Výsledky vyhledávání - "Dutta Anupam"

Akademický článek

Management of a patient with factor X deficiency with FEIBA: a case report

Publikováno v: The Journal of Haemophilia Practice, Vol 10, Iss 1, Pp 68-73 (2023)

Hereditary factor X (FX) deficiency is a rare autosomal recessive disorder that increases bleeding tendencies, ranging from epistaxis to intracranial haemorrhage (ICH), which can be life-threatening. Single factor concentrates are recommended for tre

Externí odkaz: https://doaj.org/article/7272ec6bebcf4693a715acf70b96dee9

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Akademický článek

Clinical and radiological assessment of joints in people with haemophilia in Assam, Northeast India: a cross-sectional study

Autor: Dhal Bhabani Sankar, Dutta Anupam, Das Arijit, Borpatragohain Dhrubajyoti, Sharma Adity, Kashyap Arnav

Publikováno v: The Journal of Haemophilia Practice, Vol 10, Iss 1, Pp 11-19 (2023)

Despite the availability of factor replacement therapy, including prophylaxis, to treat and prevent bleeding, haemophilic arthropathy continues to be the most common complication of haemophilia and significantly impairs the quality of life in people

Externí odkaz: https://doaj.org/article/b383485d4699412eb69a1cb895ff673f

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Akademický článek

Treatment of a patient with severe haemophilia A presenting with left extra pleural haematoma and diagnosed with inhibitors – case report

Autor: Das Arijit, Dutta Anupam, BBV Ramanan, Sreeraj Sanchu TK

Publikováno v: The Journal of Haemophilia Practice, Vol 9, Iss 1, Pp 79-84 (2022)

Haemophilia is an inherited X-linked bleeding disorder characterised by a deficiency or absence of clotting factor VIII (haemophilia A) or IX (haemophilia B), which can cause musculoskeletal bleeding. The standard treatment for haemophilia is with fa

Externí odkaz: https://doaj.org/article/8537a72753cb4d34a2dcd13ff31e93ee

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Akademický článek

Improvement in school absence after factor replacement in students with haemophilia in Upper Assam, India

Autor: Dutta Anupam, Boruah Dipjyoti, Dutta Taniya Sarkar, Boruah Angshuman, Dhal Bhabani Shankar

Publikováno v: The Journal of Haemophilia Practice, Vol 7, Iss 1, Pp 136-142 (2020)

Patients with haemophilia who are not adequately treated experience a lifetime burden of joint complications and loss of functional ability due to repeated bleeding episodes caused by low levels of clotting factor VIII or IX in the blood. These compl

Externí odkaz: https://doaj.org/article/d0acb26ee92d4d6c967750355fa16e2c

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Akademický článek

Haemostatic action of a topical foam-based patch (VELSEAL-T) in haemophiliac patients with external bleeding

Autor: Dutta Anupam, Dutta Taniya Sarkar, Das Anup Kumar, Dey Pranoy

Publikováno v: The Journal of Haemophilia Practice, Vol 7, Iss 1, Pp 78-84 (2020)

Haemophilia is an X-linked congenital bleeding disorder due to deficiency of coagulation factor VIII (in haemophilia A) or factor IX (in haemophilia B) caused by mutations of the respective clotting factor genes. Treatment involves the administration

Externí odkaz: https://doaj.org/article/b24060676c60441db10837601546b6ce

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