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of 16
pro vyhledávání: '"Prakash Manikka Lakshmanan"'
Autor:
Radha Sarawagi, Sathya Narayanan, Prakash Manikka Lakshmanan, Sunitha Vellathussery Chakkalakkoombil
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 8, Pp RD03-RD04 (2014)
We report three cases of Hirayama disease, cervical flexion myelopathy presenting as unilateral or bilateral asymmetric muscular atrophy of forearm and hand involving C7 - T1 myotomes in young males. MRI revealed asymmetric cord atrophy, altered sig
Externí odkaz:
https://doaj.org/article/938680fda280470e945baacfbad6d9df
Publikováno v:
Asian Journal of Medical Radiological Research. 7
Publikováno v:
American Journal of Roentgenology. 203:1001-1005
The purpose of this study was to compare the in vitro effects of date syrup with those of other contrast agents by qualitative and quantitative analysis and in vivo evaluation of the use of date syrup to improve the quality of MRCP images.Phantoms co
Autor:
Ajit Kumar Reddy, Prakash Manikka Lakshmanan, Siddarth Ragupathi, Annitha Elavarasi Jayamohan
Publikováno v:
BMJ case reports. 2014
A three-and-half-year-old child with developmental delay presented to the paediatric department with a 2-day history of high-grade fever with chills and rigours. There was associated weakness of the right upper and lower limbs with an episode of seiz
Publikováno v:
The Journal of Medical Sciences. 2:68-69
Scrotal cystocele is a type of urinary bladder hernia, where the bladder herniates into the scrotum. They are not common and constitute to less than 4% of the hernias and bear a gender predilection toward males with history of lower urinary tract sym
Autor:
Annitha Elavarasi Jayamohan, Ajit Kumar Reddy, Sathya Narayanan Renganathan, Prakash Manikka Lakshmanan
Publikováno v:
BMJ case reports. 2014
Introduction Congenital rubella syndrome (CRS) is a spectrum of clinical findings in a patient that results from primary maternal infection with rubella virus. Diagnosis is usually made clinically but imaging findings can prompt the diagnosis in appr
Publikováno v:
BMJ case reports. 2014
Splenogonadal fusion is a rare congenital anomaly. We present the case of a 6-year-old boy who presented with a left inguinoscrotal swelling. With a clinical diagnosis of left congenital inguinal hernia the patient was taken up for explorative laparo
Autor:
Sathya Narayanan, Prakash Manikka Lakshmanan, Sunitha Vellathussery Chakkalakkoombil, Radha Sarawagi
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 8, Pp RD03-RD04 (2014)
We report three cases of Hirayama disease, cervical flexion myelopathy presenting as unilateral or bilateral asymmetric muscular atrophy of forearm and hand involving C7 - T1 myotomes in young males. MRI revealed asymmetric cord atrophy, altered sign
Publikováno v:
Case Reports. 2014:bcr2014204899-bcr2014204899
Macrodystrophia lipomatosa (MDL), a rare non-hereditary congenital disorder of localised gigantism, is characterised by progressive proliferation of all mesenchymal elements, with a disproportionate increase in fibroadipose tissue. We report a case o
Publikováno v:
Case Reports. 2014:bcr2014203686-bcr2014203686
Lipoma arborescens is a rare condition of unknown aetiology with benign diffuse villous proliferation of the synovium characterised by replacement of the subsynovial tissue by mature adipocytes. The knee is the most commonly involved joint.1 A 56-yea