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Mustafa Sahin

Showing results (531-540 of 554) with videos related to

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Pediatric Neurology|October 8, 2025
Neurodevelopmental Outcomes From the PREVeNT TrialSarah E O'Kelley, Jamie K Capal, Tarrant O McPherson, et al.
Pediatric Neurology|March 29, 2026
Early Vigabatrin Treatment Before Seizure Onset Decreased Interictal Epileptiform Discharges Over the Duration of the PREVeNT StudyTarrant O McPherson, E Martina Bebin, Laura S Farach, et al.
Journal of Neurodevelopmental Disorders|September 14, 2023
International consensus recommendations for the identification and treatment of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)Petrus J de Vries, Tosca-Marie Heunis, Stephanie Vanclooster, et al.
Science (New York, N.Y.)|July 26, 2008
Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndromeNoriko Miyake, John Chilton, Maria Psatha, et al.
Nature Medicine|September 25, 2019
A framework for the investigation of rare genetic disorders in neuropsychiatryStephan J Sanders, Mustafa Sahin, Joseph Hostyk, et al.
Archives of Gynecology and Obstetrics|August 30, 2024
Sensitivity of frozen section analysis in patients with ovarian adult granulosa cell tumor, a multi-center studyIsin Ureyen, Tayfun Toptas, Alp Tokalıoğlu, et al.
Pediatric Neurology|August 20, 2023
Development and Feasibility of the Self-Report Quantified Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders Checklist (TAND-SQ)Tosca-Marie Heunis, Nola Chambers, Stephanie Vanclooster, et al.
Human Molecular Genetics|January 10, 2020
Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein traffickingRobert Behne, Julian Teinert, Miriam Wimmer, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 14, 2020
Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profileKrinio Giannikou, Zachary Zhu, Jaegil Kim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2024
The characterization of new de novo CACNA1G variants affecting the intracellular gate of Cav3.1 channel broadens the spectrum of neurodevelopmental phenotypes in SCA42NDLeila Qebibo, Amaël Davakan, Mathilde Nesson-Dauphin, et al.
Pageof 56

Showing results (531-540 of 554) with videos related to

Sort By:
Pageof 56
Pediatric Neurology|October 8, 2025
Neurodevelopmental Outcomes From the PREVeNT TrialSarah E O'Kelley, Jamie K Capal, Tarrant O McPherson, et al.
Pediatric Neurology|March 29, 2026
Early Vigabatrin Treatment Before Seizure Onset Decreased Interictal Epileptiform Discharges Over the Duration of the PREVeNT StudyTarrant O McPherson, E Martina Bebin, Laura S Farach, et al.
Journal of Neurodevelopmental Disorders|September 14, 2023
International consensus recommendations for the identification and treatment of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)Petrus J de Vries, Tosca-Marie Heunis, Stephanie Vanclooster, et al.
Science (New York, N.Y.)|July 26, 2008
Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndromeNoriko Miyake, John Chilton, Maria Psatha, et al.
Nature Medicine|September 25, 2019
A framework for the investigation of rare genetic disorders in neuropsychiatryStephan J Sanders, Mustafa Sahin, Joseph Hostyk, et al.
Archives of Gynecology and Obstetrics|August 30, 2024
Sensitivity of frozen section analysis in patients with ovarian adult granulosa cell tumor, a multi-center studyIsin Ureyen, Tayfun Toptas, Alp Tokalıoğlu, et al.
Pediatric Neurology|August 20, 2023
Development and Feasibility of the Self-Report Quantified Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders Checklist (TAND-SQ)Tosca-Marie Heunis, Nola Chambers, Stephanie Vanclooster, et al.
Human Molecular Genetics|January 10, 2020
Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein traffickingRobert Behne, Julian Teinert, Miriam Wimmer, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 14, 2020
Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profileKrinio Giannikou, Zachary Zhu, Jaegil Kim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2024
The characterization of new de novo CACNA1G variants affecting the intracellular gate of Cav3.1 channel broadens the spectrum of neurodevelopmental phenotypes in SCA42NDLeila Qebibo, Amaël Davakan, Mathilde Nesson-Dauphin, et al.
Pageof 56