Topaloglu H - 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: topaloglu h. 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

Occidental type cerebromuscular dystrophy: a report of eleven cases.

Topaloğlu H, Yalaz K, Renda Y, Cağlar M, Göğüs S, Kale G, Gücüyener K, Nurlu G. Topaloğlu H, et al. J Neurol Neurosurg Psychiatry. 1991 Mar;54(3):226-9. doi: 10.1136/jnnp.54.3.226. J Neurol Neurosurg Psychiatry. 1991. PMID: 2030350 Free PMC article.

3

Classification of congenital muscular dystrophy.

Topaloğlu H, Renda Y, Yalaz K, Gücuyener K, Cağlar M, Göğüş G, Kale G. Topaloğlu H, et al. J Pediatr. 1990 Jul;117(1 Pt 1):166-7. doi: 10.1016/s0022-3476(05)82466-7. J Pediatr. 1990. PMID: 2370606 No abstract available.

4

Congenital muscular dystrophy (non-Fukuyama type) in Turkey: a clinical and pathological evaluation.

Topaloğlu H, Yalaz K, Renda Y, Kale G, Cağlar M, Göğüş S. Topaloğlu H, et al. Brain Dev. 1989;11(5):341-4. doi: 10.1016/s0387-7604(89)80066-x. Brain Dev. 1989. PMID: 2817300

5

Good clinical observation is essential before molecular studies.

Topaloglu H, Tan E, Dinçer P, Erdem S, Akçören Z. Topaloglu H, et al. Lancet. 1995 Dec 2;346(8988):1490. doi: 10.1016/s0140-6736(95)92507-4. Lancet. 1995. PMID: 7491011 No abstract available.

6

Left ventricular structure and function by echocardiography in congenital muscular dystrophy.

Cil E, Topaloğlu H, Cağlar M, Ozme S. Cil E, et al. Among authors: topaloglu h. Brain Dev. 1994 Jul-Aug;16(4):301-3. doi: 10.1016/0387-7604(94)90027-2. Brain Dev. 1994. PMID: 7818025 Clinical Trial.

7

Cerebellar ataxia associated with hypogonadotropic hypogonadism and chorioretinopathy: a poorly recognized association.

Erdem E, Kiratli H, Erbaş T, Varli K, Eldem B, Akalin S, Tan E, Topaloglu H, Gedikoglu G. Erdem E, et al. Among authors: topaloglu h. Clin Neurol Neurosurg. 1994 Feb;96(1):86-91. doi: 10.1016/0303-8467(94)90036-1. Clin Neurol Neurosurg. 1994. PMID: 8187389 Review.

8

Deletion analysis of Duchenne muscular dystrophy.

Erdem H, Ayter S, Ozgüç M, Topçu M, Topaloğlu H, Renda Y. Erdem H, et al. Among authors: topaloglu h. Turk J Pediatr. 1993 Jan-Mar;35(1):15-21. Turk J Pediatr. 1993. PMID: 8236513

9

An unusual case of Duchenne muscular dystrophy.

Topaloğlu H, Dinçer P, Göğüş S, Ayter S, Topçu M. Topaloğlu H, et al. Brain Dev. 1993 Jul-Aug;15(4):313-5. doi: 10.1016/0387-7604(93)90032-4. Brain Dev. 1993. PMID: 8250158

10

Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients.

Dinçer P, Topaloğlu H, Ayter S, Ozgüç M, Taşdemir HA, Renda Y. Dinçer P, et al. Among authors: topaloglu h. Brain Dev. 1996 Mar-Apr;18(2):91-4. doi: 10.1016/0387-7604(95)00128-x. Brain Dev. 1996. PMID: 8733896 Clinical Trial.

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