Search Results - "Sivera, R"

OP08.09: Objective comparison of craniofacial features in FGR and normally grown fetuses using statistical shape modelling from 3D ultrasound by Clark, A.E., Sivera, R., Dall'Asta, A., Schievano, S., Lees, C.

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OP08.01: Development of a statistical model from 3D ultrasound to describe growth of the fetal face with gestation by Clark, A.E., Sivera, R., Dall'Asta, A., Schievano, S., Lees, C.

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VP18.03: Objective analysis of shape vector changes in fetuses with cleft lip using statistical shape modelling from three‐dimensional ultrasound by Clark, A.E., Sivera, R., Dall'Asta, A., Schievano, S., Lees, C.

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VP18.09: Quantification of craniofacial abnormalities in thanatophoric dysplasia and Cornelia de lange syndrome from three‐dimensional ultrasound by Clark, A.E., Sivera, R., Dall'Asta, A., Schievano, S., Lees, C.

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OP09.03: From three‐dimensional (3D) ultrasound to 3D shape model of the fetal face: determining a normal reference standard by Clark, A.E., Sivera, R., Dall'Asta, A., Schievano, S., Lees, C.

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VP17.07: Quantification of fetal craniofacial abnormalities in Trisomy 21 and 18 from three‐dimensional ultrasound scans by Clark, A.E., Sivera, R., Dall'Asta, A., Schievano, S., Lees, C.

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Developing and testing an algorithm for automatic segmentation of the fetal face from three-dimensional ultrasound images by Clark, A E, Biffi, B, Sivera, R, Dall'Asta, A, Fessey, L, Wong, T-L, Paramasivam, G, Dunaway, D, Schievano, S, Lees, C C

“…Fetal craniofacial abnormalities are challenging to detect and diagnose on prenatal ultrasound (US). Image segmentation and computer analysis of…”
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The EGR2 gene is involved in axonal Charcot−Marie−Tooth disease by Sevilla, T., Sivera, R., Martínez-Rubio, D., Lupo, V., Chumillas, M. J., Calpena, E., Dopazo, J., Vílchez, J. J., Palau, F., Espinós, C.

“…Background and purpose A three‐generation family affected by axonal Charcot−Marie−Tooth disease (CMT) was investigated with the aim of discovering genetic…”
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Autoimmunity as a prognostic factor in sporadic adult onset cerebellar ataxia by Sivera, R., Martín, N., Boscá, I., Sevilla, T., Muelas, N., Azorín, I., Vílchez, J. J., Bolonio, M., Donat, E., Ribes-Koninckx, C., Bataller, L.

“…Cerebellar adult onset ataxia is a heterogeneous condition. The aim of this study was to ascertain if there is a heightened autoimmune background in patients…”
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Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease by Berciano, J, Sevilla, T, Casasnovas, C, Sivera, R, Vílchez, J J, Infante, J, Ramón, C, Pelayo-Negro, A L, Illa, I

“…Charcot-Marie-Tooth disease (CMT) is the most frequent form of inherited neuropathy. In accordance with the inheritance pattern and degree of slowing of motor…”
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The ventricular septal defect in tetralogy of Fallot: A multi-centre morphological and statistical shape analysis study by Sabarigirivasan, V, Sivera, R S, Crucean, A C, Cook, A C

“…Abstract Background Ventricular septal defects (VSDs) in Tetralogy of Fallot (TOF) are often thought to be ‘large and unrestricted’ but experience suggests…”
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Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease by Berciano, J., Sevilla, T., Casasnovas, C., Sivera, R., Vílchez, J.J., Infante, J., Ramón, C., Pelayo-Negro, A.L., Illa, I.

“…Charcot-Marie-Tooth disease (CMT) is the most frequent form of inherited neuropathy. In accordance with the inheritance pattern and degree of slowing of motor…”
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Guía diagnóstica en el paciente con enfermedad de Charcot-Marie-Tooth by Berciano, J, Sevilla, T, Casasnovas, C, Sivera, R, Vílchez, J.J, Infante, J, Ramón, C, Pelayo-Negro, A.L, Illa, I

“…Resumen Introducción La enfermedad de Charcot-Marie-Tooth (CMT) es la neuropatía hereditaria más frecuente. Clásicamente dividida según su patrón de herencia y…”
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OC 26.4 A Microfluidic Approach in TTP Highlights the Need to Normalise ADAMTS13 Activity Levels in Clinical Remission by Constantinescu-Bercu, A., de Groot, R., Dragunaite, B., Sivera, R., Vanhoorelbeke, K., McCann, S., Scully, M.

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Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study by Ortega Suero, G, Abenza Abildúa, M J, Serrano Munuera, C, Rouco Axpe, I, Arpa Gutiérrez, F J, Adarmes Gómez, A D, Rodríguez de Rivera, F J, Quintans Castro, B, Posada Rodríguez, I, Vadillo Bermejo, A, Domingo Santos, Á, Blanco Vicente, E, Infante Ceberio, I, Pardo Fernández, J, Costa Arpín, E, Painous Martí, C, Muñoz, J E, Mir Rivera, P, Montón Álvarez, F, Bataller Alberola, L, Gascón Bayarri, J, Casasnovas Pons, C, Vélez Santamaría, V, López Munain, A, Fernández García Eulate, G, Gazulla Abío, J, Sanz Gallego, I, Rojas Bartolomé, L, Ayo Martín, Ó, Segura Martín, T, González Mingot, C, Baraldés Rovira, M, Sivera Mascaró, R, Cubo Delgado, E, Echevarría Íñiguez, A, Vázquez Sánchez, F, Bártulos Iglesias, M, Casadevall Codina, M T, Martínez Fernández, E M, Labandeira Guerra, C, Alemany Perna, B, Carvajal Hernández, A, Fernández Moreno, C, Palacín Larroy, M, Caballol Pons, N, Ávila Rivera, A, Navacerrada Barrero, F J, Lobato Rodríguez, R, Sobrido Gómez, M J

“…Ataxia and hereditary spastic paraplegia are rare neurodegenerative syndromes. We aimed to determine the prevalence of these disorders in Spain in 2019. We…”
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Vestibular impairment in Charcot-Marie-Tooth disease type 4C by Pérez-Garrigues, Herminio, Sivera, Rafael, Vílchez, Juan Jesús, Espinós, Carmen, Palau, Francesc, Sevilla, Teresa

“…Charcot-Marie-Tooth disease type 4C (CMT4C) is a hereditary neuropathy with prominent unsteadiness. The objective of the current study is to determine whether…”
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Mapa epidemiológico transversal de las ataxias y paraparesias espásticas hereditarias en España by Ortega Suero, G., Abenza Abildúa, M.J., Serrano Munuera, C., Rouco Axpe, I., Arpa Gutiérrez, F.J., Adarmes Gómez, A.D., Rodríguez de Rivera, F.J., Quintans Castro, B., Posada Rodríguez, I., Vadillo Bermejo, A., Domingo Santos, Á., Blanco Vicente, E., Infante Ceberio, I., Pardo Fernández, J., Costa Arpín, E., Painous Martí, C., Muñoz, J.E., Mir Rivera, P., Montón Álvarez, F., Bataller Alberola, L., Gascón Bayarri, J., Casasnovas Pons, C., Vélez Santamaría, V., López de Munain, A., Fernández-Eulate, G., Gazulla Abío, J., Sanz Gallego, I., Rojas Bartolomé, L., Ayo Martín, Ó., Segura Martín, T., González Mingot, C., Baraldés Rovira, M., Sivera Mascaró, R., Cubo Delgado, E., Echavarría Íñiguez, A., Vázquez Sánchez, F., Bártulos Iglesias, M., Casadevall Codina, M.T., Martínez Fernández, E.M., Labandeira Guerra, C., Alemany Perna, B., Carvajal Hernández, A., Fernández Moreno, C., Palacín Larroy, M., Caballol Pons, N., Ávila Rivera, A., Navacerrada Barrero, F.J., Lobato Rodríguez, R., Sobrido Gómez, M.J.

“…Las ataxias (AT) y paraparesias espásticas hereditarias (PEH) son síndromes neurodegenerativos raros. Nos proponemos conocer la prevalencia de las AT y PEH en…”
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A Geometric Interpretation of the Chern Classes by Sivera, Rafael

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A Geometric Interpretation of the Chern Classes by Sivera, Rafael

“…Let $f_\xi: M \rightarrow BU$ be a classifying map of the stable complex bundle $\xi$ over the weakly complex manifold $M$. If $\tau$ is the stable right…”
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