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Items: 7

1.

Screening of novel restless legs syndrome-associated genes in French-Canadian families.

Akçimen F, Spiegelman D, Dionne-Laporte A, Gan-Or Z, Dion PA, Rouleau GA.

Neurol Genet. 2018 Dec 20;4(6):e296. doi: 10.1212/NXG.0000000000000296. eCollection 2018 Dec.

PMID:
30637332
2.

Assessment of the corticospinal fiber integrity in mirror movement disorder.

Solmaz B, Özyurt MG, Ata DB, Akçimen F, Shabsog M, Türker KS, Dalçik H, Algin O, Başak AN, Özgür M, Çavdar S.

J Clin Neurosci. 2018 Aug;54:69-76. doi: 10.1016/j.jocn.2018.06.001. Epub 2018 Jun 12.

PMID:
29907388
3.

Clinical and molecular characterization and response to acitretin in three families with Sjögren-Larsson syndrome.

Vural S, Vural A, Akçimen F, Bağci IS, Tunca C, Gündoğdu Eken A, Ruzicka T, Başak AN.

Int J Dermatol. 2018 Jul;57(7):843-848. doi: 10.1111/ijd.14013. Epub 2018 Apr 27.

PMID:
29704247
4.

ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree.

Tunca C, Akçimen F, Coşkun C, Gündoğdu-Eken A, Kocoglu C, Çevik B, Bekircan-Kurt CE, Tan E, Başak AN.

Eur J Hum Genet. 2018 May;26(5):745-748. doi: 10.1038/s41431-018-0107-5. Epub 2018 Feb 16.

PMID:
29453415
5.

A new splice-site mutation in SLC12A6 causing Andermann syndrome with motor neuronopathy.

Akçakaya NH, Yapıcı Z, Tunca Cİ, Tektürk P, Akçimen F, Başak AN.

J Neurol Neurosurg Psychiatry. 2018 Oct;89(10):1123-1125. doi: 10.1136/jnnp-2017-317319. Epub 2017 Dec 21. No abstract available.

PMID:
29269506
6.

Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients.

Mitropoulos K, Merkouri Papadima E, Xiromerisiou G, Balasopoulou A, Charalampidou K, Galani V, Zafeiri KV, Dardiotis E, Ralli S, Deretzi G, John A, Kydonopoulou K, Papadopoulou E, di Pardo A, Akcimen F, Loizedda A, Dobričić V, Novaković I, Kostić VS, Mizzi C, Peters BA, Basak N, Orrù S, Kiskinis E, Cooper DN, Gerou S, Drmanac R, Bartsakoulia M, Tsermpini EE, Hadjigeorgiou GM, Ali BR, Katsila T, Patrinos GP.

Hum Genomics. 2017 Dec 8;11(1):30. doi: 10.1186/s40246-017-0126-2.

7.

Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11.

Iskender C, Kartal E, Akcimen F, Kocoglu C, Ozoguz A, Kotan D, Eraksoy M, Parman YG, Basak AN.

Neurol Genet. 2015 Oct 8;1(3):e25. doi: 10.1212/NXG.0000000000000025. eCollection 2015 Oct.

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