المؤلفون: Graifman, Jordana L., Lippa, Natalie C., Mulhern, Maureen S., Bergner, Amanda L., Sands, Tristan T.

المصدر: Epilepsia ; volume 64, issue 4, page 986-997 ; ISSN 0013-9580 1528-1167

الإتاحة: https://doi.org/10.1111/epi.17534Test

المؤلفون: Kutsa, Oksana, Terry, Alissa, Bodurtha, Joann, Caggana, Michele, Gonzalez, Carlos, Lopez, Enrique, Frangenberg, Maria, Burgos, Coralaidee, Arciniegas-Medina, Norma, Bergner, Amanda, Raspa, Melissa

المصدر: Genetics in Medicine Open ; volume 1, issue 1, page 100431 ; ISSN 2949-7744

الإتاحة: https://doi.org/10.1016/j.gimo.2023.100431Test
https://api.elsevier.com/content/article/PII:S2949774423004314?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2949774423004314?httpAccept=text/plainTest

المؤلفون: Wolters, Pamela L, Martin, Staci, Merker, Vanessa L, Tonsgard, James H, Solomon, Sondra E, Baldwin, Andrea, Bergner, Amanda L, Walsh, Karin, Thompson, Heather L, Gardner, Kathy L, Hingtgen, Cynthia M, Schorry, Elizabeth, Dudley, William N, Franklin, Barbara

المصدر: Neurology. 87(7_Supplement_1)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Clinical Sciences, Clinical Research, Chronic Pain, Neurosciences, Pain Research, Clinical Trials and Supportive Activities, Good Health and Well Being, Clinical Trials as Topic, Disability Evaluation, Humans, Neurofibromatoses, Pain, Pain Measurement, Patient Reported Outcome Measures, Self Report, REiNS International Collaboration, Cognitive Sciences, Neurology & Neurosurgery, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7vr8t379Test

المؤلفون: Steigerwald, Connolly G., Bertolini, Carina, McElhiney, Martin, Bergner, Amanda L., Harms, Matthew B., Harrington, Elizabeth A.

المصدر: Journal of Genetic Counseling ; ISSN 1059-7700 1573-3599

الإتاحة: https://doi.org/10.1002/jgc4.1890Test

المؤلفون: Martin, Bree E, Sands, Tristan, Bier, Louise, Bergner, Amanda, Boehme, Amelia K, Lippa, Natalie

المصدر: Journal of Medical Genetics ; volume 61, issue 7, page 645-651 ; ISSN 0022-2593 1468-6244

الإتاحة: https://doi.org/10.1136/jmg-2023-109450Test

المؤلفون: Temares, Dani S., Liang, Lusha W., Bergner, Amanda L., Reilly, Muredach P., Kalia, Isha

المصدر: Journal of Community Genetics; Apr2024, Vol. 15 Issue 2, p119-127, 9p

المؤلفون: Freiman, Andrew, Rekab, Aisha, Bergner, Amanda L., Pereira, Elaine M., Lin, Yuhuan, Ahimaz, Priyanka

المصدر: American Journal of Medical Genetics. Part A; Apr2024, Vol. 194 Issue 4, p1-11, 11p

المؤلفون: Ahimaz, Priyanka, Bergner, Amanda L., Florido, Michelle E., Harkavy, Nina, Bhattacharyya, Sriya

المصدر: American Journal of Medical Genetics. Part A; Apr2024, Vol. 194 Issue 4, p1-5, 5p

المؤلفون: Plotkin, Scott, Messiaen, Ludwine, Legius, Eric, Pancza, Patrice, Avery, Robert, Blakeley, Jaishri, Babovic-Vuksanovic, Dusica, Ferner, Rosalie, Fisher, Michael, Friedman, Jan, Giovannini, Marco, Gutmann, David, Hanemann, Clemens Oliver, Kalamarides, Michel, Kehrer-Sawatzki, Hildegard, Korf, Bruce, Mautner, Victor-Felix, Maccollin, Mia, Papi, Laura, Rauen, Katherine, Riccardi, Vincent, Schorry, Elizabeth, Smith, Miriam, Stemmer-Rachamimov, Anat, Stevenson, David, Ullrich, Nicole, Viskochil, David, Wimmer, Katharina, Yohay, Kaleb, Huson, Susan, Wolkenstein, Pierre, Evans, D. Gareth, Anten, Monique, Aylsworth, Arthur, Baralle, Diana, Barbarot, Sebastien, Barker, Fred, Ben-Shachar, Shay, Bergner, Amanda, Bessis, Didier, Blanco, Ignacio, Cassiman, Catherine, Ciavarelli, Patricia, Clementi, Maurizio, Frébourg, Thierry, Gomes, Alicia, Halliday, Dorothy, Helen Hanson Arvid Heiberg, Chris Hammond, Joly, Pascal, Jordan, Justin, Karajannis, Matthias, Kroshinsky, Daniela, Larralde, Margarita, Lázaro, Conxi, Le, Lu, Link, Michael, Listernick, Robert, Mallucci, Conor, Merker, Vanessa, Moertel, Christopher, Mueller, Amy, Ngeow, Joanne, Oostenbrink, Rianne, Packer, Roger, Parry, Allyson, Peltonen, Juha, Pichard, Dominique, Poppe, Bruce, Rezende, Nilton, Rodrigues, Luiz Oswaldo, Rosser, Tena, Ruggieri, Martino, Serra, Eduard, Steinke-Lange, Verena, Stivaros, Stavros Michael, Taylor, Amy, Toelen, Jaan, Tonsgard, James, Trevisson, Eva, Upadhyaya, Meena, Varan, Ali, Wilson, Meredith, Wu, Hao, Zadeh, Gelareh

المساهمون: Johns Hopkins University School of Medicine Baltimore, Mayo Clinic Rochester, Department of Neurology, GSTT, Guys Hospital, University of North Carolina Chapel Hill (UNC), University of North Carolina System (UNC), David Geffen School of Medicine Los Angeles, University of California Los Angeles (UCLA), University of California (UC)-University of California (UC), Universität Ulm - Ulm University Ulm, Allemagne, Department of Maxillofacial Surgery Hamburg-Eppendorf, Universitaetsklinikum Hamburg-Eppendorf = University Medical Center Hamburg-Eppendorf Hamburg (UKE), Università degli Studi di Firenze = University of Florence = Université de Florence (UniFI), Physiopathologie des Adaptations Nutritionnelles (PhAN), Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Nantes Université - UFR de Médecine et des Techniques Médicales (Nantes Univ - UFR MEDECINE), Nantes Université - pôle Santé, Nantes Université (Nantes Univ)-Nantes Université (Nantes Univ)-Nantes Université - pôle Santé, Nantes Université (Nantes Univ)-Nantes Université (Nantes Univ)

المصدر: ISSN: 1098-3600.

مصطلحات موضوعية: [SDV]Life Sciences [q-bio]

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35674741; hal-04076910; https://hal.inrae.fr/hal-04076910Test; https://hal.inrae.fr/hal-04076910/documentTest; https://hal.inrae.fr/hal-04076910/file/2022_Plotkin_genetics%20in%20medecine.pdfTest; PUBMED: 35674741; WOS: 000855692500017

الإتاحة: https://doi.org/10.1016/j.gim.2022.05.007Test
https://hal.inrae.fr/hal-04076910Test
https://hal.inrae.fr/hal-04076910/documentTest
https://hal.inrae.fr/hal-04076910/file/2022_Plotkin_genetics%20in%20medecine.pdfTest

المؤلفون: Legius, Eric, Messiaen, Ludwine, Wolkenstein, Pierre, Pancza, Patrice, Avery, Robert A., Berman, Yemima, Blakeley, Jaishri, Babovic-Vuksanovic, Dusica, Cunha, Karin Soares, Ferner, Rosalie, Fisher, Michael J., Friedman, Jan M., Gutmann, David H., Kehrer-Sawatzki, Hildegard, Korf, Bruce R., Mautner, Victor, Peltonen, Sirkku, Rauen, Katherine A., Riccardi, Vincent, Schorry, Elizabeth, Stemmer-Rachamimov, Anat, Stevenson, David A., Tadini, Gianluca, Ullrich, Nicole J., Viskochil, David, Wimmer, Katharina, Yohay, Kaleb, Gomes, Alicia, Jordan, Justin T., Merker, Vanessa L., Smith, Miriam J., Stevenson, David, Anten, Monique, Aylsworth, Arthur, Baralle, Diana, Barbarot, Sebastien, Barker, Fred, Ben-Shachar, Shay, Bergner, Amanda, Bessis, Didier, Blanco, Ignacio, Cassiman, Catherine, Ciavarelli, Patricia, Clementi, Maurizio, Frébourg, Thierry, Giovannini, Marco, Halliday, Dorothy, Wu, Hao, Evans, D. Gareth

وصف الملف: text

العلاقة: https://eprints.soton.ac.uk/453413/1/1_s2.0_S1098360021050747_main.pdfTest; International Consensus Group on Neurofibromatosis Diagnostic Criteria (I-NF-DC) (2021) Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation. Genetics in Medicine, 23 (8), 1506-1513. (doi:10.1038/s41436-021-01170-5 ).

الإتاحة: https://doi.org/10.1038/s41436-021-01170-5Test
https://eprints.soton.ac.uk/453413Test/
https://eprints.soton.ac.uk/453413/1/1_s2.0_S1098360021050747_main.pdfTest