Zobrazeno 1 - 10 of 17 pro vyhledávání: '"Mounika, Endrakanti"'
1
Akademický článek
Multidisciplinary team for genetic disorders – Integration with clinicians and health-care professionals
Autor: Mounika Endrakanti, Neerja Gupta
Publikováno v: Apollo Medicine, Vol 20, Iss 2, Pp 144-147 (2023)
Individuals with genetic disorders present with multisystem, complex, and special health care needs. Although limited treatment options are available for most genetic conditions, ensuring continued ongoing surveillance and rehabilitative care is quin
Externí odkaz: https://doaj.org/article/03d1fcc2a2c5497293aba9aafbf1c89a
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5
Akademický článek
Right Internal Jugular Vein Phlebectasia: A Rare Cause of Neck Swelling
Autor: Deepanjan Bhattacharya, Mounika Endrakanti, Rakesh Kumar
Publikováno v: Case Reports in Pediatrics, Vol 2017 (2017)
Internal jugular vein (IJV) phlebectasia is a rare condition presenting as a self-reducible soft tissue swelling of the neck due to fusiform dilation of the venous wall. We report the case of a 7-year-old boy who presented with painless soft mass in
Externí odkaz: https://doaj.org/article/d6b5497793b74434b2906f054fe9a581
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6
Late-onset cobalamin C disease: rare but treatable
Autor: Aminu Aliyar, Mounika Endrakanti, Rajesh K Singh, Arunmozhimaran Elavarasi, Neerja Gupta, Deepti Vibha, Manjari Tripathi
Publikováno v: Practical neurology.
Cobalamin C disease is the most common inborn error of cobalamin metabolism, resulting from mutations in methylmalonic aciduria and homocystinuria type C protein (MMACHC) gene. There is associated elevation of homocysteine and methylmalonic acid and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a1b1f08334ae019269fbb7e3fa0121
https://pubmed.ncbi.nlm.nih.gov/35803728
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Plný text Recenzováno Digitální knihovna AV ČR
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