Creatine and Creatine Deficiency Syndromes: Biochemical and Clinical Aspects
Nasrallah, Fahmi, BS, Feki, Moncef, MD, Kaabachi, Naziha, PhD
Published in Pediatric neurology (01.03.2010)
Published in Pediatric neurology (01.03.2010)
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Journal Article
Spectrum of Organic Aciduria Diseases in Tunisia: A 35-year Retrospective Study
Jelassi, Awatef, Nasrallah, Fahmi, Talbi, Emna, Hammami, Mohamed Bassem, Ghodbane, Rihab, Sanhaji, Haifa, Feki, Moncef, Kaabachi, Naziha, Hadj-Taieb, Sameh
Published in Saudi journal of medicine & medical sciences (01.01.2024)
Published in Saudi journal of medicine & medical sciences (01.01.2024)
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Journal Article
Biochemical and Clinical Profiles of 52 Tunisian Patients Affected by Zellweger Syndrome
Nasrallah, Fahmi, Zidi, Wiem, Feki, Moncef, Kacem, Samia, Tebib, Neji, Kaabachi, Naziha
Published in Pediatrics and neonatology (01.12.2017)
Published in Pediatrics and neonatology (01.12.2017)
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Journal Article
Non-ketotic hyperglycinaemia: a frequent, but poorly diagnosed and managed genetic disorder in Tunisia
Nasrallah, Fahmi, Ben Chehida, Amel, Kraoua, Ichraf, Hadj-Taieb, Sameh, Sanhaji, Haifa, Tebib, Neji, Feki, Moncef, Kaabachi, Naziha
Published in Archives of disease in childhood (01.03.2021)
Published in Archives of disease in childhood (01.03.2021)
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Journal Article
Altered Semen Quality is Associated with Decreased Semen Docosahexaenoic Acid and Increased Oleic Acid Levels
Nasrallah, Fahmi, Taieb, Sameh H, Sethoum, Mohamed M, Omar, Souheil, Aribia, Hamadi B, Sanhaji, Haifa, Feki, Moncef
Published in Clinical laboratory (Heidelberg) (01.01.2020)
Published in Clinical laboratory (Heidelberg) (01.01.2020)
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Journal Article
Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria
Jellouli, Nadege Kammoun, Hadj Salem, Ikhlass, Ellouz, Emna, Kamoun, Zeineb, kamoun, Fatma, tlili, Abdelaziz, Kaabachi, Naziha, Triki, Chanez, Fakhfakh, Faiza
Published in Journal of human genetics (01.04.2014)
Published in Journal of human genetics (01.04.2014)
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Journal Article
Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease
Kammoun Jellouli, Nadege, Hadj Salem, Ikhlass, Ellouz, Emna, Louhichi, Nacim, tlili, Abdelaziz, Kammoun, Fatma, Triki, Chanez, Fakhfakh, Faiza
Published in Gene (25.01.2013)
Published in Gene (25.01.2013)
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Journal Article
Clinical and Biochemical Profile of Tyrosinemia Type 1 in Tunisia
Nasrallah, Fahmi, Hammami, Mohamed Bessem, Ben Rhouma, Hanen, Fradj, Sondes Hadj, Azzouz, Hatem, Omar, Souheil, Feki, Moncef, Ben Youssef, Ilhem Turki, Messaoud, Taieb, Tebib, Neji, Kaabachi, Naziha
Published in Clinical laboratory (Heidelberg) (2015)
Published in Clinical laboratory (Heidelberg) (2015)
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Journal Article
Guanidinoacetate methyltransferase (GAMT) deficiency in two Tunisian siblings: clinical and biochemical features
Nasrallah, Fahmi, Kraoua, Ichraf, Joncquel-Chevalier Curt, Marie, Bout, Marie-Adelaïde, Taieb, Sameh Hadj, Feki, Moncef, Khouja, Néziha, Briand, Gilbert, Kaabachi, Naziha
Published in Clinical laboratory (Heidelberg) (2012)
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Published in Clinical laboratory (Heidelberg) (2012)
Journal Article
Valproate adverse effects on creatine metabolism and transport in a patient under drug therapy
Nasrallah, Fahmi, Vamecq, Joseph, Kraoua, Ichraf, Joncquel-Chevalier Curt, Marie, Feki, Moncef, Omar, Souheil, Briand, Gilbert, Turki Ben Youssef, Ilhem, Kaabachi, Naziha
Published in Iranian journal of neurology (03.04.2014)
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Published in Iranian journal of neurology (03.04.2014)
Journal Article