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Quoted phrase not found in phrase index: "11p partial monosomy syndrome"
Page 1
Wilms tumor: an update.
Al-Hussain T, Ali A, Akhtar M. Al-Hussain T, et al. Adv Anat Pathol. 2014 May;21(3):166-73. doi: 10.1097/PAP.0000000000000017. Adv Anat Pathol. 2014. PMID: 24713986 Review.
Germline mutation in WT1 may be associated with syndromic conditions such as WAGR and Denys-Drash syndromes. Perilobar rests and their corresponding tumors usually have loss of imprinting/loss of heterozygosity involving WT2, which contains several parentally imprinted gen …
Germline mutation in WT1 may be associated with syndromic conditions such as WAGR and Denys-Drash syndromes. Perilobar rests and thei …
Wilms' tumor management.
Wu HY, Snyder HM 3rd, D'Angio GJ. Wu HY, et al. Curr Opin Urol. 2005 Jul;15(4):273-6. doi: 10.1097/01.mou.0000172403.69890.eb. Curr Opin Urol. 2005. PMID: 15928519 Review.
Patients with Wilms' tumor, aniridia, major genitourinary malformations, and mental retardation, the WAGR syndrome, have a 50% chance of unexplained end-stage renal disease 20 years after treatment. SUMMARY: Less aggressive means of diagnosis and treatment for Wilms …
Patients with Wilms' tumor, aniridia, major genitourinary malformations, and mental retardation, the WAGR syndrome, have a 50% …
Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience.
Hol JA, Jongmans MCJ, Sudour-Bonnange H, Ramírez-Villar GL, Chowdhury T, Rechnitzer C, Pal N, Schleiermacher G, Karow A, Kuiper RP, de Camargo B, Avcin S, Redzic D, Wachtel A, Segers H, Vujanic GM, van Tinteren H, Bergeron C, Pritchard-Jones K, Graf N, van den Heuvel-Eibrink MM; International Society of Pediatric Oncology Renal Tumor Study Group (SIOP-RTSG). Hol JA, et al. Cancer. 2021 Feb 15;127(4):628-638. doi: 10.1002/cncr.33304. Epub 2020 Nov 4. Cancer. 2021. PMID: 33146894 Free PMC article.
BACKGROUND: WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays) is a rare contiguous gene deletion syndrome with a 45% to 60% risk of developing Wilms tumor (WT). ...Disease spread to other organs (metastases) did …
BACKGROUND: WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays) is a rare contig …
Obesity in Childhood and Adolescence, Genetic Factors.
Kostovski M, Tasic V, Laban N, Polenakovic M, Danilovski D, Gucev Z. Kostovski M, et al. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017 Dec 1;38(3):121-133. doi: 10.2478/prilozi-2018-0013. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017. PMID: 29668472 Free article.
Childhood obesity is also widespread in Macedonia. Metabolic syndrome, dyslipidemia and carbohydrate intolerance are found in significant numbers. ...Some of the children are either dysmorphic, or slightly retarded. We have already described patients with Prader-Willi s …
Childhood obesity is also widespread in Macedonia. Metabolic syndrome, dyslipidemia and carbohydrate intolerance are found in signifi …
Neuropsychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorder.
Nishizawa H, Motobayashi M, Akahane M, Wakui K, Kitazawa N, Inaba Y, Fukushima Y, Kosho T. Nishizawa H, et al. Brain Dev. 2022 Mar;44(3):229-233. doi: 10.1016/j.braindev.2021.11.006. Epub 2021 Dec 6. Brain Dev. 2022. PMID: 34876316 Free article.
BACKGROUND: Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome is a contiguous gene deletion syndrome caused by a de novo deletion including the 11p13 region. Although autism spectrum disorder (ASD) is frequently observed …
BACKGROUND: Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome is a contiguous gene delet …
Risk factors for post-nephrectomy hypotension in pediatric patients.
Nishi K, Kamei K, Ogura M, Sato M, Ishiwa S, Shioda Y, Kiyotani C, Matsumoto K, Nozu K, Ishikura K, Ito S. Nishi K, et al. Pediatr Nephrol. 2021 Nov;36(11):3699-3709. doi: 10.1007/s00467-021-05115-7. Epub 2021 May 14. Pediatr Nephrol. 2021. PMID: 33988732
The diagnoses were isolated Wilms tumor, neuroblastoma, congenital nephrotic syndrome, Denys-Drash syndrome, WAGR (Wilms tumor, aniridia, genitourinary malformations, and mental retardation) syndrome, and autosomal recessive polycystic kidney disease i …
The diagnoses were isolated Wilms tumor, neuroblastoma, congenital nephrotic syndrome, Denys-Drash syndrome, WAGR (Wilm …
Malformations, genetic abnormalities, and Wilms tumor.
Dumoucel S, Gauthier-Villars M, Stoppa-Lyonnet D, Parisot P, Brisse H, Philippe-Chomette P, Sarnacki S, Boccon-Gibod L, Rossignol S, Baumann C, Aerts I, Bourdeaut F, Doz F, Orbach D, Pacquement H, Michon J, Schleiermacher G. Dumoucel S, et al. Pediatr Blood Cancer. 2014 Jan;61(1):140-4. doi: 10.1002/pbc.24709. Epub 2013 Aug 23. Pediatr Blood Cancer. 2014. PMID: 23970395
Genetically proven tumor predisposition syndromes (n = 14) frequently observed were syndromes associated with alterations of the chromosome WT1 region such as WAGR (n = 6) and Denys-Drash syndromes (n = 3), syndromes associated with alterations of the WT2 region (Beckwith- …
Genetically proven tumor predisposition syndromes (n = 14) frequently observed were syndromes associated with alterations of the chromosome …
Genetic and hereditary aspects of childhood obesity.
Farooqi IS. Farooqi IS. Best Pract Res Clin Endocrinol Metab. 2005 Sep;19(3):359-74. doi: 10.1016/j.beem.2005.04.004. Best Pract Res Clin Endocrinol Metab. 2005. PMID: 16150380 Review.
Clinical and molecular evidence for the role of androgens and WT1 in testis descent.
Lim HN, Hughes IA, Hawkins JR. Lim HN, et al. Mol Cell Endocrinol. 2001 Dec 20;185(1-2):43-50. doi: 10.1016/s0303-7207(01)00631-1. Mol Cell Endocrinol. 2001. PMID: 11738793 Review.
Whereas subjects with severe, moderate or mild abnormalities and an unknown aetiology, had similar testis positions. The Denys-Drash and WAGR syndrome group had a greater proportion of maldescended testes than the AR mutation (P=0.013) and unknown aetiology groups ( …
Whereas subjects with severe, moderate or mild abnormalities and an unknown aetiology, had similar testis positions. The Denys-Drash and …
Results of Treatment for Patients With Multicentric or Bilaterally Predisposed Unilateral Wilms Tumor (AREN0534): A report from the Children's Oncology Group.
Ehrlich PF, Chi YY, Chintagumpala MM, Hoffer FA, Perlman EJ, Kalapurakal JA, Tornwall B, Warwick A, Shamberger RC, Khanna G, Hamilton TE, Gow KW, Paulino AC, Gratias EJ, Mullen EA, Geller JI, Grundy PE, Fernandez CV, Dome JS. Ehrlich PF, et al. Cancer. 2020 Aug 1;126(15):3516-3525. doi: 10.1002/cncr.32958. Epub 2020 May 27. Cancer. 2020. PMID: 32459384 Free PMC article. Clinical Trial.
BACKGROUND: A primary objective of Children's Oncology Group study AREN0534 (Treatment for Patients With Multicentric or Bilaterally Predisposed, Unilateral Wilms Tumor) was to facilitate partial nephrectomy in 25% of children with bilaterally predisposed unilateral tumors …
BACKGROUND: A primary objective of Children's Oncology Group study AREN0534 (Treatment for Patients With Multicentric or Bilaterally Predisp …
52 results