Haliloğlu G - Search Results

1

3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures.

Coşkun T, Aydin HI, Kiliç M, Dursun A, Haliloğlu G, Topaloğlu H, Karli-Oğuz K, de Koning TJ. Coşkun T, et al. Among authors: haliloglu g. Turk J Pediatr. 2009 Nov-Dec;51(6):587-92. Turk J Pediatr. 2009. PMID: 20196394

2

Molybdenum cofactor deficiency: report of three cases presenting as hypoxic-ischemic encephalopathy.

Topcu M, Coskun T, Haliloglu G, Saatci I. Topcu M, et al. Among authors: haliloglu g. J Child Neurol. 2001 Apr;16(4):264-70. doi: 10.1177/088307380101600406. J Child Neurol. 2001. PMID: 11332461

3

D-glyceric aciduria in a six-month-old boy presenting with West syndrome and autistic behaviour.

Topcu M, Saatci I, Haliloglu G, Kesimer M, Coskun T. Topcu M, et al. Among authors: haliloglu g. Neuropediatrics. 2002 Feb;33(1):47-50. doi: 10.1055/s-2002-23600. Neuropediatrics. 2002. PMID: 11930278

4

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

5

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

6

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

7

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

8

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

9

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.

10

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

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