المؤلفون: MacMullen LE; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States of America., George-Sankoh I; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States of America; Department of Bioinformatics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States of America., Stanley K; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States of America., McCormick EM; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States of America., Muraresku CC; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States of America., Goldstein A; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States of America; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, United States of America., Zolkipli-Cunningham Z; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States of America; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, United States of America., Falk MJ; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States of America; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, United States of America. Electronic address: falkm@chop.edu.

المصدر: Molecular genetics and metabolism [Mol Genet Metab] 2024 May; Vol. 142 (1), pp. 108348. Date of Electronic Publication: 2024 Feb 16.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE

مواضيع طبية MeSH: Patient Reported Outcome Measures* , Mitochondrial Diseases*/genetics , Mitochondrial Diseases*/therapy , Quality of Life*, Humans ; Male ; Female ; Adult ; Child ; Adolescent ; Middle Aged ; Young Adult ; Child, Preschool ; Prospective Studies ; Infant ; Surveys and Questionnaires ; Aged ; Fatigue ; Rare Diseases/genetics ; Rare Diseases/therapy ; Evidence Gaps

المؤلفون: Elander J; Otorhinolaryngology, Head and Neck Surgery, Department of Clinical Sciences Lund, Lund University, Skåne University Hospital, 221 85 Lund, Sweden., McCormick EM; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, 19104, PA, USA., Värendh M; Otorhinolaryngology, Head and Neck Surgery, Department of Clinical Sciences Lund, Lund University, Skåne University Hospital, 221 85 Lund, Sweden., Stenfeldt K; Otorhinolaryngology, Head and Neck Surgery, Department of Clinical Sciences Lund, Lund University, Skåne University Hospital, 221 85 Lund, Sweden; Logopedics, Phoniatrics and Audiology, Department of Clinical Sciences Lund, Lund University, 221 85 Lund, Sweden., Ganetzky RD; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, 19104, PA, USA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, 19104, PA, USA., Goldstein A; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, 19104, PA, USA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, 19104, PA, USA., Zolkipli-Cunningham Z; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, 19104, PA, USA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, 19104, PA, USA., MacMullen LE; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, 19104, PA, USA., Xiao R; Division of Biostatistics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, 19146, PA, USA., Falk MJ; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, 19104, PA, USA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, 19104, PA, USA. Electronic address: falkm@chop.edu., Ehinger JK; Otorhinolaryngology, Head and Neck Surgery, Department of Clinical Sciences Lund, Lund University, Skåne University Hospital, 221 85 Lund, Sweden; Mitochondrial Medicine, Department of Clinical Sciences Lund, Lund University, 221 84 Lund, Sweden. Electronic address: johannes.ehinger@med.lu.se.

المصدر: Molecular genetics and metabolism [Mol Genet Metab] 2022 Nov; Vol. 137 (3), pp. 230-238. Date of Electronic Publication: 2022 Sep 19.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE

مواضيع طبية MeSH: Mitochondrial Diseases*/complications , Mitochondrial Diseases*/genetics , Hearing Loss, Sensorineural*/genetics , Hearing Loss, Sensorineural*/diagnosis, Young Adult ; Humans ; Child ; DNA, Mitochondrial/genetics ; Retrospective Studies ; Mitochondria/genetics

المؤلفون: Karaa A; Department of Genetics, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA., MacMullen LE; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., Campbell JC; Minovia Therapeutics, Cambridge, MA 02138, USA., Christodoulou J; Murdoch Children's Research Institute and Department of Paediatrics, University of Melbourne, Melbourne, Victoria 3052, Australia., Cohen BH; Department of Pediatrics and the Rebecca D. Considine Research Institute, Akron Children's Hospital, Akron, OH 44308, USA., Klopstock T; Friedrich-Baur Institute, Department of Neurology, University Hospital, LMU, Munich 80336, Germany; German Center for Neurodegenerative Diseases (DZNE), Munich 80336, Germany; Munich Cluster for Systems Neurology (SyNergy), Munich 80336, Germany; German Network for Mitochondrial Disorders (mitoNET), Munich 80336, Germany., Koga Y; Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume 830-0011, Japan., Lamperti C; UO Genetics and Neurogenetics, Fondazione IRCCS Instituto Neurologico C. Besta, Milan 20126, Italy., van Maanen R; Khondrion BV., Nijmegen 6525 EX, The Netherlands., McFarland R; WCMR Newcastle University, Newcastle NE1 7RU, UK., Parikh S; Cleveland Clinic Foundation, Cleveland, OH 44195, USA., Rahman S; UCL Great Ormond Street Institute of Child Health and Great Ormond, Street Hospital for Children NHS Foundation Trust, London WC1N 1EH, UK., Scaglia F; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA; Joint BCM-CUHK Center of Medical Genetics, Prince of Wales Hospital, Hong Kong SAR NT, China., Sherman AV; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA., Yeske P; United Mitochondrial Disease Foundation, Pittsburgh, PA 15239, USA., Falk MJ; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

المصدر: Advanced genetics (Hoboken, N.J.) [Adv Genet (Hoboken)] 2022 Mar; Vol. 3 (1). Date of Electronic Publication: 2021 Dec 19.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Wiley Periodicals Inc Country of Publication: United States NLM ID: 101774320 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2641-6573 (Electronic) Linking ISSN: 26416573 NLM ISO Abbreviation: Adv Genet (Hoboken) Subsets: PubMed not MEDLINE

المؤلفون: Titone MK; Department of Psychology, Temple University, Philadelphia, PA, United States. Electronic address: madison.titone@temple.edu., Goel N; Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, IL, United States., Ng TH; Department of Psychology, Temple University, Philadelphia, PA, United States., MacMullen LE; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States., Alloy LB; Department of Psychology, Temple University, Philadelphia, PA, United States.

المصدر: Journal of affective disorders [J Affect Disord] 2022 Feb 01; Vol. 298 (Pt A), pp. 17-25. Date of Electronic Publication: 2021 Oct 30.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.

بيانات الدورية: Publisher: Elsevier/North-Holland Biomedical Press Country of Publication: Netherlands NLM ID: 7906073 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-2517 (Electronic) Linking ISSN: 01650327 NLM ISO Abbreviation: J Affect Disord Subsets: MEDLINE

مواضيع طبية MeSH: Bipolar Disorder*/epidemiology , Melatonin*, Adult ; Circadian Rhythm ; Ecological Momentary Assessment ; Female ; Humans ; Impulsive Behavior ; Male ; Sleep ; Young Adult

المؤلفون: Yamazaki EM; Biological Rhythms Research Laboratory, Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, IL, United States., Rosendahl-Garcia KM; Siemens Healthineers, Inc., Mountain View, CA, United States., Casale CE; Biological Rhythms Research Laboratory, Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, IL, United States., MacMullen LE; Division of Sleep and Chronobiology, Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States., Ecker AJ; Division of Sleep and Chronobiology, Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States., Kirkpatrick JN; Division of Cardiology, Department of Medicine, University of Washington, Seattle, WA, United States., Goel N; Biological Rhythms Research Laboratory, Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, IL, United States.

المصدر: Frontiers in physiology [Front Physiol] 2022 Jan 11; Vol. 12, pp. 795321. Date of Electronic Publication: 2022 Jan 11 (Print Publication: 2021).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101549006 Publication Model: eCollection Cited Medium: Print ISSN: 1664-042X (Print) Linking ISSN: 1664042X NLM ISO Abbreviation: Front Physiol Subsets: PubMed not MEDLINE

المؤلفون: Yamazaki EM; Biological Rhythms Research Laboratory, Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, IL, United States., Antler CA; Biological Rhythms Research Laboratory, Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, IL, United States., Casale CE; Biological Rhythms Research Laboratory, Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, IL, United States., MacMullen LE; Division of Sleep and Chronobiology, Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States., Ecker AJ; Division of Sleep and Chronobiology, Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States., Goel N; Biological Rhythms Research Laboratory, Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, IL, United States.

المصدر: Frontiers in physiology [Front Physiol] 2021 Nov 29; Vol. 12, pp. 782860. Date of Electronic Publication: 2021 Nov 29 (Print Publication: 2021).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101549006 Publication Model: eCollection Cited Medium: Print ISSN: 1664-042X (Print) Linking ISSN: 1664042X NLM ISO Abbreviation: Front Physiol Subsets: PubMed not MEDLINE

المؤلفون: Flickinger J; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, USA., Fan J; Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA., Wellik A; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., Ganetzky R; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA., Goldstein A; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA., Muraresku CC; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., Glanzman AM; Department of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, USA., Ballance E; Department of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, USA., Leonhardt K; Department of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, PA, USA., McCormick EM; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., Soreth B; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., Nguyen S; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., Gornish J; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., George-Sankoh I; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., Peterson J; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., MacMullen LE; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., Vishnubhatt S; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., McBride M; Cardiovascular Exercise Physiology Laboratory, Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA., Haas R; Metabolic and Mitochondrial Disease Center, La Jolla, CA, USA.; Department of Neurosciences, University of California San Diego School of Medicine, La Jolla, CA, USA., Falk MJ; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA., Xiao R; Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA., Zolkipli-Cunningham Z; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

المصدر: JCSM clinical reports [JCSM Clin Rep] 2021 Oct; Vol. 6 (4), pp. 109-127. Date of Electronic Publication: 2021 Aug 30.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Charité - Universitätsmedizin Berlin Country of Publication: Germany NLM ID: 101739435 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2521-3555 (Electronic) Linking ISSN: 25213555 NLM ISO Abbreviation: JCSM Clin Rep Subsets: PubMed not MEDLINE

المؤلفون: Titone MK; Department of Psychology, Temple University, 1701 N 13th St, Philadelphia, PA, USA. madison.titone@temple.edu., McArthur BA; Department of Psychology, University of Calgary, Calgary, AB, Canada., Ng TH; Department of Psychology, Temple University, 1701 N 13th St, Philadelphia, PA, USA., Burke TA; Department of Psychiatry and Human Behavior, Alpert Medical School Brown University, Providence, RI, USA., McLaughlin LE; Department of Psychology, Temple University, 1701 N 13th St, Philadelphia, PA, USA., MacMullen LE; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA., Goel N; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.; Department of Psychiatry and Behavioral Sciences, Rush University Medical Center, Chicago, IL, USA., Alloy LB; Department of Psychology, Temple University, 1701 N 13th St, Philadelphia, PA, USA.

المصدر: Scientific reports [Sci Rep] 2020 Aug 13; Vol. 10 (1), pp. 13731. Date of Electronic Publication: 2020 Aug 13.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.

بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE

مواضيع طبية MeSH: Bipolar Disorder/*etiology , Bipolar Disorder/*physiopathology , Circadian Rhythm/*physiology , Sleep/*physiology, Actigraphy/methods ; Adolescent ; Adult ; Bipolar Disorder/metabolism ; Female ; Humans ; Male ; Melatonin/metabolism ; Polysomnography/methods ; Prospective Studies ; Racial Groups ; Self Report ; Sex Factors ; Time Factors ; Young Adult