Haliloglu G - Search Results

1

Balci B, Aurino S, Haliloglu G, Talim B, Erdem S, Akcören Z, Tan E, Caglar M, Richard I, Nigro V, Topaloglu H, Dincer P. Balci B, et al. Among authors: haliloglu g. Eur J Pediatr. 2006 May;165(5):293-8. doi: 10.1007/s00431-005-0046-3. Epub 2006 Jan 13. Eur J Pediatr. 2006. PMID: 16411092

2

Gender prevalence in childhood multiple sclerosis and myasthenia gravis.

Haliloglu G, Anlar B, Aysun S, Topcu M, Topaloglu H, Turanli G, Yalnizoglu D. Haliloglu G, et al. J Child Neurol. 2002 May;17(5):390-2. doi: 10.1177/088307380201700516. J Child Neurol. 2002. PMID: 12150589

3

Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature.

Haliloglu G, Chattopadhyay A, Skorodis L, Manzur A, Mercuri E, Talim B, Akçören Z, Renda Y, Muntoni F, Topaloğlu H. Haliloglu G, et al. Neuropediatrics. 2002 Dec;33(6):314-9. doi: 10.1055/s-2002-37087. Neuropediatrics. 2002. PMID: 12571787

4

FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cysts.

Topaloglu H, Brockington M, Yuva Y, Talim B, Haliloglu G, Blake D, Torelli S, Brown SC, Muntoni F. Topaloglu H, et al. Among authors: haliloglu g. Neurology. 2003 Mar 25;60(6):988-92. doi: 10.1212/01.wnl.0000052996.14099.dc. Neurology. 2003. PMID: 12654965

5

Mutation analysis of TSC2 gene in 33 Turkish familial cases with tuberous sclerosis.

Apak A, Haliloğlu G, Köse G, Yilmaz E, Anlar B, Aysun S. Apak A, et al. Among authors: haliloglu g. Turk J Pediatr. 2003 Jan-Mar;45(1):1-5. Turk J Pediatr. 2003. PMID: 12718362

6

A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan.

Dinçer P, Balci B, Yuva Y, Talim B, Brockington M, Dinçel D, Torelli S, Brown S, Kale G, Haliloglu G, Gerçeker FO, Atalay RC, Yakicier C, Longman C, Muntoni F, Topaloglu H. Dinçer P, et al. Among authors: haliloglu g. Neuromuscul Disord. 2003 Dec;13(10):771-8. doi: 10.1016/s0960-8966(03)00161-5. Neuromuscul Disord. 2003. PMID: 14678799

7

Effect of topiramate on enlargement of head in Canavan disease: a new option for treatment of megalencephaly.

Topçu M, Yalnizoğlu D, Saatçi I, Haliloğlu G, Topaloğlu H, Senbil N, Onol S, Coşkun T. Topçu M, et al. Among authors: haliloglu g. Turk J Pediatr. 2004 Jan-Mar;46(1):67-71. Turk J Pediatr. 2004. PMID: 15074377

8

Glycosylation defects in muscular dystrophies.

Haliloğlu G, Topaloğlu H. Haliloğlu G, et al. Curr Opin Neurol. 2004 Oct;17(5):521-7. doi: 10.1097/00019052-200410000-00002. Curr Opin Neurol. 2004. PMID: 15367856 Review.

9

An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene.

Balci B, Uyanik G, Dincer P, Gross C, Willer T, Talim B, Haliloglu G, Kale G, Hehr U, Winkler J, Topaloğlu H. Balci B, et al. Among authors: haliloglu g. Neuromuscul Disord. 2005 Apr;15(4):271-5. doi: 10.1016/j.nmd.2005.01.013. Neuromuscul Disord. 2005. PMID: 15792865

10

L-2-hydroxyglutaric aciduria: a report of 29 patients.

Topçu M, Aydin OF, Yalçinkaya C, Haliloğlu G, Aysun S, Anlar B, Topaloğlu H, Turanli G, Yalnizoğlu D, Kesimer M, Coşkun T. Topçu M, et al. Among authors: haliloglu g. Turk J Pediatr. 2005 Jan-Mar;47(1):1-7. Turk J Pediatr. 2005. PMID: 15884621

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