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Peter Young

Showing results (61-70 of 272) with videos related to

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Journal of Sleep Research|September 9, 2014
Modafinil in the treatment of idiopathic hypersomnia without long sleep time--a randomized, double-blind, placebo-controlled studyGeert Mayer, Heike Benes, Peter Young, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 8, 2020
Two mutations in the nicotinic acetylcholine receptor subunit A4 (CHRNA4) in a family with autosomal dominant sleep-related hypermotor epilepsyLisa Langenbruch, Saskia Biskup, Peter Young, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|October 27, 2017
Musculoskeletal/Radiological Manifestations of Mucolipidosis II (I-Cell disease) in late Adolescence/Early AdulthoodAli Gholamrezanezhad, Dayna Weinert, Christos Kosmas, et al.
Glia|April 30, 2017
Sodium-dependent Vitamin C transporter 2 deficiency impairs myelination and remyelination after injury: Roles of collagen and demethylationDominik Röhr, Hartmut Halfter, Jörg B Schulz, et al.
Sleep & Breathing = Schlaf & Atmung|November 21, 2020
Disorders of sleep in spinal and bulbar muscular atrophy (Kennedy's disease)Lisa Langenbruch, Salvador Perez-Mengual, Christian Glatz, et al.
Frontiers in Microbiology|December 3, 2021
Introducing a Novel, Broad Host Range Temperate Phage Family Infecting <i>Rhizobium leguminosarum</i> and BeyondSam Ford, Sara Moeskjær, Peter Young, et al.
Cureus|May 30, 2023
Rare Paget's Disease Associated With Breast Cancer in a 70-Year-Old MaleMegan Bradley, Brittany Miles, Peter Young, et al.
Frontiers in Aging Neuroscience|December 2, 2010
COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary InterventionAnja Veronica Witte, Stefanie Jansen, Anja Schirmacher, et al.
Cureus|November 29, 2023
Distinguishing Fibroepithelial Lesions Requires Clinical, Imaging, and Pathology CorrelationMegan Bradley, Brittany Miles, Peter Young, et al.
Muscle & Nerve|February 22, 2011
Report of a novel mutation in the PMP22 gene causing an axonal neuropathyBurkhard Gess, Astrid Jeibmann, Anja Schirmacher, et al.
Pageof 28

Showing results (61-70 of 272) with videos related to

Sort By:
Pageof 28
Journal of Sleep Research|September 9, 2014
Modafinil in the treatment of idiopathic hypersomnia without long sleep time--a randomized, double-blind, placebo-controlled studyGeert Mayer, Heike Benes, Peter Young, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 8, 2020
Two mutations in the nicotinic acetylcholine receptor subunit A4 (CHRNA4) in a family with autosomal dominant sleep-related hypermotor epilepsyLisa Langenbruch, Saskia Biskup, Peter Young, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|October 27, 2017
Musculoskeletal/Radiological Manifestations of Mucolipidosis II (I-Cell disease) in late Adolescence/Early AdulthoodAli Gholamrezanezhad, Dayna Weinert, Christos Kosmas, et al.
Glia|April 30, 2017
Sodium-dependent Vitamin C transporter 2 deficiency impairs myelination and remyelination after injury: Roles of collagen and demethylationDominik Röhr, Hartmut Halfter, Jörg B Schulz, et al.
Sleep & Breathing = Schlaf & Atmung|November 21, 2020
Disorders of sleep in spinal and bulbar muscular atrophy (Kennedy's disease)Lisa Langenbruch, Salvador Perez-Mengual, Christian Glatz, et al.
Frontiers in Microbiology|December 3, 2021
Introducing a Novel, Broad Host Range Temperate Phage Family Infecting <i>Rhizobium leguminosarum</i> and BeyondSam Ford, Sara Moeskjær, Peter Young, et al.
Cureus|May 30, 2023
Rare Paget's Disease Associated With Breast Cancer in a 70-Year-Old MaleMegan Bradley, Brittany Miles, Peter Young, et al.
Frontiers in Aging Neuroscience|December 2, 2010
COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary InterventionAnja Veronica Witte, Stefanie Jansen, Anja Schirmacher, et al.
Cureus|November 29, 2023
Distinguishing Fibroepithelial Lesions Requires Clinical, Imaging, and Pathology CorrelationMegan Bradley, Brittany Miles, Peter Young, et al.
Muscle & Nerve|February 22, 2011
Report of a novel mutation in the PMP22 gene causing an axonal neuropathyBurkhard Gess, Astrid Jeibmann, Anja Schirmacher, et al.
Pageof 28