Seven M - Search Results

1

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.

Karaca E, Harel T, Pehlivan D, Jhangiani SN, Gambin T, Coban Akdemir Z, Gonzaga-Jauregui C, Erdin S, Bayram Y, Campbell IM, Hunter JV, Atik MM, Van Esch H, Yuan B, Wiszniewski W, Isikay S, Yesil G, Yuregir OO, Tug Bozdogan S, Aslan H, Aydin H, Tos T, Aksoy A, De Vivo DC, Jain P, Geckinli BB, Sezer O, Gul D, Durmaz B, Cogulu O, Ozkinay F, Topcu V, Candan S, Cebi AH, Ikbal M, Yilmaz Gulec E, Gezdirici A, Koparir E, Ekici F, Coskun S, Cicek S, Karaer K, Koparir A, Duz MB, Kirat E, Fenercioglu E, Ulucan H, Seven M, Guran T, Elcioglu N, Yildirim MS, Aktas D, Alikaşifoğlu M, Ture M, Yakut T, Overton JD, Yuksel A, Ozen M, Muzny DM, Adams DR, Boerwinkle E, Chung WK, Gibbs RA, Lupski JR. Karaca E, et al. Among authors: seven m. Neuron. 2015 Nov 4;88(3):499-513. doi: 10.1016/j.neuron.2015.09.048. Neuron. 2015. PMID: 26539891 Free PMC article.

2

An Evaluation of DNA Methylation Levels and Sleep in Relation to Hot Flashes: A Cross-Sectional Study.

Ozcivit Erkan IB, Seyisoglu HH, Benbir Senel G, Karadeniz D, Ozdemir F, Kalayci A, Seven M, Gokmen Inan N. Ozcivit Erkan IB, et al. Among authors: seven m. J Clin Med. 2024 Jun 15;13(12):3502. doi: 10.3390/jcm13123502. J Clin Med. 2024. PMID: 38930031 Free PMC article.

3

A family presenting Goltz syndrome (focal dermal hypoplasia) in three generations.

Seven M, Suyugül Z, Yüksel A, Geçkinli B, Hacihanefioğlu S, Cenani A. Seven M, et al. Turk J Pediatr. 1998 Oct-Dec;40(4):593-601. Turk J Pediatr. 1998. PMID: 10028871

4

Neuroimaging findings of four patients with Sandhoff disease.

Yüksel A, Yalçinkaya C, Işlak C, Gündüz E, Seven M. Yüksel A, et al. Among authors: seven m. Pediatr Neurol. 1999 Aug;21(2):562-5. doi: 10.1016/s0887-8994(99)00041-7. Pediatr Neurol. 1999. PMID: 10465144

5

Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.

Yüksel A, Seven M, Deviren A, Söylemez MA, Hacihanefioğlu S, Ulutin T, Cenani A. Yüksel A, et al. Among authors: seven m. Genet Couns. 1999;10(3):265-9. Genet Couns. 1999. PMID: 10546098

6

The effects of carbamazepine and valproic acid on the erythrocyte glutathione, glutathione peroxidase, superoxide dismutase and serum lipid peroxidation in epileptic children.

Cengiz M, Yüksel A, Seven M. Cengiz M, et al. Among authors: seven m. Pharmacol Res. 2000 Apr;41(4):423-5. doi: 10.1006/phrs.1999.0603. Pharmacol Res. 2000. PMID: 10704266 Clinical Trial.

7

A variant of Cenani-Lenz type syndactyly.

Seven M, Yüksel A, Ozkiliç A, Elçioğlu N. Seven M, et al. Genet Couns. 2000;11(1):41-7. Genet Couns. 2000. PMID: 10756427

8

Infantile-onset megalencephalic leucoencephalopathy in two siblings.

Soylu H, Yüksel A, Kutlu NO, Aydinli M, Seven M, Mocan H. Soylu H, et al. Among authors: seven m. J Paediatr Child Health. 2000 Dec;36(6):598-602. doi: 10.1046/j.1440-1754.2000.00522.x. J Paediatr Child Health. 2000. PMID: 11115041

9

A case of symbrachydactyly with oligodactyly.

Seven M, Yuksel A, Ozkilic A. Seven M, et al. Genet Couns. 2001;12(1):77-83. Genet Couns. 2001. PMID: 11332981

10

Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocation.

Yuksel A, Seven M, Karaman B, Yilmaz S, Deviren A, Hacihanefioglu S, Basaran S. Yuksel A, et al. Among authors: seven m. Clin Dysmorphol. 2002 Jan;11(1):39-42. doi: 10.1097/00019605-200201000-00008. Clin Dysmorphol. 2002. PMID: 11822704

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