Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene
Texto completo
Figure
Documento similar
The purpose of this study is to report a new surgical technique and the comparative clinical outcomes in patients with primary tenorrhaphy rupture or chronic flexor digitorum
The aim of this study was to evaluate retrospectively the sensitivity of three different serological tests used in real clinical practice for the screening and diagnosis of
Conclusions: This study shows that growth retardation and rickets were the most prevalent clinical manifestations at diagnosis in a large series of Spanish pediatric patients with
The aim of this study is to provide new rational and objective indices that accurate- ly quantify the morphogeometric changes associated to the clinical evidence of corne- al
Proceeding with the picture described above, our purpose in this pa- per is to study the notions of local rigidity, bifurcation instants, and stability for a family of open sets {Ω γ
In this study, we propose a model that explains the relation between family variables (re- lationship with parents and family activities) and Personal Positive Youth
Objective: The objective of this study was to compare the clinical outcomes and complications of a consecutive series of patients with proximal humerus fractures (PHF) treated
The aim of this study is to evaluate the effectiveness and efficiency of acenocoumarol dosing algorithm developed by our group, and that include demographic, clinical and