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Managing Clinical Trials for Alzheimer's Disease During the COVID-19 Crisis: Experience at Fundació ACE in Barcelona, Spain.
J Alzheimers Dis. 2020;77(4):1805-1813. doi: 10.3233/JAD-200750.
J Alzheimers Dis. 2020.
PMID: 32986671
Free PMC article.
Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48).
Genis D, Ortega-Cubero S, San Nicolás H, Corral J, Gardenyes J, de Jorge L, López E, Campos B, Lorenzo E, Tonda R, Beltran S, Negre M, Obón M, Beltran B, Fàbregas L, Alemany B, Márquez F, Ramió-Torrentà L, Gich J, Volpini V, Pastor P.
Genis D, et al. Among authors: de jorge l.
Neurology. 2018 Nov 20;91(21):e1988-e1998. doi: 10.1212/WNL.0000000000006550. Epub 2018 Oct 31.
Neurology. 2018.
PMID: 30381368
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New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32.
Serrano-Munuera C, Corral-Juan M, Stevanin G, San Nicolás H, Roig C, Corral J, Campos B, de Jorge L, Morcillo-Suárez C, Navarro A, Forlani S, Durr A, Kulisevsky J, Brice A, Sánchez I, Volpini V, Matilla-Dueñas A.
Serrano-Munuera C, et al. Among authors: de jorge l.
JAMA Neurol. 2013 Jun;70(6):764-71. doi: 10.1001/jamaneurol.2013.2311.
JAMA Neurol. 2013.
PMID: 23700170
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A novel small deletion in PMP22 causes a mild hereditary neuropathy with liability to pressure palsies phenotype.
Casasnovas C, Banchs I, De Jorge L, Antónia Albertí M, Martínez-Campo Y, Povedano M, Montero J, Volpini V.
Casasnovas C, et al. Among authors: de jorge l.
Muscle Nerve. 2012 Jan;45(1):135-8. doi: 10.1002/mus.22201.
Muscle Nerve. 2012.
PMID: 22190321
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The metabotropic glutamate receptor 1, GRM1: evaluation as a candidate gene for inherited forms of cerebellar ataxia.
Rossi PI, Vaccari CM, Terracciano A, Doria-Lamba L, Facchinetti S, Priolo M, Ayuso C, De Jorge L, Gimelli S, Santorelli FM, Ravazzolo R, Puliti A.
Rossi PI, et al. Among authors: de jorge l.
J Neurol. 2010 Apr;257(4):598-602. doi: 10.1007/s00415-009-5380-3. Epub 2009 Nov 19.
J Neurol. 2010.
PMID: 19924463
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Diagnosis of Charcot-Marie-Tooth disease.
Banchs I, Casasnovas C, Albertí A, De Jorge L, Povedano M, Montero J, Martínez-Matos JA, Volpini V.
Banchs I, et al. Among authors: de jorge l.
J Biomed Biotechnol. 2009;2009:985415. doi: 10.1155/2009/985415. Epub 2009 Oct 8.
J Biomed Biotechnol. 2009.
PMID: 19826499
Free PMC article.
Review.
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Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies.
Bernal S, Solans T, Gamundi MJ, Hernan I, de Jorge L, Carballo M, Navarro R, Tizzano E, Ayuso C, Baiget M.
Bernal S, et al. Among authors: de jorge l.
Clin Genet. 2008 Apr;73(4):360-6. doi: 10.1111/j.1399-0004.2008.00963.x. Epub 2008 Feb 20.
Clin Genet. 2008.
PMID: 18294254
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