Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Doaa I. Sadik"'
Autor:
Hind Alsharhan, Amir A. Ahmed, Naser M. Ali, Ahmad Alahmad, Buthaina Albash, Reem M. Elshafie, Sumaya Alkanderi, Usama M. Elkazzaz, Parakkal Xavier Cyril, Rehab M. Abdelrahman, Alaa A. Elmonairy, Samia M. Ibrahim, Yasser M. E. Elfeky, Doaa I. Sadik, Sara D. Al-Enezi, Ayman M. Salloum, Yadav Girish, Mohammad Al-Ali, Dina G. Ramadan, Rasha Alsafi, May Al-Rushood, Laila Bastaki
Publikováno v:
International Journal of Neonatal Screening, Vol 7, Iss 3, p 56 (2021)
Kuwait is a small Arabian Gulf country with a high rate of consanguinity and where a national newborn screening program was expanded in October 2014 to include a wide range of endocrine and metabolic disorders. A retrospective study conducted between
Externí odkaz:
https://doaj.org/article/54db8a5df6094413847ca59116a38202
Autor:
Parakkal Xavier Cyril, Laila Bastaki, Rehab M Abdelrahman, Naser M Ali, Yasser M E Elfeky, Ahmad Alahmad, Amir A Ahmed, Yadav Girish, Dina G Ramadan, Sumaya Alkanderi, Usama M Elkazzaz, Rasha Alsafi, Sara D Al-Enezi, Reem M Elshafie, Alaa A Elmonairy, Mohammad Al-Ali, Hind Alsharhan, Doaa I. Sadik, Buthaina Albash, Ayman M Salloum, Samia M Ibrahim, May Al-Rushood
Publikováno v:
International Journal of Neonatal Screening
International Journal of Neonatal Screening, Vol 7, Iss 56, p 56 (2021)
Volume 7
Issue 3
International Journal of Neonatal Screening, Vol 7, Iss 56, p 56 (2021)
Volume 7
Issue 3
Kuwait is a small Arabian Gulf country with a high rate of consanguinity and where a national newborn screening program was expanded in October 2014 to include a wide range of endocrine and metabolic disorders. A retrospective study conducted between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f9ef2c4fcf72551e37e3ff92e96f59
https://pubmed.ncbi.nlm.nih.gov/34449519
https://pubmed.ncbi.nlm.nih.gov/34449519
Publikováno v:
Middle East Journal of Medical Genetics. 5:41-44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65c9f63282abaec22c3fd3b85f37650e
https://doi.org/10.1097/01.mxe.0000484370.71282.15
https://doi.org/10.1097/01.mxe.0000484370.71282.15
Autor:
Doaa I. Sadik, Hala Y. Yousef, Mohamed G. Khallaf, Hadil Alrohaif, Muneef Al-Hathal, Laila Bastaki
Publikováno v:
Middle East Journal of Medical Genetics. 4:28-30
We report a male newborn with a rarely described congenital limb deficiency, fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome. This syndrome consists of shortening and anterior bowing of the lower limbs at the distal third of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e938fb72741dfc94fa5cb6bbe275391e
https://doi.org/10.1097/01.mxe.0000456627.22542.40
https://doi.org/10.1097/01.mxe.0000456627.22542.40
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 11, No 2 (2010)
Ellis–van Creveld syndrome (EVC) is a chondroectodermal dysplasia. The tetrad of cardinal features includes disproportionate dwarfism, bilateral postaxial polydactyl of hands, hidrotic ectodermal dysplasia, and congenital cardiac malformations. Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9a0ca6380f6283ac51c959deed16bb9
Autor:
Doaa I. Sadik, Rabah M. Shawky
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 12, No 1 (2011)
According to the World Health Organization the term congenital anomaly includes any morphological, functional, biochemical or molecular defects that may develop in the embryo and fetus from conception until birth, present at birth, whether detected a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96bd6de8028e5e9c93ddfacd26c46270