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Browsing Journal Publications by Issue Date

Browsing Journal Publications by Issue Date

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  • Geetha Krishnanand; Manpreet Kaur; Rao, Ravikala V.; Monappa, Vidya (Wolters Kluwer-Medknow, 2007)
  • Pervatikar, S. K.; Rao, Ravikala V.; Dinesh, U. S.; Parameswaraiah, S. (Wolters Kluwer-Medknow, 2009-04)
  • Pervatikar, S. K.; Rao, Ravikala V.; Dinesh, U. S. (Wolters Kluwer-Medknow, 2009-04)
  • Jayakumar, Nirmala M.; Parshawnath, H. A.; Patil, A. M. (Al Ameen Medical College, Bijapur, 2010)
    Chordoma, lesion derived from the notochord, represents about 4% of the primary malignant bone tumours. Males are affected more commonly than females and it is very rare in children;the peak incidence is in the sixth ...
  • Parshawnath, H. A.; Kulkarni, Padmaja R.; Rao, Ravikala V.; Joshi, Shyamsundar K.; Patil, Preetam B. (Wolters Kluwer-Medknow, 2010-04)
  • Pathan, Zaheer Abbas Ali Khan; Dinesh, U. S.; Rao, Ravikala V. (Wolters Kluwer-Medknow, 2010-07)
    Endometriosis is the presence of functioning endometrium outside the uterus. Endometriosis rarely occurs in the abdominal wall. Majority of abdominal wall endometriosis occur in or adjacent to surgical scars, following ...
  • Kamat, Girish C.; Grampurohit, Vandana U.; Myageri, Aneel; Shettar, Chidendra M. (Hindawi Publishing Corporation, 2011)
    Xanthogranulomatous osteomyelitis is a very rare form of chronic osteomyelitis which presents like a bone tumor. Three cases of xanthogranulomatous osteomyelitis have been described previously in the literature. We present ...
  • Grampurohit, Vandana U.; Rao, Ravikala V.; Dinesh, U. S. (Al Ameen Medical College, Bijapur, 2011)
    A ganglioneuroma is a very rare neoplasm in the gastrointestinal tract and a benign neoplasm of sympathetic nervous system. They predominantly affect the colon and rectum and are rare to arise in gall bladder. Gastrointestinal ...
  • Parinitha, S. S.; Jayakumar, Nirmala M.; Yaliwal, Laxmi V. (Manipal Colleges of Medical Sciences, 2011)
    We report a rare case of prolapsed omentum presenting as mass per vagina in a 24 year old unmarried female follow- ing dilatation and curettage for termination of pregnancy by unqualified physician. Patient presented to ...
  • Grampurohit, Vandana U.; Dinesh, U. S.; Rao, Ravikala V. (Wolters Kluwer-Medknow, 2011-04)
    Xeroderma pigmentosum is a genodermatosis characterized by photosensitivity and the development of cutaneous and internal malignancies at an early age. The basic defect underlying the clinical manifestations is a nucleotide ...
  • Grampurohit, Vandana U.; Dinesh, U. S.; Rao, Ravikala V. (Wolters Kluwer-Medknow, 2011-04)
  • Kamat, Girish C. (South African Academy of Family Physicians, 2011-05)
    Background: Lymphadenopathy is a rather common clinical finding in a primary healthcare setting, and may be due to inflammatory lesions and tumours. Correlation between clinical findings and laboratory data is essential ...
  • Grampurohit, Vandana U.; Myageri, Aneel; Rao, Ravikala V. (Wolters Kluwer-Medknow, 2011-05)
    Primary synovial sarcoma (SS) of kidney is very rare and difficult to diagnose. Here, we present a case of a 21-year-old female clinically diagnosed as renal cell carcinoma. Right nephrectomy specimen showed a cystic ...
  • Kulkarni, Padmaja R.; Rao, Ravikala V.; Alur, Mohan B.; Joshi, Shyamsundar K. (Wolters Kluwer-Medknow, 2011-07)
    Iniencephaly is a rare neural tube defect characterized by extreme retroflexion of the head with the absence of neck due to spinal deformities. The important features that help us to diagnose a case of iniencephaly are ...
  • Grampurohit, Vandana U.; Naidu, Nirmala R.; Rao, Ravikala V.; Desai, Rathnamala M. (Society for Basic Medical Sciences, 2011-07)
    Carpenter syndrome (Acrocephalopolysyndactyly Type II) is a rare autosomal recessive syndrome characterized by acrocephaly, facial dysmorphism and polysyndactyly. There is marked phenotypic variability noted in this ...
  • Grampurohit, Vandana U.; Dinesh, U. S.; Rao, Ravikala V. (Wolters Kluwer-Medknow, 2011-10)
    Nodular hidradenoma is an established entity as a skin adnexal tumor arising from eccrine sweat glands. A skin adnexal tumor located in the breast is unusual and is one of the differential diagnoses for subareolar breast ...
  • Hephzibah, Rani S.; Kanbur, Deepak (Wolters Kluwer-Medknow, 2012)
    he Chediak Higashi Syndrome (CHS) is a rare autosomal recessive disease characterized by partial oculo-cutaneous albinism, frequent pyogenic infections, presence of giant granules in leucocytes and other granule containing ...
  • Parinitha, S. S.; Kulkarni, M. H. (Australian Medical Association, 2012)
    Abstract Background HIV infection is associated with a wide range of haematological abnormalities. Methods and Objectives The objectives in this study were to study haematological changes in HIV patients and to ...
  • Kamat, Girish C.; Myageri, Aneel; Rao, Ravikala V. (Hindawi Publishing Corporation, 2012)
    Osteonevus of Nanta is a rare histopathological finding in which there is an ectopic bone formation in intradermal nevus. Very few cases have been reported so far in the literature. We present a case of osteonevus of ...
  • Pathan, Zaheer Abbas Ali Khan; Chaudappa, J. S.; Parshawnath, H. A.; Lakshmi, D. K. B. (Indian Journal of Research and Reports in Medical Sciences, 2012-01)
    Cardiac tamponade as the first presenting symptom of metastatic malignancy is very rare. A 45 year male presented with dyspnea and productive cough. Chest X-ray, echocardiogram and ECG showed pericardial effusion with ...

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