Neurobiologia molecular
NEUROMOL
Hospital Universitario La Fe
Valencia, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario La Fe (10)
2010
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Perivascular nerve fiber α-synuclein regulates contractility of mouse aorta: A link to autonomic dysfunction in Parkinson's disease
Neurochemistry International, Vol. 56, Núm. 8, pp. 991-998
2009
2008
2007
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A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation
European Journal of Human Genetics, Vol. 15, Núm. 1, pp. 29-34
2004
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Localization of MRX82: A new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family
American Journal of Medical Genetics, Vol. 131 A, Núm. 2, pp. 174-178
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Screening for Microdeletions of the X-Chromosome in Non-Specific Mental Retardation [2]
American Journal of Medical Genetics
2003
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Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome
Clinical Genetics, Vol. 64, Núm. 6, pp. 491-496
2001
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Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2
American Journal of Medical Genetics, Vol. 102, Núm. 2, pp. 200-204
1995
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Fertilization and early embryology: Morphometric characterization of normal and abnormal human zygotes
Human Reproduction, Vol. 10, Núm. 9, pp. 2339-2342