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Journal of Diabetes and Its Complications|June 17, 2016
Nocturnal blood pressure is associated with the progression of microvascular complications and hypertension in patients with type 1 diabetes mellitusIsabel Mateo-Gavira, Francisco J Vílchez-López, María V García-Palacios, et al.Journal of Human Hypertension|August 19, 2016
Early blood pressure alterations are associated with pro-inflammatory markers in type 1 diabetes mellitusI Mateo-Gavira, F J Vílchez-López, M V García-Palacios, et al.European Journal of Neurology|September 17, 2024
ITPR3-associated neuropathy: Report of a further family with adult onset intermediate Charcot-Marie-Tooth diseaseJavier Cabello-Murgui, Jesús Jiménez-Jiménez, Juan J Vílchez, et al.Nature Genetics|December 18, 2001
The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A diseaseAna Cuesta, Laia Pedrola, Teresa Sevilla, et al.European Journal of Neurology|July 25, 2015
The EGR2 gene is involved in axonal Charcot-Marie-Tooth diseaseT Sevilla, R Sivera, D Martínez-Rubio, et al.Neurologia (Barcelona, Spain)|November 1, 1995
[Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure]A Pou Serradell, J M Espadaler, J M Aragonés, et al.Journal of Neurology|October 11, 2011
Autoimmunity as a prognostic factor in sporadic adult onset cerebellar ataxiaR Sivera, N Martín, I Boscá, et al.Journal of the Peripheral Nervous System : JPNS|January 5, 2011
Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot-Marie-Tooth diseaseRafael Sivera, Carmen Espinós, Juan J Vílchez, et al.Revista De Neurologia|March 26, 2015
[Guidelines for monitoring late-onset Pompe disease.Sociedad Española de Medicina Interna (SEMI), Sociedad Española de Neurología (SEN) y Sociedad Española de Neumología y CirugíaTorácica (SEPAR)]Eduardo Gutiérrez-Rivas, Isabel Illa, Samuel I Pascual-Pascual, et al.Clinical Genetics|March 15, 2011
Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patientsN Muelas, P Hackman, H Luque, et al.Pageof 8