Laura Jorge

Institut d'Investigació Biomédica de Bellvitge — Spain

Neuroscience · Life Sciences

7h-index336citations14works2.02yr avg
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Research Topics

Genetic Neurodegenerative Diseases(6), Mitochondrial Function and Pathology(4), Neurological diseases and metabolism(4), Neutropenia and Cancer Infections(2), Hereditary Neurological Disorders(2)

Publications14 total

Late-onset vestibulocerebellar ataxia: clinical and genetic studies in a long follow-up series of 50 patients
Journal of Neurology·2025· 2 cited
Short Course of Antibiotic Therapy for Gram-Negative Bacilli Bacteremia in Patients with Cancer and Hematopoietic Stem Cell Transplantation: Less Is Possible
Microorganisms·2023· 7 citedOpen Access
Evaluación de la implementación de un Programa de Uso Optimizado de Antimicrobianos en la pandemia de COVID-19
Actualizaciones en Sida e Infectología·2021Open Access
Managing Clinical Trials for Alzheimer’s Disease During the COVID-19 Crisis: Experience at Fundació ACE in Barcelona, Spain
Journal of Alzheimer s Disease·2020· 4 citedOpen Access
CLINICAL USEFULNESS OF BROCHOALVEOLAR LAVAGE IN THE MANAGEMENT OF PULMONARY INFILTRATES IN ADULTS WITH HAEMATOLOGICAL MALIGNANCIES AND STEM CELL TRANSPLANTATION
Mediterranean Journal of Hematology and Infectious Diseases·2020· 7 citedOpen Access
Heterozygous <i>STUB1</i> mutation causes familial ataxia with cognitive affective syndrome (SCA48)
Neurology·2018· 101 cited
[Levofloxacin prophylaxis in neutropenic patients].
PubMed·2017· 3 cited
[Etiology and antimicrobial resistance of uncomplicated urinary tract infections].
PubMed·2017· 5 cited
New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32
JAMA Neurology·2013· 45 cited
Autosomal dominant late onset ataxia linked to a new locus: Last but not least
2011
A novel small deletion in PMP22 causes a mild hereditary neuropathy with liability to pressure palsies phenotype
Muscle & Nerve·2011· 15 cited
The metabotropic glutamate receptor 1, GRM1: evaluation as a candidate gene for inherited forms of cerebellar ataxia
Journal of Neurology·2009· 18 cited
Diagnosis of Charcot‐Marie‐Tooth Disease
BioMed Research International·2009· 86 citedOpen Access
Analysis of the involvement of the <i>NR2E3</i> gene in autosomal recessive retinal dystrophies
Clinical Genetics·2008· 43 cited

Frequent Co-authors

Vı́ctor Volpini(5), Héctor San Nicolás(4), Pablo Bonvehí(4), Elena Temporiti(4), Fabián Herrera(4), Berta Campos(3), David Genı́s(2), Jordi Corral(2), Josep Gardenyes(2), María Obón(2), Berta Alemany(2), Fabián Márquez(2), Isabel Banchs(2), Carlos Casasnovas(2), Jordi Montero(2), Carmen Serrano(2), Marc Corral‐Juan(2), Giovanni Stévanin(2), Carles Roig(2), Sylvie Forlani(2)