Güngör M - Search Results

1

Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children.

Öz Tunçer G, Sanri A, Aydin S, Hergüner ÖM, Özgün N, Kömür M, İçağasioğlu DF, Toker RT, Yilmaz S, Arslan EA, Güngör M, Kutluk G, Erol İ, Mert GG, Polat BG, Aksoy A. Öz Tunçer G, et al. Among authors: gungor m. J Neuromuscul Dis. 2023;10(5):915-924. doi: 10.3233/JND-230046. J Neuromuscul Dis. 2023. PMID: 37355912 Free PMC article.

2

A multicenter study of radiologically isolated syndrome in children and adolescents: Can we predict the course?

Yılmaz D, Teber S, Gültutan P, Yıldırım M, Bektaş Ö, Alikılıç D, Güngör M, Kara B, Öncel İ, Dilek TD, Saltık S, Kanmaz S, Yılmaz S, Tekgül H, Çavuşoğlu D, Karaoğlu P, Yılmaz Ü, Orak SA, Güngör O, Anlar B. Yılmaz D, et al. Among authors: gungor m, gungor o. Mult Scler Relat Disord. 2023 Nov;79:104948. doi: 10.1016/j.msard.2023.104948. Epub 2023 Aug 26. Mult Scler Relat Disord. 2023. PMID: 37659352

3

Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5.

Aylan Gelen S, Kara B, Eser Şimsek I, Güngör M, Zengin E, Sarper N. Aylan Gelen S, et al. Among authors: gungor m. J Pediatr Genet. 2021 Nov 2;13(1):50-56. doi: 10.1055/s-0041-1736560. eCollection 2024 Mar. J Pediatr Genet. 2021. PMID: 38567175 Free PMC article.

4

Acute flaccid myelitis outbreak through 2016-2018: A multicenter experience from Turkey.

Ünver O, Türkdoğan D, Güler S, Kipoğlu O, Güngör M, Paketçi C, Çarman KB, Öztürk G, Genç HM, Özkan M, Dündar NO, Işık U, Karatoprak E, Kılıç B, Özkale M, Bayram E, Yarar C, Sözen HG, Sağer G, Güneş AS, Kahraman Koytak P, Karadağ Saygı E, Ekinci G, Saltık S, Çalışkan M, Kara B, Yiş U, Aydınlı N. Ünver O, et al. Among authors: gungor m. Eur J Paediatr Neurol. 2021 Jan;30:113-120. doi: 10.1016/j.ejpn.2020.10.011. Epub 2020 Nov 4. Eur J Paediatr Neurol. 2021. PMID: 33218883

5

Angioedema-like presentation as the presenting finding of juvenile myositis and juvenile dermatomyositis in 2 patients.

Karaca Ö, Güngör M, Sakarya Güneş A, Eser Şimşek I, Anık Y, Kara B. Karaca Ö, et al. Among authors: gungor m. Int J Rheum Dis. 2022 May;25(5):617-625. doi: 10.1111/1756-185X.14311. Epub 2022 Mar 3. Int J Rheum Dis. 2022. PMID: 35238477

6

Clinical and electrophysiological predictors of behavioral disorders in patients with benign childhood epilepsy with centrotemporal spikes.

Özgen Y, Güngör M, Kutlu M, Kara B. Özgen Y, et al. Among authors: gungor m. Epilepsy Behav. 2021 Aug;121(Pt A):108037. doi: 10.1016/j.yebeh.2021.108037. Epub 2021 May 28. Epilepsy Behav. 2021. PMID: 34058495

7

Management and behavior-modifying recommendation effects in childhood headache.

Gungor M, Guler MA, Karagoz YS. Gungor M, et al. Pediatr Int. 2023 Jan;65(1):e15406. doi: 10.1111/ped.15406. Pediatr Int. 2023. PMID: 36326638

8

Recurrent Blistering Skin Lesions and Reversible Monocular Abducens Paralysis in a Patient with CD59 Deficiency.

Güngör M, Demirsoy E, Güneş AS, Anık Y, Kara B. Güngör M, et al. Neuropediatrics. 2022 Apr;53(2):140-142. doi: 10.1055/s-0041-1742160. Epub 2022 Jan 28. Neuropediatrics. 2022. PMID: 35098522

9

Early-onset rapidly progressive myoclonic epilepsy associated with G392R likely pathogenic variant in SERPINI1.

Kara B, Sarıkaya CE, Bayrak YE, Güneş AS, Güngör M, Yeşil G. Kara B, et al. Among authors: gungor m. Seizure. 2020 Aug;80:181-182. doi: 10.1016/j.seizure.2020.06.022. Epub 2020 Jun 16. Seizure. 2020. PMID: 32599536 Free article. No abstract available.

10

Monogenic lupus due to spondyloenchondrodysplasia with spastic paraparesis and intracranial calcification: case-based review.

Kara B, Ekinci Z, Sahin S, Gungor M, Gunes AS, Ozturk K, Adrovic A, Cefle A, Inanç M, Gul A, Kasapcopur O. Kara B, et al. Among authors: gungor m. Rheumatol Int. 2020 Nov;40(11):1903-1910. doi: 10.1007/s00296-020-04653-x. Epub 2020 Jul 20. Rheumatol Int. 2020. PMID: 32691099 Free PMC article. Review.

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