Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
4 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis.
Front Genet. 2022 Jun 24;13:938814. doi: 10.3389/fgene.2022.938814. eCollection 2022.
Front Genet. 2022.
PMID: 35812760
Free PMC article.
ITPA Related Developmental Encephalopathy: Key Role of Neuroimaging.
Çavuşoğlu D, Kulali MA, Dündar NO, Gokaslan CO, Aydin K.
Çavuşoğlu D, et al. Among authors: kulali ma.
Ann Indian Acad Neurol. 2022 Jan-Feb;25(1):133-134. doi: 10.4103/aian.aian_999_21. Epub 2022 Feb 18.
Ann Indian Acad Neurol. 2022.
PMID: 35342253
Free PMC article.
No abstract available.
Item in Clipboard
Hemoglobin A1C can differentiate subjects with GCK mutations among patients suspected to have MODY.
Yılmaz Uzman C, Erbaş İM, Giray Bozkaya Ö, Paketçi A, Çağlayan AO, Abacı A, Kulalı MA, Böber E, Kekilli A, Çinleti T, Erçal MD, Demir K.
Yılmaz Uzman C, et al. Among authors: kulali ma.
J Pediatr Endocrinol Metab. 2022 Oct 5;35(12):1528-1536. doi: 10.1515/jpem-2022-0381. Print 2022 Dec 16.
J Pediatr Endocrinol Metab. 2022.
PMID: 36197956
Item in Clipboard
Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p.Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother.
Koca SB, Kulali MA, Göğüş B, Demirbilek H.
Koca SB, et al. Among authors: kulali ma.
Arch Endocrinol Metab. 2024 Jan 29;68:e210305. doi: 10.20945/2359-4292-2021-0305.
Arch Endocrinol Metab. 2024.
PMID: 38289143
Free PMC article.
Item in Clipboard
Cite
Cite