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American Journal of Medical Genetics. Part A|December 18, 2022
T2 olivary nuclei hyperintensities: A characteristic neuroimaging finding in FIG4-related leukoencephalopathyHaseena Sait, Arya Shambhavi, Manmohan Pandey, et al.Indian Journal of Pediatrics|March 13, 2021
Monogenic Lupus with IgA Nephropathy Caused by Spondyloenchondrodysplasia with Immune DysregulationHaseena Sait, Harikrishnan Gangadharan, Aviral Gupta, et al.Journal of the ASEAN Federation of Endocrine Societies|December 2, 2024
Effect of Maternal Iodine Excess during Pregnancy on Neonatal Thyroid Function and Neurodevelopmental Status at 12 WeeksDeepashree K Rao, Ankur Jindal, Aashima Dabas, et al.Clinical Genetics|April 30, 2025
Spectrum of Inherited Childhood-Onset Dystonia: Case Series of 19 Families With Genotype and Phenotype Characterization Highlighting the Treatable CausesNaik Adarsha, Arya Shambhavi, Haseena Sait, et al.The Indian Journal of Radiology & Imaging|September 24, 2021
Loes Score: Clinical and Radiological Profile of 22 Patients of X-Linked Adrenoleukodystrophy: Case Series from a Single CenterSomesh Kumar, Haseena Sait, Sunil K Polipalli, et al.Clinical Genetics|July 12, 2025
Molecular and Clinical Landscape of Osteogenesis Imperfecta: Unraveling Autosomal Recessive Forms, Therapeutic Outcomes, and Bone Mineral Density in CarriersHaseena Sait, Naik Adarsha, Amita Moirangthem, et al.Indian Pediatrics|July 7, 2019
Association Between Neonatal Thyroid Stimulating Hormone Status and Maternal Urinary Iodine StatusHaseena Sait, Seema Kapoor, Ankur Jindal, et al.Journal of Pediatric Genetics|April 3, 2024
Inborn Errors of Ketogenesis: Novel Variants, Clinical Presentation, and Follow-Up in a Series of Four PatientsHaseena Sait, Somya Srivastava, Somesh Kumar, et al.European Journal of Medical Genetics|May 14, 2022
Deciphering the molecular landscape of microcephaly in 87 Indian families by exome sequencingSuzena Masih, Amita Moirangthem, Arya Shambhavi, et al.European Journal of Medical Genetics|May 4, 2021
Phenotypic and genotypic spectrum of CTSK variants in a cohort of twenty-five Indian patients with pycnodysostosisHaseena Sait, Priyanka Srivastava, Neerja Gupta, et al.Pageof 3