DISTROFIA DE STEINERT PDF

La enfermedad de Steinert es una rara miopatía hereditaria caracterizada por debilidad muscular generalizada, miotonía y afección multisistémica. Aunque los . Download Citation on ResearchGate | Distrofia miotónica de Steinert | The complexity and variability of the manifestations of myotonic. Distrofia miotónica o enfermedad de Steinert: estudio clínico-histopatológico de tres casos de una família. Arq. Neuro-Psiquiatr. [online]. , vol, n

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You can change the settings or obtain more information by clicking here. Antenatal and preoperative genetic and clinical assessment in myotonic dystrophy. Am J Obstet Gynecol, 82pp. Lancet,pp.

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Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Ultras Obstet Gyneacol [en distrofix. Computations for prenatal prediction of myotonic dystrophy. Toko-Gin Pract, 61pp.

Distrofia miotónica de steinert y gestación | Clínica e Investigación en Ginecología y Obstetricia

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Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. Prenat Diagn, 11pp. Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy. Neurophysiol Clin, 21pp.

Neurology, 42pp. Are you a health professional able to prescribe or dispense dustrofia

Las Palmas de Gran Canaria. Congenital myotonic dystrophy [abstract]. Prenat Diagn, 13pp.

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Curr Opin Neurol, 10pp. A report of two cases and a review of the literature. Anaesth Intensive Care, 27pp. Eguiluz aW. Principios de medicina interna, pp. Prenatal diagnosis of myotonic dystrophy by direct mutation analysis. Tidsskr Nor Laegeforen,pp.

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