Miriam Almendrote
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Explore the profile of Miriam Almendrote including associated specialties, affiliations and a list of published articles.
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16
Citations
71
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Recent Articles
1.
Carbayo A, Borrego-Ecija S, Turon-Sans J, Cortes-Vicente E, Molina-Porcel L, Gascon-Bayarri J, et al.
Brain
. 2024 Jan;
147(7):2357-2367.
PMID: 38227807
Amyotrophic lateral sclerosis (ALS) is a devastating motor neuron disease (MND) that shares a common clinical, genetic and pathologic spectrum with frontotemporal dementia (FTD). It is highly heterogeneous in its...
2.
Koehorst E, Odria R, Capo J, Nunez-Manchon J, Arbex A, Almendrote M, et al.
Biomedicines
. 2022 Jun;
10(6).
PMID: 35740394
Myotonic dystrophy type 1 (DM1) is a progressive, non-treatable, multi-systemic disorder. To investigate the contribution of epigenetics to the complexity of DM1, we compared DNA methylation profiles of four annotated...
3.
Koehorst E, Nunez-Manchon J, Ballester-Lopez A, Almendrote M, Lucente G, Arbex A, et al.
J Clin Med
. 2021 Dec;
10(23).
PMID: 34884222
Myotonic Dystrophy type 1 (DM1) is a muscular dystrophy with a multi-systemic nature. It was one of the first diseases in which repeat associated non-ATG (RAN) translation was described in...
4.
Lucente G, Corral J, Rodriguez-Esparragoza L, Castaner S, Ortiz H, Piqueras A, et al.
Front Neurol
. 2021 Nov;
12:755432.
PMID: 34790163
Previously published retrospective series show a high prevalence of fecal incontinence (FI) in stroke patients. We aimed to analyze in a prospective series the current incidence of FI in acute...
5.
Ballester-Lopez A, Koehorst E, Linares-Pardo I, Nunez-Manchon J, Almendrote M, Lucente G, et al.
Genes (Basel)
. 2020 Nov;
11(11).
PMID: 33171734
Myotonic Dystrophy type 1 (DM1) is characterized by a high genetic and clinical variability. Determination of the genetic variability in DM1 might help to determine whether there is an association...
6.
Alvarez M, Lucente G, Martinez L, Almendrote M, Ramos A, Broto J, et al.
Ann Vasc Surg
. 2020 Sep;
70:569.e1-569.e4.
PMID: 32927034
Ischemic lumbosacral plexopathy secondary to an acute aortic dissection is a rare condition that is usually unilateral and frequently accompanied by a simultaneous spinal cord infarction. The functional prognosis relies...
7.
Ballester-Lopez A, Nunez-Manchon J, Koehorst E, Linares-Pardo I, Almendrote M, Lucente G, et al.
Neurol Genet
. 2020 Aug;
6(4):e484.
PMID: 32802949
Objective: We aimed to determine whether 3D imaging reconstruction allows identifying molecular:clinical associations in myotonic dystrophy type 1 (DM1). Methods: We obtained myoblasts from 6 patients with DM1 and 6...
8.
Ballester-Lopez A, Linares-Pardo I, Koehorst E, Nunez-Manchon J, Pintos-Morell G, Coll-Canti J, et al.
Genes (Basel)
. 2020 Jul;
11(7).
PMID: 32645888
The number of cytosine-thymine-guanine (CTG) repeats ('CTG expansion size') in the 3'untranslated region (UTR) region of the -protein kinase () gene is a hallmark of myotonic dystrophy type 1 (DM1),...
9.
Ballester-Lopez A, Koehorst E, Almendrote M, Martinez-Pineiro A, Lucente G, Linares-Pardo I, et al.
Hum Mutat
. 2019 Oct;
41(2):420-431.
PMID: 31608518
Carriage of interruptions in CTG repeats of the myotonic dystrophy protein kinase gene has been associated with a broad spectrum of myotonic dystrophy type 1 (DM1) phenotypes, mostly mild. However,...
10.
Alonso-Perez J, Segovia S, Dominguez-Gonzalez C, Olive M, Mendoza Grimon M, Fernandez-Torron R, et al.
Med Clin (Barc)
. 2019 Jun;
154(3):80-85.
PMID: 31253477
Introduction And Objectives: Pompe disease is a rare autosomal recessive disorder produced by a deficiency of acid maltase. This deficit produces an accumulation of glycogen in tissues. Clinically it is...