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Rajeev Rahi Manoj Biswas Rahul Khanna A. K. Khanna 《The Indian journal of surgery》2010,72(2):138-139
We report a rare case of extragonadal germ cell tumour in a 55-year-old man. He presented with a painless mass in right inguinal
region, a few days after hernioplasty for right direct inguinal hernia, which caused diagnostic difficulties and treatment
problems. 相似文献
94.
Aparna Mitra Lalita A. Shevde Rajeev S. Samant 《Clinical & experimental metastasis》2009,26(6):559-567
HSP40 (DNAJ) is an understudied family of co-chaperones. The human genome codes for over 41 members of HSP40 family that reside
at distinct intracellular locations. Despite their large numbers, little is known about their physiologic roles. Recent research
has revealed involvement of some of the DNAJ family members in various types of cancers. In this article we summarize the
information about the involvement of human DNAJ family members in various aspects of cancer biology. Furthermore we discuss
the potential role of the J domain of DNAJ proteins in cancer biology. 相似文献
95.
Dnyanesh Arun Limaye Anil Yashvant Nimbkar Rajeev Jain Mansoor Ahmad 《Phytotherapy research : PTR》1995,9(1):37-40
The aqueous extract of stem bark of Moriga pterygosperma (Family Moraingaceae) was investigated for its effect on various pharmacological parameters. In cardiovascular profile at lower concentrations (1–10 ng) it produced a dose dependent positive inotropic effect (n = 3, 1.29 ± 0.021 for 10 ng) and at higher concentrations (0.1–1 μg) a dose dependent negative inotropic effect (n = 3, 0.53 ± 0.033 for 1 μg) on the isolated frog heart. It also produced a dose dependent hypotensive effect on dog blood pressure (n = 3, 82 ± 0.98 for 20 mg/kg). It failed to elicit any effect on isolated guinea-pig ileum, rat stomach fundus or frog rectus abdominis muscle. 相似文献
96.
Genitourinary tuberculosis is an important cause of morbidity in developing and developed countries. We describe a case of extensive genitourinary tuberculosis in which there was complete destruction of the right kidney, stricture of the entire left ureter and an autocystectomized bladder. He presented in azotemia with urinary incontinence and was managed by right nephroureterectomy, ileal replacement of left ureter and ileal neobladder after a preliminary nephrostomy and antituberculous chemotherapy. 相似文献
97.
Panda A Sudan R Nainiwal S 《American journal of ophthalmology》2002,133(4):590; author reply 590-590; author reply 591
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Sudan R Khokhar S Sony P 《Journal of cataract and refractive surgery》2002,28(8):1308-9; author reply 1309
100.
Prion diseases is another name for a group of 'transmissible spongiform encephalopathies'. Creutzfeldt-Jakob disease, the first prion disease described in humans, occurs in sporadic, familial or iatrogenic form. Other transmissible spongiform encephalopathies in humans such as familial Creutzfeldt-]akob disease, Gerstmann-Str?ussler-Scheinker disease and fatal familial Insomnia have been shown to be associated with specific prion protein gene mutations. In 1996, a new variant of Creutzfeldt-Jakob disease was reported in the United Kingdom among young patients with unusual clinical features and unique neuropathological findings. This new form could be due to transmission to humans of the agent causing bovine spongiform encephalopathy. While examination of brain tissue is the key to making a diagnosis, it is not always possible antemortem. Immunological tests such as ELISA or western blot assays along with tests for 1 4-3-3 protein in the cerebrospinal fluid remain the main tools of diagnosis. Conventional disinfection and sterilization practices are Ineffective for these agents. The unusual properties of prions pose a challenge for treatment, surveillance and control of these diseases. 相似文献