Maria-Isabel Moreno-Carralero
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Explore the profile of Maria-Isabel Moreno-Carralero including associated specialties, affiliations and a list of published articles.
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12
Citations
82
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Recent Articles
1.
Moreno-Risco M, Mendez M, Moreno-Carralero M, Lopez-Moreno A, Vagace-Valero J, Moran-Jimenez M
Case Rep Pediatr
. 2022 Apr;
2022:7743748.
PMID: 35449524
Hemochromatosis type 2 or juvenile hemochromatosis has an early onset of severe iron overload resulting in organ manifestation such as liver fibrosis, cirrhosis, cardiomyopathy, arthropathy, hypogonadism, diabetes, osteopathic medicine, and...
2.
Moreno-Carralero M, Arrizabalaga-Amuchastegui B, Sanchez-Calero-Guilarte J, Morado-Arias M, Velasco-Valdazo A, de-la-Iglesia-Inigo S, et al.
Int J Lab Hematol
. 2018 Jul;
41(1):e5-e9.
PMID: 30019527
No abstract available.
3.
Moreno-Carralero M, Horta-Herrera S, Morado-Arias M, Ricard-Andres M, Lemes-Castellano A, Abio-Calvete M, et al.
Eur J Haematol
. 2018 Jun;
101(3):368-378.
PMID: 29901818
Introduction: Congenital dyserythropoietic anemias (CDA) are characterized by hyporegenerative anemia with inadequate reticulocyte values, ineffective erythropoiesis, and hemolysis. Distinctive morphology of bone marrow erythroblasts and identification of causative genes allow...
4.
de-la-Iglesia-Inigo S, Moreno-Carralero M, Lemes-Castellano A, Molero-Labarta T, Mendez M, Moran-Jimenez M
Clin Case Rep
. 2017 Mar;
5(3):248-252.
PMID: 28265383
Congenital dyserythropoietic anemias (CDAs) are displayed by ineffective erythropoiesis. The wide variety of phenotypes observed in CDA patients makes differential diagnosis difficult; identification of the genetic variants is crucial in...
5.
Mendez M, Moreno-Carralero M, Morado-Arias M, Fernandez-Jimenez M, de la Iglesia Inigo S, Moran-Jimenez M
Mol Genet Genomic Med
. 2016 Jun;
4(3):273-82.
PMID: 27247955
Background: X-linked sideroblastic anemia (XLSA) is a disorder characterized by decreased heme synthesis and mitochondrial iron overload with ringed sideroblasts in bone marrow. XLSA is caused by mutations in the...
6.
Galicia-Poblet G, Cid-Paris E, Lopez-Andres N, Losada-Pajares A, Jurado-Lopez J, Moreno-Carralero M, et al.
J Pediatr Gastroenterol Nutr
. 2015 Mar;
63(6):e205-e207.
PMID: 25742196
No abstract available.
7.
Moreno-Carralero M, Munoz-Munoz J, Cuadrado-Grande N, Lopez-Rodriguez R, Jose Hernandez-Alfaro M, del-Castillo-Rueda A, et al.
Am J Hematol
. 2014 Mar;
89(7):689-94.
PMID: 24644245
Ferroportin disease is an inherited disorder of iron metabolism and is caused by mutations in the ferroportin gene (SLC40A1). We present a patient with hyperferritinemia, iron overload in the liver...
8.
del-Castillo-Rueda A, Moreno-Carralero M, Cuadrado-Grande N, Alvarez-Sala-Walther L, Enriquez-de-Salamanca R, Mendez M, et al.
Gene
. 2012 Aug;
508(1):15-20.
PMID: 22890139
Hereditary hemochromatosis causes iron overload and is associated with a variety of genetic and phenotypic conditions. Early diagnosis is important so that effective treatment can be administered and the risk...
9.
The homozygous mutation G75R in the human SLC11A2 gene leads to microcytic anaemia and iron overload
Barrios M, Moreno-Carralero M, Cuadrado-Grande N, Baro M, Vivanco J, Moran-Jimenez M
Br J Haematol
. 2012 Feb;
157(4):514-6.
PMID: 22313374
No abstract available.
10.
del-Castillo-Rueda A, Moreno-Carralero M, Alvarez-Sala-Walther L, Cuadrado-Grande N, Enriquez-de-Salamanca R, Mendez M, et al.
Eur J Haematol
. 2010 Dec;
86(3):260-4.
PMID: 21175851
The most common form of hemochromatosis is caused by mutations in the HFE gene. Rare forms of the disease are caused by mutations in other genes. We present a patient...