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

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 1
2000 2
2001 2
2002 1
2003 1
2004 3
2006 5
2007 10
2008 4
2009 5
2010 7
2011 3
2012 6
2013 7
2014 13
2015 16
2016 14
2017 14
2018 11
2019 5
2020 2
2021 7
2022 11
2023 6
2024 15
2025 7

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

140 results

Results by year

Filters applied: . Clear all
Page 1
Expanding the Mutational Landscape and Clinical Phenotype of CHD2-Related Encephalopathy.
Clara-Hwang A, Stefani S, Lau T, Scala M, Aynekin B, Bernardo P, Madia F, Bakhtadze S, Kaiyrzhanov R, Maroofian R, Zara F, Srinivasan VM, Gowda V, Guliyeva U, Montavont A, Poulat AL, Güleç A, Berger C, Ville DM, de Bellescize J, Cabet S, Wonneberger A, Schulz A, Rodriguez-Palmero A, Chatron N, Lesca G, Per H, Goel H, Brown J, Frey T, Steindl K, Rauch A, Severino M, Houlden H, Nicolaides P, Striano P, Efthymiou S. Clara-Hwang A, et al. Among authors: per h. Neurol Genet. 2024 Jul 11;10(4):e200168. doi: 10.1212/NXG.0000000000200168. eCollection 2024 Aug. Neurol Genet. 2024. PMID: 39035822 Free PMC article.
DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans.
Azizoglu ZB, Babayeva R, Haskologlu ZS, Acar MB, Ayaz-Guner S, Okus FZ, Alsavaf MB, Can S, Basaran KE, Canatan MF, Ozcan A, Erkmen H, Leblebici CB, Yilmaz E, Karakukcu M, Kose M, Canoz O, Özen A, Karakoc-Aydiner E, Ceylaner S, Gümüş G, Per H, Gumus H, Canatan H, Ozcan S, Dogu F, Ikinciogullari A, Unal E, Baris S, Eken A. Azizoglu ZB, et al. Among authors: per h. J Clin Immunol. 2024 Aug 9;44(8):175. doi: 10.1007/s10875-024-01777-8. J Clin Immunol. 2024. PMID: 39120629 Free PMC article.
Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort.
Bektaş Ö, Gülşen M, Dursun OB, Tekin A, Yüksel D, Demir E, Öztürk G, Saltık S, Hergüler Ö, Özçelik AA, Tan H, Özgör B, Ekici A, Yüksel MF, Şahin S, Duman Ö, Kömür M, Baydan F, Yıldız EP, Kara B, Yiş U, Kanmaz S, Çarman KB, Arslan EA, Canpolat M, Güven AS, Öztuncer G, Ünalp A, Ardıçlı D, Karaduman AA, Zararsız G, Deda G; Turkish SMA Study Group. Bektaş Ö, et al. Front Neurol. 2025 Mar 27;16:1541507. doi: 10.3389/fneur.2025.1541507. eCollection 2025. Front Neurol. 2025. PMID: 40212617 Free PMC article.
Optic neuritis in Turkish children and adolescents: A multicenter retrospective study.
Direk MÇ, Besen Ş, Öncel İ, Günbey C, Özdoğan O, Orgun LT, Sahin S, Cansu A, Yıldız N, Kanmaz S, Yılmaz S, Tekgül H, Türkdoğan D, Ünver O, Thomas GÖ, Başıbüyük S, Yılmaz D, Kurt AN, Gültutan P, Özsoy Ö, Yiş U, Kurul SH, Güngör S, Özgör B, Karadağ M, Dündar NO, Gençpınar P, Bildik O, Orak SA, Kabur ÇÇ, Kara B, Karaca Ö, Canpolat M, Gümüş H, Per H, Yılmaz Ü, Karaoğlu P, Ersoy Ö, Tosun A, Öztürk SB, Yüksel D, Atasoy E, Gücüyener K, Yıldırım M, Bektaş Ö, Çavuşoğlu D, Yarar Ç, Güngör O, Mert GG, Sarıgeçili E, Edizer S, Çetin İD, Aydın S, Diler B, Özdemir AA, Erol İ, Okuyaz Ç, Anlar B. Direk MÇ, et al. Among authors: per h. Mult Scler Relat Disord. 2024 Jan;81:105149. doi: 10.1016/j.msard.2023.105149. Epub 2023 Nov 26. Mult Scler Relat Disord. 2024. PMID: 38096730
Corrigendum to "Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes" [Europ. J. Paediatr. Neurol. 41 (2022) 8-18 doi.org/10.1016/j.ejpn.2022.08.006].
Yılmaz Ü, Gücüyener K, Yavuz M, Ibrahim Oncel, Canpolat M, Saltık S, Ünver O, Çıtak Kurt AN, Tosun A, Yılmaz S, Özgör B, İlknur Erol, Öztoprak Ü, Elitez DA, Çobanoğulları Direk M, Bodur M, Teber S, Anlar B; Turkish Pediatric Multiple Sclerosis Study Group. Yılmaz Ü, et al. Eur J Paediatr Neurol. 2024 Dec 2:S1090-3798(24)00172-7. doi: 10.1016/j.ejpn.2024.11.006. Online ahead of print. Eur J Paediatr Neurol. 2024. PMID: 39627061 No abstract available.
Restless leg syndrome in children with celiac disease.
Işıkay S, Işıkay N, Per H, Çarman KB, Kocamaz H. Işıkay S, et al. Among authors: per h. Turk J Pediatr. 2018;60(1):70-75. doi: 10.24953/turkjped.2018.01.010. Turk J Pediatr. 2018. PMID: 30102482 Free article.
140 results