Literature DB >> 9249628

An atypical case of partial merosin deficiency congenital muscular dystrophy.

A Prelle, G P Comi, C Rigoletto, A Turconi, G Felisari, P Ciscato, F Fortunato, S Messina, N Bresolin, M Mora, M Moggio, G Scarlato.   

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Year:  1997        PMID： 9249628     DOI： 10.1007/s004150050110

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  4 in total

Review 1.  The congenital muscular dystrophies: recent advances and molecular insights.

Authors:  Jerry R Mendell; Daniel R Boué; Paul T Martin
Journal:  Pediatr Dev Pathol       Date:  2006 Nov-Dec

Review 2.  The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review.

Authors:  K J Jones; G Morgan; H Johnston; V Tobias; R A Ouvrier; I Wilkinson; K N North
Journal:  J Med Genet       Date:  2001-10       Impact factor: 6.318

3.  Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjects.

Authors:  Elisabetta D'Adda; Monica Sciacco; Maria Elisa Fruguglietti; Veronica Crugnola; Valeria Lucchini; Filippo Martinelli-Boneschi; Chiara Zecca; Costanza Lamperti; Giacomo Pietro Comi; Nereo Bresolin; Maurizio Moggio; Alessandro Prelle
Journal:  J Neurol       Date:  2006-06-13       Impact factor: 4.849

4.  Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related Diseases.

Authors:  Isabelle Nelson; Tanya Stojkovic; Valérie Allamand; France Leturcq; Henri-Marc Bécane; Dominique Babuty; Annick Toutain; Christophe Béroud; Pascale Richard; Norma B Romero; Bruno Eymard; Rabah Ben Yaou; Gisèle Bonne
Journal:  J Neuromuscul Dis       Date:  2015-09-02
  4 in total

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