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Journal of Neurodevelopmental Disorders|December 17, 2019
Early white matter development is abnormal in tuberous sclerosis complex patients who develop autism spectrum disorderAnna K Prohl, Benoit Scherrer, Xavier Tomas-Fernandez, et al.
Journal of Neurodevelopmental Disorders|March 24, 2022
Validation of a computational phenotype for finding patients eligible for genetic testing for pathogenic PTEN variants across three centersCartik Kothari, Siddharth Srivastava, Youssef Kousa, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|August 12, 2021
Clinical Characteristics and Outcomes of COVID-19 Patients with Overweight and Obesity: Turkish Nationwide Cohort Study (TurCObesity)Ibrahim Sahin, Cem Haymana, Tevfik Demir, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
AKT-mediated phosphorylation of TSC2 controls stimulus- and tissue-specific mTORC1 signaling and organ growthYann Cormerais, Samuel C Lapp, Krystle C Kalafut, et al.
Cell|October 30, 2010
EphB-mediated degradation of the RhoA GEF Ephexin5 relieves a developmental brake on excitatory synapse formationSeth S Margolis, John Salogiannis, David M Lipton, et al.
Pediatric Neurology|June 9, 2016
Advances and Future Directions for Tuberous Sclerosis Complex Research: Recommendations From the 2015 Strategic Planning ConferenceMustafa Sahin, Elizabeth P Henske, Brendan D Manning, et al.
Annals of Clinical and Translational Neurology|March 19, 2024
Exploring the neurological features of individuals with germline PTEN variants: A multicenter studyAndrew Dhawan, Sarah Baitamouni, Darren Liu, et al.
Pediatric Neurology|February 29, 2020
Diffusion Tensor Imaging Abnormalities in the Uncinate Fasciculus and Inferior Longitudinal Fasciculus in Phelan-McDermid SyndromeJulia Bassell, Siddharth Srivastava, Anna K Prohl, et al.
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