Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Michael Nester"'
Autor:
Maysoon Alsagob, Mustafa A. Salih, Muddathir H. A. Hamad, Yusra Al-Yafee, Jawaher Al-Zahrani, Albandary Al-Bakheet, Michael Nester, Nadia Sakati, Salma M. Wakil, Ali AlOdaib, Dilek Colak, Namik Kaya
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-6 (2019)
Abstract 15q13.3 syndrome is associated with a wide spectrum of neurological disorders. Among a cohort of 150 neurodevelopmental cases, we identified two patients with two close proximity interstitial hemizygous deletions on chromosome 15q13. Using h
Externí odkaz:
https://doaj.org/article/74f03fe71e934a9d8b9467422ded30d0
Autor:
Bashayer Al-Mubarak, Mohamed Abouelhoda, Aisha Omar, Hesham AlDhalaan, Mohammed Aldosari, Michael Nester, Hussain. A. Alshamrani, Mohamed El-Kalioby, Ewa Goljan, Renad Albar, Shazia Subhani, Asma Tahir, Sultana Asfahani, Alaa Eskandrani, Ahmed Almusaiab, Amna Magrashi, Jameela Shinwari, Dorota Monies, Nada Al Tassan
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Abstract Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with genetic and clinical heterogeneity. The interplay of de novo and inherited rare variants has been suspected in the development of ASD. Here, we applied whole exome
Externí odkaz:
https://doaj.org/article/4a24e0c676b241eea3acb7405d21bc23
Autor:
Michael Nester, Noha Aljehani, Najla Al-Marzouki, Salah Baz, Haya F. Al-Joudi, Lina Mincari, Tariq Abalkhail, Camellia Al-Ibrahim, Jason Brandt
Publikováno v:
Journal of the International Neuropsychological Society. 25:761-771
Objectives: This study provides a standardized Arabic language neuropsychological test battery and tests its ability to distinguish patients with left and right hemisphere epileptic foci who are candidates for surgical resection. Methods: An Arabic l
Autor:
Maysaa W. Buraik, Jeremy L. Varnham, Hayfaa A. Wahabi, Waleed Al-Twaijri, Yasser S. Amer, Amr Jamal, Saleh M. AlSalehi, Samia M. Alhabib, Fatimah Alhaidar, Fahad A. Bashiri, Michael Nester, Mohammad Ghaziuddin, Hadeel Fakhri Daghash, Abdulkarim Alhossein, Khalid Alburikan, Haya F. Al-Joudi, Nouf Al Backer, Omar Almodayfer, Turki Homod Albatti, Yasser A. Ad-Dab’bagh, Hesham Aldhalaan, Muddathir H. Hamad
Publikováno v:
Child and Adolescent Psychiatry and Mental Health
Child and Adolescent Psychiatry and Mental Health, Vol 15, Iss 1, Pp 1-16 (2021)
Child and Adolescent Psychiatry and Mental Health, Vol 15, Iss 1, Pp 1-16 (2021)
BackgroundWe recently adapted the published National Institute for Health and Care Excellence (NICE) Attention deficit hyperactivity disorder (ADHD) diagnosis and management guideline to the Saudi Arabian context. It has been postulated that adaptati
Autor:
Yusra Alyafee, Salma M. Wakil, N. Kaya, Michael Nester, Muddathir H. Hamad, Dilek Colak, Maysoon Alsagob, Ali Al-Odaib, Nadia Sakati, Mustafa A. Salih, Jawaher Al-Zahrani, Albandary Al-Bakheet
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-6 (2019)
Molecular Cytogenetics
Molecular Cytogenetics
15q13.3 syndrome is associated with a wide spectrum of neurological disorders. Among a cohort of 150 neurodevelopmental cases, we identified two patients with two close proximity interstitial hemizygous deletions on chromosome 15q13. Using high-densi
Autor:
Tahreer Al-Rajudi, Chafica Eltabache, Rola Elkhatib, Iman Al-Saleh, Reem Al-Rouqi, Michael Nester, Mai Abduljabbar
Publikováno v:
International Journal of Hygiene and Environmental Health. 219:129-141
This cross-sectional study analyzed mercury (Hg) levels in healthy Saudi mothers and their infants (age 3-12 months) and examined the influence of Hg on the infants' neurodevelopment using screening tools, such as the Denver Developmental Screening T
Autor:
Gheid Abuharb, Abeer Al-Mostafa, Rabab Allam, Zahra Al-Sahlawi, Maaly Abdel-Fattah, Hamad Al-Zaidan, Alain Verloes, Khushnooda Ramzan, Michael Nester, Faiqa Imtiaz, Ola Khalifa
Publikováno v:
European Journal of Medical Genetics. 58:293-299
Donnai-Barrow syndrome (DBS; MIM 222448) is characterized by typical craniofacial anomalies (major hypertelorism with bulging eyes), high grade myopia, deafness and low molecular weight proteinuria. The disorder results from mutations in the low dens
Autor:
HOWE, CHARLES W.
Publikováno v:
Ballou's Pictorial; 10/24/1857, Vol. 13 Issue 17, p266-266, 3/4p
Autor:
Laila Al-alwan, Mohammad Al-Dosari, Albandary Al-Bakheet, Mehmet S. Inan, Ali Al-Odaib, Aziza Chedrawi, Pinar Ozand, Muhammad Al-Owain, Nada AbuDheim, Dilek Colak, Namik Kaya, Michael Nester, Zohair Al-Hassnan, Banan Al-Younes, Hesham Aldhalaan
Publikováno v:
Genomics. 97:19-28
Rett syndrome (RTT) is an X-linked neurodevelopmental disorder characterized by derangements in nervous system especially in cognition and behavior. The present study aims to understand the molecular underpinnings of two subtypes of RTT, classic RTT
Autor:
Reem Al-Rouqi, Iman Al-Saleh, Chafica Eltabache, Mai Abduljabbar, Michael Nester, Tahreer Al-Rajudi, Rola Elkhatib
Publikováno v:
Environmental Monitoring and Assessment. 187
A total of 1016 healthy Saudi mothers and their respective infants (aged 3-12 months) were recruited from 57 Primary Health Care Centers (PHCCs) in Riyadh, Saudi Arabia, to evaluate the extent of mercury (Hg) exposure and predict its sources in the h