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 NCBI Filters

Results by year

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

Year Number of Results
2012 1
2015 2
2016 2
2017 1
2019 1
2020 3
2021 2
2022 2
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

13 results

Results by year

Filters applied: . Clear all
Page 1
Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies.
Habibi I, Falfoul Y, Tran HV, El Matri K, Chebil A, El Matri L, Schorderet DF. Habibi I, et al. Among authors: falfoul y. Front Cell Dev Biol. 2021 Feb 5;9:625560. doi: 10.3389/fcell.2021.625560. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33634125 Free PMC article.
Rhabdomyolysis-associated acute kidney injury in a teenager: Answers.
Jellouli M, Boussetta A, Hajji M, Falfoul Y, Kacem LH, Abderrahim E, Gargah T. Jellouli M, et al. Among authors: falfoul y. Pediatr Nephrol. 2023 Jul;38(7):2061-2064. doi: 10.1007/s00467-022-05767-z. Epub 2022 Oct 10. Pediatr Nephrol. 2023. PMID: 36214888 No abstract available.
Rhabdomyolysis-associated acute kidney injury in a teenager: Questions.
Jellouli M, Boussetta A, Hajji M, Falfoul Y, Kacem LH, Abderrahim E, Gargah T. Jellouli M, et al. Among authors: falfoul y. Pediatr Nephrol. 2023 Jul;38(7):2057-2059. doi: 10.1007/s00467-022-05766-0. Epub 2022 Oct 10. Pediatr Nephrol. 2023. PMID: 36214886 No abstract available.
Genetic spectrum of retinal dystrophies in Tunisia.
Habibi I, Falfoul Y, Turki A, Hassairi A, El Matri K, Chebil A, Schorderet DF, El Matri L. Habibi I, et al. Among authors: falfoul y. Sci Rep. 2020 Jul 8;10(1):11199. doi: 10.1038/s41598-020-67792-y. Sci Rep. 2020. PMID: 32641690 Free PMC article.
Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB).
Habibi I, Falfoul Y, Todorova MG, Wyrsch S, Vaclavik V, Helfenstein M, Turki A, Matri KE, Matri LE, Schorderet DF. Habibi I, et al. Among authors: falfoul y. Genes (Basel). 2019 Nov 21;10(12):953. doi: 10.3390/genes10120953. Genes (Basel). 2019. PMID: 31766397 Free PMC article.
13 results