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Page 1
Autism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects.
J Child Neurol. 2016 Jun;31(7):843-9. doi: 10.1177/0883073815623636. Epub 2016 Jan 12.
J Child Neurol. 2016.
PMID: 26759449
Phenylketonuria is still a major cause of mental retardation in Tunisia despite the possibility of treatment.
Khemir S, El Asmi M, Sanhaji H, Feki M, Jemaa R, Tebib N, Dhondt JL, Ben Dridi MF, Mebazaa A, Kaabachi N.
Khemir S, et al.
Clin Neurol Neurosurg. 2011 Nov;113(9):727-30. doi: 10.1016/j.clineuro.2011.07.016. Epub 2011 Sep 8.
Clin Neurol Neurosurg. 2011.
PMID: 21862209
Item in Clipboard
Phenylketonuria in Tunisian institutions for the mentally handicapped.
Khemir S, Tebib N, Nasrallah F, Ben Nour F, Mizouni H, Elasmi M, Sanhaji H, Jemaa R, Feki M, Ben Dridi MF, Mebazaa A, Kaabachi N.
Khemir S, et al.
Arch Dis Child. 2009 Aug;94(8):647-8. doi: 10.1136/adc.2008.143081.
Arch Dis Child. 2009.
PMID: 19628886
No abstract available.
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A novel 22bp deletion in a Tunisian phenylketonuria family.
Khemir S, Siala H, Azzouz H, Tebib N, Dhondt JL, Messaoud T, Abdelhak S, Ben Dridi MF, Kaabachi N.
Khemir S, et al.
Pathol Biol (Paris). 2012 Dec;60(6):e87-9. doi: 10.1016/j.patbio.2012.03.007. Epub 2012 May 7.
Pathol Biol (Paris). 2012.
PMID: 22572109
Item in Clipboard
[Molecular diagnosis of fragile X syndrome].
Ben Jemaa L, Khemir S, Maazoul F, Richard L, Beldjord C, Chaabouni M, Chaabouni H.
Ben Jemaa L, et al. Among authors: khemir s.
Tunis Med. 2008 Nov;86(11):973-7.
Tunis Med. 2008.
PMID: 19213487
French.
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Screening of three Mediterranean phenylketonuria mutations in Tunisian families.
Khemir S, Siala H, Taieb SH, Cherif W, Azzouz H, Kéfi R, Abdelhak S, Khouja N, Tebib N, Massaoud T, Ben Dridi MF, Kaabachi N.
Khemir S, et al.
J Genet. 2012;91(1):91-4. doi: 10.1007/s12041-012-0140-z.
J Genet. 2012.
PMID: 22546830
Free article.
No abstract available.
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