Kendirci M - Search Results

1

An autosomal recessive adducted thumb-club foot syndrome observed in Turkish cousins.

Dundar M, Demiryilmaz F, Demiryilmaz I, Kumandas S, Erkilic K, Kendirci M, Tuncel M, Ozyazgan I, Tolmie JL. Dundar M, et al. Among authors: kendirci m. Clin Genet. 1997 Jan;51(1):61-4. doi: 10.1111/j.1399-0004.1997.tb02417.x. Clin Genet. 1997. PMID: 9084938

2

Congenital alacrima in a patient with G (Opitz Frias) syndrome.

Dundar M, Erkihç K, Demiryilmaz F, Küçükaydin M, Kendirci M, Okur H, Kazez A. Dundar M, et al. Among authors: kendirci m. Hum Genet. 1996 Apr;97(4):540-2. doi: 10.1007/BF02267083. Hum Genet. 1996. PMID: 8834259

3

Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.

Caglayan AO, Demiryilmaz F, Kendirci M, Ozyazgan I, Akalin H, Bittmann S. Caglayan AO, et al. Among authors: kendirci m. Genet Couns. 2009;20(2):173-9. Genet Couns. 2009. PMID: 19650415

4

The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other Neurological Disorders in Classical Phenotype of Glucose Transporter 1 Deficiency Syndrome.

Gumus H, Bayram AK, Kardas F, Canpolat M, Çağlayan AO, Kumandas S, Kendirci M, Per H. Gumus H, et al. Among authors: kendirci m. Neuropediatrics. 2015 Oct;46(5):313-20. doi: 10.1055/s-0035-1558435. Epub 2015 Aug 12. Neuropediatrics. 2015. PMID: 26267703

5

Glutaric Acidemia Type 1: A Case of Infantile Stroke.

Kaya Ozcora GD, Gokay S, Canpolat M, Kardaş F, Kendirci M, Kumandaş S. Kaya Ozcora GD, et al. Among authors: kendirci m. JIMD Rep. 2018;38:7-12. doi: 10.1007/8904_2017_26. Epub 2017 Apr 15. JIMD Rep. 2018. PMID: 28411331 Free PMC article.

6

Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation.

Sarıkaya E, Kendirci M, Demir M, Dündar M. Sarıkaya E, et al. Among authors: kendirci m. J Clin Res Pediatr Endocrinol. 2023 Nov 22;15(4):426-430. doi: 10.4274/jcrpe.galenos.2022.2021-12-19. Epub 2022 Apr 12. J Clin Res Pediatr Endocrinol. 2023. PMID: 35410112 Free PMC article.

7

Increased Serum Phthalates (MEHP, DEHP) and Bisphenol A Concentrations in Children With Autism Spectrum Disorder: The Role of Endocrine Disruptors in Autism Etiopathogenesis.

Kardas F, Bayram AK, Demirci E, Akin L, Ozmen S, Kendirci M, Canpolat M, Oztop DB, Narin F, Gumus H, Kumandas S, Per H. Kardas F, et al. Among authors: kendirci m. J Child Neurol. 2016 Apr;31(5):629-35. doi: 10.1177/0883073815609150. Epub 2015 Oct 8. J Child Neurol. 2016. PMID: 26450281

8

An assessment of the relation between vitamin D levels and electroencephalogram (EEG) changes in migraine patients.

Canpolat M, Topcu A, Kardas F, Ipekten F, Per H, Gumus H, Ozturk A, Acer H, Kaya Ozcora GD, Kendirci M, Kumandas S. Canpolat M, et al. Among authors: kendirci m. Bratisl Lek Listy. 2022;123(2):92-99. doi: 10.4149/BLL_2022_014. Bratisl Lek Listy. 2022. PMID: 35065584

9

Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency.

Akin L, Rizzoti K, Gregory LC, Corredor B, Le Quesne Stabej P, Williams H, Buonocore F, Mouilleron S, Capra V, McGlacken-Byrne SM, Martos-Moreno GÁ, Azmanov DN, Kendirci M, Kurtoglu S, Suntharalingham JP, Galichet C, Gustincich S, Tasic V, Achermann JC, Accogli A, Filipovska A, Tuilpakov A, Maghnie M, Gucev Z, Gonen ZB, Pérez-Jurado LA, Robinson I, Lovell-Badge R, Argente J, Dattani MT. Akin L, et al. Among authors: kendirci m. Genet Med. 2022 Feb;24(2):384-397. doi: 10.1016/j.gim.2021.09.019. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906446 Free PMC article.

10

Neurofibromatosis type 1 with overlap Turner syndrome and Klinefelter syndrome.

Hatipoglu N, Kurtoglu S, Kendirci M, Keskin M, Per H. Hatipoglu N, et al. Among authors: kendirci m. J Trop Pediatr. 2010 Feb;56(1):69-72. doi: 10.1093/tropej/fmp053. Epub 2009 Jul 3. J Trop Pediatr. 2010. PMID: 19578129

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