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

Year Number of Results
1987 2
1994 3
1996 1
1997 1
2001 1
2002 1
2005 6
2006 5
2007 2
2008 2
2010 2
2011 2
2013 3
2014 4
2017 2
2018 2
2019 3
2020 3
2021 2
2022 0
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37 results
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Page 1
[Duodenojejunal trichobezoar].
Alouini R, Allani M, Arfaoui D, Arbi N, Tlili-Graiess K. Alouini R, et al. Among authors: tlili graiess k. Presse Med. 2005 Sep 24;34(16 Pt 1):1178-9. doi: 10.1016/s0755-4982(05)84146-6. Presse Med. 2005. PMID: 16208267 French. No abstract available.
Embryopathy Associated With a Vitamin Therapy.
Tabarki B, AlHashem A, Tlili-Graiess K. Tabarki B, et al. Among authors: tlili graiess k. Pediatr Neurol. 2018 Dec;89:73-74. doi: 10.1016/j.pediatrneurol.2018.07.012. Epub 2018 Aug 4. Pediatr Neurol. 2018. PMID: 30442439 No abstract available.
PHACES syndrome associated with carcinoid endobronchial tumor.
Mama N, H'mida D, Lahmar I, Yacoubi MT, Tlili-Graiess K. Mama N, et al. Among authors: tlili graiess k. Pediatr Radiol. 2014 May;44(5):621-4. doi: 10.1007/s00247-013-2820-0. Epub 2013 Dec 13. Pediatr Radiol. 2014. PMID: 24337788 Review.
MR imaging of intracranial hemangiopericytomas.
Mama N, Ben Abdallah A, Hasni I, Kadri K, Arifa N, Ladib M, Tlili-Graiess K. Mama N, et al. Among authors: tlili graiess k. J Neuroradiol. 2014 Dec;41(5):296-306. doi: 10.1016/j.neurad.2013.10.007. Epub 2014 Jan 8. J Neuroradiol. 2014. PMID: 24412027
Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndrome.
AlKalaf HY, AlHashem AM, AlSaleh NS, AlJohar NM, Abo Thneen AM, ElGhezal HM, Bouhjar IB, Tlili-Graiess K, Sahari AH, Tabarki BM. AlKalaf HY, et al. Among authors: tlili graiess k. Neurosciences (Riyadh). 2020 Aug;25(4):287-291. doi: 10.17712/nsj.2020.4.20200045. Neurosciences (Riyadh). 2020. PMID: 33130809 Free PMC article.
Mutations in phospholipase C eta-1 (PLCH1) are associated with holoprosencephaly.
Drissi I, Fletcher E, Shaheen R, Nahorski M, Alhashem AM, Lisgo S, Fernández-Jaén A, Schon K, Tlili-Graiess K, Smithson SF, Lindsay S, J Sharpe H, Alkuraya FS, Woods G. Drissi I, et al. Among authors: tlili graiess k. J Med Genet. 2021 Apr 5:jmedgenet-2020-107237. doi: 10.1136/jmedgenet-2020-107237. Online ahead of print. J Med Genet. 2021. PMID: 33820834 Free article.
Neuroregression, coarse features, and oligosaccharides in urines.
BoAli AY, Tlili-Graiess K, AlHashem AM, Tabarki BM. BoAli AY, et al. Among authors: tlili graiess k. Neurosciences (Riyadh). 2017 Oct;22(4):325-327. doi: 10.17712/nsj.2017.4.20170193. Neurosciences (Riyadh). 2017. PMID: 29057862 Free PMC article. No abstract available.
37 results