Post-transplantation HTLV-1 myelopathy in three recipients from a single donor

JJZ Imirizaldu, JCG Esteban, IR Axpe… - Journal of Neurology …, 2003 - jnnp.bmj.com
Objectives: This paper reports for the first time three cases of infection by HTLV-I via organ
transplantation; all the organs coming from the same asymptomatic infected donor. The …

[HTML][HTML] A systematic review of social cognition in hereditary ataxia patients: Evidence from neuroimaging studies

M Pallarès-Sastre, M García, I Rouco-Axpe, I Amayra - Brain Research, 2024 - Elsevier
Cerebellar ataxias represent a heterogeneous group of complex conditions in which
cerebellum and connectivity networks are compromised (Manto et al., 2020, Palau and Arpa …

[HTML][HTML] Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study

GO Suero, MJA Abildúa, CS Munuera, IR Axpe… - Neurología (English …, 2023 - Elsevier
Introduction Ataxia and hereditary spastic paraplegia are rare neurodegenerative
syndromes. We aimed to determine the prevalence of these disorders in Spain in 2019 …

Neuropsychological profile of hereditary ataxias: study of 38 patients

M García, I Rouco-Axpe, I Amayra… - Archives of Clinical …, 2022 - academic.oup.com
Hereditary ataxias are a heterogeneous group of disorders characterized by degeneration of
the cerebellum and its connections. It is known that patients with ataxia can manifest a broad …

Hypomagnesemia: a treatable cause of ataxia with cerebellar edema

I Rouco Axpe, J Almeida Velasco, JG Barreiro Garcia… - The Cerebellum, 2017 - Springer
There are a wide variety of causes of cerebellar ataxia including toxics, vitamin deficiencies,
infections, autoimmune diseases, neoplasms, and genetic disorders [1]. To date, cases of …

[HTML][HTML] Practical recommendations for the clinical evaluation of patients with hereditary ataxia and hereditary spastic paraplegia

FJA Gutiérrez, MJA Abildúa, IR Axpe… - Neurología (English …, 2022 - Elsevier
Hereditary ataxia (HA) and hereditary spastic paraplegia (HSP) are rare diseases; as such,
they are rarely managed in general neurology consultations. We present a set of brief …

[HTML][HTML] Mapa epidemiológico transversal de las ataxias y paraparesias espásticas hereditarias en España

GO Suero, MJA Abildúa, CS Munuera, IR Axpe… - Neurología, 2023 - Elsevier
Introducción Las ataxias (AT) y paraparesias espásticas hereditarias (PEH) son síndromes
neurodegenerativos raros. Nos proponemos conocer la prevalencia de las AT y PEH en …

Patología cerebrovascular en un hospital terciario. Situación actual y puntos de mejora

…, J Barcena Llona, I Rouco Axpe… - Rev. neurol.(Ed …, 2005 - pesquisa.bvsalud.org
Introduction. Caring for patients suffering from a cerebrovascular diseases requires a large
quantity of resources which must be optimised. The aim of this study is to analyse the …

Demencia rápidamente progresiva asociada a anticuerpos anti-carboxilasa del ácido glutámico: a propósito de un caso

J Martin Prieto, I Rouco Axpe… - … (Barc., Ed. impr.), 2022 - pesquisa.bvsalud.org
https://pdf. sciencedirectassets. com/280280/1-s2. 0-S0213485321X00035/1-s2. 0-
S0213485321000669/main. pdf? X-Amz-Security-Token= IQoJb3JpZ2luX2VjEKf% 2F …

Cerebrovascular disease in a tertiary care hospital. The current situation and points to be improved

…, J Barcena-Llona, I Rouco-Axpe… - Revista de …, 2005 - europepmc.org
Results 936 patients were admitted to hospital with a diagnosis of stroke. 80.22%
corresponded to acute ischaemic strokes (27.14% lacunar, 18.57% transient ischaemic …