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Maria-Jose Moran-Jimenez

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Articles 13
Citations 44
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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.
Cervera Bravo A, Osuna Marco M, Moran-Jimenez M, Martin-Hernandez E
J Pediatr Hematol Oncol . 2021 Mar; 43(8):e1238-e1240. PMID: 33661177
Atypical microcytic anemias are rare diseases of iron/heme metabolism that can be diagnostically challenging. We report the case of a 2-year-old twin boy with neurodevelopmental delay and persistent microcytosis in...
3.
Moran-Jimenez M, Borrero-Corte M, Jara-Rubio F, Garcia-Pastor I, Diaz-Diaz S, Castelbon-Fernandez F, et al.
Genes (Basel) . 2020 Aug; 11(8). PMID: 32806544
Acute intermittent porphyria (AIP) results from a decreased activity of hepatic hydroxymethylbilane synthase (HMBS), the third enzyme in the heme biosynthetic pathway. AIP is an autosomal dominant disorder with incomplete...
4.
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.
5.
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...
6.
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...
7.
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...
8.
Lillo-Triguero L, Del Castillo A, Moran-Jimenez M, Guzman-De Villoria J, Guillem A, Peraita-Adrados R
Sleep Med . 2014 Jun; 15(8):1004-5. PMID: 24951089
No abstract available.
9.
Vegh I, Santiuste A, Colina F, Bor L, Bermejo C, Aragon A, et al.
J Gastroenterol Hepatol . 2007 Nov; 22(12):2303-9. PMID: 18031395
Background And Aim: Expression of biomarkers and probable allelic alterations were studied in esophagus tissue samples from patients with esophageal carcinoma. Methods: A total of 116 esophagus tissue samples were...
10.
Navarro S, del Hoyo P, Campos Y, Abitbol M, Moran-Jimenez M, Garcia-Bravo M, et al.
Exp Dermatol . 2005 Jan; 14(1):26-33. PMID: 15660916
Mitochondrial dysfunction might play a role in the pathogenesis of liver damage in erythropoietic protoporphyria (EPP). Changes in mitochondrial respiratory chain activities were evaluated in the Fech(m1pas)/Fech(m1pas) mouse model for...