Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sameh Khemir"'
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 54, Iss 2 (2018)
ABSTRACT The present study investigates the effect of cinnamon (Cinnamomum zeylanicumon) powder supplementation on glucose levels, lipid profiles, and oxidative stress parameters in alloxan-induced diabetic rats. Diabetes was induced in adult male Wi
Externí odkaz:
https://doaj.org/article/9a566ec4cdf2481ba983d28e4a5b9ad3
Autor:
Taieb Messaoud, Hatem Azzouz, Naziha Kaabachi, Sonia Abdelhak, Ahlem Belhaj, Neji Tebib, Sameh Khemir, Amel Bedoui, Maherzia Ferchichi, Soumeyya Halayem, Asma Guedria, Hajer Siala
Publikováno v:
Journal of Child Neurology
Journal of Child Neurology, SAGE Publications (UK and US), 2016, 31 (7), pp.843--849. ⟨10.1177/0883073815623636⟩
Journal of Child Neurology, SAGE Publications (UK and US), 2016, 31 (7), pp.843--849. ⟨10.1177/0883073815623636⟩
Autism has been reported in untreated patients with phenylketonuria. The authors aimed to explore autism in 15 Tunisian and 4 Algerian phenylketonuria patients, and report their clinical, biochemical and molecular peculiarities. The Childhood Autism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b1998934f9dfa1e21fc74f4bce451e0
https://hal-riip.archives-ouvertes.fr/pasteur-01469443
https://hal-riip.archives-ouvertes.fr/pasteur-01469443
Autor:
Monia Allal El Asmi, Riadh Jemaa, Jean Louis Dhondt, Moncef Feki, Haifa Sanhaji, Marie Françoise Ben Dridi, Sameh Khemir, Naziha Kaabachi, Neji Tebib, Abderraouf Mebazaa
Publikováno v:
Clinical Neurology and Neurosurgery. 113:727-730
Background and objective Accumulation of phenylalanine following a deficiency of phenylalanine hydroxylase activity generates a brain damage with mental retardation: phenylketonuria (PKU). In the developing countries, where PKU systematic neonatal sc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23d96a240e5ccf0a52b4525ab29b09e5
https://doi.org/10.1016/j.clineuro.2011.07.016
https://doi.org/10.1016/j.clineuro.2011.07.016
Autor:
Neji Tebib, Marie Françoise Ben Dridi, Taieb Massaoud, Wafa Cherif, Sameh Hadj Taieb, Rym Kefi, Sonia Abdelhak, Naziha Khouja, Naziha Kaabachi, Hatem Azzouz, Hajer Siala, Sameh Khemir
Phenylketonuria (PKU; OMIM 261600) is an autosomal recessive disease caused by the liver phenylalanine hydroxylase (PAH) enzyme (EC1.14.16.1) deficiency. If untreated, causes mental retardation. The incidence in Caucasian population is approximately
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42fe67ed40bde2b27067a6faa8314c1c
https://hal.archives-ouvertes.fr/hal-01358543
https://hal.archives-ouvertes.fr/hal-01358543
Autor:
Hajer Siala, Hatem Azzouz, Neji Tebib, J.L. Dhondt, Sameh Khemir, Taieb Messaoud, Sonia Abdelhak, M.F. Ben Dridi, Neziha Kaabachi
Publikováno v:
Pathologie-biologie. 60(6)
Phenylketonuria (PKU) is an autosomal recessive metabolic disorder caused by a deficiency of phenylalanine hydroxylase. To date, more than 530 mutations in the PAH gene have been reported. In Tunisia, this disease seems to be the result of point muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a66b39f135f7905c14663e8594d4c3a
https://pubmed.ncbi.nlm.nih.gov/22572109
https://pubmed.ncbi.nlm.nih.gov/22572109
Autor:
Neziha Kaabachi, Alexandre Mebazaa, F Ben Nour, H. Sanhaji, H Mizouni, M.F. Ben Dridi, Fehmi Nasrallah, Riadh Jemaa, Moncef Feki, Monia Elasmi, Sameh Khemir, Neji Tebib
Publikováno v:
Archives of Disease in Childhood. 94:647-648
Phenylketonuria (PKU) is the most frequent inherited metabolic disorder and results in progressive mental retardation. The incidence of PKU varies widely in neonates: it is high in Turkey (1:2600) and Ireland (1:4500) and low in Japan (1:125 000).1 T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cded535d5bc100e6ca557b8bb8766f8
https://doi.org/10.1136/adc.2008.143081
https://doi.org/10.1136/adc.2008.143081
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