Zobrazeno 1 - 10
of 162 248
pro vyhledávání: '"A. Woodhouse"'
It was the home of a knight, a baron, a viscount, two marquises and nine earls. The family had estates not only in South Yorkshire, but also in North Yorkshire, the Midlands and Ireland, at their greatest extent covering nearly 120,000 acres. One hea
Autor:
John R. Christensen
A cold case comes back to haunt the small town of Valley-Wood. We follow the life of Brendan Gibbons who returns to reconnect with old friends. The townsfolk live a life of quiet effort until it is upturned by outsiders and innuendo. Secrets are bein
Autor:
Gaskins, Richard1
Publikováno v:
Victoria University of Wellington Law Review. 2023, Vol. 54 Issue 4, p833-855. 23p.
Autor:
Wakim, Victor1,2 victorwakim@gmail.com, Dassouki, Mohammad El3, Azar, Ahlam2, Hani, Abeer2,3, Mehawej, Cybel4, Chouery, Eliane4, Baroudi, Marie-Jeanne5, Wakim, Gerard2
Publikováno v:
Journal of Rare Diseases. 7/23/2024, Vol. 3 Issue 1, p1-9. 9p.
Autor:
McLay, Geoff1
Publikováno v:
Victoria University of Wellington Law Review. 2023, Vol. 54 Issue 4, p857-881. 25p.
Autor:
Victor Wakim, Mohammad El Dassouki, Ahlam Azar, Abeer Hani, Cybel Mehawej, Eliane Chouery, Marie-Jeanne Baroudi, Gerard Wakim
Publikováno v:
Journal of Rare Diseases, Vol 3, Iss 1, Pp 1-9 (2024)
Abstract Woodhouse-Sakati syndrome (WSS) is a rare eponymous disease described by Drs. Woodhouse and Sakati in 1983 as a syndrome of hypogonadism, alopecia, diabetes mellitus, intellectual disability, and ECG abnormalities. A couple of years later, a
Externí odkaz:
https://doaj.org/article/045fb9851fc5441092bef97e2e4fc97e
Autor:
Amosova, Maria1 amosova_m_v@staff.sechenov.ru, Poluboyarinova, Irina1, Fadeev, Valentin1, Asanov, Aliy2
Publikováno v:
JCEM Case Reports. Aug2024, Vol. 2 Issue 8, p1-5. 5p.
Autor:
Rebecca Eilish Irvine, Arshia Ahmad
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-5 (2024)
Abstract Background Woodhouse-Sakati Syndrome (WSS) is a rare autosomal recessive condition caused by biallelic pathogenic variants in the DCAF17 gene, with fewer than 200 cases reported in the literature. Symptoms first emerge in middle-late adolesc
Externí odkaz:
https://doaj.org/article/92749792a783457d8f180e2dda121c43
Akademický článek
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Autor:
Bakhsh, Hanadi1,2 (AUTHOR) 8ebtesamalmajed@gmail.com, Alqntash, Norah1 (AUTHOR), Almajed, Ebtesam1 (AUTHOR)
Publikováno v:
Life (2075-1729). Oct2023, Vol. 13 Issue 10, p2022. 8p.