Persones / Equip Humà

Cristina Jou Muñoz

Buscador de publicacions

Publicacions

  • Ulate-Campos A, Petanas-Argemi J, Rebollo M, Jou-Munoz C, Sierra-March C, Armstrong-Moron J and Fons-Estupina C.

    Adrenoleucodistrofia ligada al X con patron radiologico atipico.

    REVISTA DE NEUROLOGIA . 66(7): 237-240. Nº de cites: 4

    [doi:10.33588/rn.6607.2017498]

  • Soria Gondek A, Julià V, Jou-Munoz C, Salvador-Hernandez H, Rovira-Zurriaga C and Tarrado X.

    Adolescent Hydrocele Carrying a Surprise: A Case of Papillary Cystadenoma of the Epididymis

    UROLOGY . 112: 172-175. Nº de cites: 2

    [doi:10.1016/j.urology.2017.10.040]

  • Rodríguez-García MA, Del Rio-Baquero LM, Ortez-Gonzalez CI, Jou-Munoz C, Vigo-Morancho M, Medina J, Febrer A, Ramon-Krauel M, Diaz-Manera J, Olive-Valls M, González-Mera L, Nascimento-Osorio A and Jimenez-Mallebrera C.

    Differences in Adipose Tissue and Lean Mass Distribution in Patients with Collagen VI Related Myopathies Are Associated with Disease Severity and Physical Ability

    FRONTIERS IN AGING NEUROSCIENCE . 9: 268-268. Nº de cites: 4

    [doi:10.3389/fnagi.2017.00268]

  • Romero-Moya D, Santos-Ocaña C, Castaño J, Garrabou G, Rodríguez-Gómez JA, Ruiz-Bonilla V, Bueno C, González-Rodriguez P, Giorgetti A, Perdiguero E, Prieto C, Moren-Nuñez C, Fernández-Ayala DJ, Cascajo MV, Velasco I, Canals JM, Montero-Sanchez R, Yubero-Siles D, Jou-Munoz C, López-Barneo J, Cardellach F, Muñoz-Cánoves P, Artuch-Iriberri R, Navas P and Menéndez P.

    Genetic Rescue of Mitochondrial and Skeletal Muscle Impairment in an Induced Pluripotent Stem Cells Model of Coenzyme Q10 Deficiency

    Stem Cells . 35(7): 1687-1703. Nº de cites: 24

    [doi:10.1002/stem.2634]

  • González-Fernández S, Sabra S, Oltra M, Parra-Hernandez JA, Jou-Munoz C, Gonzalez-Bosquet E and Gómez-Roig MD.

    Case report of recurrent abdominal wall endometrioma at the same location after nine years of its first excision

    Journal of Fertilization: in vitro - IVF - Worldwide, Reproductive Mediicne, Genetics & Stem Cell Biology . 5: 1.

    [doi:10.4172/2375-4508.1000198]

  • Fernández-Marmiesse A, Carrascosa-Romero MC, Alfaro Ponce B, Nascimento-Osorio A, Ortez-Gonzalez CI, Romero N, Palacios L, Jimenez-Mallebrera C, Jou-Munoz C, Gouveia S and Couce ML.

    Homozygous truncating mutation in prenatally expressed skeletal isoform of TTN gene results in arthrogryposis multiplex congenita and myopathy without cardiac involvement

    NEUROMUSCULAR DISORDERS . 27(2): 188-192. Nº de cites: 29

    [doi:10.1016/j.nmd.2016.11.002]

  • Llano-Diez M, Ortez CI, Gay JA, Alvarez-Cabado L, Jou-Munoz C, Medina J, Nascimento-Osorio A and Jimenez-Mallebrera C.

    Digital PCR quantification of miR-30c and miR-181a as serum biomarkers for Duchenne muscular dystrophy

    NEUROMUSCULAR DISORDERS . 27(1): 15-23. Nº de cites: 26

    [doi:10.1016/j.nmd.2016.11.003]

  • Yubero-Siles D, Adin A, Montero-Sanchez R, Jou-Munoz C, Jimenez-Mallebrera C, Garcia-Cazorla A, Nascimento-Osorio A, O'Callaghan-Gordo M, Montoya J, Gort L, Navas P, Ribes A, Ugarte MD and Artuch-Iriberri R.

    A statistical algorithm showing coenzyme Q10 and citrate synthase as biomarkers for mitochondrial respiratory chain enzyme activities

    SCIENTIFIC REPORTS . 6: 15-15. Nº de cites: 12

    [doi:10.1038/s41598-016-0008-1]

  • Nascimento-Osorio A, Ortez-Gonzalez CI, Jou-Munoz C, O'Callaghan-Gordo M, Ramos F and Garcia-Cazorla A.

    Neuromuscular Manifestations in Mitochondrial Diseases in Children.

    SEMINARS IN PEDIATRIC NEUROLOGY . 23(4): 290-305. Nº de cites: 6

    [doi:10.1016/j.spen.2016.11.004]

  • Figueras-Nart I, Vicente-Villa MA, Sánchez-Schmidt J, Jou-Munoz C, Bordas-Orpinell X, Celis-Passini VP, Cruz-Martínez O and González-Enseñat MA.

    Langerhans cell histiocytosis presenting as fingernail changes.

    JAAD case reports . 2(6): 485-487.

    [doi:10.1016/j.jdcr.2016.05.005]