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G.O.3

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.793-793

Selcen, D

2014

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Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment

Lancet neurology, 2015-05, Vol.14 (5), p.461-461

2015

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Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients

Brain (London, England : 1878), 2004-02, Vol.127 (2), p.439-451

2004

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Myasthenic syndrome caused by plectinopathy

Neurology, 2011-01, Vol.76 (4), p.327-336

2011

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Zaspopathy in a large classic late-onset distal myopathy family

Brain (London, England : 1878), 2007-06, Vol.130 (6), p.1477-1484

2007

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Recurrent respiratory failure in a patient with nemaline and myofibrillar myopathy features

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S191-S191

2016

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Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patients

Neurology, 2009-07, Vol.73 (3), p.228-235

2009

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Coexisting TIA1 and MYH7 distal myopathy

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S280-S280

2015

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LRP4 myasthenia: Investigation of a second kinship reveals impaired development and maintenance of the neuromuscular junction

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S186-S187

2015

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Myofibrillar myopathies

Current opinion in neurology, 2008-10, Vol.21 (5), p.585-589

Selcen, Duygu

2008

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Online social capital: Understanding e-impulse buying in practice

Journal of retailing and consumer services, 2009, Vol.16 (4), p.320-328

2009

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G.O.3: Severe congenital actin related myofibrillar myopathy

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.793-793

Selcen, D.

2014

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O.21 Congenital Myasthenic Syndrome (CMS), autophagic myopathy, and cognitive dysfunction caused by mutations in DPAGT1

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.851-851

2013

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73P Peripheral neuropathy in myofibrillar myopathies (MFM) and MFM gene-related myopathies

Neuromuscular disorders : NMD, 2024-10, Vol.43, p.104441, Article 104441.427

2024

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INV37 Cytoskeletal myopathies – an overview

European journal of paediatric neurology, 2007, Vol.11, p.16-16

Selcen, D

2007

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Myofibrillar myopathies

Current opinion in neurology, 2010-10, Vol.23 (5), p.477-481

Selcen, Duygu

2010

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Mutations in ZASP define a novel form of muscular dystrophy in humans

Annals of neurology, 2005-02, Vol.57 (2), p.269-276

2005

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Mutations in myotilin cause myofibrillar myopathy

Neurology, 2004-04, Vol.62 (8), p.1363-1371

2004

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O.23 A novel desmin mutation causes autosomal recessive limb girdle muscular dystrophy without features of myofibrillar myopathy

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.851-852

2013

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P5.52 Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.740-740

2011

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Myofibrillar myopathy caused by novel dominant negative αB-crystallin mutations

Annals of neurology, 2003-12, Vol.54 (6), p.804-810

2003

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205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2015-03, Vol.25 (3), p.268-272

2015

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C.I.4 Myofibrillar myopathies

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.832-832

2007

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SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES: P.189 Diverse cohort of spinraza-treated spinal muscular atrophy patients at Mayo Clinic Rochester for theranostic biomarker discovery

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S102-S102

2020

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SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S102

2020

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G.O.3

Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment

Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients

Myasthenic syndrome caused by plectinopathy

Zaspopathy in a large classic late-onset distal myopathy family

Recurrent respiratory failure in a patient with nemaline and myofibrillar myopathy features

Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patients

Coexisting TIA1 and MYH7 distal myopathy

LRP4 myasthenia: Investigation of a second kinship reveals impaired development and maintenance of the neuromuscular junction

Myofibrillar myopathies

Online social capital: Understanding e-impulse buying in practice

G.O.3: Severe congenital actin related myofibrillar myopathy

O.21 Congenital Myasthenic Syndrome (CMS), autophagic myopathy, and cognitive dysfunction caused by mutations in DPAGT1

73P Peripheral neuropathy in myofibrillar myopathies (MFM) and MFM gene-related myopathies

INV37 Cytoskeletal myopathies – an overview

Myofibrillar myopathies

Mutations in ZASP define a novel form of muscular dystrophy in humans

Mutations in myotilin cause myofibrillar myopathy

O.23 A novel desmin mutation causes autosomal recessive limb girdle muscular dystrophy without features of myofibrillar myopathy

P5.52 Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy

Myofibrillar myopathy caused by novel dominant negative αB-crystallin mutations

205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands

C.I.4 Myofibrillar myopathies

SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES: P.189 Diverse cohort of spinraza-treated spinal muscular atrophy patients at Mayo Clinic Rochester for theranostic biomarker discovery

SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES

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