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1
Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis
Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis
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Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis

Jen, Joanna C. ; Chan, Wai-Man ; Bosley, Thomas M. ; Wan, Jijun ; Carr, Janai R. ; Rüb, Udo ; Shattuck, David ; Salamon, Georges ; Kudo, Lili C. ; Ou, Jing ; Doris D. M. Lin ; Mustafa A. M. Salih ; Kansu, Tülay ; al Dhalaan, Hesham ; al Zayed, Zayed ; MacDonald, David B. ; Stigsby, Bent ; Plaitakis, Andreas ; Dretakis, Emmanuel K. ; Gottlob, Irene ; Pieh, Christina ; Traboulsi, Elias I. ; Wang, Qing ; Wang, Lejin ; Andrews, Caroline ; Yamada, Koki ; Demer, Joseph L. ; Karim, Shaheen ; Alger, Jeffry R. ; Geschwind, Daniel H. ; Deller, Thomas ; Sicotte, Nancy L. ; Nelson, Stanley F. ; Baloh, Robert W. ; Engle, Elizabeth C.

Science (American Association for the Advancement of Science), 2004-06, Vol.304 (5676), p.1509-1513 [Periódico revisado por pares]

Washington, DC: American Association for the Advancement of Science

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2
A novel X-linked disorder with developmental delay and autistic features
A novel X-linked disorder with developmental delay and autistic features
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A novel X-linked disorder with developmental delay and autistic features

Kaya, Namik ; Colak, Dilek ; Albakheet, Albandary ; Al-Owain, Mohammad ; Abu-Dheim, Nada ; Al-Younes, Banan ; Al-Zahrani, Jawaher ; Mukaddes, Nahit M. ; Dervent, Aysin ; Al-Dosari, Naji ; Al-Odaib, Ali ; Kayaalp, Inci V. ; Al-Sayed, Moeenaladin ; Al-Hassnan, Zuhair ; Nester, Michael J. ; Al-Dosari, Mohammad ; Al-Dhalaan, Hesham ; Chedrawi, Aziza ; Gunoz, Hulya ; Karakas, Bedri ; Sakati, Nadia ; Alkuraya, Fowzan S. ; Gascon, Generaso G. ; Ozand, Pinar T.

Annals of neurology, 2012-04, Vol.71 (4), p.498-508 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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3
Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations
Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations
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Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations

Abu-Amero, Khaled K ; Dhalaan, Hesham al ; Zayed, Zayed al ; Hellani, Ali ; Bosley, Thomas M

Journal of the neurological sciences, 2009-01, Vol.276 (1), p.22-26 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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4
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report
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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Abu-Amero, Khaled K ; Al-Dhalaan, Hesham ; Bohlega, Saeed ; Hellani, Ali ; Taylor, Robert W

Journal of medical case reports, 2009-10, Vol.3 (1), p.77-77, Article 77 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Feasibility of Responsive Teaching With Mothers and Young Children With Autism in Saudi Arabia
Feasibility of Responsive Teaching With Mothers and Young Children With Autism in Saudi Arabia
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Feasibility of Responsive Teaching With Mothers and Young Children With Autism in Saudi Arabia

Alquraini, Turki ; Al-Odaib, Ali ; Al-Dhalaan, Hesham ; Merza, Haniah ; Mahoney, Gerald

Journal of early intervention, 2018-12, Vol.40 (4), p.304-316 [Periódico revisado por pares]

Los Angeles, CA: SAGE Publications

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6
Relationship-based Intervention with Young Children with Autism in Saudi Arabia: Impediments and Consequences of Parenting Stress and Depression
Relationship-based Intervention with Young Children with Autism in Saudi Arabia: Impediments and Consequences of Parenting Stress and Depression
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Relationship-based Intervention with Young Children with Autism in Saudi Arabia: Impediments and Consequences of Parenting Stress and Depression

Alquraini, Turki ; Al-Odaib, Ali ; Al-Dhalaan, Hesham ; Merza, Haniah ; Mahoney, Gerald

International journal of disability, development, and education, 2019-05, Vol.66 (3), p.233-248 [Periódico revisado por pares]

Abingdon: Routledge

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7
Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways
Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways
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Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways

Aldosary, Mazhor ; Al-Bakheet, AlBandary ; Al-Dhalaan, Hesham ; Almass, Rawan ; Alsagob, Maysoon ; Al-Younes, Banan ; AlQuait, Laila ; Mustafa, Osama Mufid ; Bulbul, Mustafa ; Rahbeeni, Zuhair ; Alfadhel, Majid ; Chedrawi, Aziza ; Al-Hassnan, Zuhair ; AlDosari, Mohammed ; Al-Zaidan, Hamad ; Al-Muhaizea, Mohammad A ; AlSayed, Moeenaldeen D ; Salih, Mustafa A ; AlShammari, Mai ; Faiyaz-Ul-Haque, Muhammad ; Chishti, Mohammad Azhar ; Al-Harazi, Olfat ; Al-Odaib, Ali ; Kaya, Namik ; Colak, Dilek

Omics (Larchmont, N.Y.), 2020-03, Vol.24 (3), p.16-171 [Periódico revisado por pares]

United States: Mary Ann Liebert, Inc., publishers

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8
Seizure outcomes after hemispherectomy for drug resistant epilepsy in childhood and adolescence
Seizure outcomes after hemispherectomy for drug resistant epilepsy in childhood and adolescence
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Seizure outcomes after hemispherectomy for drug resistant epilepsy in childhood and adolescence

Khateeb, Mashael ; Al.Thubaiti, Ibrahim ; Al.Otaibi, Faisal ; Al.Dhalaan, Hesham ; Abalkhail, Tariq ; Baz, Salah

Interdisciplinary neurosurgery : Advanced techniques and case management, 2019-12, Vol.18, p.100483, Article 100483 [Periódico revisado por pares]

Elsevier B.V

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9
Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways
Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways
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Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways

Colak, Dilek ; Al-Dhalaan, Hesham ; Nester, Michael ; AlBakheet, AlBandary ; Al-Younes, Banan ; Al-Hassnan, Zohair ; Al-Dosari, Mohammad ; Chedrawi, Aziza ; Al-Owain, Muhammad ; AbuDheim, Nada ; Al-Alwan, Laila ; Al-Odaib, Ali ; Ozand, Pinar ; Inan, Mehmet Sait ; Kaya, Namik

Genomics (San Diego, Calif.), 2011, Vol.97 (1), p.19-28 [Periódico revisado por pares]

Amsterdam: Elsevier Inc

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10
Sphingolipid Activator Protein B Deficiency: Report of 9 Saudi Patients and Review of the Literature
Sphingolipid Activator Protein B Deficiency: Report of 9 Saudi Patients and Review of the Literature
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Sphingolipid Activator Protein B Deficiency: Report of 9 Saudi Patients and Review of the Literature

Al-Hassnan, Zuhair N. ; Al Dhalaan, Hesham ; Patay, Zoltan ; Faqeih, Eissa ; Al-Owain, Mohammed ; Al-Duraihem, Adel ; Faiyaz-Ul-Haque, Mohammed

Journal of child neurology, 2009-12, Vol.24 (12), p.1513-1519 [Periódico revisado por pares]

Los Angeles, CA: SAGE Publications

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