Zobrazeno 1 - 10
of 187
pro vyhledávání: '"Si, Pascual Pascual"'
Autor:
Si, Pascual-Pascual, Nascimento A, Cm, Fernandez-Llamazares, CONSTANCIO MEDRANO-LOPEZ, Villalobos-Pinto E, Martinez-Moreno M, Ley M, Manrique-Rodriguez S, Blasco-Alonso J
Publikováno v:
REVISTA DE NEUROLOGIA
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Europe PubMed Central
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Europe PubMed Central
Infantile-onset Pompe disease has a fatal prognosis in the short term unless it is diagnosed at an early stage and enzyme replacement therapy is not started as soon as possible. A group of specialists from different disciplines involved in this disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4647bfcaa670c1e8302a693341a23485
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10065
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10065
Autor:
Mc, Miranda-Herrero, Si, Pascual-Pascual, Barredo-Valderrama E, María Vázquez López, de Castro-De Castro P
Publikováno v:
Europe PubMed Central
Visuospatial functions are very important in learning process and development of abstract thought during childhood. Several studies show that preterm and low birth weight infants obtain lower scores in test that assess cognitive functions, specially
Autor:
I, Pascual Castroviejo, Si, Pascual Pascual, R, Velázquez Fragua, J, Viaño, J M, Garcia Segura
Publikováno v:
Neurologia (Barcelona, Spain). 22(10)
To describe the clinical and imaging findings of 20 patients (12 women and 8 men) with brain stem tumors associated with neurofibromatosis type 1 (NF1).All patients were first time studied before 11 years old. Clinical and magnetic resonance (MR) stu
Publikováno v:
Europe PubMed Central
To report two new patients with cerebrofaciothoracic dysplasia (Pascual-Castroviejo type I syndrome).We present two boys of 16 months and 9 years of age who were studied because of facial features, costovertebral defects and psychomotor delay.Both pa
Publikováno v:
Neuropediatrics. 37
Publikováno v:
Neurologia (Barcelona, Spain). 20(3)
To present a patient of 35 years with Costello syndrome.A male consulted at 11 months of age because of psychomotor delay and peculiar face.The main clinic features corresponded to the cutis laxa disease, although the picture and the results of the p
Autor:
Pascual-Castroviejo I, Viaño J, Roche C, Martínez-Bermejo A, Martínez-Fernández V, Arcas J, Si, Pascual-Pascual, López-Martín V, Tendero A, Alberto Fernández-Jaén, Quijano S
Publikováno v:
Europe PubMed Central
To present the fitest classification and the imaging peculiarities of the malformations of cortical development, most of which have been related with the epilepsy origin.The study is based on an anatomical-histological classification scheme that show
Autor:
Ma, Martínez-Granero, Si, Pascual Pascual, Fernando Baquero-Artigao, de Ceano Vivas M, Pascual-Castroviejo I
Publikováno v:
Europe PubMed Central
We report clinical and electrophysiologic findings for two members of a family with a history of hereditary amyotrophic neuralgia, emphasizing the early onset in both patients, the great variation in symptoms within the same family and the poor funct
Publikováno v:
Europe PubMed Central
Seventeen cases of growing cranial fractures in infancy are presented, eleven males and six females. Seventy per cent of the cases suffered a traumatic episode before one year of life. Thirteen of the total group experienced surgical intervention in
Autor:
Pascual-Castroviejo I, Si, Pascual-Pascual, Gutiérrez-Molina M, Saarinen A, Th, Joensuu, Bayés M, Bru Cormand
Publikováno v:
Europe PubMed Central
The objective [corrected] is to present a case of muscle-eye-brain (MEB) disease with genetic study.We studied an affected male from the age of 7 months to 21 years. During this time, clinical, analytical, neurophysiological (EEG, EMG, visual evoked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4fe484fe5b5c40e58fffc0fd268d1d11
http://europepmc.org/abstract/med/15954036
http://europepmc.org/abstract/med/15954036