Compact power splitter with harmonic suppression based on inductively loaded slow‐wave transmission lines
Selga, J., Coromina, J., Vélez, P., Fernández‐Prieto, A., Martinez‐Ros, A. J., Bonache, J., Aznar‐Ballesta, F., Martín, F.
Published in Microwave and optical technology letters (01.06.2018)
Published in Microwave and optical technology letters (01.06.2018)
Get full text
Journal Article
Mutation analysis of Wilson disease in the Spanish population - identification of a prevalent substitution and eight novel mutations in the ATP7B gene
Margarit, E, Bach, V, Gómez, D, Bruguera, M, Jara, P, Queralt, R, Ballesta, F
Published in Clinical genetics (01.07.2005)
Published in Clinical genetics (01.07.2005)
Get full text
Journal Article
A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures
Ezquerra, M, Carnero, C, Blesa, R, Gelpí, J L, Ballesta, F, Oliva, R
Published in Neurology (01.02.1999)
Published in Neurology (01.02.1999)
Get more information
Journal Article
CHROMOSOMAL ABNORMALITIES AND POLYMORPHISMS IN INFERTILE MEN
PENNA VIDEAU, S, ARAUJO, H, BALLESTA, F, BALLESCA, J. L, VANRELL, J. A
Published in Archives of andrology (2001)
Published in Archives of andrology (2001)
Get full text
Journal Article
Dentatorubropallidoluysian atrophy in a Spanish family: a clinical, radiological, pathological, and genetic study
Muñoz, E, Milà, M, Sánchez, A, Latorre, P, Ariza, A, Codina, M, Ballesta, F, Tolosa, E
Published in Journal of neurology, neurosurgery and psychiatry (01.12.1999)
Published in Journal of neurology, neurosurgery and psychiatry (01.12.1999)
Get full text
Journal Article
Conference Proceeding
Differential Microfluidic Sensors based on Electroinductive-Wave (EIW) Transmission Lines
Gil, M., Velez, P., Aznar-Ballesta, F., Mesegar-Ruiz, A., Munoz-Enano, J., Martin, F.
Published in 2020 Fourteenth International Congress on Artificial Materials for Novel Wave Phenomena (Metamaterials) (27.09.2020)
Published in 2020 Fourteenth International Congress on Artificial Materials for Novel Wave Phenomena (Metamaterials) (27.09.2020)
Get full text
Conference Proceeding
Fragile X syndrome and the (CGG)n mutation : two families with discordant MZ twins
KRUYER, H, MILA, M, GLOVER, G, CARBONELL, P, BALLESTA, F, ESTIVILL, X
Published in American journal of human genetics (01.03.1994)
Get full text
Published in American journal of human genetics (01.03.1994)
Journal Article
Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization
FANTES, J. A, BICKMORE, W. A, FLETCHER, J. M, BALLESTA, F, HANSON, M, VAN HEYNINGEN, V
Published in American journal of human genetics (01.12.1992)
Get full text
Published in American journal of human genetics (01.12.1992)
Journal Article
Sporadic orofaciodigital syndrome type I presenting as end-stage renal disease
COLL, E, TORRA, R, PASCUAL, J, BOTEY, A, ARA, J, PEREZ, L, BALLESTA, F, DARNELL, A
Published in Nephrology, dialysis, transplantation (01.05.1997)
Published in Nephrology, dialysis, transplantation (01.05.1997)
Get full text
Journal Article
Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements
Soler, Anna, Margarit, Ester, Carrió, Ana, Costa, Dolors, Queralt, Rosa, Ballesta, Francisca
Published in Journal of medical genetics (01.04.1999)
Published in Journal of medical genetics (01.04.1999)
Get full text
Journal Article
Systemic sarcoidosis with spleen involvement
RODRÍGUEZ-GARCÍA, J L, PICAZO, J, MIRA, C, BALLESTA, F, GARCÍA-NIETO, J C, PRIETO, E
Published in Postgraduate medical journal (01.04.2001)
Published in Postgraduate medical journal (01.04.2001)
Get full text
Journal Article
Apolipoprotein E ϵ4 alleles and meiotic origin of non-disjunction in Down syndrome children and in their corresponding fathers and mothers
Ezquerra, M, Ballesta, F, Queralt, R, Aledo, R, Gómez, D, Guitart, M, Egozcue, J, Ascaso, C, Oliva, R
Published in Neuroscience letters (22.05.1998)
Published in Neuroscience letters (22.05.1998)
Get full text
Journal Article
Trichothiodystrophy associated with urologic malformation and primary hypercalciuria
MALVEHY, J, FERRANDO, J, SOLER, J, TUNEU, A, BALLESTA, F, ESTRACH, T
Published in Pediatric dermatology (01.11.1997)
Published in Pediatric dermatology (01.11.1997)
Get full text
Journal Article
Assaying the granulocyte-macrophage colony-stimulating factor (GM-CSF) as a mitogen of immature cells in fetal blood cultures
Costa, D., Borrell, A., Jou, J. M., Besón, I., Soler, A., Carrió, A., Margarit, E., Caballín, R., Ballesta, F., Fortuny, A.
Published in Prenatal diagnosis (01.01.1999)
Published in Prenatal diagnosis (01.01.1999)
Get full text
Journal Article
Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families
Milà, M, Kruyer, H, Glover, G, Sánchez, A, Carbonell, P, Castellví-Bell, S, Volpini, V, Rossell, J, Gabarrón, J, López, I
Published in Human genetics (01.10.1994)
Published in Human genetics (01.10.1994)
Get more information
Journal Article
Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36)
Templado, C, Navarro, J, Requena, R, Benet, J, Ballesta, F, Egozcue, J
Published in Human genetics (01.01.1990)
Published in Human genetics (01.01.1990)
Get more information
Journal Article
Cytogenetic Studies in Fetal Blood
Costa, D., Borrell, A., Soler, A., Carrió, A., Margarit, E., Ballesta, F., Puerto, B., Caballín, M.R., Fortuny, A.
Published in Fetal diagnosis and therapy (01.05.1998)
Published in Fetal diagnosis and therapy (01.05.1998)
Get full text
Journal Article
Autologous hemopoietic reconstitution after fetal liver infusion in patients with bone marrow failure : consequence or coincidence ?
SIERRA, J, BADELL, I, CUBELLS, J, MARTINEZ DE LA RIBA, A, BALLESTA, F, ROZMAN, C, GRANENA, A, GARCIA, J, MARIN, P, VALLS, A, CARRERAS, E, TORRAS, A, ROVIRA, M, PUJOL, E
Published in Bone marrow transplantation (Basingstoke) (01.04.1992)
Get full text
Published in Bone marrow transplantation (Basingstoke) (01.04.1992)
Journal Article
Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls
Sánchez, Mayka, Bruguera, Miquel, Bosch, Jaume, Rodés, Joan, Ballesta, Francisca, Oliva, Rafael
Published in Journal of hepatology (01.11.1998)
Published in Journal of hepatology (01.11.1998)
Get full text
Journal Article