P. Serdaroğlu-Oflazer

Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease

U. Giger, Y. Parman, Hüseyin Demirci, 2017, Neuromuscular Disorders.

Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies

P. Sharafi, P. Korkusuz, H. Topaloglu, 2014, Neuromuscular Disorders.

Pathophysiology of protein aggregation and extended phenotyping in filaminopathy.

I. Ferrer, M. Tegenthoff, J. Bilbao, 2012, Brain : a journal of neurology.

A frameshift mutation of ERLIN2 in recessive intellectual disability, motor dysfunction and multiple joint contractures.

A. Tolun, B. Kara, E. Orhan, 2011, Human molecular genetics.

Oculopharyngodistal myopathy is a distinct entity

K. Bushby, Y. Parman, Hanns Lochmüller, 2011, Neurology.

Emery-Dreifuss Muscular Dystrophy: Nuclear Envelopathies

F. Deymeer, H. Durmuş, P. Serdaroğlu-Oflazer, 2014 .

Neuromuscular endplate pathology in recessive desminopathies

A. Franke, U. Schlötzer-Schrehardt, Y. Parman, 2016, Neurology.

Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up

A. Engel, B. Kara, F. Deymeer, 2017, Neuromuscular Disorders.

Effects of prior treatment with simvastatin on skeletal muscle structure and mitochondrial enzyme activities during early phases of sepsis.

H. Yorulmaz, E. Ozkok, G. Ates, 2014, International journal of clinical and experimental pathology.