Zobrazeno 1 - 10 of 51 pro vyhledávání: '"Haseena, Sait"'
1
Akademický článek
Effect of Maternal Iodine Excess during Pregnancy on Neonatal Thyroid Function and Neurodevelopmental Status at 12 Weeks
Autor: Deepashree K Rao, Ankur Jindal, Aashima Dabas, Haseena Sait, Sangeeta Yadav, Seema Kapoor
Publikováno v: Journal of the ASEAN Federation of Endocrine Societies (2024)
Objective. This study aims to determine the effect of iodine excess in pregnant mothers on thyroid function, growth and neurodevelopment in the neonates when assessed at 12 weeks of age. Methodology. This prospective study enrolled term neonates wi
Externí odkaz: https://doaj.org/article/0b5a242152bc412aa8137b36caf43ace
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2
Akademický článek
Loes Score: Clinical and Radiological Profile of 22 Patients of X-Linked Adrenoleukodystrophy: Case Series from a Single Center
Autor: Somesh Kumar, Haseena Sait, Sunil K. Polipalli, Gaurav S. Pradhan, Sumit Pruthi, Seema Kapoor
Publikováno v: Indian Journal of Radiology and Imaging, Vol 31, Iss 02, Pp 383-390 (2021)
Introduction X-linked adrenoleukodystrophy (X-ALD) is a devastating disease with a wide spectrum of presentation ranging from asymptomatic to a rapidly progressive childhood cerebral form. The gene responsible for adrenoleukodystrophy is ABCD1 gene,
Externí odkaz: https://doaj.org/article/da0850d3ef7b4764be4161a91db41f38
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3
Akademický článek
Dental phenotype of multiple impacted supernumerary teeth in Wiedemann–Steiner syndrome
Autor: Priyanka Verma, Seema Kapoor, Haseena Sait, Sujoy Ghosh, Sunita Gupta
Publikováno v: Journal of Cleft Lip Palate and Craniofacial Anomalies, Vol 7, Iss 1, Pp 59-63 (2020)
Wiedemann–Steiner syndrome (WSS) is a rare autosomal dominant disorder characterized by short stature, intellectual disability, developmental delay, hypertrichosis cubiti, and dysmorphic facial features (thick eyebrows with a lateral flare, long ey
Externí odkaz: https://doaj.org/article/a4f625bf1a5944d4a46b715e200b7061
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9
Haemophilia management programme: Transformation during COVID-19
Autor: Haseena Sait, Shruti M. Sajjan, Shubha R. Phadke
Publikováno v: The Indian journal of medical research. 155(6)
Haemophilia is a debilitating bleeding disorder with significant comorbidities affecting the quality of life. In India, the management of these individuals is still limited to on-demand institutional treatment with coagulant factors. In this study, w
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d67b997f1004b259d957184275330184
https://pubmed.ncbi.nlm.nih.gov/36124495
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10
Inborn Errors of Ketogenesis: Novel Variants, Clinical Presentation, and Follow-Up in a Series of Four Patients
Autor: Haseena Sait, Somya Srivastava, Somesh Kumar, Bijo Varughese, Manmohan Pandey, Manjunath Venkatramaiah, Parul Chaudhary, Amita Moirangthem, Kausik Mandal, Seema Kapoor
Publikováno v: Journal of Pediatric Genetics.
Inborn errors of ketogenesis are rare disorders that result in acute and fulminant decompensation during lipolytic stress, particularly in infants and children. These include mitochondrial 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) synthase (HMGCS) def
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a6e36d4528417fc588c92b9eea84a15e
https://doi.org/10.1055/s-0042-1749362
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