Works in Orphanet Journal of Rare Diseases, 2024, Vol 19, Issue 1

Results: 425

Patient and parent knowledge, understanding, and concerns after a new diagnosis of Ehlers Danlos syndrome.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03517-y
By:
- Jones, Jordan T.;
- Black, Lora L.;
- Black, William R.
Publication type:
Article
VIPAS39 related arthrogryposis-renal dysfunction-cholestasis syndrome—case report and systematic review.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03486-2
By:
- Kafol, Jan;
- Gnidovec Strazisar, Barbara;
- Drole Torkar, Ana;
- Homan, Matjaz;
- Bertok, Sara;
- Mlinaric, Matej;
- Sikonja, Jaka;
- Kovač, Jernej;
- Perkovic Benedik, Mirjana;
- Kersnik Levart, Tanja;
- Zerjav Tansek, Mojca;
- Praprotnik, Marina;
- Battelino, Tadej;
- Debeljak, Maruša;
- Groselj, Urh
Publication type:
Article
Clinical efficacy of efgartigimod combined with intravenous methylprednisolone in the acute phase of neuromyelitis optica spectrum disorders.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03501-6
By:
- Yang, Wenjing;
- Chen, Pei;
- Guo, Jiaxuan;
- Feng, Huiyu;
- Huang, Xin
Publication type:
Article
α-mannosidosis diagnosis in Brazilian patients with MPS-like symptoms.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03419-z
By:
- Marins, Maryana;
- Curiati, Marco Antonio;
- Gomes, Caio Perez;
- Martin, Renan Paulo;
- Nicolicht-Amorim, Priscila;
- Yamamoto, Joyce Umbelino da Silva;
- D'Almeida, Vânia;
- Martins, Ana Maria;
- Pesquero, João Bosco
Publication type:
Article
Safety and efficacy of omaveloxolone v/s placebo for the treatment of Friedreich's ataxia in patients aged more than 16 years: a systematic review.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03474-6
By:
- Umrao, Ankita;
- Pahuja, Monika;
- Chatterjee, Nabendu Sekhar
Publication type:
Article
Two-year follow-up after drug desensitization in mucopolysaccharidosis.
Published in:
2024
By:
- Spataro, Federico;
- Ria, Roberto;
- Chaoul, Nada;
- Solimando, Antonio Giovanni;
- Desantis, Vanessa;
- Vacca, Angelo;
- Di Bona, Danilo;
- Girolamo, Attilio Di;
- Macchia, Luigi
Publication type:
Letter
Novel biallelic variants in IREB2 cause an early-onset neurodegenerative disorder in a Chinese pedigree.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03465-7
By:
- Guo, Zhenglong;
- Huo, Dawei;
- Shao, Yingying;
- Yang, Wenke;
- Wang, Jinming;
- Zhang, Yuwei;
- Xiao, Hai;
- Hao, Bingtao;
- Liao, Shixiu
Publication type:
Article
Risdiplam utilization, adherence, and associated health care costs for patients with spinal muscular atrophy: a United States retrospective claims database analysis.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03399-0
By:
- Patel, Anish;
- Toro, Walter;
- Yang, Min;
- Song, Wei;
- Desai, Raj;
- Ye, Mingchen;
- Tabatabaeepour, Nadia;
- Dabbous, Omar
Publication type:
Article
Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matter.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03507-0
By:
- Castiglioni, Silvia;
- Pezzoli, Laura;
- Pezzani, Lidia;
- Lettieri, Antonella;
- Di Fede, Elisabetta;
- Cereda, Anna;
- Ancona, Silvia;
- Gallina, Andrea;
- Colombo, Elisa Adele;
- Parodi, Chiara;
- Grazioli, Paolo;
- Taci, Esi;
- Milani, Donatella;
- Iascone, Maria;
- Massa, Valentina;
- Gervasini, Cristina
Publication type:
Article
Multi-stakeholder sessions on major innovation topics in rare disease clinical trials.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03482-6
By:
- Bodden, Daniel;
- Schoenen, Stefanie;
- Wied, Stephanie;
- Verbeeck, Johan;
- Dirani, Maya;
- Abou Daya, Hiba;
- Heussen, Nicole;
- Molenberghs, Geert;
- Hilgers, Ralf-Dieter;
- Nabbout, Rima
Publication type:
Article
Impact of enzyme replacement therapy on clinical manifestations in females with Fabry disease.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03503-4
By:
- Lenders, Malte;
- Nowak, Albina;
- Cybulla, Markus;
- Kaufeld, Jessica;
- Köhn, Anja Friederike;
- Muschol, Nicole Maria;
- Kurschat, Christine;
- Brand, Eva
Publication type:
Article
When care hurts: parents' experiences of caring for a child with epidermolysis bullosa.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03502-5
By:
- Daae, Elisabeth;
- Feragen, Kristin Billaud;
- Naerland, Terje;
- von der Lippe, Charlotte
Publication type:
Article
A cross-sectional and longitudinal evaluation of serum creatinine as a biomarker in spinal muscular atrophy.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03515-0
By:
- Zhao, Xin;
- Gong, Zhenxiang;
- Luo, Han;
- Li, Zehui;
- Gao, Rong;
- Yang, Kangqin;
- Deng, Wenhua;
- Peng, Sirui;
- Ba, Li;
- Liu, Yang;
- Zhang, Min
Publication type:
Article
Multisystem clinicopathologic and genetic analysis of MELAS.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03511-4
By:
- Xu, Shuai;
- Jiang, Jialiu;
- Chang, Leilei;
- Zhang, Biao;
- Zhu, Xiaolei;
- Niu, Fengnan
Publication type:
Article
Expanding the phenotypic and genetic spectrum of GTPBP3 deficiency: findings from nine Chinese pedigrees.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03469-3
By:
- Xie, Yaojun;
- Li, Keyi;
- Yang, Li;
- Zeng, Xiaofei;
- Chen, Zhehui;
- Ma, Xue;
- Zhang, Luyi;
- Zhou, Yuwei;
- Jin, Liqin;
- Yang, Yanling;
- Lou, Xiaoting
Publication type:
Article
PHARC syndrome: an overview.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03418-0
By:
- Harutyunyan, Lusine;
- Callaerts, Patrick;
- Vermeer, Sascha
Publication type:
Article
Liver transplantation in a boy with TFAM mutation associated mtDNA depletion syndrome.
Published in:
2024
By:
- Zhao, Jing;
- Chen, Lian;
- Wang, Ni;
- Xie, Xin-bao
Publication type:
Letter
Application of four pricing models for orphan medicines: a case study for lumasiran.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03446-w
By:
- Rosenberg, Noa;
- Manders, Evert;
- van den Berg, Sibren;
- Deesker, Lisa J.;
- Garrelfs, Sander F.;
- de Visser, Saco J.;
- Groothoff, Jaap W.;
- Hollak, Carla E. M.
Publication type:
Article
Minimal encephalopathy in hereditary hemorrhagic telangiectasia patients with portosystemic vascular malformations.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03493-3
By:
- Villanueva, B.;
- Cañabate, A.;
- Torres-Iglesias, R.;
- Cerdà, P.;
- Gamundí, E.;
- Ordi, Q.;
- Alba, E.;
- Sanz-Astier, L. A.;
- Iriarte, A.;
- Ribas, J.;
- Castellote, J.;
- Pintó, X.;
- Riera-Mestre, A.
Publication type:
Article
Diagnosis of Diamond-Blackfan anemia in adulthood: case series and review of the literature.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03490-6
By:
- Versino, Francesco;
- Bianchi, Paola;
- Fermo, Elisa;
- Barcellini, Wilma;
- Fattizzo, Bruno
Publication type:
Article
Quality of life after idiopathic multicentric Castleman disease in China: a cross-sectional, multi-center survey of patient reported outcome and caregiver reported outcome.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03450-0
By:
- Chen, Jia;
- Zhang, Miao-yan;
- Gao, Yu-han;
- Zhang, Lu;
- Li, Jian
Publication type:
Article
Exploring molecular spectrum in thai patients with maple syrup urine disease: unveiling a common variant.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03411-7
By:
- Lakkhana, Panisara;
- Tim-Aroon, Thipwimol;
- Khongkraparn, Arthaporn;
- Noojarern, Saisuda;
- Wongkittichote, Parith;
- Wichajarn, Khunton;
- Kuptanon, Chulaluck;
- Boonyawat, Boonchai;
- Suphapeetiporn, Kanya;
- Wejaphikul, Karn;
- Seo, GoHun;
- Wattanasirichaigoon, Duangrurdee
Publication type:
Article
Quality of life and unmet needs in patients with fabry disease: a qualitative study.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03412-6
By:
- Morales, Montserrat;
- Cruz, Jordi;
- Brignani, Eduardo;
- Acuña, Laura;
- Lázaro, Esther;
- Soria, Cristina
Publication type:
Article
The clinical and biochemical effectiveness and safety of cholic acid treatment for bile acid synthesis defects: a systematic review.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03449-7
By:
- Polak, Yasmin;
- van Dussen, Laura;
- Kemper, E. Marleen;
- Vaz, Frédéric M.;
- Klouwer, Femke C. C.;
- Engelen, Marc;
- Hollak, Carla E. M.
Publication type:
Article
Neuronal ceroid lipofuscinoses type 7 (CLN7): a case series reporting cross sectional and retrospective clinical data to evaluate validity of standardized tools to assess disease progression, quality of life, and adaptive skills.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03448-8
By:
- Kayani, Saima;
- BordesEdgar, Veronica;
- Lowden, Andrea;
- Nettesheim, Emily R.;
- Dahshi, Hamza;
- Messahel, Souad;
- Minassian, Berge A.;
- Greenberg, Benjamin M.
Publication type:
Article
A novel homozygous intronic variant in CDT1 that alters splicing causes Meier–Gorlin syndrome, and a review of published mutations and growth hormone treatments.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03430-4
By:
- Li, Qing;
- Wu, Yichi;
- Meng, Fucheng;
- Li, Zhuxi;
- Zhan, Di;
- Luo, Xiaoping
Publication type:
Article
Role of carglumic acid in the long-term management of propionic and methylmalonic acidurias.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03468-4
By:
- Yap, Sufin;
- Gasperini, Serena;
- Matsumoto, Shirou;
- Feillet, François
Publication type:
Article
Patients with Darier disease have an increased risk of keratinocyte carcinoma: a Swedish registry-based nationwide cohort study.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03497-z
By:
- Inci, Rahime;
- Gillstedt, Martin;
- Kallionpää, Roope A.;
- Peltonen, Sirkku;
- Polesie, Sam
Publication type:
Article
Review of clinical trials and guidelines for children and youth with mucopolysaccharidosis: outcome selection and measurement.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03364-x
By:
- Howie, Alison H.;
- Tingley, Kylie;
- Inbar-Feigenberg, Michal;
- Mitchell, John J.;
- Angel, Kim;
- Gentle, Jenifer;
- Smith, Maureen;
- Offringa, Martin;
- Butcher, Nancy J.;
- Campeau, Philippe M.;
- Chakraborty, Pranesh;
- Chan, Alicia;
- Fergusson, Dean;
- Mamak, Eva;
- McClelland, Peyton;
- Mercimek-Andrews, Saadet;
- Mhanni, Aizeddin;
- Moazin, Zeinab;
- Rockman-Greenberg, Cheryl;
- Rupar, C. Anthony
Publication type:
Article
Health care costs of home care enzyme replacement therapy for patients with lysosomal storage diseases in Germany.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03492-4
By:
- Heinrich, Ria;
- Claus, Franziska;
- Schoenfelder, Tonio
Publication type:
Article
Retrospective longitudinal study on the long-term impact of COVID-19 infection on polysomnographic evaluation in patients with Prader-Willi syndrome.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03447-9
By:
- Braun, Sina;
- Laemmer, Constanze;
- Schulte, Sandra;
- Gohlke, Bettina
Publication type:
Article
Quality of care for people with differences of sex development (DSD) in Germany.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03467-5
By:
- Maike, Schnoor;
- Andreas, Heidenreich;
- Martina, Jürgensen;
- Ulla, Döhnert;
- Olaf, Hiort;
- Alexander, Katalinic
Publication type:
Article
Global longitudinal strain in pre-symptomatic patients with mutation for transthyretin amyloidosis.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03473-7
By:
- Canciello, Grazia;
- Tozza, Stefano;
- Todde, Gaetano;
- Nolano, Maria;
- Borrelli, Felice;
- Palumbo, Giovanni;
- Lombardi, Raffaella;
- Cassano, Emanuele;
- Acampa, Wanda;
- Esposito, Giovanni;
- Manganelli, Fiore;
- Losi, Maria Angela
Publication type:
Article
A natural history study of pediatric patients with early onset of GM1 gangliosidosis, GM2 gangliosidoses, or gaucher disease type 2 (RETRIEVE).
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03409-1
By:
- Héron, Bénédicte;
- Batzios, Spyros;
- Mengel, Eugen;
- Giugliani, Roberto;
- Patterson, Marc;
- Gautschi, Matthias;
- Cornelisse, Peter;
- Trokan, Luba;
- Schwierin, Barbara;
- Rohrbach, Marianne
Publication type:
Article
Meeting abstracts from the 12th European Conference on Rare Diseases and Orphan Products.
Published in:
2024
Publication type:
Abstract
Hospital administrators as forgotten partners in rare disease care: a call to action by the international hospital federation’s global rare pediatric disease network.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03459-5
By:
- Stoesz, Andrea;
- Joers, Barbara;
- Gaviglio, Amy
Publication type:
Article
Systematic quantitative modeling of the natural history of Aicardi syndrome: A cross sectional study of 245 published cases.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03375-8
By:
- Urban, Oliver Y.;
- Driedger, Jan H.;
- Garbade, Sven F.;
- Hoffmann, Georg F.;
- Kölker, Stefan;
- Ries, Markus;
- Syrbe, Steffen
Publication type:
Article
Lung function in adult patients with osteogenesis imperfecta: a cohort study.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03452-y
By:
- Lenoir, Alexandra;
- Aubry-Rozier, Bérengère;
- Bregou, Aline;
- Gonzalez Rodriguez, Elena;
- Paquier, Célia;
- Tanniger, Joëlle;
- Faouzi, Mohamed;
- Lazor, Romain
Publication type:
Article
Prevalence and clinical characteristics of incontinentia pigmenti: a nationwide population-based study.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03480-8
By:
- Herlin, Laura Krogh;
- Schmidt, Sigrun Alba Johannesdottir;
- Mogensen, Trine H.;
- Sommerlund, Mette
Publication type:
Article
Clinical spectrum and molecular basis in 19 Chinese patients with 46, XY disorder of sexual development caused by NR5A1 mutations.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03472-8
By:
- Xu, Yue;
- Liu, Xuemeng;
- Liu, Yang;
- Zhu, Hui;
- Wu, Jing;
- Han, Bing;
- Ling, Shiying;
- Cao, Ren;
- Yao, Haijun;
- Chen, Yan;
- Liu, Yu;
- Rao, Yamin;
- Liu, Xiaoyu;
- Zhao, Shuangxia;
- Song, Huaidong;
- Qiao, Jie
Publication type:
Article
Nomogram for predicting pregnancy-related relapse of myasthenia gravis.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03466-6
By:
- Su, Manqiqige;
- Liu, Xiaoqing;
- Wu, Zongtai;
- Song, Jie;
- Huan, Xiao;
- Zhong, Huahua;
- Zhao, Rui;
- Zhao, Chongbo;
- Zhang, Yali;
- Luo, Sushan
Publication type:
Article
Diagnostic flow analysis of tuberous sclerosis complex in Japan: a retrospective claims database study.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03460-y
By:
- Okanishi, Tohru;
- Fujimori, Ikuo;
- Yamada, Mariko;
- Tajima, Takumi;
- Wataya-Kaneda, Mari;
- Seyama, Kuniaki;
- Hatano, Takashi
Publication type:
Article
Quality of life and caregiving burden associated with parenting a person with Duchenne/Becker muscular dystrophy in Poland.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03481-7
By:
- Domaradzki, Jan;
- Walkowiak, Dariusz
Publication type:
Article
The challenges of hepatic epithelioid hemangioendothelioma: the diagnosis and current treatments of a problematic tumor.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03354-z
By:
- Atyah, Manar Mikhail;
- Sun, Yongliang;
- Yang, Zhiying
Publication type:
Article
Off-label use of medicines in South Africa: a review.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03476-4
By:
- Ngcobo, N. N.;
- Mathibe, L. J.
Publication type:
Article
Shifting focus from ideality to reality: a qualitative study on how quality of life is defined by premanifest and manifest Huntington's disease gene expansion carriers.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03461-x
By:
- van Lonkhuizen, Pearl J. C.;
- Heemskerk, Anne-Wil;
- Slutter, Leanne;
- van Duijn, Erik;
- de Bot, Susanne T.;
- Chavannes, Niels H.;
- Meijer, Eline;
- on behalf of the HEALTHE-RND consortium;
- Vegt, Niko;
- Chavannes, Niels;
- Heemskerk, Anne- Wil;
- Feleus, Stephanie;
- Arendts, Esther C;
- Putman, Amy;
- Landwehrmeyer, G. Bernhard;
- Mühlbäck, Alzbeta;
- Frank, Wiebke;
- Steck, Franziska;
- Klempíř, Jiří;
- Konvalinková, Romama
Publication type:
Article
The development for emerging biomarkers of lymphangioleiomyomatosis.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03455-9
By:
- Huang, Liting;
- Xiao, Ying;
- Yang, Lulu;
- Ren, Siying
Publication type:
Article
Navigating health policies and programs in India: exploring opportunities to improve rare disease management and orphan drug research.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03377-6
By:
- Mishra, Sangita;
- Bhat, Deepa;
- Venkatesh, M. P.
Publication type:
Article
Neurocognitive functioning in adults with neurofibromatosis type 1- a nationwide population-based study.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03454-w
By:
- Doser, Karoline;
- Jepsen, Jens Richardt Møllegaard;
- Kenborg, Line;
- Miskowiak, Kamilla Woznica;
- Albieri, Vanna;
- Dalton, Susanne Oksbjerg;
- Krøyer, Anja;
- Hove, Hanne;
- Østergaard, John R.;
- Johansen, Christoffer;
- Sørensen, Sven Asger;
- Mulvihill, John;
- Falck Winther, Jeanette;
- Bidstrup, Pernille Envold
Publication type:
Article
A therapeutic approach to pantothenate kinase associated neurodegeneration: a pilot study.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03453-x
By:
- Pereira, Alessandra;
- Fischinger Moura de Souza, Carolina;
- Álvarez-Córdoba, Mónica;
- Reche-López, Diana;
- Sánchez-Alcázar, José Antonio
Publication type:
Article