting and Cancer
    Benjamin Tycko · 1999 · Results and problems in cell differentiation
27. Systemic and maxillofacial characteristics of patients with Beckwith-Wiedemann syndrome not treated with glossectomy
    Akiko Kawafuji, Naoto Suda, Naoko Ichikawa · 2011 · American Journal of Orthodontics and Dentofacial Orthopedics
28. Growth, bone maturation and pubertal development in children with the EMG‐syndrome
    Wolfgang G. Sippell, C. J. Partsch, H. ‐R. Wiedemann · 1989 · Clinical Genetics
29. Clinical features in the Wiedemann‐Beckwith syndrome
    Roberto Martinezy Martinez · 1996 · Clinical Genetics
30. Manifestation of alveolar rhabdomyosarcoma as primary cutaneous lesions in a neonate with Beckwith-Wiedemann syndrome
    Minoru Kuroiwa, Jun Sakamoto, Akira Shimada · 2009 · Journal of Pediatric Surgery
31. Wilms' tumor and related abnormalities in the fetus and newborn
    Kevin E. Bove · 1999 · Seminars in Perinatology
32. Genetic background of adrenocortical tumor development
    Magnus Kjellman, Catharina Larsson, Martin Bäckdahl · 2001 · World Journal of Surgery
33. A less‐invasive approach with orthodontic treatment in Beckwith–Wiedeman patients
    Aldo Giancotti, G Romanini, Raffaella Di Girolamo · 2002 · Orthodontics and Craniofacial Research
34. Opsoclonus-myoclonus with Beckwith-Wiedemann syndrome and hepatoblastoma
    Angus A. Wilfong, Julie T. Parke, John A. McCrary · 1992 · Pediatric Neurology
35. Bilateral hemorrhagic adrenal cysts in an incomplete form of Beckwith-Wiedemann syndrome: MRI and prenatal US findings
    Rahşan Göçmen, Ceyla Başaran, Muşturay Karçaaltıncaba · 2005 · Abdominal Imaging
36. Successful laparoscopic operation of bilateral pheochromocytoma in a patient with Beckwith-Wiedemann syndrome
    L Bémurat, Philippe Gosse, P. Ballanger, Patrick Tauzin-Fin, Pascal Barat, Didier Lacombe, P Lemétayer, Jacques Clémenty · 2002 · Journal of Human Hypertension
37. Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13
    Philippe Couillin, Martine Azoulay, I. Henry et al. · 1989 · Human Genetics
38. Advances in overgrowth syndromes: clinical classification to molecular delineation in Sotos syndrome and Beckwith-Wiedemann syndrome
    Cheryl S. Cytrynbaum, Adam C. Smith, Tamar N. Rubin · 2005 · Current Opinion in Pediatrics
39. Congenital Hepatoblastoma and Beckwith-Wiedemann Syndrome: A Case Study Including DNA Ploidy Profiles of Tumor and Adrenal Cytomegaly
    Roberto Orozco, J. Adelia McBride, Blaise E. Favara, Ann Steele, John Brown, Peter Steele · 1991 · Pediatric Pathology
40. Neuroblastoma in a child with Wiedemann–Beckwith syndrome
    David A. Chitayat, Jan M. Friedman, James E. Dimmick · 1990 · American Journal of Medical Genetics
41. Congenital Pancreatoblastoma
    Karen M. Chisholm, Christopher H. Hsu, Michael J. J. Kim · 2012 · Journal of Pediatric Hematology/Oncology
42. Atypical macrocephaly-cutis marmorata telangiectatica congenita with retinoblastoma
    Ida Vanessa Döederlein Schwartz, T mis M. Felix, Mariluce Riegel, Lavínia Schüler‐Faccini · 2002 · Clinical Dysmorphology
43. Prenatally Detected Cystic Adrenal Mass Associated with Beckwith-Wiedemann Syndrome
    Thierry Merrot, Jochen Christoph Walz, Robert Anastasescu · 2004 · Fetal Diagnosis and Therapy
44. Bilateral multiple adrenal pseudocysts associated with incomplete Beckwith-Wiedemann syndrome
    Arbay Ö. Çiftçi, Ahmet Bedii Salman, Feridun Cahit Tanyel · 1997 · Journal of Pediatric Surgery
45. Simultaneous Occurrence of Pancreatoblastoma and Neuroblastoma in a Newborn With Beckwith-Wiedemann Syndrome
    Stefania Sorrentino, Massimo Conte, Paolo Nozza · 2010 · Journal of Pediatric Hematology/Oncology
46. Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child
    Lourenço Sbragia-Neto, Antônio Aldo Melo Filho, Gil Guerra‐Júnior, Sofia Helena Valente de Lemos‐Marini, Maria Tereza Matias Baptista, Patrácia Sabino de Matos, Antônio Gonçalves de Oliveira-Filho, Joaquim Murray Bustorff‐Silva · 2000 · Journal of Pediatric Surgery
47. Cystic Adrenal Masses in the Neonate Associated with Hemihypertrophy and the Relation to the Beckwith-Wiedemann Syndrome
    Gary R. Walton, Benjamin C.H. Peng, Walter E. Berdon, Margaret H. Collins, Terry W. Hensle · 1991 · The Journal of Urology
48. Congenital abnormalities and clinical features associated with Wilms’ tumour: A comprehensive study from a centre serving a large population
    A. Ng, Annie Griffiths, Tim James Cole · 2007 · European Journal of Cancer
49. Review Article: Genomic imprinting: concept and clinical consequences
    Marcel M. A. M. Mannens, Marielle M. Alders · 1999 · Annals of Medicine
50. Analysis of gene dosage on chromosome 11 in children suffering from Beckwith-Wiedemann syndrome
    Paul N. Schofield, Sten Lindham, W. Engstr�m · 1989 · European Journal of Pediatrics
51. Therapy for non-Hodgkin lymphoma in children with primary immunodeficiency: Analysis of 19 patients from the BFM trials
    Kathrin Seidemann, Markus Tiemann, G�nter Henze, Axel Sauerbrey, Susanna M�ller, Alfred Reiter · 1999 · Medical and Pediatric Oncology
52. Genetics of Wilms' tumor: A blend of aberrant development and genomic imprinting
    Claudine Junien, Isabelle Henry · 1994 · Kidney International
53. Medullary sponge kidneys and unilateral Wilms tumour in a child with Beckwith-Wiedemann syndrome
    Rolf Beetz, Otto Schofer, Hubertus N. Riedmiller, R. Schumacher, Peter Gutjahr · 1991 · European Journal of Pediatrics
54. Preclinical Models of Adrenocortical Cancer
    Andrew J. H. Sedlack, Samual J. Hatfield, Suresh Kumar, Yasuhiro Arakawa, Nitin Roper, Nai-Yun Sun, Naris Nilubol, Katja Kiseljak‐Vassiliades, Chuong D. Hoang, Emily K. Bergsland et al. · 2023 · Cancers
55. Cutaneous vascular anomalies in the neonatal period
    Kristen P. Hook · 2013 · Seminars in Perinatology
56. Presence of Vascular Anomalies with Congenital Hemihypertrophy and Wilms Tumor: An Evidence‐Based Evaluation
    Roopal V. Kundu, Ilona J. Frieden · 2003 · Pediatric Dermatology
57. Chest wall hamartoma with Wiedemann-Beckwith syndrome: Clinical report and brief review of chromosome 11p15.5-related tumors
    Roy E. Jonas, Virginia E. Kimonis · 2001 · American Journal of Medical Genetics
58. A possible relationship between Beckwith‐Wiedemann syndrome, urinary tract anomaly and prune belly syndrome
    Hiroshi Watanabe, Tatsuhiro Yamanaka · 1990 · Clinical Genetics
59. Insulin-like growth factor 2 cannot be linked to a familial form of Beckwith-Wiedemann syndrome
    Anders Nyström, F Hedborg, R Ohlsson · 1994 · European Journal of Pediatrics
60. Germ cell nuclear antigen (GCNA1) expression does not require a gonadal environment or steroidogenic factor 1: Examination of GCNA1 in ectopic germ cells and inFtz-f1 null mice
    Danhua Wang, Yayoi Ikeda, Keith L. Parker, George C. Enders · 1997 · Molecular Reproduction and Development
61. Genetics of Wilms Tumor
    Max J. Coppes, Christine E. Campbell, Bryan Williams · 1995 · Molecular biology intelligence unit
62. Wiedemann‐Beckwith syndrome, imprinting, IGF2, and H19: Implications for hemihyperplasia, associated neoplasms, and overgrowth
    M. Michael Cohen · 1994 · American Journal of Medical Genetics
63. Beckwith–Wiedemann and IMAGe syndromes: two very different diseases caused by mutations on the same gene
    Monica Rosa Miozzo, Donatella Milani, Lidia Pezzani · 2014 · The Application of Clinical Genetics
64. Early presentation of right adrenal mass, hepatoblastoma and hepatic cavernous haemangioma in Beckwith-Wiedemann Syndrome.
    Siao Hean Teh, G B Ong · 2007 · PubMed
65. Beckwith—Wiedemann syndrome in a child with Chiari I malformation
    Richard Shane Tubbs, Walter Jerry Oakes · 2005 · Journal of neurosurgery
66. Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 gene
    John Kenneth Cowell, Natalie Groves, Paul Nigel Baird · 1993 · British Journal of Cancer
67. Renal cell carcinoma as a second malignant neoplasm in a patient with non-syndromic hemihypertrophy and previous Wilms tumor
    Greg Kraushaar, Sheldon Wiebe · 2005 · Pediatric Radiology
68. Alterations of H19 Imprinting and IGF2 Replication Timing Are Infrequent in Beckwith–Wiedemann Syndrome
    Jeremy Andrew Squire, Madeline Li, Sandra M. Perlikowski, Yan Ling Fei, Jane Bayani, Zong Mei Zhang, Rosanna Weksberg · 2000 · Genomics
69. A Third Case of Cardiac Neoplasm in a Fetus with Beckwith-Wiedemann Syndrome: Epicardial Angiofibroma
    Daniel Satgé, Evelyne Vidalo, François Desfarges, Bernard de Geeter · 2004 · Fetal Diagnosis and Therapy
70. Addition of H19 ‘Loss of Methylation Testing’ for Beckwith-Wiedemann Syndrome (BWS) Increases the Diagnostic Yield
    Jochen K. Lennerz, Robert J. Timmerman, Dorothy Katherine Grange, Michael Rutledge DeBaun, Andrew P. Feinberg, Barbara A. Zehnbauer · 2010 · Journal of Molecular Diagnostics
71. A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith–Wiedemann syndrome
    Silvia Russo, Monica Mencarelli, Florinda Cavalleri · 2003 · Molecular and Cellular Probes
72. Adrenal masses associated with Beckwith Wiedemann syndrome in the newborn
    Devendra Taide, Pradnya Suhas Bendre, Rajeev Gurunath Redkar · 2010 · African Journal of Paediatric Surgery
73. Origins of ... familial cancer: histopathological perspectives.
    Jeremy R. Jass · 1997 · Journal of Clinical Pathology
74. 11p15.5-Specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis
    Anne Puech, L. Ahnine, H.‐J. Lüdecke et al. · 1992 · Genomics
75. Human Diseases and Genomic Imprinting
    Judith G. Hall · 1999 · Results and problems in cell differentiation
76. Neuroblastoma in a patient with the Beckwith–Wiedemann syndrome (BWS)
    Grace Yoon, Gail E. Graham, Rosanna Weksberg, H. Penney Gaul, Michael Rutledge DeBaun, Max J. Coppes · 2002 · Medical and Pediatric Oncology
77. Umbilical cord blood transplantation
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78. Beckwith–Wiedemann syndrome associated with congenital hypothyroidism in a preterm neonate: a case report and literature review
    G I Ramadan, NL Kennea · 2009 · Journal of Perinatology
79. Clinical treatment of oral manifestations of Beckwith-Wiedeman syndrome in a child
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80. Beckwith–Wiedemann‐like macroglossia and 18q23 haploinsufficiency
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81. Balanced reciprocal translocation (X;20) limited to Wilms' tumor in a Wiedemann-Beckwith syndrome
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82. Constitutional H19 hypermethylation in a patient with isolated cardiac tumor
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83. Case report: Urinary bladder rhabdomyosarcoma associated with Beckwith-Wiedemann syndrome
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84. B eckwith‐ W iedemann Syndrome and Hemihyperplasia
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85. Recurrent, bilateral, and metastatic pheochromocytoma in a young patient with Beckwith-Wiedemann syndrome: A genetic link?
    Tiffany N. Caza, Jared Manwaring, Jonathan Riddell · 2017 · Canadian Urological Association Journal
86. Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome
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87. The two‐hit model for Wilms' tumor: Where are we 30 years later?
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88. Focal nodular hyperplasia in a child with Beckwith–Wiedemann syndrome
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89. Disseminated Alveolar Rhabdomyosarcoma in a Child With Spinal Muscular Atrophy
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90. The IGF2 methylation score for adrenocortical cancer: an ENSAT validation study
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91. Ectopic spleen and left-sided vena cava in Beckwith–Wiedemann syndrome
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92. Molecular analysis of patients with Wiedemann-Beckwith syndrome I. Gene dosage on the short arm of chromosome 11
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93. Is intensive follow‐up for early detection of tumors effective in children with Beckwith‐Wiedemann syndrome?
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94. Adrenocortical tumors in childhood: A report of four cases
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95. Genetic epidemiology of childhood cancer
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96. Beckwith-Wiedemann syndrome and isolated hemihyperplasia
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97. A macrosomic newborn with a cystic adrenal mass
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98. Isolated hemihyperplasia in an infant: an overlooked sign for wilms tumor development.
    Kamer Mutafoğlu, Emre Çeçen, Handan Çakmakçı · 2010 · Europe PMC (PubMed Central)
99. Pediatric Urologic Oncology
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100. Overgrowth Syndromes
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