Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Laura Ventura-Espejo"'
Autor:
Laura Ventura-Espejo, Inés Gracia-Darder, Silvia Escribá-Bori, Eva Regina Amador-González, Ana Martín-Santiago, Jan Ramakers
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-7 (2021)
Abstract Background H syndrome (HS) is a rare autoinflammatory disease caused by a mutation in the solute carrier family 29, member 3 (SCL29A3) gene. It has a variable clinical presentation and little phenotype-genotype correlation. The pathognomonic
Externí odkaz:
https://doaj.org/article/3ef28ee92e6f4e1cb24842a11bb17c1d
Autor:
Silvia Escribá-Bori, Jan Ramakers, Eva Regina Amador-González, Laura Ventura-Espejo, Ana Martín-Santiago, Inés Gracia-Darder
Publikováno v:
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-7 (2021)
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-7 (2021)
Abstract Background H syndrome (HS) is a rare autoinflammatory disease caused by a mutation in the solute carrier family 29, member 3 (SCL29A3) gene. It has a variable clinical presentation and little phenotype-genotype correlation. The pathognomonic
Autor:
Patricia Martínez-Cepas, Joana María Riera-Llodrá, Nadal Riutord-Arrom, Antonio Rosell-Camps, Laura Ventura-Espejo
Publikováno v:
Laboratory medicine. 51(4)
Benign pancreatic hyperenzymemia, also known as Gullo’s syndrome, is a little-known syndrome first described in 1996 in patients studied for an elevation of pancreatic enzymes while otherwise being asymptomatic. We describe the case of a 2-year-old
Autor:
Ventura-Espejo, Laura1 (AUTHOR), Gracia-Darder, Inés2 (AUTHOR), Escribá-Bori, Silvia1 (AUTHOR), Amador-González, Eva Regina3 (AUTHOR), Martín-Santiago, Ana2 (AUTHOR), Ramakers, Jan1,4 (AUTHOR) jan.ramakers@ssib.es
Publikováno v:
Pediatric Rheumatology. 6/30/2021, Vol. 19 Issue 1, p1-7. 7p.