Yalnizoğlu D - Search Results

1

Vigabatrin in pediatric patients with refractory epilepsy.

Turanli G, Celebi A, Yalnizoğlu D, Topçu M, Topaloğlu H, Banu A, Aysun S. Turanli G, et al. Among authors: yalnizoglu d. Turk J Pediatr. 2006 Jan-Mar;48(1):25-30. Turk J Pediatr. 2006. PMID: 16562782

2

Fatal agranulocytosis developed in the course of carbamazepine therapy. A case report and review of the literature.

Olcay L, Pekcan S, Yalnizoğlu D, Büyükpamukçu M, Yalaz K. Olcay L, et al. Among authors: yalnizoglu d. Turk J Pediatr. 1995 Jan-Mar;37(1):73-7. Turk J Pediatr. 1995. PMID: 7732613 Review.

3

Analysis of "pure" congenital muscular dystrophies in thirty-eight cases. How different is the classical type 1 from the occidental type cerebromuscular dystrophy?

Topaloğlu H, Kale G, Yalnizoğlu D, Taşdemir AH, Karaduman A, Topçu M, Kotiloğlu E. Topaloğlu H, et al. Among authors: yalnizoglu d. Neuropediatrics. 1994 Apr;25(2):94-100. doi: 10.1055/s-2008-1071593. Neuropediatrics. 1994. PMID: 8072682

4

Deletions in the survival motor neuron gene in Turkish spinal muscular atrophy patients.

Erdem H, Pehlivan S, Topaloğlu H, Yalnizoğlu D, Akçören Z. Erdem H, et al. Among authors: yalnizoglu d. J Inherit Metab Dis. 1996;19(6):724-8. doi: 10.1007/BF01799161. J Inherit Metab Dis. 1996. PMID: 8982943 No abstract available.

5

Hypothalamic hamartoma with gelastic epilepsy, precocious puberty and polydactyly.

Turanli G, Aynaci M, Yalnizoğlu D, Renda Y. Turanli G, et al. Among authors: yalnizoglu d. Turk J Pediatr. 1996 Oct-Dec;38(4):533-6. Turk J Pediatr. 1996. PMID: 8993186

6

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey.

Dinçer P, Leturcq F, Richard I, Piccolo F, Yalnizoglu D, de Toma C, Akçören Z, Broux O, Deburgrave N, Brenguier L, Roudaut C, Urtizberea JA, Jung D, Tan E, Jeanpierre M, Campbell KP, Kaplan JC, Beckmann JS, Topaloglu H. Dinçer P, et al. Among authors: yalnizoglu d. Ann Neurol. 1997 Aug;42(2):222-9. doi: 10.1002/ana.410420214. Ann Neurol. 1997. PMID: 9266733

7

Neuronal migration disorders. Part I: Terminology, classification, pathophysiology, EEG and epilepsy.

Turanli G, Yalnizoğlu D, Renda Y. Turanli G, et al. Among authors: yalnizoglu d. Turk J Pediatr. 1998 Oct-Dec;40(4):473-80. Turk J Pediatr. 1998. PMID: 10028855 Review.

8

Rasmussen encephalitis in childhood.

Topçu M, Turanli G, Aynaci FM, Yalnizoglu D, Saatçi I, Yigit A, Genç D, Söylemezoglu F, Bertan V, Akalin N. Topçu M, et al. Among authors: yalnizoglu d. Childs Nerv Syst. 1999 Aug;15(8):395-402; discussion 403. doi: 10.1007/s003810050423. Childs Nerv Syst. 1999. PMID: 10447611

9

Intestinal involvement and vasculopathy in von Recklinghausen's neurofibromatosis.

Göğüş S, Sarikayalar F, Akçören Z, Yalnizoğlu D, Hiçsönmez A. Göğüş S, et al. Among authors: yalnizoglu d. Turk J Pediatr. 1997 Jan-Mar;39(1):117-22. Turk J Pediatr. 1997. PMID: 10868203

10

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. Among authors: yalnizoglu d. J Child Neurol. 2002 May;17(5):390-2. doi: 10.1177/088307380201700516. J Child Neurol. 2002. PMID: 12150589

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