Search Results - "Haliloglu G"

Two patients with ‘Dropped head syndrome’ due to mutations in LMNA or SEPN1 genes

Authors: D'Amico, A. Haliloglu, G. Richard, P. et al.

Source: Neuromuscular Disorders. Sep2005, Vol. 15 Issue 8, p521-524. 4p.

C.P.3.07 Muscle pathology in alpha-dystroglycanopathies with central nervous system malformation

Authors: Talim, B. Haliloglu, G. Orhan, D. et al.

Source: Neuromuscular Disorders. Oct2007, Vol. 17 Issue 9/10, p871-872. 2p.

P.P.4 06 Limb-girdle muscular dystrophy and mental retardation (LGMD2M) has a heterogeneous background

Authors: Haliloglu, G. Balci, B. Talim, B. et al.

Source: Neuromuscular Disorders. Oct2006, Vol. 16 Issue 9/10, p679-680. 2p.

P.P.1 06 Magnetic resonance imaging and spectroscopy findings in a patient with partial merosin deficiency

Authors: Haliloglu, G. Oguz, K. Karli Ozturk, A. et al.

Source: Neuromuscular Disorders. Oct2006, Vol. 16 Issue 9/10, p663-664. 2p.

P.75 - Congenital myasthenic syndrome due to COLQ mutations: Clues for diagnosis.

Authors: Haliloglu, G. Demirci, T. Alikasifoglu, M. et al.

Source: Neuromuscular Disorders. Oct2016 Supplement 2, Vol. 26, pS112-S112. 1p.

P.58 - Arthrogryposis multiplex congenita (AMC): Spectrum and classification at a tertiary referral center.

Authors: Oncel, I. Haliloglu, G. Utine, E. et al.

Source: Neuromuscular Disorders. Oct2016 Supplement 2, Vol. 26, pS107-S107. 1p.

G.P.67 - Expanding the pathological phenotype in megaconial congenital muscular dystrophy.

Authors: Haliloglu, G. Talim, B. Aktas, D. et al.

Source: Neuromuscular Disorders. Oct2015 Supplement 2, Vol. 25, pS206-S206. 1p.

G.P.334 - Etiological yield of muscle biopsy in the newborn period.

Authors: Serdaroglu, E. Haliloglu, G. Talim, B. et al.

Source: Neuromuscular Disorders. Oct2015 Supplement 2, Vol. 25, pS286-S286. 1p.

G.P.386 - DMD registry in Turkey: Highlights.

Authors: Topaloğlu, H. Haliloglu, G. Yilmaz, O. et al.

Source: Neuromuscular Disorders. Oct2015 Supplement 2, Vol. 25, pS301-S301. 1p.

G.P.17.03 Muscle histopathology in asymptomatic children with incidentally detected high CK

Authors: Talim, B. Haliloglu, G. Akcoren, Z. et al.

Source: Neuromuscular Disorders. Sep2009, Vol. 19 Issue 8/9, p655-655. 1p.

P.P.1 05 Magnetic resonance imaging findings in a newborn with merosin-deficient congenital muscular dystrophy

Authors: Haliloglu, G. Oguz, K. Karli Orhan, D. et al.

Source: Neuromuscular Disorders. Oct2006, Vol. 16 Issue 9/10, p663-663. 1p.

Hypertrophic olivary degeneration in children: four new cases and a review of the literature with an emphasis on the MRI findings.

Authors: Sanverdi, S. E. Oguz, K. K. Haliloglu, G.

Source: British Journal of Radiology. May2012, Vol. 85 Issue 1013, p511-516. 6p.

G.P.233: Neuroblastoma in a patient with spinal muscular atrophy (SMA) Type I: Is it just a coincidence?

Authors: Sag, E. Sen, H. Susam Haliloglu, G. et al.

Source: Neuromuscular Disorders. Oct2014, Vol. 24 Issue 9/10, p886-887. 2p.

P.331 - Utility of a next-generation sequencing (NGS)-based neuromuscular disease gene panel in an investigation of 30 families with early-onset presentation from a tertiary pediatric neuromuscular clinic.

Authors: Ardicli, D. Nowak, K. Haliloglu, G. et al.

Source: Neuromuscular Disorders. Oct2017 Supplement 2, Vol. 27, pS196-S196. 1p.

G.P.3.04 Clinical spectrum of cytochrome-c-oxidase deficiency in children

Authors: Koksal, B. Talim, B. Haliloglu, G. et al.

Source: Neuromuscular Disorders. Oct2008, Vol. 18 Issue 9/10, p752-753. 2p.

P.172 - Solving a puzzle: Incidentally detected high creatine kinase level combined with a family history of cardiomyopathy and sudden unexplained death leading to diagnosis of LMNA mutation.

Authors: Genc, H. Maras Ardicli, D. Haliloglu, G. et al.

Source: Neuromuscular Disorders. Oct2016 Supplement 2, Vol. 26, pS138-S139. 1p.

G.P.222 - Nonsense mutation dystrophinopathy: How mutation-specific treatments changed our clinical practice?

Authors: Ardicli, D. Konuskan, B. Haliloglu, G. et al.

Source: Neuromuscular Disorders. Oct2015 Supplement 2, Vol. 25, pS253-S253. 1p.

G.P.24: Cardiomyopathy in childhood: Results from a single tertiary care center.

Authors: Batu, E. Pehlivanturk, M. Haliloglu, G. et al.

Source: Neuromuscular Disorders. Oct2014, Vol. 24 Issue 9/10, p801-801. 1p.

G.P.2.01 Frequency of different forms of congenital muscular dystrophies in a referral center

Authors: Talim, B. Akcoren, Z. Haliloglu, G. et al.

Source: Neuromuscular Disorders. Oct2008, Vol. 18 Issue 9/10, p735-735. 1p.

98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE: 26–28th October, 2001, Naarden, The Netherlands

Authors: Muntoni, F. Bertini, E. Bönnemann, C. et al.

Source: Neuromuscular Disorders. Nov2002, Vol. 12 Issue 9, p889. 8p.