Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sona B Nair"'
Autor:
Bipin P Kulkarni, Sona B Nair, Manasi Vijapurkar, Leenam Mota, Sharda Shanbhag, Shehnaz Ali, Shrimati D Shetty, Kanjaksha Ghosh
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e108683 (2014)
BackgroundThough rare in occurrence, patients with rare bleeding disorders (RBDs) are highly heterogeneous and may manifest with severe bleeding diathesis. Due to the high rate of consanguinity in many caste groups, these autosomal recessive bleeding
Externí odkaz:
https://doaj.org/article/e4d25ae4a78646f6a6fc35a903eaf86b
Publikováno v:
Hemoglobin. 46:269-271
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afd2593e0a407244864ed89ecd667e6b
https://doi.org/10.1080/03630269.2022.2122497
https://doi.org/10.1080/03630269.2022.2122497
Autor:
Sona B. Nair
Publikováno v:
Journal of Rare Diseases Research & Treatment. 3:9-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6e868c6fe85543b6b2d59a8fdd4480f
https://doi.org/10.29245/2572-9411/2018/3.1161
https://doi.org/10.29245/2572-9411/2018/3.1161
Publikováno v:
Hemoglobin. 42(5-6)
We here report a case of a 23-year-old female from Mumbai, Maharashtra, India who was detected to carry the α chain variant Hb J-Norfolk [HBA2: c.173G>A (or HBA1]. She had no clinical symptoms and was referred to us for routine investigations and sc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7642e49f722749f202f84ef6cd45b181
https://pubmed.ncbi.nlm.nih.gov/30646764
https://pubmed.ncbi.nlm.nih.gov/30646764
Autor:
Arundhati S. Athalye, Sona B. Nair, Raju Khubchandani, Ivona Aksentijevich, Pallavi Pimpale Chavan
Publikováno v:
Clinical rheumatology. 38(2)
Neonatal-Onset Multisystem Inflammatory Disease (NOMID) or Chronic Infantile Neurologic Cutaneous Articular (CINCA) syndrome is a monogenic autoinflammatory disorder characterized by urticarial skin rash, fever, chronic meningitis and joint manifesta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddb8fc437f6677018393a9787705384a
https://pubmed.ncbi.nlm.nih.gov/30066283
https://pubmed.ncbi.nlm.nih.gov/30066283
Publikováno v:
Hemoglobin. 37:277-284
The aim of this study was to identify the molecular defects leading to the variable clinical and hematological presentation of four patients with Hb H disease. Investigations included a complete blood count, high performance liquid chromatography (HP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dc48a8b21209458fa3f4ed9571ae4b5
https://doi.org/10.3109/03630269.2013.774284
https://doi.org/10.3109/03630269.2013.774284
Publikováno v:
Journal of Clinical Pathology; Jul2012, Vol. 65 Issue 7, p654-659, 6p