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  1. AU="Cyriac, Sanju"
  2. AU="Axtmayer, Jossette"
  3. AU="Sato, Shusuke"
  4. AU="Debasis Mondal"
  5. AU="Hollingsworth, Neal A"
  6. AU=Restifo Nicholas P AU=Restifo Nicholas P
  7. AU="Farmer, Claire"
  8. AU="Hyeong, Seok-Ki"
  9. AU=Sathananthan A Henry
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  11. AU="Abouelkhair, Mohamed A"
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  15. AU="Gill, J L"
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  20. AU="Bovino, Antonio"
  21. AU="Deseri, Luca"
  22. AU="Cunningham, C W"
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  26. AU="Xie, Hong-Guang"
  27. AU="Ford, Paul Leicester"
  28. AU="Garver-Daniels, N. E."
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  30. AU="Inoue, Kazunori"
  31. AU="Tüzün, Funda"
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  33. AU="Puche-Cañas, Emilio"
  34. AU="Rahim, Faraan O"
  35. AU="Barritt, Andrew W"

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  1. Artikel: Durable Response with Single-Agent Pembrolizumab in a Patient with Metastatic Melanoma.

    Cyriac, Sanju / Toms, Ajith / Thomas, Sunitha

    South Asian journal of cancer

    2021  Band 11, Heft 1, Seite(n) 82–83

    Sprache Englisch
    Erscheinungsdatum 2021-11-11
    Erscheinungsland India
    Dokumenttyp Case Reports
    ZDB-ID 2719571-5
    ISSN 2278-4306 ; 2278-330X
    ISSN (online) 2278-4306
    ISSN 2278-330X
    DOI 10.1055/s-0041-1731911
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Durable Response with Single-Agent Pembrolizumab in a Patient with Metastatic Melanoma

    Cyriac, Sanju / Toms, Ajith / Thomas, Sunitha

    South Asian Journal of Cancer

    2021  Band 11, Heft 01, Seite(n) 82–83

    Sprache Englisch
    Erscheinungsdatum 2021-11-11
    Verlag Thieme Medical and Scientific Publishers Pvt. Ltd.
    Erscheinungsort Stuttgart ; New York
    Dokumenttyp Artikel
    ZDB-ID 2719571-5
    ISSN 2278-4306 ; 2278-330X ; 2278-4306
    ISSN (online) 2278-4306
    ISSN 2278-330X ; 2278-4306
    DOI 10.1055/s-0041-1731911
    Datenquelle Thieme Verlag

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  3. Artikel ; Online: PAX8-Positive Intrahepatic Cholangiocarcinoma-a Rare and Hardly Recognized Entity.

    Mathew, Rishi Philip / Sleeba, Teena / Abraham, Latha K / Cyriac, Sanju / Toms, Ajith

    Journal of gastrointestinal cancer

    2021  Band 52, Heft 3, Seite(n) 1102–1105

    Mesh-Begriff(e) Bile Duct Neoplasms/diagnostic imaging ; Bile Duct Neoplasms/genetics ; Bile Duct Neoplasms/pathology ; Cholangiocarcinoma/diagnostic imaging ; Cholangiocarcinoma/genetics ; Cholangiocarcinoma/pathology ; Female ; Humans ; Middle Aged ; PAX8 Transcription Factor/genetics
    Chemische Substanzen PAX8 Transcription Factor ; PAX8 protein, human
    Sprache Englisch
    Erscheinungsdatum 2021-01-06
    Erscheinungsland United States
    Dokumenttyp Case Reports ; Journal Article
    ZDB-ID 2452514-5
    ISSN 1941-6636 ; 1559-0739 ; 1941-6628 ; 1537-3649
    ISSN (online) 1941-6636 ; 1559-0739
    ISSN 1941-6628 ; 1537-3649
    DOI 10.1007/s12029-020-00571-0
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Follicular dendritic cell sarcoma of the neck with an aggressive and fatal course

    Cyriac Sanju / Praveenkumar David / Majhi Urmila / Sagar T

    Journal of Cancer Research and Therapeutics, Vol 6, Iss 1, Pp 114-

    2010  Band 116

    Abstract: Dendritic cell neoplasms are rare malignancies described with an increased frequency. They often involve the lymph nodes, but extranodal presentations are also described. The disease often has an indolent course. Surgery is the main modality though ... ...

    Abstract Dendritic cell neoplasms are rare malignancies described with an increased frequency. They often involve the lymph nodes, but extranodal presentations are also described. The disease often has an indolent course. Surgery is the main modality though chemotherapy and radiation have also been tried. We present here a case of a 69-year-old male diagnosed to have follicular dendritic cell sarcoma of the neck which had a rapid and fatal course inspite of chemotherapy and radiotherapy. More studies are required to assess the biology of this rare tumor.
    Schlagwörter Dendritic cell neoplasm ; immunohistochemistry ; sarcoma ; Neoplasms. Tumors. Oncology. Including cancer and carcinogens ; RC254-282 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Oncology ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Sprache Englisch
    Erscheinungsdatum 2010-01-01T00:00:00Z
    Verlag Medknow Publications
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  5. Artikel ; Online: Ataxia telangiectasia

    Seshachalam Arun / Cyriac Sanju / Reddy Neelesh / Gnana Sagar

    Indian Journal of Human Genetics, Vol 16, Iss 1, Pp 39-

    Family management

    2010  Band 42

    Abstract: Ataxia telangiectasia (AT) is a rare autosomal recessive disease resulting in progressive degeneration of multiple systems in the body. Both A-T homozygote and heterozygote are at increased risk of developing malignancy. We report a family in which three ...

    Abstract Ataxia telangiectasia (AT) is a rare autosomal recessive disease resulting in progressive degeneration of multiple systems in the body. Both A-T homozygote and heterozygote are at increased risk of developing malignancy. We report a family in which three generations were affected by this disorder. Our index case is a 12-year-old female child, born of second degree consanguineous marriage diagnosed to have ataxia telangiectasia at the age of four years, now presented with fever and neck swelling of one month duration. Family history suggestive of ataxia telangiectasia in maternal uncle and younger sibling was present. History of premature coronary artery disease and death in paternal grandfather was present. On evaluation, child was diagnosed to have Alk negative anaplastic large T cell lymphoma. Management included genetic counseling, examination of all the family members, identification of A-T homozygote and providing appropriate care, regular surveillance of the heterozygote for malignancy.
    Schlagwörter Ataxia Telangiectasia ; family management ; malignancy ; Genetics ; QH426-470 ; Biology (General) ; QH301-705.5 ; Science ; Q ; DOAJ:Genetics ; DOAJ:Biology ; DOAJ:Biology and Life Sciences
    Thema/Rubrik (Code) 900
    Sprache Englisch
    Erscheinungsdatum 2010-01-01T00:00:00Z
    Verlag Medknow Publications
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  6. Artikel ; Online: Clinicopathological analysis and outcome of primary mediastinal malignancies - A report of 91 cases from a single institute

    Dubashi Biswajit / Cyriac Sanju / Tenali Sagar

    Annals of Thoracic Medicine, Vol 4, Iss 3, Pp 140-

    2009  Band 142

    Abstract: Background: Primary mediastinal malignancies are uncommon. They can originate from any mediastinal organ or tissue but most commonly arise from thymic, neurogenic, lymphatic, germinal or mesenchymal tissues. Objectives: The aim of this study was to ... ...

    Abstract Background: Primary mediastinal malignancies are uncommon. They can originate from any mediastinal organ or tissue but most commonly arise from thymic, neurogenic, lymphatic, germinal or mesenchymal tissues. Objectives: The aim of this study was to review the clinical presentations, diagnostic methods adopted, the histologies and the treatment outcomes of this rare subset of tumors. Materials and Methods: Case records of 91 patients in the period 1993-2006 at our institute were retrospectively analyzed. Patients with primary mediastinal mass and supraclavicular nodes were included for the analysis. Patients with primary, extrathoracic disease of the lung and peripheral adenopathy were excluded. Actuarial method was used for calculating the disease-free survival and overall survival. Results: Primary mediastinal tumors were seen commonly in males with mean age of 37.48 ± 17.04 years. As many as 97% of patients were symptomatic at presentation. Superior venacaval obstruction (SVCO) was seen in 28% of the patients. As many as 50% of the patients were diagnosed by a fine-needle aspiration or Trucut biopsy, while 28% of the patients required thoracotomy for a diagnosis. Majority of the tumors had anterior mediastinal presentation. Pleural effusion was seen in 20% of the patients, but diagnosis was obtained in only 1%. In adults, thymoma (39%), lymphoma (30%) and germ cell tumor (15%) were the common tumors. In the pediatric population, lymphoma, PNET and neuroblastoma were the common tumors. The 5-year DFS and OS are 50% and 55%, respectively. Conclusion: Primary mediastinal tumors are a challenge to the treating physician because of their unique presentation in the form of medical emergencies, like superior venacaval obstruction and stridor. Diagnosis may require invasive procedures like thoracotomy. Treatment and outcome depend on the histologic subtypes.
    Schlagwörter Germ cell tumor ; lymphoma ; primary mediastinal tumor ; thymoma ; Diseases of the respiratory system ; RC705-779 ; Specialties of internal medicine ; RC581-951 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Internal medicine ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Thema/Rubrik (Code) 610
    Sprache Englisch
    Erscheinungsdatum 2009-01-01T00:00:00Z
    Verlag Medknow Publications
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  7. Artikel ; Online: Choriocarcinoma with arterial and venous thrombosis

    Cyriac Sanju / Sagar T / Mahajan Vandana

    Neurology India, Vol 57, Iss 4, Pp 505-

    2009  Band 507

    Schlagwörter Neurology. Diseases of the nervous system ; RC346-429 ; Neurosciences. Biological psychiatry. Neuropsychiatry ; RC321-571 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Neurology ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Sprache Englisch
    Erscheinungsdatum 2009-01-01T00:00:00Z
    Verlag Medknow Publications
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  8. Artikel ; Online: Immune hemolytic anemia in a patient with tuberculous lymphadenitis.

    Nandennavar, Manjunath / Cyriac, Sanju / Krishnakumar / Sagar, Tg

    Journal of global infectious diseases

    2011  Band 3, Heft 1, Seite(n) 89–91

    Abstract: Anemia in tuberculosis is usually anemia of chronic disease. Severe hemolytic anemia is exceedingly rare in tuberculosis patients. We report a patient diagnosed with tubercular lymphadenitis complicated by Coomb's positive hemolytic anemia. Patient ... ...

    Abstract Anemia in tuberculosis is usually anemia of chronic disease. Severe hemolytic anemia is exceedingly rare in tuberculosis patients. We report a patient diagnosed with tubercular lymphadenitis complicated by Coomb's positive hemolytic anemia. Patient responded well to antituberculous treatment. Hematological parameters improved after initiation of antituberculosis treatment. To the best of our knowledge, this is the first case from India of an adult patient with tuberculous lymphadenitis presenting with Coomb's positive hemolytic anemia.
    Sprache Englisch
    Erscheinungsdatum 2011-03-18
    Erscheinungsland India
    Dokumenttyp Case Reports
    ZDB-ID 2545454-7
    ISSN 0974-8245 ; 0974-777X
    ISSN (online) 0974-8245
    ISSN 0974-777X
    DOI 10.4103/0974-777X.77303
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Primary Burkitt′s lymphoma of the ovary

    Cyriac Sanju / Srinivas Lakshmi / Mahajan Vandana / Sundersingh Shirley / Sagar T

    African Journal of Paediatric Surgery, Vol 7, Iss 2, Pp 120-

    2010  Band 121

    Schlagwörter Pediatrics ; RJ1-570 ; Medicine ; R ; DOAJ:Pediatrics ; DOAJ:Medicine (General) ; DOAJ:Health Sciences ; Surgery ; RD1-811 ; DOAJ:Surgery
    Sprache Englisch
    Erscheinungsdatum 2010-01-01T00:00:00Z
    Verlag Medknow Publications
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  10. Artikel: L-asparaginase induced fatal cortical venous thrombosis in acute lymphoblastic leukemia.

    Cyriac, Sanju / Sagar, T G / Shashidhar, Karpurmath V

    Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

    2010  Band 26, Heft 1, Seite(n) 8–11

    Abstract: L-asparaginase has become an integral part in the treatment of acute lymphoblastic leukemia. The major worry of using L-asparaginase is thromboembolism. The case presented here is a 21-year-old lady who developed fatal cortical venous thrombosis during ... ...

    Abstract L-asparaginase has become an integral part in the treatment of acute lymphoblastic leukemia. The major worry of using L-asparaginase is thromboembolism. The case presented here is a 21-year-old lady who developed fatal cortical venous thrombosis during induction phase of treatment for ALL. Early recognition is very important to treat this potentially catastrophic yet treatable complication.
    Sprache Englisch
    Erscheinungsdatum 2010-08-04
    Erscheinungsland India
    Dokumenttyp Journal Article
    ZDB-ID 2422370-0
    ISSN 0974-0449 ; 0971-4502
    ISSN (online) 0974-0449
    ISSN 0971-4502
    DOI 10.1007/s12288-010-0005-7
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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