Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Manuel Parrón"'
Autor:
María D. Lledín, Manuel Parrón-Pajares, Ana Morais, Francisco Hernández-Oliveros, Jose I. Botella-Carretero, Loreto Hierro
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
BackgroundSarcopenia in adult cirrhotic patients is associated with increased morbidity and mortality whereas in children it is still being studied. Anthropometric variables in cirrhotic children are not reliable for assessing muscle mass as they may
Externí odkaz:
https://doaj.org/article/a45557e6b368480f8ee54c1e3377107e
Autor:
Francisca Diaz-Gonzalez, Javier M. Sacedo-Gutiérrez, Stephen R. F. Twigg, Eduardo Calpena, Fernando E. Carceller-Benito, Manuel Parrón-Pajares, Fernando Santos-Simarro, Karen E. Heath
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
Introduction: Saethre-Chotzen syndrome, a craniosynostosis syndrome characterized by the premature closure of the coronal sutures, dysmorphic facial features and limb anomalies, is caused by haploinsufficiency of TWIST1. Although the majority of vari
Externí odkaz:
https://doaj.org/article/e827ad7f17224d91878b038e166912a2
Autor:
Nelson M. Buitrago Sánchez, Javier M. Saceda Gutiérrez, María I. Esteban Rodríguez, Manuel Parrón Pajares
Publikováno v:
Anales de Pediatría, Vol 93, Iss 5, Pp 349-351 (2020)
Externí odkaz:
https://doaj.org/article/7dcddb4e131b41a99b737f9ae7624b90
Akademický článek
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Autor:
Marta Pacio‐Miguez, Manuel Parrón‐Pajares, Christopher T. Gordon, Fernando Santos‐Simarro, Carmen Rodríguez Jiménez, Rocio Mena, Inmaculada Rueda Arenas, Victoria Eugenia F. Montaño, María Fernández, Mario Solís, Ángela del Pozo, Jeanne Amiel, Sixto García‐Miñaur, María Palomares‐Bralo
Publikováno v:
American Journal of Medical Genetics Part A. 188:2819-2824
Autor:
Francisca Díaz‐González, Manuel Parrón‐Pajares, Elsa Lucas‐Castro, Silvia Modamio‐HØybjØr, Lucia Sentchordi‐Montané, Verónica Seidel, Pablo Prieto, Guillermo Tarraso‐Urios, Marta Codina‐Sola, Anna M. Cueto‐González, Mary J. Ballesta‐Martínez, Fernando Santos‐Simarro, Sergio B. Sousa, Karen E. Heath
Publikováno v:
Clinical Genetics.
Autor:
Silvia Modamio-Høybjør, Isabel González-Casado, Angel Campos-Barros, Francisca Díaz-González, José Antonio Bermúdez de la Vega, Fernando Santos-Simarro, Atilano Carcavilla, Ana C Barreda-Bonis, Carolina de la Torre, Purificación Ros-Pérez, Inés Mulero-Collantes, Sara Benito-Sanz, Angela del Pozo, Mario Solís, Jesús González de Buitrago Amigo, Julián Nevado, Lucia Sentchordi-Montané, André M. Travessa, Pablo Prieto, Miriam Aza-Carmona, Pilar Bahíllo-Curieses, Elena Vallespín, Jaime Cruz-Rojo, Manuel Parrón-Pajares, Joaquín Ramírez-Fernández, Karen E. Heath, Pablo Ruiz-Ocaña, Carlos Goetz, Carolina Bezanilla-López
Publikováno v:
European Journal of Endocrinology. 185:691-705
Objective Next generation sequencing (NGS) has expanded the diagnostic paradigm turning the focus to the growth plate. The aim of the study was to determine the prevalence of variants in genes implicated in skeletal dysplasias in probands with short
Autor:
André M. Travessa, Manuel Parrón-Pajares, Ana Berta Sousa, Teresa Mirco, Karen E. Heath, Francisca Díaz-González, Filipa Oliveira-Ramos
Publikováno v:
American Journal of Medical Genetics Part A. 182:2715-2721
Spondyloepiphyseal dysplasia type Stanescu (SED-S) is a very rare type II collagenopathy. We describe an 8-year-old boy who presented with short trunk, C2-C3 vertebral fusion, hand, foot, leg and thigh pain, stiffness and limited joint mobility, and
Autor:
Fernando Santos-Simarro, Aude Annick Suter, Uwe Kornak, Wiebke Hülsemann, Rosario Ramos-Mejia, Victoria Huckstadt, Angela Abad Perez, Stefan Mundlos, Pernille Mathiesen Toerring, Manuel Parrón-Pajares, Manuel Holtgrewe, Oliver Bartsch, Karen E. Heath, Nadja Ehmke, Martin A. Mensah
Publikováno v:
American Journal of Medical Genetics Part A
Suter, A A, Santos-Simarro, F, Toerring, P M, Abad Perez, A, Ramos-Mejia, R, Heath, K E, Huckstadt, V, Parrón-Pajares, M, Mensah, M A, Hülsemann, W, Holtgrewe, M, Mundlos, S, Kornak, U, Bartsch, O & Ehmke, N 2020, ' Variable pulmonary manifestations in Chitayat syndrome : Six additional affected individuals ', American Journal of Medical Genetics, Part A, vol. 182, no. 9, pp. 2068-2076 . https://doi.org/10.1002/ajmg.a.61735
Suter, A A, Santos-Simarro, F, Toerring, P M, Abad Perez, A, Ramos-Mejia, R, Heath, K E, Huckstadt, V, Parrón-Pajares, M, Mensah, M A, Hülsemann, W, Holtgrewe, M, Mundlos, S, Kornak, U, Bartsch, O & Ehmke, N 2020, ' Variable pulmonary manifestations in Chitayat syndrome : Six additional affected individuals ', American Journal of Medical Genetics, Part A, vol. 182, no. 9, pp. 2068-2076 . https://doi.org/10.1002/ajmg.a.61735
Hand hyperphalangism leading to shortened index fingers with ulnar deviation, hallux valgus, mild facial dysmorphism and respiratory compromise requiring assisted ventilation are the key features of Chitayat syndrome. This condition results from the
Publikováno v:
American Journal of Medical Genetics Part A. 182:628-631
Mesoaxial synostotic syndactyly with phalangeal reduction (MSSD) is an extremely rare autosomal recessive limb abnormality characterized by the fusion of third and fourth fingers. To date, only homozygous missense and frameshift mutations have been r