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Search Results - Najla, Gribaa
Search Results - Najla, Gribaa
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A Based Bayesian Wavelet Thresholding Method to Enhance Nuclear Imaging
by
Nawrès, Khlifa
,
Najla, Gribaa
,
Imen, Mbazaa
,
Kamel, Hamruoni
Published in
International journal of biomedical imaging
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A Based Bayesian Wavelet Thresholding Method to Enhance Nuclear Imaging
by
Khlifa, Nawrès
,
Gribaa, Najla
,
Mbazaa, Imen
,
Hamruoni, Kamel
Published in
International journal of biomedical imaging
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A framework for nuclear image enhancement based on the Anscomb transform and the bayesian thresholding
by
Mbazaa, I.
,
Gribaa, N.
,
Khlifa, N.
,
Hamrouni, K.
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Conference Proceeding
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Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndrome
by
Manoubi, Wiem
,
Mahdouani, Marwa
,
Hmida, Dorra
,
Kdissa, Ameni
,
Rouissi, Aida
,
Turki, Ilhem
,
Gueddiche, Neji
,
Soyah, Najla
,
Saad, Ali
,
Bouwkamp, Christian
,
Elgersma, Ype
,
Mougou-Zerelli, Soumaya
,
Gribaa, Moez
Published in
World journal of clinical cases
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Genome Tunisia Project: paving the way for precision medicine in North Africa
by
Kammoun Rebai, Wafa
,
Trigui, Malek
,
Charfeddine, Cherine
,
Mezghani Khemakhem, Maha
,
Chaabane, Hassan
,
Mellah, Thouraya
,
Hannachi, Mariem
,
Jandoubi, Nouha
,
Bennour, Ayda
,
Chtioui, Fatma
,
Msakni, Ahlem
,
Fakhfakh, Faiza
,
Karoui, Sana
,
Hammami, Lamia
,
Achour, Ahlem
,
Ben Said, Meriem
,
Najjar, Salma
,
El Mabrouk, Haifa
,
Charfi Triki, Chahnaz
,
Bellil, Hela
,
Rjiba, Khouloud
,
Kerkeni, Nesrine
,
Jbeli, Fidaa
,
Rejeb, Imen
,
Kchaou, Sonia
,
Chouk, Hamza
,
Kamoun, Selim
,
Guirat, Manel
,
Mkaouar, Rahma
,
Boubaker, Safa
,
Ben Ayed, Ikhlas
,
Khamessi, Oussema
,
Gargouri, Hela
,
Chaouch, Melek
,
Choura, Mouna
,
Ammouss, Nihel
,
Gargouri, Raja
,
Guidara, Souhir
,
Souissi, Amal
,
Hamdi, Yosr
,
Abid, Nabil
,
Elaribi, Yasmina
,
Bouzid, Feriel
,
Jilani, Houweyda
,
Ouertani, Ines
,
Ghram, Abdeljelal
,
Mbarek, Hamdi
,
Abid, Cyrine
,
El Abed, Yasmine
,
Boujelbene, Imene
,
Cherni, Lotfi
,
Mougou, Soumaya
,
Trabelsi, Narjess
,
Souiai, Oussema
,
Skouri, Sana
,
Kraoua, Lilia
,
Hkimi, Chaima
,
Ben Marzough, Riadh
,
Hizem, Syrine
,
Younsi, Maryam
,
ElKadri, Noomen
,
Othman, Houcemeddine
,
Dimassi, Sarra
,
Gabtni, Sana
,
Neifar, Fadoua
,
M'charek, Amade
,
Trabelsi, Mediha
,
Chaker Masmoudi, Hend
,
Meddeb, Rym
,
Mahdouani, Marwa
,
Khoujet El Khil, Houssein
,
Ghedira, Kais
,
Lajmi, Yosra
,
Braham, Rihen
,
Kharrat, Maher
,
Boujemaa, Maroua
Published in
Genome medicine
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Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients
by
Amara, Abdelbasset
,
Adala, Labiba
,
Ben Charfeddine, Ilhem
,
Mamaï, Ons
,
Mili, Amira
,
Lazreg, Taheni Ben
,
H’mida, Dorra
,
Amri, Fathi
,
Salem, Najla
,
Boughammura, Lamia
,
Saad, Ali
,
Gribaa, Moez
Published in
European journal of paediatric neurology
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Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease
by
Kammoun Jellouli, Nadege
,
Hadj Salem, Ikhlass
,
Ellouz, Emna
,
Louhichi, Nacim
,
tlili, Abdelaziz
,
Kammoun, Fatma
,
Triki, Chanez
,
Fakhfakh, Faiza
Published in
Gene
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Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia
by
Ben-Abdallah-Bouhjar, Inesse
,
Hannachi, Hanene
,
Labalme, Audrey
,
Gmidène, Abir
,
Mougou, Soumaya
,
Soyah, Najla
,
Gribaa, Moez
,
Sanlaville, Damien
,
Elghezal, Hatem
,
Saad, Ali
Published in
European journal of medical genetics
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A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene
by
Fendri-Kriaa, Nourhene
,
Hsairi, Ines
,
Kifagi, Chamseddine
,
Ellouze, Emna
,
Mkaouar-Rebai, Emna
,
Triki, Chahnez
,
Fakhfakh, Faiza
Published in
Biochemical and biophysical research communications
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Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population
by
Ben Charfeddine, Ilhem
,
Ben Lazreg, Taheni
,
M'sakni, Ahlem
,
Amara, Abdelbasset
,
Mlika, Adnène
,
Chaïeb, Anouar
,
Hlel, Khalid
,
Zouari, Noura
,
Zbidi, Faïza
,
Bouguila, Jihène
,
Soyah, Najla
,
Ayedi, Abdelkarim
,
Ben Hamouda, Hechmi
,
Abroug, Saoussen
,
Boughamoura, Lamia
,
Saad, Ali
,
Gribaa, Moez
Published in
Hemoglobin
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Correlation of SMN 2, NAIP , p44 , H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients
by
Amara, Abdelbasset
,
Adala, Labiba
,
Ben Charfeddine, Ilhem
,
Mamaï, Ons
,
Mili, Amira
,
Lazreg, Taheni Ben
,
H’mida, Dorra
,
Amri, Fathi
,
Salem, Najla
,
Boughammura, Lamia
,
Saad, Ali
,
Gribaa, Moez
Published in
European journal of paediatric neurology
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