نتایج جستجو برای: wilms tumor gene 1

تعداد نتایج: 3825016  

2017
Richard H. Scott Nazneen Rahman

Wilms tumor is a primarily sporadic disease, with only 1–2 % of affected individuals having a relative with Wilms tumor. However, bilateral Wilms tumors occur in approximately 5 % of cases, and Wilms tumor has been reported in association with more than 50 different genetic disorders, pointing to an underlying predisposition in further individuals. There is conclusive evidence of an increased r...

2012
Sang Hun Lee Min Ho Bae Sung Ho Choi Jin Seok Lee Young Sam Cho Kwan Joong Joo Chil Hun Kwon Heung Jae Park

The incidence of horseshoe kidney is about 1 in 400 cases. The presence of Wilms' tumor with a horseshoe kidney is unusual, and the occurrence of Wilms' tumor in a horseshoe kidney is estimated at 0.4 to 0.9% of all Wilms' tumors. We report the case of a 5-year-old boy who presented with a stage IV Wilms' tumor in a horseshoe kidney. The patient was treated with preoperative chemotherapy follow...

Journal: :Turkish Journal of Hematology 2019

Journal: :iranian journal of child neurology 0
ahmad talebian* 1. trauma research center, kashan university of medical sciences, kashan, iran 2. department of pediatrics, kashan university of medical sciences, kashan, iran razeieh goudarzi 1. department of pediatrics, kashan university of medical sciences, kashan, iran mahdi mohammadzadeh 1. trauma research center, kashan university of medical sciences, kashan, iran 2. department of pediatrics, kashan university of medical sciences, kashan, iran azadeh sadat mirzadeh 1. department of pediatrics, kashan university of medical sciences, kashan, iran

how to cite this article: talebian a, goudarzi rm, mohammadzadeh m , mirzadeh as. vincristine-induced cranial neuropathy. iran j child neurol. 2014 winter; 8(1):66-68.   abstract vincristine (vcr) is a vinca alkaloid that is used for treatment of many malignancies. the vinca alkaloids are neurotoxic, usually causing a peripheral neuropathy, but cranial neuropathies are rare as side effects.  de...

2015
Hong-Chuan Niu Wei-Ping Zhang Ning Sun Le-Jian He Yun Peng

IntroductIon Nephrogenic rests (NRs) are abnormally persistent clusters of embryonal cells, representing microscopic dysplasias of the developing kidney. NRs are found in approximately 1% of infant kidneys at autopsy. Nephroblastomatosis signifies the presence of multiple or diffuse NRs. Both NRs and nephroblastomatosis were known as precursor lesions of Wilms’ tumor.[1] Nephroblastomatosis can...

2007
Ajit Mahale Vinaya Poornima Manish Shrestha Manish K Shrestha

The WAGR syndrome is a multiple congenital anomaly–mental retardation syndrome caused by interstitial deletion of the distal portion of chromosome 11p13. It is a contiguous gene deletion syndrome, and WAGR is an acronym for the primary features: W for Wilms tumor, A for aniridia, G for genital anomalies, and R for mental retardation. Wilms tumor and male genital anomalies are caused by deletion...

Journal: :Fertility and sterility 2009
An Coosemans Philippe Moerman Ignace Vergote Philippe R Koninckx Stefaan W Van Gool Frédéric Amant

Innervation of deep endometriosis has recently been linked to its severe pain symptoms. We demonstrated for the first time that the Wilms' tumor gene 1 is overexpressed in part of these nerves.

Journal: :Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica 2011
M E Molina Vázquez A Sánchez Abuín R Aguilar Cuesta

INTRODUCTION Minimally invasive surgery (CMI) for the treatment of malignant tumors in children begins to have a role for selected cases and reaches similar results than open surgery. We show our first two cases of Wilms tumor treated by laparoscopy describing patients and technique. MATERIAL AND METHODS Three-year-old girl with macroscopic hematuria is diagnosed of 8 cm mass in the left kidn...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Aleksandra Bielen Gary Box Lara Perryman Lynn Bjerke Sergey Popov Yann Jamin Alexa Jury Melanie Valenti Alexis de Haven Brandon Vanessa Martins Vincent Romanet Sebastien Jeay Florence I Raynaud Francesco Hofmann Simon P Robinson Suzanne A Eccles Chris Jones

We have previously demonstrated an increased DNA copy number and expression of IGF1R to be associated with poor outcome in Wilms tumors. We have now tested whether inhibiting this receptor may be a useful therapeutic strategy by using a panel of Wilms tumor cell lines. Both genetic and pharmacological targeting resulted in inhibition of downstream signaling through PI3 and MAP kinases, G(1) cel...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید