Topcu M - Search Results

1

Williams RE, Adams HR, Blohm M, Cohen-Pfeffer JL, de Los Reyes E, Denecke J, Drago K, Fairhurst C, Frazier M, Guelbert N, Kiss S, Kofler A, Lawson JA, Lehwald L, Leung MA, Mikhaylova S, Mink JW, Nickel M, Shediac R, Sims K, Specchio N, Topcu M, von Löbbecke I, West A, Zernikow B, Schulz A. Williams RE, et al. Among authors: topcu m. Pediatr Neurol. 2017 Apr;69:102-112. doi: 10.1016/j.pediatrneurol.2017.01.034. Epub 2017 Feb 4. Pediatr Neurol. 2017. PMID: 28335910 Free article. Review.

2

Evaluation of 36 patients from Turkey with neuronal ceroid lipofuscinosis: clinical, neurophysiological, neuroradiological and histopathologic studies.

Topçu M, Tan H, Yalnizoğlu D, Usubütün A, Saatçi I, Aynaci M, Anlar B, Topaloğlu H, Turanli G, Köse G, Aysun S. Topçu M, et al. Turk J Pediatr. 2004 Jan-Mar;46(1):1-10. Turk J Pediatr. 2004. PMID: 15074367

3

Infantile convulsions and paroxysmal choreoathetosis in a consanguineous family.

Demir E, Prud'homme JF, Topçu M. Demir E, et al. Among authors: topcu m. Pediatr Neurol. 2004 May;30(5):349-53. doi: 10.1016/j.pediatrneurol.2003.11.003. Pediatr Neurol. 2004. PMID: 15165638

4

Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.

Kousi M, Siintola E, Dvorakova L, Vlaskova H, Turnbull J, Topcu M, Yuksel D, Gokben S, Minassian BA, Elleder M, Mole SE, Lehesjoki AE. Kousi M, et al. Among authors: topcu m. Brain. 2009 Mar;132(Pt 3):810-9. doi: 10.1093/brain/awn366. Epub 2009 Feb 5. Brain. 2009. PMID: 19201763

5

Management of CLN1 Disease: International Clinical Consensus.

Augustine EF, Adams HR, de Los Reyes E, Drago K, Frazier M, Guelbert N, Laine M, Levin T, Mink JW, Nickel M, Peifer D, Schulz A, Simonati A, Topcu M, Turunen JA, Williams R, Wirrell EC, King S. Augustine EF, et al. Among authors: topcu m. Pediatr Neurol. 2021 Jul;120:38-51. doi: 10.1016/j.pediatrneurol.2021.04.002. Epub 2021 Apr 9. Pediatr Neurol. 2021. PMID: 34000449 Free article.

6

Unraveling neuronal ceroid lipofuscinosis type 2 (CLN2) disease: A tertiary center experience for determinants of diagnostic delay.

Ardicli D, Haliloglu G, Gocmen R, Gunbey C, Topcu M. Ardicli D, et al. Among authors: topcu m. Eur J Paediatr Neurol. 2021 Jul;33:94-98. doi: 10.1016/j.ejpn.2021.05.015. Epub 2021 Jun 4. Eur J Paediatr Neurol. 2021. PMID: 34119739

7

Neurologic features as initial presentations of childhood malignancies.

Aysun S, Topçu M, Günay M, Topaloğlu H. Aysun S, et al. Among authors: topcu m. Pediatr Neurol. 1994 Feb;10(1):40-3. doi: 10.1016/0887-8994(94)90065-5. Pediatr Neurol. 1994. PMID: 8198671

8

Dermoid tumor with persistently low CSF glucose and unusual CT and MRI findings.

Erdem G, Topçu M, Topaloğlu H, Bertan V, Arikan U. Erdem G, et al. Among authors: topcu m. Pediatr Neurol. 1994 Feb;10(1):75-7. doi: 10.1016/0887-8994(94)90074-4. Pediatr Neurol. 1994. PMID: 8198678

9

Cockayne syndrome: review of 25 cases.

Ozdirim E, Topçu M, Ozön A, Cila A. Ozdirim E, et al. Among authors: topcu m. Pediatr Neurol. 1996 Nov;15(4):312-6. doi: 10.1016/s0887-8994(96)00229-9. Pediatr Neurol. 1996. PMID: 8972530

10

Medulloblastoma in a child with the metabolic disease L-2-hydroxyglutaric aciduria.

Ozişik PA, Akalan N, Palaoğlu S, Topçu M. Ozişik PA, et al. Among authors: topcu m. Pediatr Neurosurg. 2002 Jul;37(1):22-6. doi: 10.1159/000065097. Pediatr Neurosurg. 2002. PMID: 12138215

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