Mehmet Alikasifoglu - Search Results

Year	Number of Results
2002	2
2003	2
2004	1
2005	3
2006	3
2008	5
2009	6
2010	4
2011	3
2012	3
2013	3
2014	3
2015	3
2016	3
2017	13
2018	10
2019	13
2020	11
2021	8
2022	5
2024	0

1

Reduced irisin levels in patients with acromegaly.

Sendur SN, Baykal G, Firlatan B, Aydin B, Lay I, Dagdelen S, Alikasifoglu M, Erbas T. Sendur SN, et al. Among authors: alikasifoglu m. Horm Mol Biol Clin Investig. 2022 Jul 19;43(3):251-261. doi: 10.1515/hmbci-2022-0009. eCollection 2022 Sep 1. Horm Mol Biol Clin Investig. 2022. PMID: 35851444

2

FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum.

Mroczek M, Longman C, Farrugia ME, Kapetanovic Garcia S, Ardicli D, Topaloglu H, Hernández-Laín A, Orhan D, Alikasifoglu M, Duff J, Specht S, Nowak K, Ravenscroft G, Chao K, Valivullah Z, Donkervoort S, Saade D, Bönnemann C, Straub V, Yoon G. Mroczek M, et al. Among authors: alikasifoglu m. J Med Genet. 2022 Nov;59(11):1069-1074. doi: 10.1136/jmedgenet-2021-108341. Epub 2022 Apr 7. J Med Genet. 2022. PMID: 35393337 Free PMC article.

3

Interaction between Dietary Fat Intake and Metabolic Genetic Risk Score on 25-Hydroxyvitamin D Concentrations in a Turkish Adult Population.

Isgin-Atici K, Alathari BE, Turan-Demirci B, Sendur SN, Lay I, Ellahi B, Alikasifoglu M, Erbas T, Buyuktuncer Z, Vimaleswaran KS. Isgin-Atici K, et al. Among authors: alikasifoglu m. Nutrients. 2022 Jan 17;14(2):382. doi: 10.3390/nu14020382. Nutrients. 2022. PMID: 35057563 Free PMC article.

4

Long-term effect of conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in children with PHEX mutation.

Alikasifoglu A, Unsal Y, Gonc EN, Ozon ZA, Kandemir N, Alikasifoglu M. Alikasifoglu A, et al. Among authors: alikasifoglu m. J Pediatr Endocrinol Metab. 2021 Sep 16;34(12):1573-1584. doi: 10.1515/jpem-2021-0387. Print 2021 Dec 20. J Pediatr Endocrinol Metab. 2021. PMID: 34525271

5

Investigation of Genetic Causes in a Developmental Disorder: Oculoauriculovertebral Spectrum.

Güleray N, Koşukcu C, Oğuz S, Ürel Demir G, Taşkıran EZ, Kiper PÖŞ, Utine GE, Alanay Y, Boduroğlu K, Alikaşifoğlu M. Güleray N, et al. Among authors: alikasifoglu m. Cleft Palate Craniofac J. 2022 Sep;59(9):1114-1124. doi: 10.1177/10556656211038115. Epub 2021 Aug 19. Cleft Palate Craniofac J. 2022. PMID: 34410171

6

Specific FSTL1 polymorphism may determine the risk of cardiomyopathy in patients with acromegaly.

Sendur SN, Hazirolan T, Aydin B, Lay I, Alikasifoglu M, Erbas T. Sendur SN, et al. Among authors: alikasifoglu m. Acta Cardiol. 2022 Jun;77(4):350-359. doi: 10.1080/00015385.2021.1948206. Epub 2021 Jul 8. Acta Cardiol. 2022. PMID: 34233581

7

Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features.

Kındış E, Simsek-Kiper PÖ, Koşukcu C, Taşkıran EZ, Göçmen R, Utine E, Haliloğlu G, Boduroğlu K, Alikaşifoğlu M. Kındış E, et al. Among authors: alikasifoglu m. Am J Med Genet A. 2021 Jun;185(6):1888-1896. doi: 10.1002/ajmg.a.62179. Epub 2021 Mar 22. Am J Med Genet A. 2021. PMID: 33749994

8

Genetic disorders with symptoms mimicking rheumatologic diseases: A single-center retrospective study.

Kaya Akca U, Simsek Kiper PO, Urel Demir G, Sag E, Atalay E, Utine GE, Alikasifoglu M, Boduroglu K, Bilginer Y, Ozen S. Kaya Akca U, et al. Among authors: alikasifoglu m. Eur J Med Genet. 2021 Apr;64(4):104185. doi: 10.1016/j.ejmg.2021.104185. Epub 2021 Mar 2. Eur J Med Genet. 2021. PMID: 33662637 Clinical Trial.

9

Molecular Etiology of Isolated Congenital Cataract Using Next-Generation Sequencing: Single Center Exome Sequencing Data from Turkey.

Taylan Sekeroglu H, Karaosmanoglu B, Taskiran EZ, Simsek Kiper PO, Alikasifoglu M, Boduroglu K, Coskun T, Utine GE. Taylan Sekeroglu H, et al. Among authors: alikasifoglu m. Mol Syndromol. 2020 Dec;11(5-6):302-308. doi: 10.1159/000510481. Epub 2020 Sep 9. Mol Syndromol. 2020. PMID: 33510601 Free PMC article.

10

Klotho gene G395A and C1818T polymorphisms in acromegaly: Association with clinical presentation and comorbidities.

Helvaci N, Kabacam S, Dagdelen S, Lay I, Karabulut E, Mut M, Alikasifoglu M, Erbas T. Helvaci N, et al. Among authors: alikasifoglu m. Clin Endocrinol (Oxf). 2021 Apr;94(4):598-605. doi: 10.1111/cen.14380. Epub 2020 Dec 9. Clin Endocrinol (Oxf). 2021. PMID: 33296101

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