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1. Goals for Persistent Postconcussive Symptom Treatment From Adolescent and Parent Perspectives
by Payne, Katelyn M and Prentice, Emily T and Marcynyszyn, Lyscha A and McCarty, Carolyn A
JAMA pediatrics, ISSN 2168-6203, 12/2020, Volume 174, Issue 12, pp. 1210 - 1211
Life Sciences & Biomedicine | Pediatrics | Science & Technology | Parents & parenting | Concussion | Medical treatment | Teenagers | Patient satisfaction | Symptoms
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2. Full Text Quantitative analysis of the density of trap states at the semiconductor-dielectric interface in organic field-effect transistors
by Diemer, Peter J and Lamport, Zachary A and Mei, Yaochuan and Ward, Jeremy W and Goetz, Katelyn P and Li, Wei and Payne, Marcia M and Guthold, Martin and Anthony, John E and Jurchescu, Oana D
Applied physics letters, ISSN 0003-6951, 09/2015, Volume 107, Issue 10, p. 103303
Physical Sciences | Physics | Science & Technology | Physics, Applied | Current carriers | Electrical properties | Semiconductor devices | Electric contacts | Field effect transistors | Dielectric properties | Contact resistance | Carrier mobility | Transistors | Silicon dioxide | Quantitative analysis
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3. Approach to Assessment of Parkinson Disease with Emphasis on Genetic Testing
by Payne, Katelyn and Walls, Brooke and Wojcieszek, Joanne
The Medical clinics of North America, ISSN 0025-7125, 11/2019, Volume 103, Issue 6, p. 1055
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology
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4. Full Text Collaborative care model for treatment of persistent symptoms after concussion among youth (CARE4PCS-II): Study protocol for a randomized, controlled trial
by McCarty, Carolyn A and Zatzick, Douglas and Hoopes, Teah and Payne, Katelyn and Parrish, Rebecca and Rivara, Frederick P
Trials, ISSN 1745-6215, 09/2019, Volume 20, Issue 1, pp. 567 - 567
Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Brain Concussion - physiopathology | Delivery of Health Care, Integrated | Humans | Athletic Injuries - diagnosis | Patient Care Team | Athletic Injuries - psychology | Athletic Injuries - therapy | Male | Treatment Outcome | Combined Modality Therapy | Cognitive Behavioral Therapy | Brain Concussion - therapy | Washington | Psychotropic Drugs - therapeutic use | Randomized Controlled Trials as Topic | Comparative Effectiveness Research | Brain Concussion - psychology | Time Factors | Athletic Injuries - physiopathology | Brain Concussion - diagnosis | Adolescent | Female | Referral and Consultation | Child | Usage | Sports injuries | Care and treatment | Analysis | Clinical trials | Evidence-based medicine | Teenage girls | Health aspects | Index Medicus | Adolescent health | Cognitive-behavior therapy | Concussion | Randomized trials | Collaborative care | Sports injury
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5. Full Text The progression of Wiedemann–Steiner syndrome in adulthood and two novel variants in the KMT2A gene
by Feldman, Hailey R and Dlouhy, Stephen R and Lah, Melissa D and Payne, Katelyn K and Weaver, David D
American journal of medical genetics. Part A, ISSN 1552-4825, 02/2019, Volume 179, Issue 2, pp. 300 - 305
hypertrichosis | lysine methyltransferase | KMT2A | Wiedemann–Steiner syndrome | hypertrichosis cubiti | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Microcephaly - genetics | Humans | Child, Preschool | Infant | Male | Developmental Disabilities - genetics | Contracture - genetics | Intellectual Disability - genetics | Young Adult | Facies | Adult | Female | Microcephaly - physiopathology | Musculoskeletal Abnormalities - physiopathology | Child | Abnormalities, Multiple - genetics | Contracture - physiopathology | Developmental Disabilities - physiopathology | Histone-Lysine N-Methyltransferase - genetics | Abnormalities, Multiple - physiopathology | Disease Progression | Intellectual Disability - physiopathology | Hypertrichosis - physiopathology | Phenotype | Hypertrichosis - genetics | Myeloid-Lymphoid Leukemia Protein - genetics | Musculoskeletal Abnormalities - genetics | Adolescent | Growth Disorders - genetics | Growth Disorders - physiopathology | Congenital defects | Index Medicus
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6. Full Text An Unexplained Case of Progressive Spastic Paraparesis in an Individual with Known DiGeorge Syndrome
by Dhoot, Roshni and Payne, Katelyn and Fink, John K and Pascuzzi, Robert M
Case reports in neurology, ISSN 1662-680X, 06/2020, Volume 12, Issue 2, pp. 165 - 168
Single Case – General Neurology | Ostomy | Multiple sclerosis | Hyperactivity | Intellectual disabilities | Genes | Cognitive ability | Vitamin deficiency | Ataxia | Age | spastic paraparesis | 22q11 | digeorge syndrome
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7. Full Text Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome)
by Assia Batzir, Nurit and Posey, Jennifer E and Song, Xiaofei and Akdemir, Zeynep Coban and Rosenfeld, Jill A and Brown, Chester W and Chen, Emily and Holtrop, Shannon G and Mizerik, Elizabeth and Nieto Moreno, Margarita and Payne, Katelyn and Raas‐Rothschild, Annick and Scott, Richard and Vernon, Hilary J and Zadeh, Neda and Lupski, James R and Sutton, V. Reid and Baylor-Hopkins Ctr Mendelian Genom and Baylor-Hopkins Center for Mendelian Genomics and Baylor‐Hopkins Center for Mendelian Genomics
American journal of medical genetics. Part A, ISSN 1552-4825, 01/2020, Volume 182, Issue 1, pp. 38 - 52
speech delay | developmental delay | autism | intellectual disability | POGZ | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Autistic Disorder - pathology | Microcephaly - genetics | Humans | Middle Aged | Child, Preschool | Infant | Male | Intellectual Disability - genetics | Young Adult | Microcephaly - pathology | Transposases - genetics | Adult | Female | Child | Intellectual Disability - epidemiology | Autistic Disorder - genetics | Language Development Disorders - genetics | Intellectual Disability - pathology | Language Development Disorders - pathology | Mutation - genetics | Whole Exome Sequencing | Exome - genetics | Phenotype | Adolescent | Heterozygote | Hypoplasia | Autism | Body mass index | Sleep disorders | Phenotypes | Sleep | Apnea | Microencephaly | Gait | Intellectual disabilities | Hearing loss | Index Medicus
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8. Full Text Isomerically Pure syn-Anthradithiophenes: Synthesis, Properties, and FET Performance
by Lehnherr, Dan and Waterloo, Andreas R and Goetz, Katelyn P and Payne, Marcia M and Hampel, Frank and Anthony, John E and Jurchescu, Oana D and Tykwinski, Rik R
Organic letters, ISSN 1523-7060, 07/2012, Volume 14, Issue 14, pp. 3660 - 3663
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9. Full Text Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination
by Efthymiou, Stephanie and Salpietro, Vincenzo and Malintan, Nancy and Poncelet, Mallory and Kriouile, Yamna and Fortuna, Sara and De Zorzi, Rita and Payne, Katelyn and Henderson, Lindsay and Cortese, Andrea
Brain (London, England : 1878), ISSN 0006-8950, 10/2019, Volume 142, Issue 10, pp. 2948 - 2964
Life Sciences | Immunology | Neurons and Cognition | Neurobiology | Cellular Biology | Adaptive immunology | Cell Behavior
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10. Full Text Novel Homozygous Deletion in STRADA Gene Associated With Polyhydramnios, Megalencephaly, and Epilepsy in 2 Siblings: Implications for Diagnosis and Treatment
by Nelson, Katherine and Jackman, Christopher and Bell, Jennifer and Shih, Chie-Schin and Payne, Katelyn and Dlouhy, Stephen and Walsh, Laurence
Journal of child neurology, ISSN 0883-0738, 12/2018, Volume 33, Issue 14, pp. 925 - 929
neurodevelopment | next-generation sequencing | nephrocalcinosis | seizures | neonatal seizures | autosomal recessive | epileptic encephalopathy | facial dysmorphism | Pediatrics | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology
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11. Full Text Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes
by Martinelli, Simone and Krumbach, Oliver H.F and Pantaleoni, Francesca and Coppola, Simona and Amin, Ehsan and Pannone, Luca and Nouri, Kazem and Farina, Luciapia and Dvorsky, Radovan and Lepri, Francesca and Buchholzer, Marcel and Konopatzki, Raphael and Walsh, Laurence and Payne, Katelyn and Pierpont, Mary Ella and Vergano, Samantha Schrier and Langley, Katherine G and Larsen, Douglas and Farwell, Kelly D and Tang, Sha and Mroske, Cameron and Gallotta, Ivan and Di Schiavi, Elia and della Monica, Matteo and Lugli, Licia and Rossi, Cesare and Seri, Marco and Cocchi, Guido and Henderson, Lindsay and Baskin, Berivan and Alders, Mariëlle and Mendoza-Londono, Roberto and Dupuis, Lucie and Nickerson, Deborah A and Chong, Jessica X and Meeks, Naomi and Brown, Kathleen and Causey, Tahnee and Cho, Megan T and Demuth, Stephanie and Digilio, Maria Cristina and Gelb, Bruce D and Bamshad, Michael J and Zenker, Martin and Ahmadian, Mohammad Reza and Hennekam, Raoul C and Tartaglia, Marco and Mirzaa, Ghayda M and The University of Washington Center for Mendelian Genomics and Univ Washington Ctr Mendel and University of Washington Center for Mendelian Genomics
American journal of human genetics, ISSN 0002-9297, 02/2018, Volume 102, Issue 2, pp. 309 - 320
microcephaly | mutation spectrum | exome sequencing | thrombocytopenia | Noonan syndrome | phenotypic heterogeneity | genotype-phenotype correlations | developmental anomalies | cardiac defects | functional profiling | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Usage | Care and treatment | Genetic disorders | Gene mutations | Exome sequencing | Development and progression | Research | Index Medicus | Report
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12. Full Text Charge-transfer complexes: New perspectives on an old class of compounds
by Goetz, Katelyn P and Vermeulen, Derek and Payne, Margaret E and Kloc, Christian and McNeil, Laurie E and Jurchescu, Oana D
Journal of materials chemistry. C, Materials for optical and electronic devices, ISSN 2050-7534, 05/2014, Volume 2, Issue 17, pp. 3065 - 3076
Physical Sciences | Materials Science | Technology | Materials Science, Multidisciplinary | Physics | Science & Technology | Physics, Applied
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13. Full Text Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital Malformations
by Hughes, Joel J and Alkhunaizi, Ebba and Kruszka, Paul and Pyle, Louise C and Grange, Dorothy K and Berger, Seth I and Payne, Katelyn K and Masser-Frye, Diane and Hu, Tommy and Christie, Michelle R and Clegg, Nancy J and Everson, Joshua L and Martinez, Ariel F and Walsh, Laurence E and Bedoukian, Emma and Jones, Marilyn C and Harris, Catharine Jean and Riedhammer, Korbinian M and Choukair, Daniela and Fechner, Patricia Y and Rutter, Meilan M and Hufnagel, Sophia B and Roifman, Maian and Kletter, Gad B and Delot, Emmanuele and Vilain, Eric and Lipinski, Robert J and Vezina, Chad M and Muenke, Maximilian and Chitayat, David
American journal of human genetics, ISSN 0002-9297, 01/2020, Volume 106, Issue 1, pp. 121 - 128
encephalocele | PPP1R12A | embryogenesis | omphalocele | MYPT1 | hypospadias | disorders of sex development | forebrain | holoprosencephaly | facial dysmorphism | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Abnormalities, Multiple - pathology | Humans | Myosin-Light-Chain Phosphatase - genetics | Child, Preschool | Male | Holoprosencephaly - genetics | Holoprosencephaly - pathology | Disorders of Sex Development - genetics | Gestational Age | Pregnancy | Phenotype | Urogenital Abnormalities - pathology | Disorders of Sex Development - pathology | Adolescent | Female | Mutation | Child | Abnormalities, Multiple - genetics | Urogenital Abnormalities - genetics | Embryonic development | Genetic variation | Pseudohermaphroditism | Causes of | Genetic aspects | Identification and classification | Health aspects | Holoprosencephaly | Sex differentiation disorders | Index Medicus | Report
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