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2. Practicing the Engineering Fundamentals in a Project-Based Design and 3D Printing Course

Author

Levin, Laura, Verner, Igor, Kacprzyk, Janusz, Series Editor, Gomide, Fernando, Advisory Editor, Kaynak, Okyay, Advisory Editor, Liu, Derong, Advisory Editor, Pedrycz, Witold, Advisory Editor, Polycarpou, Marios M., Advisory Editor, Rudas, Imre J., Advisory Editor, Wang, Jun, Advisory Editor, Auer, Michael E., editor, Cukierman, Uriel R., editor, Vendrell Vidal, Eduardo, editor, and Tovar Caro, Edmundo, editor

Published
2024
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3. Characterization of wound microbes in epidermolysis bullosa: A focus on Pseudomonas aeruginosa.

Author

Scollan, Margaret, Levin, Laura, Lucky, Anne, Hook, Kristen, Peoples, Kathleen, Bruckner, Anna, Feinstein, James, Pope, Elena, McCuaig, Catherine, Powell, Julie, Eichenfield, Lawrence, Levy, Moise, Diaz, Lucia, Glick, Sharon, Paller, Amy, Browning, John, and Morel, Kimberly

Subjects
epidermolysis bullosa, infection-bacterial, therapy-topical, Humans, Pseudomonas aeruginosa, Epidermolysis Bullosa
Abstract

The most common bacteria isolated from wound cultures in patients recorded in the Epidermolysis Bullosa Clinical Characterization and Outcomes Database (EBCCOD) are Staphylococcus aureus and Pseudomonas aeruginosa. Given the prevalence of P. aeruginosa in this patient population and prior research implicating P. aeruginosas potential role in carcinogenesis, we sought to further analyze patients with recorded wound cultures positive for Pseudomonas aeruginosa in the EBCCOD. We provide a descriptive analysis of this subset of patients and highlight potential avenues for future longitudinal studies that may have significant implications in our wound care management for patients with epidermolysis bullosa.

Published
2023

4. Inpatient management of epidermolysis bullosa: Consensus-based hands-on instructions for neonates and postneonates

Author

Abreu Molnar, Brenda, Levin, Laura, Yun, Duri, Morel, Kimberly, Wiss, Karen, Wieser, Julie, Ward, Christopher, Trice, Haley, Garcia-Romero, Maria Teresa, Stephenson, Allison, Provost, Adrienne, Price, Harper N., Perman, Marissa J., Moxon, Morgan, Moeves, Beth, McCuaig, Catherine C., McCarthy, Christine, Lucky, Anne W., Levy, Moise L., Lee, Michelle, Lara-Corrales, Irene, Henner, Natalia, Halliburton, Nichole, Griffith, Emily, Gorell, Emily, Glick, Sharon, Eichenfield, Lawrence, Collins, Clara, Bruckner, Anna L., Boulrice, Brenda, Bayliss, Susan, Badger, Kellie, and Paller, Amy S.

Published
2024
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8. Characterization of wound microbes in epidermolysis bullosa: Results from the epidermolysis bullosa clinical characterization and outcomes database

Author

Levin, Laura E, Shayegan, Leila H, Lucky, Anne W, Hook, Kristen P, Bruckner, Anna L, Feinstein, James A, Whittier, Susan, Lauren, Christine T, Pope, Elena, Lara‐Corrales, Irene, Wiss, Karen, McCuaig, Catherine C, Powell, Julie, Eichenfield, Lawrence F, Levy, Moise L, Diaz, Lucia, Glick, Sharon A, Paller, Amy S, Price, Harper N, Browning, John C, and Morel, Kimberly D

Subjects
Biomedical and Clinical Sciences, Clinical Sciences, Emerging Infectious Diseases, Biodefense, Infectious Diseases, Prevention, Vaccine Related, Antimicrobial Resistance, Clinical Research, Infection, Anti-Bacterial Agents, Canada, Epidermolysis Bullosa, Humans, Mupirocin, Retrospective Studies, Staphylococcal Infections, Staphylococcus aureus, cultures, epidermolysis bullosa, microbes, resistance, wound, Paediatrics and Reproductive Medicine, Dermatology & Venereal Diseases, Clinical sciences, Paediatrics
Abstract

Background/objectivesPatients with epidermolysis bullosa (EB) require care of wounds that are colonized or infected with bacteria. A subset of EB patients are at risk for squamous cell carcinoma, and bacterial-host interactions have been considered in this risk. The EB Clinical Characterization and Outcomes Database serves as a repository of information from EB patients at multiple centers in the United States and Canada. Access to this resource enabled broad-scale analysis of wound cultures.MethodsA retrospective analysis of 739 wound cultures from 158 patients from 13 centers between 2001 and 2018.ResultsOf 152 patients with a positive culture, Staphylococcus aureus (SA) was recovered from 131 patients (86%), Pseudomonas aeruginosa (PA) from 56 (37%), and Streptococcus pyogenes (GAS) from 34 (22%). Sixty-eight percent of patients had cultures positive for methicillin-sensitive SA, and 47%, methicillin-resistant SA (18 patients had cultures that grew both methicillin-susceptible and methicillin-resistant SA at different points in time). Of 15 patients with SA-positive cultures with recorded mupirocin susceptibility testing, 11 had mupirocin-susceptible SA and 6 patients mupirocin-resistant SA (2 patients grew both mupirocin-susceptible and mupirocin-resistant SA). SCC was reported in 23 patients in the entire database, of whom 10 had documented wound cultures positive for SA, PA, and Proteus species in 90%, 50%, and 20% of cases, respectively.ConclusionsSA and PA were the most commonly isolated bacteria from wounds. Methicillin resistance and mupirocin resistance were reported in 47% and 40% of patients tested, respectively, highlighting the importance of ongoing antimicrobial strategies to limit antibiotic resistance.

Published
2021

9. Focusing a Technology Teacher Education Course on Collaborative Cloud-Based Design with Onshape

Author

Cuperman, Dan, Verner, Igor Michael, Levin, Laura, Greenholts, Moshe, Rosen, Uzi, Kacprzyk, Janusz, Series Editor, Gomide, Fernando, Advisory Editor, Kaynak, Okyay, Advisory Editor, Liu, Derong, Advisory Editor, Pedrycz, Witold, Advisory Editor, Polycarpou, Marios M., Advisory Editor, Rudas, Imre J., Advisory Editor, Wang, Jun, Advisory Editor, Auer, Michael E., editor, Hortsch, Hanno, editor, Michler, Oliver, editor, and Köhler, Thomas, editor

Published
2022
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10. Assessment of the Timing of Milestone Clinical Events in Patients With Epidermolysis Bullosa From North America

Author

Feinstein, James A, Jambal, Purevsuren, Peoples, Kathleen, Lucky, Anne W, Khuu, Phuong, Tang, Jean Y, Lara-Corrales, Irene, Pope, Elena, Wiss, Karen, Hook, Kristen P, Levin, Laura E, Morel, Kimberly D, Paller, Amy S, McCuaig, Catherine C, Powell, Julie, Eichenfield, Lawrence F, Price, Harper, Levy, Moise L, Schachner, Lawrence A, Browning, John C, Bayliss, Susan, Jahnke, Marla, Shwayder, Tor, Glick, Sharon A, and Bruckner, Anna L

Subjects
Pediatric, Congenital Structural Anomalies, Clinical Research, Good Health and Well Being, Adolescent, Age Distribution, Biopsy, Needle, Canada, Child, Child, Preschool, Cohort Studies, Databases, Factual, Disease Progression, Epidermolysis Bullosa, Female, Follow-Up Studies, Genetic Predisposition to Disease, Humans, Immunohistochemistry, Incidence, Infant, Male, North America, Retrospective Studies, Risk Assessment, Severity of Illness Index, Sex Distribution, Survival Analysis, Young Adult, Clinical Sciences, Oncology and Carcinogenesis
Abstract

ImportanceChildren with epidermolysis bullosa (EB) comprise a rare population with high morbidity and mortality. An improved understanding of the clinical trajectory of patients with EB, including age at time of clinical diagnosis and major clinical events, is needed to refine best practices and improve quality of life and clinical outcomes for patients with EB.ObjectivesTo describe demographics, clinical characteristics, milestone diagnostic and clinical events (such as initial esophageal dilation), and outcomes in patients with EB using the Epidermolysis Bullosa Clinical Characterization and Outcomes Database and to determine what characteristics may be associated with overall EB severity and/or disease progression.Design, setting, and participantsThis cohort study included data on patients with EB who were enrolled in the Epidermolysis Bullosa Clinical Characterization and Outcomes Database from January 1, 2011, to June 30, 2017; 17 participating EB centers in the United States and Canada contributed data to this study.ExposuresType of EB, including recessive dystrophic epidermolysis bullosa (RDEB), junctional epidermolysis bullosa (JEB), dominant dystrophic epidermolysis bullosa (DDEB), and epidermolysis bullosa simplex (EBS).Main outcomes and measuresDemographic information, clinical characteristics (including age at onset of signs of EB and subsequent clinical diagnosis), types of diagnostic testing performed, and milestone clinical events for patients with RDEB.ResultsOf 644 enrolled patients from 17 sites included in this study, 323 were male (50.2%), with a mean (SD) age of 14.4 (11.7) years; 283 (43.9%) had RDEB, 194 (30.1%) had EBS, 104 (16.2%) had DDEB, and 63 (9.8%) had JEB. Signs of disease were present at birth in 202 patients with RDEB (71.4%), 39 with JEB (61.9%), 60 with DDEB (57.7%), and 74 with EBS (38.1%). For those with signs of disease at birth, a clinical diagnosis was made at the time of birth in 135 patients with RDEB (67.0%), 31 with DDEB (52.6%), 35 with EBS, (47.3%) and 18 with JEB (46.2%). Patients with JEB had the highest rate of any confirmatory testing (51 of 63 [81.0%]), followed by RDEB (218 of 283 [77.0%]), DDEB (71 of 104 [68.3%]), and EBS (100 of 194 [51.5%]). For all types of EB, both electron microscopy and immunofluorescence microscopy were performed at younger ages than genetic analysis. Among 283 patients with RDEB, 157 (55.5%) had esophageal dilation, 104 (36.7%) had gastrostomy tube placement, 62 (21.9%) had hand surgery, 18 (6.4%) developed squamous cell carcinoma, and 19 (6.7%) died.Conclusions and relevanceThe findings suggest that diagnostic testing for EB is more common for patients with severe phenotypes. Earlier diagnostic testing may enable improved characterizations of patients so that appropriate counseling and clinical care may be offered, especially pertaining to milestone events for those with RDEB.

Published
2019

15. A retrospective analysis of diagnostic testing in a large North American cohort of patients with epidermolysis bullosa

Author

Phillips, Gregory Scott, Huang, Amy, Augsburger, Bret D., Kaplan, Laura, Peoples, Kathleen, Bruckner, Anna L., Khuu, Phuong, Tang, Jean Y., Lara-Corrales, Irene, Pope, Elena, Wiss, Karen, Levin, Laura E., Morel, Kimberly D., Hook, Kristen P., Paller, Amy S., Eichenfield, Lawrence F., McCuaig, Catherine C., Powell, Julie, Castelo-Soccio, Leslie, Levy, Moise L., Price, Harper N., Schachner, Lawrence A., Browning, John C., Jahnke, Marla, Shwayder, Tor, Bayliss, Susan, Lucky, Anne W., and Glick, Sharon A.

Published
2022
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16. How many is too many? A review of the significant numbers in pediatric skin lesions and their recommended evaluation.

Author

Mulinda, Carly, Yun, Sonora, Fenner, Justine, Garzon, Maria C., Scollan, Margaret E., and Levin, Laura E.

Subjects
PIGMENTATION disorders, SYMPTOMS, MACULES, HEMANGIOMAS, DIAGNOSIS
Abstract

Pediatric dermatologists are frequently consulted to evaluate children for cutaneous signs of systemic disorders. Numerical thresholds of significance have been described in the dermatologic literature for various skin findings where the likelihood of an associated extracutaneous abnormality or known genetic syndrome increases significantly. Knowledge of these numerical thresholds facilitates diagnosis and management, which improves clinical outcomes and avoids severe complications. This review highlights the clinical presentation, complications, evaluation, and numerical significance, when applicable, for the following skin findings: infantile hemangiomas, capillary malformations, café‐au‐lait macules, hypopigmented macules, juvenile xanthogranulomas, pilomatricomas, and angiofibromas. [ABSTRACT FROM AUTHOR]

Published
2024
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17. Transition of care in adolescents with epidermolysis bullosa: The provider perspective.

Author

Perez, Victoria A., Mulinda, Carly, Bruckner, Anna L., Diaz, Lucia Z., Hook, Kristen P., Lara‐Corrales, Irene, Levy, Moise L., Price, Harper N., Morel, Kimberly D., and Levin, Laura E.

Subjects
TRANSITIONAL care, EPIDERMOLYSIS bullosa, PEDIATRIC dermatology, PEDIATRIC therapy, CONSORTIA
Abstract

The characteristics of epidermolysis bullosa (EB) demand higher than average provider support for transition from pediatric to adult care. We administered an online Qualtrics survey to members of the Epidermolysis Bullosa Clinical Research Consortium (EBCRC), a group of providers who care for patients with EB, in order to examine their practices and perspectives on transition of care (TOC) and identify barriers to successful implementation. Sixteen of eighteen medical centers completed the survey. Eighty‐eight percent of center representatives expressed concerns about their patients transitioning/transferring from the pediatric to adult‐centered care. Thirty‐eight percent of providers reported having a formal TOC program in place. Our findings support the desire for formal TOC programs, the need for a team‐based approach and, in particular, identification of adult providers to participate in the transition to improve this often challenging time. [ABSTRACT FROM AUTHOR]

Published
2024
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27. Comparing long‐term outcomes of children treated with new‐onset type 2 diabetes in an outpatient versus inpatient setting: A retrospective chart review.

Author

Ranganna, Adesh, Chen, Wenya, DeLacey, Sean, Lado, Juan, Levin, Laura, Swamy, Anita, and Bianco, Monica E.

Subjects
TYPE 2 diabetes, TREATMENT effectiveness, GLYCEMIC control, GLYCOSYLATED hemoglobin, ELECTRONIC health records, HYPERGLYCEMIA
Abstract

Background: Early identification and management of pediatric type 2 diabetes mellitus (T2DM) is crucial for improving long‐term outcomes. This study aimed to assess if the severity of T2DM at presentation, inferred by the location of treatment initiation (inpatient or outpatient), influences long‐term clinical outcomes. Methods: A retrospective chart review was conducted on 116 pediatric T2DM patients. Data on treatment initiation location, initial and subsequent glycated hemoglobin (HbA1c) levels, prescribed insulin, and body mass index were collected from electronic medical records. Results: Of the 116 patients, 69 were initially treated in an inpatient setting, and 47 received outpatient treatment. At treatment initiation, the inpatient group had significantly higher HbA1c levels compared to the outpatient group (p <.001), but 3 years after treatment initiation, no significant difference in HbA1c was observed between the two groups (p =.057). Prescribed insulin dosages were higher in the inpatient group at treatment initiation (p <.001) and remained higher after 3 years (p < 0.003) compared to the outpatient group. Conclusions: Pediatric patients initially treated in an inpatient setting had poorer glycemic control and higher prescribed insulin dosing at baseline. After 3 years, there was no significant difference in HbA1c levels, but patients treated as inpatients continued to have higher prescribed insulin. These findings suggest that the severity of diabetes at initial presentation may affect long‐term clinical outcomes in children with T2DM. [ABSTRACT FROM AUTHOR]

Published
2024
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29. Editorial

Author

Alvarez, Natalie, Freeman, Barry, Levin, Laura, McLeod, Kimberley, and Stephenson, Jenn

Published
2019

33. Five by Five: Big Questions for Past Editors.

Author

Rubin, Don, Filewod, Alan, Rewa, Natalie, Knowles, Ric, and Levin, Laura

Subjects
EDITORIAL boards, CANADIAN theater, SCRIPTS, ESSAYS
Abstract

The article focuses on the reflections of five former editors of Canadian Theatre Review on their editorial experiences and the challenges they faced. Topics include balancing diverse perspectives in the journal, navigating the evolution of theatre and digital formats, and CTR's significant contributions to the Canadian theatre landscape through publishing scripts, critical essays, and engaging with diverse voices.

Published
2024
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44. Exotic litter of the invasive plant Ligustrum lucidum alters enzymatic production and lignin degradation by selected saprotrophic fungi

Author

Mallerman, Julieta, Itria, Raul, Alarcon-Gutierrez, Enrique, Hernandez, Christian, Levin, Laura, and Saparrat, Mario

Subjects
Lignin -- Environmental aspects, Alien plants -- Environmental aspects, Earth sciences
Abstract

Chemical changes in leaf input to forest soils have been reported to affect decay processes. In this work, litter mass loss and decomposition constants (k) during 200 days in solid-state fermentation of the native tree Celtis tala Gill. ex Planch. and the exotic one Ligustrum lucidum Ait. with three common litter saprotrophic basidiomycetes were compared. Alterations in litter quality were characterized by solid-state [sup.13]C NMR spectroscopy, pH, soluble sugars, ammonium, proteins, and phenol content determination and were associated with extracellular lignocellulolytic enzyme production. Differences in substrate decomposition related to litter type were observed for Leratiomyces ceres, achieving a higher k in the exotic L. lucidum litter, which might be attributed to the induction of manganese peroxidase activity. Substrate preference for alkyl C and more degradation of lignified compounds were found in such substrates. Although no statistical differences in mass loss were observed for the rest of the fungi assayed, we detected changes in several of the parameters evaluated. This suggests that exotic invasions may alter ecosystem functioning by accelerating decomposition processes through an increased fungal ligninolytic activity. Key words: basidiomycetes, extracellular enzymes, solid-state fermentation, litter quality, carbon-13 cross- polarization magicangle spinning nuclear magnetic resonance. On rapporte que des changements d'ordre chimique dans l'apport des feuilles aux sols forestiers ont un impact sur les processus de decomposition. La perte de masse de la litiere et la constante de decomposition (k) ont ete comparees durant 200 jours de fermentation en milieu solide de l'espece indigene Celtis tala Gill. ex Planch. et de l'espece exotique Ligustrum lucidum Ait. avec trois basidiomycetes saprophytes communs dans la litiere. Les alterations de la qualite de la litiere ont ete caracterisees par la spectroscopie RMN du [sup.13]C en phase solide, ainsi que la mesure du pH, des sucres solubles, de l'ammonium, des proteines et de la teneur en phenol. De plus, les alterations ont ete associees a la production d'enzymes lignocellulosiques extracellulaires. Des differences dans la decomposition du substrat en lien avec le type de litiere ont ete observees avec Leratiomyces ceres qui produisait une valeur de k plus elevee dans la litiere de l'espece exotique L. lucidum, laquelle pourrait etre due a l'induction de l'activite de la manganese peroxydase. La preference du substrat pour le carbone alkyle et une meilleure degradation des composes lignifies ont ete observees dans de tels substrats. Meme si aucunes differences statistiquement significatives dans la perte de masse n'ont ete observees avec les autres champignons testes, nous avons detecte des changements chez plusieurs des parametres qui ont ete evalues. Cela indique que les invasions exotiques peuvent alterer le fonctionnement de l'ecosysteme en accelerant les processus de decomposition par le biais d'une augmentation de l'activite ligninolytique des champignons. [Traduit par la Redaction] Mots-cles: basidiomycetes, enzymes extracellulaires, fermentation en milieu solide, qualite de la litiere, resonance magnetique nucleaire par rotation a l'angle magique et polarisation croisee du carbone 13., Introduction Invasion of exotic plants in pristine terrestrial ecosystems is a major environmental problem due to alterations in the vegetal community with the consequent detrimental impact on the activity of [...]

Published
2018
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49. Considerations and consequences of allowing DNA sequence data as types of fungal taxa

Author

Zamora, Juan Carlos, Svensson, Måns, Kirschner, Roland, Olariaga, Ibai, Ryman, Svengunnar, Parra, Luis Alberto, Geml, József, Rosling, Anna, Adamčík, Slavomír, Ahti, Teuvo, Aime, M. Catherine, Ainsworth, A. Martyn, Albert, László, Albertó, Edgardo, García, Alberto Altés, Ageev, Dmitry, Agerer, Reinhard, Aguirre-Hudson, Begoña, Ammirati, Joe, Andersson, Harry, Angelini, Claudio, Antonín, Vladimír, Aoki, Takayuki, Aptroot, André, Argaud, Didier, Sosa, Blanca Imelda Arguello, Aronsen, Arne, Arup, Ulf, Asgari, Bita, Assyov, Boris, Atienza, Violeta, Bandini, Ditte, Baptista-Ferreira, João Luís, Baral, Hans-Otto, Baroni, Tim, Barreto, Robert Weingart, Beker, Henry, Bell, Ann, Bellanger, Jean-Michel, Bellù, Francesco, Bemmann, Martin, Bendiksby, Mika, Bendiksen, Egil, Bendiksen, Katriina, Benedek, Lajos, Bérešová-Guttová, Anna, Berger, Franz, Berndt, Reinhard, Bernicchia, Annarosa, Biketova, Alona Yu., Bizio, Enrico, Bjork, Curtis, Boekhout, Teun, Boertmann, David, Böhning, Tanja, Boittin, Florent, Boluda, Carlos G., Boomsluiter, Menno W., Borovička, Jan, Brandrud, Tor Erik, Braun, Uwe, Brodo, Irwin, Bulyonkova, Tatiana, Burdsall, Jr., Harold H., Buyck, Bart, Burgaz, Ana Rosa, Calatayud, Vicent, Callac, Philippe, Campo, Emanuele, Candusso, Massimo, Capoen, Brigitte, Carbó, Joaquim, Carbone, Matteo, Castañeda-Ruiz, Rafael F., Castellano, Michael A., Chen, Jie, Clerc, Philippe, Consiglio, Giovanni, Corriol, Gilles, Courtecuisse, Régis, Crespo, Ana, Cripps, Cathy, Crous, Pedro W., da Silva, Gladstone Alves, da Silva, Meiriele, Dam, Marjo, Dam, Nico, Dämmrich, Frank, Das, Kanad, Davies, Linda, De Crop, Eske, De Kesel, Andre, De Lange, Ruben, De Madrignac Bonzi, Bárbara, dela Cruz, Thomas Edison E., Delgat, Lynn, Demoulin, Vincent, Desjardin, Dennis E., Diederich, Paul, Dima, Bálint, Dios, Maria Martha, Divakar, Pradeep Kumar, Douanla-Meli, Clovis, Douglas, Brian, Drechsler-Santos, Elisandro Ricardo, Dyer, Paul S., Eberhardt, Ursula, Ertz, Damien, Esteve-Raventós, Fernando, Salazar, Javier Angel Etayo, Evenson, Vera, Eyssartier, Guillaume, Farkas, Edit, Favre, Alain, Fedosova, Anna G., Filippa, Mario, Finy, Péter, Flakus, Adam, Fos, Simón, Fournier, Jacques, Fraiture, André, Franchi, Paolo, Molano, Ana Esperanza Franco, Friebes, Gernot, Frisch, Andreas, Fryday, Alan, Furci, Giuliana, Márquez, Ricardo Galán, Garbelotto, Matteo, García-Martín, Joaquina María, Otálora, Mónica A. García, Sánchez, Dania García, Gardiennet, Alain, Garnica, Sigisfredo, Benavent, Isaac Garrido, Gates, Genevieve, da Gerlach, Alice Cruz Lima, Ghobad-Nejhad, Masoomeh, Gibertoni, Tatiana B., Grebenc, Tine, Greilhuber, Irmgard, Grishkan, Bella, Groenewald, Johannes Z., Grube, Martin, Gruhn, Gérald, Gueidan, Cécile, Gulden, Gro, Gusmão, Luis F. P., Hafellner, Josef, Hairaud, Michel, Halama, Marek, Hallenberg, Nils, Halling, Roy E., Hansen, Karen, Harder, Christoffer Bugge, Heilmann-Clausen, Jacob, Helleman, Stip, Henriot, Alain, Hernandez-Restrepo, Margarita, Herve, Raphaël, Hobart, Caroline, Hoffmeister, Mascha, Høiland, Klaus, Holec, Jan, Holien, Håkon, Hughes, Karen, Hubka, Vit, Huhtinen, Seppo, Ivančević, Boris, Jagers, Marian, Jaklitsch, Walter, Jansen, AnnaElise, Jayawardena, Ruvishika S., Jeppesen, Thomas Stjernegaard, Jeppson, Mikael, Johnston, Peter, Jørgensen, Per Magnus, Kärnefelt, Ingvar, Kalinina, Liudmila B., Kantvilas, Gintaras, Karadelev, Mitko, Kasuya, Taiga, Kautmanová, Ivona, Kerrigan, Richard W., Kirchmair, Martin, Kiyashko, Anna, Knapp, Dániel G., Knudsen, Henning, Knudsen, Kerry, Knutsson, Tommy, Kolařík, Miroslav, Kõljalg, Urmas, Košuthová, Alica, Koszka, Attila, Kotiranta, Heikki, Kotkova, Vera, Koukol, Ondřej, Kout, Jiří, Kovács, Gábor M., Kříž, Martin, Kruys, Åsa, Kučera, Viktor, Kudzma, Linas, Kuhar, Francisco, Kukwa, Martin, Kumar, T. K. Arun, Kunca, Vladimír, Kušan, Ivana, Kuyper, Thomas W., Lado, Carlos, Læssøe, Thomas, Lainé, Patrice, Langer, Ewald, Larsson, Ellen, Larsson, Karl-Henrik, Laursen, Gary, Lechat, Christian, Lee, Serena, Lendemer, James C., Levin, Laura, Lindemann, Uwe, Lindström, Håkan, Liu, Xingzhong, Hernandez, Regulo Carlos Llarena, Llop, Esteve, Locsmándi, Csaba, Lodge, Deborah Jean, Loizides, Michael, Lőkös, László, Luangsa-ard, Jennifer, Lüderitz, Matthias, Lumbsch, Thorsten, Lutz, Matthias, Mahoney, Dan, Malysheva, Ekaterina, Malysheva, Vera, Manimohan, Patinjareveettil, Marin-Felix, Yasmina, Marques, Guilhermina, Martínez-Gil, Rubén, Marson, Guy, Mata, Gerardo, Matheny, P. Brandon, Mathiassen, Geir Harald, Matočec, Neven, Mayrhofer, Helmut, Mehrabi, Mehdi, Melo, Ireneia, Mešić, Armin, Methven, Andrew S., Miettinen, Otto, Romero, Ana M. Millanes, Miller, Andrew N., Mitchell, James K., Moberg, Roland, Moreau, Pierre-Arthur, Moreno, Gabriel, Morozova, Olga, Morte, Asunción, Muggia, Lucia, González, Guillermo Muñoz, Myllys, Leena, Nagy, István, Nagy, László G., Neves, Maria Alice, Niemelä, Tuomo, Nimis, Pier Luigi, Niveiro, Nicolas, Noordeloos, Machiel E., Nordin, Anders, Noumeur, Sara Raouia, Novozhilov, Yuri, Nuytinck, Jorinde, Ohenoja, Esteri, Fiuza, Patricia Oliveira, Orange, Alan, Ordynets, Alexander, Ortiz-Santana, Beatriz, Pacheco, Leticia, Pál-Fám, Ferenc, Palacio, Melissa, Palice, Zdeněk, Papp, Viktor, Pärtel, Kadri, Pawlowska, Julia, Paz, Aurelia, Peintner, Ursula, Pennycook, Shaun, Pereira, Olinto Liparini, Daniëls, Pablo Pérez, Capella, Miquel À. Pérez-De-Gregorio, del Amo, Carlos Manuel Pérez, Gorjón, Sergio Pérez, Pérez-Ortega, Sergio, Pérez-Vargas, Israel, Perry, Brian A., Petersen, Jens H., Petersen, Ronald H., Pfister, Donald H., Phukhamsakda, Chayanard, Piątek, Marcin, Piepenbring, Meike, Pino-Bodas, Raquel, Esquivel, Juan Pablo Pinzón, Pirot, Paul, Popov, Eugene S., Popoff, Orlando, Álvaro, María Prieto, Printzen, Christian, Psurtseva, Nadezhda, Purahong, Witoon, Quijada, Luis, Rambold, Gerhard, Ramírez, Natalia A., Raja, Huzefa, Raspé, Olivier, Raymundo, Tania, Réblová, Martina, Rebriev, Yury A., García, Juan de Dios Reyes, Ripoll, Miguel Ángel Ribes, Richard, Franck, Richardson, Mike J., Rico, Víctor J., Robledo, Gerardo Lucio, Barbosa, Flavia Rodrigues, Rodriguez-Caycedo, Cristina, Rodriguez-Flakus, Pamela, Ronikier, Anna, Casas, Luis Rubio, Rusevska, Katerina, Saar, Günter, Saar, Irja, Salcedo, Isabel, Martínez, Sergio M. Salcedo, Montoya, Carlos A. Salvador, Sánchez-Ramírez, Santiago, Sandoval-Sierra, J. Vladimir, Santamaria, Sergi, Monteiro, Josiane Santana, Schroers, Hans Josef, Schulz, Barbara, Schmidt-Stohn, Geert, Schumacher, Trond, Senn-Irlet, Beatrice, Ševčíková, Hana, Shchepin, Oleg, Shirouzu, Takashi, Shiryaev, Anton, Siepe, Klaus, Sir, Esteban B., Sohrabi, Mohammad, Soop, Karl, Spirin, Viacheslav, Spribille, Toby, Stadler, Marc, Stalpers, Joost, Stenroos, Soili, Suija, Ave, Sunhede, Stellan, Svantesson, Sten, Svensson, Sigvard, Svetasheva, Tatyana Yu., Świerkosz, Krzysztof, Tamm, Heidi, Taskin, Hatira, Taudière, Adrien, Tedebrand, Jan-Olof, Lahoz, Raúl Tena, Temina, Marina, Thell, Arne, Thines, Marco, Thor, Göran, Thüs, Holger, Tibell, Leif, Tibell, Sanja, Timdal, Einar, Tkalčec, Zdenko, Tønsberg, Tor, Trichies, Gérard, Triebel, Dagmar, Tsurykau, Andrei, Tulloss, Rodham E., Tuovinen, Veera, Sosa, Miguel Ulloa, Urcelay, Carlos, Valade, François, Garza, Ricardo Valenzuela, van den Boom, Pieter, Van Vooren, Nicolas, Vasco-Palacios, Aida M., Vauras, Jukka, Santos, Juan Manuel Velasco, Vellinga, Else, Verbeken, Annemieke, Vetlesen, Per, Vizzini, Alfredo, Voglmayr, Hermann, Volobuev, Sergey, von Brackel, Wolfgang, Voronina, Elena, Walther, Grit, Watling, Roy, Weber, Evi, Wedin, Mats, Weholt, Øyvind, Westberg, Martin, Yurchenko, Eugene, Zehnálek, Petr, Zhang, Huang, Zhurbenko, Mikhail P., and Ekman, Stefan

Published
2018
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50. An investigation of vascular anomalies centers' transition of care practices

Author

Kinariwalla, Neha, primary, Scollan, Margaret E., additional, Levin, Laura E., additional, Fernandez Faith, Esteban, additional, Lee, Margaret T., additional, Powell, Julie, additional, Baselga, Eulàlia, additional, Tollefson, Megha M., additional, Lauren, Christine T., additional, Morel, Kimberly D., additional, and Garzon, Maria C., additional

Published
2023
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