Zobrazeno 1 - 10
of 422
pro vyhledávání: '"M Zein"'
Autor:
Risma Santika, M Zein Permana
Publikováno v:
Jurnal Psikologi Perseptual, Vol 6, Iss 2, Pp 101-112 (2021)
Studi ini bertujuan untuk memberikan gambaran alasan berpacaran pada individu 18-25 tahun (emerging adulthood). Desain penelitian kualitatif dengan menggunakan analisa data tematik. Pada studi ini, partisipan dipilih menggunakan metode purposive samp
Externí odkaz:
https://doaj.org/article/c33a8abf7f034369bdcfbf8bea27dd43
Autor:
Volha V. Malechka, MD, Dat Duong, PhD, Keyla D. Bordonada, MD, Amy Turriff, MS, Delphine Blain, MS, MBA, Elizabeth Murphy, PhD, Wendy J. Introne, MD, Bernadette R. Gochuico, MD, David R. Adams, MD, PhD, Wadih M. Zein, MD, Brian P. Brooks, MD, PhD, Laryssa A. Huryn, MD, Benjamin D. Solomon, MD, Robert B. Hufnagel, MD, PhD
Publikováno v:
Ophthalmology Science, Vol 3, Iss 1, Pp 100225- (2023)
Purpose: To describe the relationships between foveal structure and visual function in a cohort of individuals with foveal hypoplasia (FH) and to estimate FH grade and visual acuity using a deep learning classifier. Design: Retrospective cohort study
Externí odkaz:
https://doaj.org/article/274a7e4a1c8149b4b26877b3c0630414
Autor:
M. Zein, Reyan, Twinomurinzi, Hossana
Publikováno v:
Blockchains; Jun2024, Vol. 2 Issue 2, p107-133, 27p
Autor:
Saumil Sethna, Wadih M Zein, Sehar Riaz, Arnaud PJ Giese, Julie M Schultz, Todd Duncan, Robert B Hufnagel, Carmen C Brewer, Andrew J Griffith, T Michael Redmond, Saima Riazuddin, Thomas B Friedman, Zubair M Ahmed
Publikováno v:
eLife, Vol 10 (2021)
Usher syndrome type I (USH1) is characterized by deafness, vestibular areflexia, and progressive retinal degeneration. The protein-truncating p.Arg245* founder variant of PCDH15 (USH1F) has an ~2% carrier frequency amongst Ashkenazi Jews accounts for
Externí odkaz:
https://doaj.org/article/b6069badb6b14498bff5ec71588e5683
Autor:
Laryssa A. Huryn, Christina Torres Kozycki, Jasmine Y. Serpen, Wadih M. Zein, Ehsan Ullah, Alessandro Iannaccone, Lloyd B. Williams, Lucia Sobrin, Brian P. Brooks, H. Nida Sen, Robert B. Hufnagel, Daniel L. Kastner, Shilpa Kodati
Publikováno v:
Ophthalmology. 130:423-432
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ff71891de88a4947bf7e4cfd3daede7
https://doi.org/10.1016/j.ophtha.2022.10.026
https://doi.org/10.1016/j.ophtha.2022.10.026
Autor:
Rabia Faridi, Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy E. Turriff, Keith Pelstring, Bin Guan, Amelia Naik, Andrew J. Griffith, Samuel Mawuli Adadey, Elvis Twumasi Aboagye, Gordon A. Awandare, Robert J. Morell, Ekaterini Tsilou, Amanda G. Noyes, Laura A. G. Sulmonte, Ambroise Wonkam, Isabelle Schrauwen, Suzanne M. Leal, Hela Azaiez, Carmen C. Brewer, Sheikh Riazuddin, Robert B. Hufnagel, Michael Hoa, Wadih M. Zein, J. Karl de Dios, Thomas B. Friedman
Publikováno v:
Clinical Genetics. 103:699-703
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fa28c57eb07bd63d0020e5fb71c72c4
https://doi.org/10.1111/cge.14312
https://doi.org/10.1111/cge.14312
Autor:
Ryan H. Peretz, Wadih M. Zein, Robert B. Hufnagel, Christine Ku, Rena Godfrey, Lynne Wolfe, David Adams, William Gahl, Camilo Toro
Publikováno v:
American Journal of Medical Genetics Part A. 191:624-629
Boucher-Neuhäuser syndrome (BNHS) is characterized by chorioretinal dystrophy, hypogonadotropic hypogonadism, and cerebellar dysfunction and atrophy. The disorder has been associated with biallelic pathogenic variants in the patatin-like phospholipa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3c084e6047acf590ed02ebf6011b5fd
https://doi.org/10.1002/ajmg.a.63045
https://doi.org/10.1002/ajmg.a.63045
Autor:
Kamil, Kruczek, Zepeng, Qu, Emily, Welby, Hiroko, Shimada, Suja, Hiriyanna, Milton A, English, Wadih M, Zein, Brian P, Brooks, Anand, Swaroop
Publikováno v:
Stem Cell Reports. 17:2172-2186
Mutations in the IQ calmodulin-binding motif containing B1 (IQCB1)/NPHP5 gene encoding the ciliary protein nephrocystin 5 cause early-onset blinding disease Leber congenital amaurosis (LCA), together with kidney dysfunction in Senior-Løken syndrome.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa4d00b274ad2fa011aa359daa92838a
https://doi.org/10.1016/j.stemcr.2022.08.006
https://doi.org/10.1016/j.stemcr.2022.08.006
Autor:
Thekraiat M Al Quran, Ziad A Bataineh, Abdel-Hameed Al-Mistarehi, Anas M Zein Alaabdin, Hadeel Allan, Anood Al Qura'an, Shatha M Weshah, Anfal A Alanazi, Yousef S Khader
Publikováno v:
International Journal of General Medicine. 15:7669-7683
Thekraiat M Al Quran,1 Ziad A Bataineh,2 Abdel-Hameed Al-Mistarehi,1 Anas M Zein Alaabdin,1 Hadeel Allan,1 Anood Al Quraâan,3 Shatha M Weshah,1 Anfal A Alanazi,4 Yousef S Khader1 1Department of Public Health and Family Medicine, Faculty of Medic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a197e42a2585e89623844479e5b495fb
https://doi.org/10.2147/ijgm.s377463
https://doi.org/10.2147/ijgm.s377463
Autor:
Giuseppe Giaccone, Nicoletta Brega, Michael Shnaidman, Brett E. Houk, William D. Figg, Baskar Mannargudi, Lokesh Jain, Wadih M. Zein, Sonja Crandon, Martin Gutierrez, Shivaani Kummar, Sylvia V. Alarcon, Yeong Sang Kim, Jane B. Trepel, Ronan J. Kelly, Arun Rajan
PDF file - 191KB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b3cfd090002f0e51aba43b6fba257d0
https://doi.org/10.1158/1078-0432.22443483.v1
https://doi.org/10.1158/1078-0432.22443483.v1
