Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Beena Harikrishna"'
Publikováno v:
Ophthalmic Genetics. 42:780-783
Aim To report the earliest diagnosis of Vici syndrome in a three-week-old Omani girl. Methods A three-week-old baby girl with blond hair and agenesis of the corpus callosum was born to consanguineous parents. An older sibling with similar findings ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732c8e8aa2fc0ef1751a90f2c350149b
https://doi.org/10.1080/13816810.2021.1952621
https://doi.org/10.1080/13816810.2021.1952621
Autor:
Rana Al-Senawi, Bushra Al-Jabri, Sana Al-Zuhaibi, Faisal Al-Azri, Saif Al-Yarubi, Beena Harikrishna, Amna Al-Futaisi, Anuradha Ganesh
Publikováno v:
Oman Journal of Ophthalmology, Vol 6, Iss 3, Pp 193-198 (2013)
Background: Septo-optic dysplasia (SOD), also known as de-Morsier′s syndrome, is a rare disorder characterized by any combination of optic nerve hypoplasia (ONH), pituitary gland hypoplasia, and midline abnormalities of the brain including absence
Externí odkaz:
https://doaj.org/article/92ec78593a0046daadc288aa1e60a2ad
Autor:
Badriya, Al-Alawi, Beena, Harikrishna, Khalid, Al-Thihli, Sana, Al Zuhabi, Anuradha, Ganesh, Zainab, Al Hashami, Zeyana, Al Dhamhmani, Razan, Zadjali, Nafila B, Al Riyami, Fahad, Zadjali
Publikováno v:
Genes. 13(2)
Mucolipidosis Type IV (MLIV) is caused by a deficiency of the mucolipin cation channel encoded by Mucolipin TRP Cation Channel 1 gene (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e291a178ee77d781c3b8587c12d822b2
https://pubmed.ncbi.nlm.nih.gov/35205297
https://pubmed.ncbi.nlm.nih.gov/35205297
Autor:
Maha Mameesh, Sana Al Zuhaibi, Beena Harikrishna, Sami Al Kalbani, Patrick Scott, Khalid Al Thihli, Anuradha Ganesh
Publikováno v:
Ophthalmic Genetics. 38:544-548
To report co-occurrence of two rare recessive conditions, the membrane frizzled-related protein (MFRP)-related ocular phenotype and glycogen storage disease type 1b (GSD-1b), in three siblings in an Omani family.Biallelic mutations in the MFRP gene (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fed22f7185f06f5a3144917ce6f8dbd
https://doi.org/10.1080/13816810.2017.1323340
https://doi.org/10.1080/13816810.2017.1323340
Publikováno v:
Oman Journal of Ophthalmology, Vol 3, Iss 1, Pp 41-42 (2010)
Externí odkaz:
https://doaj.org/article/911e21b11df64117903f4ada5c85f8d1
Autor:
Sana Al-Zuahibi, Samia Al-Jabri, Faisal Al-Azri, Anuradha Ganesh, Feraz Masoud, Adil Al-Riyami, Beena Harikrishna, Abdullah Al-Mujaini, Ahmed Al-Waily
Publikováno v:
Middle East African Journal of Ophthalmology
Purpose : To investigate the efficacy and safety of oral propranolol in the management of periorbital infantile hemangioma in four subjects. Materials and Methods : Consecutive patients who presented with periorbital capillary hemangioma with vision-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98eefb0e8508511404b21d6d4a577fe4
https://pubmed.ncbi.nlm.nih.gov/22224018
https://pubmed.ncbi.nlm.nih.gov/22224018
Autor:
Amna Al-Futaisi, Faisal Al-Azri, Sana Al-Zuhaibi, Saif Al-Yarubi, Beena Harikrishna, Bushra Al-Jabri, Anuradha Ganesh, Rana Al-Senawi
Publikováno v:
Oman Journal of Ophthalmology, Vol 6, Iss 3, Pp 193-198 (2013)
Oman Journal of Ophthalmology
Oman Journal of Ophthalmology
Background: Septo-optic dysplasia (SOD), also known as de-Morsier′s syndrome, is a rare disorder characterized by any combination of optic nerve hypoplasia (ONH), pituitary gland hypoplasia, and midline abnormalities of the brain including absence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b66d3572d4a52384adda636ed859307
https://doi.org/10.4103/0974-620x.122277
https://doi.org/10.4103/0974-620x.122277
Publikováno v:
Oman Journal of Ophthalmology, Vol 3, Iss 1, Pp 41-42 (2010)
Oman Journal of Ophthalmology
Oman Journal of Ophthalmology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1eea5532b34400910d79537b49699dc5
https://doi.org/10.4103/0974-620x.60024
https://doi.org/10.4103/0974-620x.60024
Publikováno v:
Sultan Qaboos University Medical Journal. May2023, Vol. 23 Issue 2, p276-283. 8p.
Autor:
Mameesh, Maha1 (AUTHOR), Ganesh, Anuradha1 (AUTHOR) gananu@gmail.com, Harikrishna, Beena1 (AUTHOR), Al Zuhaibi, Sana1 (AUTHOR), Scott, Patrick2 (AUTHOR), Al Kalbani, Sami2 (AUTHOR), Al Thihli, Khalid2 (AUTHOR)
Publikováno v:
Ophthalmic Genetics. Dec2017, Vol. 38 Issue 6, p544-548. 5p.