Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Fulton D'Souza"'
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 2, p S20 (2017)
Externí odkaz:
https://doaj.org/article/7e19863837464600ba8eb9cbb47b9256
Publikováno v:
Journal of Pediatric Hematology/Oncology. 41:218-221
INTRODUCTION Children with chronic disorders like β thalassemia major (TM) and their care givers are known to face various psychosocial problems. This study used screening tests to detect these psychosocial issues so that prompt referral for counsel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0ab5ef21969d26d6cf0b704e52a2f31
https://doi.org/10.1097/mph.0000000000001370
https://doi.org/10.1097/mph.0000000000001370
Autor:
Tarangini Durugappa, Smitha Kongalappa, Anand Prakash, Fulton D'Souza, Sitalakshmi Subramanian, Jyothi Muni Reddy
Publikováno v:
Journal of Pediatric Hematology/Oncology. 41:e68-e71
BACKGROUND Glanzmann thrombasthenia (GT) is a globally rare inherited disorder of hemostasis. OBJECTIVES To describe the clinical profile of GT in a tertiary care center in Southern India. METHODS A retrospective chart review of all children with GT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fc7d91e3e58de6dd8318b80568345f8
https://doi.org/10.1097/mph.0000000000001367
https://doi.org/10.1097/mph.0000000000001367
Autor:
Irina Kruzhkova, Fulton D'Souza, Bruce A. Schwartz, Flora Peyvandi, C. Djambas Khayat, SD Lohade, LS Gowda, Cristina Solomon, Omid Reza Zekavat
Publikováno v:
65th Annual Meeting of the Society of Thrombosis and Haemostasis Research.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3609261565f63886abc457512597f27c
https://doi.org/10.1055/s-0041-1728095
https://doi.org/10.1055/s-0041-1728095
Autor:
Claudia Djambas Khayat, Bruce A. Schwartz, Sigurd Knaub, Latha Gowda Shamanur, Flora Peyvandi, Fulton D'Souza, Cristina Solomon, Irina Kruzhkova, Sunil Lohade, Omid Reza Zekavat
Publikováno v:
Haemophilia
Background Congenital fibrinogen deficiency (CFD) is a rare, inherited disorder affecting normal blood clotting function, where patients can experience severe and/or frequent bleeding episodes (BEs). Treatment with human fibrinogen concentrate (HFC)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bf85d9338232150ec566064c37c3d53
https://pubmed.ncbi.nlm.nih.gov/33326665
https://pubmed.ncbi.nlm.nih.gov/33326665
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 2, p S20 (2017)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32b6f40e8e5bff02a90c37f564ab26bf
http://www.sciencedirect.com/science/article/pii/S2468124517302243
http://www.sciencedirect.com/science/article/pii/S2468124517302243
Publikováno v:
The Indian Journal of Pediatrics. 74:859-861
Fanconi's anemia is one of the inherited causes of bone marrow failure. It is inherited in autosomal recessive fashion. It presents as aplastic anemia usually at the age of 7-8 yr. Leukemias and solid tumours are complications in those who manage to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4333dad717624ef32ab456679d7c2667
https://doi.org/10.1007/s12098-007-0154-3
https://doi.org/10.1007/s12098-007-0154-3
Autor:
Sylvan Rego, Sanjoy K Datta, BD Bhatia, Fulton D'Souza, Alix Collard, Sukanta Chatterjee, Jeanne-Marie Jacquet
Publikováno v:
BMC Infectious Diseases, Vol 10, Iss 1, p 298 (2010)
BMC Infectious Diseases
BMC Infectious Diseases
Background Combination vaccines improve coverage, compliance and effectively introduce new antigens to mass vaccination programmes. This was a phase III, observer-blind, randomized study of GSK Biologicals diphtheria-tetanus-whole cell pertussis vacc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1b4bdd706721161a4c2e6b9f1429df4