Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

22 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Clinical and molecular spectrum along with genotype-phenotype correlation of 25 patients diagnosed with 3 M syndrome: a study from Turkey.
Akalın A, Özalkak Ş, Yıldırım R, Karakaya AA, Kolbaşı B, Durmuşalioğlu EA, Kökali F, Ürel-Demir G, Öz V, Ünal E, Atik T, Şimşek-Kiper PÖ, Elcioglu NH. Akalın A, et al. Among authors: urel demir g. Eur J Pediatr. 2024 Dec 7;184(1):68. doi: 10.1007/s00431-024-05855-2. Eur J Pediatr. 2024. PMID: 39643721
Further defining the molecular spectrum and long-term follow-up of 17 patients with Dyggve-Melchior-Clausen and Smith-McCort dysplasia type 2.
Akalın A, Ayaz E, Soğukpınar M, Avcı-Durmuşalioğlu E, Ürel-Demir G, Yıldız AE, Atik T, Elcioglu NH, Eda Utine G, Şimşek-Kiper PÖ. Akalın A, et al. Among authors: urel demir g. Am J Med Genet A. 2024 Oct;194(10):e63785. doi: 10.1002/ajmg.a.63785. Epub 2024 Jun 11. Am J Med Genet A. 2024. PMID: 38860472
Clinical Evaluation of Pediatric Patients with Hereditary Angioedema.
Kırmızıtaş Aydoğdu A, Ürel Demir G. Kırmızıtaş Aydoğdu A, et al. Among authors: urel demir g. Tohoku J Exp Med. 2024 Jan 10;262(1):23-27. doi: 10.1620/tjem.2023.J083. Epub 2023 Oct 5. Tohoku J Exp Med. 2024. PMID: 37793880 Free article.
Neonatal ichthyosis-sclerosing cholangitis syndrome: report of a novel mutation and a review of the literature.
Demir E, Tuna Kirsaçlioğlu C, Saltik-Temizel İN, Ürel-Demir G, Karaosmanoğlu B, Taşkiran EZ, Şimşek-Kiper PÖ, Utine GE, Kuloğlu Z, Kansu A. Demir E, et al. Among authors: urel demir g. Clin Dysmorphol. 2023 Apr 1;32(2):88-91. doi: 10.1097/MCD.0000000000000451. Epub 2023 Feb 13. Clin Dysmorphol. 2023. PMID: 36779798 Review. No abstract available.
22 results