Zobrazeno 1 - 10
of 2 446
pro vyhledávání: '"11"'
Autor:
Xinglei Shen, Reginald W Dusing, Chris McClinton, Veer A Shah, Jacqueline Hill, S.S. Sood, Maryam Niroumand
Publikováno v:
Practical Radiation Oncology. 7:325-331
Purpose 11 C-acetate positron emission tomography (PET) imaging allows for the detection of occult metastatic disease that may otherwise go undetected with standard imaging for prostate cancer (PCa). The aim of this study was to evaluate lymph node c
Autor:
Cristina Morerio, Maura Acquila, Claudio Panarello, Elisa Tassano, Annamaria Rapella, Cristina Rosanda
Publikováno v:
Cancer Genetics and Cytogenetics. 171:122-125
The inv(11)(p15q22), a rare but recurrent chromosome abnormality that creates a NUP98-DDX10 fusion gene, is associated with de novo or secondary myeloid malignancies. We report a case of acute monocytic leukemia presenting this rearrangement, studied
Autor:
Marc S. Raab, Dirk Hose, Michaela Brough, Marion Moos, Friedrich W. Cremer, Claus R. Bartram, Hans Dieter Hager, Anke Moebus, Mutlu Kartal, Hartmut Goldschmidt, Frauke Bellos, Isabelle Buck, Jelena Bila, Anna Jauch
Publikováno v:
Cancer Genetics and Cytogenetics. 161:116-124
In multiple myeloma, additional copies of chromosome 11 material, reported to confer an unfavorable prognosis, have been found in 20–45% of patients. To assess the incidence and extent of chromosome 11 aberrations, we performed interphase fluoresce
Autor:
Priyanka Katwal
Publikováno v:
International Journal of Surgery Case Reports
Introduction Spontaneous rupture of the primigravid uterus is a rare but catastrophic obstetrical emergency. It usually occurs late in pregnancy or during labour, mainly in multiparous women. But, spontaneous unscarred uterine rupture in a primigravi
Autor:
Noelia Sastre, Marta Alonso-Guervós, Ana Salas-Bustamante, David Hardisson, César Álvarez-Marcos, Andrés Sampedro
Publikováno v:
Oral Oncology. 40:409-417
Squamous cell carcinoma of the pharynx and larynx (SCCPL) is a genetically complex disease and is frequently associated with nonrandom chromosomal alterations. Fifty primary SCC of the pharynx (oropharynx, n=11, and hypopharynx, n=11) and larynx (n=2
Autor:
Cleverson Luciano Trento, Anne Evelyn Oliveira Moura, Sílvia Ferreira de Sousa, Wilton Mitsunari Takeshita, Antônio Carlos Marqueti, Italo Oliveira Barbosa, Erika Rezende Silva
Publikováno v:
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 130:e222
Fibrous dysplasia (FD) is a benign fibro-osseous lesion that accounts for 2.5% of bone lesions. Herein, we present an 11-year-old female patient presented to examination with an increase in volume on the right side of the face with indeterminate evol
Publikováno v:
European Urology
European Urology, 2015, 67 (5), pp.937-942. ⟨10.1016/j.eururo.2014.12.041⟩
European Urology, Elsevier, 2015, 67 (5), pp.937-942. ⟨10.1016/j.eururo.2014.12.041⟩
European Urology, 2015, 67 (5), pp.937-942. ⟨10.1016/j.eururo.2014.12.041⟩
European Urology, Elsevier, 2015, 67 (5), pp.937-942. ⟨10.1016/j.eururo.2014.12.041⟩
Background Artificial urinary sphincter (AUS) implantation is recommended for women suffering urinary stress incontinence. Robot-assisted laparoscopy allows improved dexterity and visibility compared to traditional laparoscopy, potentially providing
Autor:
Henrique Wambier, Renata Coutinho Ribeiro, Rodrigo Kohler, Elcio Izumi Mizoguchi, Leonardo Marques Gomes, José Antonio Pinto
Publikováno v:
Brazilian Journal of Otorhinolaryngology. 79(5):564-568
Laryngomalacia is the most frequent congenital abnormality of the larynx, accounting for approximately 60-75% of congenital stridor cases. Despite its benign and self-limited aspects, 10% of cases require intervention. Currently, supraglottoplasty is
Publikováno v:
Human Immunology. 79:99
We present an 11 yr old girl who received 3 kidney transplants (KTx). She received 1st-KTx from a living donor at age 4 due to the end-stage renal disease. She had no HLA antibodies (Ab) at pre-1st-KTx, and thus pre-tx crossmatch (XM) and donor-speci
Autor:
Kit Wu, Paul Su, Richard Nicholas, Marios Politis, Paola Piccini, Richard Reynolds, Paolo Giannetti, Omar Malik, Federico Turkheimer, Shiva Keihaninejad
Publikováno v:
Neurobiology of Disease, Vol 65, Iss, Pp 203-210 (2014)
The pathophysiological correlates and the contribution to persisting disability of hypointense T1-weighted MRI lesions, black holes (BH), in multiple sclerosis (MS) are still unclear. In order to study the in vivo functional correlates of this MRI fi