Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Ferreira BF"'
Autor:
Fronza MG; Pharmacology Departament, Ribeirão Preto Medical School, University of São Paulo, São Paulo 14049-900, Brazil., Ferreira BF; Pharmacology Departament, Ribeirão Preto Medical School, University of São Paulo, São Paulo 14049-900, Brazil., Pavan-Silva I; Pharmacology Departament, Ribeirão Preto Medical School, University of São Paulo, São Paulo 14049-900, Brazil., Guimarães FS; Pharmacology Departament, Ribeirão Preto Medical School, University of São Paulo, São Paulo 14049-900, Brazil., Lisboa SF; Pharmacology Departament, Ribeirão Preto Medical School, University of São Paulo, São Paulo 14049-900, Brazil.; Biomolecular Sciences Department, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, São Paulo 14040-903, Brazil.
Publikováno v:
Molecules (Basel, Switzerland) [Molecules] 2023 Dec 22; Vol. 29 (1). Date of Electronic Publication: 2023 Dec 22.
Publikováno v:
Revista argentina de dermatología, Volume: 99, Issue: 4, Pages: 51-58, Published: DEC 2018
RESUMEN: La enfermedad de Darier es una genodermosis autosómica dominante, caracterizada por acantolisis y queratinización anormal, con hallazgos muco-cutáneos característicos, como pápulas queratóticas en el tronco superior y eritroniquismo lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______617::944b91bddbee9ed4caa985c244a01552
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S1851-300X2018000400051&lng=en&tlng=en
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S1851-300X2018000400051&lng=en&tlng=en
Autor:
Pathare, Neeti1 (AUTHOR) Neeti.Pathare@tufts.edu, MacPhail, Dylan2,3 (AUTHOR)
Publikováno v:
Physiotherapy Theory & Practice. Sept2024, Vol. 40 Issue 9, p2160-2170. 11p.
Autor:
Arhip, Loredana1,2 (AUTHOR) loredanarhip@gmail.com, Brox-Torrecilla, Noemi3 (AUTHOR), Romero, Inmaculada4 (AUTHOR), Motilla, Marta1,2 (AUTHOR), Serrano-Moreno, Clara1,2 (AUTHOR), Miguélez, María5 (AUTHOR), Cuerda, Cristina1,2,6 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 1/20/2024, Vol. 19 Issue 1, p1-9. 9p.
Autor:
de Lima DM Jr; Universidade Federal de Alagoas, Campus Arapiraca, Av. Manoel Severino Barbosa, s/n, Bom Sucesso, 57309-005, Arapiraca, AL, Brazil, juniorzootec@yahoo.com.br., de Carvalho FF, Ribeiro MN, Batista ÂM, Ferreira BF, Monteiro Pde B
Publikováno v:
Tropical animal health and production [Trop Anim Health Prod] 2014 Aug; Vol. 46 (6), pp. 995-1000. Date of Electronic Publication: 2014 May 09.
Autor:
Lin HJ; Division of Medical Genetics, Department of Pediatrics, Harbor-UCLA Medical Center, Torrance, CA 90502, USA. hlin@labiomed.org, Kwong AM, Carter JM, Ferreira BF, Austin MF, Devarajan K, Coleman RJ, Feuchtbaum LB, Lorey F, Jonas AJ
Publikováno v:
Journal of perinatology : official journal of the California Perinatal Association [J Perinatol] 2011 Jul; Vol. 31 (7), pp. 507-10.
Autor:
Setthaya, Naruemon1 (AUTHOR), Pimraksa, Kedsarin2 (AUTHOR), Damrongwiriyanupap, Nattapong3 (AUTHOR), Panias, Dimitrios4 (AUTHOR), Mekrattanachai, Pagasukon1 (AUTHOR), Chindawong, Chakkresit1 (AUTHOR)
Publikováno v:
Chemical Engineering Communications. 2023, Vol. 210 Issue 7, p1178-1194. 17p.
Autor:
Lin HJ; Division of Medical Genetics, Harbor-UCLA Medical Center, Torrance, CA 90502, USA. hlin@labiomed.org, Neidich JA, Salazar D, Thomas-Johnson E, Ferreira BF, Kwong AM, Lin AM, Jonas AJ, Levine S, Lorey F, Rosenblatt DS
Publikováno v:
The Journal of pediatrics [J Pediatr] 2009 Dec; Vol. 155 (6), pp. 924-7.
Autor:
Alapati, Akhila1 (AUTHOR), Cameron, Nathaniel1 (AUTHOR) ncameron2@kumc.edu, Gratton, Sean2,3 (AUTHOR), Stahl, Erin2,3 (AUTHOR), Champion, Mary1,2 (AUTHOR)
Publikováno v:
Journal of Ophthalmic Inflammation & Infection. 11/10/2022, Vol. 12 Issue 1, p1-5. 5p.
Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialists.
Autor:
Kalantari, Silvia1 (AUTHOR), Brezzi, Brigida2 (AUTHOR), Bracciamà, Valeria1 (AUTHOR), Barreca, Antonella3 (AUTHOR), Nozza, Paolo4 (AUTHOR), Vaisitti, Tiziana1 (AUTHOR), Amoroso, Antonio1,5 (AUTHOR), Deaglio, Silvia1,5 (AUTHOR), Manganaro, Marco2 (AUTHOR), Porta, Francesco6 (AUTHOR) francesco.porta@unito.it, Spada, Marco6 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 2/2/2022, Vol. 17 Issue 1, p1-18. 18p.