Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophy.

Author:

Palmucci L,Mongini T,Doriguzzi C,Maniscalco M,Schiffer D

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference32 articles.

1. The neurogenic scapulo-peroneal syndrome;Ricker, K.; Mertens, H.-G.;Europ Neurol,1968

2. The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome;Ricker, K.; Mertens, H.-G.;Europ Neurol,1968

3. Les amyotrophies scapulo-peroneales (a propos de deux cas de syndrome de Stark-Kaeser);Andre, J.M.; Andre, M.N.; Floquet, J.; Tridon, P.; Arnould, G.;Ann Mid Nancy,1972

4. Neurogenic scapuloperoneal syndrome in childhood;Mercelis, R.; Demeester, J.; Martin, J.-J.;J Neurol Neurosurg Psychiatry,1980

5. Facioscapulohumeral dystrophy and the scapuloperoneal syndrome;Munsat, T.L.,1986

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1. R;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

2. Identification of a New Locus for a Peculiar Form of Congenital Muscular Dystrophy with Early Rigidity of the Spine, on Chromosome 1p35-36;The American Journal of Human Genetics;1998-06

3. The rigid spine syndrome due to acid maltase deficiency;Muscle & Nerve;1997-03

4. Emery-Dreifuss syndrome: Genetic and clinical varieties;American Journal of Medical Genetics;1994-04-15

5. Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy;Journal of the Neurological Sciences;1992-09

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